IGF2 (GeneID: 742381) | Pan troglodytes
Description: insulin like growth factor 2 [Source:NCBI gene;Acc:742381]
Synonyms:
Other ID(s): ENSPTRG00000047625
Protein Accession Numbers: XP_016775671, XP_016775668, XP_016775670, XP_016775667, XP_024202671, XP_016775669, XP_016775666
Statistics:

∙ 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.
ENST00000300632 ENST00000381389 ENST00000381392 ENST00000381395 ENST00000381406 ENST00000416167 ENST00000418738 ENST00000434045 NP_000603 NP_001007140 NP_001121070 NP_001278790 NP_001278791


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
PF00049 Insulin Insulin/IGF/Relaxin family 53-84 CL0239 Insulin Mus musculus
PF00049 Insulin Insulin/IGF/Relaxin family 30-62 CL0239 Insulin Mus musculus
PF08365 IGF2_C Insulin-like growth factor II E-peptide 112-166 Mus musculus

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Spontaneous abortion Female Urogenital Diseases and Pregnancy Complications ; 0.399 0.828
Abortion, Tubal Female Urogenital Diseases and Pregnancy Complications ; 0.399 0.828
Alzheimer's Disease Nervous System Diseases ; Mental Disorders ; 0.399 0.828
Anemia Hemic and Lymphatic Diseases ; 0.399 0.828
Atherosclerosis Cardiovascular Diseases ; 0.399 0.828
Autistic Disorder Mental Disorders ; 0.399 0.828
Beckwith-Wiedemann Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.399 0.828
Bone Diseases, Developmental Musculoskeletal Diseases ; 0.399 0.828
Malignant tumor of colon Neoplasms ; Digestive System Diseases ; 0.399 0.828
Cognition Disorders Mental Disorders ; 0.399 0.828
Colonic Neoplasms Neoplasms ; Digestive System Diseases ; 0.399 0.828
Colorectal Carcinoma Neoplasms ; Digestive System Diseases ; 0.399 0.828
Colorectal Neoplasms Neoplasms ; Digestive System Diseases ; 0.399 0.828
Presenile dementia Nervous System Diseases ; Mental Disorders ; 0.399 0.828
Fetal Growth Retardation Female Urogenital Diseases and Pregnancy Complications ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Pathological Conditions, Signs and Symptoms ; 0.399 0.828
Growth Disorders Pathological Conditions, Signs and Symptoms ; 0.399 0.828
Diaphragmatic Hernia Pathological Conditions, Signs and Symptoms ; 0.399 0.828
Polyhydramnios Female Urogenital Diseases and Pregnancy Complications ; 0.399 0.828
Hypoglycemia Nutritional and Metabolic Diseases ; 0.399 0.828
Liver neoplasms Neoplasms ; Digestive System Diseases ; 0.399 0.828
Memory Disorders Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; 0.399 0.828
Nephroblastoma Neoplasms ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.399 0.828
Nerve Degeneration Pathological Conditions, Signs and Symptoms ; 0.399 0.828
Obesity Nutritional and Metabolic Diseases ; Pathological Conditions, Signs and Symptoms ; 0.399 0.828
Parkinson Disease Nervous System Diseases ; 0.399 0.828
Placenta Disorders Female Urogenital Diseases and Pregnancy Complications ; 0.399 0.828
Precancerous Conditions Neoplasms ; 0.399 0.828
Rhabdomyosarcoma Neoplasms ; 0.399 0.828
Schizophrenia Mental Disorders ; 0.399 0.828
Russell-Silver syndrome Musculoskeletal Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.399 0.828
Hepatoblastoma Neoplasms ; 0.399 0.828
Adrenocortical carcinoma Neoplasms ; Endocrine System Diseases ; 0.399 0.828
Memory impairment Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; 0.399 0.828
Fasting Hypoglycemia Nutritional and Metabolic Diseases ; 0.399 0.828
Reactive hypoglycemia Nutritional and Metabolic Diseases ; 0.399 0.828
Familial Alzheimer Disease (FAD) Nervous System Diseases ; Mental Disorders ; 0.399 0.828
Condition, Preneoplastic Neoplasms ; 0.399 0.828
Congenital hemihypertrophy N/A 0.399 0.828
Malignant neoplasm of liver Neoplasms ; Digestive System Diseases ; 0.399 0.828
Alzheimer Disease, Late Onset Nervous System Diseases ; Mental Disorders ; 0.399 0.828
Acute Confusional Senile Dementia Nervous System Diseases ; Mental Disorders ; 0.399 0.828
prenatal alcohol exposure N/A 0.399 0.828
Alzheimer's Disease, Focal Onset Nervous System Diseases ; Mental Disorders ; 0.399 0.828
Alzheimer Disease, Early Onset Nervous System Diseases ; Mental Disorders ; 0.399 0.828
Age-Related Memory Disorders Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; 0.399 0.828
Memory Disorder, Semantic Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; 0.399 0.828
Memory Disorder, Spatial Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; 0.399 0.828
Memory Loss Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; 0.399 0.828
Lewy Body Disease Nervous System Diseases ; Mental Disorders ; 0.399 0.828
Colorectal Cancer Neoplasms ; Digestive System Diseases ; 0.399 0.828
Atherogenesis Cardiovascular Diseases ; 0.399 0.828
HEMIHYPERPLASIA, ISOLATED Pathological Conditions, Signs and Symptoms ; 0.399 0.828
Liver carcinoma Neoplasms ; Digestive System Diseases ; 0.399 0.828
Bilateral Wilms Tumor Neoplasms ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.399 0.828
Intellectual Disability Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; Mental Disorders ; 0.399 0.828
GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES N/A 0.399 0.828
NO RESULT FOUND
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