MET

Summary

MET is a gene^[1].

Key Facts

• MET's instance of is recorded as gene^[2].
• MET is a type of protein-coding gene^[3].
• MET's HomoloGene ID is recorded as 206^[4].
• MET's genomic start is recorded as 116312444^[5].
• MET's genomic start is recorded as 116672196^[6].
• MET's genomic end is recorded as 116438440^[7].
• MET's genomic end is recorded as 116798377^[8].
• MET's ortholog is recorded as Met^[9].
• MET's ortholog is recorded as Met^[10].
• MET's ortholog is recorded as met^[11].
• MET's encodes is recorded as MET proto-oncogene, receptor tyrosine kinase^[12].
• MET's found in taxon is recorded as Homo sapiens^[13].
• MET's chromosome is recorded as human chromosome 7^[14].
• MET's genetic association is recorded as multiple sclerosis^[15].
• MET's genetic association is recorded as autosomal recessive nonsyndromic deafness 97^[16].
• MET's genetic association is recorded as osteofibrous dysplasia^[17].
• MET's genetic association is recorded as familial renal papillary carcinoma^[18].
• MET's strand orientation is recorded as forward strand^[19].
• MET's exact match is recorded as http://identifiers.org/ncbigene/4233^[20].
• MET's cytogenetic location is recorded as 7q31.2^[21].
• MET's expressed in is recorded as retinal pigment epithelium^[22].
• MET's expressed in is recorded as germinal epithelium^[23].
• MET's expressed in is recorded as cartilage tissue^[24].
• MET's expressed in is recorded as parietal pleura^[25].
• MET's expressed in is recorded as Achilles tendon^[26].