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Rwdd1 Gene Detail
Summary
  • Symbol
    Rwdd1
  • Name
    RWD domain containing 1
  • Synonyms
    2610002D06Rik, 2700069A07Rik
  • Feature Type
    protein coding gene
  • IDs
    MGI:1913771
    NCBI Gene: 66521
  • Alliance
  • Transcription Start Sites
    5 TSS
Location &
Maps
more
  • Sequence Map
    Chr10:33996555-34019616 bp, - strand
  • From NCBI annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 10, 18.85 cM, cytoband B1
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    70 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1913771
protein coding gene Chr10:33996555-34019624 (-)
129S1/SvImJ MGP_129S1SvImJ_G0017132
protein coding gene Chr10:32326527-32350219 (-)
A/J MGP_AJ_G0017109
protein coding gene Chr10:31480876-31503903 (-)
AKR/J MGP_AKRJ_G0017069
protein coding gene Chr10:31844843-31868915 (-)
BALB/cJ MGP_BALBcJ_G0017072
protein coding gene Chr10:31419948-31449599 (-)
C3H/HeJ MGP_C3HHeJ_G0016892
protein coding gene Chr10:32143977-32167080 (-)
C57BL/6NJ MGP_C57BL6NJ_G0017530
protein coding gene Chr10:33250175-33273490 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0015227
protein coding gene Chr10:29823864-29844668 (-)
CAST/EiJ MGP_CASTEiJ_G0016471
protein coding gene Chr10:32268377-32291882 (-)
CBA/J MGP_CBAJ_G0016866
protein coding gene Chr10:34862018-34888067 (-)
DBA/2J MGP_DBA2J_G0016971
protein coding gene Chr10:31062529-31085677 (-)
FVB/NJ MGP_FVBNJ_G0016966
protein coding gene Chr10:30569451-30592390 (-)
LP/J MGP_LPJ_G0017048
protein coding gene Chr10:32318618-32341932 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0016996
protein coding gene Chr10:35346306-35372497 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0017566
protein coding gene Chr10:31793983-31818702 (-)
PWK/PhJ MGP_PWKPhJ_G0016252
protein coding gene Chr10:30830722-30854230 (-)
SPRET/EiJ MGP_SPRETEiJ_G0016036
protein coding gene Chr10:31673493-31696425 (-)
WSB/EiJ MGP_WSBEiJ_G0016534
protein coding gene Chr10:32005395-32031522 (-)



Homology
more
  • Human Ortholog
    RWDD1, RWD domain containing 1
  • Vertebrate Orthologs
    10
  • Human Ortholog
    RWDD1, RWD domain containing 1
    Orthology source: HomoloGene, HGNC
  • Synonyms
    CGI-24, PTD013
  • Links
    NCBI Gene ID: 51389
    neXtProt AC: NX_Q9H446
    UniProt: Q9H446

  • Chr Location
    6q22.1; chr6:116571367-116593601 (+)  GRCh38.p7

Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    10 phenotypes from 1 allele in 1 genetic background
    14 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.
  • All Mutations and Alleles
    7
  • Chemically induced (other)
    1
  • Gene trapped
    2
  • Radiation induced
    1
  • Targeted
    3
  • Genomic Mutations
    2 involving Rwdd1
  • Find Mice (IMSR)
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
  • GO References
Molecular Function

carbohydrate derivative binding
cytoskeletal protein binding
DNA binding
enzyme regulator
hydrolase
ligase
lipid binding
oxidoreductase
RNA binding
signaling receptor activity
signaling receptor binding
transcription
transferase
transporter
Biological Process

carbohydrate derivative metabolism
cell death
cell differentiation
cell population proliferation
cellular component organization
establishment of localization
homeostatic process
immune system process
lipid metabolic process
nucleic acid-templated transcription
protein metabolic process
response to stimulus
signaling
system development
Cellular Component

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
non-membrane-bounded organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
synapse
vacuole
Click cells to view annotations.
Expression
less
  • cDNA Data
Interactions
less
Sequences &
Gene Models
less
Representative SequencesLengthStrain/SpeciesFlank
genomic 66521 NCBI Gene Model | MGI Sequence Detail 23062 C57BL/6J ±  kb
transcript NM_025614 RefSeq | MGI Sequence Detail 1082 C57BL/6  
polypeptide Q9CQK7 UniProt | EBI | MGI Sequence Detail 243 Not Applicable  
For the selected sequence
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 79
    Genomic 1
    cDNA 78

    Microarray probesets 4
Other
Accession IDs
less
MGI:1919836
References
more
  • Summaries
    All 37
    Gene Ontology 2
    Phenotypes 14
  • Earliest
    J:109968 Roderick TH, et al., Nineteen paracentric chromosomal inversions in mice. Genetics. 1974 Jan;76(1):109-17
  • Latest
    J:236599 Dickinson ME, et al., High-throughput discovery of novel developmental phenotypes. Nature. 2016 Sep 14;537(7621):508-514

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO)
Citing These Resources
Funding Information
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last database update
05/14/2019
MGI 6.14
The Jackson Laboratory