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1 to 13 of 13  Show
  1. 1
    "The DNA sequence and biological annotation of human chromosome 1."
    Gregory S.G., Barlow K.F., McLay K.E., Kaul R., Swarbreck D., Dunham A., Scott C.E., Howe K.L., Woodfine K., Spencer C.C.A., Jones M.C., Gillson C., Searle S., Zhou Y., Kokocinski F., McDonald L., Evans R., Phillips K.
    Bentley D.R.
    Nature 441:315-321(2006) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 5833 other entries.

  2. 2
    "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
    The MGC Project Team
    Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 50459 other entries.

  3. 3
    Cited for: PROTEIN SEQUENCE OF 1-10 AND 43-52, IDENTIFICATION BY MASS SPECTROMETRY, POLYMORPHISM, SUBUNIT, DISULFIDE BOND.
    Category: PTM / Processing, Interaction, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 and mapped to 1 other entries.

  4. 4
    Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-22 AND SER-27, IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
    Category: PTM / Processing, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 8820 other entries.

  5. 5
    "Homozygosity for a null allele of SMIM1 defines the Vel-negative blood group phenotype."
    Storry J.R., Joud M., Christophersen M.K., Thuresson B., Akerstrom B., Sojka B.N., Nilsson B., Olsson M.L.
    Nat. Genet. 45:537-541(2013) [PubMed] [Europe PMC] [Abstract]
    Cited for: POLYMORPHISM, SUBUNIT, DISULFIDE BOND, TISSUE SPECIFICITY, TOPOLOGY.
    Category: Subcellular Location, PTM / Processing, Expression, Interaction, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 and mapped to 1 other entries.

  6. 6
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 and mapped to 2 other entries.

  7. 7
    "An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome."
    Bian Y., Song C., Cheng K., Dong M., Wang F., Huang J., Sun D., Wang L., Ye M., Zou H.
    J. Proteomics 96:253-262(2014) [PubMed] [Europe PMC] [Abstract]
    Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-22, IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
    Category: PTM / Processing, Sequences.
    Tissue: Liver.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 11670 other entries.

  8. 8
    "SMIM1 is a type II transmembrane phosphoprotein and displays the Vel blood group antigen at its carboxyl-terminus."
    Arnaud L., Kelley L.P., Helias V., Cartron J.P., Ballif B.A.
    FEBS Lett. 589:3624-3630(2015) [PubMed] [Europe PMC] [Abstract]
    Cited for: PHOSPHORYLATION AT SER-6; SER-17; SER-22 AND SER-27, SUBCELLULAR LOCATION, TOPOLOGY, MUTAGENESIS OF SER-6; SER-17; SER-22; SER-27; CYS-35; CYS-43 AND 76-LYS--LYS-78, DOMAIN, REGION, ACETYLATION AT MET-1, IDENTIFICATION BY MASS SPECTROMETRY.
    Category: Subcellular Location, Pathology & Biotech, PTM / Processing, Sequences, Family & Domains.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is mapped to 2 other entries.

  9. 9
    "Impact of genetic variation in the SMIM1 gene on Vel expression levels."
    Haer-Wigman L., Stegmann T.C., Solati S., Ait Soussan A., Beckers E., van der Harst P., van Hulst-Sundermeijer M., Ligthart P., van Rhenen D., Schepers H., de Haas M., van der Schoot C.E.
    Transfusion 55:1457-1466(2015) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech, Sequences.
    Annotation: Weak Vel expression levels are caused by multiple genetic factors in SMIM1 and probably also by other genetic or environmental factors.Imported.
    Source: GeneRIF:388588.

    This publication is mapped to 3 other entries.

  10. 10
    "The c.64_80del SMIM1 allele is segregating in the Hutterite population."
    Coghlan G., Zelinski T.
    Transfusion 56:946-949(2016) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: Alleles that initially entered the population have been maintained within the population. The c.64_80del null allele of SMIM1 is one such allele thus having implications for transfusion medicine and child or maternal health.Imported.
    Source: GeneRIF:388588.

    This publication is mapped to 3 other entries.

  11. 11
    "Screening for the SMIM1*64_80 del Allele in blood donors in a population from Southern Brazil."
    Costa D.C., Dezan M., Santos T., Schinaider A.A., Schorner E.J., Levi J.E., Santos-Silva M.C.
    Transfus Med 26:355-359(2016) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: Among the 448 samples analysed 10 (2.23%) harboured the 17 bp deletion of the gene SMIM1 and all were heterozygote for the SMIM1*64_80 del allele.Imported.
    Source: GeneRIF:388588.

    This publication is mapped to 3 other entries.

  12. 12
    "SMIM1 variants rs1175550 and rs143702418 independently modulate Vel blood group antigen expression."
    Christophersen M.K., Joud M., Ajore R., Vege S., Ljungdahl K.W., Westhoff C.M., Olsson M.L., Storry J.R., Nilsson B.
    Sci Rep 7:40451-40451(2017) [PubMed] [Europe PMC] [Abstract]
    Annotation: rs1175550G and to a lesser extent rs143702418C independently increase SMIM1 and Vel antigen expression.Imported.
    Source: GeneRIF:388588.

    This publication is mapped to 3 other entries.

  13. 13
    "SMIM1 polymorphisms in a donor population from southeast Brazil and their correlation with VEL expression."
    Arnoni C.P., De Paula Vendrame T.A., Muniz J.G., Gazito D., De Medeiros Person R.D., Pereira Cortez A.J., Latini F.R.M., Castilho L.
    Blood Transfus 17:60-65(2019) [PubMed] [Europe PMC] [Abstract]
    Annotation: the present study demonstrated that although the SMIM1*64_80del allele is responsible for some variation of Vel phenotype in this donor population Vel expression is also controlled by molecular changes in SMIM1 intron 2.Imported.
    Source: GeneRIF:388588.

    This publication is mapped to 3 other entries.

1 to 13 of 13  Show
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