ANXA5 (GeneID: 308) | Homo sapiens
Description: annexin A5 [Source:HGNC Symbol;Acc:HGNC:543]
Synonyms: PP4, ANX5, HEL-S-7, RPRGL3, ENX2
Other ID(s): HGNC:543, ENSG00000164111
Protein Accession Numbers: ENST00000515017, ENST00000501272, ENST00000513728, ENST00000296511, NP_001145, ENST00000506395
Statistics: gnomAD(174) COSMIC(144)
gnomAD Variants By Annotation

∙ 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.
ENST00000296511 ENST00000501272 ENST00000506395 ENST00000513728 ENST00000515017 NP_001145


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 17-82 Mus musculus
PF00191 Annexin Annexin 248-313 Mus musculus
PF00191 Annexin Annexin 89-154 Mus musculus
PF00191 Annexin Annexin 172-238 Mus musculus

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Squamous cell carcinoma Neoplasms ; 0.49 0.69
Hepatolenticular Degeneration Digestive System Diseases ; Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Nutritional and Metabolic Diseases ; 0.49 0.69
Leukemia, Myelocytic, Acute Neoplasms ; 0.49 0.69
Liver Cirrhosis, Experimental Digestive System Diseases ; 0.49 0.69
Malignant neoplasm of stomach Neoplasms ; Digestive System Diseases ; 0.49 0.69
Mouth Neoplasms Neoplasms ; Stomatognathic Diseases ; 0.49 0.69
Acute Myeloid Leukemia, M1 Neoplasms ; 0.49 0.69
Pre-Eclampsia Female Urogenital Diseases and Pregnancy Complications ; 0.49 0.69
Stomach Neoplasms Neoplasms ; Digestive System Diseases ; 0.49 0.69
Weight Gain Pathological Conditions, Signs and Symptoms ; 0.49 0.69
Adenocarcinoma of lung (disorder) Neoplasms ; Respiratory Tract Diseases ; 0.49 0.69
Malignant neoplasm of mouth Neoplasms ; Stomatognathic Diseases ; 0.49 0.69
Hepatic Form of Wilson Disease Digestive System Diseases ; Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Nutritional and Metabolic Diseases ; 0.49 0.69
Hereditary Diffuse Gastric Cancer Neoplasms ; Digestive System Diseases ; 0.49 0.69
Acute Myeloid Leukemia (AML-M2) Neoplasms ; 0.49 0.69
PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 3 N/A 0.49 0.69
NO RESULT FOUND
feedback