|
Symbol Name ID |
Chd7
chromodomain helicase DNA binding protein 7 MGI:2444748 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Polyhydramnios |
| Disease(s) Associated with CHD7 | |
| CHARGE syndrome |
| Mouse Phenotypes | embryo phenotype |
abnormal pharyngeal arch artery morphology |
abnormal fourth pharyngeal arch artery morphology |
abnormal sixth pharyngeal arch artery morphology |
abnormal neural crest cell migration |
delayed embryo turning |
embryonic growth arrest |
embryonic growth retardation |
abnormal embryonic neuroepithelium morphology |
decreased embryonic neuroepithelium thickness |
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| Availability | Mouse Genotype | ||||||||||
| Chd7em1Jiao/Chd7em1Jiao | |||||||||||
| Chd7Gt(S20-7E1)Sor/Chd7Gt(S20-7E1)Sor | |||||||||||
| Chd7tm2a(EUCOMM)Wtsi/Chd7tm2a(EUCOMM)Wtsi | |||||||||||
| Chd7Coa1/Chd7+ | |||||||||||
| Chd7Gt(RRR136)Byg/Chd7+ | |||||||||||
| Chd7Gt(S20-7E1)Sor/Chd7+ | |||||||||||
| Chd7Gt(XK403)Byg/Chd7+ | |||||||||||
| Chd7Gt(XK403)Byg/Chd7+ H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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| Chd7Gt(XK403)Byg/Chd7+ Tg(Tbx1-cre)1Joe/0 (conditional) |
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| Chd7Gt(XK403)Byg/Chd7+ Mesp1tm2(cre)Ysa/Mesp1+ (conditional) |
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| Chd7Gt(XK403)Byg/Chd7+ Tfap2atm1(cre)Moon/Tfap2a+ (conditional) |
* | ||||||||||
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 04/16/2024 MGI 6.23 |
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