KIAA0196 (also known as strumpellin) is a human
gene.[5] The product is a protein that is a component of the
WASH complex, which regulates
actin assembly on intracellular
vesicles.[6] Mutations in KIAA0196 are implicated in some forms of
hereditary spastic paraplegia.[7]
Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–174.
doi:
10.1016/0378-1119(94)90802-8.
PMID8125298.
Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–156.
doi:
10.1016/S0378-1119(97)00411-3.
PMID9373149.
Gevaert K, Goethals M, Martens L, et al. (2004). "Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides". Nat. Biotechnol. 21 (5): 566–569.
doi:
10.1038/nbt810.
PMID12665801.
S2CID23783563.
KIAA0196 (also known as strumpellin) is a human
gene.[5] The product is a protein that is a component of the
WASH complex, which regulates
actin assembly on intracellular
vesicles.[6] Mutations in KIAA0196 are implicated in some forms of
hereditary spastic paraplegia.[7]
Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–174.
doi:
10.1016/0378-1119(94)90802-8.
PMID8125298.
Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–156.
doi:
10.1016/S0378-1119(97)00411-3.
PMID9373149.
Gevaert K, Goethals M, Martens L, et al. (2004). "Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides". Nat. Biotechnol. 21 (5): 566–569.
doi:
10.1038/nbt810.
PMID12665801.
S2CID23783563.