Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
79879
Gene name Gene Name - the full gene name approved by the HGNC.
Coiled-coil domain containing 134
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CCDC134
Synonyms (NCBI Gene) Gene synonyms aliases
OI22
Disease Acronyms (UniProt) Disease acronyms from UniProt database
OI22
Chromosome Chromosome number
22
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
22q13.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT023784 hsa-miR-1-3p Proteomics 18668040
MIRT032346 hsa-let-7b-5p Proteomics 18668040
MIRT650062 hsa-miR-500b-3p HITS-CLIP 23824327
MIRT650061 hsa-miR-4267 HITS-CLIP 23824327
MIRT650060 hsa-miR-6515-3p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001525 Process Angiogenesis IEA
GO:0001890 Process Placenta development IEA
GO:0005515 Function Protein binding IPI 22644376, 32296183
GO:0005576 Component Extracellular region IEA
GO:0005634 Component Nucleus IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
618788 26185 ENSG00000100147
Protein
UniProt ID Q9H6E4
Protein name Coiled-coil domain-containing protein 134
Protein function Molecular adapter required to prevent protein hyperglycosylation of HSP90B1: during translation, associates with nascent HSP90B1 and the STT3A catalytic component of the OST-A complex and tethers them to a specialized translocon that forms a mic
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15002 ERK-JNK_inhib 22 223 ERK and JNK pathways, inhibitor Family
Tissue specificity TISSUE SPECIFICITY: Expressed in cervical gland, cervical squamous epithelium, endometrium, stomach, kidney distal convoluted tubule, spermatogenic cells in testis, mammary gland, liver and striated muscle (at protein level) (PubMed:18087676, PubMed:23070
Sequence
Sequence length 229
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Alzheimer disease Alzheimer`s Disease rs63750215, rs28936379, rs63749851, rs63749884, rs28936380, rs63750048, rs63750579, rs63750264, rs63749964, rs63750671, rs281865161, rs63750066, rs63750399, rs63750734, rs63751039
View all (65 more)
21123754
Breast carcinoma Breast Carcinoma rs80359671, rs11540652, rs28934575, rs28897672, rs137886232, rs193922376, rs80357783, rs80359306, rs80359405, rs80359507, rs80359598, rs80358429, rs397507683, rs397515636, rs80359451
View all (71 more)
29059683
Unknown
Disease term Disease name Evidence References Source
Osteogenesis Imperfecta osteogenesis imperfecta, osteogenesis imperfecta, IIA 22 GenCC
Breast Cancer Breast Cancer Importantly, breast cancer patients bearing PRC2 LOF mutations displayed significantly worse prognosis compared with PRC2 wild-type patients GWAS, CBGDA
Carpal Tunnel Syndrome Carpal Tunnel Syndrome GWAS
Associations from Text Mining
Disease Name Relationship Type References
Alzheimer Disease Associate 31500627
Bone Diseases Associate 32181939
Growth Disorders Associate 32181939
Neoplasms Associate 18087676
Osteogenesis Imperfecta Associate 32181939
Osteogenesis imperfecta type 3 Associate 32181939
Osteoporosis pseudoglioma syndrome Associate 32181939
Pseudarthrosis Associate 32181939