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Protein Coding Gene : Mbnl3 muscleblind like splicing factor 3

Primary Identifier  MGI:2444912 Organism  mouse, laboratory
Chromosome  X NCBI Gene Number  171170
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable RNA binding activity. Acts upstream of or within negative regulation of myoblast differentiation. Predicted to be located in cytosol. Predicted to be active in cytoplasm and nucleoplasm. Is expressed in several structures, including 1st branchial arch; early conceptus; future brain; genitourinary system; and hemolymphoid system gland. Orthologous to human MBNL3 (muscleblind like splicing regulator 3).
PHENOTYPE: Mice homozygous for an allele lacking exon 2 exhibit impaired muscle regeneration. [provided by MGI curators]
  • synonyms:
  • expressed sequence AI661274,
  • E430034C16Rik,
  • MGI:2147904,
  • AI661274,
  • Mbnl3,
  • RIKEN cDNA A530038J18 gene,
  • MGI:2443528,
  • muscleblind like splicing factor 3,
  • RIKEN cDNA E430034C16 gene,
  • A530038J18Rik,
  • CHCR

Features --> Cross References

Genome

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Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

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