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Symbol
Name
ID 		Snrpb
small nuclear ribonucleoprotein B
MGI:98342
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Micrognathia
Malar flattening
Microcephaly
Long philtrum
Cleft lip
Short hard palate
Cleft soft palate
Cleft palate
High palate
Glossoptosis
Carious teeth
Pierre-Robin sequence
Downslanted palpebral fissures
Epicanthus
Disease(s) Associated with SNRPB
cerebrocostomandibular syndrome

Mouse Phenotypes
abnormal metopic suture morphology
abnormal cranium morphology
basisphenoid bone hypoplasia
Meckel's cartilage hypoplasia
frontal bone hypoplasia
interparietal bone hypoplasia
parietal bone hypoplasia
absent alisphenoid bone
abnormal temporal bone morphology
small temporal bone squamous part
absent zygomatic arch
absent hyoid bone
hyoid bone hypoplasia
abnormal jaw morphology
abnormal mandible morphology
absent mandibular angle
absent mandibular condyloid process
absent mandibular coronoid process
mandible hypoplasia
abnormal premaxilla morphology
maxilla hypoplasia
nasal bone hypoplasia
domed cranium
abnormal frontonasal prominence morphology
absent frontonasal prominence
frontonasal prominence hypoplasia
mandibular prominence hypoplasia
absent maxillary prominence
maxillary prominence hypoplasia
first pharyngeal arch hypoplasia
pharyngeal arch hypoplasia
cleft palate
abnormal nose morphology
absent nasal septum
short snout
abnormal head shape
small ears
Availability Mouse Genotype
E2f1Tg(Wnt1-cre)2Sor/E2f1+
Snrpbem1Lajm/Snrpb+  (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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory