SLC38A9
protein-coding gene in the species Homo sapiens
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SLC38A9
Summary
SLC38A9 is a gene[1].
Key Facts
- SLC38A9's instance of is recorded as gene[2].
- SLC38A9 is a type of protein-coding gene[3].
- SLC38A9's HomoloGene ID is recorded as 18139[4].
- SLC38A9's genomic start is recorded as 55625845[5].
- SLC38A9's genomic start is recorded as 54921673[6].
- SLC38A9's genomic end is recorded as 55773194[7].
- SLC38A9's genomic end is recorded as 55069022[8].
- SLC38A9's ortholog is recorded as Slc38a9[9].
- SLC38A9's ortholog is recorded as Slc38a9[10].
- SLC38A9's ortholog is recorded as F13H10.3[11].
- SLC38A9's ortholog is recorded as slc38a9[12].
- SLC38A9's encodes is recorded as Solute carrier family 38 member 9[13].
- SLC38A9's encodes is recorded as Sodium-coupled neutral amino acid transporter 9[14].
- SLC38A9's found in taxon is recorded as Homo sapiens[15].
- SLC38A9's chromosome is recorded as human chromosome 5[16].
- SLC38A9's strand orientation is recorded as reverse strand[17].
- SLC38A9's exact match is recorded as http://identifiers.org/ncbigene/153129[18].
- SLC38A9's cytogenetic location is recorded as 5q11.2[19].
- SLC38A9's expressed in is recorded as secondary oocyte[20].