Gene Gene information from NCBI Gene database.
Entrez ID 161198
Gene name C-type lectin domain containing 14A
Gene symbol CLEC14A
Synonyms (NCBI Gene)
C14orf27CEG1EGFR-5
Chromosome 14
Chromosome location 14q21.1
Summary This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signalling, glycoprotein turnover, and roles
miRNA miRNA information provided by mirtarbase database.
166
miRTarBase ID miRNA Experiments Reference
MIRT018973 hsa-miR-335-5p Microarray 18185580
MIRT607877 hsa-miR-8485 HITS-CLIP 22927820
MIRT607876 hsa-miR-329-3p HITS-CLIP 22927820
MIRT607875 hsa-miR-362-3p HITS-CLIP 22927820
MIRT607874 hsa-miR-603 HITS-CLIP 22927820
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
19
GO ID Ontology Definition Evidence Reference
GO:0001946 Process Lymphangiogenesis IEA
GO:0002040 Process Sprouting angiogenesis IEA
GO:0002042 Process Cell migration involved in sprouting angiogenesis IEA
GO:0005515 Function Protein binding IPI 27991863, 32296183
GO:0009897 Component External side of plasma membrane IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616845 19832 ENSG00000176435
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q86T13
Protein name C-type lectin domain family 14 member A (Epidermal growth factor receptor 5) (EGFR-5)
Family and domains
Sequence
MRPAFALCLLWQALWPGPGGGEHPTADRAGCSASGACYSLHHATMKRQAAEEACILRGGA
LSTVRAGAELRAVLALLRAGPGPGGGSKDLLFWVALERRRSHCTLENEPLRGFSWLSSDP
GGLESDTLQWVEEPQRSCTARRCAVLQATGGVEPAGWKEMRCHLRANGYLCKYQFEVLCP
APRPGAASNLSYRAPFQLHSAALDFSPPGTEVSALCRGQLPISVTCIADEIGARWDKLSG
DVLCPCPGRYLRAGKCAELPNCLDDLGGFACECATGFELGKDGRSCVTSGEGQPTLGGTG
VPTRRPPATATSPVPQRTWPIRVDEKLGETPLVPEQDNSVTSIPEIPRWGSQSTMSTLQM
SLQAESKATITPSGSVISKFNSTTSSATPQAFDSSSAVVFIFVSTAVVVLVILTMTVLGL
VKLCFHESPSSQPRKESMGPPGLESDPEPAALGSSSAHCTNNGVKVGDCDLRDRAEGALL
AESPLGSSDA
Sequence length 490
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
8
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
CENTRAL NERVOUS SYSTEM CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
COLOR VISION DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CORONARY VASOSPASM GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DIABETES MELLITUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Brain Diseases Associate 35641310
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Associate 18446232
★☆☆☆☆
Found in Text Mining only
CADASIL Associate 35641310
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Associate 35576868
★☆☆☆☆
Found in Text Mining only
Carcinoma Renal Cell Associate 33761933
★☆☆☆☆
Found in Text Mining only
Carcinosarcoma Associate 28088687
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 28088687, 28878328, 35576868
★☆☆☆☆
Found in Text Mining only
Prostatic Neoplasms Associate 21694441
★☆☆☆☆
Found in Text Mining only
Stroke Associate 35641310
★☆☆☆☆
Found in Text Mining only