SNAI3 - snail family transcriptional repressor 3 Gene

Also Known as SMUC; SNAIL3; ZNF293; Zfp293

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 333929

About SNAI3

Cytogenetic location: 16q24.2 Genomic coordinates (GRCh38): 16:88,677,688-88,686,507 (from NCBI)

This gene has 1 transcript (splice variant), 141 orthologues and 36 paralogues. Broad expression in lymph node (RPKM 1.8), spleen (RPKM 1.7) and 25 other tissues.

Summary

SNAI3 is a member of the SNAIL gene family, named for the Drosophila snail gene, which plays roles in mesodermal formation during embryogenesis (Katoh and Katoh, 2003 [PubMed 12579345]).[supplied by OMIM, Apr 2009]

SNAI3 Products (1)

mRNA Protein Name
NM_178310.4 NP_840101.1 zinc finger protein SNAI3

Gene Ontology

  • Molecular Function
Molecular Function GO Annotation Evidence References Source
enables sequence-specific double-stranded DNA binding IDA
IDA: Inferred from direct assay
28473536 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

SNAI3 Protein Structure

zf-C2H2

zf-C2H2: Zinc finger, C2H2 type (183 - 205)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (224 - 247)

zf-C2H2

zf-C2H2: Zinc finger, C2H2 type (265 - 288)

  • 0
  • 100
  • 200
  • 292 a.a.
Protein Preferred Names Protein Names

zinc finger protein SNAI3

  • protein snail homolog 3

Related Diseases

Diseases Alias
Parkinson Disease 7, Autosomal Recessive Early-Onset

  • Autosomal Recessive Early-Onset Parkinson Disease 7

  • PARK7

  • Parkinson'S Disease 7

  • Autosomal Recessive Early-Onset Parkinson'S Disease 7

  • Parkinson Disease 7

  • Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex Type 2

  • Autosomal Recessive Early-Onset Parkinson Disease Type 7

  • Parkinson Disease, Type 7
Waardenburg Syndrome, Type 2e

  • Waardenburg Syndrome Type 2

  • Waardenburg Syndrome Type 2e

  • WS2E

  • Waardenburg Syndrome, Type 2e, With Or Without Neurologic Involvement

  • Waardenburg Syndrome, Type Iie

  • Hypogonadotropic Hypogonadism With Anosmia And Deafness With Or Without Hypopigmentation

  • Waardenburg Syndrome Type 2e With Or Without Neurologic Involvement

  • Waardenburg Syndrome Type Iie

  • Hypogonadotropic Hypogonadism With Anosmia And Deafness, With Or Without Hypopigmentation

  • Ws2e, With Or Without Neurologic Involvement

  • Ws2e With Or Without Neurological Involvement

  • Ws 2

  • Ws Type 2

  • Ws2

  • Waardenburg Syndrome Type Ii

  • Waardenburg Syndrome 2e

  • Kallmann Syndrome And Deafness With Or Without Hypopigmentation

  • Ws2e With Or Without Neurologic Involvement

  • Waardenburg Syndrome Type 2e, Without Neurologic Involvement

  • Ws-2
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)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS13472 SNAI3 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Bos taurus SNAI3 VGNC VGNC:35049
Rattus norvegicus SNAI3 RGD RGD:1309658
Mus musculus SNAI3 MGD MGI:1353563
Canis familiaris SNAI3 VGNC VGNC:46586
Macaca mulatta SNAI3 VGNC VGNC:77735
Others SNAI3 NCBI