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Aliases for FAM20C Gene

Aliases for FAM20C Gene

  • FAM20C, Golgi Associated Secretory Pathway Kinase 2 3 5
  • Dentin Matrix Protein 4 2 3 4
  • Golgi Casein Kinase 2 3 4
  • Family With Sequence Similarity 20, Member C 2 3
  • Golgi-Enriched Fraction Casein Kinase 3 4
  • GEF-CK 3 4
  • DMP-4 3 4
  • DMP4 3 4
  • Extracellular Serine/Threonine Protein Kinase FAM20C 3
  • EC 4
  • G-CK 3
  • RNS 3

External Ids for FAM20C Gene

Previous GeneCards Identifiers for FAM20C Gene

  • GC07U900326
  • GC07P000276
  • GC07P000289
  • GC07P000290

Summaries for FAM20C Gene

Entrez Gene Summary for FAM20C Gene

  • 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]

GeneCards Summary for FAM20C Gene

FAM20C (FAM20C, Golgi Associated Secretory Pathway Kinase) is a Protein Coding gene. Diseases associated with FAM20C include Raine Syndrome and Caffey Disease. Gene Ontology (GO) annotations related to this gene include calcium ion binding and protein serine/threonine kinase activity. An important paralog of this gene is FAM20A.

UniProtKB/Swiss-Prot for FAM20C Gene

  • Golgi serine/threonine protein kinase that phosphorylates secretory pathway proteins within Ser-x-Glu/pSer motifs and plays a key role in biomineralization of bones and teeth (PubMed:22582013, PubMed:23754375, PubMed:25789606). Constitutes the main protein kinase for extracellular proteins, generating the majority of the extracellular phosphoproteome (PubMed:26091039). Mainly phosphorylates proteins within the Ser-x-Glu/pSer motif, but also displays a broader substrate specificity (PubMed:26091039). Phosphorylates casein as well as a number of proteins involved in biomineralization such as AMELX, AMTN, ENAM and SPP1 (PubMed:22582013, PubMed:25789606). In addition to its role in biomineralization, also plays a role in lipid homeostasis, wound healing and cell migration and adhesion (PubMed:26091039).

Gene Wiki entry for FAM20C Gene

Additional gene information for FAM20C Gene

No data available for CIViC summary , Tocris Summary , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for FAM20C Gene

Genomics for FAM20C Gene

GeneHancer (GH) Regulatory Elements for FAM20C Gene

Promoters and enhancers for FAM20C Gene
GeneHancer (GH) Identifier GH Type GH
GH Sources Gene Association Score Total Score TSS distance (kb) Number of Genes Away Size (kb) Transcription Factor
Binding Sites
Gene Targets
GH07J000190 Promoter/Enhancer 2.3 EPDnew FANTOM5 Ensembl ENCODE 653.9 +0.6 553 5.4 PKNOX1 MLX ARID4B SIN3A GLI4 ZNF2 ZBTB7B ZNF48 YY1 GLIS2 FAM20C ENSG00000240093 WI2-2373I1.2 SUN1 DNAAF5 ENSG00000261795 LOC100507642
GH07J000148 Promoter/Enhancer 1.7 Ensembl ENCODE dbSUPER 12.1 -42.8 -42834 3.1 PKNOX1 SMAD1 ATF1 SIN3A ZNF2 ZNF48 YY1 POLR2B GLIS2 ZFP91 LOC100507642 ENSG00000242474 LOC102723672 ENSG00000261795 FAM20C ENSG00000240093 ENSG00000242611 GC07P000154 GC07M000141
GH07J000089 Enhancer 1.4 FANTOM5 Ensembl ENCODE dbSUPER 14.4 -102.5 -102465 3.5 HDGF CTCF KLF1 ZSCAN4 MAX MNT ZIC2 ZFHX2 POLR2A EGR1 ENSG00000242611 FAM20C ENSG00000232325 LOC101929756 GC07M000089
GH07J001022 Promoter/Enhancer 2.7 EPDnew FANTOM5 Ensembl ENCODE dbSUPER 5.1 +833.7 833695 7.4 HDGF CLOCK FOXA2 SMAD1 MLX ARNT ARID4B SIN3A DMAP1 YBX1 PIR42102 C7orf50 LOC105375120 LOC101927021 CYP2W1 ZFAND2A SUN1 COX19 INTS1 DNAAF5
GH07J000219 Enhancer 0.9 ENCODE 13.5 +27.1 27069 2.2 HDAC1 FOXA2 ZFP64 ARID4B SIN3A RAD21 ZNF48 ZSCAN9 RARA THAP11 FAM20C ENSG00000249852 ENSG00000240093
- Elite GeneHancer and/or Elite GeneHancer-gene association Download GeneHancer data from 2017 publication | Request up-to-date GeneHancer data (full dataset)

GeneHancers around FAM20C on UCSC Golden Path with GeneCards custom track

Top Transcription factor binding sites by QIAGEN in the FAM20C gene promoter:
  • HOXA3
  • Pax-5
  • Sox9
  • AREB6
  • LCR-F1
  • MEF-2A
  • aMEF-2
  • FAC1
  • Meis-1
  • Meis-1a

Genomic Locations for FAM20C Gene

Genomic Locations for FAM20C Gene
67,998 bases
Plus strand
107,743 bases
Plus strand

Genomic View for FAM20C Gene

Genes around FAM20C on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
FAM20C Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for FAM20C Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for FAM20C Gene

Proteins for FAM20C Gene

  • Protein details for FAM20C Gene (UniProtKB/Swiss-Prot)

    Protein Symbol:
    Recommended name:
    Extracellular serine/threonine protein kinase FAM20C
    Protein Accession:
    Secondary Accessions:
    • A4D2Q5
    • L8B5W8
    • Q5I0W9
    • Q7Z4I0
    • Q9NPT2

    Protein attributes for FAM20C Gene

    584 amino acids
    Molecular mass:
    66234 Da
    Name=Mn(2+); Xref=ChEBI:CHEBI:29035;
    Quaternary structure:
    • Interacts with FAM20A; probably forming a heterotetramer of 2 subunits of FAM20A and 2 subunits of FAM20C.
    • Sequence=AAH40074.1; Type=Erroneous initiation; Note=Translation N-terminally extended.; Evidence={ECO:0000305}; Sequence=EAL23705.1; Type=Erroneous initiation; Note=Translation N-terminally extended.; Evidence={ECO:0000305};

    Alternative splice isoforms for FAM20C Gene


neXtProt entry for FAM20C Gene

Post-translational modifications for FAM20C Gene

  • N-glycosylation is required for folding.
  • Autophosphorylated.
  • Glycosylation at Asn470, Asn335, Ser148, isoforms=101, Ser75, isoforms=74, isoforms=47, and isoforms=41
  • Modification sites at PhosphoSitePlus

Other Protein References for FAM20C Gene

No data available for DME Specific Peptides for FAM20C Gene

Domains & Families for FAM20C Gene

Gene Families for FAM20C Gene

Human Protein Atlas (HPA):
  • Disease related genes
  • Enzymes
  • Plasma proteins
  • Potential drug targets
  • Predicted secreted proteins

Protein Domains for FAM20C Gene

Suggested Antigen Peptide Sequences for FAM20C Gene

GenScript: Design optimal peptide antigens:

Graphical View of Domain Structure for InterPro Entry



  • Belongs to the FAM20 family.
  • Belongs to the FAM20 family.
genes like me logo Genes that share domains with FAM20C: view

Function for FAM20C Gene

Molecular function for FAM20C Gene

UniProtKB/Swiss-Prot Function:
Golgi serine/threonine protein kinase that phosphorylates secretory pathway proteins within Ser-x-Glu/pSer motifs and plays a key role in biomineralization of bones and teeth (PubMed:22582013, PubMed:23754375, PubMed:25789606). Constitutes the main protein kinase for extracellular proteins, generating the majority of the extracellular phosphoproteome (PubMed:26091039). Mainly phosphorylates proteins within the Ser-x-Glu/pSer motif, but also displays a broader substrate specificity (PubMed:26091039). Phosphorylates casein as well as a number of proteins involved in biomineralization such as AMELX, AMTN, ENAM and SPP1 (PubMed:22582013, PubMed:25789606). In addition to its role in biomineralization, also plays a role in lipid homeostasis, wound healing and cell migration and adhesion (PubMed:26091039).
UniProtKB/Swiss-Prot CatalyticActivity:
ATP + a protein = ADP + a phosphoprotein.
UniProtKB/Swiss-Prot EnzymeRegulation:
Serine/threonine protein kinase activity is increased upon interaction with FAM20A.
UniProtKB/Swiss-Prot BiophysicochemicalProperties:
Kinetic parameters: KM=0.8 uM for manganese/ATP {ECO:0000269 PubMed:23754375};

Enzyme Numbers (IUBMB) for FAM20C Gene

Phenotypes From GWAS Catalog for FAM20C Gene

Gene Ontology (GO) - Molecular Function for FAM20C Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0004674 protein serine/threonine kinase activity TAS --
GO:0005509 calcium ion binding IEA --
GO:0005515 protein binding IPI 22582013
GO:0005524 ATP binding IEA --
GO:0016301 kinase activity IEA --
genes like me logo Genes that share ontologies with FAM20C: view
genes like me logo Genes that share phenotypes with FAM20C: view

Human Phenotype Ontology for FAM20C Gene

HPO Id HPO Name Alternative Ids Definition Synonyms

Animal Models for FAM20C Gene

MGI Knock Outs for FAM20C:

Animal Model Products

  • Taconic Biosciences Mouse Models for FAM20C

miRNA for FAM20C Gene

miRTarBase miRNAs that target FAM20C

Clone Products

No data available for Transcription Factor Targets and HOMER Transcription for FAM20C Gene

Localization for FAM20C Gene

Subcellular locations from UniProtKB/Swiss-Prot for FAM20C Gene

Secreted. Golgi apparatus.

Subcellular locations from

Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
COMPARTMENTS Subcellular localization image for FAM20C gene
Compartment Confidence
extracellular 5
endoplasmic reticulum 5
golgi apparatus 5
nucleus 3
mitochondrion 2
cytosol 2

Subcellular locations from the

Human Protein Atlas (HPA)
  • Cytosol (2)
  • Golgi apparatus (2)
  • Nucleoplasm (2)
See all subcellular structures

Gene Ontology (GO) - Cellular Components for FAM20C Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005576 extracellular region IEA --
GO:0005615 extracellular space IEA,IDA 22582013
GO:0005737 cytoplasm IEA --
GO:0005788 endoplasmic reticulum lumen TAS --
GO:0005794 Golgi apparatus IEA,IDA 22582013
genes like me logo Genes that share ontologies with FAM20C: view

Pathways & Interactions for FAM20C Gene

SuperPathways for FAM20C Gene

No Data Available

Gene Ontology (GO) - Biological Process for FAM20C Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0001501 skeletal system development IEA --
GO:0006468 protein phosphorylation IDA,IEA 23754375
GO:0016310 phosphorylation IEA,IBA --
GO:0030501 positive regulation of bone mineralization IEA --
GO:0031214 biomineral tissue development IMP 22582013
genes like me logo Genes that share ontologies with FAM20C: view

No data available for Pathways by source and SIGNOR curated interactions for FAM20C Gene

Drugs & Compounds for FAM20C Gene

(1) Drugs for FAM20C Gene - From: HMDB

Name Status Disease Links Group Role Mechanism of Action Clinical Trials
calcium Approved Nutra 0
genes like me logo Genes that share compounds with FAM20C: view

Transcripts for FAM20C Gene

Unigene Clusters for FAM20C Gene

Family with sequence similarity 20, member C:
Representative Sequences:

Clone Products

Alternative Splicing Database (ASD) splice patterns (SP) for FAM20C Gene

ExUns: 1a · 1b ^ 2 ^ 3a · 3b ^ 4 ^ 5
SP1: - -
SP2: -
SP3: - - - -

Relevant External Links for FAM20C Gene

GeneLoc Exon Structure for
ECgene alternative splicing isoforms for

Expression for FAM20C Gene

mRNA expression in normal human tissues from GTEx, Illumina, BioGPS, and CGAP SAGE for FAM20C Gene

mRNA expression in embryonic tissues and stem cells from LifeMap Discovery

Protein differential expression in normal tissues from HIPED for FAM20C Gene

This gene is overexpressed in Serum (48.0) and Plasma (18.1).

Integrated Proteomics: protein expression in normal tissues and cell lines from ProteomicsDB and MOPED for FAM20C Gene

Protein tissue co-expression partners for FAM20C Gene

NURSA nuclear receptor signaling pathways regulating expression of FAM20C Gene:


SOURCE GeneReport for Unigene cluster for FAM20C Gene:


mRNA Expression by UniProt/SwissProt for FAM20C Gene:

Tissue specificity: Widely expressed.

Evidence on tissue expression from TISSUES for FAM20C Gene

  • Nervous system(4.6)
  • Liver(4.2)
  • Kidney(2.3)

Phenotype-based relationships between genes and organs from Gene ORGANizer for FAM20C Gene

Germ Layers:
  • ectoderm
  • endoderm
  • mesoderm
  • cardiovascular
  • digestive
  • immune
  • integumentary
  • nervous
  • respiratory
  • skeletal muscle
  • skeleton
Head and neck:
  • brain
  • cheek
  • chin
  • ear
  • eye
  • eyelid
  • face
  • head
  • jaw
  • lip
  • mandible
  • maxilla
  • mouth
  • neck
  • nose
  • outer ear
  • pharynx
  • skull
  • tongue
  • chest wall
  • clavicle
  • diaphragm
  • heart
  • lung
  • rib
  • rib cage
  • scapula
  • sternum
  • biliary tract
  • liver
  • pelvis
  • ankle
  • arm
  • digit
  • elbow
  • femur
  • fibula
  • finger
  • foot
  • forearm
  • hand
  • hip
  • humerus
  • knee
  • lower limb
  • radius
  • shin
  • shoulder
  • thigh
  • tibia
  • toe
  • ulna
  • upper limb
  • wrist
  • blood
  • red blood cell
  • skin
  • spinal column
  • vertebrae
  • white blood cell
genes like me logo Genes that share expression patterns with FAM20C: view

No data available for mRNA differential expression in normal tissues for FAM20C Gene

Orthologs for FAM20C Gene

This gene was present in the common ancestor of animals.

Orthologs for FAM20C Gene

Organism Taxonomy Gene Similarity Type Details
(Pan troglodytes)
Mammalia LOC740357 33
  • 98.81 (n)
FAM20C 34
  • 96 (a)
(Ornithorhynchus anatinus)
Mammalia -- 34
  • 90 (a)
-- 34
  • 66 (a)
(Canis familiaris)
Mammalia FAM20C 34 33
  • 87.84 (n)
(Bos Taurus)
Mammalia FAM20C 34 33
  • 86.97 (n)
(Mus musculus)
Mammalia Fam20c 16 34 33
  • 83.71 (n)
(Rattus norvegicus)
Mammalia Fam20c 33
  • 83.42 (n)
(Monodelphis domestica)
Mammalia FAM20C 34
  • 72 (a)
(Gallus gallus)
Aves FAM20C 34 33
  • 74.3 (n)
(Anolis carolinensis)
Reptilia FAM20C 34
  • 71 (a)
tropical clawed frog
(Silurana tropicalis)
Amphibia LOC100498448 33
  • 69.53 (n)
(Danio rerio)
Actinopterygii FAM20C (1 of 2) 34
  • 72 (a)
fam20cb 34 33
  • 69.67 (n)
fruit fly
(Drosophila melanogaster)
Insecta CG31145 34
  • 25 (a)
(Caenorhabditis elegans)
Secernentea H03A11.1 34
  • 35 (a)
Species where no ortholog for FAM20C was found in the sources mined by GeneCards:
  • A. gosspyii yeast (Ashbya gossypii)
  • Actinobacteria (Mycobacterium tuberculosis)
  • African clawed frog (Xenopus laevis)
  • African malaria mosquito (Anopheles gambiae)
  • Alicante grape (Vitis vinifera)
  • alpha proteobacteria (Wolbachia pipientis)
  • amoeba (Dictyostelium discoideum)
  • Archea (Pyrococcus horikoshii)
  • baker's yeast (Saccharomyces cerevisiae)
  • barley (Hordeum vulgare)
  • beta proteobacteria (Neisseria meningitidis)
  • bread mold (Neurospora crassa)
  • Chromalveolata (Phytophthora infestans)
  • common water flea (Daphnia pulex)
  • corn (Zea mays)
  • E. coli (Escherichia coli)
  • filamentous fungi (Aspergillus nidulans)
  • Firmicute bacteria (Streptococcus pneumoniae)
  • fission yeast (Schizosaccharomyces pombe)
  • green algae (Chlamydomonas reinhardtii)
  • honey bee (Apis mellifera)
  • K. lactis yeast (Kluyveromyces lactis)
  • loblloly pine (Pinus taeda)
  • malaria parasite (Plasmodium falciparum)
  • medicago trunc (Medicago Truncatula)
  • moss (Physcomitrella patens)
  • orangutan (Pongo pygmaeus)
  • pig (Sus scrofa)
  • rainbow trout (Oncorhynchus mykiss)
  • rice (Oryza sativa)
  • rice blast fungus (Magnaporthe grisea)
  • schistosome parasite (Schistosoma mansoni)
  • sea anemone (Nematostella vectensis)
  • sea squirt (Ciona intestinalis)
  • sea squirt (Ciona savignyi)
  • sea urchin (Strongylocentrotus purpuratus)
  • sorghum (Sorghum bicolor)
  • soybean (Glycine max)
  • stem rust fungus (Puccinia graminis)
  • sugarcane (Saccharum officinarum)
  • thale cress (Arabidopsis thaliana)
  • tomato (Lycopersicon esculentum)
  • toxoplasmosis (Toxoplasma gondii)
  • Trichoplax (Trichoplax adhaerens)
  • wheat (Triticum aestivum)

Evolution for FAM20C Gene

Gene Tree for FAM20C (if available)
Gene Tree for FAM20C (if available)
Evolutionary constrained regions (ECRs) for FAM20C: view image

Paralogs for FAM20C Gene

Paralogs for FAM20C Gene

(3) SIMAP similar genes for FAM20C Gene using alignment to 1 proteins:

genes like me logo Genes that share paralogs with FAM20C: view

Variants for FAM20C Gene

Sequence variations from dbSNP and Humsavar for FAM20C Gene

SNP ID Clin Chr 07 pos Variation AA Info Type
rs145750007 benign, likely-benign, not specified, not provided 259,906(+) G/A coding_sequence_variant, genic_downstream_transcript_variant, missense_variant, non_coding_transcript_variant
rs148276213 benign, likely-pathogenic, not specified, Raine syndrome 256,004(+) T/A coding_sequence_variant, genic_downstream_transcript_variant, missense_variant, non_coding_transcript_variant
rs150401144 benign, not specified, not provided 193,245(+) G/T coding_sequence_variant, genic_upstream_transcript_variant, missense_variant, non_coding_transcript_variant
rs267606795 pathogenic, Raine syndrome 255,869(+) G/C coding_sequence_variant, genic_downstream_transcript_variant, missense_variant, non_coding_transcript_variant
rs371584776 uncertain-significance, Raine syndrome 259,905(+) C/A/T coding_sequence_variant, genic_downstream_transcript_variant, non_coding_transcript_variant, stop_gained, synonymous_variant

Structural Variations from Database of Genomic Variants (DGV) for FAM20C Gene

Variant ID Type Subtype PubMed ID
dgv1083n67 CNV gain 20364138
dgv11094n54 CNV gain 21841781
dgv11095n54 CNV gain 21841781
dgv11096n54 CNV loss 21841781
dgv11097n54 CNV gain 21841781
dgv11098n54 CNV loss 21841781
dgv11099n54 CNV gain 21841781
dgv11100n54 CNV loss 21841781
dgv11101n54 CNV loss 21841781
dgv11102n54 CNV loss 21841781
dgv11103n54 CNV loss 21841781
dgv11104n54 CNV gain 21841781
dgv11105n54 CNV loss 21841781
dgv11106n54 CNV loss 21841781
dgv11107n54 CNV loss 21841781
dgv3458n106 CNV deletion 24896259
dgv3459n106 CNV deletion 24896259
dgv6213n100 CNV gain 25217958
dgv6220n100 CNV gain 25217958
esv1006722 CNV loss 20482838
esv1021366 CNV deletion 17803354
esv1274787 CNV deletion 17803354
esv1381494 CNV insertion 17803354
esv1554494 CNV deletion 17803354
esv1593047 CNV deletion 17803354
esv1607109 CNV deletion 17803354
esv1628554 CNV insertion 17803354
esv1714082 CNV deletion 17803354
esv2248874 CNV deletion 18987734
esv23573 CNV gain 19812545
esv23578 CNV gain+loss 19812545
esv24124 CNV loss 19812545
esv24248 CNV loss 19812545
esv2436771 CNV deletion 19546169
esv25065 CNV gain+loss 19812545
esv2541261 CNV deletion 19546169
esv2656552 CNV deletion 23128226
esv2659263 CNV deletion 23128226
esv2668014 CNV deletion 23128226
esv2676774 CNV deletion 23128226
esv27148 CNV loss 19812545
esv2759498 CNV gain+loss 17122850
esv3540977 CNV deletion 23714750
esv3540979 CNV deletion 23714750
esv3611747 CNV gain 21293372
esv3611754 CNV gain 21293372
esv3611760 CNV loss 21293372
esv3611761 CNV gain 21293372
esv3611762 CNV loss 21293372
esv3611763 CNV gain 21293372
esv3611764 CNV gain 21293372
esv3611765 CNV loss 21293372
esv3611766 CNV gain 21293372
esv3891006 CNV gain 25118596
esv988948 CNV deletion 20482838
nsv1017321 CNV gain 25217958
nsv1023966 CNV loss 25217958
nsv1026359 CNV gain 25217958
nsv1074045 CNV deletion 25765185
nsv1074457 CNV deletion 25765185
nsv1074458 CNV deletion 25765185
nsv1074459 CNV deletion 25765185
nsv1074986 CNV deletion 25765185
nsv1074987 CNV deletion 25765185
nsv1110806 CNV insertion 24896259
nsv1120539 CNV tandem duplication 24896259
nsv1126087 CNV deletion 24896259
nsv1126088 CNV deletion 24896259
nsv1132030 CNV deletion 24896259
nsv1132955 CNV insertion 24896259
nsv1133394 CNV tandem duplication 24896259
nsv1142479 CNV tandem duplication 24896259
nsv1143335 CNV deletion 24896259
nsv1143336 CNV deletion 24896259
nsv1144155 CNV deletion 24896259
nsv1152897 CNV deletion 26484159
nsv428159 CNV gain 18775914
nsv464242 CNV gain 19166990
nsv464243 CNV loss 19166990
nsv471171 CNV gain 18288195
nsv523285 CNV loss 19592680
nsv605597 CNV gain 21841781
nsv605598 CNV loss 21841781
nsv605618 CNV gain+loss 21841781
nsv605630 CNV loss 21841781
nsv605631 CNV gain 21841781
nsv605634 CNV gain 21841781
nsv605643 CNV loss 21841781
nsv605666 CNV loss 21841781
nsv605673 CNV loss 21841781
nsv605675 CNV loss 21841781
nsv605677 CNV loss 21841781
nsv605686 CNV loss 21841781
nsv605687 CNV loss 21841781
nsv823947 CNV gain 20364138
nsv823952 CNV loss 20364138
nsv823953 CNV loss 20364138
nsv830875 CNV gain 17160897
nsv957054 CNV deletion 24416366

Variation tolerance for FAM20C Gene

Gene Damage Index Score: 4.11; 61.21% of all genes are more intolerant (likely to be disease-causing)

Additional Variant Information for FAM20C Gene

Human Gene Mutation Database (HGMD)
SNPedia medical, phenotypic, and genealogical associations of SNPs for

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot for FAM20C Gene

Disorders for FAM20C Gene

MalaCards: The human disease database

(6) MalaCards diseases for FAM20C Gene - From: HGMD, OMIM, ClinVar, GTR, Orphanet, Swiss-Prot, DISEASES, and GeneCards

Disorder Aliases PubMed IDs
raine syndrome
  • rns
caffey disease
  • infantile cortical hyperostosis
amelogenesis imperfecta, type ig
  • ai1g
choanal atresia, posterior
  • pca
- elite association - COSMIC cancer census association via MalaCards


  • Raine syndrome (RNS) [MIM:259775]: Autosomal recessive osteosclerotic bone dysplasia with neonatal lethal outcome. Clinical features include generalized osteosclerosis, craniofacial dysplasia and microcephaly. {ECO:0000269 PubMed:17924334, ECO:0000269 PubMed:22582013, ECO:0000269 PubMed:25789606}. Note=The disease is caused by mutations affecting the gene represented in this entry.

Additional Disease Information for FAM20C

Genetic Association Database
Human Genome Epidemiology Navigator
ATLAS of Genetics and Cytogenetics in Oncology and Haematology
genes like me logo Genes that share disorders with FAM20C: view

No data available for Genatlas for FAM20C Gene

Publications for FAM20C Gene

  1. Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone development. (PMID: 17924334) Simpson MA … Crosby AH (American journal of human genetics 2007) 2 3 4 58
  2. FAM20: an evolutionarily conserved family of secreted proteins expressed in hematopoietic cells. (PMID: 15676076) Nalbant D … Williams SC (BMC genomics 2005) 3 4 22 58
  3. Family with sequence similarity member 20C is the primary but not the only kinase for the small-integrin-binding ligand N-linked glycoproteins in bone. (PMID: 26324849) Yang X … Wang X (FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2016) 2 3 58
  4. A secretory kinase complex regulates extracellular protein phosphorylation. (PMID: 25789606) Cui J … Dixon JE (eLife 2015) 3 4 58
  5. A Single Kinase Generates the Majority of the Secreted Phosphoproteome. (PMID: 26091039) Tagliabracci VS … Dixon JE (Cell 2015) 3 4 58

Products for FAM20C Gene

Sources for FAM20C Gene

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