PEX12
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PEX12
Summary
PEX12 is a gene[1]. PEX12 ranks in the top 2% of gene entities by monthly Wikipedia readership (6 views/month).[2]
Key Facts
- PEX12's instance of is recorded as gene[3].
- PEX12 is a type of protein-coding gene[4].
- PEX12's HomoloGene ID is recorded as 240[5].
- PEX12's genomic start is recorded as 35574795[6].
- PEX12's genomic start is recorded as 33901814[7].
- PEX12's genomic end is recorded as 35578863[8].
- PEX12's genomic end is recorded as 33905882[9].
- PEX12's ortholog is recorded as Pex12[10].
- PEX12's ortholog is recorded as Pex12[11].
- PEX12's ortholog is recorded as prx-12[12].
- PEX12's ortholog is recorded as pex12[13].
- PEX12's ortholog is recorded as Pex12[14].
- PEX12's encodes is recorded as Peroxisomal biogenesis factor 12[15].
- PEX12's found in taxon is recorded as Homo sapiens[16].
- PEX12's chromosome is recorded as human chromosome 17[17].
- PEX12's genetic association is recorded as peroxisome biogenesis disorder type 3B[18].
- PEX12's genetic association is recorded as Zellweger spectrum disorder[19].
- PEX12's genetic association is recorded as Zellweger syndrome[20].
- PEX12's strand orientation is recorded as reverse strand[21].
- PEX12's exact match is recorded as http://identifiers.org/ncbigene/5193[22].
- PEX12's cytogenetic location is recorded as 17q12[23].
- PEX12's expressed in is recorded as secondary oocyte[24].
- PEX12's expressed in is recorded as Epithelium of choroid plexus[25].
- PEX12's expressed in is recorded as gonad[26].
- PEX12's expressed in is recorded as germinal epithelium[27].
Why It Matters
PEX12 ranks in the top 2% of gene entities by monthly Wikipedia readership (6 views/month).[2] PEX12 is known by 4 alternative names across languages and contexts.[28]