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Lrrc3 Gene Detail
Summary
  • Symbol
    Lrrc3
  • Name
    leucine rich repeat containing 3
  • Synonyms
    1300011L04Rik
  • Feature Type
    protein coding gene
  • IDs
    MGI:2447899
    NCBI Gene: 237387
  • Alliance
  • Transcription Start Sites
    2 TSS
Location &
Maps
more
  • Sequence Map
    Chr10:77897575-77902536 bp, - strand
  • From NCBI annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 10, 39.72 cM
  • Mapping Data
    3 experiments
Strain
Comparison
more
  • SNPs within 2kb
    20 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_2447899
protein coding gene Chr10:77897575-77902536 (-)
129S1/SvImJ MGP_129S1SvImJ_G0017410
protein coding gene Chr10:78295447-78302403 (-)
A/J MGP_AJ_G0017388
protein coding gene Chr10:75590166-75595127 (-)
AKR/J MGP_AKRJ_G0017351
protein coding gene Chr10:77611866-77616821 (-)
BALB/cJ MGP_BALBcJ_G0017350
protein coding gene Chr10:75764468-75769429 (-)
C3H/HeJ MGP_C3HHeJ_G0017173
protein coding gene Chr10:77697968-77702929 (-)
C57BL/6NJ MGP_C57BL6NJ_G0017806
protein coding gene Chr10:81080905-81085866 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0015497
protein coding gene Chr10:71942165-71947139 (-)
CAST/EiJ MGP_CASTEiJ_G0016743
protein coding gene Chr10:78023628-78028577 (-)
CBA/J MGP_CBAJ_G0017145
protein coding gene Chr10:84151013-84155972 (-)
DBA/2J MGP_DBA2J_G0017253
protein coding gene Chr10:74831259-74836220 (-)
FVB/NJ MGP_FVBNJ_G0017245
protein coding gene Chr10:74006434-74011395 (-)
LP/J MGP_LPJ_G0017324
protein coding gene Chr10:78739994-78747051 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0017272
protein coding gene Chr10:86156514-86163052 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0017848
protein coding gene Chr10:77647514-77652484 (-)
PWK/PhJ MGP_PWKPhJ_G0016525
protein coding gene Chr10:74716242-74721258 (-)
SPRET/EiJ MGP_SPRETEiJ_G0016310
protein coding gene Chr10:76866024-76870977 (-)
WSB/EiJ MGP_WSBEiJ_G0016803
protein coding gene Chr10:77628617-77633587 (-)



Homology
more
  • Human Ortholog
    LRRC3, leucine rich repeat containing 3
  • Vertebrate Orthologs
    9
  • Human Ortholog
    LRRC3, leucine rich repeat containing 3
    Orthology source: HomoloGene, HGNC
  • Synonyms
    C21orf102, C21orf30, LRRC3DN
  • Links
    NCBI Gene ID: 81543
    neXtProt AC: NX_Q9BY71
    UniProt: Q9BY71

  • Chr Location
    21q22.3; chr21:44455486-44458856 (+)  GRCh38.p7

Human Diseases
less
  • References
    2 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    22 phenotype references
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
  • GO References
Expression
less
Expression Overview

early conceptus
embryo ectoderm
embryo endoderm
embryo mesoderm
embryo mesenchyme
extraembryonic component
alimentary system
auditory system
branchial arches
cardiovascular system
connective tissue
endocrine system
exocrine system
hemolymphoid system
integumental system
limbs
liver and biliary system
musculoskeletal system
nervous system
olfactory system
reproductive system
respiratory system
urinary system
visual system
Click cells to view annotations.


  • Assay Results
  • Tissues
  • cDNA Data
  • Literature Summary
Interactions
less
Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic 237387 NCBI Gene Model | MGI Sequence Detail 4962 C57BL/6J ±  kb
transcript NM_145152 RefSeq | MGI Sequence Detail 4311 C57BL/6  
polypeptide P59034 UniProt | EBI | MGI Sequence Detail 257 Not Applicable  
For the selected sequence
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 25
    cDNA 21
    Primer pair 3
    Other 1

    Microarray probesets 5
Other
Accession IDs
less
MGI:1919013
References
more
  • Summaries
    All 48
    Developmental Gene Expression 4
    Diseases 2
    Gene Ontology 1
    Phenotypes 22
  • Earliest
    J:137335 Roderick TH, Chromosomal inversions in studies of mammalian mutagenesis. Genetics. 1979 May;92(1 Pt 1 Suppl):s121-6
  • Latest
    J:262380 Watson-Scales S, et al., Analysis of motor dysfunction in Down Syndrome reveals motor neuron degeneration. PLoS Genet. 2018 May;14(5):e1007383

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
11/06/2018
MGI 6.13
The Jackson Laboratory