PEX2
protein-coding gene in the species Homo sapiens
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PEX2
Summary
PEX2 is a gene[1].
Key Facts
- PEX2's instance of is recorded as gene[2].
- PEX2 is a type of protein-coding gene[3].
- PEX2's HomoloGene ID is recorded as 269[4].
- PEX2's genomic start is recorded as 76980258[5].
- PEX2's genomic start is recorded as 77892494[6].
- PEX2's genomic end is recorded as 77001044[7].
- PEX2's genomic end is recorded as 77913280[8].
- PEX2's ortholog is recorded as Pex2[9].
- PEX2's ortholog is recorded as Pex2[10].
- PEX2's ortholog is recorded as Pex2[11].
- PEX2's ortholog is recorded as pex2[12].
- PEX2's encodes is recorded as peroxisomal biogenesis factor 2[13].
- PEX2's found in taxon is recorded as Homo sapiens[14].
- PEX2's chromosome is recorded as human chromosome 8[15].
- PEX2's genetic association is recorded as Zellweger spectrum disorder[16].
- PEX2's genetic association is recorded as peroxisomal biogenesis disorder[17].
- PEX2's genetic association is recorded as Zellweger syndrome[18].
- PEX2's strand orientation is recorded as reverse strand[19].
- PEX2's exact match is recorded as http://identifiers.org/ncbigene/5828[20].
- PEX2's cytogenetic location is recorded as 8q21.13[21].
- PEX2's expressed in is recorded as seminal vesicula[22].
- PEX2's expressed in is recorded as ventricular zone[23].
- PEX2's expressed in is recorded as olfactory zone of nasal mucosa[24].
- PEX2's expressed in is recorded as islet of Langerhans[25].
- PEX2's expressed in is recorded as rectum[26].