Symbol
Name
ID

Ptch1
patched 1
MGI:105373

Phenotype annotations related to growth/size/body

Darker colors indicate more annotations

Human Phenotypes	Abnormality of the neck	Branchial anomaly	Short neck	Omphalocele	Congenital diaphragmatic hernia	Failure to thrive in infancy
Disease(s) Associated with PTCH1	Abnormality of the neck	Branchial anomaly	Short neck	Omphalocele	Congenital diaphragmatic hernia	Failure to thrive in infancy
holoprosencephaly
holoprosencephaly 7
nevoid basal cell carcinoma syndrome

Mouse Phenotypes

abnormal upper incisor morphology

abnormal enamel morphology

mandibular cyst

palatal shelf hypoplasia

absent palatal shelf

cleft secondary palate

shortened head

increased embryo size

omphalocele

abnormal thoracic cavity morphology

kidney cyst

dermal cyst

epidermal cyst

abnormal head morphology

increased body size

postnatal growth retardation

increased fetal size

Availability

Mouse Genotype

Ptch1^dl/Ptch1^dl

Ptch1^mes/Ptch1^mes

Ptch1^wig/Ptch1^wig

Ptch1^dl/Ptch1^tm1Mps

Ptch1^dl/Ptch1^tm1Zim

Ptch1^tm1Kmmt/Ptch1⁺

Ptch1^tm1Mps/Ptch1⁺

Ptch1^tm1Zim/Ptch1⁺

Ptch1^tm1Bjw/Ptch1^tm1Bjw
Tcf21^tm1(cre)Seq/Tcf21⁺ (conditional)

Ptch1^tm1Bjw/Ptch1^tm1Bjw
Tg(KRT14-cre)8Brn/0 (conditional)

Ptch1^tm1Hahn/Ptch1⁺
Gt(ROSA)26Sor^{tm2(cre/ERT2)Brn}/Gt(ROSA)26Sor⁺ (conditional)

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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