SLC33A1
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SLC33A1
Summary
SLC33A1 is a gene[1]. SLC33A1 ranks in the top 2% of gene entities by monthly Wikipedia readership (6 views/month).[2]
Key Facts
- SLC33A1's instance of is recorded as gene[3].
- SLC33A1 is a type of protein-coding gene[4].
- SLC33A1's HomoloGene ID is recorded as 3476[5].
- SLC33A1's genomic start is recorded as 155821024[6].
- SLC33A1's genomic start is recorded as 155538813[7].
- SLC33A1's genomic end is recorded as 155572218[8].
- SLC33A1's genomic end is recorded as 155854456[9].
- SLC33A1's ortholog is recorded as Slc33a1[10].
- SLC33A1's ortholog is recorded as Slc33a1[11].
- SLC33A1's ortholog is recorded as YBR220C[12].
- SLC33A1's ortholog is recorded as slc33a1[13].
- SLC33A1's ortholog is recorded as T26C5.3[14].
- SLC33A1's ortholog is recorded as CG9706[15].
- SLC33A1's encodes is recorded as Solute carrier family 33 member 1[16].
- SLC33A1's encodes is recorded as Acetyl-coenzyme A transporter 1[17].
- SLC33A1's found in taxon is recorded as Homo sapiens[18].
- SLC33A1's chromosome is recorded as human chromosome 3[19].
- SLC33A1's genetic association is recorded as hereditary spastic paraplegia 42[20].
- SLC33A1's genetic association is recorded as congenital cataract-hearing loss-severe developmental delay syndrome[21].
- SLC33A1's strand orientation is recorded as reverse strand[22].
- SLC33A1's exact match is recorded as http://identifiers.org/ncbigene/9197[23].
- SLC33A1's cytogenetic location is recorded as 3q25.31[24].
- SLC33A1's expressed in is recorded as corpus epididymis[25].
- SLC33A1's expressed in is recorded as body of pancreas[26].
- SLC33A1's expressed in is recorded as islet of Langerhans[27].
Why It Matters
SLC33A1 ranks in the top 2% of gene entities by monthly Wikipedia readership (6 views/month).[2] SLC33A1 is known by 7 alternative names across languages and contexts.[28]