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Plscr5 Gene Detail
Summary
  • Symbol
    Plscr5
  • Name
    phospholipid scramblase family, member 5
Location &
Maps
more
  • Sequence Map
    Chr9:92074989-92091825 bp, + strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 9, 48.33 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    636 from dbSNP Build 142
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3779462
protein coding gene Chr9:92068569-92094589 (+)
129S1/SvImJ ENSMUSG00200005059
protein coding gene Chr9:89199814-89216656 (+)
A/J ENSMUSG00195006986
protein coding gene Chr9:88454420-88471267 (+)
AKR/J ENSMUSG00220019644
protein coding gene Chr9:88834995-88851841 (+)
BALB/cJ ENSMUSG00180007031
protein coding gene Chr9:88780153-88797004 (+)
C3H/HeJ ENSMUSG00175004379
protein coding gene Chr9:89091563-89108412 (+)
C57BL/6NJ ENSMUSG00215008044
protein coding gene Chr9:89087187-89104027 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0032522
protein coding gene Chr9:88026953-88043797 (+)
CAST/EiJ ENSTCUG00005003713
protein coding gene Chr9:89014539-89031362 (+)
CBA/J ENSMUSG00210005448
protein coding gene Chr9:88968602-88985611 (+)
DBA/2J ENSMUSG00185001643
protein coding gene Chr9:89154535-89171295 (+)
FVB/NJ ENSMUSG00205004540
protein coding gene Chr9:89292828-89309592 (+)
JF1/MsJ ENSUMUG00000027762
protein coding gene Chr9:88873609-88890396 (+)
LP/J ENSMUSG00230008127
protein coding gene Chr9:89305807-89322649 (+)
NOD/ShiLtJ ENSMUSG00190010763
protein coding gene Chr9:88749597-88766436 (+)
NZO/HlLtJ ENSMUSG00225015644
protein coding gene Chr9:89455395-89472404 (+)
PWK/PhJ ENSLUMG00010002910
protein coding gene Chr9:88843628-88860330 (+)
SPRET/EiJ ENSMSPG00010002240
protein coding gene Chr9:90603447-90620188 (+)
WSB/EiJ ENSIUOG00005003555
protein coding gene Chr9:88210609-88227362 (+)



Homology
more
  • Human Ortholog
    PLSCR5, phospholipid scramblase family member 5
  • Vertebrate Orthologs
    2
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    PLSCR5, phospholipid scramblase family member 5
  • Links
    NCBI Gene ID: 389158
    UniProt: A0PG75

  • Chr Location
    3q24; chr3:146576555-146605346 (-)  GRCh38

Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    10 phenotypes from 2 alleles in 2 genetic backgrounds
    8 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.
Mice homozygous for a null allele display progressive hearing loss with cochlear outer hair cell stereocilia degeneration. Milder hearing loss is seen in heterozygous null mice.
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 differentiation
cell population proliferation
cellular component organization
DNA-templated transcription
establishment of localization
homeostatic process
immune system process
lipid metabolic process
programmed cell death
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
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
  • cDNA Data
  • Literature Summary
  • Comparison Matrix
  • Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic ENSMUSG00000095654 Ensembl Gene Model | MGI Sequence Detail 16837 C57BL/6J ±  kb
    transcript ENSMUST00000179751 Ensembl | MGI Sequence Detail 1191 Not Applicable  
    polypeptide ENSMUSP00000136181 Ensembl | MGI Sequence Detail 274 Not Applicable  
    For the selected sequence
    Protein
    Information
    less
    Molecular
    Reagents
    less
    • All nucleic 1
      cDNA 1
    References
    more
    • Summaries
      All 19
      Developmental Gene Expression 1
      Gene Ontology 2
      Phenotypes 8
    • Earliest
      J:345621 Adams DJ, et al., Genetic determinants of micronucleus formation in vivo. Nature. 2024 Mar;627(8002):130-136
    • Latest
      J:377967 Roome RB, et al., Ontogeny of the spinal cord dorsal horn. Science. 2026 Jan 8;391(6781):eadx5781

    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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    Funding Information
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    last database update
    09/08/2026
    MGI 6.24
    The Jackson Laboratory