1. Gene
  2. CELF3 - CUGBP Elav-like family member 3 Gene

CELF3 - CUGBP Elav-like family member 3 Gene

Homo sapiens

Also known as CAGH4; ERDA4; ETR-1; TNRC4; BRUNOL1

Gene ID: 11189 | Gene type: protein coding

About CELF3

Cytogenetic location: 1q21.3 Genomic coordinates (GRCh38): 1:151,700,058-151,716,803 (from NCBI)

This gene has 7 transcripts (splice variants), 278 orthologues and 6 paralogues. Biased expression in brain (RPKM 11.4), adrenal (RPKM 3.2) and 4 other tissues.

Summary

Members of the CELF/BRUNOL protein family contain two N-terminal RNA recognition motif (RRM) domains, one C-terminal RRM domain, and a divergent segment of 160-230 aa between the second and third RRM domains. Members of this protein family regulate pre-mRNA alternative splicing and may also be involved in mRNA editing, and translation. Multiple alternatively spliced transcript variants encoding different isoforms have been identified in this gene. [provided by RefSeq, Feb 2010]

CELF3 Products(5)

mRNA Protein Name
NM_001172648.4 NP_001166119.1 CUGBP Elav-like family member 3 isoform 2
NM_001172649.4 NP_001166120.1 CUGBP Elav-like family member 3 isoform 3
NM_001291106.2 NP_001278035.1 CUGBP Elav-like family member 3 isoform 4
NM_001291107.2 NP_001278036.1 CUGBP Elav-like family member 3 isoform 5
NM_007185.7 NP_009116.3 CUGBP Elav-like family member 3 isoform 1

CELF3 Protein Structure

RRM_1

RRM_1: RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain) (9 - 76)

RRM_1

RRM_1: RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain) (97 - 161)

RRM_1

RRM_1: RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain) (382 - 451)

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  • 465 a.a.
Protein Preferred Names Protein Names

CUGBP Elav-like family member 3

CAG repeat domain

Related Diseases

Diseases Alias
Specific Language Impairment

Language Impairment, Specific

Speech And Communication Disorders

Language Disorder

Communication Disorder

Language Disorders

Communication Disorders

Speech Language Disorder

Speech-Language Disorder

Communication Impairment

Speech And Language Disorder

Palmoplantar Keratoderma, Bothnian Type

PPKB

Diffuse Palmoplantar Keratoderma, Bothnian Type

Bothnian Type Palmoplantar Keratoderma

Keratoderma, Palmoplantar, Bothnian Type

Palmoplantar Keratoderma, Nonepidermolytic

Reading Disorder

Specific Reading Disorder

Reading

Dyslexia

Developmental Reading Disorder

Learning Disability

Learning Disabilities

Learning Disorders

Academic Skill Disorder

Learning Disorder

Speech Disorder

Speech Disorders

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 CELF3 VGNC VGNC:60746
Canis familiaris CELF3 VGNC VGNC:39095
Bos taurus CELF3 VGNC VGNC:27168
Macaca mulatta CELF3 VGNC VGNC:70936
Mus musculus CELF3 MGD MGI:1926034
Rattus norvegicus CELF3 RGD RGD:1563168