Search references for GTF2I. Phrases containing GTF2I
See searches and references containing GTF2I!GTF2I
Protein-coding gene in humans
transcription factor II-I is a protein that in humans is encoded by the GTF2I gene. This gene encodes a multifunctional phosphoprotein, TFII-I, with roles
GTF2I
Genetic disorder
Williams syndrome genes ASL BAZ1B BCL7B CLDN3 CLDN4 CLIP2 EIF4H ELN FZD9 FKBP6 GTF2I GTF2IRD1 HIP1 KCTD7 LAT2 LIMK1 MDH2 NCF1 NSUN5 POR RFC2 STX1A TBL2 TRIM50
Williams_syndrome
Project to catalogue genetic mutations responsible for cancer
AB; low mutational burden; enrichment of HRAS, NRAS, TP53, and recurrent GTF2I mutations were observed; expression of autoimmune targets and aneuploidy
The_Cancer_Genome_Atlas
Chinese-American neuroscientist
could reverse myelin deficits and hypersociability symptoms in mice lacking GTF2I, which may be translatable to human patients. Beckman Young Investigator
Guoping_Feng
[323] STYWYAKASTS GTF2I ENSG00000263001 GTF2I-like Known motif – In vivo/Misc source [324] VAGVDVKTSH GTF2IRD1 ENSG00000006704 GTF2I-like Known motif –
List of human transcription factors
List_of_human_transcription_factors
Internally coordinated responses of dogs to internal and external stimuli
between dogs and humans. For example, the structural variation in the GTF2I and GTF2IRD1 genes at the locus responsible for Williams-Beuren Syndrome
Dog_behavior
Family of regulator genes
shown to interact with: ACTL6A BRCA1 Bcl-2 Cyclin T1 CHD8 DNMT3A EP400 GTF2I HTATIP let-7 MAPK1 MAPK8 MAX MLH1 MYCBP2 MYCBP NMI NFYB NFYC P73 PCAF PFDN5
Myc
Kinase that plays a role in B cell development
kinase has been shown to interact with: ARID3A BLNK (SLP-65), CAV1, GNAQ, GTF2I, PLCG2, PRKD1, and SH3BP5. GRCh38: Ensembl release 89: ENSG00000010671 –
Bruton's_tyrosine_kinase
Class of benign skin and mucous membrane lesions
tumor cells contain an AHRR-NCOA2 fusion gene in 60% to 80% of cases and a GTF2I-NCOA2 or GAB1-ABL1 fusion gene in rare cases. Cellular angiofibroma is usually
Angiofibroma
Protein-coding gene in the species Homo sapiens
encoded by the GTF2IRD1 gene. The protein encoded by this gene contains five GTF2I-like repeats and each repeat possesses a potential helix-loop-helix (HLH)
GTF2IRD1
Protein-coding gene in the species Homo sapiens
RFC2, CYLN2 (CLIP-115, WBSCR4, WBSCR3), GTF2IRD1 (WBSCR11, GTF3), and GTF2I (BAP135, SPIN). Williams Beuren syndrome is a neurodevelopmental disorder
DNAJC30
Protein-coding gene in the species Homo sapiens
to be a binding partner for GTF2IRD1 (GTF2I repeat domain containing protein 1) via a yeast 2 hybrid screen. GTF2I is a gene that encodes the general transcription
FHAD1
Mammalian protein found in Homo sapiens
interact with: ASCC3, ATF6, CEBPB, CREB-binding protein, ELK4, GATA4, GTF2F1, GTF2I, Myogenin, NFYA, Nuclear receptor co-repressor 2, Promyelocytic leukemia
Serum_response_factor
Cytoplasmic biomolecular condensates of proteins and RNA occurring in cells under stress
RNA Sequence Binding Factor 1 GSPT1 eRF3 G1 To S Phase Transition 1 GTF2I GTF2I General Transcription Factor IIi GTF3C1 GTF3C1 General Transcription
Stress_granule
Medical condition
related to the increased risk of aortic dilation. An extra copy of the GTF2I gene, which encodes a transcription factor involved in brain development
7q11.23_duplication_syndrome
Protein-coding gene in the species Homo sapiens
tuberous sclerosis. MAPK3 has been shown to interact with: DUSP3, DUSP6 GTF2I, HDAC4, MAP2K1, MAP2K2, PTPN7, RPS6KA2, and SPIB. GRCh38: Ensembl release
MAPK3
Medical condition
AFST tumor cases have also been shown to be associated with GAB1-ABL1, GTF2I-NCOA2, NCOA2-ETV4, ETV4-AHRR, and NAB2-STAT6 fusion genes. The diagnosis
Angiofibroma_of_soft_tissue
German-American physician-geneticist
deleted in the neurodevelopmental disorder Williams syndrome, including the GTF2I gene, located within the 7q11.23 common deletion. Initially, her group generated
Uta_Francke
Zinc Finger 821
ACCCGGGAATGGGCGAGGC + GLIS family zinc finger 3 GLIF CGCTCCGCCCCCCAAGG - GTF2I-like repeat 4 of GTF3 GUCE CGGGATTGGGC + zinc finger protein with KRAB and
ZNF821
Protein-coding gene in the species Homo sapiens
humans is encoded by the PRKG1 gene. PRKG1 has been shown to interact with: GTF2I, ITPR1, MRVI1, RGS2, and TNNT1. GRCh38: Ensembl release 89: ENSG00000185532
PRKG1
Protein-coding gene in the species Homo sapiens
related, BUB3, CDC20, CDH1, CHD3, CHD4, DNMT1, EED, EZH2 and FKBP3, GATA4, GTF2I, HDAC10, HDAC1, HMG20B, HSPA4, Host cell factor C1, MTA1, MTA2, MXD1, Mad1
Histone_deacetylase_2
Protein-coding gene in humans
HDAC3 has been shown to interact with: CBFA2T3, CCND1, GATA1, GATA2, GPS2, GTF2I, HDAC4, HDAC5, HDAC7A, HDAC9, MAP3K7IP2, MAPK11, NCOR1, NCOR2, PPARD, PPARG
HDAC3
Protein-coding gene in the species Homo sapiens
factor II-I repeat domain-containing protein 2B NP_001003795.1 949 25 46 GTF2I repeat domain containing 2 NP_775808.2 949 24 45 EPM2A interacting protein
FAM200A
Q13889 6734 GTF2H4 HGNC:4658; Q92759 6735 GTF2H5 HGNC:21157; Q6ZYL4 6736 GTF2I HGNC:4659; P78347 6737 GTF2IRD1 HGNC:4661; Q9UHL9 6738 GTF2IRD2 HGNC:30775;
List of human protein-coding genes 3
List_of_human_protein-coding_genes_3
Protein-coding gene in the species Homo sapiens
(ABCA1). USF1 (human gene) has been shown to interact with USF2, FOSL1, and GTF2I. GRCh38: Ensembl release 89: ENSG00000158773 – Ensembl, May 2017 GRCm38:
USF1
GTF2I
GTF2I
GTF2I
GTF2I
Male
English
Anglicized form of Hebrew Adoniyah, ADONIJAH means "my Lord is Jehovah." In the bible, this is the name of the fourth son of David, and a couple of other characters.
Boy/Male
Indian, Sanskrit
Someone who has Got Everything
Boy/Male
Indian, Sanskrit
Unshaken; Firm; Resolute
Surname or Lastname
English
English : from the Middle English personal name Adkin, a pet form of Adam that was in use particularly in the English Midlands, + patronymic -s. Compare Atkins.
Girl/Female
American, Australian, Celtic, Chinese, Christian
Like a God; Female Version of Michael; Who is Like God?; Who is Like God
Boy/Male
British, English, French, German
Valley Piercer; Pierce the Vale
Girl/Female
Arabic, Muslim
Star
Surname or Lastname
English
English : variant of Higginbotham.
Male
Hebrew
(לְמוּ×ֵל) Hebrew name LEMUWEL means "by God" or "for God." In the bible, this is the name of an unknown king, possibly Solomon.Â
Girl/Female
Biblical
A cow, increasing.
GTF2I
GTF2I
GTF2I
GTF2I
GTF2I