Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
9125
Gene name Gene Name - the full gene name approved by the HGNC.
CCR4-NOT transcription complex subunit 9
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CNOT9
Synonyms (NCBI Gene) Gene synonyms aliases
CAF40, CT129, RCD-1, RCD1, RQCD1
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q35
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the highly conserved RCD1 protein family. The encoded protein is a transcriptional cofactor and a core protein of the CCR4-NOT complex. It may be involved in signal transduction as well as retinoic acid-regulated cell differe
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs267599211 C>T Likely-pathogenic Coding sequence variant, intron variant, missense variant
rs1057519955 C>T Likely-pathogenic Missense variant, coding sequence variant, intron variant
rs1057519956 T>C Likely-pathogenic Missense variant, coding sequence variant, non coding transcript variant
rs1057519957 C>G Likely-pathogenic Missense variant, coding sequence variant, non coding transcript variant
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000289 Process Nuclear-transcribed mRNA poly(A) tail shortening TAS
GO:0000932 Component P-body IBA 21873635
GO:0000932 Component P-body ISS
GO:0005154 Function Epidermal growth factor receptor binding IPI 20878056
GO:0005515 Function Protein binding IPI 18180299, 20878056, 24768540
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
612054 10445 ENSG00000144580
Protein
UniProt ID Q92600
Protein name CCR4-NOT transcription complex subunit 9 (Cell differentiation protein RQCD1 homolog) (Rcd-1)
Protein function Component of the CCR4-NOT complex which is one of the major cellular mRNA deadenylases and is linked to various cellular processes including bulk mRNA degradation, miRNA-mediated repression, translational repression during translational initiati
PDB 2FV2 , 4CRU , 4CRV , 4CT6 , 4CT7 , 5LSW , 5ONA , 5ONB , 6HOM , 6HON , 9FL8
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04078 Rcd1 25 283 Family
Tissue specificity TISSUE SPECIFICITY: Detected in spleen, thymus, prostate, testis, ovary and intestine. {ECO:0000269|PubMed:9447985}.
Sequence
Sequence length 299
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  RNA degradation   Deadenylation of mRNA
TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Gastric cancer Gastric Adenocarcinoma rs137854571, rs63751108, rs34612342, rs121908383, rs121909144, rs121909775, rs121909219, rs121909223, rs63750871, rs80359530, rs121964873, rs121913530, rs606231203, rs121918505, rs587776802
View all (244 more)
26619011
Melanoma Cutaneous Melanoma rs121913315, rs121913323, rs137853080, rs137853081, rs121909232, rs121913388, rs104894094, rs104894095, rs104894097, rs104894098, rs104894099, rs104894109, rs137854599, rs11547328, rs104894340
View all (64 more)
26619011
Associations from Text Mining
Disease Name Relationship Type References
Developmental Disabilities Associate 37092538
Diabetes Mellitus Type 2 Associate 31797865
Epilepsy Associate 37092538
Facial Dysmorphism with Multiple Malformations Associate 37092538
Hutchinson's Melanotic Freckle Associate 25544760
Intellectual Disability Associate 37092538
Melanoma Associate 25544760
Melanoma Cutaneous Malignant Associate 25544760
Mental Disorders Associate 37092538
Muscle Hypotonia Associate 37092538