FAM13C

Protein-coding gene in the species Homo sapiens
FAM13C
Identifiers
AliasesFAM13C, FAM13C1, family with sequence similarity 13 member C
External IDsMGI: 1918971; HomoloGene: 11490; GeneCards: FAM13C; OMA:FAM13C - orthologs
Gene location (Human)
Chromosome 10 (human)
Chr.Chromosome 10 (human)[1]
Chromosome 10 (human)
Genomic location for FAM13C
Genomic location for FAM13C
Band10q21.1Start59,246,130 bp[1]
End59,363,181 bp[1]
Gene location (Mouse)
Chromosome 10 (mouse)
Chr.Chromosome 10 (mouse)[2]
Chromosome 10 (mouse)
Genomic location for FAM13C
Genomic location for FAM13C
Band10|10 B5.3Start70,276,311 bp[2]
End70,394,566 bp[2]
RNA expression pattern
Bgee
HumanMouse (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
SpeciesHumanMouse
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 MbChr 10: 70.28 – 70.39 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Family with sequence similarity 13, member C is a protein that in humans is encoded by the FAM13C gene.[5]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000148541 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000043259 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: Family with sequence similarity 13, member C".

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.


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