|
Symbol Name ID |
Recql4
RecQ protein-like 4 MGI:1931028 |
| Darker colors indicate more annotations |
| Human Phenotypes | Sparse scalp hair |
Frontal bossing |
Brachycephaly |
Brachyturricephaly |
Craniosynostosis |
Coronal craniosynostosis |
Bicoronal synostosis |
Lambdoidal craniosynostosis |
Sagittal craniosynostosis |
Turricephaly |
Oxycephaly |
Micrognathia |
Mandibular prognathia |
Wide anterior fontanel |
Large fontanelles |
Long face |
Midface capillary hemangioma |
Short chin |
Flat forehead |
Prominent forehead |
Long upper lip |
Thin vermilion border |
Bifid uvula |
Cleft palate |
High palate |
High, narrow palate |
Narrow mouth |
Microdontia |
Agenesis of permanent teeth |
Supernumerary tooth |
Delayed eruption of teeth |
Hypoplasia of teeth |
Choanal stenosis |
Underdeveloped nasal alae |
Concave nasal ridge |
Depressed nasal bridge |
Prominent nasal bridge |
Short nose |
Slender nose |
Absent eyebrow |
Sparse eyebrow |
Absent eyelashes |
Sparse eyelashes |
Blepharophimosis |
Narrow palpebral fissure |
Downslanted palpebral fissures |
Epicanthus |
| Disease(s) Associated with RECQL4 | |||||||||||||||||||||||||||||||||||||||||||||||
| Baller-Gerold syndrome | |||||||||||||||||||||||||||||||||||||||||||||||
| rapadilino syndrome | |||||||||||||||||||||||||||||||||||||||||||||||
| Rothmund-Thomson syndrome |
| Mouse Phenotypes | growth retardation of incisors |
growth retardation of molars |
cleft palate |
|
| Availability | Mouse Genotype | |||
| Recql4tm1Abe/Recql4tm1Abe | ||||
| Recql4tm1Glu/Recql4tm1Glu | ||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/23/2024 MGI 6.23 |
|
|
|
||
Analysis Tools