FGD1
protein-coding gene in the species Homo sapiens
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FGD1
Summary
FGD1 is a gene[1].
Key Facts
- FGD1's instance of is recorded as gene[2].
- FGD1 is a type of protein-coding gene[3].
- FGD1's HomoloGene ID is recorded as 3282[4].
- FGD1's genomic start is recorded as 54445454[5].
- FGD1's genomic start is recorded as 54471887[6].
- FGD1's genomic end is recorded as 54522599[7].
- FGD1's genomic end is recorded as 54496234[8].
- FGD1's ortholog is recorded as Fgd1[9].
- FGD1's ortholog is recorded as Fgd1[10].
- FGD1's ortholog is recorded as fgd1[11].
- FGD1's encodes is recorded as FYVE, RhoGEF and PH domain containing 1[12].
- FGD1's encodes is recorded as FYVE, RhoGEF and PH domain containing 1 (Faciogenital dysplasia), isoform CRA_a[13].
- FGD1's found in taxon is recorded as Homo sapiens[14].
- FGD1's chromosome is recorded as human X chromosome[15].
- FGD1's genetic association is recorded as Aarskog syndrome[16].
- FGD1's strand orientation is recorded as reverse strand[17].
- FGD1's exact match is recorded as http://identifiers.org/ncbigene/2245[18].
- FGD1's cytogenetic location is recorded as Xp11.22[19].
- FGD1's expressed in is recorded as stromal cell of endometrium[20].
- FGD1's expressed in is recorded as ganglionic eminence[21].
- FGD1's expressed in is recorded as ventricular zone[22].
- FGD1's expressed in is recorded as cartilage tissue[23].
- FGD1's expressed in is recorded as postcentral gyrus[24].
- FGD1's expressed in is recorded as entorhinal cortex[25].
- FGD1's expressed in is recorded as prefrontal cortex[26].