2024-04-25 00:24:10, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001123225 442 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens synaptonemal complex central element protein 3 (SYCE3), mRNA. ACCESSION NM_001123225 XM_927380 VERSION NM_001123225.1 GI:178557812 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 442) AUTHORS Schramm,S., Fraune,J., Naumann,R., Hernandez-Hernandez,A., Hoog,C., Cooke,H.J., Alsheimer,M. and Benavente,R. TITLE A novel mouse synaptonemal complex protein is essential for loading of central element proteins, recombination, and fertility JOURNAL PLoS Genet. 7 (5), E1002088 (2011) PUBMED 21637789 REFERENCE 2 (bases 1 to 442) AUTHORS Wang,Z.Y., Tong,Q.S., Zeng,F.Q., Liu,Y., Gu,Z.H., Zheng,L.D., Cai,J.B. and Jiang,G.S. TITLE [Cloning and expression of a novel mouse testis gene TSEG-2] JOURNAL Zhonghua Nan Ke Xue 15 (2), 99-105 (2009) PUBMED 19323366 REMARK GeneRIF: Cloning and expression analysis of a similar gene in mouse. COMMENT PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence was derived from U62317.2. On Apr 9, 2008 this sequence version replaced gi:113429475. Sequence Note: The RefSeq transcript and protein were derived from genomic sequence to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on alignments. ##Evidence-Data-START## Transcript exon combination :: HY000834.1, HY001955.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025084, ERS025085 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-42 U62317.2 77555-77596 43-151 U62317.2 84049-84157 152-442 U62317.2 89052-89342 FEATURES Location/Qualifiers source 1..442 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="22" /map="22q13.33" gene 1..442 /gene="SYCE3" /gene_synonym="C22orf41; THEG2" /note="synaptonemal complex central element protein 3" /db_xref="GeneID:644186" /db_xref="HGNC:35245" exon 1..42 /gene="SYCE3" /gene_synonym="C22orf41; THEG2" /inference="alignment:Splign:1.39.8" CDS 43..309 /gene="SYCE3" /gene_synonym="C22orf41; THEG2" /note="testis highly expressed gene 2 protein; testis highly expressed protein 2" /codon_start=1 /product="synaptonemal complex central element protein 3" /protein_id="NP_001116697.1" /db_xref="GI:178557813" /db_xref="CCDS:CCDS46733.1" /db_xref="GeneID:644186" /db_xref="HGNC:35245" /translation="
MDDADPEERNYDNMLKMLSDLNKDLEKLLEEMEKISVQATWMAYDMVVMRTNPTLAESMRRLEDAFVNCKEEMEKNWQELLHETKQRL
" exon 43..151 /gene="SYCE3" /gene_synonym="C22orf41; THEG2" /inference="alignment:Splign:1.39.8" variation complement(46) /gene="SYCE3" /gene_synonym="C22orf41; THEG2" /replace="g" /replace="t" /db_xref="dbSNP:138319189" variation complement(151) /gene="SYCE3" /gene_synonym="C22orf41; THEG2" /replace="a" /replace="g" /db_xref="dbSNP:376545270" exon 152..442 /gene="SYCE3" /gene_synonym="C22orf41; THEG2" /inference="alignment:Splign:1.39.8" variation complement(159) /gene="SYCE3" /gene_synonym="C22orf41; THEG2" /replace="a" /replace="g" /db_xref="dbSNP:6009990" variation complement(190) /gene="SYCE3" /gene_synonym="C22orf41; THEG2" /replace="c" /replace="t" /db_xref="dbSNP:373086990" variation complement(210) /gene="SYCE3" /gene_synonym="C22orf41; THEG2" /replace="c" /replace="t" /db_xref="dbSNP:368389026" variation complement(211) /gene="SYCE3" /gene_synonym="C22orf41; THEG2" /replace="a" /replace="g" /db_xref="dbSNP:146628983" variation complement(236) /gene="SYCE3" /gene_synonym="C22orf41; THEG2" /replace="c" /replace="g" /db_xref="dbSNP:199824322" variation complement(241) /gene="SYCE3" /gene_synonym="C22orf41; THEG2" /replace="a" /replace="g" /db_xref="dbSNP:55829948" variation complement(246) /gene="SYCE3" /gene_synonym="C22orf41; THEG2" /replace="c" /replace="t" /db_xref="dbSNP:375410166" variation complement(305) /gene="SYCE3" /gene_synonym="C22orf41; THEG2" /replace="c" /replace="t" /db_xref="dbSNP:6009989" ORIGIN
tgggggcgccagagcaggaccggagcgcgggccaagctggagatggatgatgctgaccctgaggaaagaaactatgacaacatgctgaaaatgctgtcagatctgaataaggacttggaaaagctattagaagagatggagaaaatctcagtgcaggcgacctggatggcctatgacatggtggtgatgcgcaccaaccctacgctggccgagtccatgcgtcggctggaggatgccttcgtcaactgcaaggaggagatggagaagaactggcaagagctgctgcatgagaccaagcaaaggctgtaggccccactggcccaccacagctgccatgccaccctctgcccgtatgaagaggtcactgggggatggagctggcacccacatgaatagctgtatgcactgtacttgtttcttaataaacttatttttaagcaca
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ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:644186 -> Biological process: GO:0006915 [apoptotic process] evidence: IEA GeneID:644186 -> Biological process: GO:0007130 [synaptonemal complex assembly] evidence: ISS GeneID:644186 -> Biological process: GO:0007131 [reciprocal meiotic recombination] evidence: ISS GeneID:644186 -> Biological process: GO:0007283 [spermatogenesis] evidence: ISS GeneID:644186 -> Biological process: GO:0051301 [cell division] evidence: IEA GeneID:644186 -> Cellular component: GO:0000801 [central element] evidence: ISS GeneID:644186 -> Cellular component: GO:0005634 [nucleus] evidence: ISS GeneID:644186 -> Cellular component: GO:0005694 [chromosome] evidence: ISS
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