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Protein Coding Gene : Ssrp1 structure specific recognition protein 1

Primary Identifier  MGI:107912 Organism  mouse, laboratory
Chromosome  2 NCBI Gene Number  20833
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables chromatin binding activity. Predicted to be involved in nucleosome disassembly and regulation of chromatin organization. Predicted to act upstream of or within DNA repair and DNA replication. Predicted to be located in nucleus. Predicted to be part of FACT complex. Is expressed in several structures, including central nervous system; early conceptus; genitourinary system; hemolymphoid system; and sensory organ. Orthologous to human SSRP1 (structure specific recognition protein 1).
PHENOTYPE: Disruption of this gene is lethal resulting in death at some point between implantation and E5.5. [provided by MGI curators]
  • synonyms:
  • HMG-box-containing,
  • high mobility group protein I, related sequence 3,
  • Hmgox,
  • high mobility group protein 1, related sequence 1,
  • MGD-MRK-10749,
  • Hmg1-rs1,
  • structure specific recognition protein 1,
  • T160,
  • Ssrp1,
  • MGD-MRK-36492,
  • MGD-MRK-10799,
  • C81323,
  • expressed sequence C81323,
  • Hmgi-rs3,
  • MGD-MRK-28178,
  • MGI:2139516

Features --> Cross References

Genome

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0 CDSs

0 Exons

0 Genomic Clusters

4 Involved In Mutations

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0 Transgenic Expressors

0 UTRs

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

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

10 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

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