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2024-04-27 04:00:44, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001143993 1746 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens Ras association (RalGDS/AF-6) domain family
(N-terminal) member 7 (RASSF7), transcript variant 2, mRNA.
ACCESSION NM_001143993
VERSION NM_001143993.1 GI:221136871
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 1746)
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 1746)
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 1746)
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 1746)
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 1746)
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 1746)
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 1746)
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 1746)
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 1746)
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
AL535761.3, AP006284.2, BC106921.1 and CA315057.1.
Transcript Variant: This variant (2) has multiple differences in
the 5' UTR and 3' coding region, compared to variant 1. These
differences result in a protein (isoform 2) with a shorter and
distinct C-terminus, compared to isoform 1.
##Evidence-Data-START##
Transcript exon combination :: AL544102.3, AL549374.3 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025082, ERS025085 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-194 AL535761.3 1-194
195-334 AP006284.2 20796-20935
335-335 BC106921.1 308-308
336-892 AP006284.2 20937-21493
893-1699 AP006284.2 21906-22712
1700-1746 CA315057.1 1-47 c
FEATURES Location/Qualifiers
source 1..1746
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="11"
/map="11p15.5"
gene 1..1746
/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..63
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/inference="alignment:Splign:1.39.8"
variation 56
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:183456713"
exon 64..194
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/inference="alignment:Splign:1.39.8"
variation 65
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="c"
/db_xref="dbSNP:373449348"
CDS 71..1084
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/note="isoform 2 is encoded by transcript variant 2;
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 2"
/protein_id="NP_001137465.1"
/db_xref="GI:221136872"
/db_xref="CCDS:CCDS44506.1"
/db_xref="GeneID:8045"
/db_xref="HGNC:1166"
/db_xref="MIM:143023"
/translation="
MLLGLAAMELKVWVDGIQRVVCGVSEQTTCQEVVIALAQAIGQTGRFVLVQRLREKERQLLPQECPVGAQATCGQFASDVQFVLRRTGPSLAGRPSSDSCPPPERCLIRASLPVKPRAALGCEPRKTLTPEPAPSLSRPGPAAPVTPTPGCCTDLRGLELRVQRNAEELGHEAFWEQELRREQAREREGQARLQALSAATAEHAARLQALDAQARALEAELQLAAEAPGPPSPMASATERLHQDLAVQERQSAEVQGSLALVSRALEAAERALQAQAQELEELNRELRQCNLQQFIQQTGAALPPPPRPDRGPPGTQVGVVLGGGWEVRTWPSPTPS
"
misc_feature 92..334
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/note="Ras association (RalGDS/AF-6) domain; Region: RA;
smart00314"
/db_xref="CDD:197646"
misc_feature order(170..172,212..214)
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/note="charged pocket; other site"
/db_xref="CDD:176352"
misc_feature order(218..229,323..328)
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/note="hydrophobic patch; other site"
/db_xref="CDD:176352"
variation 77
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376543695"
variation 80
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="g"
/db_xref="dbSNP:148569950"
variation 87
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="g"
/db_xref="dbSNP:375319457"
variation 89
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200646397"
variation 100
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:143459467"
variation 101
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="c"
/db_xref="dbSNP:199741854"
variation 103
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200876114"
variation 112
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370836177"
variation 161
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="g"
/db_xref="dbSNP:200008828"
variation 172
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:202159972"
variation 175
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="c"
/db_xref="dbSNP:367694279"
variation 176
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371827786"
variation 177
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376525434"
exon 195..892
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/inference="alignment:Splign:1.39.8"
variation 207
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="g"
/db_xref="dbSNP:377067888"
variation 243
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368746449"
variation 270
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:146160844"
variation 271
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140015139"
variation 275
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371463729"
variation 284
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201793283"
variation 285
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369226507"
variation 304
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:372646867"
variation 307
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375659022"
variation 312
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="t"
/db_xref="dbSNP:371111191"
variation 335
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2242183"
variation 339
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="g"
/replace="t"
/db_xref="dbSNP:57084297"
variation 372
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200079468"
variation 374
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:151266925"
variation 383
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139307758"
variation 384
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:202178972"
variation 408
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:149920152"
variation 419
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:377366099"
variation 424
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144999609"
variation 425
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="g"
/db_xref="dbSNP:142198842"
variation 426
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373904419"
variation 427
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146119336"
variation 443
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147855052"
variation 482
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:191057277"
variation 496
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146029107"
variation 524
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201977289"
variation 537
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2242182"
variation 553
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:11246189"
variation 580
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200238355"
variation 586
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="g"
/db_xref="dbSNP:201015304"
variation 589
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200224949"
variation 598
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371927899"
variation 611
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:202059750"
variation 623
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376601467"
variation 624
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368323944"
variation 687
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:182995401"
variation 819
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375190645"
variation 823
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="g"
/db_xref="dbSNP:111862990"
variation 834
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373052565"
exon 893..1729
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/inference="alignment:Splign:1.39.8"
variation 894
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:141096443"
variation 922
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:187452674"
variation 923
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139977222"
variation 932
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:368113813"
variation 934
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="g"
/replace="t"
/db_xref="dbSNP:370578097"
variation 944
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="c"
/db_xref="dbSNP:374951882"
variation 949
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:367611875"
variation 961
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:34954482"
variation 975
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:35670527"
variation 976
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372840376"
variation 981
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:141676372"
variation 985
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150125797"
variation 993
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:34358040"
variation 1005
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374517499"
variation 1007
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139808560"
variation 1020
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199651457"
variation 1024
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:368570830"
variation 1036
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200731347"
variation 1037
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="g"
/db_xref="dbSNP:367859913"
variation 1068
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199789820"
variation 1090
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201053421"
variation 1104
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:34822421"
variation 1109
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145732118"
variation 1116
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:140192306"
variation 1123
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141908941"
variation 1164
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144683330"
variation 1165
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:148520444"
variation 1181
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="g"
/db_xref="dbSNP:142859867"
variation 1193
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201007942"
variation 1195
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200004078"
variation 1206
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201821227"
variation 1209
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="g"
/replace="t"
/db_xref="dbSNP:200991248"
variation 1215
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:370957240"
variation 1253
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="g"
/db_xref="dbSNP:368492017"
variation 1257
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200464920"
variation 1258
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:202139378"
variation 1259
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:73399077"
variation 1266
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:151072716"
variation 1269
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373789888"
variation 1274
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369335309"
variation 1275
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371569281"
variation 1294
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:374791179"
variation 1302
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:189139046"
variation 1320
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200997178"
variation 1334
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368847112"
variation 1353
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:7109278"
STS 1354..1549
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/standard_name="STS-M91083"
/db_xref="UniSTS:36055"
variation 1362
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="g"
/replace="t"
/db_xref="dbSNP:375760553"
STS 1364..1602
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/standard_name="STS-M91083"
/db_xref="UniSTS:38240"
variation 1383
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370118538"
variation 1405
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370067890"
variation 1501
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373811537"
variation 1502
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:73399078"
variation 1527
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="g"
/db_xref="dbSNP:3168185"
variation 1592
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:181071400"
variation 1656
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="a"
/replace="g"
/db_xref="dbSNP:148507933"
variation 1703
/gene="RASSF7"
/gene_synonym="C11orf13; HRAS1; HRC1"
/replace="c"
/replace="t"
/db_xref="dbSNP:184654498"
ORIGIN
cggcgctgggggcggcaggttgcggcggcgccggagcgggtctccaggctggcgagcgcccaggacaggcatgttgttgggactggcggccatggagctgaaggtgtgggtggatggcatccagcgtgtggtctgtggggtctcagagcagaccacctgccaggaagtggtcatcgcactagcccaagcaataggccagactggccgctttgtgcttgtgcagcggcttcgggagaaggagcggcagttgctgccacaagagtgtccagtgggcgcccaggccacctgcggacagtttgccagcgatgtccagtttgtcctgaggcgcacagggcccagcctagctgggaggccctcctcagacagctgtccacccccggaacgctgcctaattcgtgccagcctccctgtaaagccacgggctgcgctgggctgtgagccccgcaaaacactgacccccgagccagcccccagcctctcacgccctgggcctgcggcccctgtgacacccacaccaggctgctgcacagacctgcggggcctggagctcagggtgcagaggaatgctgaggagctgggccatgaggccttctgggagcaagagctgcgccgggagcaggcccgggagcgagagggacaggcacgcctgcaggcactaagtgcggccactgctgagcatgccgcccggctgcaggccctggacgctcaggcccgtgccctggaggctgagctgcagctggcagcggaggcccctgggcccccctcacctatggcatctgccactgagcgcctgcaccaggacctggctgttcaggagcggcagagtgcggaggtgcagggcagcctggctctggtgagccgggccctggaggcagcagagcgagccttgcaggctcaggctcaggagctggaggagctgaaccgagagctccgtcagtgcaacctgcagcagttcatccagcagaccggggctgcgctgccaccgcccccacggcctgacaggggccctcctggcactcaggtcggagtggttctggggggaggctgggaggtgaggacctggcccagccccactccaagctgacttcccaacccacagggccctctgcctccagccagagaggagtccctcctgggcgctccctctgagtcccatgctggtgcccagcctaggccccgagggtatgtctgtgccccacctccccctggggcaccgggccctcctgtggctgcagccacctcagcctgtgtcctcccgcagtggcccccatgacgcagaactcctggaggtagcagcagctcctgccccagagtggtgtcctctggcagcccagccccaggctctgtgacagcctagtgagggctgcaagaccatcctgcccggaccacagaaggagagttggcggtcacagagggctcctctgccaggcagtgggaagccctgggtttggcctcaggagctgggggtgcagtgggggactgccctagtccttgccaggtcgccagcaccctggagaagcatggggcgtagccagctcggaacttgccaggccccaaaggccacgactgcctgttggggacaggagatgcatggacagtgtgctcaagctgtgggcatgtgcttgcctgcgggagaggtccttcactgtgtgtacacagcaagagcatgtgtgtgccacttcccctaccccaacgtgaaaacctcaataaactgcccgaagcagcttgaaaaaaaaaaaaaaaaaa
//
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
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@meso_cacase at
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