SLC19A2
protein-coding gene in the species Homo sapiens
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SLC19A2
Summary
SLC19A2 is a gene[1].
Key Facts
- SLC19A2's instance of is recorded as gene[2].
- SLC19A2 is a type of protein-coding gene[3].
- SLC19A2's HomoloGene ID is recorded as 38258[4].
- SLC19A2's genomic start is recorded as 169463909[5].
- SLC19A2's genomic start is recorded as 169433147[6].
- SLC19A2's genomic end is recorded as 169455241[7].
- SLC19A2's genomic end is recorded as 169485944[8].
- SLC19A2's ortholog is recorded as Slc19a2[9].
- SLC19A2's ortholog is recorded as Slc19a2[10].
- SLC19A2's ortholog is recorded as CG17036[11].
- SLC19A2's ortholog is recorded as slc19a2[12].
- SLC19A2's ortholog is recorded as folt-1[13].
- SLC19A2's ortholog is recorded as folt-2[14].
- SLC19A2's ortholog is recorded as folt-3[15].
- SLC19A2's ortholog is recorded as CG6574[16].
- SLC19A2's ortholog is recorded as CG14694[17].
- SLC19A2's encodes is recorded as Solute carrier family 19 member 2[18].
- SLC19A2's found in taxon is recorded as Homo sapiens[19].
- SLC19A2's chromosome is recorded as human chromosome 1[20].
- SLC19A2's genetic association is recorded as thiamine-responsive megaloblastic anemia syndrome[21].
- SLC19A2's strand orientation is recorded as reverse strand[22].
- SLC19A2's exact match is recorded as http://identifiers.org/ncbigene/10560[23].
- SLC19A2's cytogenetic location is recorded as 1q24.2[24].
- SLC19A2's expressed in is recorded as secondary oocyte[25].
- SLC19A2's expressed in is recorded as gastrocnemius muscle[26].