Details for: PLEKHG5
Associated with
Other Information
Genular Protein ID: 1030804860
Symbol: PKHG5_HUMAN
Name: Pleckstrin homology domain-containing family G member 5
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 9872452
Title: Prediction of the coding sequences of unidentified human genes. XI. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.
PubMed ID: 9872452
PubMed ID: 14702039
Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.
PubMed ID: 14702039
DOI: 10.1038/ng1285
PubMed ID: 16710414
Title: The DNA sequence and biological annotation of human chromosome 1.
PubMed ID: 16710414
DOI: 10.1038/nature04727
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: 12761501
Title: Large-scale identification and characterization of human genes that activate NF-kappaB and MAPK signaling pathways.
PubMed ID: 12761501
PubMed ID: 11704860
Title: The gene for a new brain specific RhoA exchange factor maps to the highly unstable chromosomal region 1p36.2-1p36.3.
PubMed ID: 11704860
PubMed ID: 16467373
Title: A PDZ-binding motif as a critical determinant of Rho guanine exchange factor function and cell phenotype.
PubMed ID: 16467373
PubMed ID: 23777631
Title: PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot-Marie-Tooth disease.
PubMed ID: 23777631
DOI: 10.1093/hmg/ddt274
PubMed ID: 28847484
Title: The Rho-specific guanine nucleotide exchange factor Plekhg5 modulates cell polarity, adhesion, migration, and podosome organization in macrophages and osteoclasts.
PubMed ID: 28847484
PubMed ID: 17564964
Title: The nuclear factor kappaB-activator gene PLEKHG5 is mutated in a form of autosomal recessive lower motor neuron disease with childhood onset.
PubMed ID: 17564964
DOI: 10.1086/518900
PubMed ID: 23844677
Title: Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease.
PubMed ID: 23844677
Sequence Information:
- Length: 1006
- Mass: 111231
- Checksum: 2260D175D3C27D76
- Sequence:
MHYDGHVRFD LPPQGSVLAR NVSTRSCPPR TSPAVDLEEE EEESSVDGKG DRKSTGLKLS KKKARRRHTD DPSKECFTLK FDLNVDIETE IVPAMKKKSL GEVLLPVFER KGIALGKVDI YLDQSNTPLS LTFEAYRFGG HYLRVKAPAK PGDEGKVEQG MKDSKSLSLP ILRPAGTGPP ALERVDAQSR RESLDILAPG RRRKNMSEFL GEASIPGQEP PTPSSCSLPS GSSGSTNTGD SWKNRAASRF SGFFSSGPST SAFGREVDKM EQLEGKLHTY SLFGLPRLPR GLRFDHDSWE EEYDEDEDED NACLRLEDSW RELIDGHEKL TRRQCHQQEA VWELLHTEAS YIRKLRVIIN LFLCCLLNLQ ESGLLCEVEA ERLFSNIPEI AQLHRRLWAS VMAPVLEKAR RTRALLQPGD FLKGFKMFGS LFKPYIRYCM EEEGCMEYMR GLLRDNDLFR AYITWAEKHP QCQRLKLSDM LAKPHQRLTK YPLLLKSVLR KTEEPRAKEA VVAMIGSVER FIHHVNACMR QRQERQRLAA VVSRIDAYEV VESSSDEVDK LLKEFLHLDL TAPIPGASPE ETRQLLLEGS LRMKEGKDSK MDVYCFLFTD LLLVTKAVKK AERTRVIRPP LLVDKIVCRE LRDPGSFLLI YLNEFHSAVG AYTFQASGQA LCRGWVDTIY NAQNQLQQLR AQEPPGSQQP LQSLEEEEDE QEEEEEEEEE EEEGEDSGTS AASSPTIMRK SSGSPDSQHC ASDGSTETLA MVVVEPGDTL SSPEFDSGPF SSQSDETSLS TTASSATPTS ELLPLGPVDG RSCSMDSAYG TLSPTSLQDF VAPGPMAELV PRAPESPRVP SPPPSPRLRR RTPVQLLSCP PHLLKSKSEA SLLQLLAGAG THGTPSAPSR SLSELCLAVP APGIRTQGSP QEAGPSWDCR GAPSPGSGPG LVGCLAGEPA GSHRKRCGDL PSGASPRVQP EPPPGVSAQH RKLTLAQLYR IRTTLLLNST LTASEV
Genular Protein ID: 3145960689
Symbol: A0A804EMX3_HUMAN
Name: N/A
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 16710414
Title: The DNA sequence and biological annotation of human chromosome 1.
PubMed ID: 16710414
DOI: 10.1038/nature04727
Sequence Information:
- Length: 1075
- Mass: 118479
- Checksum: FEC80DA35C9023F7
- Sequence:
MGTGPGVSGR LAASRPGPGL PLRDSEPSWA GGRARDGDSQ VCHHADCQQL HRRGPLNLCE ACDSKFHSTM HYDGHVRFDL PPQGSVLARN VSTRSCPPRT SPAVDLEEEE EESSVDGKGD RKSTGLKLSK KKARRRHTDD PSKECFTLKF DLNVDIETEI VPAMKKKSLG EVLLPVFERK GIALGKVDIY LDQSNTPLSL TFEAYRFGGH YLRVKAPAKP GDEGKVEQGM KDSKSLSLPI LRPAGTGPPA LERVDAQSRR ESLDILAPGR RRKNMSEFLG EASIPGQEPP TPSSCSLPSG SSGSTNTGDS WKNRAASRFS GFFSSGPSTS AFGREVDKME QLEGKLHTYS LFGLPRLPRG LRFDHDSWEE EYDEDEDEDN ACLRLEDSWR ELIDGHEKLT RRQCHQQEAV WELLHTEASY IRKLRVIINL FLCCLLNLQE SGLLCEVEAE RLFSNIPEIA QLHRRLWASV MAPVLEKARR TRALLQPGDF LKGFKMFGSL FKPYIRYCME EEGCMEYMRG LLRDNDLFRA YITWAEKHPQ CQRLKLSDML AKPHQRLTKY PLLLKSVLRK TEEPRAKEAV VAMIGSVERF IHHVNACMRQ RQERQRLAAV VSRIDAYEVV ESSSDEVDKL LKEFLHLDLT APIPGASPEE TRQLLLEGSL RMKEGKDSKM DVYCFLFTDL LLVTKAVKKA ERTRVIRPPL LVDKIVCREL RDPGSFLLIY LNEFHSAVGA YTFQASGQAL CRGWVDTIYN AQNQLQQLRA QEPPGSQQPL QSLEEEEDEQ EEEEEEEEEE EEGEDSGTSA ASSPTIMRKS SGSPDSQHCA SDGSTETLAM VVVEPGDTLS SPEFDSGPFS SQSDETSLST TASSATPTSE LLPLGPVDGR SCSMDSAYGT LSPTSLQDFV APGPMAELVP RAPESPRVPS PPPSPRLRRR TPVQLLSCPP HLLKSKSEAS LLQLLAGAGT HGTPSAPSRS LSELCLAVPA PGIRTQGSPQ EAGPSWDCRG APSPGSGPGL VGCLAGEPAG SHRKRCGDLP SGASPRVQPE PPPGVSAQHR KLTLAQLYRI RTTLLLNSTL TASEV
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.