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Lhfpl2 Gene Detail
Summary
  • Symbol
    Lhfpl2
  • Name
    lipoma HMGIC fusion partner-like 2
  • Synonyms
    mKIAA0206, vgim
  • Feature Type
    protein coding gene
  • IDs
    MGI:2145236
    NCBI Gene: 218454
  • Gene Overview
    MyGene.info: LHFPL2
Location & Maps
more
  • Sequence Map
    Chr13:94057796-94195409 bp, + strand
  • From VEGA annotation of GRCm38

    Mouse Genome Browser

  • Download
    Sequence
      137614 bp   ±  kb flank

  • Genome Browsers
  • Genetic Map
    Chromosome 13, 49.03 cM
  • Mapping Data
    2 experiments
Homology
more
  • Human Ortholog
    LHFPL2, lipoma HMGIC fusion partner-like 2
  • Vertebrate Orthologs
    10
  • Human Ortholog
    LHFPL2, lipoma HMGIC fusion partner-like 2
    Orthology source: HGNC, HomoloGene
  • Links
    NCBI Gene ID: 10184
    neXtProt AC: NX_Q6ZUX7

  • Chr Location
    5q14.1; chr5:78485215-78648895 (-)  GRCh38.p2

Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    13 phenotypes from 1 allele in 1 genetic background
    12 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
  • All Mutations and Alleles
    5
  • Chemically induced (other)
    1
  • Gene trapped
    1
  • Spontaneous
    1
  • Targeted
    2
  • Genomic Mutations
    1 involving Lhfpl2
  • Incidental Mutations
Females homozygous for a spontaneous point mutation have a completely closed vagina, soft swelling of the perineum and buildup of viscous fluid in the uteri.
Gene Ontology
(GO)
Classifications
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  • All GO Annotations
  • GO References
Expression
less
  • cDNA Data
Interactions
less
Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic OTTMUSG00000027714 VEGA Gene Model | MGI Sequence Detail 137614 C57BL/6J ±  kb
transcript OTTMUST00000068583 VEGA | MGI Sequence Detail 3611 Not Applicable  
polypeptide OTTMUSP00000034710 VEGA | MGI Sequence Detail 222 Not Applicable  
For the selected sequence
Polymorphisms
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  • SNPs within 2kb
    1094 from dbSNP Build 142
Protein
Information
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  • UniProt
    3 Sequences
  • Protein Ontology
    PR:000009786 lipoma HMGIC fusion partner-like 2 protein
  • InterPro Domains
    IPR019372 Lipoma HMGIC fusion partner-like protein
Molecular
Reagents
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  • All nucleic 11
    cDNA 11

    Microarray probesets 7
Other
Accession IDs
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MGI:2145409, MGI:4837107
References
more
  • Summaries
    All 30
    Gene Ontology 1
    Phenotypes 12
  • Earliest
    J:80000 The FANTOM Consortium and The RIKEN Genome Exploration Research Group Phase I & II Team, Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Nature. 2002;420:563-573
  • Latest
    J:222308 Fairfield H, et al., Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders. Genome Res. 2015 Jul;25(7):948-57

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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last database update
07/19/2016
MGI 6.04
The Jackson Laboratory