MAGEL2
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MAGEL2
Summary
MAGEL2 is a gene[1]. MAGEL2 ranks in the top 2% of gene entities by monthly Wikipedia readership (8 views/month).[2]
Key Facts
- MAGEL2's instance of is recorded as gene[3].
- MAGEL2 is a type of protein-coding gene[4].
- MAGEL2's HomoloGene ID is recorded as 8460[5].
- MAGEL2's genomic start is recorded as 23888691[6].
- MAGEL2's genomic start is recorded as 23643549[7].
- MAGEL2's genomic end is recorded as 23891175[8].
- MAGEL2's genomic end is recorded as 23647867[9].
- MAGEL2's ortholog is recorded as Magel2[10].
- MAGEL2's ortholog is recorded as Magel2[11].
- MAGEL2's encodes is recorded as MAGE family member L2[12].
- MAGEL2's found in taxon is recorded as Homo sapiens[13].
- MAGEL2's chromosome is recorded as human chromosome 15[14].
- MAGEL2's genetic association is recorded as Prader-Willi syndrome due to point mutation[15].
- MAGEL2's strand orientation is recorded as reverse strand[16].
- MAGEL2's exact match is recorded as http://identifiers.org/ncbigene/54551[17].
- MAGEL2's cytogenetic location is recorded as 15q11.2[18].
- MAGEL2's expressed in is recorded as gonad[19].
- MAGEL2's expressed in is recorded as testicle[20].
- MAGEL2's expressed in is recorded as hypothalamus[21].
- MAGEL2's expressed in is recorded as Brodmann area 23[22].
- MAGEL2's expressed in is recorded as middle temporal gyrus[23].
- MAGEL2's expressed in is recorded as tibia[24].
- MAGEL2's expressed in is recorded as pituitary gland[25].
- MAGEL2's expressed in is recorded as anterior pituitary[26].
- MAGEL2's expressed in is recorded as islet of Langerhans[27].
Why It Matters
MAGEL2 ranks in the top 2% of gene entities by monthly Wikipedia readership (8 views/month).[2]