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Symbol
Name
ID

Ndst1
N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1
MGI:104719

Phenotype annotations related to skeleton

Darker colors indicate more annotations

Human Phenotypes	Mandibular prognathia
Disease(s) Associated with NDST1	Mandibular prognathia
autosomal recessive intellectual developmental disorder 46

Mouse Phenotypes		abnormal cranium morphology	absent neurocranium	absent mandible	absent facial bone	abnormal diaphragm central tendon morphology	abnormal tendon cell morphology	abnormal tendon collagen fibril morphology	delayed bone ossification
Availability	Mouse Genotype	abnormal cranium morphology	absent neurocranium	absent mandible	absent facial bone	abnormal diaphragm central tendon morphology	abnormal tendon cell morphology	abnormal tendon collagen fibril morphology	delayed bone ossification
	Ndst1^b2b2230Clo/Ndst1^b2b2230Clo
	Ndst1^tm1.1Grob/Ndst1^tm1.1Grob
	Ndst1^tm1Je/Ndst1^tm1Je Tg(Tek-cre)1Ywa/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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