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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Hand2
heart and neural crest derivatives expressed 2
MGI:103580
101 phenotypes from 18 alleles in 17 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Hand2tm1.1Majh/Hand2tm1.1Majh
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129S1/SvImJ * C57BL/6J * CBA/J * DBA/2
abnormal craniofacial bone morphology J:137726
abnormal enteric ganglia morphology J:138032
abnormal enteric nervous system morphology J:138032
abnormal enteric neuron morphology J:138032
abnormal heart development J:137726
abnormal neuron differentiation J:137726
abnormal sympathetic ganglion morphology J:137726
decreased embryo size J:137726
embryonic lethality during organogenesis, complete penetrance J:137726
normal nervous system phenotype J:137726
short mandible J:137726
Hand2tm1.1Zllr/Hand2tm1.2Zllr
Tg(Prrx1-cre)1Cjt/0
involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL
abnormal autopod morphology J:159210
abnormal digit development J:159210
abnormal forelimb zeugopod morphology J:159210
abnormal hindlimb morphology J:159210
abnormal interdigital cell death J:159210
increased apoptosis J:159210
Hand2tm1.2Zllr/Hand2tm1.2Zllr
involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL
abnormal pharyngeal arch artery morphology J:159210
dilated aortic sac J:159210
distended pericardium J:159210
embryonic growth retardation J:159210
increased embryonic tissue cell apoptosis J:159210
Hand2tm1Cse/Hand2+
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129S1/Sv * C57BL/6J * CBA/J
aberrant origin of the right subclavian artery J:155265
abnormal cell cycle J:155265
abnormal fetal cardiomyocyte proliferation J:155265
abnormal myocardial trabeculae morphology J:155265
abnormal thymus development J:155265
normal embryo phenotype J:155265
heart right ventricle hypertrophy J:155265
interrupted aortic arch J:155265
lethality throughout fetal growth and development, complete penetrance J:155265
perimembraneous ventricular septal defect J:155265
pulmonary artery stenosis J:155265
retroesophageal right subclavian artery J:155265
Hand2tm1Cse/Hand2+
Tg(Tnnt2-cre)5Blh/0
involves: 129S1/Sv * C57BL/6J * DBA/2
abnormal cardiac outflow tract development J:155265
abnormal heart ventricle morphology J:155265
decreased heart right ventricle size J:155265
embryonic lethality during organogenesis, complete penetrance J:155265
Hand2tm1Cse/Hand2+
Tg(Hoxb6-cre)#Mku/0
involves: 129S1/Sv * FVB/N
abnormal limb development J:155265
normal cardiovascular system phenotype J:155265
normal embryo phenotype J:155265
normal mortality/aging J:155265
Hand2tm1Cse/Hand2+
Tg(DBH-cre)1Cse/0
involves: 129S1/Sv
embryonic lethality during organogenesis, complete penetrance J:155265
liver vascular congestion J:155265
visceral vascular congestion J:155265
Hand2tm1Cse/Hand2tm1Cse
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6 * CBA
normal craniofacial phenotype J:149232
Hand2tm1Cse/Hand2tm1Cse
Osr2tm2(cre)Jian/Osr2+
involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6
mandible hypoplasia J:149232
Hand2tm1Cse/Hand2tm1Cse
Tg(Pitx2-cre)1Ych/0
involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6
cleft secondary palate J:149232
failure of palatal shelf elevation J:149232
Hand2tm1Cse/Hand2tm1Dsr
involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6
abnormal palatal shelf elevation J:149232
abnormal primary and secondary palatal fusion J:122604
abnormal suckling behavior J:122604
cleft secondary palate J:122604
decreased palatal shelf size J:149232
neonatal lethality, complete penetrance J:122604
palatal shelves fail to meet at midline J:149232
tongue hypoplasia J:149232
Hand2tm1Cse/Hand2tm1Dsr
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6 * CBA
abnormal adrenergic neuron morphology J:122604
abnormal blood circulation J:122604
abnormal enzyme/coenzyme level J:122604
embryonic lethality during organogenesis, complete penetrance J:122604
normal nervous system phenotype J:122604
visceral vascular congestion J:122604
Hand2tm1Dsr/Hand2tm1Dsr
involves: 129 * 129S7/SvEvBrd * C57BL/6
heart right ventricle hypoplasia J:169213
increased apoptosis J:169213
Hand2tm1Dsr/Hand2tm1Dsr
involves: 129S7/SvEvBrd
abnormal cardiac outflow tract development J:40768
abnormal first pharyngeal arch artery morphology J:40768
abnormal forelimb bud morphology J:62028
abnormal forelimb morphology J:62028
abnormal heart looping J:40768
abnormal heart ventricle morphology J:40768
abnormal pharyngeal arch artery morphology J:40768
absent heart right ventricle J:40768
absent myocardial trabeculae J:40768
absent second pharyngeal arch artery J:40768
absent trabeculae carneae J:40768
congestive heart failure J:40768
decreased cardiac muscle contractility J:40768
decreased embryo size J:40768
decreased somite size J:62028
dilated aortic sac J:40768
edema J:62028
embryonic growth retardation J:40768
embryonic lethality during organogenesis, complete penetrance J:40768
pericardial effusion J:40768
poor circulation J:62028
small forelimb buds J:62028
thin myocardium J:40768
Hand2tm1Dsr/Hand2tm1Dsr
involves: 129S7/SvEvBrd * C57BL/6
absent pharyngeal arches J:49658
congestive heart failure J:49658
decreased embryo size J:49658
embryonic growth retardation J:49658
embryonic lethality during organogenesis, complete penetrance J:49658
incomplete somite formation J:49658
increased apoptosis J:49658
pharyngeal arch hypoplasia J:49658
Hand2tm1Dsr/Hand2tm2.1Dsr
Isl1tm1(cre)Tmj/Isl1+
involves: 129 * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6
abnormal cardiac outflow tract development J:169213
embryonic lethality during organogenesis, complete penetrance J:169213
heart right ventricle hypoplasia J:169213
increased apoptosis J:169213
Hand2tm1Dsr/Hand2tm2.1Dsr
Tg(Mef2c-cre)#Blk/0
involves: 129 * 129S7/SvEvBrd * C57BL/6
abnormal tricuspid valve morphology J:169213
decreased heart right ventricle size J:169213
embryonic lethality during organogenesis, complete penetrance J:169213
heart right ventricle hypoplasia J:169213
persistent truncus arteriosus J:169213
thin myocardium J:169213
ventricular septal defect J:169213
Hand2tm1Dsr/Hand2tm2.1Dsr
Tg(Nkx2-5-cre)9Eno/0
involves: 129 * 129S7/SvEvBrd * C57BL/6
decreased heart left ventricle size J:169213
decreased heart right ventricle size J:169213
embryonic lethality during organogenesis, complete penetrance J:169213
Hand2tm1Dsr/Hand2tm2.1Dsr
Tg(Tbx1-cre)#Dsr/0
involves: 129 * 129S7/SvEvBrd * C57BL/6
abnormal cardiac outflow tract development J:169213
decreased heart right ventricle size J:169213
lethality throughout fetal growth and development, complete penetrance J:169213
Hand2tm1Majh/Hand2tm1Majh
involves: 129S1/SvImJ
abnormal craniofacial bone morphology J:137726
abnormal heart development J:137726
abnormal suckling behavior J:137726
cleft secondary palate J:137726
decreased embryo size J:137726
embryonic lethality during organogenesis, complete penetrance J:137726
normal nervous system phenotype J:137726
short mandible J:137726
Hand2tm2.1Dsr/Hand2tm2.1Dsr
involves: 129 * C57BL/6
no abnormal phenotype detected J:169213
Hand2tm2Eno/Hand2tm2Eno
involves: 129S6/SvEvTac * C57BL/6 * SJL
abnormal apical ectodermal ridge morphology J:146638
abnormal atrioventricular cushion morphology J:146638
abnormal cardiac outflow tract development J:146638
abnormal facial morphology J:146638
abnormal first pharyngeal arch morphology J:146638
abnormal heart left ventricle morphology J:146638
abnormal heart right ventricle morphology J:146638
abnormal interventricular septum morphology J:146638
abnormal jaw morphology J:146638
abnormal limb bud morphology J:146638
decreased heart right ventricle size J:146638
dilated heart left ventricle J:146638
embryonic lethality during organogenesis, complete penetrance J:146638
increased atrioventricular cushion size J:146638
Tg(Hand2)#Tshir/0
Not Specified
abnormal pollex morphology J:198239
decreased lumbar vertebrae number J:198239
hemimelia J:198239
Tg(Prrx1-Hand2)1Eno/0
involves: C57BL/6 * CBA
polydactyly J:80030
Tg(Prrx1-Hand2)2Eno/0
involves: C57BL/6 * CBA
abnormal forelimb zeugopod morphology J:80030
abnormal hindlimb zeugopod morphology J:80030
abnormal limb bone morphology J:80030
polydactyly J:80030
short limbs J:80030
Tg(Prrx1-Hand2)3Eno/0
involves: C57BL/6 * CBA
oligodactyly J:80030
polydactyly J:80030
short limbs J:80030
Tg(Prrx1-Hand2)4Eno/0
involves: C57BL/6 * CBA
normal limbs/digits/tail phenotype J:80030
Tg(Prrx1-Hand2)5Eno/0
involves: C57BL/6 * CBA
abnormal forelimb zeugopod morphology J:80030
abnormal hindlimb zeugopod morphology J:80030
abnormal limb bone morphology J:80030
polydactyly J:80030
Tg(Prrx1-Hand2)6Eno/0
involves: C57BL/6 * CBA
abnormal forelimb zeugopod morphology J:80030
abnormal hindlimb zeugopod morphology J:80030
abnormal limb bone morphology J:80030
polydactyly J:80030
Tg(Prrx1-Hand2)7Eno/0
involves: C57BL/6 * CBA
normal limbs/digits/tail phenotype J:80030
Tg(Prrx1-Hand2)8Eno/0
involves: C57BL/6 * CBA
normal limbs/digits/tail phenotype J:80030
Tg(Prrx1-Hand2/VP16)1Eno/0
involves: C57BL/6 * CBA
polydactyly J:80030

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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
04/16/2024
MGI 6.23
The Jackson Laboratory