PEX1
protein-coding gene in the species Homo sapiens
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PEX1
Summary
PEX1 is a gene[1]. PEX1 is known by 7 alternative names across languages and contexts.[2]
Key Facts
- PEX1's instance of is recorded as gene[3].
- PEX1 is a type of protein-coding gene[4].
- PEX1's HomoloGene ID is recorded as 27006[5].
- PEX1's genomic start is recorded as 92487020[6].
- PEX1's genomic start is recorded as 92116334[7].
- PEX1's genomic end is recorded as 92157845[8].
- PEX1's genomic end is recorded as 92528520[9].
- PEX1's ortholog is recorded as Pex1[10].
- PEX1's ortholog is recorded as Pex1[11].
- PEX1's ortholog is recorded as pex1[12].
- PEX1's encodes is recorded as Peroxisomal biogenesis factor 1[13].
- PEX1's found in taxon is recorded as Homo sapiens[14].
- PEX1's chromosome is recorded as human chromosome 7[15].
- PEX1's genetic association is recorded as Zellweger spectrum disorder[16].
- PEX1's genetic association is recorded as peroxisome biogenesis disorder 1B[17].
- PEX1's genetic association is recorded as Zellweger syndrome[18].
- PEX1's strand orientation is recorded as reverse strand[19].
- PEX1's exact match is recorded as http://identifiers.org/ncbigene/5189[20].
- PEX1's cytogenetic location is recorded as 7q21.2[21].
- PEX1's expressed in is recorded as Achilles tendon[22].
- PEX1's expressed in is recorded as body of pancreas[23].
- PEX1's expressed in is recorded as gastric mucosa[24].
- PEX1's expressed in is recorded as skin of leg[25].
- PEX1's expressed in is recorded as right hemisphere of cerebellum[26].
- PEX1's expressed in is recorded as skin of abdomen[27].
Why It Matters
PEX1 is known by 7 alternative names across languages and contexts.[2]