C15orf32, chromosome 15 open reading frame 32, chromosome 15 putative open reading frame 32
External IDs
HomoloGene: 89189 GeneCards: C15orf32
Gene location (Human)
Chr.
Chromosome 15 (human)[1]
Band
15q26.1
Start
92,471,654 bp[1]
End
92,501,117 bp[1]
RNA expression pattern
Bgee
Human
Mouse (ortholog)
Top expressed in
ganglionic eminence
islet of Langerhans
gastrocnemius muscle
monocyte
upper lobe of left lung
tibial nerve
n/a
More reference expression data
BioGPS
n/a
Orthologs
Species
Human
Mouse
Entrez
145858
n/a
Ensembl
ENSG00000183643
n/a
UniProt
Q32M92
n/a
RefSeq (mRNA)
NM_001301106 NM_153040
n/a
RefSeq (protein)
NP_001288035 NP_694585
n/a
Location (UCSC)
Chr 15: 92.47 – 92.5 Mb
n/a
PubMed search
[2]
n/a
Wikidata
View/Edit Human
Uncharacterized Protein C15orf32 is a protein which in humans is encoded by the C15orf32 gene and is located on chromosome 15, location 15q26.1.[3] Variants of C15orf32 have been linked to bipolar disorder,[4][5] alcohol use disorder,[6] and acute myeloid leukemia.[7]
^ abcGRCh38: Ensembl release 89: ENSG00000183643 – Ensembl, May 2017
^"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^Lee MT, Chen CH, Lee CS, Chen CC, Chong MY, Ouyang WC, et al. (May 2011). "Genome-wide association study of bipolar I disorder in the Han Chinese population". Molecular Psychiatry. 16 (5): 548–56. doi:10.1038/mp.2010.43. PMID 20386566.
^McAuley EZ, Scimone A, Tiwari Y, Agahi G, Mowry BJ, Holliday EG, et al. (2012-05-31). "Identification of sialyltransferase 8B as a generalized susceptibility gene for psychotic and mood disorders on chromosome 15q25-26". PLOS ONE. 7 (5): e38172. Bibcode:2012PLoSO...738172M. doi:10.1371/journal.pone.0038172. PMC 3364966. PMID 22693595.
^Heath AC, Whitfield JB, Martin NG, Pergadia ML, Goate AM, Lind PA, et al. (September 2011). "A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications". Biological Psychiatry. 70 (6): 513–8. doi:10.1016/j.biopsych.2011.02.028. PMC 3210694. PMID 21529783.
^Lv H, Zhang M, Shang Z, Li J, Zhang S, Lian D, Zhang R (January 2017). "Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia". Oncotarget. 8 (5): 7891–7899. doi:10.18632/oncotarget.13631. PMC 5352368. PMID 27903959.
and 2 Related for: Uncharacterized protein C15orf32 information
UncharacterizedProteinC15orf32 is a protein which in humans is encoded by the C15orf32 gene and is located on chromosome 15, location 15q26.1. Variants...
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