KIAA2022 A chromosomal aberration involving KIAA2022 is found in 2 patients with severe mental retardation (MR). Pericentric inversion inv(X)(p22.3;q13.2). The Xq13 breakpoint lies within a predicted intron of KIAA2022 gene. KIAA2022 protein is no longer expressed in these patients lymphocytes. Note: This description may include information from UniProtKB.
Protein type: DNA replication
Chromosomal Location of Human Ortholog: Xq13.3
Cellular Component:  cytoplasm
Disease: Mental Retardation, X-linked 98
Reference #:  Q5QGS0 (UniProtKB)
Alt. Names/Synonyms: K2022; KIAA2022; KIDLIA; MRX98; Neurite extension and migration factor; NEXMIF; XPN
Gene Symbols: NEXMIF
Molecular weight: 167,551 Da
Basal Isoelectric point: 6.03  Predict pI for various phosphorylation states
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Protein Structure Not Found.

Cross-references to other databases:  STRING  |  cBioPortal  |  CCLE  |  Wikipedia  |  neXtProt  |  Protein Atlas  |  BioGPS  |  Pfam  |  Phospho.ELM  |  NetworKIN  |  UniProtKB  |  Entrez-Gene  |  GenPept  |  Ensembl Gene