Gene Gene information from NCBI Gene database.
Entrez ID 119587
Gene name Carboxypeptidase X, M14 family member 2
Gene symbol CPXM2
Synonyms (NCBI Gene)
CPX2UNQ676
Chromosome 10
Chromosome location 10q26.13
miRNA miRNA information provided by mirtarbase database.
104
miRTarBase ID miRNA Experiments Reference
MIRT650450 hsa-miR-6819-3p HITS-CLIP 23824327
MIRT650449 hsa-miR-6877-3p HITS-CLIP 23824327
MIRT650448 hsa-miR-3183 HITS-CLIP 23824327
MIRT650447 hsa-miR-4723-3p HITS-CLIP 23824327
MIRT650446 hsa-miR-6769b-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
4
GO ID Ontology Definition Evidence Reference
GO:0004181 Function Metallocarboxypeptidase activity IEA
GO:0005576 Component Extracellular region IEA
GO:0006508 Process Proteolysis IEA
GO:0008270 Function Zinc ion binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617348 26977 ENSG00000121898
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8N436
Protein name Inactive carboxypeptidase-like protein X2
Protein function May be involved in cell-cell interactions.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00754 F5_F8_type_C 150 290 F5/8 type C domain Domain
PF00246 Peptidase_M14 324 632 Zinc carboxypeptidase Domain
PF13620 CarboxypepD_reg 643 719 Domain
Sequence
Sequence length 756
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
11
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
ATTENTION DEFICIT HYPERACTIVITY DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Breast ductal adenocarcinoma Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CENTRAL NERVOUS SYSTEM CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Clear cell carcinoma of kidney Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Alzheimer Disease Associate 27805002
★☆☆☆☆
Found in Text Mining only
Bone Diseases Developmental Associate 31364750
★☆☆☆☆
Found in Text Mining only
Carcinogenesis Associate 31364750, 31651348
★☆☆☆☆
Found in Text Mining only
Developmental Disabilities Associate 31651348
★☆☆☆☆
Found in Text Mining only
Lymphatic Metastasis Stimulate 31651348
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 31364750, 31651348
★☆☆☆☆
Found in Text Mining only
Osteosarcoma Associate 31651348
★☆☆☆☆
Found in Text Mining only
Personality Disorders Associate 30217166
★☆☆☆☆
Found in Text Mining only
Stomach Neoplasms Stimulate 31364750
★☆☆☆☆
Found in Text Mining only