LRSAM1
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LRSAM1
Summary
LRSAM1 is a gene[1]. LRSAM1 ranks in the top 2% of gene entities by monthly Wikipedia readership (7 views/month).[2]
Key Facts
- LRSAM1's instance of is recorded as gene[3].
- LRSAM1 is a type of protein-coding gene[4].
- LRSAM1's HomoloGene ID is recorded as 44526[5].
- LRSAM1's genomic start is recorded as 130213765[6].
- LRSAM1's genomic start is recorded as 127451489[7].
- LRSAM1's genomic end is recorded as 130265780[8].
- LRSAM1's genomic end is recorded as 127503499[9].
- LRSAM1's ortholog is recorded as Lrsam1[10].
- LRSAM1's ortholog is recorded as Lrsam1[11].
- LRSAM1's ortholog is recorded as lrsam1[12].
- LRSAM1's encodes is recorded as Leucine rich repeat and sterile alpha motif containing 1[13].
- LRSAM1's found in taxon is recorded as Homo sapiens[14].
- LRSAM1's chromosome is recorded as human chromosome 9[15].
- LRSAM1's genetic association is recorded as Charcot-Marie-Tooth disease axonal type 2P[16].
- LRSAM1's strand orientation is recorded as forward strand[17].
- LRSAM1's exact match is recorded as http://identifiers.org/ncbigene/90678[18].
- LRSAM1's cytogenetic location is recorded as 9q33.3-q34.11[19].
- LRSAM1's expressed in is recorded as apex of heart[20].
- LRSAM1's expressed in is recorded as sural nerve[21].
Why It Matters
LRSAM1 ranks in the top 2% of gene entities by monthly Wikipedia readership (7 views/month).[2]