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Fam222a Gene Detail
Summary
  • Symbol
    Fam222a
  • Name
    family with sequence similarity 222, member A
  • Synonyms
    BC057022
  • Feature Type
    protein coding gene
  • IDs
    MGI:3605543
    NCBI Gene: 433940
  • Alliance
Location &
Maps
more
  • Sequence Map
    Chr5:114568251-114613220 bp, + strand
  • From NCBI annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 5, 55.99 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    345 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3605543
protein coding gene Chr5:114568016-114613220 (+)
129S1/SvImJ MGP_129S1SvImJ_G0029940
protein coding gene Chr5:117329967-117377010 (+)
A/J MGP_AJ_G0029905
protein coding gene Chr5:112706922-112751694 (+)
AKR/J MGP_AKRJ_G0029843
protein coding gene Chr5:116281589-116328499 (+)
BALB/cJ MGP_BALBcJ_G0029916
protein coding gene Chr5:114074210-114119480 (+)
C3H/HeJ MGP_C3HHeJ_G0029636
protein coding gene Chr5:116789165-116837330 (+)
C57BL/6NJ MGP_C57BL6NJ_G0030370
protein coding gene Chr5:121853565-121904253 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0027598
protein coding gene Chr5:107529733-107577178 (+)
CAST/EiJ MGP_CASTEiJ_G0029044
protein coding gene Chr5:115731666-115776634 (+)
CBA/J MGP_CBAJ_G0029603
protein coding gene Chr5:126506583-126559491 (+)
DBA/2J MGP_DBA2J_G0029753
protein coding gene Chr5:112775633-112822071 (+)
FVB/NJ MGP_FVBNJ_G0029710
protein coding gene Chr5:111582753-111628270 (+)
LP/J MGP_LPJ_G0029842
protein coding gene Chr5:117890981-117943622 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0029741
protein coding gene Chr5:130913736-130959860 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0030411
protein coding gene Chr5:115758139-115806386 (+)
PWK/PhJ MGP_PWKPhJ_G0028758
protein coding gene Chr5:111426251-111472485 (+)
SPRET/EiJ MGP_SPRETEiJ_G0028596
protein coding gene Chr5:113296752-113351590 (+)
WSB/EiJ MGP_WSBEiJ_G0029120
protein coding gene Chr5:116339443-116391275 (+)



Homology
more
  • Human Ortholog
    FAM222A, family with sequence similarity 222 member A
  • Vertebrate Orthologs
    10
  • Human Ortholog
    FAM222A, family with sequence similarity 222 member A
    Orthology source: HomoloGene, HGNC
  • Synonyms
    C12orf34
  • Links
    NCBI Gene ID: 84915
    neXtProt AC: NX_Q5U5X8
    UniProt: Q5U5X8

  • Chr Location
    12q24.11; chr12:109714382-109770509 (+)  GRCh38.p7

Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    10 phenotype references
  • All Mutations and Alleles
    8
  • Chemically induced (other)
    1
  • Endonuclease-mediated
    1
  • Gene trapped
    4
  • Radiation induced
    1
  • Targeted
    1
  • Genomic Mutations
    2 involving Fam222a
  • Incidental Mutations
    APF , CvDC
  • Find Mice (IMSR)
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
less
Representative SequencesLengthStrain/SpeciesFlank
genomic 433940 NCBI Gene Model | MGI Sequence Detail 44970 C57BL/6J ±  kb
transcript NM_001004180 RefSeq | MGI Sequence Detail 2717 C57BL/6  
polypeptide Q6PGH4 UniProt | EBI | MGI Sequence Detail 453 Not Applicable  
For the selected sequence
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 6
    cDNA 5
    Primer pair 1

    Microarray probesets 3
References
more
  • Summaries
    All 27
    Developmental Gene Expression 1
    Phenotypes 10
  • Earliest
    J:134667 Roderick TH, et al., Two radiation-induced chromosomal inversions in mice (Mus musculus). Proc Natl Acad Sci U S A. 1970 Oct;67(2):961-7
  • Latest
    J:193641 Nakano Y, et al., A mutation in the Srrm4 gene causes alternative splicing defects and deafness in the Bronx waltzer mouse. PLoS Genet. 2012;8(10):e1002966

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
02/11/2020
MGI 6.14
The Jackson Laboratory