SLC52A2
GHB receptor coding gene in the species Homo sapiens
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SLC52A2
Summary
SLC52A2 is a gene[1]. SLC52A2 ranks in the top 0.73% of gene entities by monthly Wikipedia readership (62 views/month, #40 of 5,469).[2]
Key Facts
- SLC52A2's instance of is recorded as gene[3].
- SLC52A2 is a type of protein-coding gene[4].
- SLC52A2's HomoloGene ID is recorded as 56994[5].
- SLC52A2's genomic start is recorded as 145577795[6].
- SLC52A2's genomic start is recorded as 144333957[7].
- SLC52A2's genomic end is recorded as 145584932[8].
- SLC52A2's genomic end is recorded as 144361286[9].
- SLC52A2's ortholog is recorded as Slc52a2[10].
- SLC52A2's ortholog is recorded as Slc52a2[11].
- SLC52A2's ortholog is recorded as slc52a2[12].
- SLC52A2's encodes is recorded as Solute carrier family 52 member 2[13].
- SLC52A2's found in taxon is recorded as Homo sapiens[14].
- SLC52A2's chromosome is recorded as human chromosome 8[15].
- SLC52A2's genetic association is recorded as brown-Vialetto-van Laere syndrome 2[16].
- SLC52A2's strand orientation is recorded as forward strand[17].
- SLC52A2's exact match is recorded as http://identifiers.org/ncbigene/79581[18].
Why It Matters
SLC52A2 ranks in the top 0.73% of gene entities by monthly Wikipedia readership (62 views/month, #40 of 5,469).[2] SLC52A2 is known by 11 alternative names across languages and contexts.[19]