About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Rest
RE1-silencing transcription factor
MGI:104897
39 phenotypes from 10 alleles in 15 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Dcttm1(cre)Bee/Dct+
Resttm1.1Yasu/Rest+
involves: 129/Sv * 129S4/SvJae * C57BL/6
normal pigmentation phenotype J:230341
Dcttm1(cre)Bee/Dct+
Resttm1.1Yasu/Resttm1.1Yasu
involves: 129/Sv * 129S4/SvJae * C57BL/6
head spot J:230341
Resttm1.1Bban/Rest+
Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sor+
involves: 129S4/SvJaeSor * C57BL/6J
cochlear hair cell degeneration J:265659
impaired hearing J:265659
increased or absent threshold for auditory brainstem response J:265659
Resttm1.1Bban/Rest+
Gfi1tm1(cre)Gan/Gfi1+
involves: 129S4/SvJaeSor * 129S7/SvEvBrd * FVB/N
cochlear inner hair cell degeneration J:265659
deafness J:265659
Resttm1.1Jhsi/Resttm1.1Jhsi
involves: 129S6/SvEvTac * C57BL/6 * SJL
abnormal neuron differentiation J:174056
Resttm1.1Jhsi/Resttm1.1Jhsi
Tg(CAG-cre)13Miya/0
involves: 129S6/SvEvTac * C57BL/6 * SJL
embryonic lethality, complete penetrance J:174056
Resttm1.1Whk/Resttm1.1Whk
Tg(Six3-cre)69Frty/0
involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * DBA/2
abnormal retina ganglion layer morphology J:167071
abnormal retina progenitor cell morphology J:167071
increased retina ganglion cell number J:167071
thick retina ganglion layer J:167071
thick retina inner plexiform layer J:167071
Resttm1.1Yasu/Rest+
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129S4/SvJae * C57BL/6 * C57BL/6J * CBA/J
belly spot J:230341
normal mortality/aging J:230341
normal nervous system phenotype J:230341
Resttm1.1Yasu/Rest+
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Tg(Dct-lacZ)A12Jkn/0
involves: 129S4/SvJae * C57BL/6 * CBA
abnormal melanoblast morphology J:230341
Resttm1.1Yasu/Rest+
Tg(Mpz-cre)26Mes/0
involves: 129S4/SvJae * C57BL/6 * FVB/NTac
normal pigmentation phenotype J:230341
Resttm1.1Yasu/Rest+
Tg(KRT14-cre)1Cgn/0
involves: 129S4/SvJae * C57BL/6 * DBA/2
normal pigmentation phenotype J:230341
Resttm1.1Yasu/Rest+
Tg(Tyr-cre)1Lru/Y
involves: 129S4/SvJae * C57BL/6 * DBA/2
normal pigmentation phenotype J:230341
Resttm1.1Yasu/Resttm1.1Yasu
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129S4/SvJae * C57BL/6 * C57BL/6J * CBA/J
neonatal lethality, complete penetrance J:230341
normal nervous system phenotype J:230341
Resttm1.1Yasu/Resttm1.1Yasu
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Tg(Dct-lacZ)A12Jkn/0
involves: 129S4/SvJae * C57BL/6 * CBA
abnormal melanoblast morphology J:230341
Resttm1.1Yasu/Resttm1.1Yasu
Tg(KRT14-cre)1Cgn/0
involves: 129S4/SvJae * C57BL/6 * DBA/2
normal pigmentation phenotype J:230341
Resttm1.1Yasu/Resttm1.1Yasu
Tg(Mpz-cre)26Mes/0
involves: 129S4/SvJae * C57BL/6 * FVB/NTac
normal pigmentation phenotype J:230341
Resttm1.1Yasu/Resttm1.1Yasu
Tg(Tyr-cre)1Lru/Y
involves: 129S4/SvJae * C57BL/6 * DBA/2
normal pigmentation phenotype J:230341
Resttm1.1Yasu/Resttm1.2Yasu
Alpltm1(cre)Nagy/Alpl+
involves: 129 * C57BL/6 * C57BL/6J
decreased primordial germ cell number J:190948
increased primordial germ cell apoptosis J:190948
normal reproductive system phenotype J:190948
Resttm1.2Bban/Rest+
involves: 129S4/SvJaeSor * FVB/N
abnormal kinocilium morphology J:265659
abnormal outer hair cell stereociliary bundle morphology J:265659
abnormal utricle morphology J:265659
cochlear hair cell degeneration J:265659
cochlear inner hair cell degeneration J:265659
deafness J:265659
impaired balance J:265659
increased or absent threshold for auditory brainstem response J:265659
normal nervous system phenotype J:265659
Resttm1And/Resttm1And
involves: 129S7/SvEvBrd * C57BL/6J
abnormal midbrain development J:50169
abnormal somite development J:50169
embryonic growth retardation J:50169
embryonic lethality during organogenesis, complete penetrance J:50169
increased embryonic tissue cell apoptosis J:50169
small embryonic telencephalon J:50169
Resttm1Mlit/Resttm1Mlit
Tg(Eno2-cre)#Mlit/0
involves: 129S1/Sv * C57BL/6 * DBA
increased neuron apoptosis J:173834
Resttm1Ymat/Resttm1Ymat
involves: 129P2/OlaHsd * C57BL/6
abnormal cranial flexure morphology J:190948
abnormal forebrain morphology J:190948
decreased primordial germ cell number J:190948
embryonic lethality during organogenesis, complete penetrance J:190948
increased primordial germ cell apoptosis J:190948
Resttm2b(EUCOMM)Wtsi/Rest+
C57BL/6N-Resttm2b(EUCOMM)Wtsi/Ieg
abnormal auditory brainstem response J:211773
decreased heart rate J:211773
decreased mean platelet volume J:211773
Resttm2b(EUCOMM)Wtsi/Resttm2b(EUCOMM)Wtsi
C57BL/6N-Resttm2b(EUCOMM)Wtsi/Ieg
preweaning lethality, complete penetrance J:211773

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
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory