SLC39A12
protein-coding gene in the species Homo sapiens
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SLC39A12
Summary
SLC39A12 is a gene[1]. SLC39A12 ranks in the top 2% of gene entities by monthly Wikipedia readership (11 views/month).[2]
Key Facts
- SLC39A12's instance of is recorded as gene[3].
- SLC39A12's subclass of is recorded as protein-coding gene[4].
- SLC39A12's Entrez Gene ID is recorded as 221074[5].
- SLC39A12's HGNC gene symbol is recorded as SLC39A12[6].
- SLC39A12's HGNC ID is recorded as 20860[7].
- SLC39A12's OMIM ID is recorded as 608734[8].
- SLC39A12's HomoloGene ID is recorded as 17654[9].
- SLC39A12's RefSeq RNA ID is recorded as NM_152725[10].
- SLC39A12's RefSeq RNA ID is recorded as NM_001145195[11].
- SLC39A12's RefSeq RNA ID is recorded as NM_001282733[12].
- SLC39A12's RefSeq RNA ID is recorded as NM_001282734[13].
- SLC39A12's ortholog is recorded as Slc39a12[14].
- SLC39A12's ortholog is recorded as Slc39a12[15].
- SLC39A12's encodes is recorded as Solute carrier family 39 member 12[16].
- SLC39A12's found in taxon is recorded as Homo sapiens[17].
- SLC39A12's decreased expression in is recorded as non-small-cell lung carcinoma[18].
- SLC39A12's increased expression in is recorded as schizophrenia[19].
- SLC39A12's gene substitution association with is recorded as esophagus adenocarcinoma[20].
- SLC39A12's Google Knowledge Graph ID is recorded as /g/11d_1clhzj[21].
- SLC39A12's exact match is recorded as http://identifiers.org/ncbigene/221074[22].
- SLC39A12's UMLS CUI is recorded as C1427167[23].
- SLC39A12's cytogenetic location is recorded as 10p12.33[24].
- SLC39A12's expressed in is recorded as retinal pigment epithelium[25].
- SLC39A12's expressed in is recorded as secondary oocyte[26].
- SLC39A12's expressed in is recorded as cerebellar vermis[27].
Why It Matters
SLC39A12 ranks in the top 2% of gene entities by monthly Wikipedia readership (11 views/month).[2] SLC39A12 is known by 6 alternative names across languages and contexts.[28]