FAM19A2
protein-coding gene in the species Homo sapiens
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FAM19A2
Summary
FAM19A2 is a gene[1].
Key Facts
- FAM19A2's instance of is recorded as gene[2].
- FAM19A2 is a type of protein-coding gene[3].
- FAM19A2's HomoloGene ID is recorded as 18678[4].
- FAM19A2's genomic start is recorded as 61708259[5].
- FAM19A2's genomic start is recorded as 62102040[6].
- FAM19A2's genomic end is recorded as 62279150[7].
- FAM19A2's genomic end is recorded as 62672931[8].
- FAM19A2's ortholog is recorded as Tafa2[9].
- FAM19A2's ortholog is recorded as Tafa2[10].
- FAM19A2's encodes is recorded as TAFA chemokine like family member 2[11].
- FAM19A2's encodes is recorded as Protein FAM19A2[12].
- FAM19A2's found in taxon is recorded as Homo sapiens[13].
- FAM19A2's chromosome is recorded as human chromosome 12[14].
- FAM19A2's genetic association is recorded as chronic obstructive pulmonary disease[15].
- FAM19A2's genetic association is recorded as obesity[16].
- FAM19A2's strand orientation is recorded as reverse strand[17].
- FAM19A2's exact match is recorded as http://identifiers.org/ncbigene/338811[18].
- FAM19A2's cytogenetic location is recorded as 12q14.1[19].
- FAM19A2's expressed in is recorded as secondary oocyte[20].
- FAM19A2's expressed in is recorded as buccal mucosa cell[21].
- FAM19A2's expressed in is recorded as primary visual cortex[22].
- FAM19A2's expressed in is recorded as endothelial cell[23].
- FAM19A2's expressed in is recorded as Brodmann area 23[24].
- FAM19A2's expressed in is recorded as middle temporal gyrus[25].
- FAM19A2's expressed in is recorded as prefrontal cortex[26].