HMSD
protein-coding gene in the species Homo sapiens
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HMSD
Summary
HMSD is a gene[1].
Key Facts
- HMSD's instance of is recorded as gene[2].
- HMSD is a type of protein-coding gene[3].
- HMSD's HomoloGene ID is recorded as 129867[4].
- HMSD's genomic start is recorded as 63949301[5].
- HMSD's genomic start is recorded as 61616535[6].
- HMSD's genomic end is recorded as 63981774[7].
- HMSD's genomic end is recorded as 61649008[8].
- HMSD's encodes is recorded as Histocompatibility minor serpin domain containing[9].
- HMSD's encodes is recorded as Minor histocompatibility protein HMSD variant form[10].
- HMSD's found in taxon is recorded as Homo sapiens[11].
- HMSD's chromosome is recorded as human chromosome 18[12].
- HMSD's strand orientation is recorded as forward strand[13].
- HMSD's exact match is recorded as http://identifiers.org/ncbigene/284293[14].
- HMSD's cytogenetic location is recorded as 18q22.1[15].
- HMSD's expressed in is recorded as C1 segment[16].
- HMSD's expressed in is recorded as ventricular zone[17].
- HMSD's expressed in is recorded as substantia nigra[18].
- HMSD's expressed in is recorded as ganglionic eminence[19].
- HMSD's expressed in is recorded as hippocampus proper[20].
- HMSD's expressed in is recorded as lymph node[21].
- HMSD's expressed in is recorded as hypothalamus[22].
- HMSD's expressed in is recorded as appendix[23].
- HMSD's expressed in is recorded as primary visual cortex[24].
- HMSD's expressed in is recorded as Brodmann area 9[25].