ASCL2 - achaete-scute family bHLH transcription factor 2 Gene

Also Known as ASH2; HASH2; MASH2; bHLHa45

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 430

About ASCL2

Cytogenetic location: 11p15.5 Genomic coordinates (GRCh38): 11:2,268,498-2,270,588 (from NCBI)

This gene has 1 transcript (splice variant), 255 orthologues and 4 paralogues. Broad expression in colon (RPKM 4.3), placenta (RPKM 2.5) and 14 other tissues.

Summary

This gene is a member of the basic helix-loop-helix (BHLH) family of transcription factors. It activates transcription by binding to the E box (5'-CANNTG-3'). Dimerization with Other BHLH proteins is required for efficient DNA binding. Involved in the determination of the neuronal precursors in the peripheral nervous system and the central nervous system. [provided by RefSeq, Jul 2008]

ASCL2 Products (1)

mRNA Protein Name
NM_005170.3 NP_005161.1 achaete-scute homolog 2
Molecular Function GO Annotation Evidence References Source
enables DNA-binding transcription repressor activity, RNA polymerase II-specific IDA
IDA: Inferred from direct assay
14561729 GOA
enables E-box binding IDA
IDA: Inferred from direct assay
14561729 GOA
enables RNA polymerase II cis-regulatory region sequence-specific DNA binding IDA
IDA: Inferred from direct assay
14561729 GOA
enables sequence-specific double-stranded DNA binding IDA
IDA: Inferred from direct assay
28473536 GOA
Biological Process GO Annotation Evidence References Source
involved in negative regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
14561729 GOA
involved in response to hypoxia IEP
IEP: Inferred from expression pattern
14561729 GOA
involved in spongiotrophoblast layer development IEP
IEP: Inferred from expression pattern
12917334 GOA
Cellular Component GO Annotation Evidence References Source
located in cytoplasm IDA
IDA: Inferred from direct assay
12917334 GOA
located in nucleus IDA
IDA: Inferred from direct assay
11440538 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

ASCL2 Protein Structure

HLH

HLH: Helix-loop-helix DNA-binding domain (54 - 103)

  • 0
  • 100
  • 193 a.a.
Protein Preferred Names Protein Names

achaete-scute homolog 2

  • achaete-scute complex homolog 2

Related Diseases

Diseases Alias
Beckwith-Wiedemann Syndrome
  • Wiedemann-Beckwith Syndrome

  • BWS

  • Exomphalos-Macroglossia-Gigantism Syndrome

  • Emg Syndrome

  • Beckwith-Wiedemann Syndrome Due To Cdkn1c Mutation

  • Emg Abnormality

  • Wbs

  • Exomphalos Macroglossia Gigantism Syndrome

  • Beckwith-Wiedemann Syndrome Due To Nsd1 Mutation

  • Macroglossia Exomphalos Gigantism

Colonic Benign Neoplasm
  • Colon Neoplasm

  • Colonic Mass

  • Colonic Tumor

  • Neoplasm Of Colon

  • Neoplasm Of The Colon

  • Colonic Neoplasms

  • Colon Cancer

  • Colon Carcinoma Nos

  • Colonic Cancer

  • Metastatic Colon Cancer Nos

Microcephaly
  • Microencephaly

  • Microcephalus

  • Microcephalic

  • Nanocephaly

  • Congenital Microcephaly

  • Brain Hypoplasia

  • Brain Nondevelopment

  • Cephalic Hypoplasia

  • Undeveloped Cerebrum

  • Undeveloped Brain

  • Micrencephalon

  • Micrencephaly

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
Canis familiaris ASCL2 VGNC VGNC:38174
Bos taurus ASCL2 VGNC VGNC:26207
Felis catus ASCL2 VGNC VGNC:68332
Mus musculus ASCL2 MGD MGI:96920
Rattus norvegicus ASCL2 RGD RGD:2159
Macaca mulatta ASCL2 VGNC VGNC:70030
Others ASCL2 NCBI