Gene Gene information from NCBI Gene database.
Entrez ID 54757
Gene name FAM20A golgi associated secretory pathway pseudokinase
Gene symbol FAM20A
Synonyms (NCBI Gene)
AI1GAIGFSFP2747
Chromosome 17
Chromosome location 17q24.2
Summary This locus encodes a protein that is likely secreted and may function in hematopoiesis. A mutation at this locus has been associated with amelogenesis imperfecta and gingival hyperplasia syndrome. Alternatively spliced transcript variants have been identi
SNPs SNP information provided by dbSNP.
4
SNP ID Visualize variation Clinical significance Consequence
rs144411158 G>A,T Pathogenic 5 prime UTR variant, stop gained, coding sequence variant, synonymous variant, non coding transcript variant
rs587776911 AG>- Pathogenic 5 prime UTR variant, coding sequence variant, frameshift variant, genic upstream transcript variant, non coding transcript variant
rs587776914 T>C Pathogenic Splice acceptor variant
rs587777531 G>- Pathogenic Coding sequence variant, frameshift variant, non coding transcript variant
miRNA miRNA information provided by mirtarbase database.
236
miRTarBase ID miRNA Experiments Reference
MIRT983940 hsa-miR-1233 CLIP-seq
MIRT983941 hsa-miR-1303 CLIP-seq
MIRT983942 hsa-miR-3125 CLIP-seq
MIRT983943 hsa-miR-3150a-3p CLIP-seq
MIRT983944 hsa-miR-3150b-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
25
GO ID Ontology Definition Evidence Reference
GO:0001934 Process Positive regulation of protein phosphorylation IDA 25789606
GO:0001934 Process Positive regulation of protein phosphorylation ISS
GO:0004674 Function Protein serine/threonine kinase activity IDA 25789606
GO:0005515 Function Protein binding IPI 25789606
GO:0005576 Component Extracellular region IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
611062 23015 ENSG00000108950
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96MK3
Protein name Pseudokinase FAM20A
Protein function Pseudokinase that acts as an allosteric activator of the Golgi serine/threonine protein kinase FAM20C and is involved in biomineralization of teeth. Forms a complex with FAM20C and increases the ability of FAM20C to phosphorylate the proteins th
PDB 5WRR , 5WRS , 5YH2 , 5YH3
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF06702 Fam20C 305 522 Golgi casein kinase, C-terminal, Fam20 Family
Tissue specificity TISSUE SPECIFICITY: Highly expressed in lung and liver. Intermediate levels in thymus and ovary. {ECO:0000269|PubMed:15676076}.
Sequence
MPGLRRDRLLTLLLLGALLSADLYFHLWPQVQRQLRPRERPRGCPCTGRASSLARDSAAA
ASDPGTIVHNFSRTEPRTEPAGGSHSGSSSKLQALFAHPLYNVPEEPPLLGAEDSLLASQ
EALRYYRRKVARWNRRHKMYREQMNLTSLDPPLQLRLEASWVQFHLGINRHGLYSRSSPV
VSKLLQDMRHFPTISADYSQDEKALLGACDCTQIVKPSGVHLKLVLRFSDFGKAMFKPMR
QQRDEETPVDFFYFIDFQRHNAEIAAFHLDRILDFRRVPPTVGRIVNVTKEILEVTKNEI
LQSVFFVSPASNVCFFAKCPYMCKTEYAVCGNPHLLEGSLSAFLPSLNLAPRLSVPNPWI
RSYTLAGKEEWEVNPLYCDTVKQIYPYNNSQRLLNVIDMAIFDFLIGNMDRHHYEMFTKF
GDDGFLIHLDNARGFGRHSHDEISILSPLSQCCMIKKKTLLHLQLLAQADYRLSDVMRES
LLEDQLSPVLTEPHLLALDRRLQTILRTVEGCIVAHGQQSVI
VDGPVEQLAPDSGQANLT
S
Sequence length 541
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)
Post-translational protein phosphorylation
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
28
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Amelogenesis imperfecta type 1G Pathogenic; Likely pathogenic rs760163489, rs2143965549, rs766926330, rs746063338, rs587777530, rs139620139, rs587777531, rs2143495812, rs149970399, rs2143526006, rs762205955, rs2509578283, rs1156573190, rs762905130, rs2509578117
View all (10 more)
RCV001535979
RCV001640790
RCV001783238
RCV005014741
RCV000128612
View all (20 more)
★★★★★
ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
Acute myeloid leukemia Benign; Likely benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AMELOGENESIS IMPERFECTA Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AMELOGENESIS IMPERFECTA NEPHROCALCINOSIS Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AMELOGENESIS IMPERFECTA, TYPE IG CTD, HPO
CTD, HPO
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Amelogenesis Imperfecta Amelogenesis imperfecta Pubtator 21549343, 23434854, 25636655, 30120606, 36351670, 38546520 Associate
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Amelogenesis Imperfecta Amelogenesis imperfecta BEFREE 23434854, 24259279, 25636655, 25827751, 27281036, 28432788, 29439260, 31667691
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Amelogenesis Imperfecta Amelogenesis imperfecta HPO_DG
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Amelogenesis imperfecta local hypoplastic form Amelogenesis Imperfecta BEFREE 21990045
★☆☆☆☆
Found in Text Mining only
Amelogenesis imperfecta local hypoplastic form Amelogenesis imperfecta Pubtator 30120606, 36351670 Associate
★☆☆☆☆
Found in Text Mining only
Amelogenesis imperfecta nephrocalcinosis Amelogenesis Imperfecta UNIPROT_DG 21549343, 21990045, 23434854, 23468644, 23697977, 24196488, 24259279, 24756937, 25636655, 25789606, 25827751
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Amelogenesis imperfecta nephrocalcinosis Amelogenesis Imperfecta GENOMICS_ENGLAND_DG 22732358, 25827751
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Amelogenesis imperfecta nephrocalcinosis Amelogenesis Imperfecta BEFREE 23434854, 23468644, 24196488, 24259279, 24927635, 28298625, 30394349, 31131889
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Amelogenesis imperfecta nephrocalcinosis Amelogenesis Imperfecta ORPHANET_DG 23434854
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Amelogenesis imperfecta nephrocalcinosis Amelogenesis Imperfecta CLINVAR_DG
★★☆☆☆
Found in Text Mining + Unknown/Other Associations