VOPP1 (GeneID: 81552) | Homo sapiens
Description: VOPP1, WBP1/VOPP1 family member [Source:HGNC Symbol;Acc:HGNC:34518]
Synonyms: ECOP, GASP
Other ID(s): HGNC:34518, ENSG00000154978
Protein Accession Numbers: ENST00000453256, NP_001308172, NP_110423, ENST00000417399, ENST00000433959, NP_001271212, NP_001308178, ENST00000427700, ENST00000455023, NP_001308175, ENST00000453112, NP_001308171, NP_001308180, ENST00000414113, ENST00000428648, NP_001271211, NP_001308177, ENST00000418904, ENST00000454227, NP_001308173, ENST00000452832, NP_001271213, NP_001308179, ENST00000285279, ENST00000428097, ENST00000545390, NP_001308176
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.
ENST00000285279 ENST00000414113 ENST00000417399 ENST00000418904 ENST00000427700 ENST00000428097 ENST00000428648 ENST00000433959 ENST00000452832 ENST00000453112 ENST00000453256 ENST00000454227 ENST00000455023 ENST00000545390 NP_001271211 NP_001271212 NP_001271213 NP_001308171 NP_001308172 NP_001308173 NP_001308175 NP_001308176 You are here now! NP_001308177 NP_001308178 NP_001308179


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
NO DOMAINS EXIST

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 ; 0.815 0.138
Liver Cirrhosis, Experimental Digestive System Diseases ; 0.815 0.138
Acute Myeloid Leukemia, M1 Neoplasms ; 0.815 0.138
Acute Myeloid Leukemia (AML-M2) Neoplasms ; 0.815 0.138
NO RESULT FOUND
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