ConVarT

Gtf2i (GeneID: 14886) | Mus musculus

Description:	general transcription factor II I [Source:MGI Symbol;Acc:MGI:1202722]
Synonyms:	WBSCR6, GtfII-I, 6030441I21Rik, TFII-I, Diws1t, pin, BAP-135
Other ID(s):	MGI:1202722, ENSMUSG00000060261
Protein Accession Numbers:	XP_030110025, XP_036020702, XP_036020710, NP_001345992, XP_006504449, XP_017176167, XP_030110005, XP_030110016, XP_030110022, XP_036020699, XP_036020707, NP_001074217, NP_034495, XP_017176164, XP_030110000, XP_030110013, XP_036020696, XP_036020704, XP_036020712, NP_001345994, XP_006504454, XP_017176169, XP_030110007, XP_030110018, XP_030110024, XP_036020701, XP_036020709, NP_001345991, XP_006504448, XP_017176166, XP_030110004, XP_030110015, XP_036020698, XP_036020706, NP_001074216, NP_001345996, XP_017176163, XP_017176171, XP_030110011, XP_030110021, XP_036020695, XP_036020703, XP_036020711, NP_001345993, XP_006504452, XP_017176168, XP_030110006, XP_030110017, XP_030110023, XP_036020700, XP_036020708, NP_001074218, XP_006504447, XP_017176165, XP_030110001, XP_030110014, XP_036020697, XP_036020705, NP_001074215, NP_001345995, XP_017176162, XP_017176170, XP_030110008, XP_030110019
Statistics:	ClinVar(1) gnomAD(168) COSMIC(209)

ClinVar Pathogenicity of Variations

∙ 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.
ENST00000324896 ENST00000346152 ENST00000353920 ENST00000416070 ENST00000432143 ENST00000443166 You are here now! ENST00000573035 NP_001157108 NP_001267729 You are here now! NP_001509 NP_127492 NP_127493 NP_127494

ClinVar Data

Variation ID	Allele ID	RS Number	Variant Type	Record	Alteration	Clinicial Sig.	Last Update	Phenotypes	Cytogenetic	Review Status	RCV Acc.N.

gnomAD

Variant ID	Transcript ID	Alteration	Annotation	Allele C.	Allele N.	Allele F.	rsNumber	Flags	Filter

Post-translational Modifications (PTMs)

Gene Name	ACC ID	PTM Type	Position	Mod-rsd	Site +/-7 Aa	Mw_kd	Site grpID

Catalogue of Somatic Mutations in Cancer (COSMIC)

Gene Name	Transcript ID	Sample name	Primary Site	Primary Histology	Mutation ID	Mutation CDS	Mutation Aa	Mutation Desc.	FATHMM Prediction	FATHMM Score	Mutation Somatic Status	PUBMED PMID	Tumor Origin	Position

dbSNP

Gene ID	Transcript ID	Consequence	Position	HGVSp	Impact

Protein Domains (PFAM)

Pfam Domain	Domain Name	Description	Positions	Clan	Clan Name	Organism
NO RESULT FOUND
NO DOMAINS EXIST

List of the diseases from DisGeNET

Disease Name	Disease Category	DSI*	DPI**
Leukemia, Myelocytic, Acute	Neoplasms ;	0.565	0.655
Acute Myeloid Leukemia, M1	Neoplasms ;	0.565	0.655
Sicca Syndrome	Musculoskeletal Diseases ; Stomatognathic Diseases ; Eye Diseases ; Skin and Connective Tissue Diseases ; Immune System Diseases ;	0.565	0.655
Williams Syndrome	Nervous System Diseases ; Cardiovascular Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ;	0.565	0.655
Thymic epithelial tumor	Neoplasms ; Hemic and Lymphatic Diseases ;	0.565	0.655
Autism Spectrum Disorders	Mental Disorders ;	0.565	0.655
Sjogren's Syndrome	Musculoskeletal Diseases ; Stomatognathic Diseases ; Eye Diseases ; Skin and Connective Tissue Diseases ; Immune System Diseases ;	0.565	0.655
Acute Myeloid Leukemia (AML-M2)	Neoplasms ;	0.565	0.655
NO RESULT FOUND