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2024-04-25 05:38:05, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001944 5561 bp mRNA linear PRI 07-JUL-2013
DEFINITION Homo sapiens desmoglein 3 (DSG3), mRNA.
ACCESSION NM_001944
VERSION NM_001944.2 GI:119964717
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 5561)
AUTHORS Patel,V., Martin,D., Malhotra,R., Marsh,C.A., Doci,C.L.,
Veenstra,T.D., Nathan,C.A., Sinha,U.K., Singh,B., Molinolo,A.A.,
Rusling,J.F. and Gutkind,J.S.
TITLE DSG3 as a biomarker for the ultrasensitive detection of occult
lymph node metastasis in oral cancer using nanostructured
immunoarrays
JOURNAL Oral Oncol. 49 (2), 93-101 (2013)
PUBMED 23010602
REMARK GeneRIF: provide a proof of principle supporting that
ultrasensitive nanostructured assay systems for DSG3 can be
exploited to detect micrometastatic HNSCC lesions in lymph nodes,
which can improve the diagnosis
REFERENCE 2 (bases 1 to 5561)
AUTHORS Hartlieb,E., Kempf,B., Partilla,M., Vigh,B., Spindler,V. and
Waschke,J.
TITLE Desmoglein 2 is less important than desmoglein 3 for keratinocyte
cohesion
JOURNAL PLoS ONE 8 (1), E53739 (2013)
PUBMED 23326495
REMARK GeneRIF: Specific desmosomal cadherins contribute differently to
keratinocyte cohesion and that Dsg2 compared to Dsg3 is less
important in this context.
REFERENCE 3 (bases 1 to 5561)
AUTHORS Tsang,S.M., Brown,L., Gadmor,H., Gammon,L., Fortune,F., Wheeler,A.
and Wan,H.
TITLE Desmoglein 3 acting as an upstream regulator of Rho GTPases,
Rac-1/Cdc42 in the regulation of actin organisation and dynamics
JOURNAL Exp. Cell Res. 318 (18), 2269-2283 (2012)
PUBMED 22796473
REMARK GeneRIF: an important novel function for Dsg3 in promoting actin
dynamics through regulating Rac1 and Cdc42 activation in epithelial
cells.
REFERENCE 4 (bases 1 to 5561)
AUTHORS Di Zenzo,G., Di Lullo,G., Corti,D., Calabresi,V., Sinistro,A.,
Vanzetta,F., Didona,B., Cianchini,G., Hertl,M., Eming,R.,
Amagai,M., Ohyama,B., Hashimoto,T., Sloostra,J., Sallusto,F.,
Zambruno,G. and Lanzavecchia,A.
TITLE Pemphigus autoantibodies generated through somatic mutations target
the desmoglein-3 cis-interface
JOURNAL J. Clin. Invest. 122 (10), 3781-3790 (2012)
PUBMED 22996451
REMARK GeneRIF: The cis-adhesive interface on extracellular subdomain EC1
recognized by the pathogenic antibody PVA224 is the primary target
of the autoantibodies present in the serum of pemiphigus vulgaris
patients.
REFERENCE 5 (bases 1 to 5561)
AUTHORS Agackiran,Y., Ozcan,A., Akyurek,N., Memis,L., Findik,G. and Kaya,S.
TITLE Desmoglein-3 and Napsin A double stain, a useful
immunohistochemical marker for differentiation of lung squamous
cell carcinoma and adenocarcinoma from other subtypes
JOURNAL Appl. Immunohistochem. Mol. Morphol. 20 (4), 350-355 (2012)
PUBMED 22495379
REMARK GeneRIF: a useful immunohistochemical marker for differentiation of
lung squamous cell carcinoma and adenocarcinoma from other subtypes
REFERENCE 6 (bases 1 to 5561)
AUTHORS Roh,J.Y. and Stanley,J.R.
TITLE Plakoglobin binding by human Dsg3 (pemphigus vulgaris antigen) in
keratinocytes requires the cadherin-like intracytoplasmic segment
JOURNAL J. Invest. Dermatol. 104 (5), 720-724 (1995)
PUBMED 7738346
REFERENCE 7 (bases 1 to 5561)
AUTHORS Schafer,S., Koch,P.J. and Franke,W.W.
TITLE Identification of the ubiquitous human desmoglein, Dsg2, and the
expression catalogue of the desmoglein subfamily of desmosomal
cadherins
JOURNAL Exp. Cell Res. 211 (2), 391-399 (1994)
PUBMED 8143788
REFERENCE 8 (bases 1 to 5561)
AUTHORS Wang,Y., Amagai,M., Minoshima,S., Sakai,K., Green,K.J.,
Nishikawa,T. and Shimizu,N.
TITLE The human genes for desmogleins (DSG1 and DSG3) are located in a
small region on chromosome 18q12
JOURNAL Genomics 20 (3), 492-495 (1994)
PUBMED 8034325
REFERENCE 9 (bases 1 to 5561)
AUTHORS Arnemann,J., Spurr,N.K. and Buxton,R.S.
TITLE The human gene (DSG3) coding for the pemphigus vulgaris antigen is,
like the genes coding for the other two known desmogleins, assigned
to chromosome 18
JOURNAL Hum. Genet. 89 (3), 347-350 (1992)
PUBMED 1601426
REFERENCE 10 (bases 1 to 5561)
AUTHORS Amagai,M., Klaus-Kovtun,V. and Stanley,J.R.
TITLE Autoantibodies against a novel epithelial cadherin in pemphigus
vulgaris, a disease of cell adhesion
JOURNAL Cell 67 (5), 869-877 (1991)
PUBMED 1720352
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from DA458544.1, M76482.1,
AC021549.9, DA447747.1, AI608626.1, U51696.1, BX507120.1,
BX110234.1 and BC105997.1.
On Dec 27, 2006 this sequence version replaced gi:4503404.
Summary: Desmosomes are cell-cell junctions between epithelial,
myocardial, and certain other cell types. Desmoglein 3 is a
calcium-binding transmembrane glycoprotein component of desmosomes
in vertebrate epithelial cells. Currently, three desmoglein
subfamily members have been identified and all are members of the
cadherin cell adhesion molecule superfamily. These desmoglein gene
family members are located in a cluster on chromosome 18. This
protein has been identified as the autoantigen of the autoimmune
skin blistering disease pemphigus vulgaris. [provided by RefSeq,
Jul 2008].
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 :: AK290367.1, M76482.1 [ECO:0000332]
RNAseq introns :: mixed/partial sample support
ERS025087 [ECO:0000350]
##Evidence-Data-END##
COMPLETENESS: full length.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-40 DA458544.1 1-40
41-2842 M76482.1 15-2816
2843-2844 AC021549.9 33673-33674 c
2845-3362 M76482.1 2819-3336
3363-3572 DA447747.1 347-556
3573-3670 AI608626.1 147-244 c
3671-3818 U51696.1 373-520
3819-3916 BX507120.1 34-131
3917-4471 BX110234.1 180-734
4472-5561 BC105997.1 4-1093
FEATURES Location/Qualifiers
source 1..5561
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="18"
/map="18q12.1"
gene 1..5561
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/note="desmoglein 3"
/db_xref="GeneID:1830"
/db_xref="HGNC:3050"
/db_xref="MIM:169615"
exon 1..157
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/inference="alignment:Splign:1.39.8"
misc_feature 1
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/note="major transcription initiation site"
variation 14
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:10084010"
misc_feature 22
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/note="minor transcription initiation site"
variation 26
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:8085523"
variation 40
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:8085532"
misc_feature 62..64
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/note="upstream in-frame stop codon"
variation 64
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:2848707"
variation 76
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:73953166"
variation 80
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:372228912"
CDS 110..3109
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/note="130-kD pemphigus vulgaris antigen; desmoglein-3;
cadherin family member 6; 130 kDa pemphigus vulgaris
antigen"
/codon_start=1
/product="desmoglein-3 preproprotein"
/protein_id="NP_001935.2"
/db_xref="GI:119964718"
/db_xref="CCDS:CCDS11898.1"
/db_xref="GeneID:1830"
/db_xref="HGNC:3050"
/db_xref="MIM:169615"
/translation="
MMGLFPRTTGALAIFVVVILVHGELRIETKGQYDEEEMTMQQAKRRQKREWVKFAKPCREGEDNSKRNPIAKITSDYQATQKITYRISGVGIDQPPFGIFVVDKNTGDINITAIVDREETPSFLITCRALNAQGLDVEKPLILTVKILDINDNPPVFSQQIFMGEIEENSASNSLVMILNATDADEPNHLNSKIAFKIVSQEPAGTPMFLLSRNTGEVRTLTNSLDREQASSYRLVVSGADKDGEGLSTQCECNIKVKDVNDNFPMFRDSQYSARIEENILSSELLRFQVTDLDEEYTDNWLAVYFFTSGNEGNWFEIQTDPRTNEGILKVVKALDYEQLQSVKLSIAVKNKAEFHQSVISRYRVQSTPVTIQVINVREGIAFRPASKTFTVQKGISSKKLVDYILGTYQAIDEDTNKAASNVKYVMGRNDGGYLMIDSKTAEIKFVKNMNRDSTFIVNKTITAEVLAIDEYTGKTSTGTVYVRVPDFNDNCPTAVLEKDAVCSSSPSVVVSARTLNNRYTGPYTFALEDQPVKLPAVWSITTLNATSALLRAQEQIPPGVYHISLVLTDSQNNRCEMPRSLTLEVCQCDNRGICGTSYPTTSPGTRYGRPHSGRLGPAAIGLLLLGLLLLLLAPLLLLTCDCGAGSTGGVTGGFIPVPDGSEGTIHQWGIEGAHPEDKEITNICVPPVTANGADFMESSEVCTNTYARGTAVEGTSGMEMTTKLGAATESGGAAGFATGTVSGAASGFGAATGVGICSSGQSGTMRTRHSTGGTNKDYADGAISMNFLDSYFSQKAFACAEEDDGQEANDCLLIYDNEGADATGSPVGSVGCCSFIADDLDDSFLDSLGPKFKKLAEISLGVDGEGKEVQPPSKDSGYGIESCGHPIEVQQTGFVKCQTLSGSQGASALSTSGSVQPAVSIPDPLQHGNYLVTETYSASGSLVQPSTAGFDPLLTQNVIVTERVICPISSVPGNLAGPTQLRGSHTMLCTEDPCSRLI
"
sig_peptide 110..178
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/inference="COORDINATES: ab initio prediction:SignalP:4.0"
misc_feature 254..256
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/experiment="experimental evidence, no additional details
recorded"
/note="proteolytic cleavage site; modified site"
/db_xref="HPRD:00653"
mat_peptide 257..3106
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/product="desmoglein-3"
misc_feature 293..568
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/note="Cadherin tandem repeat domain; Region:
Cadherin_repeat; cd11304"
/db_xref="CDD:206637"
misc_feature order(293..298,455..457,461..463,554..556,560..565)
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/note="Ca2+ binding site [ion binding]; other site"
/db_xref="CDD:206637"
misc_feature 602..898
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/note="Cadherin tandem repeat domain; Region:
Cadherin_repeat; cd11304"
/db_xref="CDD:206637"
misc_feature order(611..616,785..787,791..793,884..886,890..895)
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/note="Ca2+ binding site [ion binding]; other site"
/db_xref="CDD:206637"
misc_feature 920..1240
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/note="Cadherin tandem repeat domain; Region:
Cadherin_repeat; cd11304"
/db_xref="CDD:206637"
misc_feature order(941..946,1115..1117,1121..1123,1235..1237)
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/note="Ca2+ binding site [ion binding]; other site"
/db_xref="CDD:206637"
misc_feature 1313..1582
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/note="Cadherin tandem repeat domain; Region:
Cadherin_repeat; cd11304"
/db_xref="CDD:206637"
misc_feature order(1460..1462,1466..1468,1568..1570,1574..1579)
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/note="Ca2+ binding site [ion binding]; other site"
/db_xref="CDD:206637"
misc_feature 1955..2029
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (P32926.2);
transmembrane region"
misc_feature 2450..2452
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/experiment="experimental evidence, no additional details
recorded"
/note="proteolytic cleavage site; modified site"
/db_xref="HPRD:02799"
misc_feature 2837..2914
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (P32926.2);
Region: Desmoglein repeat 1"
misc_feature 2915..3007
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (P32926.2);
Region: Desmoglein repeat 2"
variation 114
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:202064914"
variation 118
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="g"
/replace="t"
/db_xref="dbSNP:201263431"
variation 129
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:2848706"
exon 158..193
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/inference="alignment:Splign:1.39.8"
variation 169
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="g"
/db_xref="dbSNP:146619619"
variation 174
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="c"
/db_xref="dbSNP:374855339"
variation 175
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:141345290"
variation 185
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="c"
/db_xref="dbSNP:369569611"
exon 194..325
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/inference="alignment:Splign:1.39.8"
variation 251
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:150234659"
variation 257
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="g"
/db_xref="dbSNP:377534879"
variation 282
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="g"
/db_xref="dbSNP:369832448"
variation 295
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:201860338"
variation 309
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:141767923"
exon 326..481
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/inference="alignment:Splign:1.39.8"
variation 366
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:138945214"
variation 388
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:73412299"
variation 425
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:200254801"
variation 454
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:7240789"
variation 455
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:137884016"
variation 459
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:371200207"
variation 478
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:374985207"
exon 482..626
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/inference="alignment:Splign:1.39.8"
variation 540
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:62095186"
variation 541
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:199717956"
variation 543
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:199792976"
variation 600
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:143575814"
variation 621
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:373067281"
exon 627..793
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/inference="alignment:Splign:1.39.8"
variation 644
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="g"
/db_xref="dbSNP:373672775"
variation 712
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:147164010"
variation 746
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:201738168"
variation 755
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:140361176"
variation 763
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:142808551"
variation 765
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="g"
/replace="t"
/db_xref="dbSNP:150764801"
variation 788
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="c"
/db_xref="dbSNP:1870642"
exon 794..922
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/inference="alignment:Splign:1.39.8"
variation 800
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:149952914"
variation 810
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:144692416"
variation 815
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:139510343"
variation 818
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="g"
/replace="t"
/db_xref="dbSNP:375964770"
variation 850
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:185193655"
variation 859
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:376604598"
variation 893
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="g"
/db_xref="dbSNP:190778464"
variation 913
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:199928630"
variation 918
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="c"
/db_xref="dbSNP:369605824"
exon 923..1108
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/inference="alignment:Splign:1.39.8"
variation 932
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="c"
/db_xref="dbSNP:144335146"
variation 969
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:370472156"
variation 1060
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:146580140"
variation 1063
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:199886124"
variation 1070
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:377262567"
variation 1073
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="c"
/db_xref="dbSNP:369821354"
variation 1087
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="t"
/db_xref="dbSNP:373365493"
variation 1103
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:202206106"
exon 1109..1380
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/inference="alignment:Splign:1.39.8"
variation 1120
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:113083364"
variation 1124
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:376501967"
variation 1136
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:141272063"
variation 1194
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:73414212"
variation 1229
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="g"
/replace="t"
/db_xref="dbSNP:369572434"
variation 1235
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:372851025"
variation 1248
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:146025709"
variation 1259
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:142415015"
variation 1260
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:377115190"
variation 1312
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="g"
/db_xref="dbSNP:200719096"
variation 1314
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:185975223"
variation 1323
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="t"
/db_xref="dbSNP:151296663"
variation 1341
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="g"
/db_xref="dbSNP:369082931"
variation 1343
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="c"
/db_xref="dbSNP:370854938"
variation 1346
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:191249015"
variation 1359
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:140632761"
exon 1381..1520
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/inference="alignment:Splign:1.39.8"
variation 1384
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:113090917"
variation 1392
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:182644997"
variation 1395
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:200258412"
variation 1399
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="c"
/db_xref="dbSNP:150482301"
variation 1400
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:137948279"
variation 1432
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:201873300"
variation 1441
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:141972001"
variation 1458
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:200049726"
variation 1517
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:183983864"
exon 1521..1745
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/inference="alignment:Splign:1.39.8"
variation 1527
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:200551780"
variation 1539
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:138773767"
variation 1549
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:199540300"
variation 1600
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:377026548"
variation 1601
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:145720587"
variation 1634
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:16961975"
variation 1635
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="g"
/replace="t"
/db_xref="dbSNP:149262687"
variation 1663
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:368620189"
variation 1691
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="c"
/db_xref="dbSNP:201769930"
variation 1699
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:372705160"
variation 1720
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:375966622"
variation 1721
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:144565301"
variation 1735
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="t"
/db_xref="dbSNP:61730310"
exon 1746..2006
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/inference="alignment:Splign:1.39.8"
variation 1753
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:373234061"
variation 1771
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:141811164"
variation 1772
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="g"
/db_xref="dbSNP:376204787"
variation 1782
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="g"
/db_xref="dbSNP:370252237"
variation 1790
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:202080143"
variation 1832
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:61730311"
variation 1844
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="g"
/db_xref="dbSNP:139950299"
variation 1896
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="g"
/replace="t"
/db_xref="dbSNP:374203777"
variation 1941
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:149889527"
variation 1967
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:370583301"
variation 1975
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:375825713"
variation 1981
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="g"
/replace="t"
/db_xref="dbSNP:368265771"
exon 2007..2146
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/inference="alignment:Splign:1.39.8"
variation 2036
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="g"
/replace="t"
/db_xref="dbSNP:377007515"
variation 2056
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:148588573"
variation 2061
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="g"
/replace="t"
/db_xref="dbSNP:113457225"
variation 2074
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:368643122"
variation 2080
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:146051232"
variation 2112
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="c"
/db_xref="dbSNP:202143131"
variation 2120
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="t"
/db_xref="dbSNP:182313668"
variation 2126
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:370800025"
exon 2147..2210
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/inference="alignment:Splign:1.39.8"
variation 2156
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:200076592"
variation 2177..2178
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace=""
/replace="cccc"
/db_xref="dbSNP:376666272"
exon 2211..2494
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/inference="alignment:Splign:1.39.8"
variation 2226
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:61730313"
variation 2227
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:72925163"
variation 2245
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:373824344"
variation 2253
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:367712383"
variation 2275
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="c"
/db_xref="dbSNP:145838961"
variation 2277
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:371194800"
variation 2299
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:148978830"
variation 2312
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:142902378"
variation 2316
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="g"
/db_xref="dbSNP:201074636"
variation 2317
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:61730312"
variation 2356
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="c"
/db_xref="dbSNP:142612259"
variation 2357
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:201588689"
variation 2391
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="g"
/replace="t"
/db_xref="dbSNP:376410069"
variation 2417
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="c"
/db_xref="dbSNP:199507618"
variation 2421
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:111986709"
variation 2433
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="c"
/db_xref="dbSNP:370014020"
variation 2441
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="g"
/db_xref="dbSNP:373896941"
variation 2442
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="t"
/db_xref="dbSNP:138055234"
variation 2446
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:149941394"
variation 2447
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:368819436"
variation 2457
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:200927289"
variation 2493
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="t"
/db_xref="dbSNP:145985329"
exon 2495..5551
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/inference="alignment:Splign:1.39.8"
variation 2504
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="g"
/replace="t"
/db_xref="dbSNP:138770793"
variation 2515
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:141813094"
variation 2521
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:117661169"
variation 2522
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:201790264"
STS 2537..3457
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/standard_name="DSG3__4783"
/db_xref="UniSTS:462883"
variation 2562
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="c"
/db_xref="dbSNP:74446711"
variation 2570
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:148716637"
variation 2579
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:141490338"
variation 2582
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="g"
/db_xref="dbSNP:150853711"
variation 2586
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="g"
/db_xref="dbSNP:61730314"
variation 2590
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:200747593"
variation 2591
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:144985839"
variation 2599
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:150042139"
variation 2613
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="g"
/replace="t"
/db_xref="dbSNP:11873969"
variation 2708
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:377333848"
variation 2711
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="c"
/db_xref="dbSNP:200561595"
variation 2739
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:370660821"
variation 2742
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="g"
/replace="t"
/db_xref="dbSNP:199891567"
variation 2749
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="g"
/replace="t"
/db_xref="dbSNP:184857075"
variation 2759
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="g"
/replace="t"
/db_xref="dbSNP:375554890"
variation 2764
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="g"
/db_xref="dbSNP:376551522"
variation 2802
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:147711163"
variation 2830
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:141058045"
variation 2843
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:1380866"
variation 2856
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:147783261"
variation 2867
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="g"
/db_xref="dbSNP:148820666"
variation 2875
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:372187590"
variation 2887
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:369434504"
variation 2911
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:199984290"
variation 2934
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:141527621"
variation 2939
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="g"
/replace="t"
/db_xref="dbSNP:376372895"
variation 2987
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:73414241"
variation 2994
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="g"
/db_xref="dbSNP:370978123"
STS 3001..3297
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/standard_name="GDB:189554"
/db_xref="UniSTS:155592"
variation 3001
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="g"
/db_xref="dbSNP:138907681"
variation 3028
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:201418907"
variation 3056
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:200805179"
variation 3057
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:141447616"
variation 3059
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="g"
/replace="t"
/db_xref="dbSNP:374782833"
variation 3061
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="g"
/replace="t"
/db_xref="dbSNP:200152106"
variation 3067
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:140762325"
STS 3097..3282
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/standard_name="RH76240"
/db_xref="UniSTS:87304"
variation 3156
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="c"
/db_xref="dbSNP:199737898"
variation 3206
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="t"
/db_xref="dbSNP:78419295"
variation 3241
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:113513813"
variation 3259
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="g"
/replace="t"
/db_xref="dbSNP:371285512"
variation 3283
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:371049003"
variation 3285
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:138256538"
variation 3351
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:1466379"
variation 3496
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:149644500"
variation 3530
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:72925171"
variation 3536
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:189420121"
STS 3549..3651
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/standard_name="D11S3114"
/db_xref="UniSTS:152207"
variation 3605
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:181938639"
STS 3633..3722
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/standard_name="D8S2279"
/db_xref="UniSTS:473907"
STS 3658..3814
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/standard_name="PMC156606P4"
/db_xref="UniSTS:271411"
STS 3658..3805
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/standard_name="PMC156606P3"
/db_xref="UniSTS:271410"
STS 3668..3805
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/standard_name="PMC156606P2"
/db_xref="UniSTS:271409"
variation 3671
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:113791745"
variation 3737..3741
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace=""
/replace="agcgg"
/db_xref="dbSNP:373094837"
variation 3748
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="g"
/db_xref="dbSNP:112711163"
variation 3749
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:189388599"
variation 3777
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="g"
/db_xref="dbSNP:35241223"
variation 3814..3816
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace=""
/replace="a"
/db_xref="dbSNP:35721182"
variation 3834..3835
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace=""
/replace="a"
/db_xref="dbSNP:71829469"
variation 3834
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:114266245"
variation 3834
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace=""
/replace="g"
/replace="t"
/db_xref="dbSNP:34015762"
variation 3899
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:181832700"
variation 3966
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:371610760"
variation 4034..4036
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace=""
/replace="atc"
/db_xref="dbSNP:145502964"
variation 4308
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="c"
/db_xref="dbSNP:79900999"
variation 4309
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:114295935"
variation 4313
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="g"
/db_xref="dbSNP:374744413"
variation 4329
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:142722891"
variation 4446
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:147349647"
variation 4534
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:115536425"
variation 4595
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="g"
/db_xref="dbSNP:148431272"
variation 4605
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:2298613"
variation 4714
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:142537598"
variation 4733
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:185185604"
variation 4736
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:189701787"
variation 4737
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:116119612"
variation 4747
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="t"
/db_xref="dbSNP:77917204"
variation 4801
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:2298614"
variation 4938
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:77990754"
variation 5119
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:150567597"
variation 5185
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:77344536"
variation 5188
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:369856553"
variation 5261
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="g"
/db_xref="dbSNP:139549747"
variation 5270
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="a"
/replace="c"
/db_xref="dbSNP:373746073"
variation 5273
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:75200426"
variation 5358
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:9950036"
variation 5383
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="g"
/replace="t"
/db_xref="dbSNP:11541769"
variation 5480
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:11541770"
polyA_signal 5515..5520
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
polyA_signal 5527..5532
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
variation 5529
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
/replace="c"
/replace="t"
/db_xref="dbSNP:56294225"
polyA_signal 5539..5544
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
polyA_site 5551
/gene="DSG3"
/gene_synonym="CDHF6; PVA"
ORIGIN
aaagcagcagagacgctgcagagggcttttcttagacatcaactgcagacggctggcaggatagaagcagcggctcacttggactttttcaccagggaaatcagagacaatgatggggctcttccccagaactacaggggctctggccatcttcgtggtggtcatattggttcatggagaattgcgaatagagactaaaggtcaatatgatgaagaagagatgactatgcaacaagctaaaagaaggcaaaaacgtgaatgggtgaaatttgccaaaccctgcagagaaggagaagataactcaaaaagaaacccaattgccaagattacttcagattaccaagcaacccagaaaatcacctaccgaatctctggagtgggaatcgatcagccgccttttggaatctttgttgttgacaaaaacactggagatattaacataacagctatagtcgaccgggaggaaactccaagcttcctgatcacatgtcgggctctaaatgcccaaggactagatgtagagaaaccacttatactaacggttaaaattttggatattaatgataatcctccagtattttcacaacaaattttcatgggtgaaattgaagaaaatagtgcctcaaactcactggtgatgatactaaatgccacagatgcagatgaaccaaaccacttgaattctaaaattgccttcaaaattgtctctcaggaaccagcaggcacacccatgttcctcctaagcagaaacactggggaagtccgtactttgaccaattctcttgaccgagagcaagctagcagctatcgtctggttgtgagtggtgcagacaaagatggagaaggactatcaactcaatgtgaatgtaatattaaagtgaaagatgtcaacgataacttcccaatgtttagagactctcagtattcagcacgtattgaagaaaatattttaagttctgaattacttcgatttcaagtaacagatttggatgaagagtacacagataattggcttgcagtatatttctttacctctgggaatgaaggaaattggtttgaaatacaaactgatcctagaactaatgaaggcatcctgaaagtggtgaaggctctagattatgaacaactacaaagcgtgaaacttagtattgctgtcaaaaacaaagctgaatttcaccaatcagttatctctcgataccgagttcagtcaaccccagtcacaattcaggtaataaatgtaagagaaggaattgcattccgtcctgcttccaagacatttactgtgcaaaaaggcataagtagcaaaaaattggtggattatatcctgggaacatatcaagccatcgatgaggacactaacaaagctgcctcaaatgtcaaatatgtcatgggacgtaacgatggtggatacctaatgattgattcaaaaactgctgaaatcaaatttgtcaaaaatatgaaccgagattctactttcatagttaacaaaacaatcacagctgaggttctggccatagatgaatacacgggtaaaacttctacaggcacggtatatgttagagtacccgatttcaatgacaattgtccaacagctgtcctcgaaaaagatgcagtttgcagttcttcaccttccgtggttgtctccgctagaacactgaataatagatacactggcccctatacatttgcactggaagatcaacctgtaaagttgcctgccgtatggagtatcacaaccctcaatgctacctcggccctcctcagagcccaggaacagatacctcctggagtataccacatctccctggtacttacagacagtcagaacaatcggtgtgagatgccacgcagcttgacactggaagtctgtcagtgtgacaacaggggcatctgtggaacttcttacccaaccacaagccctgggaccaggtatggcaggccgcactcagggaggctggggcctgccgccatcggcctgctgctccttggtctcctgctgctgctgttggccccccttctgctgttgacctgtgactgtggggcaggttctactgggggagtgacaggtggttttatcccagttcctgatggctcagaaggaacaattcatcagtggggaattgaaggagcccatcctgaagacaaggaaatcacaaatatttgtgtgcctcctgtaacagccaatggagccgatttcatggaaagttctgaagtttgtacaaatacgtatgccagaggcacagcggtggaaggcacttcaggaatggaaatgaccactaagcttggagcagccactgaatctggaggtgctgcaggctttgcaacagggacagtgtcaggagctgcttcaggattcggagcagccactggagttggcatctgttcctcagggcagtctggaaccatgagaacaaggcattccactggaggaaccaataaggactacgctgatggggcgataagcatgaattttctggactcctacttttctcagaaagcatttgcctgtgcggaggaagacgatggccaggaagcaaatgactgcttgttgatctatgataatgaaggcgcagatgccactggttctcctgtgggctccgtgggttgttgcagttttattgctgatgacctggatgacagcttcttggactcacttggacccaaatttaaaaaacttgcagagataagccttggtgttgatggtgaaggcaaagaagttcagccaccctctaaagacagcggttatgggattgaatcctgtggccatcccatagaagtccagcagacaggatttgttaagtgccagactttgtcaggaagtcaaggagcttctgctttgtccacctctgggtctgtccagccagctgtttccatccctgaccctctgcagcatggtaactatttagtaacggagacttactcggcttctggttccctcgtgcaaccttccactgcaggctttgatccacttctcacacaaaatgtgatagtgacagaaagggtgatctgtcccatttccagtgttcctggcaacctagctggcccaacgcagctacgagggtcacatactatgctctgtacagaggatccttgctcccgtctaatatgaccagaatgagctggaataccacactgaccaaatctggatctttggactaaagtattcaaaatagcatagcaaagctcactgtattgggctaataatttggcacttattagcttctctcataaactgatcacgattataaattaaatgtttgggttcataccccaaaagcaatatgttgtcactcctaattctcaagtactattcaaattgtagtaaatcttaaagtttttcaaaaccctaaaatcatattcgccaggaaattttcctaaacattcttaagcttctatttttcccctgccaaaggaaggtgtttatcattttaaaatgcaatgtgatttagtggattaagcaggagcgctggttcttgtctccattgccttttcttatatcattgataatgatgtaagaatcacaaggggccgggcgcggtggctcacgcctgtaatcccagcactttgggaggccgaggcaggtggatcatgaggtcaggagatcgagaccatcctggctaacaaggtgaaaccccgtctctactaaaaatacaaaaaattagccgggcgcagtggcgggcgcctgtagtcccagctactcgggaggctgaggcaggagaatggcatgaacccgggaagcggagcttgcagtgagccgagattgcgccactgcagtccgcagtccggcctgggcgacagagcgagactccgtctcaaaaaaaaaaaaaaaaaaagaatcacaaggtatttgctaaagcattttgagctgcttggaaaaagggaagtagttgcagtagagtttcttccatcttcttggtgctgggaagccatatatgtgtcttttactcaagctaaggggtataagcttatgtgttgaatttgctacatctatatttcacatattctcacaataagagaattttgaaatagaaatatcatagaacatttaagaaagtttagtataaataatattttgtgtgttttaatccctttgaagggatctatccaaagaaaatattttacactgagctccttcctacacgtctcagtaacagatcctgtgttagtctttgaaaatagctcattttttaaatgtcagtgagtagatgtagcatacatatgatgtataatgacgtgtattatgttaacaatgtctgcagattttgtaggaatacaaaacatggccttttttataagcaaaacgggccaatgactagaataacacatagggcaatctgtgaatatgtattataagcagcattccagaaaagtagttggtgaaataattttcaagtcaaaaagggatatggaaagggaattatgagtaacctctattttttaagccttgcttttaaattaaacagctacagccatttaagccttgaggataataaagcttgagagtaataatgttaggttagcaaaggtttagatgtatcacttcatgcatgctaccatgatagtaatgcagctcttcgagtcatttctggtcattcaagatattcacccttttgcccatagaaagcaccctacctcacctgcttactgacattgtcttagctgatcacaagatcattatcagcctccattattccttactgtatataaaatacagagttttatattttcctttcttcgtttttcaccatattcaaaacctaaatttgtttttgcagatggaatgcaaagtaatcaagtgtttgtgctttcacctagaagggtgtggtcctgaaggaaagaggtcccctaaatatcccccaccctggtgctcctccctctccctggtaccctgactaccaggaagtcaggtgctagagcagctggagaagtgcaggcagcctgtgcttccacagatgggggtgctgctgcaacaaggctttcaatgtgcccatcttaggtgggagaagctagatcctgtgcagcagcctggtaagtcctgaggaggttccattgctcttcctgctgctgtcctttgcttctcaacggtggctcgctctacagtctagagcacatgcagctaacttgtgcctctgcttatgcatgagggttaaattaacaaccataaccttcatttgaagttcaaaggtgtattcaggatcctcaaagcattttaaccttgccgcttaaaacccaatttaccgtgaaatgggaattttgctgcattgttaaactgtagtggaaaccatgctatagtaataaaggttatataagagagaaattgaaattaaatgtgtttttaaatttcaaaaaaaaatcaatctttaggatgacttaaaaattgatttgccatgtaaaatgtatctgcattttttacacaaaacttgttttaagcataaaattttaaaactgtactacttgatgtattatacattttgaaccatatgtattaaaccataaacagtataatgttgttataataaaacaggcaataaatttataaataaaagctgaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:1830 -> Molecular function: GO:0005509 [calcium ion binding] evidence: IEA
GeneID:1830 -> Biological process: GO:0006915 [apoptotic process] evidence: TAS
GeneID:1830 -> Biological process: GO:0006921 [cellular component disassembly involved in execution phase of apoptosis] evidence: TAS
GeneID:1830 -> Biological process: GO:0007156 [homophilic cell adhesion] evidence: IEA
GeneID:1830 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
GeneID:1830 -> Cellular component: GO:0005886 [plasma membrane] evidence: TAS
GeneID:1830 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA
GeneID:1830 -> Cellular component: GO:0030057 [desmosome] evidence: IEA
by
@meso_cacase at
DBCLS
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