PEX14
protein-coding gene in the species Homo sapiens
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PEX14
Summary
PEX14 is a gene[1].
Key Facts
- PEX14's instance of is recorded as gene[2].
- PEX14 is a type of protein-coding gene[3].
- PEX14's HomoloGene ID is recorded as 37936[4].
- PEX14's genomic start is recorded as 10472288[5].
- PEX14's genomic start is recorded as 10532345[6].
- PEX14's genomic end is recorded as 10630758[7].
- PEX14's genomic end is recorded as 10690815[8].
- PEX14's ortholog is recorded as Pex14[9].
- PEX14's ortholog is recorded as Pex14[10].
- PEX14's ortholog is recorded as Pex14[11].
- PEX14's ortholog is recorded as pex14[12].
- PEX14's encodes is recorded as Peroxisomal biogenesis factor 14[13].
- PEX14's found in taxon is recorded as Homo sapiens[14].
- PEX14's chromosome is recorded as human chromosome 1[15].
- PEX14's genetic association is recorded as breast cancer[16].
- PEX14's genetic association is recorded as Zellweger spectrum disorder[17].
- PEX14's strand orientation is recorded as forward strand[18].
- PEX14's exact match is recorded as http://identifiers.org/ncbigene/5195[19].
- PEX14's cytogenetic location is recorded as 1p36.22[20].
- PEX14's expressed in is recorded as bronchial epithelial cell[21].
- PEX14's expressed in is recorded as parotid gland[22].
- PEX14's expressed in is recorded as right lobe of liver[23].
- PEX14's expressed in is recorded as pancreatic ductal cell[24].
- PEX14's expressed in is recorded as prefrontal cortex[25].
- PEX14's expressed in is recorded as urinary bladder[26].