PSMB10
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 16[11]
- Cytogenetic location
- 16q22.1[14]
- Expressed in
- granulocyte, monocyte, blood, spleen, mucosa of transverse colon, duodenum, putamen, appendix, substantia nigra, apex of heart[15][16][17][18][19][20][21][22][23][24]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- Crohn's disease[12]
- HomoloGene ID
- 20616[3]
- Strand orientation
- reverse strand[13]
🏷️ Also known as
en beta2i
en LMP10
en MECL1
en PRAAS5
en proteasome 20S subunit beta 10
en proteasome subunit beta 10
en PSMB10
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000205220
- Ensembl transcript ID
- ENST00000575556, ENST00000358514, ENST00000570304, ENST00000570985, ENST00000574576
- Entrez Gene ID
- 5699
- Exact match
- identifiers.org
- Freebase ID
- /m/02kgnkn
- HGNC ID
- 9538
- HGNC gene symbol
- PSMB10
- Microsoft Academic ID (discontinued)
- 2781255752
- OMIM ID
- 176847
- RefSeq RNA ID
- NM_002801
- UMLS CUI
- C1419011
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