ANXA4 (GeneID: 307) | Homo sapiens
Description: annexin A4 [Source:HGNC Symbol;Acc:HGNC:542]
Synonyms: ZAP36, P4-X, ANX4, PIG28, P32.5, PAP-II, HEL-S-274
Other ID(s): HGNC:542, ENSG00000196975
Protein Accession Numbers: NP_001307629, ENST00000536030, NP_001352425, NP_001307627, ENST00000409920, NP_001307631, NP_001144, ENST00000394295
Statistics: ClinVar(6) gnomAD(269) COSMIC(243)
ClinVar Pathogenicity of Variations help

∙ 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.
ENST00000394295 You are here now! ENST00000409920 ENST00000536030 NP_001144 You are here now! NP_001307627 You are here now! NP_001307629 NP_001307631 NP_001352425 You are here now!


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
PF00191 Annexin Annexin 153-219 Homo sapiens
PF00191 Annexin Annexin 229-294 Homo sapiens
PF00191 Annexin Annexin 20-82 Homo sapiens
PF00191 Annexin Annexin 79-135 Homo sapiens

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Carcinoma Neoplasms ; 0.636 0.448
Renal Cell Carcinoma Neoplasms ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; 0.636 0.448
Leukemia, Myelocytic, Acute Neoplasms ; 0.636 0.448
Liver Cirrhosis, Experimental Digestive System Diseases ; 0.636 0.448
Liver neoplasms Neoplasms ; Digestive System Diseases ; 0.636 0.448
Animal Mammary Neoplasms Neoplasms ; Animal Diseases ; 0.636 0.448
Mammary Neoplasms, Experimental Neoplasms ; 0.636 0.448
Acute Myeloid Leukemia, M1 Neoplasms ; 0.636 0.448
Neoplasm Metastasis Neoplasms ; Pathological Conditions, Signs and Symptoms ; 0.636 0.448
Precancerous Conditions Neoplasms ; 0.636 0.448
Prostatic Neoplasms Neoplasms ; Male Urogenital Diseases ; 0.636 0.448
Anaplastic carcinoma Neoplasms ; 0.636 0.448
Carcinoma, Spindle-Cell Neoplasms ; 0.636 0.448
Undifferentiated carcinoma Neoplasms ; 0.636 0.448
Carcinomatosis Neoplasms ; 0.636 0.448
Conventional (Clear Cell) Renal Cell Carcinoma Neoplasms ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; 0.636 0.448
Condition, Preneoplastic Neoplasms ; 0.636 0.448
Malignant neoplasm of liver Neoplasms ; Digestive System Diseases ; 0.636 0.448
Malignant neoplasm of prostate Neoplasms ; Male Urogenital Diseases ; 0.636 0.448
Mammary Carcinoma, Animal Neoplasms ; Animal Diseases ; 0.636 0.448
Chromophobe Renal Cell Carcinoma Neoplasms ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; 0.636 0.448
Sarcomatoid Renal Cell Carcinoma Neoplasms ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; 0.636 0.448
Collecting Duct Carcinoma of the Kidney Neoplasms ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; 0.636 0.448
Papillary Renal Cell Carcinoma Neoplasms ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; 0.636 0.448
Acute Myeloid Leukemia (AML-M2) Neoplasms ; 0.636 0.448
Liver carcinoma Neoplasms ; Digestive System Diseases ; 0.636 0.448
NO RESULT FOUND
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