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2025-11-01 10:57:29, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001256304 2191 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens dystrobrevin, beta (DTNB), transcript variant 7, mRNA.
ACCESSION NM_001256304
VERSION NM_001256304.1 GI:372626415
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 2191)
AUTHORS Broderick,P., Chubb,D., Johnson,D.C., Weinhold,N., Forsti,A.,
Lloyd,A., Olver,B., Ma,Y.P., Dobbins,S.E., Walker,B.A.,
Davies,F.E., Gregory,W.A., Child,J.A., Ross,F.M., Jackson,G.H.,
Neben,K., Jauch,A., Hoffmann,P., Muhleisen,T.W., Nothen,M.M.,
Moebus,S., Tomlinson,I.P., Goldschmidt,H., Hemminki,K., Morgan,G.J.
and Houlston,R.S.
TITLE Common variation at 3p22.1 and 7p15.3 influences multiple myeloma
risk
JOURNAL Nat. Genet. 44 (1), 58-61 (2012)
PUBMED 22120009
REMARK Publication Status: Online-Only
REFERENCE 2 (bases 1 to 2191)
AUTHORS Artegiani,B., Labbaye,C., Sferra,A., Quaranta,M.T., Torreri,P.,
Macchia,G., Ceccarini,M., Petrucci,T.C. and Macioce,P.
TITLE The interaction with HMG20a/b proteins suggests a potential role
for beta-dystrobrevin in neuronal differentiation
JOURNAL J. Biol. Chem. 285 (32), 24740-24750 (2010)
PUBMED 20530487
REMARK GeneRIF: beta-dystrobrevin interacts with the HMG20 proteins iBRAF
and BRAF35
REFERENCE 3 (bases 1 to 2191)
AUTHORS Gudbjartsson,D.F., Walters,G.B., Thorleifsson,G., Stefansson,H.,
Halldorsson,B.V., Zusmanovich,P., Sulem,P., Thorlacius,S.,
Gylfason,A., Steinberg,S., Helgadottir,A., Ingason,A.,
Steinthorsdottir,V., Olafsdottir,E.J., Olafsdottir,G.H.,
Jonsson,T., Borch-Johnsen,K., Hansen,T., Andersen,G., Jorgensen,T.,
Pedersen,O., Aben,K.K., Witjes,J.A., Swinkels,D.W., den Heijer,M.,
Franke,B., Verbeek,A.L., Becker,D.M., Yanek,L.R., Becker,L.C.,
Tryggvadottir,L., Rafnar,T., Gulcher,J., Kiemeney,L.A., Kong,A.,
Thorsteinsdottir,U. and Stefansson,K.
TITLE Many sequence variants affecting diversity of adult human height
JOURNAL Nat. Genet. 40 (5), 609-615 (2008)
PUBMED 18391951
REFERENCE 4 (bases 1 to 2191)
AUTHORS Nazarian,R., Starcevic,M., Spencer,M.J. and Dell'Angelica,E.C.
TITLE Reinvestigation of the dysbindin subunit of BLOC-1 (biogenesis of
lysosome-related organelles complex-1) as a dystrobrevin-binding
protein
JOURNAL Biochem. J. 395 (3), 587-598 (2006)
PUBMED 16448387
REMARK GeneRIF: results suggest that dysbindin assembled into BLOC-1 is
not a physiological binding partner of the dystrobrevins, likely
due to engagement of its dystrobrevin-binding region in
interactions with other subunits
REFERENCE 5 (bases 1 to 2191)
AUTHORS Hillman,R.T., Green,R.E. and Brenner,S.E.
TITLE An unappreciated role for RNA surveillance
JOURNAL Genome Biol. 5 (2), R8 (2004)
PUBMED 14759258
REFERENCE 6 (bases 1 to 2191)
AUTHORS Piluso,G., Mirabella,M., Ricci,E., Belsito,A., Abbondanza,C.,
Servidei,S., Puca,A.A., Tonali,P., Puca,G.A. and Nigro,V.
TITLE Gamma1- and gamma2-syntrophins, two novel dystrophin-binding
proteins localized in neuronal cells
JOURNAL J. Biol. Chem. 275 (21), 15851-15860 (2000)
PUBMED 10747910
REFERENCE 7 (bases 1 to 2191)
AUTHORS Blake,D.J., Hawkes,R., Benson,M.A. and Beesley,P.W.
TITLE Different dystrophin-like complexes are expressed in neurons and
glia
JOURNAL J. Cell Biol. 147 (3), 645-658 (1999)
PUBMED 10545507
REFERENCE 8 (bases 1 to 2191)
AUTHORS Puca,A.A., Nigro,V., Piluso,G., Belsito,A., Sampaolo,S.,
Quaderi,N., Rossi,E., Di Iorio,G., Ballabio,A. and Franco,B.
TITLE Identification and characterization of a novel member of the
dystrobrevin gene family
JOURNAL FEBS Lett. 425 (1), 7-13 (1998)
PUBMED 9540997
REFERENCE 9 (bases 1 to 2191)
AUTHORS Peters,M.F., O'Brien,K.F., Sadoulet-Puccio,H.M., Kunkel,L.M.,
Adams,M.E. and Froehner,S.C.
TITLE beta-dystrobrevin, a new member of the dystrophin family.
Identification, cloning, and protein associations
JOURNAL J. Biol. Chem. 272 (50), 31561-31569 (1997)
PUBMED 9395493
REFERENCE 10 (bases 1 to 2191)
AUTHORS Straub,V. and Campbell,K.P.
TITLE Muscular dystrophies and the dystrophin-glycoprotein complex
JOURNAL Curr. Opin. Neurol. 10 (2), 168-175 (1997)
PUBMED 9146999
REMARK Review article
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from DQ160290.1 and BC016655.1.
Summary: This gene encodes dystrobrevin beta, a component of the
dystrophin-associated protein complex (DPC). The DPC consists of
dystrophin and several integral and peripheral membrane proteins,
including dystroglycans, sarcoglycans, syntrophins and dystrobrevin
alpha and beta. The DPC localizes to the sarcolemma and its
disruption is associated with various forms of muscular dystrophy.
Dystrobrevin beta is thought to interact with syntrophin and the
DP71 short form of dystrophin. Alternatively spliced transcript
variants encoding different isoforms have been identified.
[provided by RefSeq, Jul 2008].
Transcript Variant: This variant (7) lacks two in-frame exons in
the coding region, compared to variant 1. The resulting isoform (7)
lacks two internal segments, 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##
RNAseq introns :: mixed/partial sample support ERS025081, ERS025082
[ECO:0000350]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-1804 DQ160290.1 1-1804
1805-2191 BC016655.1 1835-2221
FEATURES Location/Qualifiers
source 1..2191
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="2"
/map="2p24"
gene 1..2191
/gene="DTNB"
/note="dystrobrevin, beta"
/db_xref="GeneID:1838"
/db_xref="HGNC:3058"
/db_xref="MIM:602415"
CDS 1..1809
/gene="DTNB"
/note="isoform 7 is encoded by transcript variant 7;
DTN-B; beta-dystrobrevin"
/codon_start=1
/product="dystrobrevin beta isoform 7"
/protein_id="NP_001243233.1"
/db_xref="GI:372626416"
/db_xref="GeneID:1838"
/db_xref="HGNC:3058"
/db_xref="MIM:602415"
/translation="
MIEESGNKRKTMAEKRQLFIEMRAQNFDVIRLSTYRTACKLRFVQKRCNLHLVDIWNMIEAFRDNGLNTLDHTTEISVSRLETVISSIYYQLNKRLPSTHQISVEQSISLLLNFMIAAYDSEGRGKLTVFSVKAMLATMCGGKMLDKLRYVFSQMSDSNGLMIFSKFDQFLKEVLKLPTAVFEGPSFGYTEHSVRTCFPQQRKIMLNMFLDTMMADPPPQCLVWLPLMHRLAHVENVFHPVECSYCRCESMMGFRYRCQQCHNYQLCQNCFWRGHAGGPHSNQHQMKEHSSWKSPAKKLSHAISKSLGCVPTREPPHPVFPEQPEKPLDLAHIVPPRPLTNMNDTMVSHMSSGVPTPTKRLQYSQDIPSHLADEHALIASYVARLQHCARVLDSPSRLDEEHRLIARYAARLAAEAGNVTRPPTDLSFNFDANKQQRQLIAELENKNREILQEIQRLRLEHEQASQPTPEKAQQNPTLLAELRLLRQRKDELEQRMSALQESRRELMVQLEELMKLLKAQATGSPHTSPTHGGGRPMPMPVRSTSAGSTPTHCPQDSLSGVGGDVQEAFAQGTRRNLRNDLLVAADSITNTMSSLVKELHSG
"
misc_feature 40..420
/gene="DTNB"
/note="EF hand; Region: efhand_1; pfam09068"
/db_xref="CDD:149945"
misc_feature 430..696
/gene="DTNB"
/note="EF-hand; Region: efhand_2; pfam09069"
/db_xref="CDD:149946"
misc_feature 721..867
/gene="DTNB"
/note="Zinc finger, ZZ type. Zinc finger present in
dystrophin and dystrobrevin. The ZZ motif coordinates two
zinc ions and most likely participates in ligand binding
or molecular scaffolding. Dystrophin attaches actin
filaments to an integral membrane...; Region:
ZZ_dystrophin; cd02334"
/db_xref="CDD:30238"
misc_feature order(727..729,736..738,772..774,781..783,799..801,
808..810,838..840,850..852)
/gene="DTNB"
/note="Zinc-binding sites [ion binding]; other site"
/db_xref="CDD:30238"
misc_feature order(727..729,736..738,799..801,808..810)
/gene="DTNB"
/note="zinc cluster 1 [ion binding]; other site"
/db_xref="CDD:30238"
misc_feature order(730..732,763..765,769..771,787..789,793..795)
/gene="DTNB"
/note="putative charged binding surface; other site"
/db_xref="CDD:30238"
misc_feature order(766..768,811..813,856..858,865..867)
/gene="DTNB"
/note="putative hydrophobic binding surface; other site"
/db_xref="CDD:30238"
misc_feature order(772..774,781..783,838..840,850..852)
/gene="DTNB"
/note="zinc cluster 2 [ion binding]; other site"
/db_xref="CDD:30238"
misc_feature 1195..1344
/gene="DTNB"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (O60941.1);
Region: Syntrophin-binding region"
misc_feature <1318..1542
/gene="DTNB"
/note="Seryl-tRNA synthetase N-terminal domain; Region:
Seryl_tRNA_N; pfam02403"
/db_xref="CDD:202232"
exon 1..67
/gene="DTNB"
/inference="alignment:Splign:1.39.8"
exon 68..148
/gene="DTNB"
/inference="alignment:Splign:1.39.8"
exon 149..362
/gene="DTNB"
/inference="alignment:Splign:1.39.8"
exon 363..448
/gene="DTNB"
/inference="alignment:Splign:1.39.8"
exon 449..603
/gene="DTNB"
/inference="alignment:Splign:1.39.8"
exon 604..709
/gene="DTNB"
/inference="alignment:Splign:1.39.8"
exon 710..876
/gene="DTNB"
/inference="alignment:Splign:1.39.8"
exon 877..1001
/gene="DTNB"
/inference="alignment:Splign:1.39.8"
exon 1002..1079
/gene="DTNB"
/inference="alignment:Splign:1.39.8"
exon 1080..1169
/gene="DTNB"
/inference="alignment:Splign:1.39.8"
exon 1170..1257
/gene="DTNB"
/inference="alignment:Splign:1.39.8"
variation 1253
/gene="DTNB"
/replace="a"
/replace="t"
/db_xref="dbSNP:34836260"
exon 1258..1343
/gene="DTNB"
/inference="alignment:Splign:1.39.8"
exon 1344..1457
/gene="DTNB"
/inference="alignment:Splign:1.39.8"
exon 1458..1554
/gene="DTNB"
/inference="alignment:Splign:1.39.8"
exon 1555..1714
/gene="DTNB"
/inference="alignment:Splign:1.39.8"
exon 1715..1804
/gene="DTNB"
/inference="alignment:Splign:1.39.8"
exon 1805..1838
/gene="DTNB"
/inference="alignment:Splign:1.39.8"
exon 1839..2149
/gene="DTNB"
/inference="alignment:Splign:1.39.8"
STS 1906..2142
/gene="DTNB"
/standard_name="RH80433"
/db_xref="UniSTS:93073"
polyA_site 2149
/gene="DTNB"
ORIGIN
atgattgaggaaagtgggaacaagcggaagaccatggcagagaagaggcagctgttcatagaaatgcgtgctcagaattttgatgtcatacgactatcaacttacagaacagcctgcaaattacgatttgtacaaaaacgatgcaaccttcatcttgttgatatctggaacatgattgaagccttccgagacaatggccttaatacactggaccataccaccgagatcagtgtgtcccgcctcgaaactgtcatctcctccatctactatcagttgaacaagcgccttccttctactcaccaaattagtgtggaacaatctatcagcctcctcctcaactttatgattgctgcatatgacagtgagggccgaggcaagttgacggtattttcagttaaagctatgttagcaaccatgtgtggtggaaaaatgctggacaaattgagatatgttttctcccagatgtcagattccaatggcttaatgatatttagcaagtttgaccagtttctgaaggaagttctgaagctcccaacagctgtctttgaagggccatcttttggttacacagagcactcagtccgcacctgttttccacagcagagaaagataatgctaaatatgtttttagacacaatgatggctgaccctcctccccagtgccttgtctggctacctctcatgcacaggcttgcccatgttgagaatgtcttccatcccgtggagtgctcctactgccgatgtgagagtatgatgggtttccggtaccgatgccagcagtgccacaactatcagctctgccagaattgcttttggcgtggccatgccggcggccctcacagcaaccagcaccagatgaaggagcattcctcttggaaatctcctgcaaagaagctgagccatgcaattagtaaatctttggggtgtgtacccacgagagaacccccgcatcctgtttttcctgagcaaccagagaaaccacttgaccttgcacatatagttcctcctcgccctctgactaatatgaatgacaccatggttagccacatgtcctctggagtgcccactcccaccaagaggttacagtatagccaggatatacccagtcacttggccgatgagcatgcgctgatagcctcctatgtggcccgtctgcagcactgtgcacgtgttctggacagtcctagccgactggatgaggaacaccgtcttatagctcgctatgctgcccggctggctgcagaagcaggaaacgtgactcgtcctcccactgacttgagctttaactttgatgccaacaaacaacaaagacagcttattgcagaactggaaaacaaaaacagagagatcctgcaggagattcagcgtctccgcctggaacacgagcaggcctcccagcccacccctgagaaggcacagcagaaccccacgctgctggcagagctgcggctgctgaggcaaaggaaggatgaactggagcagaggatgtcggccctgcaggagagcaggcgggagctgatggtccagctggaagagctgatgaagttgctgaaggctcaggccacagggtcaccacatacatcgcccacccatggaggcggccggccaatgcccatgccagtgcgctccacgtctgccggctccacccccacccactgtccgcaggactcgctgagcggagtcgggggagacgtgcaggaggccttcgcacaaggtacgaggagaaacctccgcaatgacctgctggtggcagctgactccatcaccaacaccatgtcatccctggtgaaggagctccattcaggttagcagaggagccggacacagaggaagctcaggcacagaggacgaggagcaagctggcgccgacatggcgaaggcaaggtcttcccccagaggcacattcctctccatctttccaccgcacacctggaccaggcttgcaggctgccagacgtcactccacccgccagggagaggggagccagagccggtgggaagcggggaggggctgcgtggcacagctagtgggcctccccctgcacagccctgcatgtactagcaccttcatcactcccctcagggcatggtctcatctccgcatcaggaattcacctggaggttgaaaagagaaaagaaaaagcaccaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:1838 -> Molecular function: GO:0005509 [calcium ion binding] evidence: IEA
GeneID:1838 -> Molecular function: GO:0008270 [zinc ion binding] evidence: IEA
GeneID:1838 -> Cellular component: GO:0005737 [cytoplasm] evidence: IEA
GeneID:1838 -> Cellular component: GO:0045202 [synapse] evidence: IEA
by
@meso_cacase at
DBCLS
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