PEX26
protein-coding gene in the species Homo sapiens
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PEX26
Summary
PEX26 is a gene[1].
Key Facts
- PEX26's instance of is recorded as gene[2].
- PEX26 is a type of protein-coding gene[3].
- PEX26's HomoloGene ID is recorded as 9922[4].
- PEX26's genomic start is recorded as 18560689[5].
- PEX26's genomic start is recorded as 18077923[6].
- PEX26's genomic end is recorded as 18613905[7].
- PEX26's genomic end is recorded as 18105396[8].
- PEX26's ortholog is recorded as Pex26[9].
- PEX26's ortholog is recorded as Pex26[10].
- PEX26's ortholog is recorded as pex26[11].
- PEX26's encodes is recorded as Peroxisomal biogenesis factor 26[12].
- PEX26's encodes is recorded as Peroxisomal biogenesis factor 26 isoform 1[13].
- PEX26's found in taxon is recorded as Homo sapiens[14].
- PEX26's chromosome is recorded as human chromosome 22[15].
- PEX26's genetic association is recorded as Zellweger spectrum disorder[16].
- PEX26's genetic association is recorded as peroxisomal biogenesis disorder[17].
- PEX26's genetic association is recorded as Zellweger syndrome[18].
- PEX26's strand orientation is recorded as forward strand[19].
- PEX26's exact match is recorded as http://identifiers.org/ncbigene/55670[20].
- PEX26's cytogenetic location is recorded as 22q11.21[21].
- PEX26's expressed in is recorded as mucosa of transverse colon[22].
- PEX26's expressed in is recorded as tendon of biceps brachii[23].
- PEX26's expressed in is recorded as islet of Langerhans[24].
- PEX26's expressed in is recorded as prefrontal cortex[25].
- PEX26's expressed in is recorded as rectum[26].