Entity Details

Primary name RIPP2_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ5TAB7
EntryNameRIPP2_HUMAN
FullNameProtein ripply2
TaxID9606
Evidenceevidence at protein level
Length128
SequenceStatuscomplete
DateCreated2007-10-23
DateModified2021-06-02

Ontological Relatives

GenesRIPPLY2

GO terms

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GOName
GO:0000122 negative regulation of transcription by RNA polymerase II
GO:0001503 ossification
GO:0001756 somitogenesis
GO:0005634 nucleus
GO:0007219 Notch signaling pathway
GO:0007368 determination of left/right symmetry
GO:0009880 embryonic pattern specification
GO:0032525 somite rostral/caudal axis specification
GO:0036342 post-anal tail morphogenesis
GO:0060349 bone morphogenesis

Subcellular Location

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Subcellular Location
Nucleus

Domains

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DomainNameCategoryType
IPR028127 Ripply familyFamilyFamily

Diseases

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Disease IDSourceNameDescription
616566 OMIMSpondylocostal dysostosis 6, autosomal recessive (SCDO6)A form of spondylocostal dysostosis, a condition of variable severity associated with vertebral and rib segmentation defects. The main skeletal malformations include fusion of vertebrae, hemivertebrae, fusion of certain ribs, and other rib malformations. Deformity of the chest and spine (severe scoliosis, kyphoscoliosis and lordosis) is a natural consequence of the malformation and leads to a dwarf-like appearance. As the thorax is small, infants frequently have respiratory insufficiency and repeated respiratory infections resulting in life-threatening complications in the first year of life. The disease is caused by variants affecting the gene represented in this entry.