MYNN
protein-coding gene in the species Homo sapiens
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MYNN
Summary
MYNN is a gene[1].
Key Facts
- MYNN's instance of is recorded as gene[2].
- MYNN is a type of protein-coding gene[3].
- MYNN's HomoloGene ID is recorded as 10253[4].
- MYNN's genomic start is recorded as 169490619[5].
- MYNN's genomic start is recorded as 169773396[6].
- MYNN's genomic end is recorded as 169789716[7].
- MYNN's genomic end is recorded as 169507504[8].
- MYNN's ortholog is recorded as Mynn[9].
- MYNN's ortholog is recorded as Mynn[10].
- MYNN's encodes is recorded as Myoneurin[11].
- MYNN's encodes is recorded as Myoneurin[12].
- MYNN's found in taxon is recorded as Homo sapiens[13].
- MYNN's chromosome is recorded as human chromosome 3[14].
- MYNN's genetic association is recorded as chronic lymphocytic leukemia[15].
- MYNN's genetic association is recorded as multiple sclerosis[16].
- MYNN's genetic association is recorded as colorectal cancer[17].
- MYNN's strand orientation is recorded as forward strand[18].
- MYNN's exact match is recorded as http://identifiers.org/ncbigene/55892[19].
- MYNN's cytogenetic location is recorded as 3q26.2[20].
- MYNN's expressed in is recorded as buccal mucosa cell[21].
- MYNN's expressed in is recorded as secondary oocyte[22].
- MYNN's expressed in is recorded as testicle[23].
- MYNN's expressed in is recorded as Achilles tendon[24].
- MYNN's expressed in is recorded as ventricular zone[25].
- MYNN's expressed in is recorded as amniotic fluid[26].