C9orf78

Uncharacterized protein C9orf78 is a protein that in humans is encoded by the C9orf78 gene.^[5][6][7]

C9orf78
Identifiers
Aliases	C9orf78, HCA59, HSPC220, bA409K20.3, chromosome 9 open reading frame 78, CSU2, TLS1
External IDs	MGI: 2385132; HomoloGene: 9551; GeneCards: C9orf78; OMA:C9orf78 - orthologs
Gene location (Human) Chr. Chromosome 9 (human)[1] Band 9q34.11 Start 129,827,290 bp[1] End 129,835,863 bp[1]
Gene location (Mouse) Chr. Chromosome 2 (mouse)[2] Band 2|2 B Start 30,862,189 bp[2] End 30,872,213 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in monocyte Achilles tendon C1 segment gastrocnemius muscle anterior cingulate cortex tibial arteries Descending thoracic aorta gonad stromal cell of endometrium gastric mucosa Top expressed in neural layer of retina dentate gyrus of hippocampal formation granule cell cerebellum hypothalamus olfactory bulb tail of embryo cerebellar cortex granulocyte ovary superior frontal gyrus More reference expression data BioGPS More reference expression data
Gene ontology Molecular function protein binding Cellular component nucleoplasm cytosol nucleus spliceosomal complex Biological process regulation of mRNA splicing, via spliceosome Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 51759 227707 Ensembl ENSG00000136819 ENSMUSG00000026851 UniProt Q9NZ63 Q3TQI7 RefSeq (mRNA) NM_016520 NM_144885 RefSeq (protein) NP_057604 NP_659134 Location (UCSC) Chr 9: 129.83 – 129.84 Mb Chr 2: 30.86 – 30.87 Mb PubMed search [3] [4]
Wikidata
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