2024-11-23 00:17:48, GGRNA.v2 : RefSeq release 226 (Sep, 2024)
LOCUS NM_001100901 2135 bp mRNA linear ROD 23-MAR-2023 DEFINITION Rattus norvegicus syntrophin, alpha 1 (Snta1), mRNA. ACCESSION NM_001100901 XM_001064932 XM_342548 VERSION NM_001100901.1 KEYWORDS RefSeq; RefSeq Select. SOURCE Rattus norvegicus (Norway rat) ORGANISM Rattus norvegicus Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Rattus. REFERENCE 1 (bases 1 to 2135) AUTHORS Kim JE, Yeo SI, Ryu HJ, Kim MJ, Kim DS, Jo SM and Kang TC. TITLE Astroglial loss and edema formation in the rat piriform cortex and hippocampus following pilocarpine-induced status epilepticus JOURNAL J Comp Neurol 518 (22), 4612-4628 (2010) PUBMED 20886625 REFERENCE 2 (bases 1 to 2135) AUTHORS Lanciotti A, Brignone MS, Camerini S, Serafini B, Macchia G, Raggi C, Molinari P, Crescenzi M, Musumeci M, Sargiacomo M, Aloisi F, Petrucci TC and Ambrosini E. TITLE MLC1 trafficking and membrane expression in astrocytes: role of caveolin-1 and phosphorylation JOURNAL Neurobiol Dis 37 (3), 581-595 (2010) PUBMED 19931615 REFERENCE 3 (bases 1 to 2135) AUTHORS Cheng J, Van Norstrand DW, Medeiros-Domingo A, Valdivia C, Tan BH, Ye B, Kroboth S, Vatta M, Tester DJ, January CT, Makielski JC and Ackerman MJ. TITLE Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium current JOURNAL Circ Arrhythm Electrophysiol 2 (6), 667-676 (2009) PUBMED 20009079 REFERENCE 4 (bases 1 to 2135) AUTHORS Wu G, Ai T, Kim JJ, Mohapatra B, Xi Y, Li Z, Abbasi S, Purevjav E, Samani K, Ackerman MJ, Qi M, Moss AJ, Shimizu W, Towbin JA, Cheng J and Vatta M. TITLE alpha-1-syntrophin mutation and the long-QT syndrome: a disease of sodium channel disruption JOURNAL Circ Arrhythm Electrophysiol 1 (3), 193-201 (2008) PUBMED 19684871 REFERENCE 5 (bases 1 to 2135) AUTHORS Ueda K, Valdivia C, Medeiros-Domingo A, Tester DJ, Vatta M, Farrugia G, Ackerman MJ and Makielski JC. TITLE Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex JOURNAL Proc Natl Acad Sci U S A 105 (27), 9355-9360 (2008) PUBMED 18591664 REFERENCE 6 (bases 1 to 2135) AUTHORS Thomas GD, Shaul PW, Yuhanna IS, Froehner SC and Adams ME. TITLE Vasomodulation by skeletal muscle-derived nitric oxide requires alpha-syntrophin-mediated sarcolemmal localization of neuronal Nitric oxide synthase JOURNAL Circ Res 92 (5), 554-560 (2003) PUBMED 12600881 REFERENCE 7 (bases 1 to 2135) AUTHORS Hagiwara Y, Sasaoka T, Araishi K, Imamura M, Yorifuji H, Nonaka I, Ozawa E and Kikuchi T. TITLE Caveolin-3 deficiency causes muscle degeneration in mice JOURNAL Hum Mol Genet 9 (20), 3047-3054 (2000) PUBMED 11115849 REFERENCE 8 (bases 1 to 2135) AUTHORS Adams ME, Kramarcy N, Krall SP, Rossi SG, Rotundo RL, Sealock R and Froehner SC. TITLE Absence of alpha-syntrophin leads to structurally aberrant neuromuscular synapses deficient in utrophin JOURNAL J Cell Biol 150 (6), 1385-1398 (2000) PUBMED 10995443 REFERENCE 9 (bases 1 to 2135) AUTHORS Ort T, Maksimova E, Dirkx R, Kachinsky AM, Berghs S, Froehner SC and Solimena M. TITLE The receptor tyrosine phosphatase-like protein ICA512 binds the PDZ domains of beta2-syntrophin and nNOS in pancreatic beta-cells JOURNAL Eur J Cell Biol 79 (9), 621-630 (2000) PUBMED 11043403 REFERENCE 10 (bases 1 to 2135) AUTHORS Peters MF, Kramarcy NR, Sealock R and Froehner SC. TITLE beta 2-Syntrophin: localization at the neuromuscular junction in skeletal muscle JOURNAL Neuroreport 5 (13), 1577-1580 (1994) PUBMED 7819523 COMMENT PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence was derived from BC169101.1. On or before Sep 14, 2008 this sequence version replaced XM_001064932.1, XM_342548.3. 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 :: BC169101.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMN06621351 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## RefSeq Select criteria :: based on conservation, expression, longest protein ##RefSeq-Attributes-END## FEATURES Location/Qualifiers source 1..2135 /organism="Rattus norvegicus" /mol_type="mRNA" /db_xref="taxon:10116" /chromosome="3" /map="3q41" gene 1..2135 /gene="Snta1" /note="syntrophin, alpha 1" /db_xref="GeneID:362242" /db_xref="RGD:1307068" exon 1..402 /gene="Snta1" /inference="alignment:Splign:2.1.0" CDS 111..1610 /gene="Snta1" /note="syntrophin, acidic 1" /codon_start=1 /product="alpha-1-syntrophin" /protein_id="NP_001094371.1" /db_xref="GeneID:362242" /db_xref="RGD:1307068" /translation="
MASGRRAPRTGLLELRSGAGSGAGGERWQRVLLTLAEDALTVSPADGEPGPEPEPAQLNGAAEPGAASPQLPEALLLQRRRVTVRKADAGGLGISIKGGRENKMPILISKIFKGLAADQTEALFVGDAILSVNGEDLSSATHDEAVQALKKTGKEVVLEVKYMKEVSPYFKNSAGGTSVGWDSPPASPLQRQPSSPGPQPRNLNEAKHVSLKMAYVSRRCTPTDPEPRYLEICAADGQDTLFLRAKDEASARSWAGAIQAQISTFIPWVKDELQALLTATGTAGSQDIKQIGWLTEQLPSGGTAPTLALLTEKELLLYCSLPQTREALSRPARTAPLIATRLVHSGPSKGSVPYDAELSFALRTGTRHGVDTHLFSVESPQELAAWTRQLVDGCHRAAEGVQEVSTACTWNGRPCNLSVHIDKGFTLWAAEPGATRAVLLRQPFEKLQMSSDDGMSLLFLDFGGAEGEIQLDLHSCPKTMVFIIHSFLSAKVTRLGLLA"
misc_feature 348..596 /gene="Snta1" /note="PDZ domain of syntrophins, and related domains; Region: PDZ_syntrophin-like; cd06801" /db_xref="CDD:467262" misc_feature order(381..401,435..437,444..446,534..536,546..548, 555..560) /gene="Snta1" /note="peptide binding site [polypeptide binding]; other site" /db_xref="CDD:467262" misc_feature <726..902 /gene="Snta1" /note="Syntrophin Split Pleckstrin homology (PH) domain; Region: PHsplit_syntrophin; cd01258" /db_xref="CDD:269960" misc_feature 984..1295 /gene="Snta1" /note="PH domain; Region: PH; pfam00169" /db_xref="CDD:459697" exon 403..588 /gene="Snta1" /inference="alignment:Splign:2.1.0" exon 589..793 /gene="Snta1" /inference="alignment:Splign:2.1.0" exon 794..1001 /gene="Snta1" /inference="alignment:Splign:2.1.0" exon 1002..1132 /gene="Snta1" /inference="alignment:Splign:2.1.0" exon 1133..1329 /gene="Snta1" /inference="alignment:Splign:2.1.0" exon 1330..1517 /gene="Snta1" /inference="alignment:Splign:2.1.0" exon 1518..2099 /gene="Snta1" /inference="alignment:Splign:2.1.0" ORIGIN
gtggcggctggctctgctgccccgccgccctctgccctgggcgctgggtcggagcgggccgggtacggcgggaccgggcgagcgcagcgtactgggacttcgaggcgaagatggcgtcaggcaggcgcgctccgcgcaccgggttgctagaactgcgctccggggcgggctccggggcgggtggtgagcggtggcagcgggtgttgctcactctggcggaggacgcgctgaccgtgagccccgccgacggcgagcccggcccggagcccgagcccgcgcagctcaacggcgccgctgagcccggcgcggcgtccccacagctgccagaggcgctgctgctccagcggcgccgcgtgacggtgcgcaaggccgacgccggcgggctcggcatcagcatcaagggaggccgggaaaacaagatgcctattctcatttccaagatcttcaaggggctggcagcagaccagacggaggccctctttgtcggcgatgccatcctctctgtgaatggtgaagatttgtcctctgccacccatgatgaagcagtacaggccctcaagaagacgggcaaggaggttgtgttggaggttaagtatatgaaggaggtctcaccgtatttcaagaattctgctggtgggacctccgttggctgggactcacctcctgcctcgcctcttcagcgtcagccttcttcccctggcccccaaccccggaacctcaatgaggccaaacatgtatctttgaagatggcgtatgtctcaaggaggtgtacccccactgacccggagcccaggtatctggagatctgtgcagcagatggccaggacactctcttcttgagggccaaggatgaggccagtgcaaggtcatgggcaggtgccatccaagctcagatcagcacatttataccttgggtcaaggatgagctgcaggcgctgctgacagccacaggtacagctgggagccaggacatcaagcagattggctggctcacggaacagttgcccagtgggggtacagcaccaaccctggccctgctgactgagaaggagctgctcctctactgctctctcccccagactcgagaggccctgagcaggccggcccgcactgccccgctcattgccaccaggctggtgcactcaggcccttccaagggctcagtgccctatgatgcagagctctcctttgccctgcgcacgggtacacgccacggtgtggacactcacctgttcagtgtggagtcgccgcaggagctggcagcctggacccgacagttggtggatggctgtcaccgggctgctgaaggtgtgcaagaagtgtctacagcctgcacgtggaatggccgtccctgcaacctatccgtgcacattgacaagggcttcacactgtgggcagctgagccaggagcaacccgagctgtgctgctccgacagccctttgagaaacttcagatgtcatcagatgatggcatgagtctccttttcctggactttgggggtgctgaaggagagatccagctggacctgcattcgtgtcccaaaaccatggtctttatcatccactctttcctgtctgccaaggtcacccgcttggggctcttggcctagaagttgtcaggtgaactaggcctgaagaggaacgttcatcttgtgacctgacccgtccttctgctgactgcctgctcatctgtgggctgagggaagggagaggaggggaactagggcctcagagaccaacctgaggaagcagaactcagacctgggacagtgagtctggcttgtgatggggcagccttcctactgctcacctccaccagtgcctttcgaagagagatattttgtgtacacagaagccattccgaggctgggacctgaccctgtggggatccatcccatctccagtcaacagcagagctgccacgcctcctggaggcccctaagccaccctgagatctctgcagatggagtcttctgggtcagtggcaagaggaggaagaggagcctttctgttcactctcccttgggccctgagggctgtctgggctctctcctcctctctctccttcctcttgataataaacagcctgtgagcacataaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
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Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
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