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28 Possible Causes for CDH10, human, protein

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  • Amegakaryocytic Thrombocytopenia

    In this article, the authors addressed the limitations on control cells, the human cell line K562 and primary umbilical cord blood CD34 stem cells from StemExpress, before[stemexpress.com] MYB, NKX2-3, NCK1, CDKN3, NQO1, NFATC1, CECR2, CDK3, CD22, CD1D, NKX3-1, NFIB, NEK7, NEK6, CDH20, CDKN1A, CDK10, CCND3, NEK4, CDK8, CDC42, NAB1, CDK1, NFATC3, CD276, MTDH, CDH10[mendelian.co] We investigated whether the point mutation also affected the physical protein-protein interaction between HoxA11 and Meis1b.[ncbi.nlm.nih.gov]

  • Congenital Hypotrichosis with Juvenile Macular Dystrophy

    Preparation Note The full-length extracellular domain of human CDH3 gene (108 - 645 aa) was constructed with 29 N-terminal T7/HIS-tag and expressed in E. coli as inclusion[sigmaaldrich.com] CDH18A; COL17A1; CDH7; CADM2A Cell-Cell communication KIRREL3L; ANG; ITGB1B.1; CDH12A; CDH18; CDH8; SPTBN1; DSCAMA; PLECA; KIRREL3 Cell-cell junction organization ANG; CDH6; CDH10[creativebiomart.net] [provided by RefSeq, Nov 2015] Cadherins are calcium-dependent cell adhesion proteins.[genecards.org]

  • Hereditary Hypotrichosis with Recurrent Skin Vesicles

    The critical role of these desmosomal proteins in epithelial integrity has been illustrated by their disruption in mouse models and human diseases.[ncbi.nlm.nih.gov] · Desmocollin ( DSC1 , DSC2 , DSC3 ) Protocadherin PCDH1 Unconventional/ungrouped T-cadherin · CDH4 · CDH5 · CDH6 · CDH8 · CDH11 · CDH12 · CDH15 · CDH16 · CDH17 · CDH9 · CDH10[en.academic.ru] Human Molecular Genetics 9: 2761–2766.[els.net]

  • Rosselli-Gulienetti Syndrome

    Hypertension 2015 The goal of this study was to determine whether and how adenosine affects the proliferation of human coronary artery smooth… (More) Morris Teubal 2008 1[semanticscholar.org] Autism CADM1 CDH10 CDH9 NRCAM PCDH10 ROBO1 ROBO2 Breast Carcinoma CADM1 CDH1 CDH5 DSC3 NRCAM PCDHGB6 Colorectal Cancer CDH1 CDH5 CDH7 FAT1 NRCAM RET Liver Cirrhosis, Experimental[selfdecode.com] Here, protein domains act as modules, each with a particular and independent function, that can be mixed together to produce genes encoding new proteins with novel properties[wikivisually.com]

  • Autosomal Dominant Myopia 22

    Below is a table of dominant and recessive traits shown in humans.[sciencebrainwaves.com] Six candidate genes CDH6 , CDH10 , CDH12 , PDZD2 , GOLPH3 , and ZFR at this high myopia locus were selected on the basis of their function to screen for gene mutations by[molvis.org] Phosphoprotein Proteomic databases PTM databases Expression i Gene expression databases Organism-specific databases Interaction i Subunit structure i Binary interactions i Protein-protein[uniprot.org]

  • Autosomal Recessive Myopia 18

    Below is a table of dominant and recessive traits shown in humans.[sciencebrainwaves.com] Six candidate genes CDH6 , CDH10 , CDH12 , PDZD2 , GOLPH3 , and ZFR at this high myopia locus were selected on the basis of their function to screen for gene mutations by[molvis.org] The encoded preproprotein is proteolytically processed to generate the mature protein, which may regulate hemostatic balance and function as a tumor suppressor.[genecards.org]

  • Familial Congenital Mirror Movements 2

    Human RAD51 shows predominant expression in testis, ovary, and lymphoid tissue.[sigmaaldrich.com] MYB, NKX2-3, NCK1, CDKN3, NQO1, NFATC1, CECR2, CDK3, CD22, CD1D, NKX3-1, NFIB, NEK7, NEK6, CDH20, CDKN1A, CDK10, CCND3, NEK4, CDK8, CDC42, NAB1, CDK1, NFATC3, CD276, MTDH, CDH10[mendelian.co] Multiple protein interactions have been demonstrated for the mammalian Rad51 protein.[mskcc.org]

  • Autosomal Dominant Myopia Type 24

    Below is a table of dominant and recessive traits shown in humans.[sciencebrainwaves.com] Six candidate genes CDH6 , CDH10 , CDH12 , PDZD2 , GOLPH3 , and ZFR at this high myopia locus were selected on the basis of their function to screen for gene mutations by[molvis.org] Additional Disease Information for SLC39A5 No data available for Genatlas for SLC39A5 Gene The mammalian Zip5 protein is a zinc transporter that localizes to the basolateral[genecards.org]

  • Usher Syndrome Type 1K

    Usher syndrome (USH) is an autosomal recessive disorder considered as the most common cause of hereditary deaf-blindness in human, accounting for over 50% of individuals who[mafiadoc.com] […] cDNA 4932438H23 gene chr18_ _50115628 0.047 Dmxl1 Dmx-like 1 chr8_-_70498472 0.045 NM_177698 Psd3 pleckstrin and Sec7 domain containing 3 chr15_ _18750083 0.045 NM_009865 Cdh10[ismara.unibas.ch] […] network component harmonin 1 102,207,096 102,256,779 RGD:8547536 RGD:8554872 RGD:8695937 RGD:8695939 RGD:8694458 RGD:8694457 G Ush1g USH1 protein network component sans 10[rgd.mcw.edu]

  • X-Linked Susceptibility to Asperger Syndrome 1

    Human Neuroligin 3 / NLGN3 Gene ORF cDNA clone expression plasmid, N-Flag tag Human Neuroligin 3 / NLGN3 Gene ORF cDNA clone expression plasmid, C-His tag Human Neuroligin[sinobiological.com] […] substantial differences in the extent and quality of symptoms. [17] Genome-wide association studies (GWAS) have implicated the region on chromosome 5p14.1 between CDH9 and CDH10[emedicine.medscape.com] The encoded protein belongs to a family of neuronal cell surface proteins.[mybiosource.com]