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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:

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

by @meso_cacase at DBCLS
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