SLC2A4 (GeneID: 6517) | Homo sapiens
Description: solute carrier family 2 member 4 [Source:HGNC Symbol;Acc:HGNC:11009]
Synonyms: GLUT4
Other ID(s): HGNC:11009, ENSG00000181856
Protein Accession Numbers: ENST00000570783, ENST00000317370, ENST00000572485, ENST00000424875, ENST00000571308, ENST00000317370.8, NP_001033
Statistics: gnomAD(424) COSMIC(103)
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.
ENST00000317370 ENST00000424875 ENST00000570783 ENST00000571308 ENST00000572485 NP_001033


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
Alloxan Diabetes Nutritional and Metabolic Diseases ; Endocrine System Diseases ; 0.564 0.586
Alzheimer's Disease Nervous System Diseases ; Mental Disorders ; 0.564 0.586
Presenile dementia Nervous System Diseases ; Mental Disorders ; 0.564 0.586
Diabetes Mellitus, Experimental Nutritional and Metabolic Diseases ; Endocrine System Diseases ; 0.564 0.586
Diabetes Mellitus, Non-Insulin-Dependent Nutritional and Metabolic Diseases ; Endocrine System Diseases ; 0.564 0.586
Cardiomegaly Cardiovascular Diseases ; Pathological Conditions, Signs and Symptoms ; 0.564 0.586
Insulin Resistance Nutritional and Metabolic Diseases ; 0.564 0.586
Streptozotocin Diabetes Nutritional and Metabolic Diseases ; Endocrine System Diseases ; 0.564 0.586
Familial Alzheimer Disease (FAD) Nervous System Diseases ; Mental Disorders ; 0.564 0.586
Alzheimer Disease, Late Onset Nervous System Diseases ; Mental Disorders ; 0.564 0.586
Acute Confusional Senile Dementia Nervous System Diseases ; Mental Disorders ; 0.564 0.586
Alzheimer's Disease, Focal Onset Nervous System Diseases ; Mental Disorders ; 0.564 0.586
Alzheimer Disease, Early Onset Nervous System Diseases ; Mental Disorders ; 0.564 0.586
Insulin Sensitivity Nutritional and Metabolic Diseases ; 0.564 0.586
Cardiac Hypertrophy Cardiovascular Diseases ; Pathological Conditions, Signs and Symptoms ; 0.564 0.586
INSULIN RESISTANCE, SUSCEPTIBILITY TO N/A 0.564 0.586
DIABETES MELLITUS, TYPE 2, PROTECTION AGAINST N/A 0.564 0.586
NO RESULT FOUND
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