{
  "url": "https://dantelabs.com/nl/genes/kcnv2",
  "gene": {
    "slug": "kcnv2",
    "symbol": "KCNV2",
    "name": "potassium voltage-gated channel modifier subfamily V member 2",
    "hgnc": "HGNC:19698",
    "summary": null,
    "location": "9p24.2",
    "locusType": "gene with protein product",
    "aliases": [
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    "previousSymbols": [],
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    "entrezId": 169522,
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    "uniprot": [
      "Q8TDN2"
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    "model": {
      "build": "GRCh38",
      "release": "v1.5",
      "chrom": "9",
      "start": 2717510,
      "end": 2730037,
      "strand": "+",
      "ensemblTranscript": "ENST00000382082.4",
      "refseqTranscript": "NM_133497.4",
      "ensemblProtein": "ENSP00000371514.3",
      "refseqProtein": "NP_598004.1",
      "exons": [
        {
          "start": 2717510,
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        {
          "start": 2729446,
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        "start": 2717740,
        "end": 2729727
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    },
    "grch37": {
      "build": "GRCh37",
      "release": "87",
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      "end": 2730037,
      "strand": "+"
    },
    "neighbourhood": {
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      "genes": [
        {
          "symbol": "VLDLR",
          "ensemblId": "ENSG00000147852",
          "biotype": "protein_coding",
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          "end": 2660056,
          "strand": "+",
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        },
        {
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          "strand": "-",
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        },
        {
          "symbol": "RFX3",
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      ],
      "truncated": false
    },
    "reports": [],
    "pharmacogenomics": [],
    "traits": [],
    "phenotypes": [
      {
        "slug": "astigmatism",
        "name": "Astigmatism",
        "systems": [
          "abnormality-of-the-eye"
        ],
        "url": "https://dantelabs.com/traits/astigmatism"
      },
      {
        "slug": "scotoma",
        "name": "Blind spot",
        "systems": [
          "abnormality-of-the-eye"
        ],
        "url": "https://dantelabs.com/traits/scotoma"
      },
      {
        "slug": "myopia",
        "name": "Close sighted",
        "systems": [
          "abnormality-of-the-eye"
        ],
        "url": "https://dantelabs.com/traits/myopia"
      },
      {
        "slug": "cone-cone-rod-dystrophy",
        "name": "Cone/cone-rod dystrophy",
        "systems": [
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        ],
        "url": "https://dantelabs.com/traits/cone-cone-rod-dystrophy"
      },
      {
        "slug": "strabismus",
        "name": "Cross-eyed",
        "systems": [
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        ],
        "frequency": "occasional",
        "url": "https://dantelabs.com/traits/strabismus"
      },
      {
        "slug": "reduced-visual-acuity",
        "name": "Decreased clarity of vision",
        "systems": [
          "abnormality-of-the-eye"
        ],
        "url": "https://dantelabs.com/traits/reduced-visual-acuity"
      },
      {
        "slug": "nyctalopia",
        "name": "Difficulties with night vision",
        "systems": [
          "abnormality-of-the-eye"
        ],
        "url": "https://dantelabs.com/traits/nyctalopia"
      },
      {
        "slug": "photophobia",
        "name": "Extreme sensitivity of the eyes to light",
        "systems": [
          "abnormality-of-the-eye",
          "abnormality-of-the-nervous-system"
        ],
        "url": "https://dantelabs.com/traits/photophobia"
      },
      {
        "slug": "horizontal-nystagmus",
        "name": "Horizontal nystagmus",
        "systems": [
          "abnormality-of-the-eye"
        ],
        "url": "https://dantelabs.com/traits/horizontal-nystagmus"
      },
      {
        "slug": "macular-atrophy",
        "name": "Macular atrophy",
        "systems": [
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        ],
        "frequency": "occasional",
        "url": "https://dantelabs.com/traits/macular-atrophy"
      }
    ],
    "related": [],
    "sources": null,
    "locusKind": "proteinCoding"
  },
  "variants": {
    "total": 0,
    "url": null,
    "items": []
  }
}