Gene Gene information from NCBI Gene database.
Entrez ID 116173
Gene name CKLF like MARVEL transmembrane domain containing 5
Gene symbol CMTM5
Synonyms (NCBI Gene)
CKLFSF5
Chromosome 14
Chromosome location 14q11.2
Summary This gene encodes a member of the chemokine-like factor superfamily. This family of genes encodes multi-pass membrane proteins that are similar to both the chemokine and the transmembrane 4 superfamilies of signaling molecules. The encoded protein may exh
miRNA miRNA information provided by mirtarbase database.
18
miRTarBase ID miRNA Experiments Reference
MIRT1966726 hsa-miR-3690 CLIP-seq
MIRT1966727 hsa-miR-4254 CLIP-seq
MIRT1966728 hsa-miR-4786-3p CLIP-seq
MIRT1966729 hsa-miR-4793-5p CLIP-seq
MIRT2202474 hsa-miR-149 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
8
GO ID Ontology Definition Evidence Reference
GO:0005125 Function Cytokine activity IEA
GO:0005515 Function Protein binding IPI 21516116, 25416956, 25910212, 26871637, 29892012, 30614533, 31515488, 32296183
GO:0005615 Component Extracellular space IEA
GO:0006935 Process Chemotaxis IEA
GO:0007165 Process Signal transduction IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607888 19176 ENSG00000166091
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96DZ9
Protein name CKLF-like MARVEL transmembrane domain-containing protein 5 (Chemokine-like factor superfamily member 5)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01284 MARVEL 29 155 Membrane-associating domain Domain
Tissue specificity TISSUE SPECIFICITY: Highly expressed in the brain. {ECO:0000269|PubMed:12782130}.
Sequence
MLSARDRRDRHPEEGVVAELQGFAVDKAFLTSHKGILLETELALTLIIFICFTASISAYM
AAALLEFFITLAFLFLYATQYYQRFDRINWPCLLQGHGQSGGPHPLDLLSHSAKVQPQPW
PGLTPPGWHTPAAVPWVPAPAPGFWSWLLWFICFH
SLGSSDFLRCVSAIIIFLVVSFAAV
TSRDGAAIAAFVFGIILVSIFAYDAFKIYRTEMAPGASQGDQQ
Sequence length 223
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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
ALZHEIMER DISEASE 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 Neoplasms Breast neoplasm Pubtator 32568178, 33478201 Associate
★☆☆☆☆
Found in Text Mining only
Carcinogenesis Carcinogenesis Pubtator 21841490 Inhibit
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Hepatocellular carcinoma Pubtator 36975415 Associate
★☆☆☆☆
Found in Text Mining only
Carcinoma Ovarian Epithelial Epithelial ovarian carcinoma Pubtator 21841490 Inhibit
★☆☆☆☆
Found in Text Mining only
Cervix carcinoma Cervix carcinoma BEFREE 19124004
★☆☆☆☆
Found in Text Mining only
Conventional (Clear Cell) Renal Cell Carcinoma Renal Carcinoma BEFREE 28789377
★☆☆☆☆
Found in Text Mining only
Coronary Arteriosclerosis Coronary Arteriosclerosis BEFREE 28457985
★☆☆☆☆
Found in Text Mining only
Coronary Artery Disease Coronary artery disease BEFREE 28457985
★☆☆☆☆
Found in Text Mining only
Coronary heart disease Coronary Heart Disease BEFREE 28457985
★☆☆☆☆
Found in Text Mining only
leukemia Leukemia BEFREE 21168207
★☆☆☆☆
Found in Text Mining only