Gene Gene information from NCBI Gene database.
Entrez ID 55750
Gene name Acylglycerol kinase
Gene symbol AGK
Synonyms (NCBI Gene)
CATC5CTRCT38MTDPS10MULK
Chromosome 7
Chromosome location 7q34
Summary The protein encoded by this gene is a mitochondrial membrane protein involved in lipid and glycerolipid metabolism. The encoded protein is a lipid kinase that catalyzes the formation of phosphatidic and lysophosphatidic acids. Defects in this gene have be
SNPs SNP information provided by dbSNP.
19
SNP ID Visualize variation Clinical significance Consequence
rs35269563 A>G Conflicting-interpretations-of-pathogenicity Missense variant, coding sequence variant
rs142069429 C>T Conflicting-interpretations-of-pathogenicity, uncertain-significance Genic downstream transcript variant, coding sequence variant, missense variant
rs387907024 C>T Pathogenic Coding sequence variant, stop gained
rs387907025 C>T Pathogenic Coding sequence variant, stop gained
rs542547163 G>A Pathogenic Genic downstream transcript variant, intron variant
miRNA miRNA information provided by mirtarbase database.
266
miRTarBase ID miRNA Experiments Reference
MIRT025890 hsa-miR-7-5p Microarray 19073608
MIRT031554 hsa-miR-16-5p Proteomics 18668040
MIRT043923 hsa-miR-378a-3p CLASH 23622248
MIRT042001 hsa-miR-484 CLASH 23622248
MIRT529306 hsa-miR-3691-3p PAR-CLIP 22012620
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
38
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0001727 Function Lipid kinase activity IEA
GO:0001729 Function Ceramide kinase activity IBA
GO:0001729 Function Ceramide kinase activity IEA
GO:0004143 Function ATP-dependent diacylglycerol kinase activity IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610345 21869 ENSG00000006530
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q53H12
Protein name Acylglycerol kinase, mitochondrial (hAGK) (EC 2.7.1.107) (EC 2.7.1.138) (EC 2.7.1.94) (Multiple substrate lipid kinase) (HsMuLK) (MuLK) (Multi-substrate lipid kinase)
Protein function Lipid kinase that can phosphorylate both monoacylglycerol and diacylglycerol to form lysophosphatidic acid (LPA) and phosphatidic acid (PA), respectively (PubMed:15939762). Does not phosphorylate sphingosine (PubMed:15939762). Phosphorylates cer
PDB 7CGP
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00781 DAGK_cat 62 195 Diacylglycerol kinase catalytic domain Family
Tissue specificity TISSUE SPECIFICITY: Highly expressed in muscle, heart, kidney and brain. {ECO:0000269|PubMed:15939762}.
Sequence
MTVFFKTLRNHWKKTTAGLCLLTWGGHWLYGKHCDNLLRRAACQEAQVFGNQLIPPNAQV
KKATVFLNPAACKGKARTLFEKNAAPILHLSGMDVTIVKTDYEGQAKKLLELMENTDVII
VAGGDGTLQEVVTGVLRRTDEATFSKIPIGFIPLGETSSLSHTLFAESGNKVQHITDATL
AIVKGETVPLDVLQI
KGEKEQPVFAMTGLRWGSFRDAGVKVSKYWYLGPLKIKAAHFFST
LKEWPQTHQASISYTGPTERPPNEPEETPVQRPSLYRRILRRLASYWAQPQDALSQEVSP
EVWKDVQLSTIELSITTRNNQLDPTSKEDFLNICIEPDTISKGDFITIGSRKVRNPKLHV
EGTECLQASQCTLLIPEGAGGSFSIDSEEYEAMPVEVKLLPRKLQFFCDPRKREQMLTSP
TQ
Sequence length 422
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Glycerolipid metabolism
Metabolic pathways
  Glycerophospholipid biosynthesis
Signaling by BRAF and RAF fusions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
572
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
AGK-related disorder Pathogenic rs2485391716, rs765471424 RCV003492749
RCV004541541
Autosomal recessive AGK-related phenotype Likely pathogenic; Pathogenic rs766413410 RCV000984913
Cataract 38 Pathogenic; Likely pathogenic rs1259937492, rs2116998520, rs1199705359, rs773677513, rs746709222, rs766413410, rs2485410329, rs2485501462, rs2485465829, rs2485410335, rs886041491, rs2485379262, rs139967538, rs2485379466, rs2485387302
View all (7 more)
RCV001382409
RCV001933190
RCV002044696
RCV003091648
RCV001852539
RCV000024610
RCV002847437
RCV002862667
RCV003059184
RCV003048475
RCV003765578
RCV003779486
RCV003785050
RCV003804110
RCV003817962
RCV005222702
RCV002527087
RCV005208714
RCV000696618
RCV003769020
RCV005213456
RCV005213511
Sengers syndrome Pathogenic; Likely pathogenic rs778049466, rs1259937492, rs2116998520, rs1199705359, rs2485391716, rs773677513, rs746709222, rs766413410, rs2485410329, rs2485501462, rs863223895, rs2485465829, rs2485410335, rs886041491, rs368565785
View all (23 more)
RCV001336431
RCV001382409
RCV001933190
RCV002044696
RCV002283348
RCV003091648
RCV000191059
RCV000191058
RCV002847437
RCV002862667
RCV000023811
RCV003059184
RCV003048475
RCV003765578
RCV003330156
RCV003779486
RCV003785050
RCV003804110
RCV003817962
RCV000023808
RCV000023809
RCV000023810
RCV000023812
RCV000023813
RCV000023814
RCV000023815
RCV000023816
RCV002527087
RCV000538499
RCV000578375
RCV000578454
RCV000696618
RCV000787336
RCV000985092
RCV000991387
RCV002471037
RCV001095709
RCV001268954
RCV001268953
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Developmental cataract Uncertain significance; Likely benign; Conflicting classifications of pathogenicity rs886062017, rs560194759, rs886062029, rs886062018, rs143849281, rs148553992, rs552726046, rs886062021, rs142235678, rs886062023, rs886062028, rs886062030 RCV000364867
RCV000376499
RCV000349405
RCV000266812
RCV000376564
RCV000312506
RCV000324959
RCV000404456
RCV000273641
RCV000272328
RCV000268303
RCV000402583
Familial cancer of breast Likely benign rs371220594 RCV005928694
Gastric cancer Uncertain significance rs1410173365 RCV005926791
Mitochondrial disease Conflicting classifications of pathogenicity rs367844999, rs561898521 RCV005359887
RCV005367734
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Acidosis Lactic Associate 28712726, 33476211, 36253788
Adenocarcinoma of Lung Associate 31747139
Carcinoma Ovarian Epithelial Stimulate 35934718
Carcinoma Renal Cell Associate 31900208, 37009826
Cardiomyopathies Associate 22284826, 34948281
Cardiomyopathy Hypertrophic Associate 28712724, 28712726, 33120694, 33476211
Cataract Associate 22284826, 28712724, 28712726, 33120694, 33476211, 34948281, 36253788
Cataract and cardiomyopathy Associate 22284826, 28712724, 28712726, 33120694, 33476211, 34948281, 36253788, 39824030
Death Associate 34948281
Dilatation Pathologic Associate 34948281