PCNX2
protein-coding gene in the species Homo sapiens
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PCNX2
Summary
PCNX2 is a gene[1].
Key Facts
- PCNX2's instance of is recorded as gene[2].
- PCNX2 is a type of protein-coding gene[3].
- PCNX2's HomoloGene ID is recorded as 8987[4].
- PCNX2's genomic start is recorded as 232983435[5].
- PCNX2's genomic start is recorded as 233119181[6].
- PCNX2's genomic end is recorded as 233431459[7].
- PCNX2's genomic end is recorded as 233295725[8].
- PCNX2's ortholog is recorded as Pcnx2[9].
- PCNX2's ortholog is recorded as Pcnx2[10].
- PCNX2's ortholog is recorded as pcnx2[11].
- PCNX2's encodes is recorded as Pecanex 2[12].
- PCNX2's encodes is recorded as Protein PCNX2[13].
- PCNX2's found in taxon is recorded as Homo sapiens[14].
- PCNX2's chromosome is recorded as human chromosome 1[15].
- PCNX2's strand orientation is recorded as reverse strand[16].
- PCNX2's exact match is recorded as http://identifiers.org/ncbigene/80003[17].
- PCNX2's cytogenetic location is recorded as 1q42.2[18].
- PCNX2's expressed in is recorded as buccal mucosa cell[19].
- PCNX2's expressed in is recorded as middle temporal gyrus[20].
- PCNX2's expressed in is recorded as cerebellar vermis[21].
- PCNX2's expressed in is recorded as primary visual cortex[22].
- PCNX2's expressed in is recorded as cerebellar hemisphere[23].
- PCNX2's expressed in is recorded as Brodmann area 23[24].
- PCNX2's expressed in is recorded as right hemisphere of cerebellum[25].
- PCNX2's expressed in is recorded as endothelial cell[26].