FAM13C

Family with sequence similarity 13, member C is a protein that in humans is encoded by the FAM13C gene.

FAM13C
Identifiers
Aliases	FAM13C, FAM13C1, family with sequence similarity 13 member C
External IDs	MGI: 1918971; HomoloGene: 11490; GeneCards: FAM13C; OMA:FAM13C - orthologs
Gene location (Human) Chr. Chromosome 10 (human) Band 10q21.1 Start 59,246,130 bp End 59,363,181 bp
Gene location (Mouse) Chr. Chromosome 10 (mouse) Band 10|10 B5.3 Start 70,276,311 bp End 70,394,566 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in corpus callosum inferior ganglion of vagus nerve subthalamic nucleus medulla oblongata pons internal globus pallidus superior vestibular nucleus C1 segment endothelial cell pars reticulata Top expressed in lateral septal nucleus mammillary body anterior amygdaloid area ventromedial nucleus lateral hypothalamus supraoptic nucleus secondary oocyte deep cerebellar nuclei medial vestibular nucleus subiculum More reference expression data BioGPS n/a
Orthologs Species Human Mouse Entrez 220965 71721 Ensembl ENSG00000148541 ENSMUSG00000043259 UniProt Q8NE31 Q9DBR2 RefSeq (mRNA) NM_001001971 NM_001143773 NM_001166698 NM_001347840 NM_001347842 NM_001347843 NM_001347844 NM_001347845 NM_001347846 NM_001347847 NM_001347848 NM_001347849 NM_001347850 NM_001347851 NM_001347852 NM_198215 NM_001143776 NM_001143777 NM_024244 NM_001359551 RefSeq (protein) NP_001001971 NP_001137245 NP_001160170 NP_001334769 NP_001334771 NP_001334772 NP_001334773 NP_001334774 NP_001334775 NP_001334776 NP_001334777 NP_001334778 NP_001334779 NP_001334780 NP_001334781 NP_937858 NP_001137248 NP_001137249 NP_077206 NP_001346480 Location (UCSC) Chr 10: 59.25 – 59.36 Mb Chr 10: 70.28 – 70.39 Mb PubMed search
Wikidata
View/Edit Human View/Edit Mouse

Further reading

• Wu JH, Lemaitre RN, Manichaikul A, Guan W, Tanaka T, Foy M, Kabagambe EK, Djousse L, Siscovick D, Fretts AM, Johnson C, King IB, Psaty BM, McKnight B, Rich SS, Chen YD, Nettleton JA, Tang W, Bandinelli S, Jacobs DR, Browning BL, Laurie CC, Gu X, Tsai MY, Steffen LM, Ferrucci L, Fornage M, Mozaffarian D (April 2013). "Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium". Circulation: Cardiovascular Genetics. 6 (2): 171–83. doi:10.1161/CIRCGENETICS.112.964619. PMC 3891054. PMID 23362303.
• Karasik D, Hsu YH, Zhou Y, Cupples LA, Kiel DP, Demissie S (July 2010). "Genome-wide pleiotropy of osteoporosis-related phenotypes: the Framingham Study". Journal of Bone and Mineral Research. 25 (7): 1555–63. doi:10.1002/jbmr.38. PMC 3153998. PMID 20200953.