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E030018B13Rik Gene Detail
Summary
  • Symbol
    E030018B13Rik
  • Name
    RIKEN cDNA E030018B13 gene
  • Synonyms
    LOC381994
  • Feature Type
    protein coding gene
  • IDs
    MGI:2686543
    NCBI Gene: 381994
  • Alliance
  • Transcription Start Sites
    2 TSS
Location &
Maps
more
  • Sequence Map
    Chr7:63566605-63570287 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 7, Syntenic
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    52 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_2686543
protein coding gene Chr7:63566605-63570287 (+)
129S1/SvImJ MGP_129S1SvImJ_G0032333
protein coding gene Chr7:65033625-65037311 (+)
A/J MGP_AJ_G0032312
protein coding gene Chr7:63791398-63795080 (+)
AKR/J MGP_AKRJ_G0032248
protein coding gene Chr7:65136484-65140170 (+)
BALB/cJ MGP_BALBcJ_G0032324
protein coding gene Chr7:63528911-63532799 (+)
C3H/HeJ MGP_C3HHeJ_G0032037
protein coding gene Chr7:65773743-65785785 (+)
C57BL/6NJ MGP_C57BL6NJ_G0032817
protein coding gene Chr7:67816189-67819866 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0029824
protein coding gene Chr7:66750051-66753716 (+)
CAST/EiJ MGP_CASTEiJ_G0031366
protein coding gene Chr7:56449271-56454820 (+)
CBA/J MGP_CBAJ_G0032003
protein coding gene Chr7:70015019-70020750 (+)
DBA/2J MGP_DBA2J_G0032159
protein coding gene Chr7:62523578-62530384 (+)
FVB/NJ MGP_FVBNJ_G0032113
protein coding gene Chr7:62628216-62631923 (+)
LP/J MGP_LPJ_G0032239
protein coding gene Chr7:66264938-66269630 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0032150
protein coding gene Chr7:70311455-70316322 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0032834
protein coding gene Chr7:64397577-64401748 (+)
PWK/PhJ MGP_PWKPhJ_G0031086
protein coding gene Chr7:55534000-55537697 (+)
SPRET/EiJ MGP_SPRETEiJ_G0030927
protein coding gene Chr7:51540329-51543999 (+)
WSB/EiJ MGP_WSBEiJ_G0031484
protein coding gene Chr7:64788057-64793761 (+)



Homology
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    14 phenotype references
  • All Mutations and Alleles
    5
  • Chemically induced (other)
    1
  • Radiation induced
    1
  • Targeted
    3
  • Genomic Mutations
    5 involving E030018B13Rik
  • Find Mice (IMSR)
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 381994 NCBI Gene Model | MGI Sequence Detail 3683 C57BL/6J ±  kb
transcript NM_001256311 RefSeq | MGI Sequence Detail 1015 ZRU/MplStud  
polypeptide NP_001243240 RefSeq | MGI Sequence Detail 113 ZRU/MplStud  
For the selected sequence
Protein
Information
less
  • UniProt
    1 Sequence
Molecular
Reagents
less
  • All nucleic 1
    cDNA 1
References
more
  • Summaries
    All 23
    Diseases 1
    Phenotypes 14
  • Earliest
    J:88307 Giometti CS, et al., The analysis of recessive lethal mutations in mice by using two-dimensional gel electrophoresis of liver proteins. Mutat Res. 1990 Sep;242(1):47-55
  • Latest
    J:322231 Malwade S, et al., Identification of Vulnerable Interneuron Subtypes in 15q13.3 Microdeletion Syndrome Using Single-Cell Transcriptomics. Biol Psychiatry. 2022 Apr 15;91(8):727-739

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)
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last database update
03/19/2024
MGI 6.23
The Jackson Laboratory