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Results for the Protein: NP_001073341
121114302

cullin-4B isoform 2 [Homo sapiens]

Known Diseases associated with this Protein:
  ABNORMAL GAIT
  MENTAL RETARDATION, X-LINKED, WITH SHORT STATURE, HYPOGONADISM, AND
2
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2
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Default View:

CULLIN - smart00182
Cullin_Nedd8 - pfam10557




Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
Cullin_Nedd8pfam105576.4e-39824889

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
OMIM300304.0001 Diseasep.ARG554CYSMENTAL RETARDATION, X-LINKED, WITH SHORT STATURE, HYPOGONADISM, AND||ABNORMAL GAIT
OMIM300304.0002 Diseasep.ARG370TERMENTAL RETARDATION, X-LINKED, WITH SHORT STATURE, HYPOGONADISM, AND||ABNORMAL GAIT



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