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Fam91a1 Gene Detail
Summary
  • Symbol
    Fam91a1
  • Name
    family with sequence similarity 91, member A1
  • Synonyms
    D15Ertd621e, mKIAA0493
  • Feature Type
    protein coding gene
  • IDs
    MGI:1277178
    NCBI Gene: 210998
  • Alliance
Location & Maps
more
  • Sequence Map
    Chr15:58415468-58457801 bp, + strand
  • From Ensembl annotation of GRCm38

    Mouse Genome Browser

  • Download
    Sequence
      42334 bp   ±  kb flank

  • Genome Browsers
  • Genetic Map
    Chromosome 15, 24.76 cM
  • Mapping Data
    3 experiments
Homology
more
  • Human Ortholog
    FAM91A1, family with sequence similarity 91 member A1
  • Vertebrate Orthologs
    10
  • Human Ortholog
    FAM91A1, family with sequence similarity 91 member A1
    Orthology source: HomoloGene, HGNC
  • Links
    NCBI Gene ID: 157769
    neXtProt AC: NX_Q658Y4
    UniProt: Q658Y4

  • Chr Location
    8q24.13; chr8:123768439-123815452 (+)  GRCh38.p7

Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    1 phenotype from multigenic genotypes
    26 phenotype references
Mice homozygous for a transgenic gene disruption exhibit male infertility.
Gene Ontology
(GO)
Classifications
less
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 ENSMUSG00000037119 Ensembl Gene Model | MGI Sequence Detail 42334 C57BL/6J ±  kb
transcript ENSMUST00000037270 Ensembl | MGI Sequence Detail 5621 Not Applicable  
polypeptide ENSMUSP00000036524 Ensembl | MGI Sequence Detail 837 Not Applicable  
For the selected sequence
Polymorphisms
less
  • SNPs within 2kb
    148 from dbSNP Build 142
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 12
    cDNA 11
    Primer pair 1

    Microarray probesets 5
Other
Accession IDs
less
MGI:2146170, MGI:2384813
References
more
  • Summaries
    All 49
    Developmental Gene Expression 1
    Diseases 1
    Phenotypes 26
  • Earliest
    J:109968 Roderick TH, et al., Nineteen paracentric chromosomal inversions in mice. Genetics. 1974 Jan;76(1):109-17
  • Latest
    J:233611 Hirata A, et al., Homeobox family Hoxc localization during murine palate formation. Congenit Anom (Kyoto). 2016 Jul;56(4):172-9

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
12/05/2017
MGI 6.11
The Jackson Laboratory