FANCG
protein-coding gene in the species Homo sapiens
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FANCG
Summary
FANCG is a gene[1].
Key Facts
- FANCG's instance of is recorded as gene[2].
- FANCG is a type of protein-coding gene[3].
- FANCG's HomoloGene ID is recorded as 3402[4].
- FANCG's genomic start is recorded as 35073835[5].
- FANCG's genomic start is recorded as 35073832[6].
- FANCG's genomic end is recorded as 35080013[7].
- FANCG's genomic end is recorded as 35080004[8].
- FANCG's ortholog is recorded as Fancg[9].
- FANCG's ortholog is recorded as Fancg[10].
- FANCG's ortholog is recorded as fancg[11].
- FANCG's encodes is recorded as FA complementation group G[12].
- FANCG's encodes is recorded as Fanconi anemia group G protein[13].
- FANCG's found in taxon is recorded as Homo sapiens[14].
- FANCG's chromosome is recorded as human chromosome 9[15].
- FANCG's genetic association is recorded as Fanconi anemia complementation group G[16].
- FANCG's strand orientation is recorded as reverse strand[17].
- FANCG's exact match is recorded as http://identifiers.org/ncbigene/2189[18].
- FANCG's cytogenetic location is recorded as 9p13.3[19].
- FANCG's expressed in is recorded as ventricular zone[20].
- FANCG's expressed in is recorded as ganglionic eminence[21].
- FANCG's expressed in is recorded as right hemisphere of cerebellum[22].
- FANCG's expressed in is recorded as mucosa of transverse colon[23].
- FANCG's expressed in is recorded as granulocyte[24].
- FANCG's expressed in is recorded as body of pancreas[25].
- FANCG's expressed in is recorded as left testis[26].