2. Gene
  3. ELAVL2 - ELAV like RNA binding protein 2 Gene

ELAVL2 - ELAV like RNA binding protein 2 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as HUB; HELN1; HEL-N1

Gene ID: 1993 | Gene type: protein coding

About ELAVL2

Cytogenetic location: 9p21.3 Genomic coordinates (GRCh38): 9:23,690,104-23,850,601 (from NCBI)

This gene has 8 transcripts (splice variants), 203 orthologues and 24 paralogues. Biased expression in testis (RPKM 13.9) and brain (RPKM 8.2).

Summary

In humans, the ELAV like RNA binding protein gene family has four members (ELAVL1-4). ELAVL RNA binding proteins recognize AU-rich elements in the 3' UTRs of gene transcripts and thereby regulate gene expression post-transcriptionally. The protein encoded by this gene binds to several 3' UTRs, including its own and also that of FOS, ID, and POU5F1. This gene encodes ELAVL2 and, like ELAVL3 and ELAVL4, is expressed specifically in neurons and primarily localizes to the cytoplasm. This protein also forms a cytosolic complex with the normally nuclear-localized ELAVL1 protein. Alternative splicing of this gene results in multiple transcript variants encoding distinct protein isoforms. [provided by RefSeq, Jul 2020]

ELAVL2 Products(41)

mRNA Protein Name
NM_001171195.2 NP_001164666.1 ELAV-like protein 2 isoform b
NM_001171197.2 NP_001164668.1 ELAV-like protein 2 isoform b
NM_001351455.2 NP_001338384.1 ELAV-like protein 2 isoform c
NM_001351456.2 NP_001338385.1 ELAV-like protein 2 isoform d
NM_001351457.2 NP_001338386.1 ELAV-like protein 2 isoform d
NM_001351458.2 NP_001338387.1 ELAV-like protein 2 isoform d
NM_001351459.2 NP_001338388.1 ELAV-like protein 2 isoform d
NM_001351460.2 NP_001338389.1 ELAV-like protein 2 isoform e
NM_001351461.2 NP_001338390.1 ELAV-like protein 2 isoform e
NM_001351462.2 NP_001338391.1 ELAV-like protein 2 isoform f
NM_001351463.2 NP_001338392.1 ELAV-like protein 2 isoform f
NM_001351464.2 NP_001338393.1 ELAV-like protein 2 isoform g
NM_001351465.2 NP_001338394.1 ELAV-like protein 2 isoform g
NM_001351466.2 NP_001338395.1 ELAV-like protein 2 isoform h
NM_001351467.2 NP_001338396.1 ELAV-like protein 2 isoform i
NM_001351468.2 NP_001338397.1 ELAV-like protein 2 isoform i
NM_001351469.2 NP_001338398.1 ELAV-like protein 2 isoform i
NM_001351470.2 NP_001338399.1 ELAV-like protein 2 isoform i
NM_001351471.2 NP_001338400.1 ELAV-like protein 2 isoform i
NM_001351472.2 NP_001338401.1 ELAV-like protein 2 isoform a
NM_001351473.2 NP_001338402.1 ELAV-like protein 2 isoform a
NM_001351474.2 NP_001338403.1 ELAV-like protein 2 isoform a
NM_001351475.2 NP_001338404.1 ELAV-like protein 2 isoform a
NM_001351476.2 NP_001338405.1 ELAV-like protein 2 isoform a
NM_001351477.2 NP_001338406.1 ELAV-like protein 2 isoform b
NM_001351478.2 NP_001338407.1 ELAV-like protein 2 isoform b
NM_001385693.1 NP_001372622.1 ELAV-like protein 2 isoform b
NM_001385694.1 NP_001372623.1 ELAV-like protein 2 isoform j
NM_001385695.1 NP_001372624.1 ELAV-like protein 2 isoform k
NM_001385696.1 NP_001372625.1 ELAV-like protein 2 isoform m
NM_001385697.1 NP_001372626.1 ELAV-like protein 2 isoform c
NM_001385698.1 NP_001372627.1 ELAV-like protein 2 isoform c
NM_001385699.1 NP_001372628.1 ELAV-like protein 2 isoform d
NM_001385700.1 NP_001372629.1 ELAV-like protein 2 isoform e
NM_001385701.1 NP_001372630.1 ELAV-like protein 2 isoform g
NM_001385702.1 NP_001372631.1 ELAV-like protein 2 isoform i
NM_001385703.1 NP_001372632.1 ELAV-like protein 2 isoform a
NM_001385704.1 NP_001372633.1 ELAV-like protein 2 isoform c
NM_001385705.1 NP_001372634.1 ELAV-like protein 2 isoform i
NM_001385707.1 NP_001372636.1 ELAV-like protein 2 isoform d
NM_004432.5 NP_004423.2 ELAV-like protein 2 isoform a

ELAVL2 Protein Structure

RRM_1

RRM_1: RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain) (41 - 111)

RRM_1

RRM_1: RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain) (127 - 193)

RRM_1

RRM_1: RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain) (278 - 347)

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Protein Preferred Names Protein Names

ELAV-like protein 2

ELAV (embryonic lethal, abnormal vision, Drosophila)-like 2 (Hu antigen B)

Related Diseases

Diseases Alias
Hyperinsulinemic Hypoglycemia, Familial, 4

Hyperinsulinism Due To Glutamodehydrogenase Deficiency

HHF4

Familial Hyperinsulinemic Hypoglycemia 4

Hyperinsulinemic Hypoglycemia Due To Short Chain 3-Hydroxylacyl-Coa Dehydrogenase Deficiency

Hyperinsulinism Due To Schad Deficiency

Hyperinsulinism Due To Short Chain 3-Hydroxylacyl-Coa Dehydrogenase Deficiency

Congenital Hyperinsulinism

Schad Deficiency

Persistent Hyperinsulinemic Hypoglycemia Of Infancy

Phhi

3-Hydroxyacyl-Coa Dehydrogenase Deficiency
Myotonic Disease

Myotonic Disorders

Myotonic Syndrome

Symptomatic Myotonia
Myotonic Dystrophy 1

Myotonic Dystrophy

Dystrophia Myotonica

Steinert Disease

Myotonic Dystrophy Type 1

Myotonia Atrophica

DM1

Congenital Myotonic Dystrophy

Myotonia Dystrophica

Steinert Myotonic Dystrophy

Dystrophia Myotonica 1

Dm

Steinert'S Disease

Steinert Myotonic Dystrophy Syndrome

Myotonic Dystrophy Of Steinert

Dystrophia Myotonica Type 1

Myotonic Dystrophy Congenital

Dystrophy, Myotonic, Type 1

Dm - [Dystrophia Myotonica]

Myotonic Muscular Dystrophy
Autism

Autistic Disorder

Autism Susceptibility 1

Childhood Autism

Autistic Disorder Of Childhood Onset

Infantile Autism

Kanner'S Syndrome

Autistic
Autosomal Dominant Cerebellar Ataxia

Spinocerebellar Ataxia

Adca

Pierre Marie Cerebellar Ataxia

Ataxia, Spinocerebellar

Sca

Autosomal Dominant Spinocerebellar Ataxia

Spinocerebellar Ataxias
Amyotrophic Lateral Sclerosis 1

Amyotrophic Lateral Sclerosis

ALS

Lou Gehrig Disease

Amyotrophic Lateral Sclerosis Type 1

Charcot Disease

ALS1

Amyotrophic Lateral Sclerosis, Susceptibility To

Fals

Lou Gehrig'S Disease

Mnd

Motor Neuron Disease

Familial Amyotrophic Lateral Sclerosis

Amyotrophic Lateral Sclerosis 1, Familial

Amyotrophic Lateral Sclerosis 1, Autosomal Dominant

Motor Neuron Disease, Bulbar

Motor Neurone Disease

Amyotrophic Lateral Sclerosis With Dementia

Dementia With Amyotrophic Lateral Sclerosis

Motor Neuron Disease, Amyotrophic Lateral Sclerosis

Sclerosis, Lateral, Amyotrophic

Sclerosis, Lateral, Amyotrophic, Type 1

Amyotrophic Sclerosis

Als - [Amyotrophic Lateral Sclerosis]

Wasting Palsy

Amyotrophic Paralysis

Amyotrophy Lateral Sclerosis

Wasting Paralysis

Spinal Progressive Amyotrophy

Progressive Atrophic Paralysis
Hereditary Spastic Paraplegia

Familial Spastic Paraplegia

Hereditary Spastic Paraparesis

Strumpell-Lorrain Disease

Familial Spastic Paraparesis

Hsp

Spg

Strümpell-Lorrain Disease

Spastic Paraplegia, Hereditary

French Settlement Disease

Strumpell-Lorrain Syndrome

Fsp

Spastic Paraplegia, Familial

Spastic Paraplegia Hereditary

Spastic Paraplegia 3, Autosomal Dominant

Spastic Paraparesis

Hereditary Spastic Paralysis

Familial Spastic Paralysis

Hereditary Spastic Ataxia
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
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS04295 ELAVL2 Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source ID
Canis familiaris ELAVL2 VGNC VGNC:51712
Macaca mulatta ELAVL2 VGNC VGNC:72201
Rattus norvegicus ELAVL2 RGD RGD:628611
Bos taurus ELAVL2 VGNC VGNC:52768
Mus musculus ELAVL2 MGD MGI:1100887
Felis catus ELAVL2 VGNC VGNC:61802