GCSH
protein-coding gene in the species Homo sapiens
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GCSH
Summary
GCSH is a gene[1].
Key Facts
- GCSH's instance of is recorded as gene[2].
- GCSH is a type of protein-coding gene[3].
- GCSH's HomoloGene ID is recorded as 90880[4].
- GCSH's genomic start is recorded as 81115566[5].
- GCSH's genomic start is recorded as 81081945[6].
- GCSH's genomic end is recorded as 81130008[7].
- GCSH's genomic end is recorded as 81096395[8].
- GCSH's ortholog is recorded as Gcsh[9].
- GCSH's ortholog is recorded as Gcsh[10].
- GCSH's ortholog is recorded as GCV3[11].
- GCSH's ortholog is recorded as gcsh-2[12].
- GCSH's ortholog is recorded as gcshb[13].
- GCSH's ortholog is recorded as gcsha[14].
- GCSH's ortholog is recorded as ppl[15].
- GCSH's ortholog is recorded as gcsh-1[16].
- GCSH's encodes is recorded as Glycine cleavage system protein H[17].
- GCSH's found in taxon is recorded as Homo sapiens[18].
- GCSH's chromosome is recorded as human chromosome 16[19].
- GCSH's genetic association is recorded as glycine encephalopathy[20].
- GCSH's strand orientation is recorded as reverse strand[21].
- GCSH's exact match is recorded as http://identifiers.org/ncbigene/2653[22].
- GCSH's cytogenetic location is recorded as 16q23.2[23].
- GCSH's expressed in is recorded as C1 segment[24].
- GCSH's expressed in is recorded as substantia nigra[25].
- GCSH's expressed in is recorded as amygdala[26].