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Prl7d1 Gene Detail
Summary
  • Symbol
    Prl7d1
  • Name
    prolactin family 7, subfamily d, member 1
  • Synonyms
    Plfr, PLF-RP, PRP
  • Feature Type
    protein coding gene
  • IDs
    MGI:97619
    NCBI Gene: 18814
  • Alliance
    genome feature page
  • Transcription Start Sites
    1 TSS
Location &
Maps
more
  • Sequence Map
    Chr13:27892981-27900720 bp, - strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 13, 12.60 cM
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    299 from dbSNP Build 142
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_97619
 protein coding gene Chr13:27890320-27900720 (-)
129S1/SvImJ ENSMUSG00200028371
 protein coding gene Chr13:25050073-25060466 (-)
A/J ENSMUSG00195037374
 protein coding gene Chr13:24195371-24205764 (-)
AKR/J ENSMUSG00220012449
 protein coding gene Chr13:24001465-24011862 (-)
BALB/cJ ENSMUSG00180021172
 protein coding gene Chr13:24500601-24510986 (-)
C3H/HeJ ENSMUSG00175031900
 protein coding gene Chr13:24523331-24533722 (-)
C57BL/6NJ ENSMUSG00215008378
 protein coding gene Chr13:24655212-24665611 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0018376
 protein coding gene Chr13:23360392-23367883 (-)
CAST/EiJ ENSTCUG00005009603
 protein coding gene Chr13:24683839-24694196 (-)
CBA/J ENSMUSG00210026728
 protein coding gene Chr13:24467514-24477907 (-)
DBA/2J ENSMUSG00185019166
 protein coding gene Chr13:25282380-25292781 (-)
FVB/NJ ENSMUSG00205020305
 protein coding gene Chr13:24279530-24289926 (-)
JF1/MsJ ENSUMUG00000013341
 protein coding gene Chr13:24929087-24940762 (-)
LP/J ENSMUSG00230016784
 protein coding gene Chr13:34610838-34621229 (-)
NOD/ShiLtJ ENSMUSG00190025221
 protein coding gene Chr13:24264408-24274807 (-)
NZO/HlLtJ ENSMUSG00225043946
 protein coding gene Chr13:28389979-28400378 (-)
PWK/PhJ ENSLUMG00010027115
 protein coding gene Chr13:23747535-23755957 (-)
SPRET/EiJ ENSMSPG00010023351
 protein coding gene Chr13:23708853-23717171 (-)
WSB/EiJ ENSIUOG00005016313
 protein coding gene Chr13:23845708-23856104 (-)



Homology
less
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    11 phenotypes from 2 alleles in 2 genetic backgrounds
    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
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.
Female mice homozygous for a null allele display reduced litter sizes and placental abnormalities that vary with the sex of the fetus.
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
    19
  • GO References
    7
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
    637
  • Tissues
    16
  • cDNA Data
    35
  • Literature Summary
    12
  • Comparison Matrix
    Gene Expression + Phenotype
    • Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic 18814 NCBI Gene Model | MGI Sequence Detail 7740 C57BL/6J ±  kb
    transcript NM_011120 RefSeq | MGI Sequence Detail 997 C57BL/6  
    polypeptide P04769 UniProt | EBI | MGI Sequence Detail 244 Not Applicable  
    For the selected sequence
    Protein
    Information
    less
    Molecular
    Reagents
    less
    • All nucleic 40
      cDNA 39
      Other 1

      Microarray probesets 3
    Other
    Accession IDs
    less
    MGD-MRK-13359
    References
    more
    • Summaries
      All 63
      Developmental Gene Expression 12
      Gene Ontology 7
      Phenotypes 14
    • Earliest
      J:182573 Roderick TH, Producing and detecting paracentric chromosomal inversions in mice. Mutat Res. 1971 Jan;11(1):59-69
    • Latest
      J:345621 Adams DJ, et al., Genetic determinants of micronucleus formation in vivo. Nature. 2024 Mar;627(8002):130-136
    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
    09/01/2026
    MGI 6.24     		The Jackson Laboratory