PEX7
protein-coding gene in the species Homo sapiens
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PEX7
Summary
PEX7 is a gene[1].
Key Facts
- PEX7's instance of is recorded as gene[2].
- PEX7 is a type of protein-coding gene[3].
- PEX7's HomoloGene ID is recorded as 242[4].
- PEX7's genomic start is recorded as 136822564[5].
- PEX7's genomic start is recorded as 137143717[6].
- PEX7's genomic end is recorded as 137235075[7].
- PEX7's genomic end is recorded as 136913934[8].
- PEX7's ortholog is recorded as Pex7[9].
- PEX7's ortholog is recorded as Pex7[10].
- PEX7's ortholog is recorded as pex7[11].
- PEX7's ortholog is recorded as Pex7[12].
- PEX7's encodes is recorded as peroxisomal biogenesis factor 7[13].
- PEX7's found in taxon is recorded as Homo sapiens[14].
- PEX7's chromosome is recorded as human chromosome 6[15].
- PEX7's genetic association is recorded as rhizomelic chondrodysplasia punctata type 1[16].
- PEX7's genetic association is recorded as Zellweger spectrum disorder[17].
- PEX7's genetic association is recorded as adult Refsum disease[18].
- PEX7's strand orientation is recorded as forward strand[19].
- PEX7's exact match is recorded as http://identifiers.org/ncbigene/5191[20].
- PEX7's cytogenetic location is recorded as 6q23.3[21].
- PEX7's expressed in is recorded as retinal pigment epithelium[22].
- PEX7's expressed in is recorded as sperm[23].
- PEX7's expressed in is recorded as right adrenal gland[24].
- PEX7's expressed in is recorded as right adrenal cortex[25].
- PEX7's expressed in is recorded as left adrenal gland[26].