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2024-04-24 18:56:04, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_032858 1731 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens maelstrom spermatogenic transposon silencer (MAEL),
mRNA.
ACCESSION NM_032858
VERSION NM_032858.1 GI:14249589
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 1731)
AUTHORS Xiao,L., Wang,Y., Zhou,Y., Sun,Y., Sun,W., Wang,L., Zhou,C.,
Zhou,J. and Zhang,J.
TITLE Identification of a novel human cancer/testis gene MAEL that is
regulated by DNA methylation
JOURNAL Mol. Biol. Rep. 37 (5), 2355-2360 (2010)
PUBMED 19693694
REMARK GeneRIF: These results suggest that MAEL is a novel
cancer/testis-associated gene and is regulated by DNA methylation.
REFERENCE 2 (bases 1 to 1731)
AUTHORS Ehret,G.B., O'Connor,A.A., Weder,A., Cooper,R.S. and Chakravarti,A.
TITLE Follow-up of a major linkage peak on chromosome 1 reveals
suggestive QTLs associated with essential hypertension: GenNet
study
JOURNAL Eur. J. Hum. Genet. 17 (12), 1650-1657 (2009)
PUBMED 19536175
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 3 (bases 1 to 1731)
AUTHORS Cheung,C.L., Chan,B.Y., Chan,V., Ikegawa,S., Kou,I., Ngai,H.,
Smith,D., Luk,K.D., Huang,Q.Y., Mori,S., Sham,P.C. and Kung,A.W.
TITLE Pre-B-cell leukemia homeobox 1 (PBX1) shows functional and possible
genetic association with bone mineral density variation
JOURNAL Hum. Mol. Genet. 18 (4), 679-687 (2009)
PUBMED 19064610
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 4 (bases 1 to 1731)
AUTHORS Soper,S.F., van der Heijden,G.W., Hardiman,T.C., Goodheart,M.,
Martin,S.L., de Boer,P. and Bortvin,A.
TITLE Mouse maelstrom, a component of nuage, is essential for
spermatogenesis and transposon repression in meiosis
JOURNAL Dev. Cell 15 (2), 285-297 (2008)
PUBMED 18694567
REFERENCE 5 (bases 1 to 1731)
AUTHORS Lamesch,P., Li,N., Milstein,S., Fan,C., Hao,T., Szabo,G., Hu,Z.,
Venkatesan,K., Bethel,G., Martin,P., Rogers,J., Lawlor,S.,
McLaren,S., Dricot,A., Borick,H., Cusick,M.E., Vandenhaute,J.,
Dunham,I., Hill,D.E. and Vidal,M.
TITLE hORFeome v3.1: a resource of human open reading frames representing
over 10,000 human genes
JOURNAL Genomics 89 (3), 307-315 (2007)
PUBMED 17207965
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AK027810.1.
##Evidence-Data-START##
Transcript exon combination :: AK027810.1, AK131066.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025084, ERS025085 [ECO:0000348]
##Evidence-Data-END##
FEATURES Location/Qualifiers
source 1..1731
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="1"
/map="1q24.1"
gene 1..1731
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/note="maelstrom spermatogenic transposon silencer"
/db_xref="GeneID:84944"
/db_xref="HGNC:25929"
/db_xref="HPRD:08609"
/db_xref="MIM:611368"
exon 1..203
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/inference="alignment:Splign:1.39.8"
variation 20
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="t"
/db_xref="dbSNP:367546837"
variation 24
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="t"
/db_xref="dbSNP:371448725"
variation 26
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="t"
/db_xref="dbSNP:200229017"
variation 27
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="t"
/db_xref="dbSNP:199628429"
variation 32
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:191751530"
variation 36
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="g"
/replace="t"
/db_xref="dbSNP:369323097"
variation 39
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="c"
/db_xref="dbSNP:373094105"
variation 48
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:375758244"
variation 51
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:376351090"
variation 63
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="t"
/db_xref="dbSNP:147719038"
variation 64
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="g"
/db_xref="dbSNP:201592441"
CDS 72..1376
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/note="cancer/testis antigen 128; maelstrom homolog;
spermatogenesis associated 35"
/codon_start=1
/product="protein maelstrom homolog"
/protein_id="NP_116247.1"
/db_xref="GI:14249590"
/db_xref="CCDS:CCDS1257.1"
/db_xref="GeneID:84944"
/db_xref="HGNC:25929"
/db_xref="HPRD:08609"
/db_xref="MIM:611368"
/translation="
MPNRKASRNAYYFFVQEKIPELRRRGLPVARVADAIPYCSSDWALLREEEKEKYAEMAREWRAAQGKDPGPSEKQKPVFTPLRRPGMLVPKQNVSPPDMSALSLKGDQALLGGIFYFLNIFSHGELPPHCEQRFLPCEIGCVKYSLQEGIMADFHSFINPGEIPRGFRFHCQAASDSSHKIPISNFERGHNQATVLQNLYRFIHPNPGNWPPIYCKSDDRTRVNWCLKHMAKASEIRQDLQLLTVEDLVVGIYQQKFLKEPSKTWIRSLLDVAMWDYSSNTRCKWHEENDILFCALAVCKKIAYCISNSLATLFGIQLTEAHVPLQDYEASNSVTPKMVVLDAGRYQKLRVGSSGFSHFNSSNEEQRSNTPIGDYPSRAKISGQNSSVRGRGITRLLESISNSSSNIHKFSNCDTSLSPYMSQKDGYKSFSSLS
"
misc_feature 84..272
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/note="High Mobility Group (HMG)-box is found in a variety
of eukaryotic chromosomal proteins and transcription
factors. HMGs bind to the minor groove of DNA and have
been classified by DNA binding preferences. Two
phylogenically distinct groups of Class I...; Region:
HMG-box; cd00084"
/db_xref="CDD:28965"
misc_feature order(87..89,93..98,102..107,114..119,126..128,138..140,
180..182,189..191,198..200,255..257)
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/note="DNA binding site [nucleotide binding]"
/db_xref="CDD:28965"
misc_feature 456..1043
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/note="piRNA pathway germ-plasm component; Region:
Maelstrom; pfam13017"
/db_xref="CDD:205198"
variation 76
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="g"
/db_xref="dbSNP:368453105"
variation 83
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2296837"
variation 89
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="g"
/db_xref="dbSNP:113297248"
variation 162
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="c"
/db_xref="dbSNP:141032216"
variation 165
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:373780513"
variation 177
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:200668978"
variation 192
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="g"
/replace="t"
/db_xref="dbSNP:11578336"
variation 197
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="g"
/db_xref="dbSNP:144910501"
exon 204..296
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/inference="alignment:Splign:1.39.8"
variation 217
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:144606344"
variation 224
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:187409599"
variation 249
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="g"
/db_xref="dbSNP:199731527"
variation 270
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:201306124"
exon 297..396
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/inference="alignment:Splign:1.39.8"
variation 299
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:11550694"
variation 311
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:146003706"
variation 328
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:372850622"
variation 365
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="t"
/db_xref="dbSNP:376004050"
variation 372
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:143708432"
exon 397..552
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/inference="alignment:Splign:1.39.8"
variation 431
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="t"
/db_xref="dbSNP:374077150"
variation 440
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="t"
/db_xref="dbSNP:149991521"
variation 456
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="t"
/db_xref="dbSNP:375663463"
variation 464
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:369799064"
variation 468
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="c"
/db_xref="dbSNP:182472064"
variation 469
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:113109340"
variation 498
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="t"
/db_xref="dbSNP:77327505"
variation 522
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:200919942"
exon 553..594
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/inference="alignment:Splign:1.39.8"
variation 565
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:199624416"
variation 573
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="c"
/db_xref="dbSNP:199904572"
exon 595..719
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/inference="alignment:Splign:1.39.8"
variation 603
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:374498631"
variation 611
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:142019908"
variation 618
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:367759111"
variation 686
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="t"
/db_xref="dbSNP:143074041"
variation 688
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:140068242"
variation 706
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="c"
/db_xref="dbSNP:76161896"
exon 720..774
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/inference="alignment:Splign:1.39.8"
variation 733
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="c"
/db_xref="dbSNP:369125241"
variation 742
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:370371545"
exon 775..916
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/inference="alignment:Splign:1.39.8"
variation 787
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="c"
/db_xref="dbSNP:369981337"
variation 792
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="t"
/db_xref="dbSNP:369004774"
variation 835
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:372986703"
variation 864
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="t"
/db_xref="dbSNP:377578248"
variation 905
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="t"
/db_xref="dbSNP:201245864"
exon 917..979
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/inference="alignment:Splign:1.39.8"
variation 930
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:375877930"
exon 980..1112
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/inference="alignment:Splign:1.39.8"
variation 1004
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="c"
/db_xref="dbSNP:368745228"
variation 1028
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:141798349"
variation 1042
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="t"
/db_xref="dbSNP:144722963"
variation 1055
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="t"
/db_xref="dbSNP:41270684"
variation 1079
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="g"
/db_xref="dbSNP:371451660"
variation 1080
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:140976712"
variation 1109
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="t"
/db_xref="dbSNP:149792560"
exon 1113..1188
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/inference="alignment:Splign:1.39.8"
variation 1150
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:34554682"
variation 1179
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:369912892"
exon 1189..1731
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/inference="alignment:Splign:1.39.8"
variation 1232
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="t"
/db_xref="dbSNP:146423777"
variation 1233
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="g"
/replace="t"
/db_xref="dbSNP:141476246"
variation 1234
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="t"
/db_xref="dbSNP:140844121"
variation 1236
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="t"
/db_xref="dbSNP:202037854"
variation 1255
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:138775755"
variation 1260
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="g"
/db_xref="dbSNP:138195157"
variation 1263
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="g"
/replace="t"
/db_xref="dbSNP:60327497"
variation 1274
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:202158678"
variation 1276
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:149589757"
variation 1314
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:377041536"
variation 1327
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="t"
/db_xref="dbSNP:371442590"
variation 1360
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="t"
/db_xref="dbSNP:200941748"
variation 1365
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="t"
/db_xref="dbSNP:143050038"
variation 1370
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:370018714"
variation 1627
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="g"
/db_xref="dbSNP:187047607"
variation 1684
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="c"
/replace="t"
/db_xref="dbSNP:111330073"
variation 1696
/gene="MAEL"
/gene_synonym="CT128; RP11-102C16.1; SPATA35"
/replace="a"
/replace="t"
/db_xref="dbSNP:191483563"
ORIGIN
ttagggcgggagcccggcgagggcgccggtgctttgttctgtctgaggccaggaagtttgaccgcgctgccatgccgaaccgtaaggccagccggaatgcttactatttcttcgtgcaggagaagatccccgaactacggcgacgaggcctgcctgtggctcgcgttgctgatgccatcccttactgctcctcagactgggcgcttctgagggaggaagaaaaggagaaatacgcagaaatggctcgagaatggagggccgctcagggaaaggaccctgggccctcagagaagcagaaacctgttttcacaccactgaggaggccaggcatgcttgtaccaaagcagaatgtttcacctccagatatgtcagctttgtctttaaaaggtgatcaagctctccttggaggcattttttattttttgaacatttttagccatggcgagctacctcctcattgtgaacagcgcttcctcccttgtgaaattggctgtgttaagtattctctccaagaaggtattatggcagatttccacagttttataaatcctggtgaaattccacgaggatttcgatttcattgtcaggctgcaagtgattctagtcacaagattcctatttcaaattttgaacgtgggcataaccaagcaactgtgttacaaaacctttatagatttattcatcccaacccagggaactggccacctatctactgcaagtctgatgatagaaccagagtcaactggtgtttgaagcatatggcaaaggcatcagaaatcaggcaagatctacaacttctcactgtagaggaccttgtagtggggatctaccaacaaaaatttctcaaggagccctctaagacttggattcgaagcctcctagatgtggccatgtgggattattctagcaacacaaggtgcaagtggcatgaagaaaatgatattctcttctgtgctttagctgtttgcaagaagattgcgtactgcatcagtaattctctggccactctctttggaatccagctcacagaggctcatgtaccactacaagattatgaggccagcaatagtgtgacacccaaaatggttgtattggatgcagggcgttaccagaagctaagggttgggagttcaggattctctcatttcaactcttctaatgaggaacaaagatcaaacacacccattggtgactacccatctagggcaaaaatttctggccaaaacagcagcgttcggggaagaggaattacccgcttactagagagcatttccaattcttccagcaatatccacaaattctccaactgtgacacttcactctcaccttacatgtcccaaaaagatggatacaaatctttctcttccttatcttaatgatggtactcttttcaatttctgaaaacagtaacaggcccaacttccttcttactacagtcatattaaacagatcacatcaatgacaaatgtcactactataaaaactacttaatttgtaaggaaattgtttcatagatttaaaaaaattgtggttggagagcatcttggcatttgtgctttttttcttgagggattgttctgcttcctggctgtatgatgggtatatcattaaagtttggagtcctatatgaacaaaactgacatttttagagttgtacttttgggaatgttatagattgatcattctttctcctgataataaaggtattgaatatctgttatgaaaggttct
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:84944 -> Molecular function: GO:0003677 [DNA binding] evidence: IEA
GeneID:84944 -> Biological process: GO:0000122 [negative regulation of transcription from RNA polymerase II promoter] evidence: IEA
GeneID:84944 -> Biological process: GO:0000902 [cell morphogenesis] evidence: IEA
GeneID:84944 -> Biological process: GO:0006974 [response to DNA damage stimulus] evidence: IEA
GeneID:84944 -> Biological process: GO:0007129 [synapsis] evidence: IEA
GeneID:84944 -> Biological process: GO:0007140 [male meiosis] evidence: IEA
GeneID:84944 -> Biological process: GO:0007275 [multicellular organismal development] evidence: IEA
GeneID:84944 -> Biological process: GO:0007283 [spermatogenesis] evidence: ISS
GeneID:84944 -> Biological process: GO:0009566 [fertilization] evidence: IEA
GeneID:84944 -> Biological process: GO:0030154 [cell differentiation] evidence: IEA
GeneID:84944 -> Biological process: GO:0031047 [gene silencing by RNA] evidence: ISS
GeneID:84944 -> Biological process: GO:0034587 [piRNA metabolic process] evidence: ISS
GeneID:84944 -> Biological process: GO:0043046 [DNA methylation involved in gamete generation] evidence: ISS
GeneID:84944 -> Biological process: GO:0043066 [negative regulation of apoptotic process] evidence: IEA
GeneID:84944 -> Biological process: GO:0046620 [regulation of organ growth] evidence: IEA
GeneID:84944 -> Cellular component: GO:0000785 [chromatin] evidence: IEA
GeneID:84944 -> Cellular component: GO:0001741 [XY body] evidence: IEA
GeneID:84944 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
GeneID:84944 -> Cellular component: GO:0005634 [nucleus] evidence: ISS
GeneID:84944 -> Cellular component: GO:0005730 [nucleolus] evidence: IDA
GeneID:84944 -> Cellular component: GO:0005737 [cytoplasm] evidence: ISS
GeneID:84944 -> Cellular component: GO:0030849 [autosome] evidence: IEA
GeneID:84944 -> Cellular component: GO:0033391 [chromatoid body] evidence: IEA
GeneID:84944 -> Cellular component: GO:0043186 [P granule] evidence: ISS
GeneID:84944 -> Cellular component: GO:0043231 [intracellular membrane-bounded organelle] evidence: IDA
GeneID:84944 -> Cellular component: GO:0048471 [perinuclear region of cytoplasm] evidence: IEA
GeneID:84944 -> Cellular component: GO:0071547 [piP-body] evidence: ISS
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