PEX13
protein-coding gene in the species Homo sapiens
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PEX13
Summary
PEX13 is a gene[1]. PEX13 ranks in the top 2% of gene entities by monthly Wikipedia readership (9 views/month).[2]
Key Facts
- PEX13's instance of is recorded as gene[3].
- PEX13 is a type of protein-coding gene[4].
- PEX13's HomoloGene ID is recorded as 1967[5].
- PEX13's genomic start is recorded as 61017225[6].
- PEX13's genomic start is recorded as 61244360[7].
- PEX13's genomic end is recorded as 61051990[8].
- PEX13's genomic end is recorded as 61279125[9].
- PEX13's ortholog is recorded as Pex13[10].
- PEX13's ortholog is recorded as Pex13[11].
- PEX13's ortholog is recorded as prx-13[12].
- PEX13's ortholog is recorded as Pex13[13].
- PEX13's ortholog is recorded as pex13[14].
- PEX13's encodes is recorded as Peroxisomal biogenesis factor 13[15].
- PEX13's found in taxon is recorded as Homo sapiens[16].
- PEX13's chromosome is recorded as human chromosome 2[17].
- PEX13's genetic association is recorded as Zellweger spectrum disorder[18].
- PEX13's genetic association is recorded as peroxisome biogenesis disorder 11B[19].
- PEX13's genetic association is recorded as Zellweger syndrome[20].
- PEX13's strand orientation is recorded as forward strand[21].
- PEX13's exact match is recorded as http://identifiers.org/ncbigene/5194[22].
- PEX13's cytogenetic location is recorded as 2p15[23].
- PEX13's expressed in is recorded as secondary oocyte[24].
- PEX13's expressed in is recorded as sperm[25].
- PEX13's expressed in is recorded as buccal mucosa cell[26].
- PEX13's expressed in is recorded as epithelium of nasopharynx[27].
Why It Matters
PEX13 ranks in the top 2% of gene entities by monthly Wikipedia readership (9 views/month).[2] PEX13 is known by 6 alternative names across languages and contexts.[28]