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Gene : FAM20C Homo sapiens

Name  ? FAM20C golgi associated secretory pathway kinase Cytological Location  7p22.3
Brief Description  FAM20C, golgi associated secretory pathway kinase
description  This gene encodes a member of the family of secreted protein kinases. The encoded protein binds calcium and phosphorylates proteins involved in bone mineralization. Mutations in this gene are associated with the autosomal recessive disorder Raine syndrome. [provided by RefSeq, Apr 2014]
  • synonyms:
  • FAM20C, golgi associated secretory pathway kinase,
  • family with sequence similarity 20, member C,
  • golgi casein kinase,
  • DMP-4,
  • FAM20C,
  • BC040074,
  • GEF-CK,
  • DMP4,
  • HGNC:22140,
  • RNS,
  • G-CK,
  • G-CK,
  • NM_020223,
  • dentin matrix protein 4,
  • OTTHUMG00000151401,
  • DMP4,
  • IMAGE:4942737,
  • DKFZp547D065,
  • uc003sip.4
  • identifiers:
  • 56975,
  • ENSG00000177706,
  • FAM20C

Genome feature

Region: gene ? Length: 67836  
Location: 7:192939-260774 Cyto location: 7p22.3

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Gene Report --> GWAS hit


1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Mouse Gene --> Allele [Phenotype]


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Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



76 SN Ps

5 Cross References

16 Data Sets

8 Homologues

0 Located Features

90 Rna Seq Results