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Symbol
Name
ID

Specc1l
sperm antigen with calponin homology and coiled-coil domains 1-like
MGI:1921642

Phenotype annotations related to growth/size/body

Darker colors indicate more annotations

Human Phenotypes	Omphalocele	Umbilical hernia	Short stature
Disease(s) Associated with SPECC1L
Teebi hypertelorism syndrome 1

Mouse Phenotypes		abnormal secondary palate development	delayed palatal shelf elevation	abnormal oral cavity morphology	abnormal palatal rugae morphology	cleft palate	omphalocele
Availability	Mouse Genotype	abnormal secondary palate development	delayed palatal shelf elevation	abnormal oral cavity morphology	abnormal palatal rugae morphology	cleft palate	omphalocele
	Specc1l^em2Kumc/Specc1l^em2Kumc
	Specc1l^em3Kumc/Specc1l^em3Kumc
	Specc1l^em4Kumc/Specc1l^em4Kumc
	Specc1l^em1Kumc/Specc1l^tm1Kumc
	Specc1l^em3Kumc/Specc1l⁺
	Specc1l^em4Kumc/Specc1l⁺

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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