2024-03-29 13:45:25, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_178826 4142 bp mRNA linear PRI 29-JUN-2013 DEFINITION Homo sapiens anoctamin 4 (ANO4), mRNA. ACCESSION NM_178826 VERSION NM_178826.3 GI:218084957 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 4142) AUTHORS Sherva,R., Tripodis,Y., Bennett,D.A., Chibnik,L.B., Crane,P.K., de Jager,P.L., Farrer,L.A., Saykin,A.J., Shulman,J.M. and Green,R.C. CONSRTM The GENAROADS Consortium, and The Alzheimer's Disease Neuroimaging Initiative TITLE Genome-wide association study of the rate of cognitive decline in Alzheimer's disease JOURNAL Alzheimers Dement (2013) In press PUBMED 23535033 REMARK Publication Status: Available-Online prior to print REFERENCE 2 (bases 1 to 4142) AUTHORS Hartzell,H.C., Yu,K., Xiao,Q., Chien,L.T. and Qu,Z. TITLE Anoctamin/TMEM16 family members are Ca2+-activated Cl- channels JOURNAL J. Physiol. (Lond.) 587 (PT 10), 2127-2139 (2009) PUBMED 19015192 REMARK Review article REFERENCE 3 (bases 1 to 4142) AUTHORS Katoh,M. and Katoh,M. TITLE Identification and characterization of TMEM16E and TMEM16F genes in silico JOURNAL Int. J. Oncol. 24 (5), 1345-1349 (2004) PUBMED 15067359 REFERENCE 4 (bases 1 to 4142) AUTHORS Katoh,M. and Katoh,M. TITLE FLJ10261 gene, located within the CCND1-EMS1 locus on human chromosome 11q13, encodes the eight-transmembrane protein homologous to C12orf3, C11orf25 and FLJ34272 gene products JOURNAL Int. J. Oncol. 22 (6), 1375-1381 (2003) PUBMED 12739008 COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from DA811418.1, DC325277.1, AK091591.1, DA213819.1 and AI140598.1. On Dec 16, 2008 this sequence version replaced gi:31341259. ##Evidence-Data-START## Transcript exon combination :: AK091591.1 [ECO:0000332] RNAseq introns :: mixed/partial sample support ERS025081, ERS025082 [ECO:0000350] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-12 DA811418.1 1-12 13-211 DC325277.1 1-199 212-1091 AK091591.1 1-880 1092-1145 DA213819.1 443-496 1146-4109 AK091591.1 935-3898 4110-4142 AI140598.1 1-33 c FEATURES Location/Qualifiers source 1..4142 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="12" /map="12q23.1" gene 1..4142 /gene="ANO4" /gene_synonym="TMEM16D" /note="anoctamin 4" /db_xref="GeneID:121601" /db_xref="HGNC:23837" /db_xref="MIM:610111" exon 1..432 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 98 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:191596863" variation 196 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:183373530" variation 341 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:200493332" variation 359 /gene="ANO4" /gene_synonym="TMEM16D" /replace="" /replace="t" /db_xref="dbSNP:71727090" variation 371 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:76904423" misc_feature 387..389 /gene="ANO4" /gene_synonym="TMEM16D" /note="upstream in-frame stop codon" exon 433..627 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 435 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:181677054" variation 440 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:200782384" variation 443 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:186198729" variation 456 /gene="ANO4" /gene_synonym="TMEM16D" /replace="g" /replace="t" /db_xref="dbSNP:191009660" variation 501 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:374998220" variation 508 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:373057963" variation 543 /gene="ANO4" /gene_synonym="TMEM16D" /replace="g" /replace="t" /db_xref="dbSNP:374591511" variation 547 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:111530742" variation 549 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="c" /db_xref="dbSNP:368294772" CDS 573..3335 /gene="ANO4" /gene_synonym="TMEM16D" /note="transmembrane protein 16D" /codon_start=1 /product="anoctamin-4" /protein_id="NP_849148.2" /db_xref="GI:218084958" /db_xref="CCDS:CCDS31884.1" /db_xref="GeneID:121601" /db_xref="HGNC:23837" /db_xref="MIM:610111" /translation="
MEASSSGITNGKTKVFHPVAKDVNILFDELEAVSSPCKDDDSLLHPGNLTSTSDDASRLEAGGETVPERNKSNGLYFRDGKCRIDYILVYRKSNPQTEKREVFERNIRAEGLQMEKESSLINSDIIFVKLHAPWEVLGRYAEQMNVRMPFRRKIYYLPRRYKFMSRIDKQISRFRRWLPKKPMRLDKETLPDLEENDCYTAPFSQQRIHHFIIHNKETFFNNATRSRIVHHILQRIKYEEGKNKIGLNRLLTNGSYEAAFPLHEGSYRSKNSIRTHGAENHRHLLYECWASWGVWYKYQPLDLVRRYFGEKIGLYFAWLGWYTGMLFPAAFIGLFVFLYGVTTLDHSQVSKEVCQATDIIMCPVCDKYCPFMRLSDSCVYAKVTHLFDNGATVFFAVFMAVWATVFLEFWKRRRAVIAYDWDLIDWEEEEEEIRPQFEAKYSKKERMNPISGKPEPYQAFTDKCSRLIVSASGIFFMICVVIAAVFGIVIYRVVTVSTFAAFKWALIRNNSQVATTGTAVCINFCIIMLLNVLYEKVALLLTNLEQPRTESEWENSFTLKMFLFQFVNLNSSTFYIAFFLGRFTGHPGAYLRLINRWRLEECHPSGCLIDLCMQMGIIMVLKQTWNNFMELGYPLIQNWWTRRKVRQEHGPERKISFPQWEKDYNLQPMNAYGLFDEYLEMILQFGFTTIFVAAFPLAPLLALLNNIIEIRLDAYKFVTQWRRPLASRAKDIGIWYGILEGIGILSVITNAFVIAITSDFIPRLVYAYKYGPCAGQGEAGQKCMVGYVNASLSVFRISDFENRSEPESDGSEFSGTPLKYCRYRDYRDPPHSLVPYGYTLQFWHVLAARLAFIIVFEHLVFCIKHLISYLIPDLPKDLRDRMRREKYLIQEMMYEAELERLQKERKERKKNGKAHHNEWP
" misc_feature 1482..3233 /gene="ANO4" /gene_synonym="TMEM16D" /note="Calcium-activated chloride channel; Region: Anoctamin; pfam04547" /db_xref="CDD:203044" variation 610 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:144771429" variation 611 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="g" /db_xref="dbSNP:34182255" exon 628..764 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 636 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:373885901" variation 676 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:368038308" variation 690 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:371304626" exon 765..923 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 765 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:372743717" variation 785 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:377300608" variation 787 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:141833422" variation 811 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="g" /db_xref="dbSNP:34162417" variation 850 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="c" /db_xref="dbSNP:199936621" exon 924..1024 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 1019 /gene="ANO4" /gene_synonym="TMEM16D" /replace="g" /replace="t" /db_xref="dbSNP:148065824" exon 1025..1069 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 1039 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="c" /db_xref="dbSNP:201084190" variation 1042 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:79379625" variation 1043..1044 /gene="ANO4" /gene_synonym="TMEM16D" /replace="" /replace="c" /db_xref="dbSNP:370605819" variation 1043 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="g" /db_xref="dbSNP:199907380" variation 1050 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:144445830" exon 1070..1201 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 1091 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="g" /db_xref="dbSNP:150616124" variation 1095 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:372521580" variation 1096 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:199651099" variation 1115 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:144762607" variation 1121 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:200739663" variation 1140 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="g" /db_xref="dbSNP:147507034" exon 1202..1308 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 1212 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:140116275" variation 1226 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:367676037" variation 1256 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:371829096" variation 1259 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="g" /db_xref="dbSNP:145580165" variation 1260 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:201748002" variation 1296 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="c" /db_xref="dbSNP:185164070" variation 1306 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:375891394" variation 1307 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:17030913" exon 1309..1364 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 1321 /gene="ANO4" /gene_synonym="TMEM16D" /replace="g" /replace="t" /db_xref="dbSNP:372045550" variation 1329 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:7969347" variation 1330 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:148799316" variation 1338 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:201831622" variation 1358 /gene="ANO4" /gene_synonym="TMEM16D" /replace="g" /replace="t" /db_xref="dbSNP:375375787" variation 1361 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:142484336" exon 1365..1486 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 1406 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:113453785" variation 1433 /gene="ANO4" /gene_synonym="TMEM16D" /replace="g" /replace="t" /db_xref="dbSNP:376366677" exon 1487..1621 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 1489 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:201513929" variation 1541 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:377315098" variation 1593 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:116925463" exon 1622..1718 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 1622..1623 /gene="ANO4" /gene_synonym="TMEM16D" /replace="" /replace="a" /db_xref="dbSNP:34321057" exon 1719..1779 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 1727 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:140890653" exon 1780..1862 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 1784 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:369280518" variation 1839 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:144708621" exon 1863..2003 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 1897 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:139549272" variation 1977 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:200403749" exon 2004..2168 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 2024 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:146719285" variation 2037 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:140325859" variation 2047 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:377115870" variation 2068 /gene="ANO4" /gene_synonym="TMEM16D" /replace="g" /replace="t" /db_xref="dbSNP:74724653" variation 2070 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:150353677" variation 2087 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:138063019" variation 2109 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:200715860" exon 2169..2205 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" exon 2206..2317 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 2249..2250 /gene="ANO4" /gene_synonym="TMEM16D" /replace="" /replace="a" /db_xref="dbSNP:35742697" variation 2252 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:376628514" variation 2300 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:200172974" exon 2318..2375 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" exon 2376..2473 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 2429 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:149548968" variation 2441 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:143233263" variation 2466 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:12582172" exon 2474..2616 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 2525 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:368320715" variation 2526 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:370881866" variation 2547 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="g" /db_xref="dbSNP:373890363" variation 2567 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="c" /db_xref="dbSNP:367780147" variation 2572 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="c" /db_xref="dbSNP:148308691" variation 2576 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:372248204" variation 2587 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:143089752" variation 2615 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:200042629" exon 2617..2769 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 2641 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:200708403" variation 2649 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:200450110" variation 2654 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:190167099" variation 2695 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:368069375" variation 2719 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:374151506" exon 2770..2917 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 2794 /gene="ANO4" /gene_synonym="TMEM16D" /replace="g" /replace="t" /db_xref="dbSNP:367844823" variation 2837 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:3741956" variation 2852 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:147476649" variation 2859 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:141487719" exon 2918..3037 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 2918 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:373088631" variation 2958 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:145182702" variation 3013 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:376008571" variation 3024 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="g" /db_xref="dbSNP:369625786" variation 3031 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="c" /db_xref="dbSNP:202022090" variation 3032 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:201602807" exon 3038..3143 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 3052 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:369120652" variation 3059 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:17031025" variation 3062 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="t" /db_xref="dbSNP:115686403" variation 3089 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:2271642" variation 3107 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:377515922" variation 3108 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:149861898" exon 3144..3339 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 3176 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:1055734" variation 3180 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="g" /db_xref="dbSNP:199976858" variation 3251 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:201623880" variation 3270 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:139827573" variation 3271 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:143188971" variation 3289 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:201262281" variation 3292 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="c" /db_xref="dbSNP:146684951" variation 3308 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:140291622" exon 3340..4120 /gene="ANO4" /gene_synonym="TMEM16D" /inference="alignment:Splign:1.39.8" variation 3415..3416 /gene="ANO4" /gene_synonym="TMEM16D" /replace="" /replace="tgac" /db_xref="dbSNP:149946501" variation 3415 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="c" /db_xref="dbSNP:199499102" variation 3433 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:823561" variation 3467 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:17031048" variation 3558 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="g" /db_xref="dbSNP:17031051" STS 3566..3715 /gene="ANO4" /gene_synonym="TMEM16D" /standard_name="WI-15132" /db_xref="UniSTS:8659" variation 3621 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:77565162" variation 3685 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:76262859" variation 3766 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:145035675" variation 3779 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="g" /db_xref="dbSNP:1849710" variation 3809 /gene="ANO4" /gene_synonym="TMEM16D" /replace="c" /replace="t" /db_xref="dbSNP:186029508" variation 3889..3890 /gene="ANO4" /gene_synonym="TMEM16D" /replace="" /replace="a" /db_xref="dbSNP:36003551" variation 3965 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:369607295" variation 3969 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="c" /db_xref="dbSNP:79709625" STS 3974..4107 /gene="ANO4" /gene_synonym="TMEM16D" /standard_name="SHGC-33403" /db_xref="UniSTS:66274" variation 4017 /gene="ANO4" /gene_synonym="TMEM16D" /replace="g" /replace="t" /db_xref="dbSNP:7302845" variation 4046 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:147562304" variation 4072 /gene="ANO4" /gene_synonym="TMEM16D" /replace="a" /replace="g" /db_xref="dbSNP:142660042" ORIGIN
actgatgttctctccggcagttccttccactctaaagagactccttttcatccctcttctcgcctttcctagcccagcctagtgcccaccctcccccgaccatgcctcccctgcacctggggagggggaggaccagtcctgggcgtgatgctctgagacggtggtgaaatccaccaggctgctttcactccggctcgctctccggagagtcctgttccagacttctcagggtttttacagcacaaacaactgcatacggcccgaggggaggctgaaaaggacttgtgtgtggtggttttattgcctgtcatcactttgctggcctcctcccgactggagcctggaggttcacagtggatttctttctgccgaagacaccaaggcactgaggaaggatcccttctccttctgttgactctttctatttttatggtttaagtttatctattcatggggctgaaaagcgtttgcaaatccatcaacggcgaagtgtggcaagccgcccagcgtcacgtcgtcgcctgcctgtggtcaggcattcctcactcccaccaggcagaaggtcaataaaaatggaggcaagctcttctggaatcactaatggaaaaaccaaagtcttccacccagtggccaaggatgtcaatattctttttgatgaattagaagctgtcagcagtccttgcaaagatgacgattctcttcttcaccctggaaacctgactagtacttcagatgatgccagcagattggaagccgggggagagacagtgccagaaagaaacaaatcaaatggactttactttcgagatggaaagtgtcgaattgactacatccttgtgtacagaaaatccaacccccagactgaaaagagagaagtatttgaaagaaacattagagcagaaggattgcaaatggagaaagagtcctctctaataaatagtgacattatctttgtgaagttgcatgccccatgggaagtccttggaagatatgcagaacaaatgaatgtaagaatgcctttcaggagaaaaatctattacctgccccgccgttacaagttcatgagcaggatcgataaacaaataagcaggtttcggagatggttacctaagaagccaatgaggctggacaaggagacactgccagacctggaggagaatgactgctacactgcccctttcagccagcaaaggatccatcacttcatcatacacaacaaagaaacgttcttcaacaatgccacaagaagtagaatcgtgcatcacattttacaaagaataaaatatgaagaaggaaaaaacaagattggtctgaatcgtttgcttaccaatggctcctatgaagctgcgtttcccctgcatgagggaagttatagaagtaaaaactccattcgaacccatggagcagaaaaccaccgacatctactctatgagtgctgggcctcctggggcgtgtggtataaataccaacctttggatcttgtaaggcggtactttggagagaagattgggttatattttgcctggttgggctggtacaccggcatgctcttcccagctgccttcattggattgtttgtctttttgtatggcgtcaccactctggatcacagccaagtcagtaaagaagtctgccaagctacagatatcatcatgtgtcctgtgtgtgataaatactgtccattcatgaggctgtcagacagctgtgtatatgccaaggtaacccacctttttgacaatggagccactgtcttctttgctgttttcatggcagtctgggcaacagttttcctggagttttggaaaagacggcgagcagtaattgcttatgactgggatttgatagactgggaagaagaggaggaagaaatacgaccccagtttgaagccaagtattccaagaaagagcggatgaatccaatttctggaaagccagaaccttatcaagcatttacagataaatgcagcagacttatcgtttctgcatctggaatattttttatgatctgcgtggtgattgctgccgtgttcgggatcgtcatttaccgggtggtgactgtcagcactttcgctgcctttaagtgggcgttaatcaggaataactctcaggttgcaaccacagggactgctgtgtgcatcaacttctgtatcattatgttgctgaatgtgctctatgaaaaagttgccctgcttctgacgaatttagaacagcctcgcacagagtctgagtgggagaacagcttcaccctgaaaatgtttctttttcagtttgtcaatctgaacagctccacattttacatcgcattcttcctcggaagatttacaggacacccaggtgcctacttgaggctgataaacaggtggagactagaagagtgccaccctagtggatgccttattgatctgtgtatgcaaatgggtattataatggtgctaaagcagacctggaataatttcatggaacttggctacccgttaattcagaattggtggactagaagaaaagtacgacaagaacatggacctgaaaggaaaataagtttcccacaatgggaaaaggactataaccttcagccgatgaatgcctatggactcttcgatgaatacttagaaatgattcttcagtttggattcacaactatctttgtggcagcttttcccctagcaccacttctggccttactgaataacataattgaaattcgacttgatgcttacaaatttgtcacacagtggaggagacctttagcttcaagggccaaagacataggaatttggtatggaattcttgaaggcattggaattctctctgttatcacaaatgcatttgtcatagcgataacatctgactttatccctcgcttggtgtatgcttataagtatggaccttgtgcaggccaaggagaagctgggcaaaagtgcatggttggctatgtgaatgccagcttgtctgtatttcgaatttctgactttgagaaccgatctgagcctgaatctgatggcagtgagttctcggggactcctcttaagtactgcagataccgggactaccgtgacccgcctcattcactggtgccctatggctacacactgcagttttggcatgtcctagctgctcgattagcttttatcattgtctttgagcacctcgtgttttgtataaagcacctcatttcatatctgatcccagacctcccaaaagacctaagggatcgaatgagaagagagaagtacttgattcaggagatgatgtatgaagcagaactggaacgtctccagaaggaacgaaaggagaggaagaagaatggaaaagcacaccacaacgagtggccgtgaccataaaatagtccctttccaggccaaggacctgaattctgtttacttcttctggctgtgcaaaagcacactcaagtgaatgactaaaaatgcaaccacagtgcatgttgcagataccggcggccgcaggaggggcagcatccagtagaggactggcgttggagtcacactgctgtgaaatcacgttgcagtccagcgcacaattgctatctatccatagaccattcttgaccaagcaagcatgcacattatgggcagttacattctcaagtttttaaaatcaaggggaacttgtatactgggcctgtttttcagcctgtttgctaccttttttgcattctatcccatgtgaattttacagacactgggctaaaaagggtattcagacacatggacacacattcctagaatgtcatcatatggtcctaattccatgtcaccaacaacacagacaagaccctgtttacaactttttctttccttttttttaattttagacctttctgagaagattattatatatgacatatctatagctatgtgtatggccatagatgtatttctgtgtgtacatatgtatagtcatgtattcctgcatatgtacatacaaatacagagatatataaagtacatagaaattccttacttgtaaatagccaaaaagtactgacatgagtgaattttcacatttaaatagtcatcaatatgaagccatgattaatgcttgtataatgtgatgcaataaaatttaaaataaatttctgcacatggaatattttcagctgaaaaaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:121601 -> Biological process: GO:0034220 [ion transmembrane transport] evidence: TAS GeneID:121601 -> Biological process: GO:0055085 [transmembrane transport] evidence: TAS GeneID:121601 -> Cellular component: GO:0005622 [intracellular] evidence: ISS GeneID:121601 -> Cellular component: GO:0005886 [plasma membrane] evidence: TAS GeneID:121601 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA
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