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Prr13 Gene Detail
Summary
  • Symbol
    Prr13
  • Name
    proline rich 13
  • Synonyms
    1110020C13Rik, 2010324E22Rik
  • Feature Type
    protein coding gene
  • IDs
    MGI:1913401
    NCBI Gene: 66151
  • Alliance
    genome feature page
  • Transcription Start Sites
    21 TSS
Location &
Maps
more
  • Sequence Map
    Chr15:102367605-102371241 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 15, 57.60 cM
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    150 from dbSNP Build 142
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1913401
 protein coding gene Chr15:102367463-102371241 (+)
129S1/SvImJ ENSMUSG00200049119
 protein coding gene Chr15:99592397-99596176 (+)
A/J ENSMUSG00195037795
 protein coding gene Chr15:99482062-99485851 (+)
AKR/J ENSMUSG00220048376
 protein coding gene Chr15:99452215-99455994 (+)
BALB/cJ ENSMUSG00180037952
 protein coding gene Chr15:99365023-99368802 (+)
C3H/HeJ ENSMUSG00175044820
 protein coding gene Chr15:99683909-99687702 (+)
C57BL/6NJ ENSMUSG00215047444
 protein coding gene Chr15:99408450-99412228 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0020352
 protein coding gene Chr15:96300189-96303080 (+)
CAST/EiJ ENSTCUG00005041518
 protein coding gene Chr15:98889589-98893361 (+)
CBA/J ENSMUSG00210026557
 protein coding gene Chr15:99435083-99438874 (+)
DBA/2J ENSMUSG00185040246
 protein coding gene Chr15:99452046-99455824 (+)
FVB/NJ ENSMUSG00205038395
 protein coding gene Chr15:99156803-99160580 (+)
JF1/MsJ ENSUMUG00000047263
 protein coding gene Chr15:98913968-98917744 (+)
LP/J ENSMUSG00230006259
 protein coding gene Chr15:102813408-102817187 (+)
NOD/ShiLtJ ENSMUSG00190028354
 protein coding gene Chr15:99396908-99400686 (+)
NZO/HlLtJ ENSMUSG00225027335
 protein coding gene Chr15:102993229-102997010 (+)
PWK/PhJ ENSLUMG00010046454
 protein coding gene Chr15:99123877-99127661 (+)
SPRET/EiJ ENSMSPG00010039337
 protein coding gene Chr15:100911456-100915227 (+)
WSB/EiJ ENSIUOG00005030264
 protein coding gene Chr15:99542263-99546049 (+)



Homology
more
  • Human Ortholog
    PRR13, proline rich 13
  • Vertebrate Orthologs
    3
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    PRR13, proline rich 13
  • Synonyms
    TXR1
  • Links
    NCBI Gene ID: 54458
    UniProt: Q9NZ81

  • Chr Location
    12q13.13; chr12:53441308-53446660 (+)  GRCh38
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    2 phenotypes from 1 allele in 1 genetic background
    32 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
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
    4
  • GO References
    3
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

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
membraneless organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
protein-containing complex
synapse
vacuole
Click cells to view annotations.
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
    597
  • cDNA Data
    113
  • Comparison Matrix
    Gene Expression + Phenotype
    • Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic 66151 NCBI Gene Model | MGI Sequence Detail 3637 C57BL/6J ±  kb
    transcript NM_025385 RefSeq | MGI Sequence Detail 1229 C57BL/6  
    polypeptide Q9CQJ5 UniProt | EBI | MGI Sequence Detail 137 Not Applicable  
    For the selected sequence
    Protein
    Information
    less
    Molecular
    Reagents
    less
    • All nucleic 113
      cDNA 113

      Microarray probesets 4
    Other
    Accession IDs
    less
    MGI:1919350
    References
    more
    • Summaries
      All 57
      Diseases 1
      Gene Ontology 3
      Phenotypes 32
    • Earliest
      J:7688 Lane PW, et al., Association of megacolon with a new dominant spotting gene (Dom) in the mouse. J Hered. 1984 Nov-Dec;75(6):435-9
    • Latest
      J:387680 Ahn B, et al., Disorganization of Transcriptional Regulation and Alteration of Keratin Family Gene Expression in Hairy Ear Mice. Genes (Basel). 2026 Jan 31;17(2)
    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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    Send questions and comments to User Support.     		last database update
    09/08/2026
    MGI 6.24     		The Jackson Laboratory