About   Help   FAQ
Rpl24 Gene Detail
Summary
  • Symbol
    Rpl24
  • Name
    ribosomal protein L24
  • Synonyms
    0610008L05Rik, Bst
  • Feature Type
    protein coding gene
  • IDs
    MGI:1915443
    NCBI Gene: 68193
  • Gene Overview
    MyGene.info: RPL24
Location & Maps
more
  • Sequence Map
    Chr16:55966275-55971435 bp, + strand
  • From VEGA annotation of GRCm38

    Mouse Genome Browser

  • Download
    Sequence
      5161 bp   ±  kb flank

  • Genome Browsers
  • Genetic Map
    Chromosome 16, 33.74 cM, cytoband C1
  • Mapping Data
    8 experiments
Homology
more
  • Human Ortholog
    RPL24, ribosomal protein L24
  • Vertebrate Orthologs
    10
  • Human Ortholog
    RPL24, ribosomal protein L24
    Orthology source: HomoloGene
  • Synonyms
    HEL-S-310, L24
  • Links
    NCBI Gene ID: 6152
    neXtProt AC: NX_P83731

  • Chr Location
    3q12; chr3:101681090-101686719 (-)  GRCh38.p2

Human Diseases
more
  • Diseases
    1 with Rpl24 mouse models

Human Disease Mouse Models
       Optic Atrophy 1; OPA1   OMIM: 165500 View 1 model
Click on a disease name to see all genes associated with that disease.

  • Mutations/Alleles
    1 with disease annotations
  • References
    2 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    44 phenotypes from 1 allele in 1 genetic background
    4 phenotypes from multigenic genotypes
    3 images
    20 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.
  • All Mutations and Alleles
    2
  • Spontaneous
    1
  • Targeted
    1
  • Incidental Mutations
Heterozygous mutants have short kinked tail, ventral spotting, malocclusion, white feet, and anomalies of the spine and eyes; homozygotes die in utero.
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
receptor
receptor binding
RNA binding
transcription
transferase
transporter
Biological Process

nucleic acid-templated transcription
carbohydrate derivative metabolism
cell death
cell differentiation
cell proliferation
cellular component organization
establishment of localization
homeostatic process
immune system process
lipid metabolic process
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
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
  • Tissues
  • cDNA Data
  • Literature Summary
Sequences &
Gene Models
less
Representative SequencesLengthStrain/SpeciesFlank
genomic OTTMUSG00000025840 VEGA Gene Model | MGI Sequence Detail 5161 C57BL/6J ±  kb
transcript OTTMUST00000063661 VEGA | MGI Sequence Detail 677 Not Applicable  
polypeptide OTTMUSP00000031508 VEGA | MGI Sequence Detail 157 Not Applicable  
For the selected sequence
Polymorphisms
less
  • SNPs within 2kb
    80 from dbSNP Build 142
Protein
Information
less
  • UniProt
    4 Sequences
  • Protein Ontology
    PR:000014205 60S ribosomal protein L24
  • InterPro Domains
    IPR023442 Ribosomal protein L24e, conserved site
    IPR023441 Ribosomal protein L24e domain
    IPR000988 Ribosomal protein L24e-related
    IPR011017 TRASH domain
Molecular
Reagents
less
  • All nucleic 14
    cDNA 14

    Microarray probesets 7
Other
Accession IDs
less
MGD-MRK-1677, MGI:88211
References
more
  • Summaries
    All 47
    Developmental Gene Expression 2
    Diseases 2
    Gene Ontology 8
    Phenotypes 20
  • Earliest
    J:13703 Southard JL, et al., Bst. Mouse News Lett. 1977;56:40
  • Latest
    J:223920 Riazifar H, et al., Phenotypic and functional characterization of Bst+/- mouse retina. Dis Model Mech. 2015 Aug 1;8(8):969-76

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
08/17/2016
MGI 6.05
The Jackson Laboratory