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Previous release (v1)
2026-06-24 23:05:14, GGRNA.v2 : RefSeq release 233 (Jan, 2026)
LOCUS NM_001406542 6112 bp mRNA linear PRI 01-MAY-2025
DEFINITION Homo sapiens ATPase copper transporting beta (ATP7B), transcript
variant 35, mRNA.
ACCESSION NM_001406542
VERSION NM_001406542.1
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 6112)
AUTHORS Zhang,K., Qu,C., Zhou,P., Yang,Z. and Wu,X.
TITLE Integrative analysis of the cuproptosis-related gene ATP7B in the
prognosis and immune infiltration of IDH1 wild-type glioma
JOURNAL Gene 905, 148220 (2024)
PUBMED 38286269
REMARK GeneRIF: Integrative analysis of the cuproptosis-related gene ATP7B
in the prognosis and immune infiltration of IDH1 wild-type glioma.
REFERENCE 2 (bases 1 to 6112)
AUTHORS Ruturaj, Mishra,M., Saha,S., Maji,S., Rodriguez-Boulan,E.,
Schreiner,R. and Gupta,A.
TITLE Regulation of the apico-basolateral trafficking polarity of the
homologous copper-ATPases ATP7A and ATP7B
JOURNAL J Cell Sci 137 (5) (2024)
PUBMED 38032054
REMARK GeneRIF: Regulation of the apico-basolateral trafficking polarity
of the homologous copper-ATPases ATP7A and ATP7B.
REFERENCE 3 (bases 1 to 6112)
AUTHORS Tavares,L.A., Rodrigues,R.L., Santos da Costa,C., Nascimento,J.A.,
Vargas de Carvalho,J., Nogueira de Carvalho,A., Mardones,G.A. and
daSilva,L.L.P.
TITLE AP-1gamma2 is an adaptor protein 1 variant required for
endosome-to-Golgi trafficking of the mannose-6-P receptor (CI-MPR)
and ATP7B copper transporter
JOURNAL J Biol Chem 300 (3), 105700 (2024)
PUBMED 38307383
REMARK GeneRIF: AP-1gamma2 is an adaptor protein 1 variant required for
endosome-to-Golgi trafficking of the mannose-6-P receptor (CI-MPR)
and ATP7B copper transporter.
REFERENCE 4 (bases 1 to 6112)
AUTHORS Gorukmez,O., Ozgur,T., Gorukmez,O. and Topak,A.
TITLE ATP7B Gene Variant Profile Identified by NGS in Wilson's Disease
JOURNAL Fetal Pediatr Pathol 42 (6), 891-900 (2023)
PUBMED 37737146
REMARK GeneRIF: ATP7B Gene Variant Profile Identified by NGS in Wilson's
Disease.
REFERENCE 5 (bases 1 to 6112)
AUTHORS Petrukhin,K., Lutsenko,S., Chernov,I., Ross,B.M., Kaplan,J.H. and
Gilliam,T.C.
TITLE Characterization of the Wilson disease gene encoding a P-type
copper transporting ATPase: genomic organization, alternative
splicing, and structure/function predictions
JOURNAL Hum Mol Genet 3 (9), 1647-1656 (1994)
PUBMED 7833924
REFERENCE 6 (bases 1 to 6112)
AUTHORS Petrukhin,K., Fischer,S.G., Pirastu,M., Tanzi,R.E., Chernov,I.,
Devoto,M., Brzustowicz,L.M., Cayanis,E., Vitale,E., Russo,J.J. et
al.
TITLE Mapping, cloning and genetic characterization of the region
containing the Wilson disease gene
JOURNAL Nat Genet 5 (4), 338-343 (1993)
PUBMED 8298640
REFERENCE 7 (bases 1 to 6112)
AUTHORS Bull,P.C., Thomas,G.R., Rommens,J.M., Forbes,J.R. and Cox,D.W.
TITLE The Wilson disease gene is a putative copper transporting P-type
ATPase similar to the Menkes gene
JOURNAL Nat Genet 5 (4), 327-337 (1993)
PUBMED 8298639
REMARK Erratum:[Nat Genet 1994 Feb;6(2):214]
REFERENCE 8 (bases 1 to 6112)
AUTHORS Yamaguchi,Y., Heiny,M.E. and Gitlin,J.D.
TITLE Isolation and characterization of a human liver cDNA as a candidate
gene for Wilson disease
JOURNAL Biochem Biophys Res Commun 197 (1), 271-277 (1993)
PUBMED 8250934
REFERENCE 9 (bases 1 to 6112)
AUTHORS Weiss,K.H. and Schilsky,M.
TITLE Wilson Disease
JOURNAL (in) Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE and
Amemiya A (Eds.);
GENEREVIEWS(R);
(1993)
PUBMED 20301685
REFERENCE 10 (bases 1 to 6112)
AUTHORS Klein,C., Lohmann,K., Marras,C. and Munchau,A.
TITLE Hereditary Dystonia Overview
JOURNAL (in) Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE and
Amemiya A (Eds.);
GENEREVIEWS(R);
(1993)
PUBMED 20301334
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AL139082.18, AL138821.12 and
AL162377.10.
Summary: This gene is a member of the P-type cation transport
ATPase family and encodes a protein with several membrane-spanning
domains, an ATPase consensus sequence, a hinge domain, a
phosphorylation site, and at least 2 putative copper-binding sites.
This protein is a monomer, and functions as a copper-transporting
ATPase which exports copper out of the cells, such as the efflux of
hepatic copper into the bile. Alternate transcriptional splice
variants, encoding different isoforms with distinct cellular
localizations, have been characterized. Mutations in this gene have
been associated with Wilson disease which is characterized by
copper accumulation. [provided by RefSeq, Dec 2019].
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 :: SRR14038197.2109779.1,
SRR14038195.1540031.1 [ECO:0000332]
RNAseq introns :: mixed sample support SAMEA1965299,
SAMEA1966682 [ECO:0006172]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-164 AL139082.18 29750-29913 c
165-1398 AL138821.12 33967-35200 c
1399-1656 AL138821.12 30524-30781 c
1657-1820 AL138821.12 28476-28639 c
1821-1982 AL138821.12 24904-25065 c
1983-2074 AL138821.12 17548-17639 c
2075-2202 AL138821.12 10304-10431 c
2203-2357 AL138821.12 10039-10193 c
2358-2492 AL138821.12 9694-9828 c
2493-2687 AL138821.12 6316-6510 c
2688-2870 AL138821.12 4141-4323 c
2871-3039 AL138821.12 2418-2586 c
3040-3183 AL138821.12 1113-1256 c
3184-3326 AL162377.10 168087-168229 c
3327-3530 AL162377.10 166512-166715 c
3531-3648 AL162377.10 166312-166429 c
3649-3751 AL162377.10 164629-164731 c
3752-6112 AL162377.10 161705-164065 c
FEATURES Location/Qualifiers
source 1..6112
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="13"
/map="13q14.3"
gene 1..6112
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="ATPase copper transporting beta"
/db_xref="GeneID:540"
/db_xref="HGNC:HGNC:870"
/db_xref="MIM:606882"
exon 1..164
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/inference="alignment:Splign:2.1.0"
CDS 114..4025
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/EC_number="7.2.2.8"
/note="isoform x is encoded by transcript variant 35;
copper-transporting ATPase 2; copper pump 2; ATPase, Cu++
transporting, beta polypeptide; Wilson disease-associated
protein; ATPase, Cu(2+)- transporting, beta polypeptide;
copper-transporting protein ATP7B"
/codon_start=1
/product="copper-transporting ATPase 2 isoform x"
/protein_id="NP_001393471.1"
/db_xref="GeneID:540"
/db_xref="HGNC:HGNC:870"
/db_xref="MIM:606882"
/translation="
MPEQERQITAREGASRKILSKLSLPTRAWEPAMKKSFAFDNVGYEGGLDGLGPSSQVATSTVRILGMTCQSCVKSIEDRISNLKGIISMKVSLEQGSATVKYVPSVVCLQQVCHQIGDMGFEASIAEGKAASWPSRSLPAQEAVVKLRVEGMTCQSCVSSIEGKVRKLQGVVRVKVSLSNQEAVITYQPYLIQPEDLRDHVNDMGFEAAIKSKVAPLSLGPIDIERLQSTNPKRPLSSANQNFNNSETLGHQGSHVVTLQLRIDGMHCKSCVLNIEENIGQLLGVQSIQVSLENKTAQVKYDPSCTSPVALQRAIEALPPGNFKVSLPDGAEGSGTDHRSSSSHSPGSPPRNQVQGTCSTTLIAIAGMTCASCVHSIEGMISQLEGVQQISVSLAEGTATVLYNPSVISPEELRAAIEDMGFEASVVSESCSTNPLGNHSAGNSMVQTTDGTPTSVQEVAPHTGRLPANHAPDILAKSPQSTRAVAPQKCFLQIKGMTCASCVSNIERNLQKEAGVLSVLVALMAGKAEIKYDPEVIQPLEIAQFIQDLGFEAAVMEDYAGSDGNIELTITGMTCASCVHNIESKLTRTNGITYASVALATSKALVKFDPEIIGPRDIIKIIESKTSEALAKLMSLQATEATVVTLGEDNLIIREEQVPMELVQRGDIVKVVPGGKFPVDGKVLEGNTMADESLITGEAMPVTKKPGSTVIAGSINAHGSVLIKATHVGNDTTLAQIVKLVEEAQMSKAPIQQLADRFSGYFVPFIIIMSTLTLVVWIVIGFIDFGVVQRYFPNPNKHISQTEVIIRFAFQTSITVLCIACPCSLGLATPTAVMVGTGVAAQNGILIKGGKPLEMAHKIKTVMFDKTGTITHGVPRVMRVLLLGDVATLPLRKVLAVVGTAEASSEHPLGVAVTKYCKEELGTETLGYCTDFQAVPGCGIGCKVSNVEGILAHSERPLSAPASHLNEAGSLPAEKDAVPQTFSVLIGNREWLRRNGLTISSDVSDAMTDHEMKGQTAILVAIDGVLCGMIAIADAVKQEAALAVHTLQSMGVDVVLITGDNRKTARAIATQVGINKVFAEVLPSHKVAKVQELQNKGKKVAMVGDGVNDSPALAQADMGVAIGTGTDVAIEAADVVLIRNDLLDVVASIHLSKRTVRRIRINLVLALIYNLVGIPIAAGVFMPIGIVLQPWMGSAAMAASSVSVVLSSLQLKCYKKPDLERYEAQAHGHMKPLTASQVSVHIGMDDRWRDSPRATPWDQVSYVSQVSLSSLTSDKPSRHSAAADDDGDKWSLLLNGRDEEQYI"
misc_feature 180..182
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (P35670.4); phosphorylation site"
misc_feature 294..485
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="Heavy-metal-associated domain (HMA) is a conserved
domain of approximately 30 amino acid residues found in a
number of proteins that transport or detoxify heavy
metals, for example, the CPx-type heavy metal ATPases and
copper chaperones. HMA domain...; Region: HMA; cd00371"
/db_xref="CDD:238219"
misc_feature order(312..320,327..329)
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="metal-binding site [ion binding]"
/db_xref="CDD:238219"
misc_feature 549..740
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="Heavy-metal-associated domain (HMA) is a conserved
domain of approximately 30 amino acid residues found in a
number of proteins that transport or detoxify heavy
metals, for example, the CPx-type heavy metal ATPases and
copper chaperones. HMA domain...; Region: HMA; cd00371"
/db_xref="CDD:238219"
misc_feature order(567..575,582..584)
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="metal-binding site [ion binding]"
/db_xref="CDD:238219"
misc_feature 801..860
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="propagated from UniProtKB/Swiss-Prot (P35670.4);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
misc_feature 891..1067
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="Heavy-metal-associated domain (HMA) is a conserved
domain of approximately 30 amino acid residues found in a
number of proteins that transport or detoxify heavy
metals, for example, the CPx-type heavy metal ATPases and
copper chaperones. HMA domain...; Region: HMA; cd00371"
/db_xref="CDD:238219"
misc_feature order(909..917,924..926)
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="metal-binding site [ion binding]"
/db_xref="CDD:238219"
misc_feature 1077..1178
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="propagated from UniProtKB/Swiss-Prot (P35670.4);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
misc_feature 1200..1388
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="Heavy-metal-associated domain (HMA) is a conserved
domain of approximately 30 amino acid residues found in a
number of proteins that transport or detoxify heavy
metals, for example, the CPx-type heavy metal ATPases and
copper chaperones. HMA domain...; Region: HMA; cd00371"
/db_xref="CDD:238219"
misc_feature order(1215..1223,1230..1232)
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="metal-binding site [ion binding]"
/db_xref="CDD:238219"
misc_feature 1545..1547
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (P35670.4); phosphorylation site"
misc_feature 1554..1556
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="Phosphoserine.
/evidence=ECO:0000250|UniProtKB:Q64535; propagated from
UniProtKB/Swiss-Prot (P35670.4); phosphorylation site"
misc_feature 1587..1775
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="Heavy-metal-associated domain (HMA) is a conserved
domain of approximately 30 amino acid residues found in a
number of proteins that transport or detoxify heavy
metals, for example, the CPx-type heavy metal ATPases and
copper chaperones. HMA domain...; Region: HMA; cd00371"
/db_xref="CDD:238219"
misc_feature order(1602..1610,1617..1619)
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="metal-binding site [ion binding]"
/db_xref="CDD:238219"
misc_feature 1812..1985
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="Heavy-metal-associated domain (HMA) is a conserved
domain of approximately 30 amino acid residues found in a
number of proteins that transport or detoxify heavy
metals, for example, the CPx-type heavy metal ATPases and
copper chaperones. HMA domain...; Region: HMA; cd00371"
/db_xref="CDD:238219"
misc_feature order(1830..1838,1845..1847)
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="metal-binding site [ion binding]"
/db_xref="CDD:238219"
misc_feature 1983..3689
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="P-type heavy metal-transporting ATPase, similar to
human copper-transporting ATPases, ATP7A and ATP7B;
Region: P-type_ATPase_Cu-like; cd02094"
/db_xref="CDD:319783"
misc_feature order(2574..2576,2580..2582,3618..3620)
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="putative Cu binding site [ion binding]; other site"
/db_xref="CDD:319783"
misc_feature order(2706..2714,2916..2918,3069..3077,3165..3167,
3285..3293,3351..3353,3360..3362,3369..3371,3426..3428,
3435..3437)
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="putative ATP binding site [chemical binding]; other
site"
/db_xref="CDD:319783"
exon 165..1398
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/inference="alignment:Splign:2.1.0"
exon 1399..1656
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/inference="alignment:Splign:2.1.0"
exon 1657..1820
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/inference="alignment:Splign:2.1.0"
exon 1821..1982
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/inference="alignment:Splign:2.1.0"
exon 1983..2074
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/inference="alignment:Splign:2.1.0"
exon 2075..2202
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/inference="alignment:Splign:2.1.0"
exon 2203..2357
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/inference="alignment:Splign:2.1.0"
exon 2358..2492
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/inference="alignment:Splign:2.1.0"
exon 2493..2687
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/inference="alignment:Splign:2.1.0"
exon 2688..2870
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/inference="alignment:Splign:2.1.0"
exon 2871..3039
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/inference="alignment:Splign:2.1.0"
exon 3040..3183
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/inference="alignment:Splign:2.1.0"
exon 3184..3326
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/inference="alignment:Splign:2.1.0"
exon 3327..3530
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/inference="alignment:Splign:2.1.0"
exon 3531..3648
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/inference="alignment:Splign:2.1.0"
exon 3649..3751
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/inference="alignment:Splign:2.1.0"
exon 3752..6112
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/inference="alignment:Splign:2.1.0"
regulatory 6085..6090
/regulatory_class="polyA_signal_sequence"
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="hexamer: AATAAA"
polyA_site 6112
/gene="ATP7B"
/gene_synonym="PWD; WC1; WD; WND"
/note="major polyA site"
ORIGIN
ctcacactctgcgcctcctctcccgggactttaacaccccgctctcctccaccgaccaggtgaccttttgctctgagccagatcagagaagaattcggtgtccgtgcgggacgatgcctgagcaggagagacagatcacagccagagaaggggccagtcggaaaatcttatctaagctttctttgcctacccgtgcctgggaaccagcaatgaagaagagttttgcttttgacaatgttggctatgaaggtggtctggatggcctgggcccttcttctcaggtggccaccagcacagtcaggatcttgggcatgacttgccagtcatgtgtgaagtccattgaggacaggatttccaatttgaaaggcatcatcagcatgaaggtttccctggaacaaggcagtgccactgtgaaatatgtgccatcggttgtgtgcctgcaacaggtttgccatcaaattggggacatgggcttcgaggccagcattgcagaaggaaaggcagcctcctggccctcaaggtccttgcctgcccaggaggctgtggtcaagctccgggtggagggcatgacctgccagtcctgtgtcagctccattgaaggcaaggtccggaaactgcaaggagtagtgagagtcaaagtctcactcagcaaccaagaggccgtcatcacttatcagccttatctcattcagcccgaagacctcagggaccatgtaaatgacatgggatttgaagctgccatcaagagcaaagtggctcccttaagcctgggaccaattgatattgagcggttacaaagcactaacccaaagagacctttatcttctgctaaccagaattttaataattctgagaccttggggcaccaaggaagccatgtggtcaccctccaactgagaatagatggaatgcattgtaagtcttgcgtcttgaatattgaagaaaatattggccagctcctaggggttcaaagtattcaagtgtccttggagaacaaaactgcccaagtaaagtatgacccttcttgtaccagcccagtggctctgcagagggctatcgaggcacttccacctgggaattttaaagtttctcttcctgatggagccgaagggagtgggacagatcacaggtcttccagttctcattcccctggctccccaccgagaaaccaggtccagggcacatgcagtaccactctgattgccattgccggcatgacctgtgcatcctgtgtccattccattgaaggcatgatctcccaactggaaggggtgcagcaaatatcggtgtctttggccgaagggactgcaacagttctttataatccctctgtaattagcccagaagaactcagagctgctatagaagacatgggatttgaggcttcagtcgtttctgaaagctgttctactaaccctcttggaaaccacagtgctgggaattccatggtgcaaactacagatggtacacctacatctgtgcaggaagtggctccccacactgggaggctccctgcaaaccatgccccggacatcttggcaaagtccccacaatcaaccagagcagtggcaccgcagaagtgcttcttacagatcaaaggcatgacctgtgcatcctgtgtgtctaacatagaaaggaatctgcagaaagaagctggtgttctctccgtgttggttgccttgatggcaggaaaggcagagatcaagtatgacccagaggtcatccagcccctcgagatagctcagttcatccaggacctgggttttgaggcagcagtcatggaggactacgcaggctccgatggcaacattgagctgacaatcacagggatgacctgcgcgtcctgtgtccacaacatagagtccaaactcacgaggacaaatggcatcacttatgcctccgttgcccttgccaccagcaaagcccttgttaagtttgacccggaaattatcggtccacgggatattatcaaaattattgagagcaaaacctcagaagccctggctaaactcatgtctctccaagccacagaagccaccgttgtgacccttggtgaggacaatttaatcatcagggaggagcaagtccccatggagctggtgcagcggggcgatatcgtcaaggtggtccctgggggaaagtttccagtggatgggaaagtcctggaaggcaataccatggctgatgagtccctcatcacaggagaagccatgccagtcactaagaaacccggaagcactgtaattgcggggtctataaatgcacatggctctgtgctcattaaagctacccacgtgggcaatgacaccactttggctcagattgtgaaactggtggaagaggctcagatgtcaaaggcacccattcagcagctggctgaccggtttagtggatattttgtcccatttatcatcatcatgtcaactttgacgttggtggtatggattgtaatcggttttatcgattttggtgttgttcagagatactttcctaaccccaacaagcacatctcccagacagaggtgatcatccggtttgctttccagacgtccatcacggtgctgtgcattgcctgcccctgctccctggggctggccacgcccacggctgtcatggtgggcaccggggtggccgcgcagaacggcatcctcatcaagggaggcaagcccctggagatggcgcacaagataaagactgtgatgtttgacaagactggcaccattacccatggcgtccccagggtcatgcgggtgctcctgctgggggatgtggccacactgcccctcaggaaggttctggctgtggtggggactgcggaggccagcagtgaacaccccttgggcgtggcagtcaccaaatactgtaaagaggaacttggaacagagaccttgggatactgcacggacttccaggcagtgccaggctgtggaattgggtgcaaagtcagcaacgtggaaggcatcctggcccacagtgagcgccctttgagtgcaccggccagtcacctgaatgaggctggcagccttcccgcagaaaaagatgcagtcccccagaccttctctgtgctgattggaaaccgtgagtggctgaggcgcaacggtttaaccatttctagcgatgtcagtgacgctatgacagaccacgagatgaaaggacagacagccatcctggtggctattgacggtgtgctctgtgggatgatcgcaatcgcagacgctgtcaagcaggaggctgccctggctgtgcacacgctgcagagcatgggtgtggacgtggttctgatcacgggggacaaccggaagacagccagagctattgccacccaggttggcatcaacaaagtctttgcagaggtgctgccttcgcacaaggtggccaaggtccaggagctccagaataaagggaagaaagtcgccatggtgggggatggggtcaatgactccccggccttggcccaggcagacatgggtgtggccattggcaccggcacggatgtggccatcgaggcagccgacgtcgtccttatcagaaatgatttgctggatgtggtggctagcattcacctttccaagaggactgtccgaaggatacgcatcaacctggtcctggcactgatttataacctggttgggatacccattgcagcaggtgtcttcatgcccatcggcattgtgctgcagccctggatgggctcagcggccatggcagcctcctctgtgtctgtggtgctctcatccctgcagctcaagtgctataagaagcctgacctggagaggtatgaggcacaggcgcatggccacatgaagcccctgacggcatcccaggtcagtgtgcacataggcatggatgacaggtggcgggactcccccagggccacaccatgggaccaggtcagctatgtcagccaggtgtcgctgtcctccctgacgtccgacaagccatctcggcacagcgctgcagcagacgatgatggggacaagtggtctctgctcctgaatggcagggatgaggagcagtacatctgatgacttcaggcaggcgggccggggcagggacttgcctccactcaccacaagctgagcaggacagccagcagcaggatgggctgagctagcctccagctttggggacttccgctccctggatatgtccagtcatcctgccctgcagcacgcggccttgtctgggtgcagctgggcttggcctggagaggacggccctgcctgcctcttggcctcacgggaccgtcagcatgggctttgtcttggactctagtccttggctggactgtagaaggtgagaggcgagtcaccctcctcacagacctctgcttggagtatttaggatgactgctgtgaaatggagaacagtttcatcaggaccaaaaaacctcactgggcctttccagagaactgcagacctcactgtcagggtctttctgatgacgcctgtctgtgtgcatcatgtttctgagaccacagtttacctcaggtgtgcctgttgctttcttcctgcatagtctgttcctttcttcgtacatagtctgttccttttctctcctgtgtgcttgtcagtggggacccctcgcaaccctgcctgtcacctgggagggtgggaccaatgtccttgtggtctttgctgctgctctcaggcgcttctccaatgctctggagtgtgcatttcagcttgaacctgcttcctggctcacacatccccagccagggagcttgccacactcttcttcaagttgaggagagttcttttttgcttaaagcccccttctccatggagtgttggcttctcaatagagtgttgttgctgaccagctggagtgagggcctcagagcctgacctgagagtccgtactcggcttcctgtggggtgtaggttctcgcgattcaggacgtccttccatatccctgcccagcctgtggtgcttgaaacgtttgccccatgggaaacgtatgtgtgcaggagcctccctgcacggcccaaggggcttcgttttcagtcttctgactgtcacctcgtggggttcagtagagaattcatgtgactagcgcctggccttgtgtggcttggaggaaatggtactgcccaaataggaggaaaacacagcctccctgagcctgcattctgcacgctgcccaggggcttcagaaaaggagtggccacagcaccccgaagggagcatctgtttacctggcagtggctctcagagcagcagaacgggttcagttttagactctgaagttggttgtgattgacagaaccctttgggagcaaactagtagagttggattaaattctgggtgaaacccttttctcccacacaaaatagttttagtgatttttttcattgtccattacttgccaggggcagttttagcagcacttttgatagattacgtctaatcctcccaaccaaccagcagggtagctattactgtccacattttacaggcaaggaaacaggctccaagaggctgaggactttgcccaggatgacatagccaatggacaagcagtgtctgtcagctgtgaaggcttcactcttattgtccttctaccttgaatagaagttttcctgataagaataaacgaggaaaaggtccttgcctcctggaagaacaaatctaccaggtgatctattcattgtttcaactcagaatgcacttgattcaggaggtcatctgaccttcaccttggatggttagtttcactttttacatatagtttttgcagggttttattttataaaatccaagcgcgctgttgattgtgttttccttgttttcagcccccccactccagcccgcagcacatttccgctgtccgtcagtaattgtgtcctctctttatgcttgcttggggaatgttgttttctgactaggctgatcattatctaaagaatctaattctgttgatttttaaaacttttaggaccataaacgttgtgttcatatatggacatggaaatatttatataattttatagaaaataaccttttagatggtcaaagtgtaaggagtttttttgtcagataatcatttctacttcaaaaacatttcatgcaatattagaataaagttcctgtcattcctctaaaaa
//
by
@meso_cacase at
DBCLS
This page is licensed under a
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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