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2025-05-09 17:18:22, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_022742 4221 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens coiled-coil domain containing 136 (CCDC136),
transcript variant 1, mRNA.
ACCESSION NM_022742
VERSION NM_022742.4 GI:319655555
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 4221)
AUTHORS Hendrickson,S.L., Lautenberger,J.A., Chinn,L.W., Malasky,M.,
Sezgin,E., Kingsley,L.A., Goedert,J.J., Kirk,G.D., Gomperts,E.D.,
Buchbinder,S.P., Troyer,J.L. and O'Brien,S.J.
TITLE Genetic variants in nuclear-encoded mitochondrial genes influence
AIDS progression
JOURNAL PLoS ONE 5 (9), E12862 (2010)
PUBMED 20877624
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
Publication Status: Online-Only
REFERENCE 2 (bases 1 to 4221)
AUTHORS Lim,J., Hao,T., Shaw,C., Patel,A.J., Szabo,G., Rual,J.F.,
Fisk,C.J., Li,N., Smolyar,A., Hill,D.E., Barabasi,A.L., Vidal,M.
and Zoghbi,H.Y.
TITLE A protein-protein interaction network for human inherited ataxias
and disorders of Purkinje cell degeneration
JOURNAL Cell 125 (4), 801-814 (2006)
PUBMED 16713569
REFERENCE 3 (bases 1 to 4221)
AUTHORS Lehner,B. and Sanderson,C.M.
TITLE A protein interaction framework for human mRNA degradation
JOURNAL Genome Res. 14 (7), 1315-1323 (2004)
PUBMED 15231747
REFERENCE 4 (bases 1 to 4221)
AUTHORS Zhang,X.M., Sheng,S.R., Wang,X.Y., Bin,L.H., Wang,J.R. and Li,G.Y.
TITLE Expression of tumor related gene NAG6 in gastric cancer and
restriction fragment length polymorphism analysis
JOURNAL World J. Gastroenterol. 10 (9), 1361-1364 (2004)
PUBMED 15112360
REMARK GeneRIF: Data suggest that NAG6 may represent a candidate tumor
suppressor gene at 7q31-32 loci associated with gastric carcinoma.
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
BX952188.1, AB058696.1 and AI611323.1.
On Jan 19, 2011 this sequence version replaced gi:115511011.
Transcript Variant: This variant (1) represents the longer
transcript and encodes the longer isoform (1).
##Evidence-Data-START##
Transcript exon combination :: BC150331.1, AB058696.1 [ECO:0000332]
RNAseq introns :: mixed/partial sample support
ERS025084, ERS025085 [ECO:0000350]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-49 BX952188.1 2-50
50-4217 AB058696.1 1-4168
4218-4221 AI611323.1 5-8 c
FEATURES Location/Qualifiers
source 1..4221
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="7"
/map="7q33"
gene 1..4221
/gene="CCDC136"
/gene_synonym="NAG6"
/note="coiled-coil domain containing 136"
/db_xref="GeneID:64753"
/db_xref="HGNC:22225"
/db_xref="MIM:611902"
exon 1..432
/gene="CCDC136"
/gene_synonym="NAG6"
/inference="alignment:Splign:1.39.8"
variation 59
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:73238120"
variation 64
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="c"
/db_xref="dbSNP:188002290"
misc_feature 66..68
/gene="CCDC136"
/gene_synonym="NAG6"
/note="upstream in-frame stop codon"
variation 107
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="g"
/replace="t"
/db_xref="dbSNP:191625228"
variation 231
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:377037705"
variation 367
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:371820153"
variation 393
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:368197914"
variation 397
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="g"
/replace="t"
/db_xref="dbSNP:201807209"
variation 400
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="c"
/db_xref="dbSNP:183403624"
variation 403
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:369999789"
CDS 417..3881
/gene="CCDC136"
/gene_synonym="NAG6"
/note="isoform 1 is encoded by transcript variant 1;
coiled-coil domain-containing protein 136; nasopharyngeal
carcinoma-associated gene 6 protein"
/codon_start=1
/product="coiled-coil domain-containing protein 136
isoform 1"
/protein_id="NP_073579.4"
/db_xref="GI:319655556"
/db_xref="CCDS:CCDS47704.1"
/db_xref="GeneID:64753"
/db_xref="HGNC:22225"
/db_xref="MIM:611902"
/translation="
MQAMEGEVLLPALYEEEEEEEEEEEEVEEEEEQVQKGGSVGSLSVNKHRGLSLTETELEELRAQVLQLVAELEETRELAGQHEDDSLELQGLLEDERLASAQQAEVFTKQIQQLQGELRSLREEISLLEHEKESELKEIEQELHLAQAEIQSLRQAAEDSATEHESDIASLQEDLCRMQNELEDMERIRGDYEMEIASLRAEMEMKSSEPSGSLGLSDYSGLQEELQELRERYHFLNEEYRALQESNSSLTGQLADLESERTQRATERWLQSQTLSMTSAESQTSEMDFLEPDPEMQLLRQQLRDAEEQMHGMKNKCQELCCELEELQHHRQVSEEEQRRLQRELKCAQNEVLRFQTSHSVTQNEELKSRLCTLQKKYDTSQDEQNELLKMQLQLQTELRQLKVMKSTLVENQSEKELLCRLQKLHLQHQNVTCEKEKLLERQQQLQEELQCHEAELQHLRDTVASFKESNEKDTETHAQLQEMKQLYQASKDELERQKHMYDQLEQDLLLCQLELKELKASHPIPEDKGKCANKCDTLLSRLTELQEKYKASQKEMGQLQMEQCELLEDQRRMQEEQGQLQEELHRLTLPLPKSGLLLKSQELLTKLEDLCELQLLYQGMQEEQKKLIQNQDCVLKEQLEIHEELRRFKESHFQEVLENPDDSKLAKSSKCNRNKQSKLLMEQMQALQVMYDAGQAKQELLQQEQGRLLEERKRLQADLQLCLEEMQLLQVQSPSIKMSLESYGKSYGSMVPSNENCRKTYDTTVDDNESYYKSYTSTQTSSKSFLKSYDSSTSASEAYGKSYCTTSNSSITYKKSYGSTSSSDTCQKSFVSSCTDEEPAEPEDMERFEEMVVKVLIKLQAVQAMYQISQEEHSQLQEQMEKLLAKQKDLKEELDACEREFKECMECLEKPMAPQNDKNEIKELQTKLRELQLQYQASMDEQGRLLVVQEQLEGQLQCCQEELRQLREKRPSVVKEARGKNANKNMNKNANGVKMKKVTKPCSDTSESDLETRKSLEVVLYYKASQRKLDGLAKEEEKKEEMEEEKKEVKEEAKEQCGDELVAEPADPEEAKSTEDQEENEEDKEEEEKEEDSEEEEDDADSSLESPEENNPLRLSESKKSSPTPNPPIFSLPLVGLVVISALLWCWWAETSS
"
misc_feature 3804..3866
/gene="CCDC136"
/gene_synonym="NAG6"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96JN2.3);
transmembrane region"
exon 433..687
/gene="CCDC136"
/gene_synonym="NAG6"
/inference="alignment:Splign:1.39.8"
variation 453
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="g"
/db_xref="dbSNP:372607897"
variation 482
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:192348781"
variation 496
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="t"
/db_xref="dbSNP:375637274"
variation 516
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:201497246"
variation 529
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:143537881"
variation 530
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:376755462"
variation 538
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="g"
/replace="t"
/db_xref="dbSNP:371358536"
variation 539
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:374254797"
variation 578
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:78589071"
variation 593
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:368126722"
variation 601
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:370540126"
variation 614
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:200045449"
variation 686
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:374903912"
exon 688..762
/gene="CCDC136"
/gene_synonym="NAG6"
/inference="alignment:Splign:1.39.8"
exon 763..1086
/gene="CCDC136"
/gene_synonym="NAG6"
/inference="alignment:Splign:1.39.8"
variation 782
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:201330064"
variation 834
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:200870724"
variation 842
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:368166029"
variation 862
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="c"
/db_xref="dbSNP:200585539"
variation 931
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:200189364"
variation 936
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="g"
/replace="t"
/db_xref="dbSNP:201479027"
variation 946
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:374763554"
variation 975
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:142162337"
variation 976
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:372522612"
variation 1002
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="t"
/db_xref="dbSNP:377566040"
variation 1015
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:185493260"
variation 1064
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:117874579"
variation 1068
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="g"
/db_xref="dbSNP:3816887"
variation 1079
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="g"
/db_xref="dbSNP:3816886"
exon 1087..1198
/gene="CCDC136"
/gene_synonym="NAG6"
/inference="alignment:Splign:1.39.8"
variation 1104
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:199931459"
variation 1110
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:373645281"
variation 1132
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="c"
/db_xref="dbSNP:368912903"
variation 1161
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:372216926"
variation 1168
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:193040933"
exon 1199..1364
/gene="CCDC136"
/gene_synonym="NAG6"
/inference="alignment:Splign:1.39.8"
variation 1249
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:143320390"
variation 1276
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:201808958"
variation 1290
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:200137911"
variation 1296
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="c"
/db_xref="dbSNP:367581022"
variation 1310
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="g"
/replace="t"
/db_xref="dbSNP:201520741"
variation 1314
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:373307906"
exon 1365..1505
/gene="CCDC136"
/gene_synonym="NAG6"
/inference="alignment:Splign:1.39.8"
variation 1420
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:377594781"
variation 1434
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="g"
/db_xref="dbSNP:370564304"
variation 1444
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:374412941"
variation 1448
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:142215231"
variation 1477
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:371534652"
exon 1506..1664
/gene="CCDC136"
/gene_synonym="NAG6"
/inference="alignment:Splign:1.39.8"
variation 1568
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="g"
/db_xref="dbSNP:200864528"
variation 1574
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:146397482"
variation 1597
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:138494965"
variation 1613
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:191944826"
variation 1614
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:368845976"
variation 1658
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="g"
/replace="t"
/db_xref="dbSNP:371781556"
variation 1662
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="c"
/db_xref="dbSNP:377302405"
exon 1665..1835
/gene="CCDC136"
/gene_synonym="NAG6"
/inference="alignment:Splign:1.39.8"
variation 1710
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:61746779"
variation 1715
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:377623985"
variation 1794
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="g"
/db_xref="dbSNP:374219801"
variation 1818
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:200328990"
exon 1836..2021
/gene="CCDC136"
/gene_synonym="NAG6"
/inference="alignment:Splign:1.39.8"
variation 1847
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:370349092"
variation 1850
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:374313513"
variation 1883
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="g"
/db_xref="dbSNP:369048158"
variation 1905
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:187408244"
variation 1911
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:150626171"
variation 1932
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:376521370"
variation 1934
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:370969982"
exon 2022..2216
/gene="CCDC136"
/gene_synonym="NAG6"
/inference="alignment:Splign:1.39.8"
variation 2033
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="g"
/db_xref="dbSNP:201409151"
variation 2174
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:368212477"
variation 2214
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:142055253"
exon 2217..2444
/gene="CCDC136"
/gene_synonym="NAG6"
/inference="alignment:Splign:1.39.8"
variation 2220
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="g"
/db_xref="dbSNP:367971232"
variation 2264
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="g"
/db_xref="dbSNP:61740835"
variation 2279
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="g"
/replace="t"
/db_xref="dbSNP:200890079"
variation 2288
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:376477504"
variation 2308
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:202240629"
variation 2310
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="g"
/db_xref="dbSNP:116868322"
variation 2321
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:377096915"
variation 2355
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:200892824"
variation 2356
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:202183336"
variation 2366
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:200162055"
variation 2384
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:375382998"
variation 2399
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:369412186"
variation 2436
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="c"
/db_xref="dbSNP:372613683"
variation 2437
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="g"
/replace="t"
/db_xref="dbSNP:375639275"
exon 2445..2957
/gene="CCDC136"
/gene_synonym="NAG6"
/inference="alignment:Splign:1.39.8"
variation 2461
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="g"
/replace="t"
/db_xref="dbSNP:377491251"
variation 2464
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:186600964"
variation 2477
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:61743943"
variation 2496
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:368143350"
variation 2530
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="c"
/db_xref="dbSNP:370649260"
variation 2552
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="g"
/replace="t"
/db_xref="dbSNP:61742628"
variation 2573
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:374908110"
variation 2648
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:367576294"
variation 2678
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:148305489"
variation 2784
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="t"
/db_xref="dbSNP:372761655"
variation 2793
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:377315858"
variation 2812
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:368815709"
variation 2828
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:372104350"
variation 2832
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:8180870"
variation 2850..2851
/gene="CCDC136"
/gene_synonym="NAG6"
/replace=""
/replace="t"
/db_xref="dbSNP:35530274"
variation 2850
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:376400216"
variation 2857
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:373049285"
variation 2888
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:369363208"
variation 2927
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:189804470"
exon 2958..3179
/gene="CCDC136"
/gene_synonym="NAG6"
/inference="alignment:Splign:1.39.8"
variation 2959
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:371433810"
variation 3012
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:201564680"
variation 3084
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="g"
/replace="t"
/db_xref="dbSNP:377281608"
variation 3098
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:140010464"
variation 3128
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="g"
/db_xref="dbSNP:375061729"
variation 3132
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="c"
/db_xref="dbSNP:367980353"
variation 3153
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:370442842"
variation 3167
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:369180028"
variation 3170
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:374799375"
exon 3180..3461
/gene="CCDC136"
/gene_synonym="NAG6"
/inference="alignment:Splign:1.39.8"
variation 3196
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="c"
/db_xref="dbSNP:374327276"
variation 3204
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:199769669"
variation 3250
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:61730244"
variation 3351
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:201403112"
variation 3352
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:199650087"
variation 3354
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:61730174"
variation 3359
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:371406451"
variation 3427
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:150275906"
variation 3428
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:192407933"
variation 3431
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="g"
/replace="t"
/db_xref="dbSNP:138966292"
variation 3443
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:184775299"
exon 3462..3779
/gene="CCDC136"
/gene_synonym="NAG6"
/inference="alignment:Splign:1.39.8"
variation 3523
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="t"
/db_xref="dbSNP:377595539"
variation 3528
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:201740952"
variation 3561
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="g"
/db_xref="dbSNP:4728137"
variation 3573
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:371133316"
variation 3628
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="t"
/db_xref="dbSNP:189812175"
variation 3638
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:368597564"
variation 3649
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="c"
/db_xref="dbSNP:372024334"
variation 3677
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:56979796"
variation 3706
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:143918184"
variation 3710
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:2270590"
variation 3714
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:374969434"
variation 3715
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:368985899"
variation 3719
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:201209390"
variation 3740
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:371393598"
variation 3741
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:376829002"
exon 3780..3886
/gene="CCDC136"
/gene_synonym="NAG6"
/inference="alignment:Splign:1.39.8"
variation 3782
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:369256399"
variation 3793
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:180873354"
variation 3802
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="g"
/db_xref="dbSNP:199887952"
variation 3872
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:376488298"
variation 3875
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:370532020"
exon 3887..4221
/gene="CCDC136"
/gene_synonym="NAG6"
/inference="alignment:Splign:1.39.8"
variation 4027
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="g"
/replace="t"
/db_xref="dbSNP:146581806"
STS 4049..4179
/gene="CCDC136"
/gene_synonym="NAG6"
/standard_name="D7S2100E"
/db_xref="UniSTS:39686"
variation 4150
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="a"
/replace="g"
/db_xref="dbSNP:184242384"
variation 4205
/gene="CCDC136"
/gene_synonym="NAG6"
/replace="c"
/replace="t"
/db_xref="dbSNP:188901467"
ORIGIN
agcctcttcttcactggctcccgccctctttcagtcttggccctctcctccctgtccccccggactaaatacgcacaccccctctttctttctgtgcaagcaagagggtcctggaacagcgggttctgaggaggctgggaggcagggctgagaggtggccgagagagaggagtcgcagagccgccagagtgagtcaggcacctccactgggattacagatcccagagcctcgaggagctggaagacatgtccccttctttcctctgcaccccagcccgcagccagccccccaccccccagcccctcctttctccctgctctcaggacccacagtgaccactctaggctcctatgaggcttccgagggctgtgagaggaagaagggccaacgctgggggtccctggaacgacgggggatgcaagctatggagggggaggtgttactcccagctctctatgaggaggaagaggaagaggaagaggaggaagaagaggtggaagaagaagaagaacaagtgcagaaaggtggcagtgttggctctctgtcagtcaacaagcaccggggactgagcctcacggagacagagctggaggagctgcgggctcaggtgctgcagctggtggcagaactggaggagacccgggaactggcagggcagcatgaggatgactccttggagctacaggggctcctggaggatgaacggctagccagcgcccagcaggcagaggtgttcaccaagcagatccagcagctccaaggtgagctgcgttctctacgggaggagatttccctgttagagcatgagaaagaaagcgaacttaaggaaatagaacaggaattgcatttggcccaggctgagatccagagtctgcggcaagcagcagaggattccgcaactgaacatgagagtgacatagcatccctgcaggaggatctctgccggatgcagaatgaacttgaagacatggaacgcattcggggagattatgagatggagatcgcctccctccgtgcagaaatggaaatgaagagctctgaaccatccggtagtttaggtctctcagattactctgggttacaagaagaactgcaggagctgcgggaacgctaccatttcctgaatgaggaataccgggccctgcaggagagcaacagcagcctcacggggcagcttgcagatctggagagtgagaggacacagagagcaacagagagatggctgcagtcccaaacactgagtatgacgtcagcagagtctcagacttcagaaatggatttcttagagcctgatcctgaaatgcagttgttacggcagcagctacgggatgctgaagagcagatgcatggcatgaagaacaagtgtcaggaattgtgttgtgagttggaagagctacagcatcatcgccaggtcagtgaggaggagcagaggcggctgcagagggagctcaagtgtgctcagaatgaggtgcttcggtttcagacctcccacagtgtcacccagaatgaggagctgaagtccagactctgtaccctgcagaaaaaatatgatactagccaggatgagcagaacgagctcttgaagatgcagctgcaacttcagactgagctccggcagctcaaagtcatgaaatccacacttgtagaaaaccagagtgagaaggagttactgtgccggctgcagaagctgcacctccagcaccagaacgtcacatgtgagaaggaaaagctgctggaacggcagcagcagctgcaggaggagctgcagtgccatgaggcagagctgcagcacctcagggatacggtggcctccttcaaagagagcaatgagaaggacacagagacgcacgctcagcttcaggagatgaagcagctgtaccaggccagcaaggacgagctggagcggcagaagcacatgtatgaccagctggagcaggacctcctgctctgccagctggagctgaaagagctcaaggcctcccaccccattccggaggacaaaggaaagtgtgctaataagtgtgacacactgctgtccagactgacagaattgcaggaaaagtacaaggccagccagaaggagatggggcagctgcagatggagcagtgtgagctcctggaggatcagaggaggatgcaggaggagcagggccagctgcaggaagagctgcacaggctcacactgccactgccaaagagtggcctcttactcaagagtcaggagctactcaccaagttagaagacctgtgtgagctgcagctgctctaccaaggcatgcaggaggaacagaagaagctgatacagaaccaagactgtgtattaaaagaacaattagagatccacgaagagctgcgacgtttcaaagagtctcatttccaggaagtgttggagaatcccgatgattccaaattggctaagtcctccaaatgtaatcgaaacaagcaatccaagctgctcatggagcagatgcaggccctgcaggtgatgtatgacgccggtcaggcgaagcaggagctcttgcagcaagagcaagggaggctcctagaggagcggaagaggctgcaggcagacttgcagctctgcctggaagaaatgcagctgcttcaagtccagtccccttctataaaaatgagccttgagtcctacgggaagagctatggtagcatggtccccagcaatgagaactgtcgcaagacttatgataccactgtggatgacaatgagagctattacaagagttacaccagcacccagaccagcagcaagagctttctcaagagctatgacagcagcaccagtgccagtgaggcctatgggaagagttactgcactaccagcaacagcagcattacctataagaagagttacggcagcaccagtagctctgacacctgccagaagagttttgtcagcagctgcactgacgaggaacctgctgagcctgaagacatggagcgctttgaggaaatggttgtgaaagtgctgatcaagctgcaggcggtgcaggccatgtaccagataagccaggaggaacacagccagctgcaagagcagatggaaaagttactggccaagcagaaagacctgaaggaagagctggatgcctgtgaaagggagttcaaggagtgcatggaatgccttgaaaagcccatggccccccagaacgacaagaatgagatcaaagaactgcagaccaagctgcgggagctgcagctgcaataccaggctagcatggatgagcaggggcggcttctggtagtgcaggagcagctggaggggcagctgcagtgctgccaggaggagctccgccagctcagggagaagaggccttctgttgtcaaagaagcccgggggaagaatgctaataagaacatgaacaagaatgccaatggggttaaaatgaaaaaggtgaccaagccatgctcggatacttctgagagcgaccttgagaccagaaagagtctggaggtagtgctgtactacaaggccagccagaggaaattagatggactagcaaaagaggaggaaaagaaagaggagatggaggaggaaaaaaaggaagtgaaagaggaagcaaaggagcagtgtggggatgagctagttgctgagccagcagatcctgaggaagctaaatccacagaagatcaggaggaaaatgaagaggacaaagaggaagaggagaaggaagaagacagtgaagaggaggaggatgacgccgactcttcccttgaaagtcccgaagaaaataaccccctcagactttccgagagcaaaaagtcatcccctacccccaatccccccatcttctccttgcctcttgtaggcctggtggtcatctcggctttgctctggtgctggtgggctgagacgtcgtcctaatgcagaacatgtttgggttgtggaagcctatggtattcttggctattgcagctgtggctctgtatgtgttacccaacatgcgacagcaggagtcagagttctgcctcatggagtgatggcagaccttggccagcgcgagggcagatccccagtggccaccaccctcagctttgggcaggacacactgtgccagaaccctccccatatgttccatgtgtccccatctcctcagcctcagtcacccaggctgaaaaggcttgtggggagcggctgacttccatctcctgccttgtgtaagaacctgagttccttgtaattaaatatcaactgaattacatga
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:64753 -> Cellular component: GO:0005739 [mitochondrion] evidence: IEA
GeneID:64753 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA
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DBCLS
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