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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Twist2
twist basic helix-loop-helix transcription factor 2
MGI:104685
115 phenotypes from multigenic genotypes
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Adam17tm1.1Wesh/Adam17tm1.1Wesh
Tg(Scgb1a1-rtTA)2Jaw/0
Tg(tetO-cre)1Jaw/0
Twist2tm1.1(cre)Dor/Twist2+
involves: 129X1/SvJ * C57BL/6 * FVB/N
abnormal lung saccule morphology J:210193
abnormal lung vasculature morphology J:210193
decreased cell proliferation J:210193
normal mortality/aging J:210193
Adam17tm1.1Wesh/Adam17tm1.1Wesh
Twist2tm1.1(cre)Dor/Twist2+
involves: 129X1/SvJ * C57BL/6 * FVB/N
normal respiratory system phenotype J:210193
ApcMin/Apc+
Mapkapk2tm1.1Gkl/Mapkapk2tm1.1Gkl
Twist2tm1.1(cre)Dor/Twist2+
involves: 129X1/SvJ * BALB/cJ * C57BL/6J
decreased tumor growth/size J:262876
decreased tumor incidence J:262876
Ctnna1tm1Efu/Ctnna1tm1Efu
Twist2tm1(cre)Dor/Twist2+
involves: 129X1/SvJ
abnormal skeleton development J:178499
decreased width of hypertrophic chondrocyte zone J:178499
delayed intramembranous bone ossification J:178499
Ctnnb1tm1Yy/Ctnnb1tm1Yy
Twist2tm1(cre)Dor/Twist2+
involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6
fused synovial joints J:93028
Ctnnb1tm2Kem/Ctnnb1tm2Kem
Twist2tm1(cre)Dor/Twist2+
involves: 129S1/Sv * 129X1/SvJ
abnormal bone structure J:178499
abnormal cartilage morphology J:178499
abnormal joint morphology J:178499
abnormal skeleton morphology J:178499
arrested osteoblast differentiation J:178499
ectopic cartilage J:178499
failure of bone ossification J:178499
split sternum J:178499
Epha4tm1.1Bzh/Epha4tm1.1Bzh
Tg(Hlxb9-GFP)1Tmj/0
Twist2tm1(cre)Dor/Twist2+
involves: 129S/Sv * C57BL/6J * CD-1 * FVB/N
abnormal innervation J:243785
Fgf10tm1Ska/Fgf10tm1Sms
Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+
Twist2tm1(cre)Dor/Twist2+
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * CBA
abnormal lung development J:150706
abnormal lung lobe morphology J:150706
abnormal right lung accessory lobe morphology J:150706
abnormal right lung cranial lobe morphology J:150706
abnormal right lung middle lobe morphology J:150706
impaired branching involved in bronchus morphogenesis J:150706
lung hemorrhage J:150706
pulmonary hypoplasia J:150706
small lung J:150706
small lung lobe J:150706
Fgfr1tm1Jpa/Fgfr1+
Fgfr2tm1Dor/Fgfr2tm1.1Dor
Twist2tm1(cre)Dor/Twist2+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal small intestine morphology J:139005
Fgfr1tm1Jpa/Fgfr1tm1.1Jpa
Fgfr2tm1Dor/Fgfr2+
Twist2tm1(cre)Dor/Twist2+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal small intestine morphology J:139005
Fgfr1tm1Jpa/Fgfr1tm1.1Jpa
Fgfr2tm1Dor/Fgfr2tm1.1Dor
Twist2tm1(cre)Dor/Twist2+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal digestive system physiology J:139005
abnormal small intestine crypts of Lieberkuhn morphology J:139005
abnormal small intestine morphology J:139005
Fgfr1tm1Jpa/Fgfr1tm1Jpa
Fgfr2tm1Dor/Fgfr2tm1Dor
Twist2tm1.1(cre)Dor/Twist2+
involves: 129S1/Sv * 129X1/SvJ
abnormal reproductive system physiology J:223057
genital tubercle hypoplasia J:223057
Fgfr2tm1Dor/Fgfr2tm1.1Dor
Twist2tm1(cre)Dor/Twist2+
involves: 129X1/SvJ
abnormal appendicular skeleton morphology J:90391
abnormal axial skeleton morphology J:90391
abnormal cervical vertebrae morphology J:90391
abnormal joint morphology J:90391
abnormal long bone hypertrophic chondrocyte zone J:90391
abnormal long bone metaphysis morphology J:90391
abnormal osteoblast physiology J:90391
abnormal osteoclast differentiation J:90391
abnormal skeleton development J:90391
abnormal thoracic vertebrae morphology J:90391
abnormal vertebrae development J:90391
abnormal vertebrae morphology J:90391
absent vertebral spinous process J:90391
decreased bone mineral density J:90391
decreased cell proliferation J:90391
decreased osteoblast cell number J:90391
disproportionate dwarf J:90391
domed cranium J:90391
postnatal growth retardation J:90391
short femur J:90391
Hdac8tm1.1Eno/Y
Twist2tm1(cre)Dor/Twist2+
involves: 129 * C57BL/6 * CD-1 * SJL
no abnormal phenotype detected J:150709
Kdrtm1Jrt/Kdr+
Ptentm1Hwu/Ptentm1Hwu
Twist2tm1.1(cre)Dor/Twist2+
B6.129-Twist2tm1.1(cre)Dor Kdrtm1Jrt Ptentm1Hwu
abnormal lung morphology J:192736
abnormal vasculogenesis J:192736
Lrp5tm1.1Vari/Lrp5tm1.1Vari
Lrp6tm1.1Vari/Lrp6tm1.1Vari
Twist2tm1(cre)Dor/Twist2+
involves: 129S1/Sv * 129X1/SvJ
abnormal bone ossification J:178499
abnormal bone structure J:178499
abnormal cartilage morphology J:178499
abnormal cranium morphology J:178499
abnormal epiphyseal plate morphology J:178499
abnormal limb morphology J:178499
abnormal skeleton morphology J:178499
abnormal trabecular bone morphology J:178499
decreased body size J:178499
ectopic cartilage J:178499
neonatal lethality, complete penetrance J:178499
split sternum J:178499
Lrp5tm1.1Vari/Lrp5tm1.2Vari
Twist2tm1(cre)Dor/Twist2+
involves: 129S1/Sv * 129X1/SvJ
normal skeleton phenotype J:178499
Lrp5tm1.2Vari/Lrp5tm1.2Vari
Lrp6tm1.1Vari/Lrp6tm1.1Vari
Twist2tm1(cre)Dor/Twist2+
involves: 129S1/Sv * 129X1/SvJ
abnormal bone ossification J:178499
abnormal bone structure J:178499
abnormal cartilage morphology J:178499
abnormal cranium morphology J:178499
abnormal epiphyseal plate morphology J:178499
abnormal joint morphology J:178499
abnormal limb morphology J:178499
abnormal osteoblast differentiation J:178499
abnormal skeleton morphology J:178499
abnormal trabecular bone morphology J:178499
decreased body size J:178499
decreased width of hypertrophic chondrocyte zone J:178499
ectopic cartilage J:178499
failure of bone ossification J:178499
neonatal lethality, complete penetrance J:178499
split sternum J:178499
Lrp6tm1.1Vari/Lrp6tm1.1Vari
Twist2tm1(cre)Dor/Twist2+
involves: 129S1/Sv * 129X1/SvJ
delayed bone ossification J:178499
normal skeleton phenotype J:178499
Lrp6tm1.1Vari/Lrp6tm1.2Vari
Twist2tm1(cre)Dor/Twist2+
involves: 129S1/Sv * 129X1/SvJ
delayed bone ossification J:178499
normal skeleton phenotype J:178499
Mapkapk2tm1.1Gkl/Mapkapk2tm1.1Gkl
Twist2tm1.1(cre)Dor/Twist2+
involves: 129X1/SvJ * BALB/cJ * C57BL/6
decreased incidence of tumors by chemical induction J:262876
Mef2ctm1Eno/Mef2ctm2Eno
Twist2tm1(cre)Dor/Twist2+
involves: 129S/SvEv * 129S7/SvEvBrd * 129X1/SvJ
abnormal endochondral bone ossification J:119152
abnormal trabecular bone morphology J:119152
failure of endochondral bone ossification J:119152
postnatal lethality, complete penetrance J:119152
respiratory distress J:119152
short fibula J:119152
short limbs J:119152
short tibia J:119152
Mirc32tm1.1Jtm/Mirc32tm1.1Jtm
Twist2tm1(cre)Dor/Twist2+
B6.129(Cg)-Twist2tm1.1(cre)Dor Mirc32tm1.1Jtm
abnormal colon morphology J:214382
abnormal intestinal mucosa morphology J:214382
abnormal large intestine crypts of Lieberkuhn morphology J:214382
abnormal susceptibility to induced morbidity/mortality J:214382
colonic necrosis J:214382
impaired intestine regeneration J:214382
increased susceptibility to induced colitis J:214382
intestinal ulcer J:214382
Mmp14tm1Stjw/Mmp14tm1Stjw
Twist2tm1.1(cre)Dor/Twist2+
involves: 129X1/SvJ * C57BL/6
abnormal bone ossification J:198679
abnormal cartilage morphology J:198679
abnormal hypodermis fat layer morphology J:198679
abnormal joint morphology J:198679
decreased body size J:198679
decreased body weight J:198679
decreased bone mineral density J:198679
delayed cranial suture closure J:198679
delayed intramembranous bone ossification J:198679
domed cranium J:198679
increased bone marrow adipose tissue amount J:198679
postnatal growth retardation J:198679
premature death J:198679
short snout J:198679
normal skeleton phenotype J:198679
Nfibtm2Rmg/Nfibtm2Rmg
Twist2tm1(cre)Dor/Twist2+
involves: 129S4/SvJae * 129X1/SvJ * C57BL/6
abnormal lung development J:173651
abnormal lung morphology J:173651
abnormal lung saccule morphology J:173651
abnormal respiratory system physiology J:173651
enlarged lung J:173651
perinatal lethality, complete penetrance J:173651
Ptentm1Hwu/Ptentm1Hwu
Twist2tm1.1(cre)Dor/Twist2+
B6.129-Twist2tm1.1(cre)Dor Ptentm1Hwu
abnormal lung development J:192736
abnormal lung morphology J:192736
abnormal lung vasculature morphology J:192736
abnormal lung-associated mesenchyme development J:192736
abnormal vascular development J:192736
cyanosis J:192736
decreased blood oxygen capacity J:192736
hemorrhage J:192736
lethality throughout fetal growth and development, incomplete penetrance J:192736
neonatal lethality, complete penetrance J:192736
respiratory distress J:192736
Ptpratm1c(EUCOMM)Hmgu/Ptpratm1c(EUCOMM)Hmgu
Twist2tm1.1(cre)Dor/Twist2+
involves: 129X1/SvJ * C57BL/6N
decreased susceptibility to injury J:300194
Robo1tm1Matl/Robo1tm1Matl
Robo2tm1Rilm/Robo2tm1Rilm
Twist2tm1(cre)Dor/Twist2+
involves: 129 * 129X1/SvJ
abnormal foregut morphology J:193400
diaphragmatic hernia J:193400
neonatal lethality J:193400
respiratory failure J:193400
small esophagus J:193400
Runx2tm1Mjo/Runx2+
Twist2tm1(cre)Dor/Twist2+
involves: 129X1/SvJ * C57BL/6
clavicle hypoplasia J:90056
Runx2tm1Mjo/Runx2+
Twist2tm1(cre)Dor/Twist2tm1(cre)Dor
involves: 129X1/SvJ * C57BL/6
delayed fontanelle closure J:90056
normal skeleton phenotype J:90056
small interparietal bone J:90056
Snai1tm1.1Stjw/Snai1tm1.1Stjw
Twist2tm1.1(cre)Dor/Twist2+
B6.129(SJL)-Twist2tm1.1(cre)Dor Snai1tm1.1Stjw
no abnormal phenotype detected J:214991
Tgfbr2tm1.2Hlm/Tgfbr2tm1.2Hlm
Twist2tm1(cre)Dor/Twist2+
involves: 129X1/SvJ * C57BL/6
abnormal branching involved in lung morphogenesis J:143910
abnormal bronchial cartilage morphology J:143910
abnormal bronchus morphology J:143910
abnormal lung lobe morphology J:143910
abnormal tracheal cartilage morphology J:143910
decreased tracheal cartilage ring number J:143910
dilated respiratory conducting tube J:143910
lethality throughout fetal growth and development, complete penetrance J:143910
Twist1tm1Bhr/Twist1+
Twist2tm1(cre)Dor/Twist2+
involves: 129/Sv * 129X1/SvJ
abnormal skeletal muscle morphology J:81485
cachexia J:81485
neonatal lethality, incomplete penetrance J:81485
Twist2tm1(cre)Dor/Twist2+
Wnt7btm1Parr/Wnt7btm2Amc
involves: 129S1/Sv * 129X1/SvJ
abnormal bone ossification J:117333
abnormal osteoblast differentiation J:117333
decreased width of hypertrophic chondrocyte zone J:117333

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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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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory