2024-03-28 19:17:17, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_015124 4337 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens GRAM domain containing 4 (GRAMD4), mRNA. ACCESSION NM_015124 XM_027105 VERSION NM_015124.3 GI:319738595 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 4337) AUTHORS John,K., Alla,V., Meier,C. and Putzer,B.M. TITLE GRAMD4 mimics p53 and mediates the apoptotic function of p73 at mitochondria JOURNAL Cell Death Differ. 18 (5), 874-886 (2011) PUBMED 21127500 REMARK GeneRIF: GRAMD4 induces changes in Bcl-2 and Bax protein levels Erratum:[Cell Death Differ. 2012 Mar;19(3):552] REFERENCE 2 (bases 1 to 4337) AUTHORS Stanelle,J., Tu-Rapp,H. and Putzer,B.M. TITLE A novel mitochondrial protein DIP mediates E2F1-induced apoptosis independently of p53 JOURNAL Cell Death Differ. 12 (4), 347-357 (2005) PUBMED 15565177 REMARK GeneRIF: localizes to the mitochondria, upregulated following E2F1 induction GeneRIF: DIP induces p53-independent caspase-dependent and -independent apoptosis. DIP is localized in the mitochondria. DIP accumulates upon E2F1 activation. REFERENCE 3 (bases 1 to 4337) 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 REFERENCE 4 (bases 1 to 4337) AUTHORS Stanelle,J., Stiewe,T., Theseling,C.C., Peter,M. and Putzer,B.M. TITLE Gene expression changes in response to E2F1 activation JOURNAL Nucleic Acids Res. 30 (8), 1859-1867 (2002) PUBMED 11937641 COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AB018310.2, AL096766.12 and R39786.1. On Jan 20, 2011 this sequence version replaced gi:67782363. Summary: GRAMD4 is a mitochondrial effector of E2F1 (MIM 189971)-induced apoptosis (Stanelle et al., 2005 [PubMed 15565177]).[supplied by OMIM, Jan 2011]. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. ##Evidence-Data-START## Transcript exon combination :: CR456470.1, BC129837.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025081, ERS025082 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-2033 AB018310.2 175-2207 2034-4307 AL096766.12 29377-31650 4308-4337 R39786.1 1-30 c FEATURES Location/Qualifiers source 1..4337 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="22" /map="22q13.31" gene 1..4337 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /note="GRAM domain containing 4" /db_xref="GeneID:23151" /db_xref="HGNC:29113" /db_xref="HPRD:11107" /db_xref="MIM:613691" exon 1..201 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /inference="alignment:Splign:1.39.8" variation 34 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:140504996" variation 35 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:375181598" CDS 40..1776 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /note="death-inducing-protein; death-inducing protein" /codon_start=1 /product="GRAM domain-containing protein 4" /protein_id="NP_055939.1" /db_xref="GI:67763814" /db_xref="CCDS:CCDS33672.1" /db_xref="GeneID:23151" /db_xref="HGNC:29113" /db_xref="HPRD:11107" /db_xref="MIM:613691" /translation="
MLRRLDKIRFRGHKRDDFLDLAESPNASDTECSDEIPLKVPRTSPRDSEELRDPAGPGTLIMATGVQDFNRTEFDRLNEIKGHLEIALLEKHFLQEELRKLREETNAEMLRQELDRERQRRMELEQKVQEVLKARTEEQMAQQPPKGQAQASNGAERRSQGLSSRLQKWFYERFGEYVEDFRFQPEENTVETEEPLSARRLTENMRRLKRGAKPVTNFVKNLSALSDWYSVYTSAIAFTVYMNAVWHGWAIPLFLFLAILRLSLNYLIARGWRIQWSIVPEVSEPVEPPKEDLTVSEKFQLVLDVAQKAQNLFGKMADILEKIKNLFMWVQPEITQKLYVALWAAFLASCFFPYRLVGLAVGLYAGIKFFLIDFIFKRCPRLRAKYDTPYIIWRSLPTDPQLKERSSAAVSRRLQTTSSRSYVPSAPAGLGKEEDAGRFHSTKKGNFHEIFNLTENERPLAVCENGWRCCLINRDRKMPTDYIRNGVLYVTENYLCFESSKSGSSKRNKVIKLVDITDIQKYKVLSVLPGSGMGIAVSTPSTQKPLVFGAMVHRDEAFETILSQYIKITSAAASGGDS
" misc_feature 109..111 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /experiment="experimental evidence, no additional details recorded" /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot (Q6IC98.1); phosphorylation site" misc_feature 121..123 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /experiment="experimental evidence, no additional details recorded" /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot (Q6IC98.1); phosphorylation site" misc_feature 757..819 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /inference="non-experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q6IC98.1); transmembrane region" misc_feature 1039..1101 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /inference="non-experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q6IC98.1); transmembrane region" misc_feature 1105..1167 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /inference="non-experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q6IC98.1); transmembrane region" misc_feature 1396..1608 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /note="GRAM domain; Region: GRAM; pfam02893" /db_xref="CDD:190467" variation 97 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="g" /db_xref="dbSNP:142967893" variation 100 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:367882036" variation 104 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:370713440" variation 139 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:374106125" variation 157 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="g" /replace="t" /db_xref="dbSNP:75994818" variation 170 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:140068081" variation 180 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="c" /db_xref="dbSNP:367756638" exon 202..322 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /inference="alignment:Splign:1.39.8" variation 222 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="g" /db_xref="dbSNP:200303713" exon 323..443 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /inference="alignment:Splign:1.39.8" variation 334 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:374112415" variation 357 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:147577527" variation 360 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:142065018" variation 387 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:145906275" variation 395 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:376982476" variation 403 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="t" /db_xref="dbSNP:138818823" exon 444..505 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /inference="alignment:Splign:1.39.8" variation 448 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:370294828" variation 455 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:149306643" variation 468 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="g" /replace="t" /db_xref="dbSNP:375479472" variation 497 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:376816295" exon 506..638 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /inference="alignment:Splign:1.39.8" variation 509 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:143591814" variation 510 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:148064648" variation 511 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:141819452" variation 515 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="g" /replace="t" /db_xref="dbSNP:36211078" variation 523 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:146061140" variation 542 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:201013436" variation 556 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:368538880" variation 561 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:2542040" variation 562 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:61552185" variation 570 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:141555305" variation 571 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:139348663" variation 596 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="t" /db_xref="dbSNP:372025092" variation 625 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:145387351" exon 639..664 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /inference="alignment:Splign:1.39.8" exon 665..756 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /inference="alignment:Splign:1.39.8" variation 669 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:202227527" variation 670 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:200160992" variation 681 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:16995533" variation 686 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:5769060" variation 720 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:144976533" variation 724 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:200909649" variation 756 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:147561076" exon 757..848 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /inference="alignment:Splign:1.39.8" variation 804 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:375706316" exon 849..897 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /inference="alignment:Splign:1.39.8" variation 873 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:375236476" exon 898..969 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /inference="alignment:Splign:1.39.8" variation 902 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="g" /db_xref="dbSNP:368967710" variation 954 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:372744256" variation 955 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:113662863" variation 957 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:139953287" exon 970..1013 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /inference="alignment:Splign:1.39.8" variation 979 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:377286272" variation 997 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="g" /db_xref="dbSNP:369736360" variation 1001 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="t" /db_xref="dbSNP:200752570" variation 1008 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:200059488" exon 1014..1123 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /inference="alignment:Splign:1.39.8" variation 1061 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:151176619" exon 1124..1278 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /inference="alignment:Splign:1.39.8" variation 1138 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="t" /db_xref="dbSNP:375447907" variation 1154 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:367633187" variation 1172 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:371794625" variation 1188 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:192534639" variation 1206 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="g" /db_xref="dbSNP:141113580" variation 1208 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="t" /db_xref="dbSNP:138062317" variation 1209 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:149535995" variation 1222 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:376626431" variation 1238 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:368573910" variation 1261 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:376340420" variation 1266 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:144925706" exon 1279..1423 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /inference="alignment:Splign:1.39.8" variation 1286 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:138805326" variation 1292 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:141984137" variation 1293 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:146325443" variation 1305 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:148538932" variation 1344 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:141922091" variation 1348 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:150667253" variation 1383 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:201846264" variation 1389 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:369913766" variation 1394 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:144916604" variation 1412 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:200706485" variation 1422 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:147965854" exon 1424..1517 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /inference="alignment:Splign:1.39.8" variation 1428 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:200137778" variation 1480 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="g" /replace="t" /db_xref="dbSNP:372441521" variation 1494 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:140274659" variation 1497 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="g" /db_xref="dbSNP:376984154" variation 1507 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:370970861" variation 1512 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:144224839" exon 1518..1602 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /inference="alignment:Splign:1.39.8" variation 1530 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:145491235" variation 1557 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:184410177" exon 1603..1671 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /inference="alignment:Splign:1.39.8" variation 1652 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:9627529" exon 1672..4316 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /inference="alignment:Splign:1.39.8" variation 1674 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:148851544" variation 1758 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:142588743" variation 1760 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="g" /db_xref="dbSNP:374680937" variation 1766 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="g" /replace="t" /db_xref="dbSNP:150981769" variation 1770 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:201745875" variation 1817 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="t" /db_xref="dbSNP:370777720" variation 1827 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="" /replace="c" /db_xref="dbSNP:200370294" variation 1828 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="" /replace="t" /db_xref="dbSNP:375658129" variation 1882 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:35748179" variation 1887 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:187551483" variation 2075 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:368706381" variation 2195 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:41279839" variation 2207 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:2748342" variation 2257 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:373474616" variation 2260 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="g" /replace="t" /db_xref="dbSNP:191012751" variation 2349 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:5769068" variation 2360 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:370356747" variation 2378 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:375020369" variation 2389 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:41279841" variation 2404 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:7286826" variation 2429 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:41279843" variation 2489 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:17761627" variation 2503 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:2748343" variation 2635 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:138858582" variation 2737 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="g" /db_xref="dbSNP:3209569" variation 2765 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:141975005" variation 2883 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:377261114" variation 2886 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:3747253" variation 2890 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:115392863" variation 2898 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="g" /db_xref="dbSNP:3747254" variation 2903 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:373810373" variation 2909 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:3747255" variation 3071 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:187783771" variation 3079 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="c" /db_xref="dbSNP:2542027" variation 3141 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:3747256" variation 3146 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:192461643" variation 3307 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:370212172" variation 3469 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:184541977" variation 3480 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:149526341" variation 3565 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:2542026" variation 3634 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="g" /replace="t" /db_xref="dbSNP:118128822" variation 3705 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="g" /db_xref="dbSNP:186896966" variation 3877..3878 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="" /replace="c" /db_xref="dbSNP:144223689" variation 3910 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="g" /replace="t" /db_xref="dbSNP:377537401" variation 3922 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="g" /db_xref="dbSNP:191689883" variation 3997 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:376578599" STS 4004..4203 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /standard_name="G43099" /db_xref="UniSTS:94883" STS 4033..4171 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /standard_name="RH15769" /db_xref="UniSTS:90207" STS 4073..4193 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /standard_name="A005V42" /db_xref="UniSTS:39655" STS 4073..4193 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /standard_name="G20543" /db_xref="UniSTS:39654" variation 4090 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:3179" variation 4197 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="c" /replace="t" /db_xref="dbSNP:375680943" variation 4221 /gene="GRAMD4" /gene_synonym="dA59H18.1; DIP; dJ439F8.1" /replace="a" /replace="t" /db_xref="dbSNP:184196406" ORIGIN
cgtcatgttagggtgaagcagaggacctcagtgctgaacatgctaaggaggttggacaaaatcaggttcagaggtcacaagagagatgacttcctcgatctagcggagtctccaaatgcctcggacaccgaatgcagcgacgaaatccccctgaaggtaccgcggacctcgccccgggacagcgaggagctgagggaccctgctggtccagggaccctcatcatggccacaggagtccaggactttaaccggacagagtttgatcgactgaatgagatcaaaggtcacctggaaattgccttattggaaaaacatttcttacaggaggagctccggaagctgcgagaagaaaccaacgcggagatgctgcggcaggagctggaccgcgagcggcagcggcggatggagctggagcagaaggtgcaggaggtgctgaaggccagaaccgaggagcagatggctcagcagcccccaaaagggcaggcccaggccagcaatggagcagagcgccggagccaggggctgtcctcgcgcctgcagaagtggttctacgagcggttcggggagtacgtggaggacttccggttccagcccgaggagaacactgtggagacagaggaacccctgagcgcccgcaggttaactgaaaatatgagacggctcaagcgcggtgccaagccggtcactaactttgtgaagaacctctctgccttatccgactggtactccgtctacacgtctgccattgccttcaccgtgtacatgaatgccgtgtggcatggctgggccatcccattgttcttatttctagcaattctgaggttatccctcaattacctcatcgccagggggtggcggatacagtggagcatcgtgcccgaagtgtctgagcccgtggaacctccaaaggaagacctgactgtgtctgagaagttccagctggtgctggacgtcgcccagaaagcccagaaccttttcgggaagatggctgacatcctggagaagatcaagaacttgttcatgtgggtccagccggagatcacacagaagctgtatgtggcgctctgggctgccttcctggcctcctgcttcttcccctaccgcctggtggggcttgccgtgggactctatgctggtatcaagttcttcctcattgatttcatctttaaacgctgcccgaggctgcgcgccaagtacgacacgccctatatcatctggaggagtctccccaccgacccgcagctcaaggagcgctccagcgccgcagtctcacgcaggctgcagacgacctcgtcacggagctacgtacccagcgcaccggccggcctgggtaaagaggaggacgccggtcgcttccacagcaccaagaagggcaatttccacgagatcttcaatctgacagaaaacgagcgtccgctggcggtgtgcgagaatggctggcgctgctgcctcatcaacagggaccggaagatgcccacggactacatcaggaacggggtgctctacgtcacggagaattacttgtgcttcgaaagctccaaatctgggtcctcaaagaggaacaaagtcatcaagctagtggacatcacggacatccagaagtacaaggtcctgtctgtcctcccaggctcaggcatggggattgccgtgtcgacgccatccacccagaaaccgctcgtgtttggtgccatggtgcacagggatgaggccttcgagaccattctcagccagtacatcaagatcacctcagcggcagcgtctggcggggacagctagtattgacttgcccaggacgttgctggaattttctttttctttttctttttctttttttttttttacgatttggtagtggaaacaattggacatcctcatgagcttttgcaataattctcctggacctgtggttctattgtgttgacctctgcgttttatcgaccaagaaggggccagggctcacagggacgggggtgcccctctcccacagggcacgtcaggtgcctctgagggccacccgcagactgggggagggggcagaggccctcgggggcccgtggagaagacacacaggacccctggccctgcccttctccgttccagcctggacagagaaacctctccagccaccccaagaggttctcgcaaccttgtgtcccgctctccagaggccagaagctcgtccaccaccaaagccatagctgaagagtgcggggcccttcctcctggggacagaaagatgtcgtcaaggagggacatgggggcctttcaccaaccaccgagaaacgggcctggcggccctccttcctcttacatgagaccctcctgtggcatttgcccttggtgccgggctggggccgggcgcagtgaccctgcctgcgctccacactcgctccacgggaacagagagggtgagaagggcccacccctcgcctgccctcagtgtctttggtggcaccttccttgctggcctccagggcgctcagcaccgcgtctgtaagggcctgcctgctgctctcggcctgacacgccggccaggaggtctgtagctggggaccagtaagggcacaggatggtgcaggtaaaagcacatctttctcacactttgctctttggaaggcccaggagaacatccgcgaaggctgttggaggtgctccgagcactgtggcatgtctggcacatggcccccaggctgcggttgcctgggttggttgggggaggaagtggggaggagtgttccgggaccatggtggcccaggctgcagccgcctttgggccatccgagaggctctggcagcccctgtgctttagggagcaaccgtgagccgagcccagaggcctgggcctgcactgcctgcagccgacatgcgacagcgttccctcccccgcgtgcctagccggtgccggtccgggcacagacccccccagcccccgccctgccccagggaagcctgggcttcccgggaacaaggtggcatttgtggagggagcgcccgcaggcctggtctgctggggccgcctgcgctgggctgaagggagggaaaggcggcttgggcctcctggaaggaggtggccaccccgcgggcctgcgtgtctgctggggcggatcccgcagctccctcagcttgtcctgagtcccttgggtgtcgttgagattgttgttttttgaagaaacagaagattctattttttacagcgagcaagctggttttcttatttttgtatcctttttcagatgtaatttttatctttgctccgatcctcatttgctggtgtgggtgagggatccggcggcatgggctggtttcacccccttcacgaggggccgcagagtcacacgctggtgccgggggtgctttggggggagctgcgccgatcaccagattaagcacatgtcctatcccaggcggtggagcggagcccccgtggctctggactgcgcggacgttggcgtcaggatgaccacacggcggcctttcccgaatggggacagaacccgctctgagccgtgggtctggctcctgtaggggactggctctcttggtgcaccaggggagggggacatatcccagtgaaccccaccttggcgcctgaggcaacacagggtgggcactgacccacccccaggggcggctgcagaggcagtgcccgcagacaatggccacacctctctccccagggcccggcagtgcccaaggatgggtccggggcctcggggccaatgagcgcctcttcctaggtgctgggattcagtccccaaacacagcgggaggggtccctggggcagatggggctttaccagcgtcgggtggtttagttcgagtcccttttgtggagaaagggagatgaaaactgaccacgtgccaggtgtggccgaagcccccagggagggccacattcggggagcggggggtcgggggagggccaccgactggctctgctgccagcacaggcccctccctggaagtcctcgggagcggagcgcggatcggcacgggctctgggctccccgtggagagaagctgtagtttttaccaaattgtgtacatctgggcagatgtttaatttctgtgactaatcactgaactagacgaatgttaaattttttatgtctgaagcctgagtctattttggatctgtaaataatcattgccagtgtgacttttgttcaacaaaaggattgtactgtattaagaaccgatgaaaaaaattctcctgtaacatttttttaagaaaactttgtttgtttaaagaaaaagtattgtataaattataatttttatttaaataaacctaaaatgctttgtgctaaggctcaaaaaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:23151 -> Biological process: GO:0006915 [apoptotic process] evidence: IEA GeneID:23151 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA GeneID:23151 -> Cellular component: GO:0031966 [mitochondrial membrane] evidence: IEA
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@meso_cacase at
DBCLS
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