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2024-04-26 08:45:21, GGRNA : RefSeq release 60 (20130726)
LOCUS XM_003960896 684 bp mRNA linear PRI 30-OCT-2012
DEFINITION PREDICTED: Homo sapiens late cornified envelope 4A (LCE4A), mRNA.
ACCESSION XM_003960896
VERSION XM_003960896.1 GI:410169997
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
COMMENT MODEL REFSEQ: This record is predicted by automated computational
analysis. This record is derived from a genomic sequence
(NW_001838529) annotated using gene prediction method: GNOMON,
supported by EST evidence.
Also see:
Documentation of NCBI's Annotation Process
##Genome-Annotation-Data-START##
Annotation Provider :: NCBI
Annotation Status :: Full annotation
Annotation Version :: Homo sapiens Annotation Release 104
Annotation Pipeline :: NCBI eukaryotic genome annotation pipeline
Annotation Method :: Best-placed RefSeq; Gnomon
Features Annotated :: Gene; mRNA; CDS; ncRNA
##Genome-Annotation-Data-END##
FEATURES Location/Qualifiers
source 1..684
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="1"
/sex="male"
/dev_stage="adult"
gene 1..684
/gene="LCE4A"
/note="Derived by automated computational analysis using
gene prediction method: GNOMON. Supporting evidence
includes similarity to: 2 ESTs"
/db_xref="GeneID:199834"
/db_xref="HGNC:16613"
/db_xref="MIM:612618"
CDS 41..568
/gene="LCE4A"
/codon_start=1
/product="uncharacterized protein LOC199834"
/protein_id="XP_003960945.1"
/db_xref="GI:410169998"
/db_xref="GeneID:199834"
/db_xref="HGNC:16613"
/db_xref="MIM:612618"
/translation="
MKPGGRRMSGMTPHLCNSHVLLLPLAWLIRGPAPGSIQSVFLLLASHLLCFLRDVSVAASEPTVYRNPTKMSCQQNQQQCQPPPKCPIPKYPPKCPSKCASSCPPPISSCCGSSSGGCCSSGGCGCCSSEGGGCCLSHHRHHRSHCHRPKSSNCYGSGSGQQSGGSGCCSGGGCC
"
variation 63
/gene="LCE4A"
/replace="c"
/replace="t"
/db_xref="dbSNP:190753626"
variation 79
/gene="LCE4A"
/replace="a"
/replace="g"
/db_xref="dbSNP:12033945"
variation 178
/gene="LCE4A"
/replace="g"
/replace="t"
/db_xref="dbSNP:201745923"
variation 217
/gene="LCE4A"
/replace="a"
/replace="g"
/db_xref="dbSNP:111624447"
variation 236
/gene="LCE4A"
/replace="c"
/replace="t"
/db_xref="dbSNP:144247009"
variation 242
/gene="LCE4A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1332496"
variation 252
/gene="LCE4A"
/replace="a"
/replace="t"
/db_xref="dbSNP:151125573"
variation 259
/gene="LCE4A"
/replace="a"
/replace="c"
/db_xref="dbSNP:147765240"
variation 300
/gene="LCE4A"
/replace="c"
/replace="t"
/db_xref="dbSNP:200910232"
variation 302
/gene="LCE4A"
/replace="a"
/replace="g"
/db_xref="dbSNP:41268472"
variation 310
/gene="LCE4A"
/replace="c"
/replace="g"
/db_xref="dbSNP:370378908"
variation 350
/gene="LCE4A"
/replace="c"
/replace="t"
/db_xref="dbSNP:199807622"
variation 354
/gene="LCE4A"
/replace="c"
/replace="t"
/db_xref="dbSNP:200796580"
variation 369
/gene="LCE4A"
/replace="g"
/replace="t"
/db_xref="dbSNP:371078921"
variation 372
/gene="LCE4A"
/replace="a"
/replace="g"
/db_xref="dbSNP:138799465"
variation 379..380
/gene="LCE4A"
/replace=""
/replace="agctctgggggctgctgt"
/db_xref="dbSNP:6143428"
variation 379
/gene="LCE4A"
/replace="c"
/replace="t"
/db_xref="dbSNP:200890315"
variation 380..381
/gene="LCE4A"
/replace=""
/replace="agctctgggggctgctgt"
/db_xref="dbSNP:33921874"
variation 388
/gene="LCE4A"
/replace="c"
/replace="g"
/db_xref="dbSNP:200223098"
variation 392..401
/gene="LCE4A"
/replace=""
/replace="tgtggt"
/db_xref="dbSNP:113617356"
variation 393..395
/gene="LCE4A"
/replace=""
/replace="ctgtagctctgggggctg"
/db_xref="dbSNP:11269814"
variation 395..396
/gene="LCE4A"
/replace=""
/replace="ctgtagctctgggggctg"
/db_xref="dbSNP:34855202"
variation 395
/gene="LCE4A"
/replace="c"
/replace="t"
/db_xref="dbSNP:74871420"
variation 396
/gene="LCE4A"
/replace="g"
/replace="t"
/db_xref="dbSNP:79268808"
variation 429
/gene="LCE4A"
/replace="a"
/replace="g"
/db_xref="dbSNP:118176527"
variation 436
/gene="LCE4A"
/replace="a"
/replace="t"
/db_xref="dbSNP:141839549"
variation 439
/gene="LCE4A"
/replace="c"
/replace="t"
/db_xref="dbSNP:117220394"
variation 457
/gene="LCE4A"
/replace="c"
/replace="g"
/db_xref="dbSNP:375783060"
variation 465
/gene="LCE4A"
/replace="a"
/replace="g"
/db_xref="dbSNP:199914704"
variation 486
/gene="LCE4A"
/replace="c"
/replace="t"
/db_xref="dbSNP:185961871"
variation 517
/gene="LCE4A"
/replace="c"
/replace="t"
/db_xref="dbSNP:375297518"
variation 552
/gene="LCE4A"
/replace="g"
/replace="t"
/db_xref="dbSNP:10888510"
variation 562
/gene="LCE4A"
/replace="c"
/replace="t"
/db_xref="dbSNP:4845465"
variation 573
/gene="LCE4A"
/replace="c"
/replace="g"
/db_xref="dbSNP:376871904"
variation 602
/gene="LCE4A"
/replace="c"
/replace="g"
/db_xref="dbSNP:73011196"
variation 605
/gene="LCE4A"
/replace="a"
/replace="g"
/db_xref="dbSNP:141892122"
variation 613
/gene="LCE4A"
/replace="c"
/replace="t"
/db_xref="dbSNP:376970394"
variation 656
/gene="LCE4A"
/replace="c"
/replace="t"
/db_xref="dbSNP:371845656"
ORIGIN
agaggctatctgggaagctcatcatccagctcaggaagagatgaaaccaggaggcaggagaatgtcaggcatgaccccacacttgtgcaacagccacgtcctgctcctgccattagcatggctcatccgaggcccagccccaggatccatacaaagtgtgttcctgctgctggcttctcatctgctctgcttcctaagggacgtatctgttgctgcgtctgaacccacggtttatcgaaatcccaccaagatgtcctgccagcagaaccaacagcagtgccagccccctcccaagtgtcctatccccaagtatcccccaaaatgtccctcaaagtgtgcatcctcatgcccacctccaatctcttcctgctgtggctccagctctgggggctgctgtagctctgggggctgtggttgctgcagctctgagggaggtggctgctgcctgagccaccacagacaccataggtcccactgccacagacccaagagctccaattgctatggcagtggcagtggccagcagtctgggggttctggctgctgctctggagggggctgttgctgacctggaccaggagcagcaccaaaggaattagtgggcgaaggacccattgcagcctggtgttttacctccttcactctcttgcctttcctttctgtagccccatcaattgaataaac
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:199834 -> Biological process: GO:0031424 [keratinization] evidence: IEA
by
@meso_cacase at
DBCLS
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