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MATR3

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Mammalian protein found in Homo sapiens
MATR3
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

1X4D, 1X4F

Identifiers
AliasesMATR3, ALS21, MPD2, VCPDM, matrin 3
External IDsOMIM: 164015; MGI: 1298379; HomoloGene: 7830; GeneCards: MATR3; OMA:MATR3 - orthologs
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

9782

17184

Ensembl

ENSG00000015479
ENSG00000280987

ENSMUSG00000037236

UniProt

P43243

Q8K310

RefSeq (mRNA)
NM_001194954
NM_001194955
NM_001194956
NM_001282278
NM_018834

NM_199189

NM_010771

RefSeq (protein)
NP_001181883
NP_001181884
NP_001181885
NP_001269207
NP_061322

NP_954659

NP_034901
NP_001386912
NP_001386913
NP_001386914
NP_001386915

NP_001386917
NP_001386918
NP_001386919
NP_001386920
NP_001386921
NP_001386922

Location (UCSC)n/an/a
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Matrin-3 is a protein that in humans is encoded by the MATR3 gene.

Function

The protein encoded by this gene is localized in the nuclear matrix. It may play a role in transcription or may interact with other nuclear matrix proteins to form the internal fibrogranular network. Two transcript variants encoding the same protein have been identified for this gene.

Pathology

Mutations in the Matrin 3 gene are associated with familial amyotrophic lateral sclerosis.

References

  1. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  2. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. Belgrader P, Dey R, Berezney R (Jun 1991). "Molecular cloning of matrin 3. A 125-kilodalton protein of the nuclear matrix contains an extensive acidic domain". J Biol Chem. 266 (15): 9893–9. doi:10.1016/S0021-9258(18)92902-9. PMID 2033075.
  4. ^ "Entrez Gene: MATR3 matrin 3".
  5. Johnson JO, Pioro EP, Boehringer A, Chia R, Feit H, Renton AE, Pliner HA, Abramzon Y, Marangi G, Winborn BJ, Gibbs JR, Nalls MA, Morgan S, Shoai M, Hardy J, Pittman A, Orrell RW, Malaspina A, Sidle KC, Fratta P, Harms MB, Baloh RH, Pestronk A, Weihl CC, Rogaeva E, Zinman L, Drory VE, Borghero G, Mora G, Calvo A, Rothstein JD, Drepper C, Sendtner M, Singleton AB, Taylor JP, Cookson MR, Restagno G, Sabatelli M, Bowser R, Chiò A, Traynor BJ (2014). "Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis". Nat. Neurosci. 17 (5): 664–6. doi:10.1038/nn.3688. PMC 4000579. PMID 24686783.

Further reading

PDB gallery
  • 1x4d: Solution structure of RRM domain in Matrin 3 1x4d: Solution structure of RRM domain in Matrin 3
  • 1x4f: Solution structure of the second RRM domain in Matrin 3 1x4f: Solution structure of the second RRM domain in Matrin 3


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