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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 Show/Hide all (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 Show/Hide all (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 Show/Hide all (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 Pathway Reactome Pathway
Glycerolipid metabolism Glycerophospholipid biosynthesis
Metabolic pathways Signaling by BRAF and RAF fusions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
22
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
Show/Hide Causal Diseases (6)
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
AGK-related disorder Pathogenic rs2485391716, rs765471424 RCV003492749
RCV004541541
★★★★★
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Autosomal recessive AGK-related phenotype Likely pathogenic; Pathogenic rs766413410 RCV000984913
★★★★★
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
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
View all (17 more)
★★★★★
★★★★★
ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)
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
View all (34 more)
★★★★★
★★★★★
ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)
Thyroid cancer, nonmedullary, 1 Pathogenic rs2485379466 RCV005934933
★★★★★
★★★★☆
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.
Show/Hide Unknown Diseases (16)
Phenotype Name Clinical Significance Source Reference Evidence Score
CATARACT AND CARDIOMYOPATHY — CTD, Disgenet
CTD, Disgenet
23266196
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CHRONIC KIDNEY DISEASE — GWAS catalog 40465716
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CONGENITAL CATARACT — Disgenet —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CONGENITAL CATARACT-HYPERTROPHIC CARDIOMYOPATHY-MITOCHONDRIAL MYOPATHY SYNDROME — Orphanet 22284826
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CONGENITAL TOTAL CATARACT — Disgenet —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Show/Hide Text Mining Associations (61)
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome 3-Methylglutaconic Aciduria With Sensorineural Deafness, Encephalopathy And Leigh-Like Syndrome BEFREE 25595726
★★★★★
★☆☆☆☆
Found in Text Mining only
Acidosis Lactic Lactic acidosis Pubtator 28712726, 33476211, 36253788 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Breast Carcinoma Breast Carcinoma BEFREE 23676499, 24886245
★★★★★
★☆☆☆☆
Found in Text Mining only
Carcinoma Ovarian Epithelial Epithelial ovarian carcinoma Pubtator 35934718 Stimulate
★★★★★
★☆☆☆☆
Found in Text Mining only
Carcinoma Renal Cell Renal cell carcinoma Pubtator 31900208, 37009826 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Cardiomyopathies Cardiomyopathy BEFREE 22284826
★★★★★
★☆☆☆☆
Found in Text Mining only
Cardiomyopathies Cardiomyopathy Pubtator 22284826, 34948281 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Cardiomyopathy Hypertrophic Hypertrophic cardiomyopathy Pubtator 28712724, 28712726, 33120694, 33476211 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Cataract Cataract Pubtator 22284826, 28712724, 28712726, 33120694, 33476211, 34948281, 36253788 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Cataract Cataract BEFREE 22415731, 28712724
★★★★★
★☆☆☆☆
Found in Text Mining only