2024-04-26 05:52:12, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_016454 1013 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens ER membrane protein complex subunit 4 (EMC4), mRNA. ACCESSION NM_016454 VERSION NM_016454.2 GI:24475963 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 1013) AUTHORS Christianson,J.C., Olzmann,J.A., Shaler,T.A., Sowa,M.E., Bennett,E.J., Richter,C.M., Tyler,R.E., Greenblatt,E.J., Harper,J.W. and Kopito,R.R. TITLE Defining human ERAD networks through an integrative mapping strategy JOURNAL Nat. Cell Biol. 14 (1), 93-105 (2012) PUBMED 22119785 REMARK Publication Status: Online-Only REFERENCE 2 (bases 1 to 1013) AUTHORS Ring,G., Khoury,C.M., Solar,A.J., Yang,Z., Mandato,C.A. and Greenwood,M.T. TITLE Transmembrane protein 85 from both human (TMEM85) and yeast (YGL231c) inhibit hydrogen peroxide mediated cell death in yeast JOURNAL FEBS Lett. 582 (17), 2637-2642 (2008) PUBMED 18586032 REMARK GeneRIF: TMEM85 is a complex gene that encodes a novel conserved anti-apoptotic protein. REFERENCE 3 (bases 1 to 1013) AUTHORS Girard,A., Sachidanandam,R., Hannon,G.J. and Carmell,M.A. TITLE A germline-specific class of small RNAs binds mammalian Piwi proteins JOURNAL Nature 442 (7099), 199-202 (2006) PUBMED 16751776 COMMENT PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence was derived from AF151018.1. On Nov 2, 2002 this sequence version replaced gi:7705996. ##Evidence-Data-START## Transcript exon combination :: AF151018.1, BC016348.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025081, ERS025082 [ECO:0000348] ##Evidence-Data-END## FEATURES Location/Qualifiers source 1..1013 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="15" /map="15q14" gene 1..1013 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /note="ER membrane protein complex subunit 4" /db_xref="GeneID:51234" /db_xref="HGNC:28032" /db_xref="HPRD:14233" exon 1..157 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /inference="alignment:Splign:1.39.8" misc_feature 54..56 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /note="upstream in-frame stop codon" variation 60 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="a" /replace="g" /db_xref="dbSNP:200295598" variation 65 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="a" /replace="t" /db_xref="dbSNP:376859759" variation 70 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="c" /replace="t" /db_xref="dbSNP:150984739" CDS 72..623 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /note="proliferation-inducing gene 17; cell proliferation-inducing gene 17 protein; transmembrane protein 85" /codon_start=1 /product="ER membrane protein complex subunit 4" /protein_id="NP_057538.1" /db_xref="GI:7705997" /db_xref="CCDS:CCDS10035.1" /db_xref="GeneID:51234" /db_xref="HGNC:28032" /db_xref="HPRD:14233" /translation="
MTAQGGLVANRGRRFKWAIELSGPGGGSRGRSDRGSGQGDSLYPVGYLDKQVPDTSVQETDRILVEKRCWDIALGPLKQIPMNLFIMYMAGNTISIFPTMMVCMMAWRPIQALMAISATFKMLESSSQKFLQGLVYLIGNLMGLALAVYKCQSMGLLPTHASDWLAFIEPPERMEFSGGGLLL
" misc_feature 165..167 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /experiment="experimental evidence, no additional details recorded" /note="phosphorylation site" misc_feature 192..194 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /experiment="experimental evidence, no additional details recorded" /note="phosphorylation site" misc_feature 198..200 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /experiment="experimental evidence, no additional details recorded" /note="phosphorylation site" misc_feature 228..590 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /note="Protein of unknown function (DUF1077); Region: DUF1077; pfam06417" /db_xref="CDD:219016" misc_feature 321..383 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /inference="non-experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q5J8M3.2); transmembrane region" misc_feature 459..521 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /inference="non-experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q5J8M3.2); transmembrane region" variation 93 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="g" /replace="t" /db_xref="dbSNP:1132869" variation 97 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="c" /replace="g" /db_xref="dbSNP:139134705" variation 127 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="c" /replace="t" /db_xref="dbSNP:371572098" exon 158..272 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /inference="alignment:Splign:1.39.8" variation 175 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="c" /replace="g" /db_xref="dbSNP:140809470" variation 177 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="a" /replace="g" /db_xref="dbSNP:145064675" variation 194 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="g" /replace="t" /db_xref="dbSNP:371911554" variation 235 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="c" /replace="t" /db_xref="dbSNP:79389628" variation 263 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="c" /replace="g" /db_xref="dbSNP:79609466" exon 273..426 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /inference="alignment:Splign:1.39.8" variation 296 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="a" /replace="t" /db_xref="dbSNP:200052989" variation 302 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="a" /replace="c" /db_xref="dbSNP:11544433" variation 321 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="a" /replace="g" /db_xref="dbSNP:11544434" variation 363 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="g" /replace="t" /db_xref="dbSNP:11544437" variation 406 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="a" /replace="c" /db_xref="dbSNP:181943133" variation 414 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="c" /replace="g" /db_xref="dbSNP:11544438" exon 427..587 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /inference="alignment:Splign:1.39.8" variation 437 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="a" /replace="g" /db_xref="dbSNP:377044886" variation 479 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="c" /replace="t" /db_xref="dbSNP:371080541" variation 482 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="c" /replace="t" /db_xref="dbSNP:376299788" variation 484 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="c" /replace="t" /db_xref="dbSNP:116858574" variation 554 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="a" /replace="g" /db_xref="dbSNP:368550740" variation 557 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="a" /replace="g" /db_xref="dbSNP:375492262" variation 581 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="c" /replace="t" /db_xref="dbSNP:375749312" exon 588..991 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /inference="alignment:Splign:1.39.8" variation 589 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="a" /replace="g" /db_xref="dbSNP:138144365" variation 621 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="c" /replace="t" /db_xref="dbSNP:372229813" variation 651 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="c" /replace="t" /db_xref="dbSNP:201082530" variation 659 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="a" /replace="g" /db_xref="dbSNP:374866723" variation 685 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="a" /replace="c" /db_xref="dbSNP:11544436" variation 694 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="c" /replace="t" /db_xref="dbSNP:372247843" variation 722 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="a" /replace="c" /db_xref="dbSNP:140570424" variation 723 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:112473788" variation 742..743 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="" /replace="ac" /db_xref="dbSNP:201968639" variation 743..744 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="" /replace="ct" /db_xref="dbSNP:71702457" variation 745 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="a" /replace="g" /db_xref="dbSNP:201628991" variation 813 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="c" /replace="t" /db_xref="dbSNP:7598" variation 824 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="a" /replace="c" /db_xref="dbSNP:16958862" variation 837 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="a" /replace="t" /db_xref="dbSNP:16958864" variation 866 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="g" /replace="t" /db_xref="dbSNP:147712898" variation 894 /gene="EMC4" /gene_synonym="PIG17; TMEM85" /replace="a" /replace="g" /db_xref="dbSNP:371851468" ORIGIN
acgctggtgggcctgttgtggagtacgctttggactgagaagcatcgaggctataggacgcagctgttgccatgacggcccaggggggcctggtggctaaccgaggccggcgcttcaagtgggccattgagctaagcgggcctggaggaggcagcaggggtcgaagtgaccggggcagtggccagggagactcgctctacccagtcggttacttggacaagcaagtgcctgataccagcgtgcaagagacagaccggatcctggtggagaagcgctgctgggacatcgccttgggtcccctcaaacagattcccatgaatctcttcatcatgtacatggcaggcaatactatctccatcttccctactatgatggtgtgtatgatggcctggcgacccattcaggcacttatggccatttcagccactttcaagatgttagaaagttcaagccagaagtttcttcagggtttggtctatctcattgggaacctgatgggtttggcattggctgtttacaagtgccagtccatgggactgttacctacacatgcatcggattggttagccttcattgagccccctgagagaatggagttcagtggtggaggactgcttttgtgaacatgagaaagcagcgcctggtccctatgtatttgggtcttatttacatccttctttaagcccagtggctcctcagcatactcttaaactaatcacttatgttaaaaagaaccaaaagactcttttctccatggtggggtgacaggtcctagaaggacaatgtgcatattacgacaaacacaaagaaactataccataacccaaggctgaaaataatgtagaaaactttatttttgtttccagtacagagcaaaacaacaacaaaaaaacataactatgtaaacaagagaataactgctgctaaatcaagaactgttgcagcatctcctttcaataaattaaatggttgagaacaatgcataaaaaaaaaaaaaaaaaaaaaaaaaaaaa
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ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:51234 -> Biological process: GO:0006915 [apoptotic process] evidence: IEA GeneID:51234 -> Cellular component: GO:0016021 [integral to membrane] evidence: IDA GeneID:51234 -> Cellular component: GO:0072546 [ER membrane protein complex] evidence: IDA
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