2025-05-09 20:11:16, GGRNA : RefSeq release 60 (20130726)
LOCUS NR_002221 670 bp RNA linear PRI 16-JUL-2013 DEFINITION Homo sapiens divergent-paired related homeobox pseudogene 4 (DPRXP4), non-coding RNA. ACCESSION NR_002221 VERSION NR_002221.1 GI:60593078 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 670) AUTHORS Visser,R., Koelma,N., Vijfhuizen,L., van der Wielen,M.J., Kant,S.G., Breuning,M.H., Wit,J.M. and Losekoot,M. TITLE RNF135 mutations are not present in patients with Sotos syndrome-like features JOURNAL Am. J. Med. Genet. A 149A (4), 806-808 (2009) PUBMED 19291764 REMARK GeneRIF: Observational study of gene-disease association. (HuGE Navigator) COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. This record has been curated by NCBI staff in collaboration with Anne Booth and Peter Holland. The reference sequence was derived from AC138207.3. Summary: Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This pseudogene is a member of the DPRX homeobox gene family. [provided by RefSeq, Jul 2008]. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-670 AC138207.3 144384-145053 c FEATURES Location/Qualifiers source 1..670 /organism="Homo sapiens" /mol_type="transcribed RNA" /db_xref="taxon:9606" /chromosome="17" /map="17q11.2" gene 1..670 /gene="DPRXP4" /note="divergent-paired related homeobox pseudogene 4" /pseudo /db_xref="GeneID:503645" /db_xref="HGNC:32170" misc_RNA 1..670 /gene="DPRXP4" /product="divergent-paired related homeobox pseudogene 4" /pseudo /db_xref="GeneID:503645" /db_xref="HGNC:32170" exon 1..670 /gene="DPRXP4" /inference="alignment:Splign:1.39.8" /pseudo variation 203 /gene="DPRXP4" /replace="c" /replace="t" /db_xref="dbSNP:187620040" variation 223 /gene="DPRXP4" /replace="a" /replace="c" /db_xref="dbSNP:58401536" variation 257 /gene="DPRXP4" /replace="c" /replace="g" /db_xref="dbSNP:192082071" variation 321 /gene="DPRXP4" /replace="a" /replace="g" /db_xref="dbSNP:150230306" variation 348 /gene="DPRXP4" /replace="c" /replace="t" /db_xref="dbSNP:138871368" variation 460 /gene="DPRXP4" /replace="a" /replace="g" /db_xref="dbSNP:112639565" variation 646..647 /gene="DPRXP4" /replace="" /replace="a" /replace="at" /db_xref="dbSNP:200417259" variation 656 /gene="DPRXP4" /replace="" /replace="t" /db_xref="dbSNP:67257819" ORIGIN
tattgctacttatgcctgcacctgagcccaggcacacatctggattagaagatgccaggctcagaggatcttcctaaaggcaaggaccagatgcattcacacaggaaatgaactgtgttcactgagaagcaactggaagatctgaacatcttgttcaatgagaacccatacccaaacccctgccctcagaaataaatggcctcgaaaatagacatacacccaacaatactccaggtctggttcaagaaccacagagcaaaactcaagaaagccaaataaaagcatattcagcaaaaacaagaaactccacaaccgccaataccggagggtggagtcaccaccagtgtcggcctgagaaatgcagacacactacccagattgcccaacactgctcacctgattggcctggtgtacatgggtcatcgggtaccctctttccagctcatcctgtaccccaacatcaaggtccctgcagatgacttcgttggccacagaatagtccattttggctgctgccaagctcctaacgtatatggcttctaccccattttggaatcccaagtttgggctccaagcttcaattctgactcttctgcctgttcatctctacaaagttgagagatgataaatacaaaaagtcacatgtaaaaaaaaataaatactaaaaaaa
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