Home |
Help |
Advanced search
2025-05-12 01:57:12, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001195278 10558 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens transmembrane protein 178B (TMEM178B), mRNA.
ACCESSION NM_001195278 XM_001714428 XM_001716072 XM_001716337 XM_001716921
XM_001723883 XM_001724518 XM_002344396 XM_002344427
VERSION NM_001195278.1 GI:305632806
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 10558)
AUTHORS Rose,J.E., Behm,F.M., Drgon,T., Johnson,C. and Uhl,G.R.
TITLE Personalized smoking cessation: interactions between nicotine dose,
dependence and quit-success genotype score
JOURNAL Mol. Med. 16 (7-8), 247-253 (2010)
PUBMED 20379614
REMARK GeneRIF: Clinical trial of gene-disease association and
gene-environment interaction. (HuGE Navigator)
GeneRIF: Clinical trial of gene-disease association and
gene-environment interaction. (HuGE Navigator)
Erratum:[Mol Med. 2012;18(1):729]
COMMENT PROVISIONAL REFSEQ: This record has not yet been subject to final
NCBI review. The reference sequence was derived from AC006362.2,
AC006396.1, AC005692.1 and AC073878.7.
On or before Sep 2, 2010 this sequence version replaced
gi:169171976, gi:239509055, gi:239509058, gi:169171015,
gi:169171557, gi:239743363, gi:239749266, gi:239754718.
Sequence Note: The RefSeq transcript and protein were derived from
genomic sequence because no single transcript was available for the
full length of the gene. The genomic coordinates used for the
transcript record were based on transcript and protein alignments.
##Evidence-Data-START##
RNAseq introns :: mixed/partial sample support ERS025082, ERS025083
[ECO:0000350]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-461 AC006362.2 28301-28761
462-575 AC006396.1 37437-37550
576-713 AC005692.1 43863-44000
714-10558 AC073878.7 14455-24299
FEATURES Location/Qualifiers
source 1..10558
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="7"
/map="7q34"
gene 1..10558
/gene="TMEM178B"
/note="transmembrane protein 178B"
/db_xref="GeneID:100507421"
/db_xref="HGNC:44112"
exon 1..461
/gene="TMEM178B"
/inference="alignment:Splign:1.39.8"
variation 16
/gene="TMEM178B"
/replace="c"
/replace="g"
/db_xref="dbSNP:368492073"
misc_feature 62..64
/gene="TMEM178B"
/note="upstream in-frame stop codon"
CDS 80..964
/gene="TMEM178B"
/codon_start=1
/product="transmembrane protein 178B precursor"
/protein_id="NP_001182207.1"
/db_xref="GI:305632807"
/db_xref="CCDS:CCDS59086.1"
/db_xref="GeneID:100507421"
/db_xref="HGNC:44112"
/translation="
MAAGRLLLYTGLSLALCALGMLAVAICSDHWYETDARKHRDRCKAFNTRRVDPGFIYNNNNNLPLRASRSRLDRWEGKLLRARNRRQLFAMSPADECSRQYNSTNMGLWRKCHRQGFDPEIAALIRKGEIERCTYIKYHYSSATIPRNLTFNITKTIRQDEWHALHLRRMTAGFMGMAVAIILFGWIIGVLGCCWDRGLMQYVAGLLFLMGGTFCIISLCTCVAGINFELSRYPRYLYGLPDDISHGYGWSMFCAWGGLGLTLISGFFCTLAPSVQPVPRTNYPKSRPENGTVC
"
sig_peptide 80..148
/gene="TMEM178B"
/inference="COORDINATES: ab initio prediction:SignalP:4.0"
mat_peptide 149..961
/gene="TMEM178B"
/product="Transmembrane protein 178B"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (H3BS89.1)"
misc_feature <566..877
/gene="TMEM178B"
/note="PMP-22/EMP/MP20/Claudin tight junction; Region:
Claudin_2; pfam13903"
/db_xref="CDD:222446"
misc_feature 593..655
/gene="TMEM178B"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (H3BS89.1);
transmembrane region"
misc_feature 695..757
/gene="TMEM178B"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (H3BS89.1);
transmembrane region"
misc_feature 833..895
/gene="TMEM178B"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (H3BS89.1);
transmembrane region"
variation 212
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:139501428"
variation 324
/gene="TMEM178B"
/replace="a"
/replace="c"
/db_xref="dbSNP:113786640"
variation 333
/gene="TMEM178B"
/replace="g"
/replace="t"
/db_xref="dbSNP:370682172"
variation 436..437
/gene="TMEM178B"
/replace=""
/replace="g"
/db_xref="dbSNP:200269993"
variation 436
/gene="TMEM178B"
/replace="c"
/replace="g"
/db_xref="dbSNP:477223"
exon 462..575
/gene="TMEM178B"
/inference="alignment:Splign:1.39.8"
exon 576..713
/gene="TMEM178B"
/inference="alignment:Splign:1.39.8"
variation 628
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:13233459"
variation 643
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:112679326"
exon 714..10558
/gene="TMEM178B"
/inference="alignment:Splign:1.39.8"
variation 793
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:58854811"
variation 907
/gene="TMEM178B"
/replace="a"
/replace="c"
/db_xref="dbSNP:182507206"
variation 992
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:187206014"
variation 997..998
/gene="TMEM178B"
/replace=""
/replace="at"
/db_xref="dbSNP:113071559"
variation 998..999
/gene="TMEM178B"
/replace=""
/replace="ta"
/db_xref="dbSNP:112680169"
variation 1099
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:192041678"
variation 1163
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:149177705"
variation 1219
/gene="TMEM178B"
/replace="c"
/replace="g"
/db_xref="dbSNP:184640815"
variation 1223
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:143685011"
variation 1225
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:373703440"
variation 1237
/gene="TMEM178B"
/replace="a"
/replace="t"
/db_xref="dbSNP:190318459"
variation 1279
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:376794033"
variation 1337
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:146857722"
variation 1408
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:375357851"
variation 1447
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:76916720"
variation 1448
/gene="TMEM178B"
/replace="g"
/replace="t"
/db_xref="dbSNP:140652705"
variation 1549
/gene="TMEM178B"
/replace="a"
/replace="c"
/db_xref="dbSNP:145906901"
variation 1588
/gene="TMEM178B"
/replace="a"
/replace="c"
/db_xref="dbSNP:193292616"
variation 1605
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:113413765"
variation 1610
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:369387542"
variation 1738
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:10808015"
variation 1781..1782
/gene="TMEM178B"
/replace=""
/replace="t"
/db_xref="dbSNP:75747739"
variation 1907
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:36163259"
variation 1947..1948
/gene="TMEM178B"
/replace=""
/replace="gt"
/db_xref="dbSNP:150535593"
STS 1956..1998
/gene="TMEM178B"
/standard_name="AU048745"
/db_xref="UniSTS:145195"
variation 1956..1959
/gene="TMEM178B"
/replace=""
/replace="gtgc"
/db_xref="dbSNP:150586744"
variation 1959
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:62486703"
variation 1960..1974
/gene="TMEM178B"
/replace=""
/replace="tgtgtgtgtgtgtgtg"
/db_xref="dbSNP:376779670"
variation 1960..1963
/gene="TMEM178B"
/replace=""
/replace="gtgt"
/db_xref="dbSNP:71948091"
variation 1960..1961
/gene="TMEM178B"
/replace=""
/replace="gt"
/db_xref="dbSNP:34510903"
variation 1961
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:112414062"
variation 1961
/gene="TMEM178B"
/replace=""
/replace="tgtg"
/replace="tgtgtg"
/db_xref="dbSNP:57564160"
variation 1965
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:141917843"
STS 1978..1998
/gene="TMEM178B"
/standard_name="AU048745"
/db_xref="UniSTS:145195"
variation 1983..1986
/gene="TMEM178B"
/replace=""
/replace="tgtg"
/db_xref="dbSNP:72195620"
variation 2033
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:184327192"
variation 2041
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:150284425"
variation 2045
/gene="TMEM178B"
/replace="a"
/replace="t"
/db_xref="dbSNP:189264641"
variation 2175
/gene="TMEM178B"
/replace="a"
/replace="c"
/db_xref="dbSNP:180864804"
variation 2220
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:374511960"
variation 2252
/gene="TMEM178B"
/replace="g"
/replace="t"
/db_xref="dbSNP:185321174"
variation 2345
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:113153620"
variation 2572
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:117936334"
variation 2582
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:112033999"
variation 2605
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:114156686"
variation 2681
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:58862006"
variation 2706
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:114960868"
variation 2852
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:10280774"
variation 2870
/gene="TMEM178B"
/replace="g"
/replace="t"
/db_xref="dbSNP:188641762"
variation 2898
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:112742087"
variation 2924
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:137900477"
variation 2940
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:181474822"
variation 2973
/gene="TMEM178B"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:10235351"
variation 3073
/gene="TMEM178B"
/replace="c"
/replace="g"
/db_xref="dbSNP:191942484"
variation 3091
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:73520445"
variation 3135
/gene="TMEM178B"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:184241061"
variation 3136
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:149493463"
variation 3221
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:118186034"
variation 3455
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:56786624"
variation 3475
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:145849965"
variation 3495..3496
/gene="TMEM178B"
/replace=""
/replace="ca"
/db_xref="dbSNP:111770706"
variation 3497
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:59193172"
variation 3498
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:59220463"
variation 3511
/gene="TMEM178B"
/replace="c"
/replace="g"
/db_xref="dbSNP:58189529"
variation 3619
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:187196346"
variation 3643
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:112270621"
variation 3683
/gene="TMEM178B"
/replace="a"
/replace="t"
/db_xref="dbSNP:189689724"
variation 3823
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:113124395"
variation 3825
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:368485217"
variation 3849
/gene="TMEM178B"
/replace="a"
/replace="c"
/db_xref="dbSNP:142788423"
variation 3853
/gene="TMEM178B"
/replace="a"
/replace="c"
/db_xref="dbSNP:182350860"
variation 3857
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:187083168"
variation 3991
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:147433846"
variation 4013
/gene="TMEM178B"
/replace="g"
/replace="t"
/db_xref="dbSNP:374853136"
variation 4095
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:369038692"
variation 4181
/gene="TMEM178B"
/replace="c"
/replace="g"
/db_xref="dbSNP:148469534"
variation 4237
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:141786204"
variation 4367
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:201343572"
variation 4429
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:191890900"
variation 4441
/gene="TMEM178B"
/replace="a"
/replace="c"
/db_xref="dbSNP:73520453"
variation 4566
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:183387429"
variation 4698
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:150625897"
variation 4775
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:73520456"
variation 4860
/gene="TMEM178B"
/replace="a"
/replace="c"
/db_xref="dbSNP:368459461"
variation 4866
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:113778931"
variation 4888
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:188841717"
variation 4908
/gene="TMEM178B"
/replace="a"
/replace="c"
/db_xref="dbSNP:192904189"
variation 4911
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:1881022"
variation 4947
/gene="TMEM178B"
/replace="c"
/replace="g"
/db_xref="dbSNP:369594908"
variation 5071..5072
/gene="TMEM178B"
/replace=""
/replace="g"
/db_xref="dbSNP:34382879"
variation 5131
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:139683633"
variation 5160
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:185519346"
variation 5245
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:188830050"
variation 5369
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:143725796"
variation 5419
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:202096212"
variation 5476
/gene="TMEM178B"
/replace="a"
/replace="c"
/db_xref="dbSNP:116828625"
STS 5486..5611
/gene="TMEM178B"
/standard_name="WI-16153"
/db_xref="UniSTS:23554"
variation 5515
/gene="TMEM178B"
/replace="c"
/replace="g"
/db_xref="dbSNP:62486704"
variation 5521
/gene="TMEM178B"
/replace="a"
/replace="t"
/db_xref="dbSNP:191178859"
variation 5530
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:146807829"
variation 5649
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:10231171"
variation 5687
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:116813722"
variation 5688
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:374144333"
variation 5751
/gene="TMEM178B"
/replace="a"
/replace="c"
/db_xref="dbSNP:183731013"
variation 5787
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:60551486"
variation 5846
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:55846251"
variation 5940
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:139708766"
variation 5966..5967
/gene="TMEM178B"
/replace=""
/replace="t"
/db_xref="dbSNP:367640949"
variation 5977
/gene="TMEM178B"
/replace=""
/replace="t"
/db_xref="dbSNP:58548651"
variation 5979
/gene="TMEM178B"
/replace="a"
/replace="c"
/db_xref="dbSNP:199855988"
variation 6054
/gene="TMEM178B"
/replace="c"
/replace="g"
/db_xref="dbSNP:373483989"
variation 6094
/gene="TMEM178B"
/replace="a"
/replace="t"
/db_xref="dbSNP:73169575"
variation 6210
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:144355533"
variation 6276
/gene="TMEM178B"
/replace="c"
/replace="g"
/db_xref="dbSNP:188496256"
variation 6346
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:181340332"
variation 6380
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:185160487"
variation 6457
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:145408523"
variation 6563
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:149230413"
variation 6577
/gene="TMEM178B"
/replace="g"
/replace="t"
/db_xref="dbSNP:1113682"
variation 6632
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:1405831"
variation 6698
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:190057244"
variation 6813
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:181755902"
variation 6836
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:150939195"
variation 6864
/gene="TMEM178B"
/replace="a"
/replace="c"
/db_xref="dbSNP:376248822"
variation 6874
/gene="TMEM178B"
/replace="a"
/replace="t"
/db_xref="dbSNP:113164929"
variation 6898
/gene="TMEM178B"
/replace="a"
/replace="c"
/db_xref="dbSNP:57225366"
variation 6909
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:58588454"
variation 6910
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:187247161"
variation 7033
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:370261820"
variation 7056..7057
/gene="TMEM178B"
/replace="aa"
/replace="gg"
/db_xref="dbSNP:371599432"
variation 7306
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:4726454"
variation 7319
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:145890805"
variation 7334
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:373708028"
variation 7335
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:138701212"
variation 7366
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:7799309"
variation 7492
/gene="TMEM178B"
/replace="a"
/replace="t"
/db_xref="dbSNP:77240754"
variation 7502
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:146996501"
variation 7528
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:115128582"
variation 7540
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:73520468"
variation 7541
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:80329458"
variation 7546
/gene="TMEM178B"
/replace="g"
/replace="t"
/db_xref="dbSNP:138030478"
variation 7563
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:149545315"
variation 7570
/gene="TMEM178B"
/replace="a"
/replace="c"
/db_xref="dbSNP:10239319"
variation 7580
/gene="TMEM178B"
/replace="g"
/replace="t"
/db_xref="dbSNP:191143297"
variation 7612
/gene="TMEM178B"
/replace="a"
/replace="t"
/db_xref="dbSNP:180799804"
variation 7651
/gene="TMEM178B"
/replace="c"
/replace="g"
/db_xref="dbSNP:185472709"
variation 7679
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:190231502"
variation 7767
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:183064260"
variation 7835
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:148722922"
variation 7879
/gene="TMEM178B"
/replace="c"
/replace="g"
/db_xref="dbSNP:371744072"
variation 8125
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:141920767"
variation 8314
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:111295125"
variation 8548
/gene="TMEM178B"
/replace="c"
/replace="g"
/db_xref="dbSNP:376653016"
variation 8748..8749
/gene="TMEM178B"
/replace=""
/replace="t"
/db_xref="dbSNP:34261232"
variation 8801
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:146335002"
variation 8868..8869
/gene="TMEM178B"
/replace=""
/replace="t"
/db_xref="dbSNP:35878987"
variation 8877
/gene="TMEM178B"
/replace="a"
/replace="t"
/db_xref="dbSNP:367754610"
variation 9018..9019
/gene="TMEM178B"
/replace=""
/replace="g"
/replace="gggg"
/db_xref="dbSNP:60100890"
variation 9026
/gene="TMEM178B"
/replace="g"
/replace="t"
/db_xref="dbSNP:78742571"
variation 9027
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:76054240"
variation 9029
/gene="TMEM178B"
/replace="c"
/replace="g"
/db_xref="dbSNP:62486705"
variation 9046
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:139568615"
variation 9089..9090
/gene="TMEM178B"
/replace=""
/replace="a"
/db_xref="dbSNP:35497428"
variation 9131
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:144288579"
variation 9148
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:151100159"
variation 9214
/gene="TMEM178B"
/replace="a"
/replace="t"
/db_xref="dbSNP:139861685"
variation 9232
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:149858136"
variation 9235
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:73520473"
variation 9279
/gene="TMEM178B"
/replace="g"
/replace="t"
/db_xref="dbSNP:145849457"
variation 9307..9308
/gene="TMEM178B"
/replace=""
/replace="g"
/db_xref="dbSNP:34301372"
variation 9374
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:141971937"
variation 9378
/gene="TMEM178B"
/replace="c"
/replace="g"
/db_xref="dbSNP:372626359"
variation 9489
/gene="TMEM178B"
/replace="g"
/replace="t"
/db_xref="dbSNP:58409763"
STS 9509..9714
/gene="TMEM178B"
/standard_name="RH18406"
/db_xref="UniSTS:56788"
STS 9554..9723
/gene="TMEM178B"
/standard_name="D7S2144E"
/db_xref="UniSTS:151140"
variation 9562
/gene="TMEM178B"
/replace=""
/replace="g"
/db_xref="dbSNP:368503910"
variation 9621
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:112291826"
variation 9782
/gene="TMEM178B"
/replace="g"
/replace="t"
/db_xref="dbSNP:369285741"
variation 9941
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:73520478"
variation 9946
/gene="TMEM178B"
/replace="c"
/replace="g"
/db_xref="dbSNP:188006195"
variation 9958..9959
/gene="TMEM178B"
/replace=""
/replace="ttg"
/db_xref="dbSNP:200661577"
variation 9959
/gene="TMEM178B"
/replace="g"
/replace="t"
/db_xref="dbSNP:141273106"
variation 10011
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:143490406"
variation 10020
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:191688283"
variation 10058
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:28488523"
variation 10061
/gene="TMEM178B"
/replace="a"
/replace="c"
/db_xref="dbSNP:148041325"
variation 10161
/gene="TMEM178B"
/replace="c"
/replace="t"
/db_xref="dbSNP:183521204"
variation 10246
/gene="TMEM178B"
/replace="c"
/replace="g"
/db_xref="dbSNP:10273211"
STS 10287..10387
/gene="TMEM178B"
/standard_name="D7S2119E"
/db_xref="UniSTS:151126"
variation 10288..10289
/gene="TMEM178B"
/replace=""
/replace="g"
/db_xref="dbSNP:375576316"
variation 10289..10290
/gene="TMEM178B"
/replace=""
/replace="g"
/db_xref="dbSNP:138760325"
variation 10349
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:114368882"
variation 10373
/gene="TMEM178B"
/replace="a"
/replace="c"
/db_xref="dbSNP:187686398"
variation 10428
/gene="TMEM178B"
/replace="a"
/replace="g"
/db_xref="dbSNP:1527645"
variation 10490..10491
/gene="TMEM178B"
/replace=""
/replace="at"
/db_xref="dbSNP:146428280"
variation 10491..10492
/gene="TMEM178B"
/replace=""
/replace="at"
/db_xref="dbSNP:371894930"
variation 10548
/gene="TMEM178B"
/replace="a"
/replace="t"
/db_xref="dbSNP:140814180"
ORIGIN
cgccgctttgttccgggtgcggcgagggaaggcgaggctgcggcggatcatgcccatggtgtagccgccaagcggaggcatggctgccggaaggttactgctctacactggcctctcgctagcgctctgcgccctcggcatgctggccgtggccatctgctcggaccactggtacgagacggacgccaggaagcacagggacaggtgcaaggccttcaacacccgccgggtcgaccccggcttcatttacaacaataacaacaacttgccgctccgggcgagccgctcgcgcctggaccgctgggagggcaaactcctccgggcccggaatcgccggcagctgttcgccatgagccccgcggacgagtgcagccggcagtacaactccaccaacatgggcctctggaggaagtgccaccggcagggcttcgaccccgagatcgccgccctcattcggaaaggagaaattgagcgatgtacgtacatcaaataccactactcctcagcaaccatccccaggaacctcactttcaatatcacgaagaccatccgtcaggatgagtggcatgccctacacctgcgcagaatgacggctggcttcatgggcatggcggtggccatcatcctctttggctggatcatcggcgtgctgggctgctgctgggaccgaggccttatgcagtacgtggcagggctgctcttcctcatgggaggaaccttctgcatcatttcactgtgcacctgtgtggccgggatcaactttgagctgtcacgctacccacgctacctgtacggactccctgatgacatcagccatggctatggctggtccatgttctgtgcatgggggggcctgggcctcacactcatctcgggattcttctgtaccttagccccttctgttcaacctgtcccgaggaccaactaccctaaatccagacccgagaatgggacagtgtgctaaaaaacaaacccatacatacatatatatatataaatatatatatataatatacatatataaaacaaaacaaaactaaatcaagacgatgccagtgccaaggtagagttgagttggctcaggcacctgcatctcgccggactttgtgttgcctcatctctgagatggggaaagtttttccatcctgtggctcttccatcagttcttgacttttggcttcatggtctcttgaagacagagcaaacaccaccacttgcgaccgcgtcttgatccccatcactggcgaggatggggtggtgaagggacagtggaaggggtctgaggcagcacagatgtagagaaggaagtgccacccactgggtcaacgggagaggacgccacccctaaccagtcatatcacagggtaacaaagccctcagttcctagaatgtaaccaaattattgaggccattttcagaatcacttcttctcctgctcttcctgttcggacttccttcccagcccaccagcaacacacaaggagtggaagagaaaacaaactgagaaggacgttttctctttgctgccaaacttttggaccatgtttcataggtgggaagggaagagaacatgctgagaggcaagatctgcatcaatgaaaggacgcttcggtggatgctcagacaacccagtcttaccttccagctgccttacacccagtgaaacaagaggccaccctgtccccagccgcacctgcactccctgggcagactggagccttggagtcatgctgtgatgtgtgtgtgtgggtgtgcgtgcatgtgtactttgggcggtttcctttttttcttttctaccttttaaatggaaatactgcattatgactgttgtctctcttatcactgtagtggtttcatggccccagatagaggcccagagacctagaaattgtcatgagggacaggcctataagggtgccaattctgcagctacagatccctggagtggtgtgtgtgtgcgtgtgtgtgtgtgtgtgtgtgtgtgtgtgtgtgtgtggtggatgtttcttgagcgtggggttttattgtttgtgttgtgtttttttaaattgtttctggtatagctgaaatttccagagggcagaaccaagaacaaagccactgggccagaggacccccgtggttctccacattacagctctgggactctgcacgatttagtcctctaattttggaagttcaagacacagctgggcacataagccatgagagaagagggggaacacacagttcaggagagagaagaaatgttgctctggttgctgttgtacaagaacataaaccaacaagaccttcactccccattatagaagctgtcctttgtcactggacatctcccctttccctaggggtgacctctgtacaaacgaaaggaagtgggtcacatgcagagagagcacctccatttcccatgggctcaagtttgtatgatattgtgtaaattaatgcagaactcttgactctttccatcctcttcctttccctcttgatattcaaggccatgaatcccaaaataacagtcttagtggctagcacccaaacagaggtggaataaatccaccccagtgtctcgggctcatttgagcaaattagcactgcaggtgctggcaagcaaagtcagccagagagttgtgaacgctgtaggggtgggagtctgctggagtgggctggagccgctcacagtcatctcagtgagcctgctggtgcccagcagccctggggaggccaggtgagaatccctgagctggtgtagccatggtcaactgtgtagcagagaatccccttgtttcataaacaaatatgctttgggagctttgccaggcactcagcagcctttcttccactgctgtgtaatctgtttcatttacacgtcttccaacccatcttcctaccactctcctccttttctcacctactaaccacttaccttctctctcttctatcttccaccctcatctgctcctttgaactgcgtgtatgtaattcatatctggatatgatatgacatctgatgtgcatgaatggggttgaatgtggatctctctgtatgtgtatctctctggtgcattttgtgtacgtttgtgtcagtacacacctgcacacaggtgtgggtgccctactcaagacttccttaccggggactctggtcagcttctgcaaaaggtctcatgtgtgagttccctgtgtgtgggtgtgctgggcgatagggtaaggtgtgcaacgggaaaagttgttagcttccagttggggttctaaggattatttttaaaacaaaggatttattctatgagaagggaaataattttcaggaaaacccagtttttcaattgggcattttatttctaattttctttgaaaagttagatttctcccttaaggggaagggcatacttgggcttaaggaaaagtgaagaaaagtatctcagattgagaggccttttgtcttccttccaagcgtcctgaaggggctctgccgaggaagggacagacaggttcacaagcatccatttgggggagagggcttgtctatgaccacactgaaattccagcttttttccagttgcaggagagaggggaaaaattctaaatggggaaatttgctatgaaccatttaaactttttgtaagtaatcatgtttgaggatgctggctcacagacctatcattatttatatcctctttttaaaaaaaaatcccatactttcaatgaatagattatctgctctatccaattattgtctttgtgacagacatttagcaaagcttactgcatccctttgaaaccttgagagttcctgaaatgttagaaagctcccaggaaagacgtaaacaacctgggctcaactcaccagcccagagcaggggctttgagtgacttctttgatagcaggaccagataaatacgaacacactttgggatctgatcctgctgggaagcaaaagacgcccagccacatgaccaggatagaggcccctttcagacggcaagtcctggccaatgggaggacttctcaggtgaccttgatccctctagcataagggcttgaccacagattaaaacatgtgactccaaccagttacggaagctttctggctgtgaggtagctgagggagatgaggaggaggaagagaggagccttgacttgtgaggctctgtaggtcagactctgctaactccaaatcaaagtggaacccaaccttatgagggcatttagggtcaatgacctcactaaagtcaccagccgcaaccccaggtcaagttcaaacttcttactggcatatgaacatgtatgtgctttgagctccatgcaagtcaaccttgagcctggggcccattgcaacttttatttccttccctactctactaccttgagattcaggaaagtgaggtattctacctagagagaggtcccatatctttttctccttattttgggagttacggtttcttcttctgtttccgtttcctctctctctactcactcctactttctcctgcatcaactttggtcaattaacatagacaagtgattcatctgtagagaggctcctagactccaagcagcccccttccttgttcattgtggctgtaggttttataaggaggtctgtggctccctggcatcaaaatatgaaaaataaaatctgtgcctgttccagcttcaatcctcctccaagccttagcttttcaacaaccctaccctttcaacttcagggatcatggagtcacagagactggacaactcctccaaatctagacaaagactttcttaagcgccctgagcccaggtgcatatcttcccatcagggatgagtggtcccacctagcaatgcttgcctctcctgtgacaagagggtaggatatcctaggactctgagactgggccctatatctcaatattcatccacactcatgataagatgccggaaatgaatgcactgtgtgtagctgtcttgatttagtgggaggatgtgctgcttaggtctccaaagatgcccacctgggtcaaattcagaataatgaactcaggtacatcacccagaggcatttagaatggactctctcttcacctggattatgtgctgagtgttaagtgatttttcaaatatctgggggaaggagtgggaagagatacactctggtcatcctttggtgtggtttgtgggggatacttggttgattcttgtagttaaagtgaagttgcttttctgaaaatgttccctgtcttcaggggacttacccatcccaggggacacatccatcccaggggacacagccagccctttccagggaaatacgatgtttctgagtgagaggtgatttcagtgcagataggaagagctggtgcacaccagcagggttgccttccatgccatcttccagctggtgtgggatagactaagggggcagatttttaagaaccccaccagagttgacatacacacgtgattctcgtgtctgtctctcaaagctctcaatgtctggggctgtgtttgccctcttttcattgatgctgccatgatgcaaaatgtttcttaaacattattcctggttcttagaatatgtgattactgagtattggatttctttcctgaataataactgctcattgtagaaaataagaaaaataaaatacaaaaaagactacaagatttttcataatccagtcactctgaggcatctaccgcgggcccaatccaaatggtcatgacctcaaaacttccccaatgagtgcttgtctctgggttggcagctggggccatgtgagcagtgtacaccacagaaccgcactggtctgcgttgagttgaccctgtgttcctggcagcaagagtgcagggccctgagcccccagagatagcaaagaggcctaaaagtttaatgccagaccttaggggcaggatggagcagggctaaaagatgtctctttgggcctgtctgcctgctttccttccttccttttctttcctttttttttttggtcagttgccatctcaatctaatcatagatgtaagaatgcggaagccagagtaactcactcattaagctacacttgtgtaacagttactgtaaatttcactacagctctgcactgaaatgatttgtgactctgggcactgtgtcttctccatacttgaacttcctcatctacaaaatgaggataagtgataacaccttacctcatggtatattaagggtgacaaagaaattgcaaagtgatttgcaaacatgaagtgtcatatgagttatgtatgttctaattatccctcagaagaccccccgctggaatggaattctcacatcaagtgtctgtgcctcgctgctgaaggataacccagagtgcaaggtcatctttgttgctgaacagggctggacctgtcgcacttaagcacacttaaaggattctattcttcattcaggtcccccagagaaattggctccttatttttctttacctattcctagacttccttttgtctagagccagttttgcaaagggcacttttatccatctcagttattcccagaggtgacagaatgagtaaaccatatggggcaaatagcatatatgagctaaaccagttaactgttaaccaaggcacatggtcaatgccttagtatttttttttttaattctcctaacgttatttctagctgtacattcccaaaaggaatgggtggaagcaaatcagattctgaaaggtttcaatgatctttcaagtttaggatgagaccaagtctcaaggagctgggatcttctttctcttgtcagttgctgaagccagtagcttcgtcaaaaacatatgaattcatataaggaagccctttagatggtacattcactaagacgtgtctgggtgtgatcctgtttgggaaaaacagaatcctaggttctaaacaagaaaagaacgcccttcccaaagggtccgcacactttctgctttgcagcggatcaagtgtccttgtgagggtgagacttccttcaagggaagggaagccattgctctctctgtagatagagcccagctggtaacgggggagccacccaactgcaggggggtgtatgttcaggtgtgaaaaacagaaaactgggtctgaacatgaagagttgcacagcagtagttcgaagaagctggcatctctttggcaaacaccaacctcagcaaatgcaactcctacacttcattcccaaggaccaggtgttgctccttaaggaactctgtatccctctctcctctccagaaccccattcctcccactggctgagcttttcctttcctttccgggtcacccatagaccctctccgtctgtaccagtgcgtctgtgttgtgagcgtgacgaagcctttcctgtgaagagctttcatgaactcattctcatactccttccccatttccacccatggtgtgactgttttgctattcaagactatctgtaaaaatgtacaaataaaagtgaaaactgaaaataaaggggagggagattgagattaaacaaatgcaatgatgtagcccttagttttctgaggacttctgtggacggccctaaaatcctgagttagggtgggatatgaagggagggataccattgacacaggaggtttttttctggttgtttctctcacagtcatcagtgtctgcttagaactctctgttctaaaggtttttccctgtaaagtagaatgcacttcccccaaaataaaagtaaatcagcaatgtttgaagggtcatggcaagggtcatgacaaagacctgactctggggtggcatgagtggccctgtcaccggctcactcagggccttgggggagtctcattacctcaccttgtctccacgtcttctcagccaaatggggatcaggggcttccagggctctgggggtgcgcagtccccttgtgtattttgctgctatttctagagagactttgagcccttgctagtgcgtgcttactgcatggaggtaaattaggagatgttttctctctgctactcctggcctctgctttcgcccctcagaaagtgaccttgagctagcagccagtttgcactcagagtccagagccttctatctaccgtttcattctcagattccttttcccacccactttgacgatctcattttactatcagtctctactgactgagctttgctgcactgggctggggtaggagaaagagcatccaaggagatgatgtgtgaattgctttgtaatttatgactcaccatataaatgtggcttgcagtgtcagaagcagggagtctggccaagggttgctaccaaataagactgaagatggtggaggcagtggtggcgtggaggcagtaggcagaagatgtgggttgggagcagaggtaagatgaacggagctttgggaaggacagatggcagaagcaccagaaaatcctcagcaaggcagcagagaaggatcctcaaagcagtaaccctgaagtaataggaagtaggaaagaggagcagggattaggtaaatctgcagcataaacagctgtctccctgcaggactgagaagaccagctgccccagagaggggaggcacgtcgagcttggccagtgacccaacccatgattagaggcaccttcaatcccaactttcctctcctctgctgggtcacagtgatggaaccagcttcaggaaggtagtatagaccagcgtcatccaatggaaccatgatccaagccacatatgcaatttaaaatattctagtagccacattttttaaagtccaaagaaacagctaaaatcagtgaaattaatttttagactacattttaacctaacatgtcaaaaatagtatcacttcagcatggaatcaatataaaaattactgggatattttacattcttttttccaaatgaagtcttcaaaatccaatgtgattttcctcttagaaaacatctcagtctggcccagccctatttccagtgttcaatagccacacctgactactggttgctgtataggacagcacggacttaggttcttcattaggagactgatggggggggtccttcctggtgggtcactcactgccatagctcttgtcatagctgatgaaggcaggagtgagtcttattatgttggcctagagtagaaagcacagagctatgtcgaggctgctgtctcagcctctggaagttctgcttcacctgcttagtaagaggagatgaccactcctgtggactgcatgtcccatctgcccccagagggtgtcggcgctgccccagtcatgtcccttatgacctgtccaagtcctagaggccaaagcaggtcatattcttcagctgcaggaatgtcagctactgcctcccaccccttaacctgatccccttatcatatagtggggaaggggcaggcaggccttctctctgtcaagaacaaagatctctacaacatttcgtcacctgggccagtcacctgctaatatcatctcaccaatatttggagctgttttctgaatcccttaattttcttaaatatttatcttaaagtcaaatgctataaaggagataccctgggaagggcagtggccacaggcagactgggtctcctaggaggtggtggtgttggtgacaagttctacttggactgggactcaacccaccattgcctacctctcttccctgcctggagaccttccttaggattgaagaaacctcttttgtttgtgaaaaagataggtatcgagatcttaatggagagaacagaataaaatgcaaggagccaacccctgggtattctcaaagcatttcaacggtcagtataacaaggtttgattgatttaaaatataacattctgagccctgtgttactgagcaaaaatgagctgatttggtgagtatgttttatatatggtcattagacagggaccataactgacaaaactctcaaacgcctggagtgtttatggcccaccagattattgctcagtcaatataaatttatttacctttattttaatttgcatagtgctttctgattggtcagacaaggagtggtgtgtactgcaggattctaacaatgcctctgcccttggaggcagcaattcctgtggttattggtgctaaaataagataaaatattatgttaatttgttctgatatgatgtgaataaatgtgttgtttaatcttaacaagaatgctacatcttatcagatctattgtactgtctgttccttctcataattaattaattacaggaaaggcgattcaaaccagatcttgaaactattgtgatgttctgagaggtaaatttaacagggaagtgggaggggggatgaaaagggaaattgccaggttcctgtgactttgaaaggactgaggaagcagagagcatttggggacttcactgaaactgactgcatcttgcaattttctttttcgaattggcagaaatattgtatttccattgattgaagaaaaacaagtgtctggtaattaattaaatgacttgttcatggaaaaaataaataatctgtcagttgtggaatgtaaactgattaaacaattaaataaagaagattatgttgtgtgttttaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:100507421 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA
by
@meso_cacase at
DBCLS
This page is licensed under a Creative Commons Attribution 2.1 Japan License.