MFHAS1
protein-coding gene in the species Homo sapiens
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MFHAS1
Summary
MFHAS1 is a gene[1].
Key Facts
- MFHAS1's instance of is recorded as gene[2].
- MFHAS1 is a type of protein-coding gene[3].
- MFHAS1's HomoloGene ID is recorded as 3114[4].
- MFHAS1's genomic start is recorded as 8783354[5].
- MFHAS1's genomic start is recorded as 8640864[6].
- MFHAS1's genomic end is recorded as 8751155[7].
- MFHAS1's genomic end is recorded as 8893630[8].
- MFHAS1's ortholog is recorded as Mfhas1[9].
- MFHAS1's ortholog is recorded as Mfhas1[10].
- MFHAS1's ortholog is recorded as mfhas1[11].
- MFHAS1's encodes is recorded as Malignant fibrous histiocytoma amplified sequence 1[12].
- MFHAS1's found in taxon is recorded as Homo sapiens[13].
- MFHAS1's chromosome is recorded as human chromosome 8[14].
- MFHAS1's genetic association is recorded as conduct disorder[15].
- MFHAS1's strand orientation is recorded as reverse strand[16].
- MFHAS1's exact match is recorded as http://identifiers.org/ncbigene/9258[17].
- MFHAS1's cytogenetic location is recorded as 8p23.1[18].
- MFHAS1's expressed in is recorded as saphenous vein[19].
- MFHAS1's expressed in is recorded as secondary oocyte[20].
- MFHAS1's expressed in is recorded as renal medulla[21].
- MFHAS1's expressed in is recorded as pylorus[22].
- MFHAS1's expressed in is recorded as superior surface of tongue[23].
- MFHAS1's expressed in is recorded as cardia[24].
- MFHAS1's expressed in is recorded as pericardium[25].
- MFHAS1's expressed in is recorded as vena cava[26].