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Spata31d1b Gene Detail
Summary
  • Symbol
    Spata31d1b
  • Name
    spermatogenesis associated 31 subfamily D, member 1B
  • Synonyms
    Fam75d1b, Gm4934
  • Feature Type
    protein coding gene
  • IDs
    MGI:3646080
    NCBI Gene: 238662
  • Alliance
  • Transcription Start Sites
    1 TSS
Location &
Maps
more
  • Sequence Map
    Chr13:59712284-59719289 bp, + strand
  • From NCBI annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 13, 31.87 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    62 from dbSNP Build 142
  • Strain Annotations
    11
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3646080
protein coding gene Chr13:59712284-59719295 (+)
129S1/SvImJ MGP_129S1SvImJ_G0020641
protein coding gene Chr13:59423462-59431559 (+)
A/J MGP_AJ_G0020596
protein coding gene Chr13:57205697-57213983 (+)
AKR/J no annotation
BALB/cJ MGP_BALBcJ_G0020592
protein coding gene Chr13:57468611-57475482 (+)
C3H/HeJ no annotation
C57BL/6NJ MGP_C57BL6NJ_G0021026
protein coding gene Chr13:61218509-61228941 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0018608
protein coding gene Chr13:55092731-55099835 (+)
CAST/EiJ MGP_CASTEiJ_G0019907
protein coding gene Chr13:58919901-58926486 (+)
CBA/J no annotation
DBA/2J MGP_DBA2J_G0020473
protein coding gene Chr13:56748679-56757482 (+)
FVB/NJ no annotation
LP/J MGP_LPJ_G0020549
protein coding gene Chr13:59685389-59693737 (+)
NOD/ShiLtJ no annotation
NZO/HlLtJ MGP_NZOHlLtJ_G0021069
protein coding gene Chr13:58525648-58531921 (+)
PWK/PhJ no annotation
SPRET/EiJ no annotation
WSB/EiJ MGP_WSBEiJ_G0019967
protein coding gene Chr13:58969493-58976009 (+)



Homology
more
  • Human Ortholog
    SPATA31D1, SPATA31 subfamily D member 1
  • Human Ortholog
    SPATA31D1, SPATA31 subfamily D member 1
    Orthology source: HGNC
  • Synonyms
    FAM75D1
  • Links
    NCBI Gene ID: 389763
    neXtProt AC: NX_Q6ZQQ2
    UniProt: Q6ZQQ2

  • Chr Location
    9q21.32; chr9:81987404-81995256 (+)  GRCh38.p7

Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    5 phenotype 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
  • cDNA Data
Interactions
less
Sequences &
Gene Models
less
Representative SequencesLengthStrain/SpeciesFlank
genomic 238662 NCBI Gene Model | MGI Sequence Detail 7006 C57BL/6J ±  kb
transcript NM_001167593 RefSeq | MGI Sequence Detail 4281 C57BL/6  
polypeptide NP_001161065 RefSeq | MGI Sequence Detail 1361 C57BL/6  
For the selected sequence
Protein
Information
less
  • UniProt
    1 Sequence
  • InterPro Domains
    IPR039509 SPATA31/FAM205
Molecular
Reagents
less
  • All nucleic 5
    cDNA 5
References
more
  • Summaries
    All 16
    Phenotypes 5
  • Earliest
    J:182573 Roderick TH, Producing and detecting paracentric chromosomal inversions in mice. Mutat Res. 1971 Jan;11(1):59-69
  • Latest
    J:153498 Diez-Roux G, et al., A high-resolution anatomical atlas of the transcriptome in the mouse embryo. PLoS Biol. 2011;9(1):e1000582

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
02/23/2021
MGI 6.16
The Jackson Laboratory