Gene Gene information from NCBI Gene database.
Entrez ID 2996
Gene name Glycophorin E (MNS blood group)
Gene symbol GYPE
Synonyms (NCBI Gene)
GPEGYPAMNSMiIX
Chromosome 4
Chromosome location 4q31.21
Summary The protein encoded by this gene is a sialoglycoprotein and a type I membrane protein. It is a member of a gene family with GPA and GPB genes. This encoded protein might carry the M blood group antigen. GYPA, GYPB, and GYPE are organized in tandem on chro
miRNA miRNA information provided by mirtarbase database.
48
miRTarBase ID miRNA Experiments Reference
MIRT1038905 hsa-miR-142-5p CLIP-seq
MIRT1038906 hsa-miR-340 CLIP-seq
MIRT1038907 hsa-miR-4481 CLIP-seq
MIRT1038908 hsa-miR-4658 CLIP-seq
MIRT1038909 hsa-miR-4745-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
3
GO ID Ontology Definition Evidence Reference
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane TAS 2295603, 7622054
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
138590 4705 ENSG00000197465
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P15421
Protein name Glycophorin-E
Protein function This protein is a minor sialoglycoprotein in human erythrocyte membranes.
Family and domains
Tissue specificity TISSUE SPECIFICITY: Erythrocytes.
Sequence
MYGKIIFVLLLSGIVSISASSTTGVAMHTSTSSSVTKSYISSQTNGITLINWWAMARVIF
EVMLVVVGMIILISYCIR
Sequence length 78
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
11
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Chronic lymphocytic leukemia/small lymphocytic lymphoma Benign rs1132785 RCV005898266
Colorectal cancer Benign rs1132785 RCV005898264
Familial cancer of breast Benign rs1132785, rs146400730 RCV005898257
RCV005905025
Familial pancreatic carcinoma Benign rs1132785 RCV005898262
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Huntington Disease Associate 11905993
Respiratory Distress Syndrome Associate 34898369
Rett Syndrome Associate 24419315