SPTSSB
protein-coding gene in the species Homo sapiens
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SPTSSB
Summary
SPTSSB is a gene[1].
Key Facts
- SPTSSB's instance of is recorded as gene[2].
- SPTSSB is a type of protein-coding gene[3].
- SPTSSB's HomoloGene ID is recorded as 64463[4].
- SPTSSB's genomic start is recorded as 161062580[5].
- SPTSSB's genomic start is recorded as 161344798[6].
- SPTSSB's genomic end is recorded as 161372880[7].
- SPTSSB's genomic end is recorded as 161090668[8].
- SPTSSB's ortholog is recorded as Sptssb[9].
- SPTSSB's ortholog is recorded as Sptssb[10].
- SPTSSB's ortholog is recorded as sptssb[11].
- SPTSSB's encodes is recorded as Serine palmitoyltransferase small subunit B[12].
- SPTSSB's found in taxon is recorded as Homo sapiens[13].
- SPTSSB's chromosome is recorded as human chromosome 3[14].
- SPTSSB's strand orientation is recorded as reverse strand[15].
- SPTSSB's exact match is recorded as http://identifiers.org/ncbigene/165679[16].
- SPTSSB's cytogenetic location is recorded as 3q26.1[17].
- SPTSSB's expressed in is recorded as testicle[18].
- SPTSSB's expressed in is recorded as skin of abdomen[19].
- SPTSSB's expressed in is recorded as skin of leg[20].
- SPTSSB's expressed in is recorded as primary visual cortex[21].
- SPTSSB's expressed in is recorded as islet of Langerhans[22].
- SPTSSB's expressed in is recorded as skin of arm[23].
- SPTSSB's expressed in is recorded as cerebellar cortex[24].
- SPTSSB's expressed in is recorded as cerebellar hemisphere[25].
- SPTSSB's expressed in is recorded as Brodmann area 9[26].