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  "url": "https://dantelabs.com/cs/genes/rims2",
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          "ensemblId": "ENSG00000155096",
          "biotype": "protein_coding",
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        {
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        {
          "symbol": "ATP6V1C1",
          "ensemblId": "ENSG00000155097",
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        {
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          "ensemblId": "ENSG00000164929",
          "biotype": "protein_coding",
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          "strand": "+",
          "slug": "baalc"
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        {
          "symbol": "FZD6",
          "ensemblId": "ENSG00000164930",
          "biotype": "protein_coding",
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          "slug": "fzd6"
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        {
          "symbol": "CTHRC1",
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          "biotype": "protein_coding",
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        {
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        {
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        {
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          "ensemblId": "ENSG00000164934",
          "biotype": "protein_coding",
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        {
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          "ensemblId": "ENSG00000147647",
          "biotype": "protein_coding",
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        {
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          "biotype": "protein_coding",
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          "slug": "dcstamp"
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        {
          "symbol": "LRP12",
          "ensemblId": "ENSG00000147650",
          "biotype": "protein_coding",
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        {
          "symbol": "ZFPM2",
          "ensemblId": "ENSG00000169946",
          "biotype": "protein_coding",
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          "strand": "+",
          "slug": "zfpm2"
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      ],
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    "reports": [
      {
        "slug": "congenital-stationary-night-blindness",
        "name": "Congenital Stationary Night Blindness",
        "diseases": [
          {
            "mondoId": "MONDO:0016293",
            "name": "Congenital Stationary Night Blindness",
            "genes": 16,
            "inheritance": null,
            "description": "A group of mostly non-progressive retinal conditions, including Oguchi disease, caused by changes in genes such as NYX, CACNA1F, TRPM1, GRM6, GPR179 and SAG, often with nystagmus or short-sightedness.",
            "management": "A genetic diagnosis explains the symptoms, helps distinguish the condition from progressive retinal diseases and informs family counselling.",
            "evidence": {
              "gencc": [
                "Franklin by Genoox"
              ],
              "acmgSf": false,
              "inheritance": [
                "autosomal-recessive"
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            },
            "sameAsReport": true,
            "broad": false
          }
        ],
        "url": "https://dantelabs.com/cs/conditions/congenital-stationary-night-blindness"
      }
    ],
    "pharmacogenomics": [],
    "traits": [],
    "phenotypes": [
      {
        "slug": "anxiety",
        "name": "Anxiety",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "occasional",
        "url": "https://dantelabs.com/traits/anxiety"
      },
      {
        "slug": "ataxia",
        "name": "Ataxia",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/ataxia"
      },
      {
        "slug": "autistic-behavior",
        "name": "Autism spectrum disorder",
        "systems": [
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        "frequency": "very-frequent",
        "url": "https://dantelabs.com/traits/autistic-behavior"
      },
      {
        "slug": "reduced-visual-acuity",
        "name": "Decreased clarity of vision",
        "systems": [
          "abnormality-of-the-eye"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/reduced-visual-acuity"
      },
      {
        "slug": "delayed-speech-and-language-development",
        "name": "Delayed speech and language development",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/delayed-speech-and-language-development"
      },
      {
        "slug": "photophobia",
        "name": "Extreme sensitivity of the eyes to light",
        "systems": [
          "abnormality-of-the-eye",
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/photophobia"
      },
      {
        "slug": "global-developmental-delay",
        "name": "Global developmental delay",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "url": "https://dantelabs.com/traits/global-developmental-delay"
      },
      {
        "slug": "hyperglycemia",
        "name": "High blood sugar",
        "systems": [
          "abnormality-of-metabolism-homeostasis"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/hyperglycemia"
      },
      {
        "slug": "nystagmus",
        "name": "Involuntary, rapid, rhythmic eye movements",
        "systems": [
          "abnormality-of-the-eye"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/nystagmus"
      },
      {
        "slug": "optic-disc-pallor",
        "name": "Optic disc pallor",
        "systems": [
          "abnormality-of-the-eye"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/optic-disc-pallor"
      },
      {
        "slug": "retinal-thinning-on-oct",
        "name": "Retinal thinning",
        "systems": [
          "abnormality-of-the-eye"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/retinal-thinning-on-oct"
      }
    ],
    "related": [
      {
        "slug": "cabp4",
        "symbol": "CABP4",
        "name": "calcium binding protein 4",
        "shared": 1,
        "url": "https://dantelabs.com/cs/genes/cabp4"
      },
      {
        "slug": "cacna1f",
        "symbol": "CACNA1F",
        "name": "calcium voltage-gated channel subunit alpha1 F",
        "shared": 1,
        "url": "https://dantelabs.com/cs/genes/cacna1f"
      },
      {
        "slug": "gnat1",
        "symbol": "GNAT1",
        "name": "G protein subunit alpha transducin 1",
        "shared": 1,
        "url": "https://dantelabs.com/cs/genes/gnat1"
      },
      {
        "slug": "gnb3",
        "symbol": "GNB3",
        "name": "G protein subunit beta 3",
        "shared": 1,
        "url": "https://dantelabs.com/cs/genes/gnb3"
      },
      {
        "slug": "gpr179",
        "symbol": "GPR179",
        "name": "G protein-coupled receptor 179",
        "shared": 1,
        "url": "https://dantelabs.com/cs/genes/gpr179"
      },
      {
        "slug": "grk1",
        "symbol": "GRK1",
        "name": "G protein-coupled receptor kinase 1",
        "shared": 1,
        "url": "https://dantelabs.com/cs/genes/grk1"
      },
      {
        "slug": "grm6",
        "symbol": "GRM6",
        "name": "glutamate metabotropic receptor 6",
        "shared": 1,
        "url": "https://dantelabs.com/cs/genes/grm6"
      },
      {
        "slug": "gucy2d",
        "symbol": "GUCY2D",
        "name": "guanylate cyclase 2D, retinal",
        "shared": 1,
        "url": "https://dantelabs.com/cs/genes/gucy2d"
      },
      {
        "slug": "lrit3",
        "symbol": "LRIT3",
        "name": "leucine rich repeat, Ig-like and transmembrane domains 3",
        "shared": 1,
        "url": "https://dantelabs.com/cs/genes/lrit3"
      },
      {
        "slug": "nyx",
        "symbol": "NYX",
        "name": "nyctalopin",
        "shared": 1,
        "url": "https://dantelabs.com/cs/genes/nyx"
      },
      {
        "slug": "pde6b",
        "symbol": "PDE6B",
        "name": "phosphodiesterase 6B",
        "shared": 1,
        "url": "https://dantelabs.com/cs/genes/pde6b"
      },
      {
        "slug": "rho",
        "symbol": "RHO",
        "name": "rhodopsin",
        "shared": 1,
        "url": "https://dantelabs.com/cs/genes/rho"
      }
    ],
    "sources": {
      "bundleId": "2026.10.17-8666dff2",
      "panel": "2026-10-17",
      "acmgSf": "SF v3.2"
    },
    "locusKind": "proteinCoding"
  },
  "variants": {
    "total": 0,
    "url": null,
    "items": []
  }
}