PEX10
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 1[11]
- Cytogenetic location
- 1p36.32[16]
- Expressed in
- parotid gland, tendon of biceps brachii, C1 segment, right adrenal cortex, left adrenal gland, left adrenal cortex, amygdala, internal globus pallidus, left testis, right testis[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- Zellweger spectrum disorder, peroxisome biogenesis disorder 6B, Zellweger syndrome[12][13][14]
- HomoloGene ID
- 5671[3]
- Strand orientation
- reverse strand[15]
🏷️ Also known as
en PBD6B
en NALD
en PBD6A
en RNF69
en peroxisomal biogenesis factor 10
en PEX10
ar PEX١٠
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000157911
- Ensembl transcript ID
- ENST00000515760, ENST00000288774, ENST00000447513, ENST00000502666, ENST00000507596, ENST00000508384, ENST00000510434, ENST00000514502, ENST00000650293
- Entrez Gene ID
- 5192
- Exact match
- identifiers.org
- Freebase ID
- /m/03g_v62
- HGNC ID
- 8851
- HGNC gene symbol
- PEX10
- Microsoft Academic ID (discontinued)
- 2779192100
- OMIM ID
- 602859
- RefSeq RNA ID
- NM_002617, NM_153818, XM_011541576, NM_001374425, NM_001374426, NM_001374427, NR_164636, XM_047422539
- UMLS CUI
- C1418470
🔗 Connections
Expressed in 2
Chromosome 1
Found in taxon 1
Genetic association 1
Instance of 1
← Genetic association 1
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