Not currently registered for phenotyping at IMPC

Phenotyping is currently not planned for a knockout strain of this gene.

Gene Summary

paternally expressed 10
MyEF-3 like,  Edr,  HB-1,  Mart2,  MyEF-3,  Mar2,  Rtl2,  MEF3L

IMPC Data Collections

  • No Body Weight Data
  • No Embryo Imaging Data
  • No Viability Data

IMPC Phenotype Summary

Not Significant
Not tested


The IMPC applies a panel of phenotyping screens to characterise single-gene knockout mice by comparison to wild types. Click on the different tabs to visualise significant phenotypes identified by the IMPC, as well as all data that was measured.

lacZ Expression

Expression data not available

Associated Images

Images submitted by IMPC centres for a selection of procedures. Each set of images is available to view in our image comparator.

Phenotype associated images not available

Human diseases caused by Peg10 mutations

The analysis uses data from IMPC, along with published data on other mouse mutants, in comparison to human disease reports in OMIM, Orphanet, and DECIPHER.

Phenotype comparisons summarize the similarity of mouse phenotypes with human disease phenotypes.

No human diseases associated to this gene by orthology or annotation.

The table below shows human diseases predicted to be associated to Peg10 by phenotypic similarity.

Disease Similarity of
Matching phenotypes Source
Placental Insufficiency
Abnormal placenta morphology, Preeclampsia, Small placenta, Eclampsia, Abnormal umbilical cord bl... ORPHA:439167
Growth Delay Due To Insulin-Like Growth Factor Type 1 Deficiency
Severe intrauterine growth retardation, Short stature, Severe postnatal growth retardation, Small... ORPHA:73272
Silver-Russell Syndrome Due To A Point Mutation
Small placenta, Postnatal growth retardation, Oligohydramnios, Intrauterine growth retardation ORPHA:397590
Kagami-Ogata Syndrome Due To Maternal 14Q32.2 Hypermethylation
Polyhydramnios, Postnatal growth retardation, Umbilical hernia, Large placenta ORPHA:254534
Fetal Akinesia Deformation Sequence 1
Stillbirth, Fetal akinesia sequence, Short umbilical cord, Small placenta, Polyhydramnios, Intrau... OMIM:208150
Neu-Laxova Syndrome 1
Intrauterine growth retardation, Short umbilical cord, Hydranencephaly, Small placenta, Polyhydra... OMIM:256520
Kagami-Ogata Syndrome Due To Maternal 14Q32.2 Microdeletion
Polyhydramnios, Umbilical hernia, Postnatal growth retardation, Intrauterine growth retardation, ... ORPHA:254528
Restrictive Dermopathy
Short umbilical cord, Small placenta, Polyhydramnios, Premature delivery because of cervical insu... ORPHA:1662
Mosaic Trisomy 16
Single umbilical artery, Preeclampsia, Maternal diabetes, Intrauterine growth retardation, Premat... ORPHA:1708
Greenberg Dysplasia
Disproportionate short-limb short stature, Echogenic fetal bowel, Hydrops fetalis, Nonimmune hydr... OMIM:215140
Kagami-Ogata Syndrome
Polyhydramnios, Postnatal growth retardation, Premature birth, Large placenta ORPHA:254519
Trichohepatoenteric Syndrome 1
Short stature, Abnormalities of placenta or umbilical cord, Polyhydramnios, Intrauterine growth r... OMIM:222470
Restrictive Dermopathy 1
Premature rupture of membranes, Stillbirth, Short umbilical cord, Neonatal death, Spontaneous cho... OMIM:275210
Meckel Syndrome, Type 1
Breech presentation, Occipital encephalocele, Anencephaly, Oligohydramnios, Intrauterine growth r... OMIM:249000
Kagami-Ogata Syndrome Due To Paternal Uniparental Disomy Of Chromosome 14
Postnatal growth retardation, Short stature, Polyhydramnios, Spinal dysraphism, Growth delay, Int... ORPHA:96334
Beckwith-Wiedemann Syndrome
Subchorionic septal cyst, Polyhydramnios, Umbilical hernia, Premature birth, Large placenta ORPHA:116


Summary table of phenotypes displayed during the Histopathology procedure which are considered significant. Full histopathology data table, including submitted images, can be accessed by clicking any row in this table.

There is no histopathology data for Peg10

IMPC related publications

The table below lists publications which used either products generated by the IMPC or data produced by the phenotyping efforts of the IMPC. These publications have also been associated to Peg10.

No publications found that use IMPC mice or data for Peg10.

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