{
  "url": "https://dantelabs.com/fr/genes/gsn",
  "gene": {
    "slug": "gsn",
    "symbol": "GSN",
    "name": "gelsolin",
    "hgnc": "HGNC:4620",
    "summary": null,
    "location": "9q33.2",
    "locusType": "gene with protein product",
    "aliases": [
      "DKFZp313L0718"
    ],
    "previousSymbols": [],
    "ensemblId": "ENSG00000148180",
    "entrezId": 2934,
    "omim": [
      "137350"
    ],
    "uniprot": [
      "P06396"
    ],
    "model": {
      "build": "GRCh38",
      "release": "v1.5",
      "chrom": "9",
      "start": 121268162,
      "end": 121332842,
      "strand": "+",
      "ensemblTranscript": "ENST00000432226.7",
      "refseqTranscript": "NM_198252.3",
      "ensemblProtein": "ENSP00000404226.2",
      "refseqProtein": "NP_937895.1",
      "exons": [
        {
          "start": 121268162,
          "end": 121268219
        },
        {
          "start": 121281470,
          "end": 121281562
        },
        {
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        },
        {
          "start": 121302911,
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        },
        {
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        },
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        },
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        },
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        },
        {
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          "end": 121321401
        },
        {
          "start": 121324554,
          "end": 121324644
        },
        {
          "start": 121326512,
          "end": 121326682
        },
        {
          "start": 121327308,
          "end": 121327482
        },
        {
          "start": 121328891,
          "end": 121329015
        },
        {
          "start": 121329238,
          "end": 121329315
        },
        {
          "start": 121331388,
          "end": 121331448
        },
        {
          "start": 121332434,
          "end": 121332842
        }
      ],
      "cds": {
        "start": 121301972,
        "end": 121332603
      }
    },
    "grch37": {
      "build": "GRCh37",
      "release": "87",
      "chrom": "9",
      "start": 123970072,
      "end": 124095121,
      "strand": "+"
    },
    "neighbourhood": {
      "release": "116",
      "start": 120800502,
      "end": 121800501,
      "genes": [
        {
          "symbol": "B3GALT9",
          "ensemblId": "ENSG00000214654",
          "biotype": "protein_coding",
          "start": 120792403,
          "end": 120801787,
          "strand": "+",
          "slug": "b3galt9"
        },
        {
          "symbol": "PSMD5",
          "ensemblId": "ENSG00000095261",
          "biotype": "protein_coding",
          "start": 120815496,
          "end": 120843388,
          "strand": "-",
          "slug": "psmd5"
        },
        {
          "symbol": "PHF19",
          "ensemblId": "ENSG00000119403",
          "biotype": "protein_coding",
          "start": 120854422,
          "end": 120894903,
          "strand": "-",
          "slug": "phf19"
        },
        {
          "symbol": "TRAF1",
          "ensemblId": "ENSG00000056558",
          "biotype": "protein_coding",
          "start": 120902393,
          "end": 120931875,
          "strand": "-",
          "slug": "traf1"
        },
        {
          "symbol": "C5",
          "ensemblId": "ENSG00000106804",
          "biotype": "protein_coding",
          "start": 120932987,
          "end": 121075195,
          "strand": "-",
          "slug": "c5"
        },
        {
          "symbol": "CNTRL",
          "ensemblId": "ENSG00000119397",
          "biotype": "protein_coding",
          "start": 121074660,
          "end": 121177786,
          "strand": "+",
          "slug": "cntrl"
        },
        {
          "symbol": "RAB14",
          "ensemblId": "ENSG00000119396",
          "biotype": "protein_coding",
          "start": 121178133,
          "end": 121223014,
          "strand": "-",
          "slug": "rab14"
        },
        {
          "symbol": "STOM",
          "ensemblId": "ENSG00000148175",
          "biotype": "protein_coding",
          "start": 121328424,
          "end": 121370304,
          "strand": "-",
          "slug": "stom"
        },
        {
          "symbol": "GGTA1",
          "ensemblId": "ENSG00000204136",
          "biotype": "protein_coding",
          "start": 121444988,
          "end": 121513399,
          "strand": "-",
          "slug": "ggta1"
        },
        {
          "symbol": "DAB2IP",
          "ensemblId": "ENSG00000136848",
          "biotype": "protein_coding",
          "start": 121567057,
          "end": 121785530,
          "strand": "+",
          "slug": "dab2ip"
        }
      ],
      "truncated": false
    },
    "reports": [
      {
        "slug": "hereditary-amyloidosis-145",
        "name": "Amylose héréditaire",
        "diseases": [
          {
            "mondoId": "MONDO:0018634",
            "name": "Amylose héréditaire",
            "genes": 12,
            "inheritance": "autosomal-dominant",
            "description": "L'amylose héréditaire désigne un groupe d'affections génétiques qui constituent l'un des sous-types d'amyloses. Elle se caractérise par l'accumulation anormale d'une protéine appelée substance amyloïde dans plusieurs organes du corps, altérant leur structure tissulaire et leur fonctionnement. Dans l'amylose héréditaire, ces dépôts amyloïdes touchent le plus souvent les tissus du cœur, des reins et du système nerveux. Bien que certains symptômes puissent se manifester dès l'enfance, la plupart des personnes concernées ne développent de signes qu'à l'âge adulte.\n\nIl existe de nombreuses formes d'amylose héréditaire, associées à différentes mutations génétiques et protéines anormales. La forme la plus fréquente est l'amylose à transthyrétine (ATTR), une affection dans laquelle les dépôts d'amyloïde sont majoritairement constitués de transthyrétine, une protéine produite par le foie. Parmi les autres formes d'amylose héréditaire, on retrouve notamment l'amylose à apolipoprotéine AI (A ApoAI), l'amylose à gelsoline (A Gel), l'amylose à lysozyme (A Lys), l'amylose à cystatine C (A Cys), l'amylose à chaîne Aα du fibrinogène (A Fib) et l'amylose à apolipoprotéine AII (A ApoAII).",
            "management": "Tafamidis (stabilisateur cinétique), patisiran (ARNi), vutrisiran (ARNi), inotersen (oligonucléotide antisens), transplantation hépatique",
            "evidence": {
              "gencc": [
                "G2P",
                "Labcorp Genetics (formerly Invitae)",
                "PanelApp Australia"
              ],
              "acmgSf": false,
              "inheritance": [
                "autosomal-dominant",
                "autosomal-recessive"
              ]
            },
            "sameAsReport": true,
            "broad": false
          }
        ],
        "url": "https://dantelabs.com/fr/conditions/hereditary-amyloidosis-145"
      },
      {
        "slug": "hereditary-corneal-dystrophies",
        "name": "Dystrophies cornéennes héréditaires",
        "diseases": [
          {
            "mondoId": "MONDO:0018102",
            "name": "Dystrophie cornéenne",
            "genes": 19,
            "inheritance": null,
            "description": "Groupe d'affections héréditaires touchant une ou plusieurs couches de la cornée, notamment la dystrophie endothéliale de Fuchs (souvent liée à une expansion de répétitions dans le gène TCF4), les dystrophies granuleuses et réticulaires liées au gène TGFBI, ainsi que des formes plus rares causées par des gènes tels que SLC4A11, COL8A2, ZEB1 et CHST6.",
            "management": "Il est généralement recommandé aux porteurs de variants du gène TGFBI d'éviter la chirurgie réfractive au laser (LASIK ou PRK), qui peut aggraver les dépôts. Une greffe de cornée peut rétablir la vision dans les formes avancées de la maladie.",
            "evidence": {
              "gencc": [
                "G2P",
                "Labcorp Genetics (formerly Invitae)",
                "PanelApp Australia"
              ],
              "acmgSf": false,
              "inheritance": [
                "autosomal-dominant",
                "autosomal-recessive"
              ]
            },
            "sameAsReport": false,
            "broad": false
          }
        ],
        "url": "https://dantelabs.com/fr/conditions/hereditary-corneal-dystrophies"
      }
    ],
    "pharmacogenomics": [],
    "traits": [],
    "phenotypes": [
      {
        "slug": "arrhythmia",
        "name": "Abnormal heart rate",
        "systems": [
          "abnormality-of-the-cardiovascular-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/arrhythmia"
      },
      {
        "slug": "abnormal-spleen-morphology",
        "name": "Abnormal spleen morphology",
        "systems": [
          "abnormality-of-the-cardiovascular-system",
          "abnormality-of-the-digestive-system",
          "abnormality-of-the-immune-system"
        ],
        "frequency": "occasional",
        "url": "https://dantelabs.com/traits/abnormal-spleen-morphology"
      },
      {
        "slug": "abnormality-of-the-eye",
        "name": "Abnormality of the eye",
        "systems": [],
        "frequency": "very-frequent",
        "url": "https://dantelabs.com/traits/abnormality-of-the-eye"
      },
      {
        "slug": "abnormality-of-the-nervous-system",
        "name": "Abnormality of the nervous system",
        "systems": [],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/abnormality-of-the-nervous-system"
      },
      {
        "slug": "ataxia",
        "name": "Ataxia",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/ataxia"
      },
      {
        "slug": "facial-palsy",
        "name": "Bell's palsy",
        "systems": [
          "abnormality-of-head-or-neck",
          "abnormality-of-the-musculoskeletal-system",
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/facial-palsy"
      },
      {
        "slug": "blepharochalasis",
        "name": "Blepharochalasis",
        "systems": [
          "abnormality-of-head-or-neck",
          "abnormality-of-metabolism-homeostasis"
        ],
        "frequency": "occasional",
        "url": "https://dantelabs.com/traits/blepharochalasis"
      },
      {
        "slug": "bruising-susceptibility",
        "name": "Bruising susceptibility",
        "systems": [
          "abnormality-of-blood-and-blood-forming-tissues",
          "abnormality-of-the-cardiovascular-system",
          "abnormality-of-the-integument"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/bruising-susceptibility"
      },
      {
        "slug": "bulbar-palsy",
        "name": "Bulbar palsy",
        "systems": [
          "abnormality-of-the-musculoskeletal-system",
          "abnormality-of-the-nervous-system"
        ],
        "url": "https://dantelabs.com/traits/bulbar-palsy"
      },
      {
        "slug": "bulbar-signs",
        "name": "Bulbar signs",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "very-rare",
        "url": "https://dantelabs.com/traits/bulbar-signs"
      },
      {
        "slug": "cardiac-amyloidosis",
        "name": "Cardiac amyloidosis",
        "systems": [
          "abnormality-of-metabolism-homeostasis",
          "abnormality-of-the-cardiovascular-system"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/cardiac-amyloidosis"
      },
      {
        "slug": "cataract",
        "name": "Clouding of the lens of the eye",
        "systems": [
          "abnormality-of-the-eye"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/cataract"
      },
      {
        "slug": "constrictive-median-neuropathy",
        "name": "Constrictive median neuropathy",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/constrictive-median-neuropathy"
      },
      {
        "slug": "corneal-ulceration",
        "name": "Corneal ulceration",
        "systems": [
          "abnormality-of-the-eye"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/corneal-ulceration"
      },
      {
        "slug": "sensory-neuropathy",
        "name": "Damage to nerves that sense feeling",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "occasional",
        "url": "https://dantelabs.com/traits/sensory-neuropathy"
      },
      {
        "slug": "optic-neuropathy",
        "name": "Damaged optic nerve",
        "systems": [
          "abnormality-of-the-eye"
        ],
        "frequency": "occasional",
        "url": "https://dantelabs.com/traits/optic-neuropathy"
      },
      {
        "slug": "orthostatic-hypotension",
        "name": "Decrease in blood pressure upon standing up",
        "systems": [
          "abnormality-of-the-cardiovascular-system",
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/orthostatic-hypotension"
      },
      {
        "slug": "reduced-visual-acuity",
        "name": "Decreased clarity of vision",
        "systems": [
          "abnormality-of-the-eye"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/reduced-visual-acuity"
      },
      {
        "slug": "decreased-heart-rate-variability",
        "name": "Decreased heart rate variability",
        "systems": [
          "abnormality-of-the-cardiovascular-system"
        ],
        "url": "https://dantelabs.com/traits/decreased-heart-rate-variability"
      },
      {
        "slug": "xerostomia",
        "name": "Decreased salivary flow",
        "systems": [
          "abnormality-of-head-or-neck"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/xerostomia"
      },
      {
        "slug": "deficit-in-phonologic-short-term-memory",
        "name": "Deficit in phonologic short-term memory",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "very-rare",
        "url": "https://dantelabs.com/traits/deficit-in-phonologic-short-term-memory"
      },
      {
        "slug": "depression",
        "name": "Depression",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "very-rare",
        "url": "https://dantelabs.com/traits/depression"
      },
      {
        "slug": "dermatological-manifestations-of-systemic-disorders",
        "name": "Dermatological manifestations of systemic disorders",
        "systems": [
          "abnormality-of-the-integument"
        ],
        "frequency": "very-frequent",
        "url": "https://dantelabs.com/traits/dermatological-manifestations-of-systemic-disorders"
      },
      {
        "slug": "dysarthria",
        "name": "Difficulty articulating speech",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "occasional",
        "url": "https://dantelabs.com/traits/dysarthria"
      },
      {
        "slug": "diffuse-skin-atrophy",
        "name": "Diffuse skin atrophy",
        "systems": [
          "abnormality-of-the-integument"
        ],
        "frequency": "occasional",
        "url": "https://dantelabs.com/traits/diffuse-skin-atrophy"
      },
      {
        "slug": "cardiomyopathy",
        "name": "Disease of the heart muscle",
        "systems": [
          "abnormality-of-the-cardiovascular-system"
        ],
        "frequency": "occasional",
        "url": "https://dantelabs.com/traits/cardiomyopathy"
      },
      {
        "slug": "distal-peripheral-sensory-neuropathy",
        "name": "Distal peripheral sensory neuropathy",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/distal-peripheral-sensory-neuropathy"
      },
      {
        "slug": "bilateral-ptosis",
        "name": "Drooping of both upper eyelids",
        "systems": [
          "abnormality-of-the-eye"
        ],
        "frequency": "very-frequent",
        "url": "https://dantelabs.com/traits/bilateral-ptosis"
      },
      {
        "slug": "keratoconjunctivitis-sicca",
        "name": "Dry eye syndrome",
        "systems": [
          "abnormality-of-head-or-neck",
          "abnormality-of-the-cardiovascular-system",
          "abnormality-of-the-eye",
          "abnormality-of-the-immune-system"
        ],
        "frequency": "very-frequent",
        "url": "https://dantelabs.com/traits/keratoconjunctivitis-sicca"
      },
      {
        "slug": "dry-skin",
        "name": "Dry skin",
        "systems": [
          "abnormality-of-the-integument"
        ],
        "frequency": "very-frequent",
        "url": "https://dantelabs.com/traits/dry-skin"
      },
      {
        "slug": "edema",
        "name": "Fluid retention",
        "systems": [
          "abnormality-of-metabolism-homeostasis"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/edema"
      },
      {
        "slug": "generalized-amyloid-deposition",
        "name": "Generalized amyloid deposition",
        "systems": [
          "abnormality-of-metabolism-homeostasis"
        ],
        "url": "https://dantelabs.com/traits/generalized-amyloid-deposition"
      },
      {
        "slug": "glaucoma",
        "name": "Glaucoma",
        "systems": [
          "abnormality-of-the-eye"
        ],
        "frequency": "occasional",
        "url": "https://dantelabs.com/traits/glaucoma"
      },
      {
        "slug": "cutis-laxa",
        "name": "Hanging skin",
        "systems": [
          "abnormality-of-the-integument"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/cutis-laxa"
      },
      {
        "slug": "hearing-impairment",
        "name": "Hearing impairment",
        "systems": [
          "abnormality-of-the-ear"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/hearing-impairment"
      },
      {
        "slug": "proteinuria",
        "name": "High urine protein levels",
        "systems": [
          "abnormality-of-metabolism-homeostasis",
          "abnormality-of-the-genitourinary-system"
        ],
        "frequency": "occasional",
        "url": "https://dantelabs.com/traits/proteinuria"
      },
      {
        "slug": "pruritus",
        "name": "Itching",
        "systems": [
          "abnormality-of-the-integument"
        ],
        "frequency": "occasional",
        "url": "https://dantelabs.com/traits/pruritus"
      },
      {
        "slug": "lattice-corneal-dystrophy",
        "name": "Lattice corneal dystrophy",
        "systems": [
          "abnormality-of-the-eye"
        ],
        "frequency": "very-frequent",
        "url": "https://dantelabs.com/traits/lattice-corneal-dystrophy"
      },
      {
        "slug": "myokymia",
        "name": "Myokymia",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/myokymia"
      },
      {
        "slug": "nephrotic-syndrome",
        "name": "Nephrotic syndrome",
        "systems": [
          "abnormality-of-the-genitourinary-system"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/nephrotic-syndrome"
      },
      {
        "slug": "orthostatic-hypotension-due-to-autonomic-dysfunction",
        "name": "Orthostatic hypotension due to autonomic dysfunction",
        "systems": [
          "abnormality-of-the-cardiovascular-system",
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "occasional",
        "url": "https://dantelabs.com/traits/orthostatic-hypotension-due-to-autonomic-dysfunction"
      },
      {
        "slug": "sleep-apnea",
        "name": "Pauses in breathing while sleeping",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "occasional",
        "url": "https://dantelabs.com/traits/sleep-apnea"
      },
      {
        "slug": "polyneuropathy",
        "name": "Peripheral nerve disease",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/polyneuropathy"
      },
      {
        "slug": "nail-dystrophy",
        "name": "Poor nail formation",
        "systems": [
          "abnormality-of-the-integument"
        ],
        "frequency": "very-rare",
        "url": "https://dantelabs.com/traits/nail-dystrophy"
      },
      {
        "slug": "dysphagia",
        "name": "Poor swallowing",
        "systems": [
          "abnormality-of-the-digestive-system",
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/dysphagia"
      },
      {
        "slug": "regional-abnormality-of-skin",
        "name": "Regional abnormality of skin",
        "systems": [
          "abnormality-of-the-integument"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/regional-abnormality-of-skin"
      },
      {
        "slug": "renal-insufficiency",
        "name": "Renal failure",
        "systems": [
          "abnormality-of-the-genitourinary-system"
        ],
        "url": "https://dantelabs.com/traits/renal-insufficiency"
      },
      {
        "slug": "renal-glomerular-amyloid-deposition",
        "name": "Renal glomerular amyloid deposition",
        "systems": [
          "abnormality-of-metabolism-homeostasis",
          "abnormality-of-the-genitourinary-system"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/renal-glomerular-amyloid-deposition"
      },
      {
        "slug": "respiratory-tract-infection",
        "name": "Respiratory tract infection",
        "systems": [
          "abnormality-of-the-respiratory-system"
        ],
        "frequency": "very-rare",
        "url": "https://dantelabs.com/traits/respiratory-tract-infection"
      },
      {
        "slug": "sparse-hair",
        "name": "Sparse hair",
        "systems": [
          "abnormality-of-the-integument"
        ],
        "frequency": "occasional",
        "url": "https://dantelabs.com/traits/sparse-hair"
      },
      {
        "slug": "stage-5-chronic-kidney-disease",
        "name": "Stage 5 chronic kidney disease",
        "systems": [
          "abnormality-of-the-genitourinary-system"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/stage-5-chronic-kidney-disease"
      },
      {
        "slug": "urolithiasis",
        "name": "Urolithiasis",
        "systems": [
          "abnormality-of-the-genitourinary-system"
        ],
        "frequency": "occasional",
        "url": "https://dantelabs.com/traits/urolithiasis"
      },
      {
        "slug": "visual-impairment",
        "name": "Visual impairment",
        "systems": [
          "abnormality-of-the-eye"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/visual-impairment"
      },
      {
        "slug": "tongue-atrophy",
        "name": "Wasting of the tongue",
        "systems": [
          "abnormality-of-head-or-neck"
        ],
        "frequency": "occasional",
        "url": "https://dantelabs.com/traits/tongue-atrophy"
      },
      {
        "slug": "ophthalmoparesis",
        "name": "Weakness of muscles controlling eye movement",
        "systems": [
          "abnormality-of-the-eye"
        ],
        "frequency": "occasional",
        "url": "https://dantelabs.com/traits/ophthalmoparesis"
      }
    ],
    "related": [
      {
        "slug": "apoa1",
        "symbol": "APOA1",
        "name": "apolipoprotein A1",
        "shared": 1,
        "url": "https://dantelabs.com/fr/genes/apoa1"
      },
      {
        "slug": "apoa4",
        "symbol": "APOA4",
        "name": "apolipoprotein A4",
        "shared": 1,
        "url": "https://dantelabs.com/fr/genes/apoa4"
      },
      {
        "slug": "app",
        "symbol": "APP",
        "name": "amyloid beta precursor protein",
        "shared": 1,
        "url": "https://dantelabs.com/fr/genes/app"
      },
      {
        "slug": "b2m",
        "symbol": "B2M",
        "name": "beta-2-microglobulin",
        "shared": 1,
        "url": "https://dantelabs.com/fr/genes/b2m"
      },
      {
        "slug": "chst6",
        "symbol": "CHST6",
        "name": "carbohydrate sulfotransferase 6",
        "shared": 1,
        "url": "https://dantelabs.com/fr/genes/chst6"
      },
      {
        "slug": "col17a1",
        "symbol": "COL17A1",
        "name": "collagen type XVII alpha 1 chain",
        "shared": 1,
        "url": "https://dantelabs.com/fr/genes/col17a1"
      },
      {
        "slug": "col8a2",
        "symbol": "COL8A2",
        "name": "collagen type VIII alpha 2 chain",
        "shared": 1,
        "url": "https://dantelabs.com/fr/genes/col8a2"
      },
      {
        "slug": "cst3",
        "symbol": "CST3",
        "name": "cystatin C",
        "shared": 1,
        "url": "https://dantelabs.com/fr/genes/cst3"
      },
      {
        "slug": "dcn",
        "symbol": "DCN",
        "name": "decorin",
        "shared": 1,
        "url": "https://dantelabs.com/fr/genes/dcn"
      },
      {
        "slug": "fga",
        "symbol": "FGA",
        "name": "fibrinogen alpha chain",
        "shared": 1,
        "url": "https://dantelabs.com/fr/genes/fga"
      },
      {
        "slug": "gpnmb",
        "symbol": "GPNMB",
        "name": "glycoprotein nmb",
        "shared": 1,
        "url": "https://dantelabs.com/fr/genes/gpnmb"
      },
      {
        "slug": "grhl2",
        "symbol": "GRHL2",
        "name": "grainyhead like transcription factor 2",
        "shared": 1,
        "url": "https://dantelabs.com/fr/genes/grhl2"
      }
    ],
    "sources": {
      "bundleId": "2026.10.17-8666dff2",
      "panel": "2026-10-17",
      "acmgSf": "SF v3.2"
    },
    "locusKind": "proteinCoding"
  },
  "variants": {
    "total": 0,
    "url": null,
    "items": []
  }
}