RBM20 RNA binding motif protein 20 [Homo sapiens (human)] - Gene

Summary

Official Symbol: RBM20provided by HGNC
Official Full Name: RNA binding motif protein 20provided by HGNC
Primary source: HGNC:HGNC:27424
See related: Ensembl:ENSG00000203867 MIM:613171; AllianceGenome:HGNC:27424
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Summary: This gene encodes a protein that binds RNA and regulates splicing. Mutations in this gene have been associated with familial dilated cardiomyopathy. [provided by RefSeq, Apr 2014]
Expression: Biased expression in heart (RPKM 10.3), salivary gland (RPKM 1.2) and 5 other tissues See more
Orthologs: mouse all
NEW: Try the new Gene table
Try the new Transcript table

Genomic context

Location:: 10q25.2

Exon count:: 17

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	10	NC_000010.11 (110643245..110839468)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	10	NC_060934.1 (111526746..111723237)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	10	NC_000010.10 (112404094..112599226)

Chromosome 10 - NC_000010.11 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

Go to the top of the page Help

Go to reference sequence details

Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Expression

Go to the top of the page Help

See details

Project title: HPA RNA-seq normal tissues
Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
BioProject: PRJEB4337
Publication: PMID 24309898
Analysis date: Wed Apr 4 07:08:55 2018

Bibliography

Go to the top of the page Help

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

[Research progress on the expression of the RBM20 gene in dilated cardiomyopathy].
Title: [Research progress on the expression of the RBM20 gene in dilated cardiomyopathy].
Risks of Ventricular Arrhythmia and Heart Failure in Carriers of RBM20 Variants.
Title: Risks of Ventricular Arrhythmia and Heart Failure in Carriers of RBM20 Variants.
I536T variant of RBM20 affects splicing of cardiac structural proteins that are causative for developing dilated cardiomyopathy.
Title: I536T variant of RBM20 affects splicing of cardiac structural proteins that are causative for developing dilated cardiomyopathy.
SR Protein Kinases Regulate the Splicing of Cardiomyopathy-Relevant Genes via Phosphorylation of the RSRSP Stretch in RBM20.
Title: SR Protein Kinases Regulate the Splicing of Cardiomyopathy-Relevant Genes via Phosphorylation of the RSRSP Stretch in RBM20.
RBM20(S639G) mutation is a high genetic risk factor for premature death through RNA-protein condensates.
Title: RBM20(S639G) mutation is a high genetic risk factor for premature death through RNA-protein condensates.
Cardiomyopathy-associated mutations in the RS domain affect nuclear localization of RBM20.
Title: Cardiomyopathy-associated mutations in the RS domain affect nuclear localization of RBM20.
RBM20 Is a Candidate Gene for Hypertrophic Cardiomyopathy.
Title: RBM20 Is a Candidate Gene for Hypertrophic Cardiomyopathy.
Gain-of-function cardiomyopathic mutations in RBM20 rewire splicing regulation and re-distribute ribonucleoprotein granules within processing bodies.
Title: Gain-of-function cardiomyopathic mutations in RBM20 rewire splicing regulation and re-distribute ribonucleoprotein granules within processing bodies.
The Combined Human Genotype of Truncating TTN and RBM20 Mutations Is Associated with Severe and Early Onset of Dilated Cardiomyopathy.
Title: The Combined Human Genotype of Truncating TTN and RBM20 Mutations Is Associated with Severe and Early Onset of Dilated Cardiomyopathy.
Phenotype and progression among patients with dilated cardiomyopathy and RBM20 mutations.
Title: Phenotype and progression among patients with dilated cardiomyopathy and RBM20 mutations.

Submit: New GeneRIF Correction See all GeneRIFs (35)

Phenotypes

Go to the top of the page Help

Find tests for this gene in the NIH Genetic Testing Registry (GTR)

Review eQTL and phenotype association data in this region using PheGenI

Associated conditions

Description	Tests
Dilated cardiomyopathy 1DD MedGen: C2750995 OMIM: 613172 GeneReviews: Dilated Cardiomyopathy Overview	Compare labs
Primary dilated cardiomyopathy MedGen: C0007193 GeneReviews: Dilated Cardiomyopathy Overview	Compare labs

Variation

Go to the top of the page Help

See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Interactions

Go to the top of the page Help

Products	Interactant	Other Gene	Complex	Source	Pubs	Description

General gene information

Go to the top of the page Help

Markers

SHGC-54184 (e-PCR)
- UniSTS:75046

SHGC-145640 (e-PCR)
- UniSTS:174698

SHGC-147317 (e-PCR)
- UniSTS:175737

SHGC-82989 (e-PCR)
- UniSTS:101273

SHGC-80917 (e-PCR)
- UniSTS:102556

WI-10472 (e-PCR)
- UniSTS:42446

WI-11215 (e-PCR)
- UniSTS:41168

Gene Ontology Provided by GOA

Function	Evidence Code	Pubs
enables RNA binding	ISS Inferred from Sequence or Structural Similarity more info
enables mRNA binding	IBA Inferred from Biological aspect of Ancestor more info
enables pre-mRNA intronic binding	IDA Inferred from Direct Assay more info	PubMed
enables protein binding	IPI Inferred from Physical Interaction more info	PubMed
enables splicing factor binding	IDA Inferred from Direct Assay more info	PubMed
enables zinc ion binding	IEA Inferred from Electronic Annotation more info

Process	Evidence Code	Pubs
involved_in heart formation	IDA Inferred from Direct Assay more info	PubMed
involved_in heart formation	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in negative regulation of mRNA splicing, via spliceosome	IDA Inferred from Direct Assay more info	PubMed
involved_in negative regulation of mRNA splicing, via spliceosome	ISS Inferred from Sequence or Structural Similarity more info
involved_in positive regulation of RNA splicing	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in regulation of RNA splicing	IBA Inferred from Biological aspect of Ancestor more info
involved_in regulation of alternative mRNA splicing, via spliceosome	IEA Inferred from Electronic Annotation more info
involved_in regulation of mRNA splicing, via spliceosome	IDA Inferred from Direct Assay more info	PubMed
involved_in regulation of mRNA splicing, via spliceosome	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in spliceosome-depend formation of circular RNA	IDA Inferred from Direct Assay more info	PubMed

Component	Evidence Code	Pubs
located_in cytoplasmic ribonucleoprotein granule	IDA Inferred from Direct Assay more info	PubMed
is_active_in nucleus	IBA Inferred from Biological aspect of Ancestor more info
is_active_in nucleus	IDA Inferred from Direct Assay more info	PubMed

General protein information

Go to the top of the page Help

Preferred Names: RNA-binding protein 20

Names: probable RNA-binding protein 20

NCBI Reference Sequences (RefSeq)

Go to the top of the page Help

NEW Try the new Transcript table

RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

NG_021177.1 RefSeqGene

Range

5001..200075

Download

GenBank, FASTA, Sequence Viewer (Graphics), LRG_382

mRNA and Protein(s)

NM_001134363.3 → NP_001127835.2 RNA-binding protein 20

Status: REVIEWED

Source sequence(s)

AL359260, EU822950, KF459660

Consensus CDS

CCDS44477.1

UniProtKB/Swiss-Prot

A6NIP5, B5A868, Q5JVI1, Q5T481

Related

ENSP00000358532.3, ENST00000369519.4

Conserved Domains (3) summary

smart00451
Location:1159 → 1193

ZnF_U1; U1-like zinc finger

cd12685
Location:518 → 593

RRM_RBM20; RNA recognition motif of vertebrate RNA-binding protein 20 (RBM20)

pfam08648
Location:612 → 706

DUF1777; Protein of unknown function (DUF1777)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

NC_000010.11 Reference GRCh38.p14 Primary Assembly

Range

110643245..110839468

Download

GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

XM_017016103.3 → XP_016871592.1 RNA-binding protein 20 isoform X1
XM_017016104.3 → XP_016871593.1 RNA-binding protein 20 isoform X2

Conserved Domains (3) summary

smart00451
Location:1031 → 1065

ZnF_U1; U1-like zinc finger

cd12685
Location:390 → 465

RRM_RBM20; RNA recognition motif of vertebrate RNA-binding protein 20 (RBM20)

pfam08648
Location:484 → 578

DUF1777; Protein of unknown function (DUF1777)
XM_047425116.1 → XP_047281072.1 RNA-binding protein 20 isoform X2