SLC2A4 (GeneID: 468443) | Pan troglodytes
Description: solute carrier family 2 member 4 [Source:HGNC Symbol;Acc:HGNC:11009]
Synonyms:
Other ID(s):
Protein Accession Numbers: XP_024205972
Statistics: ClinVar(2) gnomAD(492) COSMIC(143) PTM(6)
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.
ENST00000317370 You are here now! ENST00000424875 ENST00000570783 ENST00000571308 ENST00000572485 NP_001033 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
PF00083 Sugar_tr Sugar (and other) transporter 27-483 CL0015 MFS Homo sapiens

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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