ABT1 - activator of basal transcription 1 Gene

Also Known as Esf2; hABT1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 29777

About ABT1

Cytogenetic location: 6p22.2 Genomic coordinates (GRCh38): 6:26,596,953-26,600,739 (from NCBI)

This gene has 1 transcript (splice variant) and 194 orthologues. Ubiquitous expression in bone marrow (RPKM 4.4), lymph node (RPKM 3.9) and 25 other tissues.

Summary

Basal transcription of genes by RNA polymerase II requires the interaction of TATA-binding protein (TBP) with the core region of class II promoters. Studies in mouse suggest that the protein encoded by this gene likely activates basal transcription from class II promoters by interaction with TBP and the class II promoter DNA. [provided by RefSeq, Jul 2008]

ABT1 Products (1)

mRNA Protein Name
NM_013375.4 NP_037507.1 activator of basal transcription 1
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
19299493 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
Protein Preferred Names Protein Names

activator of basal transcription 1

  • TATA-binding protein-binding protein

ABT1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
ABT1 Q9ULW3 CCDC136 Homo sapiens Q96JN2-2 25416956
Intra
ABT1 Q9ULW3 FAM9B Homo sapiens Q8IZU0 25416956
Intra
ABT1 Q9ULW3 FAM9B Homo sapiens Q8IZU0 25416956
Intra
ABT1 Q9ULW3 RNF151 Homo sapiens Q2KHN1 32296183
Intra
ABT1 Q9ULW3 RNF151 Homo sapiens Q2KHN1 32296183
Intra
ABT1 Q9ULW3 KANK2 Homo sapiens Q63ZY3 32296183
Intra
ABT1 Q9ULW3 KANK2 Homo sapiens Q63ZY3 32296183
Intra
ABT1 Q9ULW3 EMD Homo sapiens P50402 32296183
Intra
ABT1 Q9ULW3 EMD Homo sapiens P50402 25416956
Intra
ABT1 Q9ULW3 EMD Homo sapiens P50402 32296183
Intra
ABT1 Q9ULW3 CDCA7L Homo sapiens Q96GN5 25416956
Intra
ABT1 Q9ULW3 SYNE4 Homo sapiens Q8N205 25416956
Intra
ABT1 Q9ULW3 SYNE4 Homo sapiens Q8N205 25416956
Intra
ABT1 Q9ULW3 CEP70 Homo sapiens Q8NHQ1 32296183
Intra
ABT1 Q9ULW3 CEP70 Homo sapiens Q8NHQ1 32296183
Intra
ABT1 Q9ULW3 CEP70 Homo sapiens Q8NHQ1 25416956
Intra
ABT1 Q9ULW3 DVL3 Homo sapiens Q92997 32296183
Intra
ABT1 Q9ULW3 DVL3 Homo sapiens Q92997 32296183
Intra
ABT1 Q9ULW3 LZTS2 Homo sapiens Q9BRK4 25416956
Intra
ABT1 Q9ULW3 LZTS2 Homo sapiens Q9BRK4 25416956
Intra
ABT1 Q9ULW3 LZTS2 Homo sapiens Q9BRK4 25416956
Intra
ABT1 Q9ULW3 PICK1 Homo sapiens Q9NRD5 32296183
Intra
ABT1 Q9ULW3 PICK1 Homo sapiens Q9NRD5 32296183
Intra
ABT1 Q9ULW3 TSPYL2 Homo sapiens Q9H2G4 33961781
Intra
ABT1 Q9ULW3 TSPYL2 Homo sapiens Q9H2G4 32296183
Intra
ABT1 Q9ULW3 TSPYL2 Homo sapiens Q9H2G4 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 1
  • Smard1

  • DSMA1

  • Sianrf

  • Dhmn6

  • Spinal Muscular Atrophy With Respiratory Distress 1

  • HMN6

  • Severe Infantile Axonal Neuropathy With Respiratory Failure

  • Autosomal Recessive Distal Spinal Muscular Atrophy 1

  • Diaphragmatic Spinal Muscular Atrophy

  • Spinal Muscular Atrophy With Respiratory Distress Type 1

  • Neuronopathy, Distal Hereditary Motor, Type Vi

  • Hmn Vi

  • Neuronopathy, Severe Infantile Axonal, With Respiratory Failure

  • Distal Spinal Muscular Atrophy 1

  • Autosomal Recessive Spinal Muscular Atrophy With Respiratory Distress

  • Distal Hereditary Motor Neuropathy Type 6

  • Distal-Hmn Type 6

  • Severe Infantile Axonal Neuropathy With Respiratory Failure Type 1

  • Spinal Muscular Atrophy, Diaphragmatic

  • Distal Hereditary Motor Neuronopathy Type Vi

  • Distal Spinal Muscular Atrophy Type 1

  • Hmnvi

  • Spinal Muscular Atrophy With Respiratory Distress

  • Autosomal Recessive Distal Spinal Muscular Atrophy Type 1

  • Neuronopathy, Distal Hereditary Motor, 6

  • Dhmn Vi

  • Distal Hereditary Motor Neuropathy Type Vi

  • Severe Infantile Axonal Neuronopathy With Respiratory Failure

  • Spinal Muscular Atrophy Distal Autosomal Recessive 1

  • Atrophy, Muscular, Spinal, Distal, Type 1

Autosomal Recessive Distal Hereditary Motor Neuronopathy
  • Autosomal Recessive Distal Spinal Muscular Atrophy

Spinocerebellar Ataxia 17
  • Spinocerebellar Ataxia Type 17

  • SCA17

  • Huntington Disease-Like 4

  • Hdl4

  • Olivopontocerebellar Atrophy V

  • Cerebelloparenchymal Disorder Ii

  • Opca5

  • Cpd2

  • Sca 17

  • Ataxia, Spinocerebellar, Type 17

Acute Diarrhea
Essential Thrombocythemia
  • Essential Thrombocytosis

  • Familial Thrombocytosis

  • Hemorrhagic Thrombocythemia

  • Hereditary Thrombocythemia

  • Primary Thrombocytosis

  • Idiopathic Thrombocythemia

  • Primary Thrombocythemia

  • Thrombocythemia, Essential

  • Essential Thrombocythaemia

  • Et

  • Familial Thrombocythemia

  • Thrombocythemia Essential

Autosomal Dominant Cerebellar Ataxia
  • Spinocerebellar Ataxia

  • Adca

  • Pierre Marie Cerebellar Ataxia

  • Ataxia, Spinocerebellar

  • Sca

  • Autosomal Dominant Spinocerebellar Ataxia

  • Spinocerebellar Ataxias

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

Orthologs Information

Species Symbol Source ID
Felis catus ABT1 VGNC VGNC:102372
Rattus norvegicus ABT1 RGD RGD:1310785
Mus musculus ABT1 MGD MGI:1353636
Bos taurus ABT1 VGNC VGNC:25514
Macaca mulatta ABT1 VGNC VGNC:69448
Canis familiaris ABT1 VGNC VGNC:37485
Others ABT1 NCBI