CREBBP (GeneID: 1387) | Homo sapiens
Description: CREB binding protein [Source:HGNC Symbol;Acc:HGNC:2348]
Synonyms: RSTS1, CBP, RSTS, KAT3A
Other ID(s): HGNC:2348, ENSG00000005339
Protein Accession Numbers: ENST00000262367, NP_004371, ENST00000572134, ENST00000382070, NP_001073315, ENST00000571826, ENST00000262367.5, ENST00000573517, ENST00000570939
Statistics:

∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000262367 ENST00000382070 ENST00000570939 ENST00000571826 ENST00000572134 ENST00000573517 NP_001073315 NP_004371


import_contactsClinVar Data
Variation ID filter_list Allele ID filter_list RS Number filter_list Variant Type filter_list Record filter_list Alteration filter_list Clinicial Sig. filter_list Last Update filter_list Phenotypes filter_list Cytogenetic filter_list Review Status filter_list RCV Acc.N. filter_list

healinggnomAD
Variant ID filter_list Transcript ID filter_list Alteration filter_list Annotation filter_list Allele C. filter_list Allele N. filter_list Allele F. filter_list rsNumber filter_list Flagsfilter_list Filter filter_list

placePost-translational Modifications (PTMs)
Gene Name filter_list ACC ID filter_list PTM Type filter_list Position filter_list Mod-rsd filter_list Site +/-7 Aa filter_list Mw_kd filter_list Site grpID filter_list

blur_onCatalogue of Somatic Mutations in Cancer (COSMIC)
Gene Name filter_list Transcript ID filter_list Sample name filter_list Primary Site filter_list Primary Histology filter_list Mutation ID filter_list Mutation CDS filter_list Mutation Aa filter_list Mutation Desc. filter_list FATHMM Prediction filter_list FATHMM Score filter_list Mutation Somatic Status filter_list PUBMED PMID filter_list Tumor Origin filter_list Position filter_list

chrome_reader_modedbSNP
Gene ID filter_list Transcript ID filter_list Consequence filter_list Position filter_list HGVSp filter_list Impact filter_list

format_align_centerProtein Domains (PFAM)
Pfam Domain filter_list Domain Name filter_list Description filter_list Positions filter_list Clan filter_list Clan Name filter_list Organism filter_list
NO RESULT FOUND
PF00439 Bromodomain Bromodomain 1095-1181 Mus musculus
PF00569 ZZ Zinc finger, ZZ type 1702-1743 CL0006 C1 Mus musculus
PF02135 zf-TAZ TAZ zinc finger 353-429 Mus musculus
PF02135 zf-TAZ TAZ zinc finger 1773-1844 Mus musculus
PF02172 KIX KIX domain 586-666 CL0589 KIX_like Mus musculus
PF06001 DUF902 Domain of Unknown Function (DUF902) 1193-1232 Mus musculus
PF08214 HAT_KAT11 Histone acetylation protein 1343-1651 CL0257 Acetyltrans Mus musculus
PF09030 Creb_binding Creb binding 2014-2115 Mus musculus

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Bipolar Disorder Mental Disorders ; 0.451 0.862
Malignant neoplasm of urinary bladder Neoplasms ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; 0.451 0.862
Bladder Neoplasm Neoplasms ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; 0.451 0.862
Squamous cell carcinoma Neoplasms ; 0.451 0.862
Carcinoma, Transitional Cell Neoplasms ; 0.451 0.862
Adenoid Cystic Carcinoma Neoplasms ; 0.451 0.862
Endogenous depression Mental Disorders ; 0.451 0.862
Leukemia, Myelocytic, Acute Neoplasms ; 0.451 0.862
Lymphoma, Follicular Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.451 0.862
Lymphoma, Non-Hodgkin Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.451 0.862
Osteogenesis Imperfecta Musculoskeletal Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Skin and Connective Tissue Diseases ; 0.451 0.862
Prostatic Neoplasms Neoplasms ; Male Urogenital Diseases ; 0.451 0.862
Rubinstein-Taybi Syndrome Musculoskeletal Diseases ; Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.451 0.862
Schizophrenia Mental Disorders ; 0.451 0.862
Sezary Syndrome Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.451 0.862
Diffuse Large B-Cell Lymphoma Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.451 0.862
Lymphoma, Large-Cell, Follicular Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.451 0.862
Lymphoma, Mixed-Cell, Follicular Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.451 0.862
Lymphoma, Small Cleaved-Cell, Follicular Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.451 0.862
Small cell carcinoma of lung Neoplasms ; Respiratory Tract Diseases ; 0.451 0.862
Adenocarcinoma of lung (disorder) Neoplasms ; Respiratory Tract Diseases ; 0.451 0.862
Squamous cell carcinoma of esophagus Neoplasms ; Digestive System Diseases ; 0.451 0.862
Malignant neoplasm of prostate Neoplasms ; Male Urogenital Diseases ; 0.451 0.862
Primary microcephaly N/A 0.451 0.862
AMYOTROPHIC LATERAL SCLEROSIS 1 Nervous System Diseases ; Nutritional and Metabolic Diseases ; 0.451 0.862
Amyotrophic Lateral Sclerosis, Sporadic Nervous System Diseases ; Nutritional and Metabolic Diseases ; 0.451 0.862
CHROMOSOME 16p13.3 DELETION SYNDROME, PROXIMAL N/A 0.451 0.862
Lymphoma, Follicular, Grade 1 Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.451 0.862
Lymphoma, Follicular, Grade 3 Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.451 0.862
Lymphoma, Follicular, Grade 2 Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.451 0.862
Precursor Cell Lymphoblastic Leukemia Lymphoma Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.451 0.862
Intellectual Disability Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; Mental Disorders ; 0.451 0.862
Radial club hand N/A 0.451 0.862
Acute myeloid leukemia with t(8;16)(p11;p13) translocation N/A 0.451 0.862
NO RESULT FOUND
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