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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Twsg1
twisted gastrulation BMP signaling modulator 1
MGI:2137520
94 phenotypes from 6 alleles in 9 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Tg(Sox10-cre)1Wdr/0
Twsg1tm1Aptr/Twsg1tm1Aptr
involves: C57BL/6 * CBA
abnormal frontonasal prominence morphology J:173627
abnormal telencephalon development J:173627
fused first pharyngeal arch J:173627
small first pharyngeal arch J:173627
Twsg1tm1.1Mboc/Twsg1tm1.1Mboc
129S/SvEv-Twsg1tm1.1Mboc
abnormal craniofacial morphology J:88784
abnormal jaw morphology J:88784
abnormal vertebral arch morphology J:88784
decreased body size J:88784
decreased body weight J:88784
lethality at weaning, incomplete penetrance J:88784
neonatal lethality, incomplete penetrance J:88784
Twsg1tm1.1Mboc/Twsg1tm1.1Mboc
B6.129S7-Twsg1tm1.1Mboc
abnormal cervical vertebrae morphology J:88784
abnormal craniofacial development J:88784
abnormal craniofacial morphology J:88784
abnormal head morphology J:88784
abnormal submandibular gland development J:144153
absent submandibular gland J:144153
agnathia J:88784
anophthalmia J:88784
cyclopia J:88784
decreased mouth size J:144153
fused first pharyngeal arch J:88784
lowered ear position J:144153
microphthalmia J:88784
perinatal lethality, incomplete penetrance J:88784
postnatal lethality, complete penetrance J:88784
single external naris J:88784
Twsg1tm1.1Mboc/Twsg1tm1.1Mboc
involves: 129S7/SvEvBrd * C57BL/6 * FVB/N
abnormal caudal vertebrae morphology J:88784
abnormal cervical vertebrae morphology J:88784
abnormal foregut morphology J:88784
abnormal gait J:88784
abnormal oropharynx morphology J:88784
abnormal thoracic vertebrae morphology J:88784
abnormal vertebrae morphology J:88784
abnormal vertebral arch morphology J:88784
abnormal vertebral lamina morphology J:88784
abnormal vertebral spinous process morphology J:88784
alobar holoprosencephaly J:88784
decreased body size J:88784
decreased body weight J:88784
decreased caudal vertebrae number J:88784
delayed bone ossification J:88784
hindlimb paralysis J:88784
kinked tail J:88784
premature death J:88784
short tail J:88784
Twsg1tm1Dgen/Twsg1tm1Dgen
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
decreased body length J:101679
decreased body mass index J:101679
decreased body weight J:101679
kinked tail J:101679
weight loss J:101679
Twsg1tm1Ecan/Twsg1tm1Ecan
involves: 129 * C57BL/6
abnormal skeleton development J:137597
abnormal skeleton morphology J:137597
abnormal tail morphology J:137597
decreased body size J:137597
decreased bone mineral content J:137597
decreased bone trabecula number J:137597
decreased bone volume J:137597
decreased circulating osteocalcin level J:137597
decreased trabecular bone volume J:137597
kinked tail J:137597
prenatal lethality, incomplete penetrance J:137597
short femur J:137597
short tail J:137597
Twsg1tm1Emdr/Twsg1tm1Emdr
involves: 129 * C57BL/6 * SJL
prenatal lethality, incomplete penetrance J:141243
Twsg1tm1Emdr/Twsg1tm1Emdr
involves: 129X1/SvJ * C57BL/6 * SJL
abnormal caudal vertebrae morphology J:90398
abnormal intervertebral disk development J:90398
abnormal tail morphology J:90398
abnormal vertebral arch development J:90398
decreased body weight J:90398
kinked tail J:90398
persistence of notochord tissue J:90398
short tail J:90398
Twsg1tm1Nosa/Twsg1tm1Nosa
involves: 129P2/OlaHsd * C57BL/6
abnormal B cell differentiation J:82738
abnormal bone marrow cell morphology/development J:82738
abnormal gait J:82738
abnormal intervertebral disk morphology J:82738
abnormal intramembranous bone ossification J:82738
abnormal kidney development J:82738
abnormal limb bone morphology J:82738
abnormal long bone epiphyseal plate morphology J:82738
abnormal long bone epiphyseal plate proliferative zone J:82738
abnormal skeleton development J:82738
abnormal spleen development J:82738
abnormal thymus development J:82738
abnormal timing of postnatal eyelid opening J:82738
cachexia J:82738
decreased body size J:82738
decreased bone mineral density of femur J:82738
decreased bone mineral density of lumbar vertebrae J:82738
decreased double-positive T cell number J:82738
decreased erythrocyte cell number J:82738
decreased immature B cell number J:82738
decreased lymphocyte cell number J:82738
decreased pre-B cell number J:82738
decreased pro-B cell number J:82738
decreased spleen white pulp amount J:82738
decreased splenocyte number J:82738
decreased thymocyte number J:82738
decreased width of hypertrophic chondrocyte zone J:82738
delayed endochondral bone ossification J:82738
disproportionate dwarf J:82738
increased granulocyte number J:82738
increased monocyte cell number J:82738
increased single-positive T cell number J:82738
increased thymocyte apoptosis J:82738
internal hemorrhage J:82738
kinked tail J:82738
neonatal lethality, incomplete penetrance J:82738
postnatal growth retardation J:82738
premature death J:82738
pulmonary fibrosis J:82738
subarachnoid hemorrhage J:82738
thin neurocranium J:82738
thrombocytopenia J:82738
thymus atrophy J:82738
tremors J:82738

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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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory