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Frg2f9 Pseudogene Detail
Summary
  • Symbol
    Frg2f9
  • Name
    FSHD region gene 2 family member 9
  • Synonyms
    Gm6232
  • Feature Type
    pseudogene
  • IDs
    MGI:3779574
    NCBI Gene: 621487
  • Alliance
Location &
Maps
more
  • Sequence Map
    Chr14:106701914-106703185 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 14, 56.16 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    73 from dbSNP Build 142
  • Strain Annotations
    1
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3779574
pseudogene Chr14:106701914-106703185 (+)
129S1/SvImJ no annotation
A/J no annotation
AKR/J no annotation
BALB/cJ no annotation
C3H/HeJ no annotation
C57BL/6NJ no annotation
CAROLI/EiJ no annotation
CAST/EiJ no annotation
CBA/J no annotation
DBA/2J no annotation
FVB/NJ no annotation
LP/J no annotation
NOD/ShiLtJ no annotation
NZO/HlLtJ no annotation
PWK/PhJ no annotation
SPRET/EiJ no annotation
WSB/EiJ no annotation



Homology
more
  • Human Ortholog
    FRG2, FSHD region gene 2
  • Vertebrate Orthologs
    2
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    FRG2, FSHD region gene 2
  • Synonyms
    FRG2A
  • Links
    NCBI Gene ID: 448831
    neXtProt AC: NX_Q64ET8
    UniProt: Q64ET8

  • Chr Location
    4q35.2; chr4:190024367-190027257 (-)  GRCh38

  • Human Ortholog
    FRG2B, FSHD region gene 2 family member B
  • Links
    NCBI Gene ID: 441581
    neXtProt AC: NX_Q96QU4
    UniProt: Q96QU4

  • Chr Location
    10q26.3; chr10:133623895-133626795 (-)  GRCh38

Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    4 phenotype references
  • All Mutations and Alleles
    2
  • Chemically induced (other)
    1
  • Radiation induced
    1
  • Genomic Mutations
    2 involving Frg2f9
  • Find Mice (IMSR)
Gene Ontology
(GO)
Classifications
less
Molecular Function

No experimental evidence to support Molecular Function annotation, following literature review. See J:73796.
Biological Process

No experimental evidence to support Biological Process annotation, following literature review. See J:73796.
Cellular Component

No experimental evidence to support Cellular Component annotation, following literature review. See J:73796.
Sequences &
Gene Models
less
  • All Sequences
  • RefSeq
Representative SequencesLengthStrain/SpeciesFlank
genomic 621487 NCBI Gene Model | MGI Sequence Detail 1272 C57BL/6J ±  kb
For the selected sequence
References
more
  • Summaries
    All 8
    Phenotypes 4
  • Earliest
    J:67314 Roix J, et al., Molecular and functional mapping of the piebald deletion complex on mouse chromosome 14. Genetics. 2001 Feb;157(2):803-15

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Funding Information
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory