2025-05-09 17:17:29, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001253837 3082 bp mRNA linear PRI 16-JUN-2013 DEFINITION Homo sapiens polycystic kidney disease 2-like 1 (PKD2L1), transcript variant 2, mRNA. ACCESSION NM_001253837 VERSION NM_001253837.1 GI:359465611 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 3082) AUTHORS Wu,J.H., Lemaitre,R.N., Manichaikul,A., Guan,W., Tanaka,T., Foy,M., Kabagambe,E.K., Djousse,L., Siscovick,D., Fretts,A.M., Johnson,C., King,I.B., Psaty,B.M., McKnight,B., Rich,S.S., Chen,Y.D., Nettleton,J.A., Tang,W., Bandinelli,S., Jacobs,D.R. Jr., Browning,B.L., Laurie,C.C., Gu,X., Tsai,M.Y., Steffen,L.M., Ferrucci,L., Fornage,M. and Mozaffarian,D. TITLE Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium JOURNAL Circ Cardiovasc Genet 6 (2), 171-183 (2013) PUBMED 23362303 REFERENCE 2 (bases 1 to 3082) AUTHORS Adachi,R., Sasaki,Y., Morita,H., Komai,M., Shirakawa,H., Goto,T., Furuyama,A. and Isono,K. TITLE Behavioral analysis of Drosophila transformants expressing human taste receptor genes in the gustatory receptor neurons JOURNAL J. Neurogenet. 26 (2), 198-205 (2012) PUBMED 22794107 REMARK GeneRIF: This study demonistrated that human PKD2L play the role of food preference behavior. REFERENCE 3 (bases 1 to 3082) AUTHORS Molland,K.L., Paul,L.N. and Yernool,D.A. TITLE Crystal structure and characterization of coiled-coil domain of the transient receptor potential channel PKD2L1 JOURNAL Biochim. Biophys. Acta 1824 (3), 413-421 (2012) PUBMED 22193359 REMARK GeneRIF: Trimerization may be important for both homo- and possibly heteromeric assemblies of PKD2L1. REFERENCE 4 (bases 1 to 3082) AUTHORS Comuzzie,A.G., Cole,S.A., Laston,S.L., Voruganti,V.S., Haack,K., Gibbs,R.A. and Butte,N.F. TITLE Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population JOURNAL PLoS ONE 7 (12), E51954 (2012) PUBMED 23251661 REFERENCE 5 (bases 1 to 3082) AUTHORS Demirkan,A., van Duijn,C.M., Ugocsai,P., Isaacs,A., Pramstaller,P.P., Liebisch,G., Wilson,J.F., Johansson,A., Rudan,I., Aulchenko,Y.S., Kirichenko,A.V., Janssens,A.C., Jansen,R.C., Gnewuch,C., Domingues,F.S., Pattaro,C., Wild,S.H., Jonasson,I., Polasek,O., Zorkoltseva,I.V., Hofman,A., Karssen,L.C., Struchalin,M., Floyd,J., Igl,W., Biloglav,Z., Broer,L., Pfeufer,A., Pichler,I., Campbell,S., Zaboli,G., Kolcic,I., Rivadeneira,F., Huffman,J., Hastie,N.D., Uitterlinden,A., Franke,L., Franklin,C.S., Vitart,V., Nelson,C.P., Preuss,M., Bis,J.C., O'Donnell,C.J., Franceschini,N., Witteman,J.C., Axenovich,T., Oostra,B.A., Meitinger,T., Hicks,A.A., Hayward,C., Wright,A.F., Gyllensten,U., Campbell,H. and Schmitz,G. CONSRTM DIAGRAM Consortium; CARDIoGRAM Consortium; CHARGE Consortium; EUROSPAN consortium TITLE Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations JOURNAL PLoS Genet. 8 (2), E1002490 (2012) PUBMED 22359512 REFERENCE 6 (bases 1 to 3082) AUTHORS Veldhuisen,B., Spruit,L., Dauwerse,H.G., Breuning,M.H. and Peters,D.J. TITLE Genes homologous to the autosomal dominant polycystic kidney disease genes (PKD1 and PKD2) JOURNAL Eur. J. Hum. Genet. 7 (8), 860-872 (1999) PUBMED 10602361 REFERENCE 7 (bases 1 to 3082) AUTHORS Chen,X.Z., Vassilev,P.M., Basora,N., Peng,J.B., Nomura,H., Segal,Y., Brown,E.M., Reeders,S.T., Hediger,M.A. and Zhou,J. TITLE Polycystin-L is a calcium-regulated cation channel permeable to calcium ions JOURNAL Nature 401 (6751), 383-386 (1999) PUBMED 10517637 REFERENCE 8 (bases 1 to 3082) AUTHORS Tsiokas,L., Arnould,T., Zhu,C., Kim,E., Walz,G. and Sukhatme,V.P. TITLE Specific association of the gene product of PKD2 with the TRPC1 channel JOURNAL Proc. Natl. Acad. Sci. U.S.A. 96 (7), 3934-3939 (1999) PUBMED 10097141 REFERENCE 9 (bases 1 to 3082) AUTHORS Wu,G., Hayashi,T., Park,J.H., Dixit,M., Reynolds,D.M., Li,L., Maeda,Y., Cai,Y., Coca-Prados,M. and Somlo,S. TITLE Identification of PKD2L, a human PKD2-related gene: tissue-specific expression and mapping to chromosome 10q25 JOURNAL Genomics 54 (3), 564-568 (1998) PUBMED 9878261 REFERENCE 10 (bases 1 to 3082) AUTHORS Nomura,H., Turco,A.E., Pei,Y., Kalaydjieva,L., Schiavello,T., Weremowicz,S., Ji,W., Morton,C.C., Meisler,M., Reeders,S.T. and Zhou,J. TITLE Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defects JOURNAL J. Biol. Chem. 273 (40), 25967-25973 (1998) PUBMED 9748274 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AF073481.1, BC025665.1, DQ084244.1 and AF053316.1. Summary: This gene encodes a member of the polycystin protein family. The encoded protein contains multiple transmembrane domains, and cytoplasmic N- and C-termini. The protein may be an integral membrane protein involved in cell-cell/matrix interactions. This protein functions as a calcium-regulated nonselective cation channel. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]. Transcript Variant: This variant (2) uses an alternate splice junction at the 5' end of coding exon compared to variant 1, that causes a frameshift. The resulting isoform (2) has a shorter and distinct N-terminus compared to isoform 1. 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 :: DQ084244.1 [ECO:0000332] RNAseq introns :: mixed/partial sample support ERS025081, ERS025082 [ECO:0000350] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-303 AF073481.1 1-303 304-546 BC025665.1 1-243 547-755 DQ084244.1 1-209 756-3070 BC025665.1 431-2745 3071-3082 AF053316.1 2539-2550 FEATURES Location/Qualifiers source 1..3082 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="10" /map="10q24" gene 1..3082 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /note="polycystic kidney disease 2-like 1" /db_xref="GeneID:9033" /db_xref="HGNC:9011" /db_xref="MIM:604532" exon 1..618 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /inference="alignment:Splign:1.39.8" misc_feature 487..489 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /note="upstream in-frame stop codon" CDS 547..2823 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /note="isoform 2 is encoded by transcript variant 2; transient receptor potential cation channel, subfamily P, member 3; polycystin-L; polycystic kidney disease 2-like 1 protein; polycystin-L1; polycystin-2L1; polycystin-2 homolog" /codon_start=1 /product="polycystic kidney disease 2-like 1 protein isoform 2" /protein_id="NP_001240766.1" /db_xref="GI:359465612" /db_xref="GeneID:9033" /db_xref="HGNC:9011" /db_xref="MIM:604532" /translation="
MNPRRRHTGPRCPAAASISVKASEASLPCPLGLWGTTLTENTAENRELYIKTTLRELLVYIVFLVDICLLTYGMTSSSAYYYTKVMSELFLHTPSDTGVSFQAISSMADFWDFAQGPLLDSLYWTKWYNNQSLGHGSHSFIYYENMLLGVPRLRQLKVRNDSCVVHEDFREDILSCYDVYSPDKEEQLPFGPFNGTAWTYHSQDELGGFSHWGRLTSYSGGGYYLDLPGSRQGSAEALRALQEGLWLDRGTRVVFIDFSVYNANINLFCVLRLVVEFPATGGAIPSWQIRTVKLIRYVSNWDFFIVGCEVIFCVFIFYYVVEEILELHIHRLRYLSSIWNILDLVVILLSIVAVGFHIFRTLEVNRLMGKLLQQPNTYADFEFLAFWQTQYNNMNAVNLFFAWIKIFKYISFNKTMTQLSSTLARCAKDILGFAVMFFIVFFAYAQLGYLLFGTQVENFSTFIKCIFTQFRIILGDFDYNAIDNANRILGPAYFVTYVFFVFFVLLNMFLAIINDTYSEVKEELAGQKDELQLSDLLKQGYNKTLLRLRLRKERVSDVQKVLQGGEQEIQFEDFTNTLRELGHAEHEITELTATFTKFDRDGNRILDEKEQEKMRQDLEEERVALNTEIEKLGRSIVSSPQGKSGPEAARAGGWVSGEEFYMLTRRVLQLETVLEGVVSQIDAVGSKLKMLERKGWLAPSPGVKEQAIWKHPQPAPAVTPDPWGVQGGQESEVPYKREEEALEERRLSRGEIPTLQRS
" misc_feature 841..2106 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /note="Polycystin cation channel; Region: PKD_channel; pfam08016" /db_xref="CDD:203839" variation 581 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /replace="a" /replace="g" /db_xref="dbSNP:569511" exon 619..754 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /inference="alignment:Splign:1.39.8" exon 755..882 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /inference="alignment:Splign:1.39.8" exon 883..1136 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /inference="alignment:Splign:1.39.8" variation 1021 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /replace="c" /replace="t" /db_xref="dbSNP:2305383" exon 1137..1361 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /inference="alignment:Splign:1.39.8" exon 1362..1590 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /inference="alignment:Splign:1.39.8" variation 1582 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /replace="a" /replace="g" /db_xref="dbSNP:2278842" exon 1591..1761 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /inference="alignment:Splign:1.39.8" exon 1762..1943 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /inference="alignment:Splign:1.39.8" exon 1944..2064 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /inference="alignment:Splign:1.39.8" exon 2065..2163 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /inference="alignment:Splign:1.39.8" exon 2164..2285 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /inference="alignment:Splign:1.39.8" exon 2286..2412 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /inference="alignment:Splign:1.39.8" exon 2413..2531 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /inference="alignment:Splign:1.39.8" exon 2532..2655 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /inference="alignment:Splign:1.39.8" exon 2656..2740 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /inference="alignment:Splign:1.39.8" exon 2741..3073 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" /inference="alignment:Splign:1.39.8" polyA_signal 3051..3056 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" polyA_site 3073 /gene="PKD2L1" /gene_synonym="PCL; PKD2L; PKDL; TRPP3" ORIGIN
cagcatcgccttttcctcccgtttctccttccactcccagctccacatcctcctcctattctcccctctcccctcttcaaacccccaccttccagttccctcacctcccctttcggctggtcccctggggcttgcagcaagagggagagagagctcctgacaggattgatggtccttccccaccctgtcctctcatccgctccctccccagcaggcacagacatccccctacaaaaggcaggagcccaggctgtgtggaaacagctgctctcagacgcctttccatttgctctctgctggctaggctgggctgtgcctctgctccctcttcctctagctgagagtgggcacctggggtaccgggcccccccacctcattccccatgaatgctgtgggaagtcctgaggggcaggagctgcaaaagctggggagtggagcctgggacaaccccgcctacagtggtcccccttccccacacgggacgctgagagtctgcaccatctccagcacggggcctctccagccccaacccaagaagcctgaagatgaaccccaggagacggcatacaggacccaggtgtccagctgctgcctccatatctgtcaaggcatcagaggcatctctcccatgccccttaggactttggggaacaaccctgactgagaacacagctgagaaccgggaactttatatcaagaccaccctgagggagctgttggtatatattgtgttcctggtggacatctgtctactgacctatggaatgacaagctccagtgcttattactacaccaaagtgatgtctgagctcttcttacatactccatcagacactggagtctcctttcaggccatcagcagcatggcggacttctgggattttgcccagggcccactactggacagtttgtattggaccaaatggtacaacaaccagagcctgggccatggctcccactccttcatctactatgagaacatgctgctgggggttccgaggctgcggcagctaaaggtccgcaatgactcctgtgtggtgcatgaagacttccgggaggacattctgagctgctatgatgtctactctccagacaaagaagaacaactcccctttgggcccttcaatggcacagcgtggacataccactcgcaggatgagttggggggcttctcccactggggcaggctcacaagctacagcggaggtggctactacctggaccttccaggatcccgacagggtagtgcagaggctctccgggcccttcaggaggggctgtggctggacaggggcactcgagtggtgttcatcgacttctcagtctacaatgccaatatcaatcttttctgtgtcctgaggctggtggtggagtttccagctacaggaggtgccatcccatcctggcaaatccgcacagtcaagctgatccgctatgtcagcaactgggacttctttatcgttggctgtgaggtcatcttctgcgtcttcatcttctactatgtggtggaagagatcctggagctccacattcaccggcttcgctacctcagcagcatctggaacatactggacctggtggtcatcttgctctccattgtggctgtgggcttccacatattccgaaccctcgaggtgaatcggctcatggggaagctcctgcagcagccaaacacgtatgcagactttgagttcctcgccttctggcagacacagtacaacaacatgaatgctgtcaacctcttcttcgcctggatcaagatattcaagtacatcagcttcaacaaaaccatgacccagctctcctccacgctggcccgctgtgccaaggacatcctgggcttcgccgtcatgttcttcattgttttcttcgcctatgcccaactcggctacctgcttttcgggacccaagtggaaaactttagcactttcatcaagtgcattttcactcagttccggataatcctcggggactttgactacaatgctatcgacaatgccaaccgcatcctgggccctgcctactttgtcacctatgtcttcttcgtcttcttcgtgctcctgaacatgttcctggccatcatcaatgacacatattcagaggtcaaggaggagctggctggacagaaggatgagctgcaactttctgacctcctgaaacagggctacaacaagaccctactaagactgcgtctgaggaaggagagggtttcggatgtgcagaaggtcctgcagggtggggagcaggagatccagtttgaggatttcaccaacaccttaagggaactgggacacgcagagcatgaaatcactgagctcacggccaccttcaccaagtttgacagagatgggaatcgtattctggatgagaaggaacaggaaaaaatgcgacaggacctggaggaagagagggtggccctcaacactgagattgagaaactaggccgatctattgtgagcagcccacaaggcaaatcgggtccagaggctgccagagcaggaggctgggtttcaggagaagaattctacatgctcacaaggagagttctgcagctggagactgtcctggaaggagtagtgtcccagattgatgctgtaggctcaaagctgaaaatgctggagaggaaggggtggctggctccctccccaggcgtgaaggaacaagctatttggaagcacccgcagccagccccagctgtgaccccagacccctggggagtccagggtgggcaggagagtgaggttccctataaaagagaagaggaagccttagaggagaggagactctcccgtggtgagattccaacgttgcagaggagttaagtgtgaggcactcccggagcaaagtctatgaaggatcttctgcaagaggctgcctcctggtccactgaacctggaaactgagtgggctttaaccaggagataaaaatggagcctgaagggaatcaggcaaggaaatgaactcaggattcagagatctttgaattaatatgtggtgggttctgacattattcttccataagaccatgtgggtttccatggtggctatcaataaaactccttaggaaaacttaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:9033 -> Molecular function: GO:0005227 [calcium activated cation channel activity] evidence: IDA GeneID:9033 -> Molecular function: GO:0005261 [cation channel activity] evidence: IDA GeneID:9033 -> Molecular function: GO:0005262 [calcium channel activity] evidence: IBA GeneID:9033 -> Molecular function: GO:0005272 [sodium channel activity] evidence: IDA GeneID:9033 -> Molecular function: GO:0005509 [calcium ion binding] evidence: ISS GeneID:9033 -> Molecular function: GO:0005515 [protein binding] evidence: IPI GeneID:9033 -> Molecular function: GO:0008092 [cytoskeletal protein binding] evidence: IPI GeneID:9033 -> Molecular function: GO:0008324 [cation transmembrane transporter activity] evidence: ISS GeneID:9033 -> Molecular function: GO:0015269 [calcium-activated potassium channel activity] evidence: IDA GeneID:9033 -> Molecular function: GO:0033040 [sour taste receptor activity] evidence: ISS GeneID:9033 -> Molecular function: GO:0042802 [identical protein binding] evidence: ISS GeneID:9033 -> Molecular function: GO:0051371 [muscle alpha-actinin binding] evidence: IPI GeneID:9033 -> Molecular function: GO:0051393 [alpha-actinin binding] evidence: IPI GeneID:9033 -> Biological process: GO:0001581 [detection of chemical stimulus involved in sensory perception of sour taste] evidence: ISS GeneID:9033 -> Biological process: GO:0006812 [cation transport] evidence: ISS GeneID:9033 -> Biological process: GO:0035725 [sodium ion transmembrane transport] evidence: IDA GeneID:9033 -> Biological process: GO:0050982 [detection of mechanical stimulus] evidence: IBA GeneID:9033 -> Biological process: GO:0070588 [calcium ion transmembrane transport] evidence: IBA GeneID:9033 -> Biological process: GO:0071468 [cellular response to acidity] evidence: ISS GeneID:9033 -> Biological process: GO:0071805 [potassium ion transmembrane transport] evidence: IDA GeneID:9033 -> Cellular component: GO:0005783 [endoplasmic reticulum] evidence: ISS GeneID:9033 -> Cellular component: GO:0005886 [plasma membrane] evidence: IMP GeneID:9033 -> Cellular component: GO:0009986 [cell surface] evidence: ISS GeneID:9033 -> Cellular component: GO:0016021 [integral to membrane] evidence: NAS GeneID:9033 -> Cellular component: GO:0043231 [intracellular membrane-bounded organelle] evidence: IDA
by
@meso_cacase at
DBCLS
This page is licensed under a Creative Commons Attribution 2.1 Japan License.