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2024-04-26 01:02:08, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001143994 1471 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens Ras association (RalGDS/AF-6) domain family
(N-terminal) member 7 (RASSF7), transcript variant 3, mRNA.
ACCESSION NM_001143994
VERSION NM_001143994.1 GI:221136875
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 1471)
AUTHORS Djos,A., Martinsson,T., Kogner,P. and Caren,H.
TITLE The RASSF gene family members RASSF5, RASSF6 and RASSF7 show
frequent DNA methylation in neuroblastoma
JOURNAL Mol. Cancer 11, 40 (2012)
PUBMED 22695170
REMARK GeneRIF: The RASSF gene family members RASSF5, RASSF6 and RASSF7
show frequent DNA methylation in neuroblastoma.
Publication Status: Online-Only
REFERENCE 2 (bases 1 to 1471)
AUTHORS Takahashi,S., Ebihara,A., Kajiho,H., Kontani,K., Nishina,H. and
Katada,T.
TITLE RASSF7 negatively regulates pro-apoptotic JNK signaling by
inhibiting the activity of phosphorylated-MKK7
JOURNAL Cell Death Differ. 18 (4), 645-655 (2011)
PUBMED 21278800
REMARK GeneRIF: RASSF7 acts in concert with N-Ras to constitute a
stress-sensitive temporary mechanism of apoptotic regulation.
REFERENCE 3 (bases 1 to 1471)
AUTHORS Recino,A., Sherwood,V., Flaxman,A., Cooper,W.N., Latif,F., Ward,A.
and Chalmers,A.D.
TITLE Human RASSF7 regulates the microtubule cytoskeleton and is required
for spindle formation, Aurora B activation and chromosomal
congression during mitosis
JOURNAL Biochem. J. 430 (2), 207-213 (2010)
PUBMED 20629633
REMARK GeneRIF: RASSF7 regulates the microtubule cytoskeleton and is
required for spindle formation, Aurora B activation and chromosomal
congression during mitosis.
REFERENCE 4 (bases 1 to 1471)
AUTHORS Lescai,F., Blanche,H., Nebel,A., Beekman,M., Sahbatou,M.,
Flachsbart,F., Slagboom,E., Schreiber,S., Sorbi,S., Passarino,G.
and Franceschi,C.
TITLE Human longevity and 11p15.5: a study in 1321 centenarians
JOURNAL Eur. J. Hum. Genet. 17 (11), 1515-1519 (2009)
PUBMED 19367319
REMARK GeneRIF: Observational study and meta-analysis of gene-disease
association. (HuGE Navigator)
REFERENCE 5 (bases 1 to 1471)
AUTHORS Sherwood,V., Manbodh,R., Sheppard,C. and Chalmers,A.D.
TITLE RASSF7 is a member of a new family of RAS association
domain-containing proteins and is required for completing mitosis
JOURNAL Mol. Biol. Cell 19 (4), 1772-1782 (2008)
PUBMED 18272789
REFERENCE 6 (bases 1 to 1471)
AUTHORS Tsang,H.T., Connell,J.W., Brown,S.E., Thompson,A., Reid,E. and
Sanderson,C.M.
TITLE A systematic analysis of human CHMP protein interactions:
additional MIT domain-containing proteins bind to multiple
components of the human ESCRT III complex
JOURNAL Genomics 88 (3), 333-346 (2006)
PUBMED 16730941
REFERENCE 7 (bases 1 to 1471)
AUTHORS Iarmolinskii,D.G., Kartel,N.A., Ermak,G., Demidchik,Iu.E. and
Figge,J.
TITLE [Study of HRas1 minisatellite frequencies in children with thyroid
papillary cancer]
JOURNAL Tsitol. Genet. 38 (1), 9-14 (2004)
PUBMED 15098441
REMARK GeneRIF: 'rare' alleles of HRas1 minisatellite are associated with
increased risk of papillary thyroid cancer formation in children
and adolescents after Chernobyl accident
REFERENCE 8 (bases 1 to 1471)
AUTHORS Morris,J.A., Kandpal,G., Ma,L. and Austin,C.P.
TITLE DISC1 (Disrupted-In-Schizophrenia 1) is a centrosome-associated
protein that interacts with MAP1A, MIPT3, ATF4/5 and NUDEL:
regulation and loss of interaction with mutation
JOURNAL Hum. Mol. Genet. 12 (13), 1591-1608 (2003)
PUBMED 12812986
REFERENCE 9 (bases 1 to 1471)
AUTHORS Weitzel,J.N., Kasperczyk,A., Mohan,C. and Krontiris,T.G.
TITLE The HRAS1 gene cluster: two upstream regions recognizing
transcripts and a third encoding a gene with a leucine zipper
domain
JOURNAL Genomics 14 (2), 309-319 (1992)
PUBMED 1339391
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
BC106921.1, BC106922.1 and CA315057.1.
Transcript Variant: This variant (3) lacks an exon in the 3' coding
region, compared to variant 1. This difference results in a
frameshift and a protein (isoform 3) with a shorter and distinct
C-terminus, compared to isoform 1.
##Evidence-Data-START##
Transcript exon combination :: BC106922.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025087, ERS025092 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-300 BC106921.1 9-308
301-1393 BC106922.1 309-1401
1394-1471 CA315057.1 1-78 c
FEATURES Location/Qualifiers
source 1..1471
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="11"
/map="11p15.5"
gene 1..1471
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/note="Ras association (RalGDS/AF-6) domain family
(N-terminal) member 7"
/db_xref="GeneID:8045"
/db_xref="HGNC:1166"
/db_xref="MIM:143023"
exon 1..28
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/inference="alignment:Splign:1.39.8"
variation 28
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace=""
/replace="g"
/db_xref="dbSNP:142735008"
exon 29..159
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/inference="alignment:Splign:1.39.8"
variation 30
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="c"
/db_xref="dbSNP:373449348"
CDS 36..998
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/note="isoform 3 is encoded by transcript variant 3;
HRAS1-related cluster-1; Ras association (RalGDS/AF-6)
domain family 7; ras association domain-containing protein
7; HRAS1-related cluster protein 1"
/codon_start=1
/product="ras association domain-containing protein 7
isoform 3"
/protein_id="NP_001137466.1"
/db_xref="GI:221136876"
/db_xref="CCDS:CCDS44505.1"
/db_xref="GeneID:8045"
/db_xref="HGNC:1166"
/db_xref="MIM:143023"
/translation="
MLLGLAAMELKVWVDGIQRVVCGVSEQTTCQEVVIALAQAIGQTGRFVLVQRLREKERQLLPQECPVGAQATCGQFASDVQFVLRRTGPSLAGRPSSDSCPPPERCLIRASLPVKPRAALGCEPRKTLTPEPAPSLSRPGPAAPVTPTPGCCTDLRGLELRVQRNAEELGHEAFWEQELRREQAREREGQARLQALSAATAEHAARLQALDAQARALEAELQLAAEAPGPPSPMASATERLHQDLAVQERQSAEVQGSLALVSRALEAAERALQAQAQELEELNRELRQCNLQQFIQQTGAALPPPPRPDRGPPGTQWPP
"
misc_feature 57..299
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/note="Ras association (RalGDS/AF-6) domain; Region: RA;
smart00314"
/db_xref="CDD:197646"
misc_feature order(135..137,177..179)
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/note="charged pocket; other site"
/db_xref="CDD:176352"
misc_feature order(183..194,288..293)
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/note="hydrophobic patch; other site"
/db_xref="CDD:176352"
variation 42
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376543695"
variation 45
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="g"
/db_xref="dbSNP:148569950"
variation 52
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="g"
/db_xref="dbSNP:375319457"
variation 54
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200646397"
variation 65
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:143459467"
variation 66
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="c"
/db_xref="dbSNP:199741854"
variation 68
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200876114"
variation 77
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370836177"
variation 126
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="g"
/db_xref="dbSNP:200008828"
variation 137
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:202159972"
variation 140
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="c"
/db_xref="dbSNP:367694279"
variation 141
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371827786"
variation 142
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376525434"
exon 160..857
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/inference="alignment:Splign:1.39.8"
variation 172
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="g"
/db_xref="dbSNP:377067888"
variation 208
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368746449"
variation 235
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:146160844"
variation 236
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140015139"
variation 240
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371463729"
variation 249
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201793283"
variation 250
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369226507"
variation 269
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:372646867"
variation 272
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375659022"
variation 277
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="t"
/db_xref="dbSNP:371111191"
variation 300
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2242183"
variation 304
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="g"
/replace="t"
/db_xref="dbSNP:57084297"
variation 337
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200079468"
variation 339
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:151266925"
variation 348
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139307758"
variation 349
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:202178972"
variation 373
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:149920152"
variation 384
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:377366099"
variation 389
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144999609"
variation 390
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="g"
/db_xref="dbSNP:142198842"
variation 391
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373904419"
variation 392
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146119336"
variation 408
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147855052"
variation 447
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:191057277"
variation 461
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146029107"
variation 489
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201977289"
variation 502
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2242182"
variation 518
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:11246189"
variation 545
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200238355"
variation 551
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="g"
/db_xref="dbSNP:201015304"
variation 554
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200224949"
variation 563
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371927899"
variation 576
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:202059750"
variation 588
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376601467"
variation 589
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368323944"
variation 652
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:182995401"
variation 784
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375190645"
variation 788
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="g"
/db_xref="dbSNP:111862990"
variation 799
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373052565"
exon 858..986
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/inference="alignment:Splign:1.39.8"
variation 859
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:141096443"
variation 887
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:187452674"
variation 888
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139977222"
variation 897
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:368113813"
variation 899
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="g"
/replace="t"
/db_xref="dbSNP:370578097"
variation 909
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="c"
/db_xref="dbSNP:374951882"
variation 914
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:367611875"
variation 926
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:34954482"
variation 940
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:35670527"
variation 941
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372840376"
variation 946
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:141676372"
variation 950
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150125797"
variation 958
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:34358040"
variation 970
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374517499"
variation 972
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139808560"
variation 985
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199651457"
exon 987..1454
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/inference="alignment:Splign:1.39.8"
variation 991
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:151072716"
variation 994
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373789888"
variation 999
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369335309"
variation 1000
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371569281"
variation 1019
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:374791179"
variation 1027
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:189139046"
variation 1045
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200997178"
variation 1059
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368847112"
variation 1078
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:7109278"
STS 1079..1274
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/standard_name="STS-M91083"
/db_xref="UniSTS:36055"
variation 1087
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="g"
/replace="t"
/db_xref="dbSNP:375760553"
STS 1089..1327
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/standard_name="STS-M91083"
/db_xref="UniSTS:38240"
variation 1108
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370118538"
variation 1130
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370067890"
variation 1226
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373811537"
variation 1227
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:73399078"
variation 1252
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="g"
/db_xref="dbSNP:3168185"
variation 1317
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:181071400"
variation 1381
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:148507933"
variation 1428
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:184654498"
ORIGIN
ggggagggggcagtgtcctccgagccaggacaggcatgttgttgggactggcggccatggagctgaaggtgtgggtggatggcatccagcgtgtggtctgtggggtctcagagcagaccacctgccaggaagtggtcatcgcactagcccaagcaataggccagactggccgctttgtgcttgtgcagcggcttcgggagaaggagcggcagttgctgccacaagagtgtccagtgggcgcccaggccacctgcggacagtttgccagcgatgtccagtttgtcctgaggcgcacagggcccagcctagctgggaggccctcctcagacagctgtccacccccggaacgctgcctaattcgtgccagcctccctgtaaagccacgggctgcgctgggctgtgagccccgcaaaacactgacccccgagccagcccccagcctctcacgccctgggcctgcggcccctgtgacacccacaccaggctgctgcacagacctgcggggcctggagctcagggtgcagaggaatgctgaggagctgggccatgaggccttctgggagcaagagctgcgccgggagcaggcccgggagcgagagggacaggcacgcctgcaggcactaagtgcggccactgctgagcatgccgcccggctgcaggccctggacgctcaggcccgtgccctggaggctgagctgcagctggcagcggaggcccctgggcccccctcacctatggcatctgccactgagcgcctgcaccaggacctggctgttcaggagcggcagagtgcggaggtgcagggcagcctggctctggtgagccgggccctggaggcagcagagcgagccttgcaggctcaggctcaggagctggaggagctgaaccgagagctccgtcagtgcaacctgcagcagttcatccagcagaccggggctgcgctgccaccgcccccacggcctgacaggggccctcctggcactcagtggcccccatgacgcagaactcctggaggtagcagcagctcctgccccagagtggtgtcctctggcagcccagccccaggctctgtgacagcctagtgagggctgcaagaccatcctgcccggaccacagaaggagagttggcggtcacagagggctcctctgccaggcagtgggaagccctgggtttggcctcaggagctgggggtgcagtgggggactgccctagtccttgccaggtcgccagcaccctggagaagcatggggcgtagccagctcggaacttgccaggccccaaaggccacgactgcctgttggggacaggagatgcatggacagtgtgctcaagctgtgggcatgtgcttgcctgcgggagaggtccttcactgtgtgtacacagcaagagcatgtgtgtgccacttcccctaccccaacgtgaaaacctcaataaactgcccgaagcagcttgaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:8045 -> Molecular function: GO:0003677 [DNA binding] evidence: NAS
GeneID:8045 -> Biological process: GO:0006355 [regulation of transcription, DNA-dependent] evidence: NAS
GeneID:8045 -> Biological process: GO:0006915 [apoptotic process] evidence: IEA
GeneID:8045 -> Biological process: GO:0007165 [signal transduction] evidence: IEA
GeneID:8045 -> Cellular component: GO:0005634 [nucleus] evidence: NAS
GeneID:8045 -> Cellular component: GO:0005737 [cytoplasm] evidence: IEA
GeneID:8045 -> Cellular component: GO:0005815 [microtubule organizing center] evidence: IEA
by
@meso_cacase at
DBCLS
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