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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 embryo

Darker colors indicate more annotations

Human Phenotypes	Single umbilical artery
Disease(s) Associated with SPECC1L	Single umbilical artery
Teebi hypertelorism syndrome 1

Mouse Phenotypes		abnormal cranial neural crest cell migration	abnormal neural crest cell delamination	abnormal neural tube closure
Availability	Mouse Genotype	abnormal cranial neural crest cell migration	abnormal neural crest cell delamination	abnormal neural tube closure
	Specc1l^em3Kumc/Specc1l^em3Kumc
	Specc1l^em4Kumc/Specc1l^em4Kumc
	Specc1l^{Gt(DTM096)Byg}/Specc1l^{Gt(DTM096)Byg}
	Specc1l^{Gt(RRH048)Byg}/Specc1l^{Gt(RRH048)Byg}
	Specc1l^{Gt(DTM096)Byg}/Specc1l^{Gt(RRH048)Byg}

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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