RCBTB1
protein-coding gene in the species Homo sapiens
Facts
9 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 13[7]
- Cytogenetic location
- 13q14.2[9]
- Found in taxon
- Homo sapiens[6]
- Genetic association
- retinal dystrophy with or without extraocular anomalies[8]
- HomoloGene ID
- 10061[3]
🏷️ Also known as
en CLLD7
en CLLL7
en GLP
en RCBTB1
en RCC1 and BTB domain containing protein 1
en RDEOA
🔖 Identifiers · 9
- Ensembl gene ID
- ENSG00000136144
- Entrez Gene ID
- 55213
- Exact match
- identifiers.org
- Freebase ID
- /m/03hgnfp
- HGNC ID
- 18243
- HGNC gene symbol
- RCBTB1
- OMIM ID
- 607867
- RefSeq RNA ID
- NM_018191, XM_005266441, XM_011535133, XM_011535134, XM_011535135, XM_011535136, XR_245392, XR_941613, XR_001749596, XR_001749597
- UMLS CUI
- C1425391
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