Gene Gene information from NCBI Gene database.
Entrez ID 56265
Gene name Carboxypeptidase X, M14 family member 1
Gene symbol CPXM1
Synonyms (NCBI Gene)
CPX1CPXM
Chromosome 20
Chromosome location 20p13
Summary This gene likely encodes a member of the carboxypeptidase family of proteins. Cloning of a comparable locus in mouse indicates that the encoded protein contains a discoidin domain and a carboxypeptidase domain, but the protein appears to lack residues nec
miRNA miRNA information provided by mirtarbase database.
6
miRTarBase ID miRNA Experiments Reference
MIRT907810 hsa-miR-1236 CLIP-seq
MIRT907811 hsa-miR-1247 CLIP-seq
MIRT907812 hsa-miR-3127-3p CLIP-seq
MIRT907813 hsa-miR-3183 CLIP-seq
MIRT907814 hsa-miR-4684-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
11
GO ID Ontology Definition Evidence Reference
GO:0004180 Function Carboxypeptidase activity IEA
GO:0004181 Function Metallocarboxypeptidase activity IEA
GO:0005576 Component Extracellular region IEA
GO:0005615 Component Extracellular space IBA
GO:0005615 Component Extracellular space IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
609555 15771 ENSG00000088882
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96SM3
Protein name Probable carboxypeptidase X1 (EC 3.4.17.-) (Metallocarboxypeptidase CPX-1)
Protein function May be involved in cell-cell interactions. No carboxypeptidase activity was found yet (By similarity).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00754 F5_F8_type_C 130 271 F5/8 type C domain Domain
PF00246 Peptidase_M14 305 613 Zinc carboxypeptidase Domain
PF13620 CarboxypepD_reg 624 701 Domain
Sequence
Sequence length 734
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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)
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
EBV-positive nodal T- and NK-cell lymphoma Likely benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MAJOR DEPRESSIVE DISORDER GWAS catalog
★★☆☆☆
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
Breast Carcinoma Breast Carcinoma BEFREE 30072699
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Breast neoplasm Pubtator 27993161, 30072699, 33499882 Associate
★☆☆☆☆
Found in Text Mining only
Leiomyoma Leiomyoma Pubtator 36948524 Associate
★☆☆☆☆
Found in Text Mining only
Leukemia Leukemia Pubtator 32078680 Associate
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of breast Breast Cancer BEFREE 30072699
★☆☆☆☆
Found in Text Mining only
Melanoma Melanoma Pubtator 36224027 Associate
★☆☆☆☆
Found in Text Mining only
Myelodysplastic Syndromes Myelodysplastic syndrome Pubtator 32078680 Associate
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 30072699
★☆☆☆☆
Found in Text Mining only
Scleroderma Systemic Systemic sclerosis Pubtator 33253093 Stimulate
★☆☆☆☆
Found in Text Mining only
Thyroid Cancer Papillary Papillary thyroid cancer Pubtator 30072699 Associate
★☆☆☆☆
Found in Text Mining only