PEX13
protein-coding gene in the species Homo sapiens
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Summary
PEX13 is a gene[1]. PEX13 is a type of protein-coding gene[2].
Key Facts
- HomoloGene ID: 1967[3]
- Genomic start: 61017225[4], 61244360[5]
- Genomic end: 61051990[6], 61279125[7]
- Ortholog: Pex13[8], prx-13[9]
- Encodes: Peroxisomal biogenesis factor 13[10]
- Found in taxon: Homo sapiens[11]
- Chromosome: human chromosome 2[12]
- Genetic association: Zellweger spectrum disorder[13], peroxisome biogenesis disorder 11B[14], Zellweger syndrome[15]
- Strand orientation: forward strand[16]
- Cytogenetic location: 2p15[17]
- Expressed in: secondary oocyte[18], sperm[19], buccal mucosa cell[20], epithelium of nasopharynx[21], germinal epithelium[22], visceral pleura[23], Achilles tendon[24], gonad[25], mucosa of paranasal sinus[26], ventricular zone[27]