GTF2H1 - general transcription factor IIH subunit 1 Gene

Also Known as P62; BTF2; TFB1; TFIIH

生物種: Homo sapiens

遺伝子タイプ: protein coding
遺伝子ID: 2965

About GTF2H1

Cytogenetic location: 11p15.1 Genomic coordinates (GRCh38): 11:18,322,567-18,367,045 (from NCBI)

This gene has 16 transcripts (splice variants), 1 gene allele and 219 orthologues. Ubiquitous expression in testis (RPKM 18.1), thyroid (RPKM 12.6) and 25 other tissues.

Summary

Enables Thyroid Hormone Receptor binding activity. Involved in positive regulation of transcription, DNA-templated and transcription by RNA polymerase II. Located in nucleoplasm. Part of transcription factor TFIIH core complex and transcription factor TFIIH holo complex. [provided by Alliance of Genome Resources, Apr 2022]

GTF2H1 Products (2)

mRNA Protein Name
NM_001142307.2 NP_001135779.1 general transcription factor IIH subunit 1
NM_005316.4 NP_005307.1 general transcription factor IIH subunit 1

Gene Ontology

  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence 参考文献 由来
enables nuclear thyroid hormone receptor binding IPI
IPI: Inferred from physical interaction
15625236 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
8652557 GOA
Biological Process GO Annotation Evidence 参考文献 由来
involved in positive regulation of DNA-templated transcription IDA
IDA: Inferred from direct assay
15625236 GOA
involved in transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
9852112 GOA
involved in transcription initiation at RNA polymerase II promoter IDA
IDA: Inferred from direct assay
8692841 GOA
Cellular Component GO Annotation Evidence 参考文献 由来
part of transcription factor TFIIH core complex IDA
IDA: Inferred from direct assay
8692841 GOA
part of transcription factor TFIIH holo complex IDA
IDA: Inferred from direct assay
9852112 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

GTF2H1 Protein Structure

PH_TFIIH

PH_TFIIH: TFIIH p62 subunit, N-terminal domain (10 - 81)

BSD

BSD: BSD domain (104 - 148)

BSD

BSD: BSD domain (179 - 235)

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  • 500
  • 548 a.a.
Protein Preferred Names Protein Names

general transcription factor IIH subunit 1

  • BTF2 p62

GTF2H1 Protein-protein interaction Information

Type
タンパク質名 Protein ID Interactor Interactor Species Interactor ID Detection Method 参考文献
Intra
GTF2H1 P32780 AGTRAP Homo sapiens Q6RW13-2
Y2H Prey Pooling
32296183
Intra
GTF2H1 P32780 AGTRAP Homo sapiens Q6RW13-2
Y2H Array
32296183
Intra
GTF2H1 P32780 AGTRAP Homo sapiens Q6RW13-2
Validated Y2H
32296183
Intra
GTF2H1 P32780 GTF2H2 Homo sapiens Q13888
Anti Tag CoIP
33961781
Intra
GTF2H1 P32780 XPC Homo sapiens Q01831-1
NMR
26278177
Intra
GTF2H1 P32780 XPC Homo sapiens Q01831-1
ITC
26278177
Intra
GTF2H1 P32780 TP53 Homo sapiens P04637
Pull Down
18354501
Intra
GTF2H1 P32780 GTF2E1 Homo sapiens P29083
Y2H Array
32296183
Intra
GTF2H1 P32780 GTF2E1 Homo sapiens P29083
NMR
18354501
Intra
GTF2H1 P32780 GTF2E1 Homo sapiens P29083
Pull Down
18354501
Intra
GTF2H1 P32780 GTF2E1 Homo sapiens P29083
Y2H Prey Pooling
32296183
Intra
GTF2H1 P32780 FHL2 Homo sapiens Q14192
Validated Y2H
32296183
Intra
GTF2H1 P32780 EAF1 Homo sapiens Q96JC9
Validated Y2H
32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

GTF2H1 抗体

製品番号 製品名 アプリケーション 反応性
HY-P81322 GTF2H1 Antibody (YA1067) WB, ICC/IF, IP Human
HY-P81322A GTF2H1 Antibody (YA1067)(PBS only) WB, ICC/IF, IP Human
HY-P85475 GTF2H1 Antibody (YA5167) WB Human, Mouse, Rat, Bovine, Dog, Pig
HY-P85514 GTF2H1 Antibody (YA5206) WB, IP, ICC/IF Human

関連疾患

Diseases Alias
Rift Valley Fever

  • Rfv - [Rift Valley Fever]
Phlebotomus Fever

  • Pappataci Fever

  • Sandfly Fever

  • Sandfly-Borne Phleboviral Disease

  • Sandfly-Borne Arboviral Fever

  • Sandfly-Borne Bunyavirus Fever

  • Three Day Fever

  • Chitral Fever

  • Italy Summer Grippe

  • Italy Summer Grippe Influenza
Trichothiodystrophy

  • Ttd

  • Amish Brittle Hair Syndrome

  • Bids Syndrome

  • Brittle Hair-Intellectual Impairment-Decreased Fertility-Short Stature Syndrome

  • Ibids

  • Pibids

  • Trichothiodystrophy Syndromes
Cockayne Syndrome

  • Cockayne'S Syndrome

  • Dwarfism-Retinal Atrophy-Deafness Syndrome

  • Neill-Dingwall Syndrome

  • Progeria-Like Syndrome

  • Progeroid Nanism

  • Cs
Hermansky-Pudlak Syndrome 5

  • HPS5

  • Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial

  • Delta Storage Pool Disease

  • Hermansky-Pudlak Syndrome, Type 5

  • Platelet Storage Pool Deficiency

  • Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells
Cerebrooculofacioskeletal Syndrome 1

  • Cofs Syndrome

  • COFS1

  • Pena-Shokeir Syndrome Type 2

  • Cofs

  • Pena-Shokeir Syndrome, Type Ii

  • Cerebrooculofacioskeletal Syndrome

  • Cerebro-Oculo-Facio-Skeletal Syndrome 1

  • Pena Shokeir Syndrome Type 2
Xeroderma Pigmentosum, Complementation Group G

  • Xeroderma Pigmentosum, Group G

  • Xeroderma Pigmentosum Vii

  • Xp7

  • XPG

  • Xeroderma Pigmentosum Group G

  • Xp Group G

  • Xp, Group G

  • Xpgc

  • Xeroderma Pigmentosum, Group G/Cockayne Syndrome

  • Xeroderma Pigmentosum, Type 7

  • Xeroderma Pigmentosum Complementation Group G

  • XP-G

  • Xp-G/Cs

  • Xeroderma Pigmentosum Group G/Cockayne Syndrome
Xeroderma Pigmentosum, Variant Type

  • Xeroderma Pigmentosum

  • XPV

  • Xeroderma Pigmentosum Variant Type

  • Xeroderma Pigmentosum With Normal Dna Repair Rates

  • Photosensitivity With Defective Dna Synthesis

  • Xp

  • De Sanctis-Cacchione Syndrome

  • Desanctis-Cacchione Syndrome

  • Xeroderma Pigmentosa

  • Xerodermic Idiocy

  • Xeroderma Pigmentosum Variant

  • Xp - [Xeroderma Pigmentosum]

  • Atrophoderma Pigmentosum
Xeroderma Pigmentosum, Complementation Group C

  • Xeroderma Pigmentosum, Group C

  • XPC

  • Xpcc

  • Xeroderma Pigmentosum Iii

  • Xp3

  • Xeroderma Pigmentosum Group C

  • Xp Group C

  • Xp, Group C

  • Xeroderma Pigmentosum, Type 3

  • Xeroderma Pigmentosum Complementation Group C

  • XP-C
Uv-Sensitive Syndrome

  • Uvss

  • Uv Sensitive Syndrome

  • Ultraviolet Sensitive Syndrome
Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
製品番号 製品名
製品効果
純度
Rare Diseases
HY-RS05898 GTF2H1 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

生物種 Symbol 由来 ID
Felis catus GTF2H1 VGNC VGNC:67498
Bos taurus GTF2H1 VGNC VGNC:29695
Canis familiaris GTF2H1 VGNC VGNC:41547
Macaca mulatta GTF2H1 VGNC VGNC:73311
Mus musculus GTF2H1 MGD MGI:1277216
Rattus norvegicus GTF2H1 RGD RGD:1308225
Others GTF2H1 NCBI