Details for: WASHC5
Associated with
Other Information
Genular Protein ID: 3509084000
Symbol: WASC5_HUMAN
Name: Strumpellin
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 8724849
Title: Prediction of the coding sequences of unidentified human genes. V. The coding sequences of 40 new genes (KIAA0161-KIAA0200) deduced by analysis of cDNA clones from human cell line KG-1.
PubMed ID: 8724849
PubMed ID: 14702039
Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.
PubMed ID: 14702039
DOI: 10.1038/ng1285
PubMed ID: 15489334
Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
PubMed ID: 15489334
DOI: 10.1101/gr.2596504
PubMed ID: 18691976
Title: Kinase-selective enrichment enables quantitative phosphoproteomics of the kinome across the cell cycle.
PubMed ID: 18691976
PubMed ID: 19922875
Title: The Arp2/3 activator WASH controls the fission of endosomes through a large multiprotein complex.
PubMed ID: 19922875
PubMed ID: 20833645
Title: Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseases.
PubMed ID: 20833645
DOI: 10.1093/brain/awq222
PubMed ID: 20498093
Title: WASH and WAVE actin regulators of the Wiskott-Aldrich syndrome protein (WASP) family are controlled by analogous structurally related complexes.
PubMed ID: 20498093
PubMed ID: 21269460
Title: Initial characterization of the human central proteome.
PubMed ID: 21269460
PubMed ID: 23085491
Title: The hereditary spastic paraplegia protein strumpellin: characterisation in neurons and of the effect of disease mutations on WASH complex assembly and function.
PubMed ID: 23085491
PubMed ID: 24065355
Title: A novel mutation in KIAA0196: identification of a gene involved in Ritscher-Schinzel/3C syndrome in a First Nations cohort.
PubMed ID: 24065355
PubMed ID: 23186163
Title: Toward a comprehensive characterization of a human cancer cell phosphoproteome.
PubMed ID: 23186163
DOI: 10.1021/pr300630k
PubMed ID: 23676666
Title: The WASH complex, an endosomal Arp2/3 activator, interacts with the Hermansky-Pudlak syndrome complex BLOC-1 and its cargo phosphatidylinositol-4-kinase type IIalpha.
PubMed ID: 23676666
PubMed ID: 25944712
Title: N-terminome analysis of the human mitochondrial proteome.
PubMed ID: 25944712
PubMed ID: 17160902
Title: Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia.
PubMed ID: 17160902
DOI: 10.1086/510782
PubMed ID: 23881105
Title: Exome sequencing expands the mutational spectrum of SPG8 in a family with spasticity responsive to L-DOPA treatment.
PubMed ID: 23881105
PubMed ID: 23455931
Title: Pure adult-onset Spastic Paraplegia caused by a novel mutation in the KIAA0196 (SPG8) gene.
PubMed ID: 23455931
PubMed ID: 25454649
Title: A novel strumpellin mutation and potential pitfalls in the molecular diagnosis of hereditary spastic paraplegia type SPG8.
PubMed ID: 25454649
Sequence Information:
- Length: 1159
- Mass: 134286
- Checksum: D6156D359981FC5F
- Sequence:
MLDFLAENNL CGQAILRIVS CGNAIIAELL RLSEFIPAVF RLKDRADQQK YGDIIFDFSY FKGPELWESK LDAKPELQDL DEEFRENNIE IVTRFYLAFQ SVHKYIVDLN RYLDDLNEGV YIQQTLETVL LNEDGKQLLC EALYLYGVML LVIDQKIEGE VRERMLVSYY RYSAARSSAD SNMDDICKLL RSTGYSSQPG AKRPSNYPES YFQRVPINES FISMVIGRLR SDDIYNQVSA YPLPEHRSTA LANQAAMLYV ILYFEPSILH THQAKMREIV DKYFPDNWVI SIYMGITVNL VDAWEPYKAA KTALNNTLDL SNVREQASRY ATVSERVHAQ VQQFLKEGYL REEMVLDNIP KLLNCLRDCN VAIRWLMLHT ADSACDPNNK RLRQIKDQIL TDSRYNPRIL FQLLLDTAQF EFILKEMFKQ MLSEKQTKWE HYKKEGSERM TELADVFSGV KPLTRVEKNE NLQAWFREIS KQILSLNYDD STAAGRKTVQ LIQALEEVQE FHQLESNLQV CQFLADTRKF LHQMIRTINI KEEVLITMQI VGDLSFAWQL IDSFTSIMQE SIRVNPSMVT KLRATFLKLA SALDLPLLRI NQANSPDLLS VSQYYSGELV SYVRKVLQII PESMFTSLLK IIKLQTHDII EVPTRLDKDK LRDYAQLGPR YEVAKLTHAI SIFTEGILMM KTTLVGIIKV DPKQLLEDGI RKELVKRVAF ALHRGLIFNP RAKPSELMPK LKELGATMDG FHRSFEYIQD YVNIYGLKIW QEEVSRIINY NVEQECNNFL RTKIQDWQSM YQSTHIPIPK FTPVDESVTF IGRLCREILR ITDPKMTCHI DQLNTWYDMK THQEVTSSRL FSEIQTTLGT FGLNGLDRLL CFMIVKELQN FLSMFQKIIL RDRTVQDTLK TLMNAVSPLK SIVANSNKIY FSAIAKTQKI WTAYLEAIMK VGQMQILRQQ IANELNYSCR FDSKHLAAAL ENLNKALLAD IEAHYQDPSL PYPKEDNTLL YEITAYLEAA GIHNPLNKIY ITTKRLPYFP IVNFLFLIAQ LPKLQYNKNL GMVCRKPTDP VDWPPLVLGL LTLLKQFHSR YTEQFLALIG QFICSTVEQC TSQKIPEIPA DVVGALLFLE DYVRYTKLPR RVAEAHVPNF IFDEFRTVL
Genular Protein ID: 3941736881
Symbol: E7EQI7_HUMAN
Name: N/A
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 16421571
Title: DNA sequence and analysis of human chromosome 8.
PubMed ID: 16421571
DOI: 10.1038/nature04406
PubMed ID: 18691976
Title: Kinase-selective enrichment enables quantitative phosphoproteomics of the kinome across the cell cycle.
PubMed ID: 18691976
PubMed ID: 21269460
Title: Initial characterization of the human central proteome.
PubMed ID: 21269460
PubMed ID: 23186163
Title: Toward a comprehensive characterization of a human cancer cell phosphoproteome.
PubMed ID: 23186163
PubMed ID: 25944712
Title: N-terminome analysis of the human mitochondrial proteome.
PubMed ID: 25944712
Sequence Information:
- Length: 1011
- Mass: 117066
- Checksum: 5810C6A99389134C
- Sequence:
MLLVIDQKIE GEVRERMLVS YYRYSAARSS ADSNMDDICK LLRSTGYSSQ PGAKRPSNYP ESYFQRVPIN ESFISMVIGR LRSDDIYNQV SAYPLPEHRS TALANQAAML YVILYFEPSI LHTHQAKMRE IVDKYFPDNW VISIYMGITV NLVDAWEPYK AAKTALNNTL DLSNVREQAS RYATVSERVH AQVQQFLKEG YLREEMVLDN IPKLLNCLRD CNVAIRWLML HTADSACDPN NKRLRQIKDQ ILTDSRYNPR ILFQLLLDTA QFEFILKEMF KQMLSEKQTK WEHYKKEGSE RMTELADVFS GVKPLTRVEK NENLQAWFRE ISKQILSLNY DDSTAAGRKT VQLIQALEEV QEFHQLESNL QVCQFLADTR KFLHQMIRTI NIKEEVLITM QIVGDLSFAW QLIDSFTSIM QESIRVNPSM VTKLRATFLK LASALDLPLL RINQANSPDL LSVSQYYSGE LVSYVRKVLQ IIPESMFTSL LKIIKLQTHD IIEVPTRLDK DKLRDYAQLG PRYEVAKLTH AISIFTEGIL MMKTTLVGII KVDPKQLLED GIRKELVKRV AFALHRGLIF NPRAKPSELM PKLKELGATM DGFHRSFEYI QDYVNIYGLK IWQEEVSRII NYNVEQECNN FLRTKIQDWQ SMYQSTHIPI PKFTPVDESV TFIGRLCREI LRITDPKMTC HIDQLNTWYD MKTHQEVTSS RLFSEIQTTL GTFGLNGLDR LLCFMIVKEL QNFLSMFQKI ILRDRTVQDT LKTLMNAVSP LKSIVANSNK IYFSAIAKTQ KIWTAYLEAI MKVGQMQILR QQIANELNYS CRFDSKHLAA ALENLNKALL ADIEAHYQDP SLPYPKEDNT LLYEITAYLE AAGIHNPLNK IYITTKRLPY FPIVNFLFLI AQLPKLQYNK NLGMVCRKPT DPVDWPPLVL GLLTLLKQFH SRYTEQFLAL IGQFICSTVE QCTSQKIPEI PADVVGALLF LEDYVRYTKL PRRVAEAHVP NFIFDEFRTV L
Database document:
This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.