2025-05-12 01:37:40, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001001663 507 bp mRNA linear PRI 18-APR-2013 DEFINITION Homo sapiens transmembrane protein 211 (TMEM211), mRNA. ACCESSION NM_001001663 XM_170994 VERSION NM_001001663.1 GI:48717248 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 507) AUTHORS Collins,J.E., Wright,C.L., Edwards,C.A., Davis,M.P., Grinham,J.A., Cole,C.G., Goward,M.E., Aguado,B., Mallya,M., Mokrab,Y., Huckle,E.J., Beare,D.M. and Dunham,I. TITLE A genome annotation-driven approach to cloning the human ORFeome JOURNAL Genome Biol. 5 (10), R84 (2004) PUBMED 15461802 COMMENT PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence was derived from CR456388.1. On Aug 30, 2004 this sequence version replaced gi:51475972. ##Evidence-Data-START## Transcript exon combination :: CR456388.1, BC130647.1 [ECO:0000332] ##Evidence-Data-END## FEATURES Location/Qualifiers source 1..507 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="22" /map="22q11.23" gene 1..507 /gene="TMEM211" /gene_synonym="bA9F11.1" /note="transmembrane protein 211" /db_xref="GeneID:255349" /db_xref="HGNC:33725" /db_xref="HPRD:17327" exon 1..13 /gene="TMEM211" /gene_synonym="bA9F11.1" /inference="alignment:Splign:1.39.8" exon 14..152 /gene="TMEM211" /gene_synonym="bA9F11.1" /inference="alignment:Splign:1.39.8" CDS 26..415 /gene="TMEM211" /gene_synonym="bA9F11.1" /codon_start=1 /product="transmembrane protein 211 precursor" /protein_id="NP_001001663.1" /db_xref="GI:48717249" /db_xref="CCDS:CCDS33624.1" /db_xref="GeneID:255349" /db_xref="HGNC:33725" /db_xref="HPRD:17327" /translation="
MLLGGWLLLAFNAIFLLSWAVAPKGLCPRRSSVPMPGVQAVAATAMIVGLLIFPIGLASPFIKEVCEASSMYYGGKCRLGWGYMTAILNAVLASLLPIISWPHTTKVQGRTIIFSSATERIIFVPEMNK
" sig_peptide 26..85 /gene="TMEM211" /gene_synonym="bA9F11.1" /inference="COORDINATES: ab initio prediction:SignalP:4.0" misc_feature <140..313 /gene="TMEM211" /gene_synonym="bA9F11.1" /note="PMP-22/EMP/MP20/Claudin family; Region: PMP22_Claudin; cl15797" /db_xref="CDD:210197" variation complement(41) /gene="TMEM211" /gene_synonym="bA9F11.1" /replace="c" /replace="t" /db_xref="dbSNP:112354981" variation complement(48) /gene="TMEM211" /gene_synonym="bA9F11.1" /replace="c" /replace="t" /db_xref="dbSNP:199584302" variation complement(73) /gene="TMEM211" /gene_synonym="bA9F11.1" /replace="c" /replace="g" /db_xref="dbSNP:376083488" variation complement(81) /gene="TMEM211" /gene_synonym="bA9F11.1" /replace="c" /replace="g" /db_xref="dbSNP:371111926" variation complement(84) /gene="TMEM211" /gene_synonym="bA9F11.1" /replace="a" /replace="c" /db_xref="dbSNP:7292477" variation complement(103) /gene="TMEM211" /gene_synonym="bA9F11.1" /replace="a" /replace="g" /db_xref="dbSNP:376553259" variation complement(112) /gene="TMEM211" /gene_synonym="bA9F11.1" /replace="c" /replace="g" /db_xref="dbSNP:138723870" exon 153..507 /gene="TMEM211" /gene_synonym="bA9F11.1" /inference="alignment:Splign:1.39.8" variation complement(169) /gene="TMEM211" /gene_synonym="bA9F11.1" /replace="g" /replace="t" /db_xref="dbSNP:73157942" variation complement(213) /gene="TMEM211" /gene_synonym="bA9F11.1" /replace="a" /replace="g" /db_xref="dbSNP:376332479" variation complement(214) /gene="TMEM211" /gene_synonym="bA9F11.1" /replace="a" /replace="g" /db_xref="dbSNP:201030375" variation complement(223) /gene="TMEM211" /gene_synonym="bA9F11.1" /replace="c" /replace="t" /db_xref="dbSNP:146817251" variation complement(237) /gene="TMEM211" /gene_synonym="bA9F11.1" /replace="g" /replace="t" /db_xref="dbSNP:372256324" variation complement(264) /gene="TMEM211" /gene_synonym="bA9F11.1" /replace="a" /replace="g" /db_xref="dbSNP:34889393" variation complement(279) /gene="TMEM211" /gene_synonym="bA9F11.1" /replace="c" /replace="g" /db_xref="dbSNP:148065388" variation complement(310) /gene="TMEM211" /gene_synonym="bA9F11.1" /replace="c" /replace="t" /db_xref="dbSNP:371967395" variation complement(319) /gene="TMEM211" /gene_synonym="bA9F11.1" /replace="c" /replace="t" /db_xref="dbSNP:372889091" variation complement(406) /gene="TMEM211" /gene_synonym="bA9F11.1" /replace="a" /replace="g" /db_xref="dbSNP:201918677" variation complement(407) /gene="TMEM211" /gene_synonym="bA9F11.1" /replace="a" /replace="g" /db_xref="dbSNP:143636353" variation complement(444) /gene="TMEM211" /gene_synonym="bA9F11.1" /replace="c" /replace="t" /db_xref="dbSNP:115941615" variation complement(453) /gene="TMEM211" /gene_synonym="bA9F11.1" /replace="a" /replace="g" /db_xref="dbSNP:200512627" variation complement(488) /gene="TMEM211" /gene_synonym="bA9F11.1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:55763948" ORIGIN
ctttgcctggaaggtctcagctgtgatgctcctcggaggctggctcctgttggccttcaatgcaattttcctcctgtcttgggctgtggcccccaaagggctgtgcccaaggagaagcagtgttccaatgccaggggtgcaggcagtggcagctactgccatgattgtgggtctgctgattttcccaatcggccttgcctccccattcatcaaggaagtgtgcgaagcctcctccatgtattatggtgggaagtgccggctgggttggggttacatgactgctatcctcaatgcagtcctggccagcctcctgcccatcatcagctggccccacacaaccaaggtccaagggaggaccatcatcttctccagtgccaccgagagaatcatctttgtgccagaaatgaacaaataaaaatctcctgggagtagcacaaagggcacactccagagttttatgaaatcatcatgtagccaacttcaaatcccatctctgctccttcttgc
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:255349 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA
by
@meso_cacase at
DBCLS
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