TCEAL3 - transcription elongation factor A like 3 Gene

Also Known as WEX8

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 85012

About TCEAL3

This gene has 4 transcripts (splice variants), 120 orthologues and 8 paralogues. Ubiquitous expression in prostate (RPKM 39.3), brain (RPKM 35.9) and 25 other tissues.

Summary

This gene encodes a member of the transcription elongation factor A (SII)-like (TCEAL) gene family. Members of this family contain TFA domains and may function as nuclear phosphoproteins that modulate transcription in a promoter context-dependent manner. Multiple family members are located on the X chromosome. Alternative splicing results in multiple transcript variants encoding a single isoform. [provided by RefSeq, Jul 2008]

TCEAL3 Products (2)

mRNA Protein Name
NM_001006933.2 NP_001006934.1 transcription elongation factor A protein-like 3
NM_032926.3 NP_116315.1 transcription elongation factor A protein-like 3

TCEAL3 Protein Structure

BEX

BEX: Brain expressed X-linked like family (1 - 173)

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

transcription elongation factor A protein-like 3

  • TCEA-like protein 3

Related Diseases

Diseases Alias
Severe Congenital Neutropenia 7
  • Autosomal Recessive Severe Congenital Neutropenia Due To Csf3r Deficiency

  • Scn7

Pelizaeus-Merzbacher Disease
  • PMD

  • HLD1

  • Pelizaeus-Merzbacher Brain Sclerosis

  • Leukodystrophy, Hypomyelinating, 1

  • Diffuse Familial Brain Sclerosis

  • Pelizaeus Merzbacher Brain Sclerosis

  • Sudanophilic Leukodystrophy, Paelizeus-Merzbacher Type

  • Cockayne-Pelizaeus-Merzbacher Disease

  • Hypomyelinating Leukodystrophy 1

  • Leukodystrophy, Sudanophilic

  • Pelizaeus Merzbacher Disease

  • Hypomyelinating Leukodystrophy, 1

  • Sudanophilic Leukodystrophy

  • Pelizaeus-Merzbacher Disease, Connatal Form

  • Connatal Pmd

  • Pelizaeus-Merzbacher Disease Type Ii

  • Severe Pmd

  • Null Syndrome

  • Plp1 Null Syndrome

  • Pelizaeus-Merzbacher Disease, Null Syndrome

  • Brain Sclerosis Diffuse Familial

  • Sudanophilic Leukodystrophy Paelizeus-Merzbacher Type

  • Leukodystrophy Hypomyelinating 1

  • Diffuse Cerebral Sclerosis Of Schilder

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
Mus musculus TCEAL3 MGD MGI:1913354
Rattus norvegicus TCEAL3 RGD RGD:1562504