|
Symbol Name ID |
Snrpb
small nuclear ribonucleoprotein B MGI:98342 |
| Darker colors indicate more annotations |
| Human Phenotypes | Micrognathia |
Malar flattening |
Microcephaly |
Clinodactyly of the 5th finger |
Short humerus |
Congenital hip dislocation |
Elbow flexion contracture |
Calcaneal epiphyseal stippling |
Anomalous rib insertion to vertebrae |
10 pairs of ribs |
11 pairs of ribs |
Rib gap |
Posterior rib gap |
Bell-shaped thorax |
Thoracic hypoplasia |
Kyphosis |
Scoliosis |
Cerebral calcification |
| 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 tracheal cartilage morphology |
ectopic cartilage |
ectopic bone |
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| Availability | Mouse Genotype | ||||||||||||||||||||||||||
| E2f1Tg(Wnt1-cre)2Sor/E2f1+ Snrpbem1Lajm/Snrpb+ (conditional) |
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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 04/30/2024 MGI 6.23 |
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