Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
312
Gene name Gene Name - the full gene name approved by the HGNC.
Annexin A13
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ANXA13
Synonyms (NCBI Gene) Gene synonyms aliases
ANX13, ISA
Chromosome Chromosome number
8
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
8q24.13
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the annexin family. Members of this calcium-dependent phospholipid-binding protein family play a role in the regulation of cellular growth and in signal transduction pathways. The specific function of this gene has not yet be
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT786408 hsa-miR-1 CLIP-seq
MIRT786409 hsa-miR-105 CLIP-seq
MIRT786410 hsa-miR-1227 CLIP-seq
MIRT786411 hsa-miR-206 CLIP-seq
MIRT786412 hsa-miR-3673 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001786 Function Phosphatidylserine binding IDA 27676605
GO:0005509 Function Calcium ion binding IBA 21873635
GO:0005509 Function Calcium ion binding IDA 27676605
GO:0005544 Function Calcium-dependent phospholipid binding IDA 27676605
GO:0005615 Component Extracellular space HDA 22664934
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602573 536 ENSG00000104537
Protein
UniProt ID P27216
Protein name Annexin A13 (Annexin XIII) (Annexin-13) (Intestine-specific annexin) (ISA)
Protein function [Isoform A]: Binds to membranes enriched in phosphatidylserine or phosphatidylglycerol in a calcium-dependent manner (PubMed:27676605, PubMed:30610115). Half-maximal membrane binding requires about 60 uM calcium. Does not bind to membranes that
PDB 6B3I
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00191 Annexin 18 83 Annexin Family
PF00191 Annexin 90 155 Annexin Family
PF00191 Annexin 173 239 Annexin Family
PF00191 Annexin 249 314 Annexin Family
Tissue specificity TISSUE SPECIFICITY: Detected in epithelial cells in colon and jejunum (at protein level). Detected in epithelial cells in jejunum. {ECO:0000269|PubMed:1530946}.
Sequence
Sequence length 316
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Breast carcinoma Breast Carcinoma rs80359671, rs11540652, rs28934575, rs28897672, rs137886232, rs193922376, rs80357783, rs80359306, rs80359405, rs80359507, rs80359598, rs80358429, rs397507683, rs397515636, rs80359451
View all (71 more)
29059683
Unknown
Disease term Disease name Evidence References Source
Breast Cancer Breast Cancer Importantly, breast cancer patients bearing PRC2 LOF mutations displayed significantly worse prognosis compared with PRC2 wild-type patients GWAS, CBGDA
Associations from Text Mining
Disease Name Relationship Type References
Carcinoma Pancreatic Ductal Associate 26644413
Carcinoma Renal Cell Associate 37464398
Cholangiocarcinoma Associate 26644413
Colorectal Neoplasms Associate 28423508
Glomerulosclerosis Focal Segmental Associate 34675284
Lupus Nephritis Associate 26110394
Lymphatic Metastasis Associate 28423508
Neoplasm Metastasis Associate 28423508
Neoplasms Associate 28423508