CBX7
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 22[13]
- Cytogenetic location
- 22q13.1[16]
- Expressed in
- cerebellar vermis, paraflocculus of cerebellum, Brodmann area 10, right hemisphere of cerebellum, frontal pole, gastric mucosa, middle frontal gyrus, pons, right coronary artery, right frontal lobe[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- multiple myeloma[14]
- HomoloGene ID
- 65296[3]
- Strand orientation
- reverse strand[15]
🏷️ Also known as
en CBX7
en chromobox 7
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000100307
- Ensembl transcript ID
- ENST00000216133, ENST00000401405, ENST00000434260, ENST00000475962, ENST00000477827, ENST00000482294, ENST00000490741
- Entrez Gene ID
- 23492
- Exact match
- identifiers.org
- Freebase ID
- /m/0hncd43
- HGNC ID
- 1557
- HGNC gene symbol
- CBX7
- OMIM ID
- 608457
- RefSeq RNA ID
- NM_175709, NM_001346743, NM_001346744
- UMLS CUI
- C1413162
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