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Symbol
Name
ID
Shh
sonic hedgehog
MGI:98297
Phenotype annotations related to nervous system
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Dandy-Walker malformation
Microcephaly
Encephalocele
Anosmia
Hyposmia
Aganglionic megacolon
Decreased response to growth hormone stimulation test
Anterior hypopituitarism
Panhypopituitarism
Spasticity
Abnormal nervous system morphology
Hydrocephalus
Ventriculomegaly
Aplasia/Hypoplasia of the corpus callosum
Aplasia/Hypoplasia of the cerebellum
Holoprosencephaly
Spinal dysraphism
Spinal cord tumor
Abnormality of neuronal migration
Chorea
Cognitive impairment
Intellectual disability
Intellectual disability, mild
Dystonia
Global developmental delay
Specific learning disability
Seizure
Disease(s) Associated with SHH
Hirschsprung's disease
holoprosencephaly
holoprosencephaly 3
polydactyly
solitary median maxillary central incisor

Mouse Phenotypes
nervous system phenotype
seizures
abnormal neural tube morphology
absent floor plate
spina bifida
abnormal nervous system morphology
abnormal enteric neuron morphology
abnormal hippocampus development
abnormal telencephalon development
abnormal cerebellum development
abnormal cerebellar lobule formation
abnormal cerebellum external granule cell layer morphology
thin external granule cell layer
holoprosencephaly
abnormal brain interneuron morphology
decreased brain weight
increased forebrain size
decreased midbrain size
increased midbrain size
decreased brain size
enlarged brain ventricles
abnormal choroid plexus morphology
abnormal corpus callosum morphology
abnormal forebrain morphology
disorganized thalamus
absent diencephalon
abnormal telencephalon morphology
absent olfactory bulb
small olfactory bulb
abnormal cerebellum morphology
abnormal cerebellar cortex morphology
abnormal cerebellar Purkinje cell layer
decreased Purkinje cell number
abnormal cerebellar granule layer morphology
abnormal cerebellar granule cell morphology
abnormal cerebellar molecular layer
absent cerebellar lobules
small cerebellum
cerebellum hypoplasia
abnormal postnatal subventricular zone morphology
abnormal glial cell morphology
abnormal astrocyte morphology
abnormal embryonic/fetal subventricular zone morphology
abnormal lateral ganglionic eminence morphology
abnormal medial ganglionic eminence morphology
abnormal vestibulocochlear ganglion morphology
absent vestibulocochlear ganglion
loss of dopaminergic neurons
abnormal motor neuron morphology
decreased motor neuron number
decreased neuron number
increased neuron number
abnormal retina ganglion cell morphology
abnormal spinal cord interneuron morphology
abnormal ventral interneuron 2 morphology
abnormal ventral interneuron 3 morphology
abnormal optic nerve morphology
abnormal spinal cord lateral motor column morphology
decreased spinal cord size
abnormal synaptic dopamine release
Availability Mouse Genotype
Shhtm1.1Rseg/Shhtm1.1Rseg
Shhtm1Amc/Shhtm1Amc
Shhtm1Chg/Shhtm1Chg
Shhtm1Ptch/Shhtm1Ptch
Shhtm3(cre)Chg/Shhtm3(cre)Chg
Shhtm1Amc/Shhtm1.1Rseg
Shhtm1Chg/Shh+
Tg(Shh)#Dje/0
Tg(KRT14-Shh)#Cobm/0
Tg(Shh)#Dje/0
Shhtm1Ahk/Shhtm1Ahk
Slc6a3tm1(cre)Xz/Slc6a3+  (conditional)
Shhtm2Amc/Shhtm2Amc
Tg(Nes-cre)1Kln/0  (conditional)
Olig2tm1(cre)Tmj/Olig2+
Shhtm2Amc/Shhtm2Amc  (conditional)
*
Shhtm2Chg/Shh+
Edil3Tg(Sox2-cre)1Amc/Edil3+  (conditional)
Shhtm1(EGFP/cre)Cjt/Shhtm2Amc  (conditional)
Shhtm1Amc/Shhtm2Amc
Tg(Thy1-cre)703Vaw/?  (conditional)
Shhtm2Amc/Shhtm3Amc
Tg(Pcp2-cre)1Amc/0  (conditional)
Shhtm2Amc/Shhtm3Amc
Tg(Pax2-cre)1Amc/0  (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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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory