GRIFIN
protein-coding gene in the species Homo sapiens
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GRIFIN
Summary
GRIFIN is a gene[1].
Key Facts
- GRIFIN's instance of is recorded as gene[2].
- GRIFIN is a type of protein-coding gene[3].
- GRIFIN's genomic start is recorded as 2474728[4].
- GRIFIN's genomic end is recorded as 2476894[5].
- GRIFIN's found in taxon is recorded as Homo sapiens[6].
- GRIFIN's chromosome is recorded as human chromosome 7[7].
- GRIFIN's strand orientation is recorded as reverse strand[8].
- GRIFIN's exact match is recorded as http://identifiers.org/ncbigene/402635[9].
- GRIFIN's cytogenetic location is recorded as 7p22.3[10].
- GRIFIN's expressed in is recorded as gonad[11].
- GRIFIN's expressed in is recorded as stromal cell of endometrium[12].
- GRIFIN's expressed in is recorded as skin of leg[13].
- GRIFIN's expressed in is recorded as granulocyte[14].
- GRIFIN's expressed in is recorded as skin of abdomen[15].
- GRIFIN's expressed in is recorded as right hemisphere of cerebellum[16].
- GRIFIN's expressed in is recorded as hypothalamus[17].
- GRIFIN's expressed in is recorded as left uterine tube[18].
- GRIFIN's expressed in is recorded as substantia nigra[19].
- GRIFIN's expressed in is recorded as nucleus accumbens[20].