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Previous release (v1)
2024-05-01 12:18:37, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_001276331 628 bp mRNA linear PRI 27-DEC-2022
DEFINITION Homo sapiens late cornified envelope 1C (LCE1C), transcript variant
2, mRNA.
ACCESSION NM_001276331
VERSION NM_001276331.2
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 628)
AUTHORS Luck K, Kim DK, Lambourne L, Spirohn K, Begg BE, Bian W, Brignall
R, Cafarelli T, Campos-Laborie FJ, Charloteaux B, Choi D, Cote AG,
Daley M, Deimling S, Desbuleux A, Dricot A, Gebbia M, Hardy MF,
Kishore N, Knapp JJ, Kovacs IA, Lemmens I, Mee MW, Mellor JC,
Pollis C, Pons C, Richardson AD, Schlabach S, Teeking B, Yadav A,
Babor M, Balcha D, Basha O, Bowman-Colin C, Chin SF, Choi SG,
Colabella C, Coppin G, D'Amata C, De Ridder D, De Rouck S,
Duran-Frigola M, Ennajdaoui H, Goebels F, Goehring L, Gopal A,
Haddad G, Hatchi E, Helmy M, Jacob Y, Kassa Y, Landini S, Li R, van
Lieshout N, MacWilliams A, Markey D, Paulson JN, Rangarajan S,
Rasla J, Rayhan A, Rolland T, San-Miguel A, Shen Y, Sheykhkarimli
D, Sheynkman GM, Simonovsky E, Tasan M, Tejeda A, Tropepe V,
Twizere JC, Wang Y, Weatheritt RJ, Weile J, Xia Y, Yang X,
Yeger-Lotem E, Zhong Q, Aloy P, Bader GD, De Las Rivas J, Gaudet S,
Hao T, Rak J, Tavernier J, Hill DE, Vidal M, Roth FP and Calderwood
MA.
TITLE A reference map of the human binary protein interactome
JOURNAL Nature 580 (7803), 402-408 (2020)
PUBMED 32296183
REFERENCE 2 (bases 1 to 628)
AUTHORS Sun L, Cao Y, He N, Han J, Hai R, Arlud S, He B, Wu W, Li L, Su X,
Cui H, Zhao W, Chao B, Liu D, Sun Z and Huang Y.
TITLE Association between LCE gene polymorphisms and psoriasis vulgaris
among Mongolians from Inner Mongolia
JOURNAL Arch Dermatol Res 310 (4), 321-327 (2018)
PUBMED 29397434
REMARK GeneRIF: genetic polymorphism is associated with psoriasis vulgaris
among Mongolians from Inner Mongolia
REFERENCE 3 (bases 1 to 628)
AUTHORS Yabuta N, Ota C, Sasakura T, Naito Y, Okuzaki D, Fukushima K and
Nojima H.
TITLE Late cornified envelope 1C (LCE1C), a transcriptional target of
TAp63 phosphorylated at T46/T281, interacts with PRMT5
JOURNAL Sci Rep 8 (1), 4892 (2018)
PUBMED 29559659
REMARK GeneRIF: Luciferase reporter assays using the promoter region of
the LCE1C gene confirmed that the phosphorylations of
TAp63-T46/T281 contributed to full transcriptional activation of
the LCE1C gene. LCE1C interacted with protein arginine
methyltransferase 5 (PRMT5) and translocated it from the nucleus to
the cytoplasm.
Publication Status: Online-Only
REFERENCE 4 (bases 1 to 628)
AUTHORS Bowes J, Flynn E, Ho P, Aly B, Morgan AW, Marzo-Ortega H, Coates L,
McManus R, Ryan AW, Kane D, Korendowych E, McHugh N, FitzGerald O,
Packham J, Bruce IN and Barton A.
TITLE Variants in linkage disequilibrium with the late cornified envelope
gene cluster deletion are associated with susceptibility to
psoriatic arthritis
JOURNAL Ann Rheum Dis 69 (12), 2199-2203 (2010)
PUBMED 20643763
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 5 (bases 1 to 628)
AUTHORS Jackson B, Tilli CM, Hardman MJ, Avilion AA, MacLeod MC, Ashcroft
GS and Byrne C.
TITLE Late cornified envelope family in differentiating
epithelia--response to calcium and ultraviolet irradiation
JOURNAL J Invest Dermatol 124 (5), 1062-1070 (2005)
PUBMED 15854049
REMARK GeneRIF: paper describing nomenclature changes and expression in
range of tissues and in response to UV
REFERENCE 6 (bases 1 to 628)
AUTHORS Marshall D, Hardman MJ, Nield KM and Byrne C.
TITLE Differentially expressed late constituents of the epidermal
cornified envelope
JOURNAL Proc Natl Acad Sci U S A 98 (23), 13031-13036 (2001)
PUBMED 11698679
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AL353779.11.
On Jun 2, 2019 this sequence version replaced NM_001276331.1.
Transcript Variant: This variant (2) lacks an in-frame segment
compared to variant 1. The resulting isoform (2) has the same N-
and C-termini but is shorter compared to isoform 1.
Sequence Note: The RefSeq transcript and protein were derived from
genomic sequence to make the sequence consistent with the reference
genome assembly. The genomic coordinates used for the transcript
record were based on alignments.
##Evidence-Data-START##
Transcript exon combination :: AA029646.1 [ECO:0000332]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-51 AL353779.11 91004-91054 c
52-115 AL353779.11 89838-89901 c
116-628 AL353779.11 89235-89747 c
FEATURES Location/Qualifiers
source 1..628
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="1"
/map="1q21.3"
gene 1..628
/gene="LCE1C"
/gene_synonym="LEP3"
/note="late cornified envelope 1C"
/db_xref="GeneID:353133"
/db_xref="HGNC:HGNC:29464"
/db_xref="MIM:612605"
exon 1..51
/gene="LCE1C"
/gene_synonym="LEP3"
/inference="alignment:Splign:2.1.0"
variation 2
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1201420114"
variation 6
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1047018122"
variation 10
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:577274560"
variation 15
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252947394"
variation 16
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:929764049"
variation 18
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/db_xref="dbSNP:563618743"
variation 19
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="g"
/replace="t"
/db_xref="dbSNP:919793944"
variation 21
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652350081"
variation 24
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652350024"
variation 29
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1235328743"
variation 30..32
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1476069301"
variation 30
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:543654250"
variation 31
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652349854"
variation 35
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="g"
/replace="t"
/db_xref="dbSNP:2101588033"
variation 40..41
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1652349718"
variation 42
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:973818211"
variation 43
/gene="LCE1C"
/gene_synonym="LEP3"
/replace=""
/replace="g"
/db_xref="dbSNP:779797924"
variation 46
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1464034015"
variation 47
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:937131942"
variation 49
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:922955940"
variation 50
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:541923804"
variation 51
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:554876729"
exon 52..115
/gene="LCE1C"
/gene_synonym="LEP3"
/inference="alignment:Splign:2.1.0"
variation 52
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:772872756"
variation 54
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1374919058"
variation 60..61
/gene="LCE1C"
/gene_synonym="LEP3"
/replace=""
/replace="ac"
/db_xref="dbSNP:1652313128"
variation 60
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:764848536"
variation 62
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:17624493"
variation 63
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:756695380"
variation 64
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:751224806"
variation 67
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:375935802"
variation 69
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:775504023"
variation 71..74
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="g"
/replace="gatg"
/db_xref="dbSNP:1303843171"
CDS 72..338
/gene="LCE1C"
/gene_synonym="LEP3"
/note="isoform 2 is encoded by transcript variant 2; late
envelope protein 3; late cornified envelope protein 1C"
/codon_start=1
/product="late cornified envelope protein 1C isoform 2"
/protein_id="NP_001263260.1"
/db_xref="GeneID:353133"
/db_xref="HGNC:HGNC:29464"
/db_xref="MIM:612605"
/translation="
MSCQQSQQQCQPPPNVSSGGCCGSSSGGSCGSSSGGCCSSGGGGCCLSHHRRRRSHCHRPQSSGCCSQPSGGSSCCGGGSGQHSGGCC"
variation 76
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:771170567"
variation 77
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:139069429"
variation 78
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1346724469"
variation 79
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1309452653"
variation 81..98
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="cagcagagccagcagcag"
/replace="cagcagagccagcagcagagccagcagcag"
/db_xref="dbSNP:2101587239"
variation 82
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:778176107"
variation 83
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:756283945"
variation 84
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1399132761"
variation 85
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652311045"
variation 88
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:748601190"
variation 89
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1361165739"
variation 90
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:781421464"
variation 98
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/db_xref="dbSNP:373823062"
variation 100
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1361366944"
variation 103
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652310235"
variation 105..109
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="ccccc"
/replace="ccccccc"
/db_xref="dbSNP:1652309898"
variation 105
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1300829674"
variation 107
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1349658712"
variation 109
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1052019392"
variation 112
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1434106846"
variation 113
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380993768"
variation 114
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:755301041"
variation 115
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1044914690"
exon 116..628
/gene="LCE1C"
/gene_synonym="LEP3"
/inference="alignment:Splign:2.1.0"
variation 116
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:776767449"
variation 119..148
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="cagctccggaggctgctgtggctccagctc"
/replace="cagctccggaggctgctgtggctccagctccggaggctgctgtggctc
cagctc"
/db_xref="dbSNP:755608024"
variation 119
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/db_xref="dbSNP:768892178"
variation 120
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1424192407"
variation 124..125
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="cc"
/db_xref="dbSNP:763594949"
variation 125
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:747442143"
variation 126
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:780385036"
variation 128
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:372416698"
variation 131
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1031491975"
variation 133..178
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="gctgtggctccagctctggggg"
/replace="gctgtggctccagctctgggggcagctgtggctccagctctggggg"
/replace="gctgtggctccagctctgggggcagctgtggctccagctctgggggca
gctgtggctccagctctggggg"
/db_xref="dbSNP:752311639"
variation 134
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:746381820"
variation 140
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:999890851"
variation 146
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1370662305"
variation 148
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/db_xref="dbSNP:779438640"
variation 149
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756743626"
variation 150
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1271693906"
variation 152
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:753370924"
variation 153
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1319225339"
variation 154
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652302529"
variation 155
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:148874685"
variation 156
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:755811433"
variation 157
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1325994997"
variation 158
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1323018263"
variation 168
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:752335872"
variation 169
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652301970"
variation 170
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200339777"
variation 171..197
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="tctggggga"
/replace="tctgggggatgctgcagttctggggga"
/db_xref="dbSNP:767242134"
variation 172
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:2101587023"
variation 173
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652301801"
variation 174
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1416299402"
variation 175
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1369001286"
variation 177
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1323672259"
variation 178
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:534849272"
variation 179
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:565723067"
variation 181
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="g"
/replace="t"
/db_xref="dbSNP:146157684"
variation 186
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:761838249"
variation 191
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1460381884"
variation 192
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/db_xref="dbSNP:150691692"
variation 193
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1198900688"
variation 194
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1455322676"
variation 196
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1250687086"
variation 199
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:768924444"
variation 200
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1570862768"
variation 209
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:760901253"
variation 210
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:775624987"
variation 213
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:202080650"
variation 218
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652298655"
variation 219
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:897982826"
variation 221
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:746185600"
variation 222
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652298382"
variation 223
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:779340672"
variation 224
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:549773903"
variation 225
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:771441994"
variation 226
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:748802687"
variation 228
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:777347540"
variation 229
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:755616563"
variation 230
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:747831816"
variation 232
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/db_xref="dbSNP:2101586952"
variation 233
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1389635773"
variation 235
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1395621558"
variation 236
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652297582"
variation 239
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1172666833"
variation 240
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:201333896"
variation 242..243
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1557838997"
variation 242
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:754868295"
variation 244
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:751337361"
variation 247
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652297105"
variation 248
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:766294594"
variation 249
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1439902925"
variation 251
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1213885706"
variation 253
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1570862656"
variation 255
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652296681"
variation 258
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:112500812"
variation 260
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1570862651"
variation 262
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652296455"
variation 265
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1235003747"
variation 266
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:2101586920"
variation 268..281
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="g"
/replace="gcagccagccctcg"
/db_xref="dbSNP:1275538191"
variation 269..274
/gene="LCE1C"
/gene_synonym="LEP3"
/replace=""
/replace="cagcca"
/db_xref="dbSNP:759109278"
variation 272
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:758343976"
variation 277..283
/gene="LCE1C"
/gene_synonym="LEP3"
/replace=""
/replace="cctcggg"
/db_xref="dbSNP:750879799"
variation 277
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:2101586915"
variation 278
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1257411121"
variation 279
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652296139"
variation 280
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200121117"
variation 281..286
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="ggggg"
/replace="gggggg"
/replace="ggggggg"
/db_xref="dbSNP:765643412"
variation 281
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:200605256"
variation 282
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1279674492"
variation 283
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:931565459"
variation 284
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:368153386"
variation 285
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:775714867"
variation 286
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:767707238"
variation 289
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/db_xref="dbSNP:759862182"
variation 291
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1334826281"
variation 292
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652294530"
variation 293
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:760746628"
variation 295
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="g"
/replace="t"
/db_xref="dbSNP:377075809"
variation 298
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:115724302"
variation 299
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1311714433"
variation 302
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:551622346"
variation 303
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:747638102"
variation 304
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:781031344"
variation 305
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:372400123"
variation 306
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1286984751"
variation 308
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:779913339"
variation 309
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201754622"
variation 310
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:750408036"
variation 311
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="g"
/replace="t"
/db_xref="dbSNP:765113175"
variation 313
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756237878"
variation 314
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/db_xref="dbSNP:752746104"
variation 315
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1173330660"
variation 317
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:367971555"
variation 319
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1652292504"
variation 322
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1431799250"
variation 324
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:968583720"
variation 326
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:774367291"
variation 329
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:766794610"
variation 330
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652292025"
variation 331
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1017739317"
variation 332
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:201538693"
variation 333
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:773903042"
variation 336
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:770392039"
variation 337
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1292162758"
variation 341
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652291548"
variation 342
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:761481026"
variation 345
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1346604317"
variation 346
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:776268603"
variation 347
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:767993345"
variation 351
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:73018626"
variation 354
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:771926294"
variation 357
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:745644373"
variation 359
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:376188566"
variation 360
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652290596"
variation 362
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1048534"
variation 363
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:999323258"
variation 364
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652290024"
variation 366
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="t"
/db_xref="dbSNP:531919609"
variation 368
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:563162977"
variation 372
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="g"
/replace="t"
/db_xref="dbSNP:754969018"
variation 374..375
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2101586761"
variation 374
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1273618948"
variation 375
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:367658244"
variation 376
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201367303"
variation 378
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1272401605"
variation 380
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1207823041"
variation 382
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1215085178"
variation 383
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:763414543"
variation 385
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1439057279"
variation 394
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:201054908"
variation 397
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368758259"
variation 398
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652288588"
variation 401..405
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="ct"
/replace="ctcct"
/db_xref="dbSNP:1652288522"
variation 406
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1395659977"
variation 407
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:949521522"
variation 412
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652288339"
variation 414
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1331909894"
variation 415
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="g"
/replace="t"
/db_xref="dbSNP:570994530"
variation 424
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1284721716"
variation 425
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1052360232"
variation 429
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1466702566"
variation 431
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652287996"
variation 433
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1163724358"
variation 435
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1200551008"
variation 437
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1246885685"
variation 439
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652287726"
variation 445
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:942788604"
variation 448
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652287520"
variation 450
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="t"
/db_xref="dbSNP:137884439"
variation 454
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652287383"
variation 455
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:183795360"
variation 456
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:572081202"
variation 464
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:753771252"
variation 466
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652287082"
variation 467
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="t"
/db_xref="dbSNP:529271349"
variation 471
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1048535"
variation 475
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652286722"
variation 478
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652286660"
variation 480
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/db_xref="dbSNP:1652286593"
variation 482
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1365950771"
variation 486
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:918805114"
variation 490
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1325815495"
variation 494
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="t"
/db_xref="dbSNP:978708963"
variation 497
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:968950410"
variation 499
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:910426018"
variation 505
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652286141"
variation 507
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1441727782"
variation 512
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1180075029"
variation 516
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1437556888"
variation 517
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:972879312"
variation 518
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1652283748"
variation 519
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652283683"
variation 522
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652283627"
variation 524
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:986270331"
variation 529
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1570862298"
variation 532
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:538785806"
variation 534
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:938893301"
variation 539
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:928799216"
variation 544
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="aa"
/db_xref="dbSNP:144897268"
variation 545
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1459197641"
variation 546
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652283112"
variation 547
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1436905076"
variation 551
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1201998128"
variation 553
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:865980563"
variation 554
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1216024155"
variation 555
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1187144841"
variation 559
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1652282168"
variation 565
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="g"
/replace="t"
/db_xref="dbSNP:1415530208"
variation 567
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:954455280"
variation 571
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652281987"
variation 575
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652281936"
variation 578
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652281893"
variation 580..583
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="aatg"
/replace="aatgaatg"
/db_xref="dbSNP:1652281658"
variation 580
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652281814"
variation 581
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1030103897"
variation 582
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652281711"
variation 589
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1652281594"
variation 592
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1471865938"
variation 593
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652281459"
variation 594
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:373672565"
variation 595
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:4845487"
variation 598
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1306343745"
variation 599
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557838755"
variation 604
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:1372798074"
regulatory 607..612
/regulatory_class="polyA_signal_sequence"
/gene="LCE1C"
/gene_synonym="LEP3"
/note="hexamer: ATTAAA"
variation 611
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1652280798"
variation 613
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1232373308"
variation 614
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1557838750"
variation 617
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="t"
/db_xref="dbSNP:1016514756"
variation 625
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:916250066"
variation 626
/gene="LCE1C"
/gene_synonym="LEP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:1329385702"
polyA_site 628
/gene="LCE1C"
/gene_synonym="LEP3"
/note="major polyA site"
ORIGIN
atccactcacctcccgaggtgctgaaggaccctgtgctgcctgtgaccccgctcctgaatccgccaccaagatgtcctgccagcagagccagcagcagtgccagccccctcccaatgtcagctccggaggctgctgtggctccagctctgggggcagctgtggctccagctctgggggatgctgcagttctgggggaggtggctgctgcctgagccaccacaggcgccgtaggtcccactgccacagaccccagagctctggctgctgcagccagccctcggggggctccagctgctgtggcggggggagtggccagcactctggaggctgctgctgaagtggaccctgagcctagaagagcagaatccaggaccgcaaactgccaaggacatcccccttctcctactaggcctgcctgagaggctcacaggtccaagggaaagctctgaacttgccaagagcatatcttttccctggagtccagaaactcagatcctctcctggatctccattcactggccttggacctcacctttgtggctaccctcccacgctctgtctaagcccctagcttactcaatgtcatttgcagcgtgcatctgctgattaaaggactaaaacaaggaa
//
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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