Incidental Mutation 'IGL01867:Ets1'
ID178566
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ets1
Ensembl Gene ENSMUSG00000032035
Gene NameE26 avian leukemia oncogene 1, 5' domain
SynonymsTpl1, Ets-1, p51Ets-1, p42Ets-1
Accession Numbers
Is this an essential gene? Probably essential (E-score: 0.910) question?
Stock #IGL01867
Quality Score
Status
Chromosome9
Chromosomal Location32636221-32757820 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 32734159 bp
ZygosityHeterozygous
Amino Acid Change Aspartic acid to Glycine at position 234 (D234G)
Ref Sequence ENSEMBL: ENSMUSP00000138951 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000034534] [ENSMUST00000050797] [ENSMUST00000184364] [ENSMUST00000184887]
Predicted Effect possibly damaging
Transcript: ENSMUST00000034534
AA Change: D234G

PolyPhen 2 Score 0.880 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000034534
Gene: ENSMUSG00000032035
AA Change: D234G

DomainStartEndE-ValueType
SAM_PNT 53 136 2.56e-48 SMART
low complexity region 266 278 N/A INTRINSIC
ETS 334 419 1.98e-57 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000050797
AA Change: D234G

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000051303
Gene: ENSMUSG00000032035
AA Change: D234G

DomainStartEndE-ValueType
SAM_PNT 53 136 2.56e-48 SMART
ETS 247 332 1.98e-57 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000183879
Predicted Effect probably benign
Transcript: ENSMUST00000184364
SMART Domains Protein: ENSMUSP00000139107
Gene: ENSMUSG00000032035

DomainStartEndE-ValueType
low complexity region 50 62 N/A INTRINSIC
ETS 118 203 1.98e-57 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000184887
AA Change: D234G

PolyPhen 2 Score 0.985 (Sensitivity: 0.74; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000138951
Gene: ENSMUSG00000032035
AA Change: D234G

DomainStartEndE-ValueType
SAM_PNT 53 136 2.56e-48 SMART
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the ETS family of transcription factors, which are defined by the presence of a conserved ETS DNA-binding domain that recognizes the core consensus DNA sequence GGAA/T in target genes. These proteins function either as transcriptional activators or repressors of numerous genes, and are involved in stem cell development, cell senescence and death, and tumorigenesis. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.[provided by RefSeq, Jul 2011]
PHENOTYPE: Homozygotes for targeted null mutations exhibit reduced numbers of peripheral CD8+ T cells, impaired TCR-mediated activation of both CD4+ and CD8+ T cells, increased numbers of IgM-secreting plasma cells, and severely impaired NK cell development. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc10 T C 17: 46,324,438 E213G probably benign Het
Akap6 T C 12: 52,888,008 L761P probably damaging Het
Bbs7 A C 3: 36,573,547 L697R probably benign Het
Cd74 G A 18: 60,808,280 R99H probably benign Het
Cpne6 A G 14: 55,513,680 N182S probably benign Het
Cyp4f17 A G 17: 32,528,083 H429R probably benign Het
Dact2 A T 17: 14,195,670 M756K probably damaging Het
Fam196b A G 11: 34,403,065 E369G probably benign Het
Fat3 A C 9: 16,377,901 S109A probably benign Het
Fras1 G T 5: 96,588,131 M528I probably benign Het
Gm10718 A T 9: 3,025,118 Y194F probably benign Het
Gtf3c1 A G 7: 125,662,376 F1189L probably benign Het
Ift81 A T 5: 122,602,676 probably benign Het
Lag3 A G 6: 124,910,906 S22P probably benign Het
Mos G T 4: 3,870,845 Q324K probably benign Het
Mtx2 T A 2: 74,876,389 V236E probably damaging Het
Naip6 T C 13: 100,300,312 T568A probably benign Het
Olfr175-ps1 A G 16: 58,823,974 F245S probably damaging Het
Olfr780 T C 10: 129,321,716 I31T probably benign Het
Olfr781 T A 10: 129,333,363 L161M probably damaging Het
Olfr794 G A 10: 129,570,827 M57I possibly damaging Het
Olfr920 A C 9: 38,755,898 D70A probably damaging Het
Pcid2 A G 8: 13,078,243 V386A probably benign Het
Pde8b T C 13: 95,100,938 D116G probably damaging Het
Plxnc1 A G 10: 94,798,146 V1365A possibly damaging Het
Prex2 G T 1: 11,098,503 C241F probably benign Het
Prr23a2 A G 9: 98,857,060 E157G probably benign Het
Ptpn4 A T 1: 119,675,599 H836Q probably benign Het
Ptprd C T 4: 76,243,647 R117H probably damaging Het
Rab11fip4 T C 11: 79,683,390 S102P probably benign Het
Slc44a1 G T 4: 53,536,405 V194F probably damaging Het
Synm T A 7: 67,733,474 H1480L probably benign Het
Tmem63a A G 1: 180,956,005 Y175C possibly damaging Het
Trmt61a C T 12: 111,678,716 R29C probably benign Het
Ubap1 C T 4: 41,379,236 T150I probably benign Het
Uimc1 T C 13: 55,075,401 M353V probably benign Het
Usp34 T C 11: 23,384,411 M1135T possibly damaging Het
Vmn1r25 A C 6: 57,979,211 L31R probably damaging Het
Wtap T C 17: 12,969,455 E186G probably benign Het
Wwc2 T G 8: 47,883,580 N216H probably benign Het
Zhx1 A T 15: 58,054,445 M135K probably damaging Het
Other mutations in Ets1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00733:Ets1 APN 9 32752926 intron probably benign
IGL00899:Ets1 APN 9 32752808 missense probably damaging 1.00
IGL01615:Ets1 APN 9 32732939 splice site probably benign
IGL02424:Ets1 APN 9 32754293 nonsense probably null
IGL03204:Ets1 APN 9 32733012 missense possibly damaging 0.64
Ecru UTSW 9 32733960 nonsense probably null
Fawn UTSW 9 32752857 nonsense probably null
R0479:Ets1 UTSW 9 32730180 missense probably damaging 1.00
R0659:Ets1 UTSW 9 32738293 missense probably damaging 1.00
R0839:Ets1 UTSW 9 32734061 nonsense probably null
R5009:Ets1 UTSW 9 32732999 missense possibly damaging 0.85
R5590:Ets1 UTSW 9 32728798 splice site probably benign
R6367:Ets1 UTSW 9 32733960 nonsense probably null
R6423:Ets1 UTSW 9 32738315 missense probably damaging 0.97
R6517:Ets1 UTSW 9 32752797 critical splice acceptor site probably null
R6584:Ets1 UTSW 9 32733997 missense probably damaging 1.00
R7347:Ets1 UTSW 9 32733032 splice site probably null
R7414:Ets1 UTSW 9 32752857 nonsense probably null
R7688:Ets1 UTSW 9 32696424 missense probably benign 0.10
Posted On2014-05-07