CEBPD (GeneID: 464163) | Pan troglodytes
Description: CCAAT enhancer binding protein delta [Source:VGNC Symbol;Acc:VGNC:12001]
Synonyms:
Other ID(s): ENSPTRG00000042020
Protein Accession Numbers: XP_003951307
Statistics: gnomAD(257) COSMIC(32) PTM(7)
Post translational modifications (PTM) by Type
14%71%14%10010090908080707060605050404030302020101000
Acetylation
Phosphorylation
Sumoylation
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∙ 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.
ENST00000408965 You are here now! NP_005186 You are here now!


import_contactsClinVar Data

healinggnomAD
64%33%10010090908080707060605050404030302020101000
Frameshift Variant
Inframe Deletion
Inframe Insertion
Missense Variant
Stop Gained
Synonymous Variant
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placePost-translational Modifications (PTMs)
14%71%14%10010090908080707060605050404030302020101000
Acetylation
Phosphorylation
Sumoylation
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blur_onCatalogue of Somatic Mutations in Cancer (COSMIC)
3%3%41%44%9%10010090908080707060605050404030302020101000
Deletion - Frameshift
Deletion - In Frame
Substitution - Coding Silent
Substitution - Missense
Unknown
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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
PF07716 bZIP_2 Basic region leucine zipper 190-243 CL0018 bZIP Homo sapiens

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Leukemia, Myelocytic, Acute Neoplasms ; 0.6 0.69
Liver Cirrhosis, Experimental Digestive System Diseases ; 0.6 0.69
Acute Myeloid Leukemia, M1 Neoplasms ; 0.6 0.69
Prolactinoma Neoplasms ; Nervous System Diseases ; Endocrine System Diseases ; 0.6 0.69
Myocardial Ischemia Cardiovascular Diseases ; 0.6 0.69
Microprolactinoma Neoplasms ; Nervous System Diseases ; Endocrine System Diseases ; 0.6 0.69
Macroprolactinoma Neoplasms ; Nervous System Diseases ; Endocrine System Diseases ; 0.6 0.69
Acute Myeloid Leukemia (AML-M2) Neoplasms ; 0.6 0.69
Liver carcinoma Neoplasms ; Digestive System Diseases ; 0.6 0.69
NO RESULT FOUND
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