IGF2R (GeneID: 703220) | Macaca mulatta
Description: insulin like growth factor 2 receptor [Source:NCBI gene;Acc:703220]
Synonyms:
Other ID(s): ENSMMUG00000015658
Protein Accession Numbers: XP_014993117
Statistics: ClinVar(25) PTM(68)
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.
ENST00000356956 ENST00000475834 NP_000867 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
PF00040 fn2 Fibronectin type II domain 1903-1942 CL0602 Kringle Homo sapiens
PF00878 CIMR Cation-independent mannose-6-phosphate receptor repeat 1031-1178 CL0226 M6PR Homo sapiens
PF00878 CIMR Cation-independent mannose-6-phosphate receptor repeat 423-573 CL0226 M6PR Homo sapiens
PF00878 CIMR Cation-independent mannose-6-phosphate receptor repeat 1322-1462 CL0226 M6PR Homo sapiens
PF00878 CIMR Cation-independent mannose-6-phosphate receptor repeat 575-716 CL0226 M6PR Homo sapiens
PF00878 CIMR Cation-independent mannose-6-phosphate receptor repeat 720-876 CL0226 M6PR Homo sapiens
PF00878 CIMR Cation-independent mannose-6-phosphate receptor repeat 1465-1599 CL0226 M6PR Homo sapiens
PF00878 CIMR Cation-independent mannose-6-phosphate receptor repeat 1603-1750 CL0226 M6PR Homo sapiens
PF00878 CIMR Cation-independent mannose-6-phosphate receptor repeat 1946-2083 CL0226 M6PR Homo sapiens
PF00878 CIMR Cation-independent mannose-6-phosphate receptor repeat 277-421 CL0226 M6PR Homo sapiens
PF00878 CIMR Cation-independent mannose-6-phosphate receptor repeat 1755-1894 CL0226 M6PR Homo sapiens
PF00878 CIMR Cation-independent mannose-6-phosphate receptor repeat 123-270 CL0226 M6PR Homo sapiens
PF00878 CIMR Cation-independent mannose-6-phosphate receptor repeat 1179-1320 CL0226 M6PR Homo sapiens
PF00878 CIMR Cation-independent mannose-6-phosphate receptor repeat 882-1026 CL0226 M6PR Homo sapiens
PF00878 CIMR Cation-independent mannose-6-phosphate receptor repeat 2085-2233 CL0226 M6PR Homo sapiens
PF00878 CIMR Cation-independent mannose-6-phosphate receptor repeat 2237-2290 CL0226 M6PR Homo sapiens

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Alzheimer's Disease Nervous System Diseases ; Mental Disorders ; 0.545 0.655
Presenile dementia Nervous System Diseases ; Mental Disorders ; 0.545 0.655
Liver Cirrhosis, Experimental Digestive System Diseases ; 0.545 0.655
Lung diseases Respiratory Tract Diseases ; 0.545 0.655
Parkinson Disease Nervous System Diseases ; 0.545 0.655
Prostatic Neoplasms Neoplasms ; Male Urogenital Diseases ; 0.545 0.655
Congenital diaphragmatic hernia Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Pathological Conditions, Signs and Symptoms ; 0.545 0.655
Congenital hernia of foramen of Morgagni Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Pathological Conditions, Signs and Symptoms ; 0.545 0.655
Congenital hernia of foramen of Bochdalek Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Pathological Conditions, Signs and Symptoms ; 0.545 0.655
Familial Alzheimer Disease (FAD) Nervous System Diseases ; Mental Disorders ; 0.545 0.655
Malignant neoplasm of prostate Neoplasms ; Male Urogenital Diseases ; 0.545 0.655
Alzheimer Disease, Late Onset Nervous System Diseases ; Mental Disorders ; 0.545 0.655
Acute Confusional Senile Dementia Nervous System Diseases ; Mental Disorders ; 0.545 0.655
Alzheimer's Disease, Focal Onset Nervous System Diseases ; Mental Disorders ; 0.545 0.655
Alzheimer Disease, Early Onset Nervous System Diseases ; Mental Disorders ; 0.545 0.655
Lewy Body Disease Nervous System Diseases ; Mental Disorders ; 0.545 0.655
Liver carcinoma Neoplasms ; Digestive System Diseases ; 0.545 0.655
NO RESULT FOUND
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