LOC124900664 (-)

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Gene Gene information from NCBI Gene database.
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Entrez ID 124900664
Gene name -
Gene symbol LOC124900664
Synonyms (NCBI Gene)
-
Chromosome 4
Chromosome location 4p16.1
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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MIM HGNC e!Ensembl
N/A N/A N/A
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Intellectual developmental disorder 61 Pathogenic rs540561511 RCV000999502
★★★★★
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)

No strongly related genes found yet for LOC124900664.

No additional diseases found yet through genes similar to LOC124900664.