FOXC1
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FOXC1
Summary
FOXC1 is a gene[1]. FOXC1 ranks in the top 2% of gene entities by monthly Wikipedia readership (13 views/month).[2]
Key Facts
- FOXC1's instance of is recorded as gene[3].
- FOXC1 is a type of protein-coding gene[4].
- FOXC1's HomoloGene ID is recorded as 20373[5].
- FOXC1's genomic start is recorded as 1610681[6].
- FOXC1's genomic start is recorded as 1609915[7].
- FOXC1's genomic end is recorded as 1613897[8].
- FOXC1's genomic end is recorded as 1614127[9].
- FOXC1's ortholog is recorded as Foxc1[10].
- FOXC1's ortholog is recorded as Foxc1[11].
- FOXC1's ortholog is recorded as foxc1a[12].
- FOXC1's encodes is recorded as Forkhead box C1[13].
- FOXC1's found in taxon is recorded as Homo sapiens[14].
- FOXC1's chromosome is recorded as human chromosome 6[15].
- FOXC1's genetic association is recorded as Axenfeld-Rieger syndrome type 3[16].
- FOXC1's genetic association is recorded as Rieger anomaly[17].
- FOXC1's genetic association is recorded as Axenfeld anomaly[18].
- FOXC1's strand orientation is recorded as forward strand[19].
- FOXC1's exact match is recorded as http://identifiers.org/ncbigene/2296[20].
- FOXC1's cytogenetic location is recorded as 6p25.3[21].
- FOXC1's expressed in is recorded as parotid gland[22].
- FOXC1's expressed in is recorded as vena cava[23].
- FOXC1's expressed in is recorded as trigeminal ganglion[24].
- FOXC1's expressed in is recorded as renal medulla[25].
- FOXC1's expressed in is recorded as palpebral conjunctiva[26].
- FOXC1's expressed in is recorded as tibia[27].
Why It Matters
FOXC1 ranks in the top 2% of gene entities by monthly Wikipedia readership (13 views/month).[2] FOXC1 is known by 11 alternative names across languages and contexts.[28]