CSRP3 (cysteine and glycine rich protein 3)

2011-03-01  

Identity

HGNC
LOCATION
11p15.1
LOCUSID
ALIAS
CLP,CMD1M,CMH12,CRP3,LMO4,MLP

Other Information

Locus ID:

NCBI: 8048
MIM: 600824
HGNC: 2472
Ensembl: ENSG00000129170

Variants:

dbSNP: 8048
ClinVar: 8048
TCGA: ENSG00000129170
COSMIC: CSRP3

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000129170ENST00000265968P50461
ENSG00000129170ENST00000265968A2TDB8
ENSG00000129170ENST00000533783P50461
ENSG00000129170ENST00000533783A2TDB8
ENSG00000129170ENST00000647990A0A3B3IRI5
ENSG00000129170ENST00000648719A0A3B3IT61
ENSG00000129170ENST00000649235P50461
ENSG00000129170ENST00000649235A2TDB8
ENSG00000129170ENST00000649842A0A3B3ISZ2

Expression (GTEx)

0
100
200
300
400
500
600
700
800

Protein levels (Protein atlas)

Not detected
Low
Medium
High

PharmGKB

Entity IDNameTypeEvidenceAssociationPKPDPMIDs
PA164713366Tumor necrosis factor alpha (TNF-alpha) inhibitorsChemicalClinicalAnnotationassociatedPD
PA443434Arthritis, RheumatoidDiseaseClinicalAnnotationassociatedPD

References

Pubmed IDYearTitleCitations
368773462023Identification and in silico characterization of CSRP3 synonymous variants in dilated cardiomyopathy.0
368773462023Identification and in silico characterization of CSRP3 synonymous variants in dilated cardiomyopathy.0
352417522022LIM domain-wide comprehensive virtual mutagenesis provides structural rationale for cardiomyopathy mutations in CSRP3.8
352417522022LIM domain-wide comprehensive virtual mutagenesis provides structural rationale for cardiomyopathy mutations in CSRP3.8
319193352020Identification of a variant hotspot in MYBPC3 and of a novel CSRP3 autosomal recessive alteration in a cohort of Polish patients with hypertrophic cardiomyopathy.5
330357022020The p.(Cys150Tyr) variant in CSRP3 is associated with late-onset hypertrophic cardiomyopathy in heterozygous individuals.5
319193352020Identification of a variant hotspot in MYBPC3 and of a novel CSRP3 autosomal recessive alteration in a cohort of Polish patients with hypertrophic cardiomyopathy.5
330357022020The p.(Cys150Tyr) variant in CSRP3 is associated with late-onset hypertrophic cardiomyopathy in heterozygous individuals.5
314061092019MLP-deficient human pluripotent stem cell derived cardiomyocytes develop hypertrophic cardiomyopathy and heart failure phenotypes due to abnormal calcium handling.25
314061092019MLP-deficient human pluripotent stem cell derived cardiomyocytes develop hypertrophic cardiomyopathy and heart failure phenotypes due to abnormal calcium handling.25
300124242018First identification of homozygous truncating CSRP3 variants in two unrelated cases with hypertrophic cardiomyopathy.7
300124242018First identification of homozygous truncating CSRP3 variants in two unrelated cases with hypertrophic cardiomyopathy.7
248609832014Muscle lim protein isoform negatively regulates striated muscle actin dynamics and differentiation.16
249344432014Human muscle LIM protein dimerizes along the actin cytoskeleton and cross-links actin filaments.32
248609832014Muscle lim protein isoform negatively regulates striated muscle actin dynamics and differentiation.16

Citation

Dessen P

CSRP3 (cysteine and glycine rich protein 3)

Atlas Genet Cytogenet Oncol Haematol. 2011-03-01

Online version: http://atlasgeneticsoncology.org/gene/52140/haematological-explorer/js/favicon/apple-touch-icon.png