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Fam151a Gene Detail
Summary
  • Symbol
    Fam151a
  • Name
    family with sequence simliarity 151, member A
  • Feature Type
    protein coding gene
  • IDs
    MGI:2657115
    NCBI Gene: 230579
  • Alliance
  • Transcription Start Sites
    1 TSS
Location &
Maps
more
  • Sequence Map
    Chr4:106733915-106748292 bp, + strand
  • From NCBI annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 4, 49.74 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    202 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_2657115
protein coding gene Chr4:106733889-106748292 (+)
129S1/SvImJ MGP_129S1SvImJ_G0028526
protein coding gene Chr4:107377188-107391590 (+)
A/J MGP_AJ_G0028489
protein coding gene Chr4:103536175-103550621 (+)
AKR/J MGP_AKRJ_G0028436
protein coding gene Chr4:106055625-106069972 (+)
BALB/cJ MGP_BALBcJ_G0028508
protein coding gene Chr4:103726190-103740888 (+)
C3H/HeJ MGP_C3HHeJ_G0028222
protein coding gene Chr4:106805338-106821727 (+)
C57BL/6NJ MGP_C57BL6NJ_G0028948
protein coding gene Chr4:111245762-111261312 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0026239
protein coding gene Chr4:98812741-98827609 (+)
CAST/EiJ MGP_CASTEiJ_G0027658
protein coding gene Chr4:104612210-104628089 (+)
CBA/J MGP_CBAJ_G0028191
protein coding gene Chr4:114840021-114854393 (+)
DBA/2J MGP_DBA2J_G0028339
protein coding gene Chr4:103154934-103169308 (+)
FVB/NJ MGP_FVBNJ_G0028307
protein coding gene Chr4:102013316-102028749 (+)
LP/J MGP_LPJ_G0028440
protein coding gene Chr4:107575633-107591619 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0028333
protein coding gene Chr4:120157638-120179101 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0028984
protein coding gene Chr4:106303869-106319726 (+)
PWK/PhJ MGP_PWKPhJ_G0027384
protein coding gene Chr4:101391714-101406186 (+)
SPRET/EiJ MGP_SPRETEiJ_G0027208
protein coding gene Chr4:103689856-103708929 (+)
WSB/EiJ MGP_WSBEiJ_G0027739
protein coding gene Chr4:106478338-106493913 (+)



Homology
more
  • Human Ortholog
    FAM151A, family with sequence similarity 151 member A
  • Vertebrate Orthologs
    8
  • Human Ortholog
    FAM151A, family with sequence similarity 151 member A
    Orthology source: HomoloGene, HGNC
  • Synonyms
    C1orf179
  • Links
    NCBI Gene ID: 338094
    neXtProt AC: NX_Q8WW52
    UniProt: Q8WW52

  • Chr Location
    1p32.3; chr1:54609177-54623527 (-)  GRCh38.p7

Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    2 phenotypes from 1 allele in 1 genetic background
    4 phenotypes from multigenic genotypes
    14 phenotype references
Homozygous knockout does not affect the retina.
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
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Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic 230579 NCBI Gene Model | MGI Sequence Detail 14378 C57BL/6J ±  kb
transcript NM_146149 RefSeq | MGI Sequence Detail 1966 FVB/N  
polypeptide Q8QZW3 UniProt | EBI | MGI Sequence Detail 608 Not Applicable  
For the selected sequence
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 7
    cDNA 7

    Microarray probesets 1
References
more
  • Summaries
    All 32
    Developmental Gene Expression 3
    Gene Ontology 1
    Phenotypes 14
  • Earliest
    J:65060 Kawai J, et al., Functional annotation of a full-length mouse cDNA collection. Nature. 2001 Feb 8;409(6821):685-90
  • Latest
    J:284934 Findlay AS, et al., Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function. Sci Rep. 2020 Jan 16;10(1):437

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)
Citing These Resources
Funding Information
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last database update
03/30/2021
MGI 6.16
The Jackson Laboratory