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CRYM

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IdentifiersAliasesCRYM, DFNA40, THBP, crystallin muExternal IDsMGI:102675 HomoloGene:1424 GeneCards:CRYM
Gene location Human
ChrChromosome 16 human
Band16p122Start21,238,874 bp
End21,303,083 bp
RNA expression pattern
More reference expression data
OrthologsSpeciesHumanMouseEntrez
Ensembl
UniProt
RefSeq mRNA

NM_001014444
NM_001888

NM_016669

RefSeq protein

NP_001879

NP_057878

Location UCSCChr 16:2124 – 213 MbChr 7:12019 – 1202 MbPubMed searchWikidata
^ "Mouse PubMed Reference:" 
  • ^ Chen H, Phillips HA, Callen DF, Kim RY, Wistow GJ, Antonarakis SE Feb 1993 "Localization of the human gene for mu-crystallin to chromosome 16p" Genomics 14 4:1115–6 doi:101016/S0888-75430580143-0 PMID 1478656 
  • ^ a b "Entrez Gene:CRYM crystallin, mu" 
  • ^ Hallen A, Cooper AJ, Jamie JF, Haynes PA, Willows RD February 2011 "Mammalian forebrain ketimine reductase identified as μ-crystallin; potential regulation by thyroid hormones" J Neurochem 118 3:no–no doi:101111/j1471-4159201107220x PMID 21332720 
  • ^ Oshima A, Suzuki S, Takumi Y, Hashizume K, Abe S, Usami S June 2006 "CRYM mutations cause deafness through thyroid hormone binding properties in the fibrocytes of the cochlea" J Med Genet 43 6:e25 doi:101136/jmg2005034397 PMC 2564543  PMID 16740909 
  • ^ Abe S, Katagiri T, Saito-Hisaminato A, Usami S, Inoue Y, Tsunoda T, Nakamura Y January 2003 "Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues" Am J Hum Genet 72 1:73–82 doi:101086/345398 PMC 420014  PMID 12471561 
  • ^ Suzuki S, Suzuki N, Mori J, Oshima A, Usami S, Hashizume K April 2007 "micro-Crystallin as an intracellular 3,5,3'-triiodothyronine holder in vivo" Mol Endocrinol 21 4:885–94 doi:101210/me2006-0403 PMID 17264173 
  • ^ Dietrich JW 2002 Der Hypophysen-Schilddrüsen-Regelkreis Entwicklung und klinische Anwendung eines nichtlinearen Modellsin German Berlin:Logos-Verlag ISBN 3-89722-850-5 
  • ^ Dietrich JW, Tesche A, Pickardt CR, Mitzdorf U 2004 "Thyrotropic Feedback Control:Evidence for an Additional Ultrashort Feedback Loop from Fractal Analysis" Cybernetics and Systems 35 4:315–31 doi:101080/01969720490443354 
  • External links

    • Human CRYM genome location and CRYM gene details page in the UCSC Genome Browser

    Further reading

    • Kim RY, Gasser R, Wistow GJ 1992 "mu-crystallin is a mammalian homologue of Agrobacterium ornithine cyclodeaminase and is expressed in human retina" Proc Natl Acad Sci USA 89 19:9292–6 doi:101073/pnas89199292 PMC 50112  PMID 1384048 
    • Vié MP, Blanchet P, Samson M, et al 1996 "High affinity thyroid hormone-binding protein in human kidney:kinetic characterization and identification by photoaffinity labeling" Endocrinology 137 11:4563–70 doi:101210/en137114563 PMID 8895318 
    • Segovia L, Horwitz J, Gasser R, Wistow G 1998 "Two roles for mu-crystallin:a lens structural protein in diurnal marsupials and a possible enzyme in mammalian retinas" Mol Vis 3:9 PMID 9285773 
    • Vié MP, Evrard C, Osty J, et al 1998 "Purification, molecular cloning, and functional expression of the human nicodinamide-adenine dinucleotide phosphate-regulated thyroid hormone-binding protein" Mol Endocrinol 11 11:1728–36 doi:101210/me11111728 PMID 9328354 
    • Loftus BJ, Kim UJ, Sneddon VP, et al 1999 "Genome duplications and other features in 12 Mb of DNA sequence from human chromosome 16p and 16q" Genomics 60 3:295–308 doi:101006/geno19995927 PMID 10493829 
    • Abe S, Katagiri T, Saito-Hisaminato A, et al 2003 "Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues" Am J Hum Genet 72 1:73–82 doi:101086/345398 PMC 420014  PMID 12471561 
    • Strausberg RL, Feingold EA, Grouse LH, et al 2003 "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences" Proc Natl Acad Sci USA 99 26:16899–903 doi:101073/pnas242603899 PMC 139241  PMID 12477932 
    • Gerhard DS, Wagner L, Feingold EA, et al 2004 "The status, quality, and expansion of the NIH full-length cDNA project:the Mammalian Gene Collection MGC" Genome Res 14 10B:2121–7 doi:101101/gr2596504 PMC 528928  PMID 15489334 
    • Reed PW, Corse AM, Porter NC, et al 2007 "Abnormal expression of mu-crystallin in facioscapulohumeral muscular dystrophy" Exp Neurol 205 2:583–6 doi:101016/jexpneurol200703009 PMID 17451686 


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      CRYM beatiful post thanks!

      29.10.2014


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