GREB1L GREB1 like retinoic acid receptor coactivator
Gene ID: 80000, updated on 18-Sep-2024Gene type: protein coding
Also known as: RHDA3; DFNA80; C18orf6; KIAA1772
- See all available tests in GTR for this gene
- Go to complete Gene record for GREB1L
- Go to Variation Viewer for GREB1L variants
Summary
Acts upstream of or within kidney development. Predicted to be integral component of membrane. Implicated in autosomal dominant nonsyndromic deafness and renal agenesis. [provided by Alliance of Genome Resources, Apr 2022]
Associated conditions
Genomic context
- Location:
- 18q11.1-q11.2
- Sequence:
- Chromosome: 18; NC_000018.10 (21242232..21526112)
- Total number of exons:
- 35
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for GREB1L variants |
Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- MedGenRelated information in MedGen
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- Variation ViewerRelated Variants
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