Gene Gene information from NCBI Gene database.
Entrez ID 84871
Gene name AGBL carboxypeptidase 4
Gene symbol AGBL4
Synonyms (NCBI Gene)
CCP6
Chromosome 1
Chromosome location 1p33
miRNA miRNA information provided by mirtarbase database.
48
miRTarBase ID miRNA Experiments Reference
MIRT771678 hsa-miR-1238 CLIP-seq
MIRT771679 hsa-miR-1254 CLIP-seq
MIRT771680 hsa-miR-1290 CLIP-seq
MIRT771681 hsa-miR-1825 CLIP-seq
MIRT771682 hsa-miR-3116 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
40
GO ID Ontology Definition Evidence Reference
GO:0004180 Function Carboxypeptidase activity IEA
GO:0004181 Function Metallocarboxypeptidase activity IBA
GO:0004181 Function Metallocarboxypeptidase activity IEA
GO:0004181 Function Metallocarboxypeptidase activity ISS
GO:0005737 Component Cytoplasm IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616476 25892 ENSG00000186094
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q5VU57
Protein name Cytosolic carboxypeptidase 6 (EC 3.4.17.24) (ATP/GTP-binding protein-like 4) (Protein deglutamylase CCP6)
Protein function Metallocarboxypeptidase that mediates protein deglutamylation of tubulin and non-tubulin target proteins. Catalyzes the removal of polyglutamate side chains present on the gamma-carboxyl group of glutamate residues within the C-terminal tail of
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF18027 Pepdidase_M14_N 46 166 Cytosolic carboxypeptidase N-terminal domain Domain
PF00246 Peptidase_M14 174 439 Zinc carboxypeptidase Domain
Sequence
Sequence length 503
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
14
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
AGBL4-related disorder Benign; Likely benign rs60977321, rs3934240, rs138271641, rs770755809, rs80256865, rs373001734, rs764055566, rs897258395, rs75333004, rs41289226 RCV003973814
RCV003977320
RCV003952188
RCV003961798
RCV003917122
RCV003939395
RCV003932051
RCV003969386
RCV003976535
RCV003981331
Lung cancer Benign rs75333004 RCV005935185
Ovarian serous cystadenocarcinoma Benign rs75333004 RCV005935183
Thymoma Benign rs75333004 RCV005935184
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Carcinoma Renal Cell Inhibit 26993597
Cerebral Infarction Associate 37370144
Glioblastoma Associate 35295612
Macular Degeneration Associate 23365078
Necrosis Associate 17293598
Triglyceride Storage Disease Type I Associate 27853278