Entity Details

Primary name K0825_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8IV33
EntryNameK0825_HUMAN
FullNameUncharacterized protein KIAA0825
TaxID9606
Evidenceevidence at protein level
Length1275
SequenceStatuscomplete
DateCreated2008-02-05
DateModified2021-06-02

Ontological Relatives

GenesKIAA0825

GO terms

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Subcellular Location

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Domains

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DomainNameCategoryType
IPR027993 Protein of unknown function DUF4495FamilyFamily

Diseases

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Disease IDSourceNameDescription
618498 OMIMPolydactyly, postaxial, A10 (PAPA10)A form of postaxial polydactyly, a condition characterized by the occurrence of supernumerary digits in the upper and/or lower extremities. In postaxial polydactyly type A, the extra digit is well-formed and articulates with the fifth or a sixth metacarpal/metatarsal. PAPA10 is an autosomal recessive condition characterized by one or more postaxial digits of the hands and/or feet. A rudimentary digit (PAP type B) may also be present. Intrafamilial variability has been observed. The disease may be caused by variants affecting the gene represented in this entry.