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2024-03-29 07:38:24, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_148960               2859 bp    mRNA    linear   PRI 24-JUN-2013
DEFINITION  Homo sapiens claudin 19 (CLDN19), transcript variant 1, mRNA.
ACCESSION   NM_148960
VERSION     NM_148960.2  GI:183979972
KEYWORDS    RefSeq.
SOURCE      Homo sapiens (human)
  ORGANISM  Homo sapiens
            Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
            Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
            Catarrhini; Hominidae; Homo.
REFERENCE   1  (bases 1 to 2859)
  AUTHORS   Al-Shibli,A., Konrad,M., Altay,W., Al Masri,O., Al-Gazali,L. and Al
            Attrach,I.
  TITLE     Familial hypomagnesemia with hypercalciuria and nephrocalcinosis
            (FHHNC): report of three cases with a novel mutation in CLDN19 gene
  JOURNAL   Saudi J Kidney Dis Transpl 24 (2), 338-344 (2013)
   PUBMED   23538362
  REMARK    GeneRIF: Case Reports: novel CLDN19 mutation in familial
            hypomagnesemia with hypercalciuria and nephrocalcinosis.
REFERENCE   2  (bases 1 to 2859)
  AUTHORS   Godron,A., Harambat,J., Boccio,V., Mensire,A., May,A.,
            Rigothier,C., Couzi,L., Barrou,B., Godin,M., Chauveau,D.,
            Faguer,S., Vallet,M., Cochat,P., Eckart,P., Guest,G., Guigonis,V.,
            Houillier,P., Blanchard,A., Jeunemaitre,X. and Vargas-Poussou,R.
  TITLE     Familial hypomagnesemia with hypercalciuria and nephrocalcinosis:
            phenotype-genotype correlation and outcome in 32 patients with
            CLDN16 or CLDN19 mutations
  JOURNAL   Clin J Am Soc Nephrol 7 (5), 801-809 (2012)
   PUBMED   22422540
  REMARK    GeneRIF: The risk of end-stage renal disease in patients with
            CLDN19 mutations was two times the risk of patients with CLDN16
            mutations. Ocular abnormalities were observed only in patients with
            CLDN19 mutations.
REFERENCE   3  (bases 1 to 2859)
  AUTHORS   Ekinci,Z., Karabas,L. and Konrad,M.
  TITLE     Hypomagnesemia-hypercalciuria-nephrocalcinosis and ocular findings:
            a new claudin-19 mutation
  JOURNAL   Turk. J. Pediatr. 54 (2), 168-170 (2012)
   PUBMED   22734304
  REMARK    GeneRIF: In a patient with consanguineous parents, history of
            disturbed organization and development of the retina, a diagnosis
            of Familial hypomagnesemia with hypercalciuria and nephrocalcinosis
            caused by claudin-19 mutation should be considered.
REFERENCE   4  (bases 1 to 2859)
  AUTHORS   Faguer,S., Chauveau,D., Cintas,P., Tack,I., Cointault,O.,
            Rostaing,L., Vargas-Poussou,R. and Ribes,D.
  TITLE     Renal, ocular, and neuromuscular involvements in patients with
            CLDN19 mutations
  JOURNAL   Clin J Am Soc Nephrol 6 (2), 355-360 (2011)
   PUBMED   21030577
  REMARK    GeneRIF: Ocular manifestations and exercise intolerance mimicking
            mild to moderate periodic paralysis are two symptoms that may occur
            in patients with familial hypomagnesemia with hypercalciuria and
            nephrocalcinosis and may indicate CLDN19 mutations.
REFERENCE   5  (bases 1 to 2859)
  AUTHORS   Lal-Nag,M. and Morin,P.J.
  TITLE     The claudins
  JOURNAL   Genome Biol. 10 (8), 235 (2009)
   PUBMED   19706201
  REMARK    Review article
REFERENCE   6  (bases 1 to 2859)
  AUTHORS   Gonzalez-Mariscal,L., Betanzos,A., Nava,P. and Jaramillo,B.E.
  TITLE     Tight junction proteins
  JOURNAL   Prog. Biophys. Mol. Biol. 81 (1), 1-44 (2003)
   PUBMED   12475568
  REMARK    Review article
REFERENCE   7  (bases 1 to 2859)
  AUTHORS   Tsukita,S. and Furuse,M.
  TITLE     Claudin-based barrier in simple and stratified cellular sheets
  JOURNAL   Curr. Opin. Cell Biol. 14 (5), 531-536 (2002)
   PUBMED   12231346
  REMARK    Review article
REFERENCE   8  (bases 1 to 2859)
  AUTHORS   Tsukita,S., Furuse,M. and Itoh,M.
  TITLE     Multifunctional strands in tight junctions
  JOURNAL   Nat. Rev. Mol. Cell Biol. 2 (4), 285-293 (2001)
   PUBMED   11283726
  REMARK    Review article
REFERENCE   9  (bases 1 to 2859)
  AUTHORS   Heiskala,M., Peterson,P.A. and Yang,Y.
  TITLE     The roles of claudin superfamily proteins in paracellular transport
  JOURNAL   Traffic 2 (2), 93-98 (2001)
   PUBMED   11247307
  REMARK    Review article
REFERENCE   10 (bases 1 to 2859)
  AUTHORS   Kniesel,U. and Wolburg,H.
  TITLE     Tight junctions of the blood-brain barrier
  JOURNAL   Cell. Mol. Neurobiol. 20 (1), 57-76 (2000)
   PUBMED   10690502
  REMARK    Review article
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from AK096063.1, BC030524.1 and
            AC098484.2.
            This sequence is a reference standard in the RefSeqGene project.
            On Apr 19, 2008 this sequence version replaced gi:22507371.
            
            Summary: The product of this gene belongs to the claudin family. It
            plays a major role in tight junction-specific obliteration of the
            intercellular space, through calcium-independent cell-adhesion
            activity. Defects in this gene are the cause of hypomagnesemia
            renal with ocular involvement (HOMGO). HOMGO is a progressive renal
            disease characterized by primary renal magnesium wasting with
            hypomagnesemia, hypercalciuria and nephrocalcinosis associated with
            severe ocular abnormalities such as bilateral chorioretinal scars,
            macular colobomata, significant myopia and nystagmus. Alternatively
            spliced transcript variants encoding distinct isoforms have been
            identified for this gene. [provided by RefSeq, Jun 2010].
            
            Transcript Variant: This variant (1) represents the shortest
            transcript, but encodes the longest isoform (a).
            
            Publication Note:  This RefSeq record includes a subset of the
            publications that are available for this gene. Please see the Gene
            record to access additional publications.
            
            ##Evidence-Data-START##
            Transcript exon combination :: AK096063.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025084, ERS025088 [ECO:0000348]
            ##Evidence-Data-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-327               AK096063.1         1-327
            328-817             BC030524.1         214-703
            818-1096            AK096063.1         818-1096
            1097-1097           AC098484.2         82833-82833         c
            1098-2859           AK096063.1         1098-2859
FEATURES             Location/Qualifiers
     source          1..2859
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="1"
                     /map="1p34.2"
     gene            1..2859
                     /gene="CLDN19"
                     /gene_synonym="HOMG5"
                     /note="claudin 19"
                     /db_xref="GeneID:149461"
                     /db_xref="HGNC:2040"
                     /db_xref="MIM:610036"
     exon            1..414
                     /gene="CLDN19"
                     /gene_synonym="HOMG5"
                     /inference="alignment:Splign:1.39.8"
     CDS             192..866
                     /gene="CLDN19"
                     /gene_synonym="HOMG5"
                     /note="isoform a is encoded by transcript variant 1;
                     claudin-19"
                     /codon_start=1
                     /product="claudin-19 isoform a"
                     /protein_id="NP_683763.2"
                     /db_xref="GI:183979973"
                     /db_xref="CCDS:CCDS471.1"
                     /db_xref="GeneID:149461"
                     /db_xref="HGNC:2040"
                     /db_xref="MIM:610036"
                     /translation="
MANSGLQLLGYFLALGGWVGIIASTALPQWKQSSYAGDAIITAVGLYEGLWMSCASQSTGQVQCKLYDSLLALDGHIQSARALMVVAVLLGFVAMVLSVVGMKCTRVGDSNPIAKGRVAIAGGALFILAGLCTLTAVSWYATLVTQEFFNPSTPVNARYEFGPALFVGWASAGLAVLGGSFLCCTCPEPERPNSSPQPYRPGPSAAAREPVVKLPASAKGPLGV
"
     misc_feature    201..737
                     /gene="CLDN19"
                     /gene_synonym="HOMG5"
                     /note="PMP-22/EMP/MP20/Claudin family; Region:
                     PMP22_Claudin; cl15797"
                     /db_xref="CDD:210197"
     misc_feature    213..275
                     /gene="CLDN19"
                     /gene_synonym="HOMG5"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8N6F1.2);
                     transmembrane region"
     misc_feature    435..497
                     /gene="CLDN19"
                     /gene_synonym="HOMG5"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8N6F1.2);
                     transmembrane region"
     misc_feature    543..605
                     /gene="CLDN19"
                     /gene_synonym="HOMG5"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8N6F1.2);
                     transmembrane region"
     misc_feature    672..734
                     /gene="CLDN19"
                     /gene_synonym="HOMG5"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8N6F1.2);
                     transmembrane region"
     exon            415..579
                     /gene="CLDN19"
                     /gene_synonym="HOMG5"
                     /inference="alignment:Splign:1.39.8"
     variation       468
                     /gene="CLDN19"
                     /gene_synonym="HOMG5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:34374110"
     exon            580..664
                     /gene="CLDN19"
                     /gene_synonym="HOMG5"
                     /inference="alignment:Splign:1.39.8"
     exon            665..817
                     /gene="CLDN19"
                     /gene_synonym="HOMG5"
                     /inference="alignment:Splign:1.39.8"
     exon            818..2859
                     /gene="CLDN19"
                     /gene_synonym="HOMG5"
                     /inference="alignment:Splign:1.39.8"
ORIGIN      
attctggagtccagagccactgcctttgctccagccgctgccgccgcaccacctctccttctctgcctctgaccctccttctcgctgctccccctgcccagctgctcctcccacctggccatgaccaaagcccctgctggcaccctggcccagctctgagtcctgggaccctcggtcctctctcctgggccatggccaactcaggcctccagctcctgggctacttcttggccctgggtggctgggtgggcatcattgctagcacagccctgccacagtggaagcagtcttcctacgcaggcgacgccatcatcactgccgtgggcctctatgaagggctctggatgtcctgcgcctcccagagcactgggcaagtgcagtgcaagctctacgactcgctgctcgccctggacggtcacatccaatcagcgcgggccctgatggtggtggccgtgctcctgggcttcgtggccatggtcctcagcgtagttggcatgaagtgtacgcgggtgggagacagcaaccccattgccaagggccgtgttgccatcgccgggggagccctcttcatcctggcaggcctctgcactttgactgctgtctcgtggtatgccaccctggtgacccaggagttcttcaacccaagcacacctgtcaatgccaggtatgaatttggcccagccctgttcgtgggctgggcctcagctggcctggccgtgctgggcggctccttcctctgctgcacatgcccggagccagagagacccaacagcagcccacagccctatcggcctggaccctctgctgctgcccgagaaccagttgttaaattgcccgcctccgccaagggccccctgggtgtgtaatgtccagtccccagccaggctctgtcccctgccatacctagactgtgtgtttcatatttttttggaaagagaagtgaacatccagccccaatcatggtatcattcggtctgtcctcagcgtggcttggacggggcctgtgtcagagtggtcagtgctgacccctggggctcttgggcagaaagatgaggagacagaggtccagggtgggttacatagcacatccagggctaagcaagaaataattcagaggtcctaccctctgtctagggacccccctcccaagcctggccttggccttggcacaaagtcctccttgataggagatcccactcactcctggaggctgcccctgaggcttggcccagctctaggagcagtccccagggtcagggagcccctggtgtggaaagaggccccaaggtagtaaaccctgcccctgttactgtgctccagagacctcctaagggaagggacagttcctggaaggccctccagctggatgctggggatcagcgataggtgaggggacacagtgtaggagctccccatgtagaaaagggaatgtggggagggcgttaggagcttgcaggcattaggactgtcctgagcaaggtctgcagcccccagctctgctcaccccgaatcctgccccttgtttccacacctaccattcctcctctcctgatccccagcatccagctgaggtccaaggtctttgtcctagaatcagagtggggaggggacagcctggggctgcccagagactgtgggtggagctgcctgctgcactcagcagtgcggtcagagaagggcttttggtcttgaagtccaggtaccatccccccttagcatacagggggaagggcctgagaggaatgtaaggaaaccagcccagatcagtcccaaggccagagtcctttgtcctacatctccctgaaccagagtgtgccctgcccctcatgctcagacctctcccaccccaaaccctctcccgggactcagtctccctggccactgcgtatcaggcttctggggaaagcatccatcacagaacctccccttccctgccacgcaccttccttggccagctccattctggcctcctccaccacctgccttgtgaccacatctcccaccacgtccccagatctcaagaacgcagctcagcttctccttcgagcttgactctgagagggaaagtgacggaaaccaagtcagatgagatgactgccatgtacactgcagtcaagggcagggaggggaggaatgacacaaatggcagggagctgctgggggactgacccctcggcgcctggcctggccggtgctgcacatccaccggggcacaacagggacttgtccagcctctggtcagaggatgtggccacctgaccctaaataggttccccagagtcctgcccctctaatgaatgagaactgcaggagtttctcctctgggtgcctgaagctatagtgcaatggttcccaaccctgcatgcacattcgaatcacctgggggcacaatgcctaggctccaaccccagacactcttatttcattggtctgggtggacctggcatcagaagtcatgtagctcctcaggggactgtagtgtgtggtcagcactgagggctcctctatgaggcctcaagcccaggtgactctgtgaggtctgcagagggagaaaagaacccacaagggaagaggtggaggtcaggcacggtggctcacgcttgtaatcccagcactttgggaggccgaggtgggtagatacctgaagtcaggagttcgagactagcctggccaatatggtaaaaccccgtgtctattaaaaatacaaaaattagctggctgtggtggtgggcacctgtaatcccagctactcgggaggctgaggcaggagaatcgcttgaactcgggaggtggaggttgcagtcagccaagatcgtgccactgcacaccatcctggatgacagagcaagactccatcac
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:149461 -> Molecular function: GO:0005198 [structural molecule activity] evidence: IEA
            GeneID:149461 -> Molecular function: GO:0042802 [identical protein binding] evidence: ISS
            GeneID:149461 -> Biological process: GO:0007601 [visual perception] evidence: IEA
            GeneID:149461 -> Biological process: GO:0016338 [calcium-independent cell-cell adhesion] evidence: ISS
            GeneID:149461 -> Biological process: GO:0019227 [neuronal action potential propagation] evidence: IEA
            GeneID:149461 -> Biological process: GO:0043297 [apical junction assembly] evidence: IEA
            GeneID:149461 -> Biological process: GO:0050896 [response to stimulus] evidence: IEA
            GeneID:149461 -> Cellular component: GO:0005634 [nucleus] evidence: IEA
            GeneID:149461 -> Cellular component: GO:0005737 [cytoplasm] evidence: IEA
            GeneID:149461 -> Cellular component: GO:0005923 [tight junction] evidence: IDA
            GeneID:149461 -> Cellular component: GO:0005923 [tight junction] evidence: ISS
            GeneID:149461 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA
            GeneID:149461 -> Cellular component: GO:0016323 [basolateral plasma membrane] evidence: IDA
            GeneID:149461 -> Cellular component: GO:0043296 [apical junction complex] evidence: IDA

by @meso_cacase at DBCLS
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