Erg (GeneID: 170909) | Rattus norvegicus
Description: ETS transcription factor ERG [Source:RGD Symbol;Acc:621108]
Synonyms:
Other ID(s): ENSRNOG00000001652
Protein Accession Numbers: XP_006248205, XP_006248204, XP_006248207, NP_596888
Statistics: ClinVar(1) PTM(23)
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.
ENST00000288319 ENST00000398897 ENST00000398905 ENST00000398907 ENST00000398910 ENST00000398911 ENST00000398919 ENST00000417133 ENST00000429727 ENST00000442448 ENST00000453032 NP_001129626 NP_001129627 NP_001230357 NP_001230358 NP_001230361 You are here now! NP_001278320 NP_001317954 NP_004440 NP_891548


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
PF00178 Ets Ets-domain 312-391 CL0123 HTH Homo sapiens
PF02198 SAM_PNT Sterile alpha motif (SAM)/Pointed domain 115-199 CL0003 SAM Homo sapiens

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
leukemia Neoplasms ; 0.511 0.69
Childhood Acute Lymphoblastic Leukemia Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.511 0.69
Leukemia, Lymphocytic, Acute, L2 Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.511 0.69
Leukemia, Myelocytic, Acute Neoplasms ; 0.511 0.69
Acute Myeloid Leukemia, M1 Neoplasms ; 0.511 0.69
Neoplastic Processes Neoplasms ; Pathological Conditions, Signs and Symptoms ; 0.511 0.69
Prostatic Neoplasms Neoplasms ; Male Urogenital Diseases ; 0.511 0.69
Extraosseous Ewings sarcoma-primitive neuroepithelial tumor N/A 0.511 0.69
Malignant neoplasm of prostate Neoplasms ; Male Urogenital Diseases ; 0.511 0.69
Ewings sarcoma Neoplasms ; 0.511 0.69
Acute Myeloid Leukemia (AML-M2) Neoplasms ; 0.511 0.69
Precursor Cell Lymphoblastic Leukemia Lymphoma Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.511 0.69
NO RESULT FOUND
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