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1700093K21Rik Gene Detail
Summary
  • Symbol
    1700093K21Rik
  • Name
    RIKEN cDNA 1700093K21 gene
  • Synonyms
    b2b3025Clo
  • Feature Type
    protein coding gene
  • IDs
    MGI:1914608
    NCBI Gene: 67358
  • Alliance
  • Transcription Start Sites
    5 TSS
Location &
Maps
more
  • Sequence Map
    Chr11:23516203-23521155 bp, - strand
  • From Ensembl annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 11, 14.32 cM, cytoband A3.3
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    9 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1914608
protein coding gene Chr11:23516203-23521317 (-)
129S1/SvImJ MGP_129S1SvImJ_G0018088
protein coding gene Chr11:21279140-21286032 (-)
A/J MGP_AJ_G0018061
protein coding gene Chr11:20448190-20453146 (-)
AKR/J MGP_AKRJ_G0018025
protein coding gene Chr11:21181253-21190209 (-)
BALB/cJ MGP_BALBcJ_G0018029
protein coding gene Chr11:20589279-20594652 (-)
C3H/HeJ MGP_C3HHeJ_G0017843
protein coding gene Chr11:21063812-21068717 (-)
C57BL/6NJ MGP_C57BL6NJ_G0018481
protein coding gene Chr11:22140409-22146732 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0016139
protein coding gene Chr11:19341385-19346235 (-)
CAST/EiJ MGP_CASTEiJ_G0017404
protein coding gene Chr11:21089705-21094613 (-)
CBA/J MGP_CBAJ_G0017817
protein coding gene Chr11:23122536-23127427 (-)
DBA/2J MGP_DBA2J_G0017927
protein coding gene Chr11:20374334-20379569 (-)
FVB/NJ MGP_FVBNJ_G0017919
protein coding gene Chr11:20153609-20158718 (-)
LP/J MGP_LPJ_G0017998
protein coding gene Chr11:21376355-21383133 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0017945
protein coding gene Chr11:23649802-23654663 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0018522
protein coding gene Chr11:21292903-21299235 (-)
PWK/PhJ MGP_PWKPhJ_G0017185
protein coding gene Chr11:20420989-20425955 (-)
SPRET/EiJ MGP_SPRETEiJ_G0016982
protein coding gene Chr11:21044175-21049757 (-)
WSB/EiJ MGP_WSBEiJ_G0017458
protein coding gene Chr11:20928294-20934255 (-)



Homology
more
  • Human Ortholog
    C2orf74, chromosome 2 open reading frame 74
  • Vertebrate Orthologs
    7
  • Human Ortholog
    C2orf74, chromosome 2 open reading frame 74
    Orthology source: HGNC, HomoloGene
  • Links
    NCBI Gene ID: 339804
    neXtProt AC: NX_A8MZ97
    UniProt: A8MZ97

  • Chr Location
    2p15; chr2:61145068-61164830 (+)  GRCh38.p7

Human Diseases
more
  • Diseases
    1 with 1700093K21Rik mouse models

Human Disease Mouse Models
      
IDs
View 1 model
Click on a disease name to see all genes associated with that disease.

  • Mutations/Alleles
    1 with disease annotations
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    7 phenotypes from 2 alleles in 2 genetic backgrounds
    9 images
    6 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
immune system
integument
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
neoplasm
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
vision/eye

Click cells to view annotations.
Mice homozygous for an ENU-induced allele exhibit congenital heart defects associated with heterotaxy, as well as thoracic and abdominal visceral organ situs anomalies, and misaligned sternal vertebrae.
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
  • GO References
Expression
less
  • cDNA Data
Interactions
less
Sequences &
Gene Models
less
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000020286 Ensembl Gene Model | MGI Sequence Detail 4953 C57BL/6J ±  kb
transcript ENSMUST00000169264 Ensembl | MGI Sequence Detail 1320 Not Applicable  
polypeptide ENSMUSP00000131204 Ensembl | MGI Sequence Detail 196 Not Applicable  
For the selected sequence
Protein
Information
less
  • UniProt
    3 Sequences
  • InterPro Domains
    IPR027813 Protein of unknown function DUF4642
Molecular
Reagents
less
  • All nucleic 17
    cDNA 17

    Microarray probesets 2
Other
Accession IDs
less
MGI:5618822
References
more
  • Summaries
    All 22
    Diseases 1
    Gene Ontology 1
    Phenotypes 6
  • Earliest
    J:137335 Roderick TH, Chromosomal inversions in studies of mammalian mutagenesis. Genetics. 1979 May;92(1 Pt 1 Suppl):s121-6
  • Latest
    J:234235 Miyata H, et al., Genome engineering uncovers 54 evolutionarily conserved and testis-enriched genes that are not required for male fertility in mice. Proc Natl Acad Sci U S A. 2016 Jul 12;113(28):7704-10

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
12/04/2018
MGI 6.13
The Jackson Laboratory