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Protein Coding Gene : Hmces 5-hydroxymethylcytosine (hmC) binding, ES cell specific

Primary Identifier  MGI:1914053 Organism  mouse, laboratory
Chromosome  6 NCBI Gene Number  232210
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Enables single-stranded DNA binding activity. Involved in double-strand break repair via alternative nonhomologous end joining; positive regulation of isotype switching; and somatic hypermutation of immunoglobulin genes. Predicted to be active in replication fork. Is expressed in several structures, including adipose tissue; genitourinary system; gut; hemolymphoid system gland; and liver. Orthologous to human HMCES (5-hydroxymethylcytosine binding, ES cell specific).
PHENOTYPE: Homozygous knockout leads to changes in DNA methylation, resulting in an altered embryonic gene expression profile and embryonic sub-lethality (lower embryonic survival). [provided by MGI curators]
  • synonyms:
  • Hmces,
  • C85376,
  • MGI:2141771,
  • 5-hydroxymethylcytosine (hmC) binding, ES cell specific,
  • expressed sequence C85376,
  • Srap1,
  • 8430410A17Rik,
  • RIKEN cDNA 8430410A17 gene

Features --> Cross References

Genome

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1 Involved In Mutations

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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

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

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