SLC26A5
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SLC26A5
Summary
SLC26A5 is a gene[1]. SLC26A5 ranks in the top 1% of gene entities by monthly Wikipedia readership (62 views/month).[2]
Key Facts
- SLC26A5's instance of is recorded as gene[3].
- SLC26A5 is a type of protein-coding gene[4].
- SLC26A5's HomoloGene ID is recorded as 69472[5].
- SLC26A5's genomic start is recorded as 103352730[6].
- SLC26A5's genomic start is recorded as 102993177[7].
- SLC26A5's genomic end is recorded as 103086624[8].
- SLC26A5's genomic end is recorded as 103446207[9].
- SLC26A5's ortholog is recorded as Slc26a5[10].
- SLC26A5's ortholog is recorded as Slc26a5[11].
- SLC26A5's ortholog is recorded as sulp-5[12].
- SLC26A5's ortholog is recorded as slc26a5[13].
- SLC26A5's ortholog is recorded as sulp-7[14].
- SLC26A5's ortholog is recorded as sulp-3[15].
- SLC26A5's ortholog is recorded as sulp-8[16].
- SLC26A5's ortholog is recorded as sulp-4[17].
- SLC26A5's ortholog is recorded as Prestin[18].
- SLC26A5's encodes is recorded as Solute carrier family 26 member 5[19].
- SLC26A5's found in taxon is recorded as Homo sapiens[20].
- SLC26A5's chromosome is recorded as human chromosome 7[21].
- SLC26A5's genetic association is recorded as autosomal recessive nonsyndromic deafness 61[22].
- SLC26A5's strand orientation is recorded as reverse strand[23].
- SLC26A5's exact match is recorded as http://identifiers.org/ncbigene/375611[24].
- SLC26A5's cytogenetic location is recorded as 7q22.1[25].
- SLC26A5's expressed in is recorded as testicle[26].
- SLC26A5's expressed in is recorded as cerebellar cortex[27].
Why It Matters
SLC26A5 ranks in the top 1% of gene entities by monthly Wikipedia readership (62 views/month).[2] SLC26A5 has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[28] SLC26A5 is known by 3 alternative names across languages and contexts.[29]