PEX26
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 22[12]
- Cytogenetic location
- 22q11.21[17]
- Encodes
- Peroxisomal biogenesis factor 26, Peroxisomal biogenesis factor 26 isoform 1[9][10]
- Expressed in
- mucosa of transverse colon, tendon of biceps brachii, islet of Langerhans, prefrontal cortex, rectum, ganglionic eminence, stromal cell of endometrium, anterior cingulate cortex, duodenum, ventricular zone[18][19][20][21][22][23][24][25][26][27]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- Zellweger spectrum disorder, peroxisomal biogenesis disorder, Zellweger syndrome[13][14][15]
- HomoloGene ID
- 9922[3]
- Strand orientation
- forward strand[16]
🏷️ Also known as
en PBD7A
en PBD7B
en peroxisomal biogenesis factor 26
en PEX26
en PEX26M1T
en Pex26pM1T
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000215193
- Ensembl transcript ID
- ENST00000329627, ENST00000399744, ENST00000428061
- Entrez Gene ID
- 55670
- Exact match
- identifiers.org
- Freebase ID
- /m/03hgntc
- HGNC ID
- 22965
- HGNC gene symbol
- PEX26
- OMIM ID
- 608666
- RefSeq RNA ID
- NM_017929, NM_001127649, NM_001199319
- UMLS CUI
- C1427818
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