ARHGAP22
protein-coding gene in the species Homo sapiens
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ARHGAP22
Summary
ARHGAP22 is a gene[1].
Key Facts
- ARHGAP22's instance of is recorded as gene[2].
- ARHGAP22 is a type of protein-coding gene[3].
- ARHGAP22's HomoloGene ID is recorded as 23292[4].
- ARHGAP22's genomic start is recorded as 49654077[5].
- ARHGAP22's genomic start is recorded as 48446036[6].
- ARHGAP22's genomic end is recorded as 48656265[7].
- ARHGAP22's genomic end is recorded as 49864310[8].
- ARHGAP22's ortholog is recorded as Arhgap22[9].
- ARHGAP22's ortholog is recorded as Arhgap22[10].
- ARHGAP22's ortholog is recorded as si:dkey-191m6.4[11].
- ARHGAP22's encodes is recorded as Rho GTPase activating protein 22[12].
- ARHGAP22's found in taxon is recorded as Homo sapiens[13].
- ARHGAP22's chromosome is recorded as human chromosome 10[14].
- ARHGAP22's genetic association is recorded as diabetic retinopathy[15].
- ARHGAP22's strand orientation is recorded as reverse strand[16].
- ARHGAP22's exact match is recorded as http://identifiers.org/ncbigene/58504[17].
- ARHGAP22's cytogenetic location is recorded as 10q11.22-q11.23[18].
- ARHGAP22's expressed in is recorded as C1 segment[19].
- ARHGAP22's expressed in is recorded as inferior olivary nucleus[20].