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1700029H14Rik Gene Detail
Summary
  • Symbol
    1700029H14Rik
  • Name
    RIKEN cDNA 1700029H14 gene
  • Feature Type
    protein coding gene
  • IDs
    MGI:1913751
    NCBI Gene: 66501
  • Alliance
  • Transcription Start Sites
    1 TSS
Location &
Maps
more
  • Sequence Map
    Chr8:13600733-13612461 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 8, 6.26 cM, cytoband A2
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    145 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1913751
protein coding gene Chr8:13600722-13612555 (-)
129S1/SvImJ MGP_129S1SvImJ_G0033383
protein coding gene Chr8:10908905-10920695 (-)
A/J MGP_AJ_G0033363
protein coding gene Chr8:10512558-10524282 (-)
AKR/J MGP_AKRJ_G0033294
protein coding gene Chr8:10798667-10810391 (-)
BALB/cJ MGP_BALBcJ_G0033364
protein coding gene Chr8:10645059-10656783 (-)
C3H/HeJ MGP_C3HHeJ_G0033077
protein coding gene Chr8:11015628-11027356 (-)
C57BL/6NJ MGP_C57BL6NJ_G0033876
protein coding gene Chr8:11283653-11295381 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0030844
protein coding gene Chr8:10012396-10024813 (-)
CAST/EiJ MGP_CASTEiJ_G0032399
protein coding gene Chr8:10771055-10782780 (-)
CBA/J MGP_CBAJ_G0033050
protein coding gene Chr8:11760611-11772335 (-)
DBA/2J MGP_DBA2J_G0033203
protein coding gene Chr8:10458034-10469758 (-)
FVB/NJ MGP_FVBNJ_G0033152
protein coding gene Chr8:10474251-10485976 (-)
LP/J MGP_LPJ_G0033297
protein coding gene Chr8:10834495-10846250 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0033186
protein coding gene Chr8:11978003-11989727 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0033893
protein coding gene Chr8:10859748-10871495 (-)
PWK/PhJ MGP_PWKPhJ_G0032112
protein coding gene Chr8:10516990-10528830 (-)
SPRET/EiJ MGP_SPRETEiJ_G0031954
protein coding gene Chr8:10752716-10764435 (-)
WSB/EiJ MGP_WSBEiJ_G0032515
protein coding gene Chr8:10896553-10908303 (-)



Homology
more
  • Human Ortholog
    C13orf46, chromosome 13 open reading frame 46
  • Vertebrate Orthologs
    2
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    C13orf46, chromosome 13 open reading frame 46
  • Links
    NCBI Gene ID: 100507747
    UniProt: A0A1B0GUA9

  • Chr Location
    chr13:113926514-113974076 (-)  GRCh38

Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    4 phenotype references
Gene Ontology
(GO)
Classifications
less
Molecular Function

No experimental evidence to support Molecular Function annotation, following literature review. See J:73796.
Biological Process

No experimental evidence to support Biological Process annotation, following literature review. See J:73796.
Cellular Component

No experimental evidence to support Cellular Component annotation, following literature review. See J:73796.
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
Sequences &
Gene Models
less
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000031452 Ensembl Gene Model | MGI Sequence Detail 11729 C57BL/6J ±  kb
transcript ENSMUST00000151400 Ensembl | MGI Sequence Detail 1216 Not Applicable  
polypeptide ENSMUSP00000120739 Ensembl | MGI Sequence Detail 240 Not Applicable  
For the selected sequence
Protein
Information
less
  • UniProt
    4 Sequences
  • InterPro Domains
    IPR040020 Uncharacterized protein C13orf46-like
Molecular
Reagents
less
  • All nucleic 26
    cDNA 26

    Microarray probesets 4
References
more
  • Summaries
    All 21
    Phenotypes 4
  • 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:274872 Ingham NJ, et al., Mouse screen reveals multiple new genes underlying mouse and human hearing loss. PLoS Biol. 2019 Apr;17(4):e3000194

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
04/16/2024
MGI 6.23
The Jackson Laboratory