Incidental Mutation 'IGL03081:Fgfr1op2'
ID417864
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Fgfr1op2
Ensembl Gene ENSMUSG00000040242
Gene NameFGFR1 oncogene partner 2
Synonyms
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.500) question?
Stock #IGL03081
Quality Score
Status
Chromosome6
Chromosomal Location146577203-146599198 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 146597319 bp
ZygosityHeterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 217 (I217F)
Ref Sequence ENSEMBL: ENSMUSP00000107292 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000037836] [ENSMUST00000058245] [ENSMUST00000067404] [ENSMUST00000111663]
Predicted Effect probably benign
Transcript: ENSMUST00000037836
SMART Domains Protein: ENSMUSP00000037316
Gene: ENSMUSG00000040242

DomainStartEndE-ValueType
Pfam:DUF837 1 142 4e-59 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000058245
SMART Domains Protein: ENSMUSP00000107289
Gene: ENSMUSG00000040242

DomainStartEndE-ValueType
Pfam:DUF837 1 142 4e-59 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000067404
AA Change: I179F

PolyPhen 2 Score 0.881 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000098352
Gene: ENSMUSG00000040242
AA Change: I179F

DomainStartEndE-ValueType
Pfam:DUF837 1 185 8.6e-80 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000111663
AA Change: I217F

PolyPhen 2 Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000107292
Gene: ENSMUSG00000040242
AA Change: I217F

DomainStartEndE-ValueType
Pfam:DUF837 2 221 2e-73 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000160697
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc2 C A 19: 43,782,402 probably benign Het
Acan T G 7: 79,098,543 S1021A probably benign Het
Adamts6 A G 13: 104,444,956 probably benign Het
Apc2 A G 10: 80,312,252 K1018E probably damaging Het
Arhgef28 A T 13: 98,029,373 probably benign Het
Atp2b1 T C 10: 98,994,813 probably benign Het
Cct6b A T 11: 82,764,169 L20* probably null Het
Cd300ld2 G A 11: 115,012,542 probably benign Het
Cdc23 T G 18: 34,636,704 K454T probably damaging Het
Cdh20 A T 1: 104,941,257 I158F probably damaging Het
Cdk14 C T 5: 4,949,527 probably benign Het
Ces1d C A 8: 93,169,718 probably null Het
Clec2i A T 6: 128,894,765 Y113F probably damaging Het
Dmpk T A 7: 19,087,533 S239T probably damaging Het
Dnah8 T C 17: 30,686,373 probably benign Het
Exoc2 A G 13: 30,900,902 Y359H probably benign Het
Eya1 A T 1: 14,183,191 F520L possibly damaging Het
Gm12258 A G 11: 58,858,259 N87D probably benign Het
Gp6 A G 7: 4,371,648 S225P probably benign Het
Hdac7 T C 15: 97,798,306 Y619C probably damaging Het
Lars A G 18: 42,210,091 I1087T probably benign Het
Lrrc37a G T 11: 103,456,595 H3091Q unknown Het
Mcm3ap T C 10: 76,470,316 S88P possibly damaging Het
Mrps23 G A 11: 88,210,217 R117Q probably benign Het
Nbea T C 3: 56,079,918 S384G probably damaging Het
Ndufs4 A T 13: 114,307,837 I135N possibly damaging Het
Noto T C 6: 85,424,109 F40S probably damaging Het
Nr5a1 A T 2: 38,710,532 V41D possibly damaging Het
Olfr914 C T 9: 38,606,870 A135V probably benign Het
Papola T A 12: 105,818,855 H415Q probably damaging Het
Pcm1 C T 8: 41,275,060 T557I probably damaging Het
Pde11a A T 2: 76,075,930 probably benign Het
Pls1 A G 9: 95,773,643 V352A probably damaging Het
Pygm T C 19: 6,388,821 S226P possibly damaging Het
Rnf17 T A 14: 56,434,371 S273R probably benign Het
Scamp2 T C 9: 57,587,127 V261A possibly damaging Het
Slc7a12 T A 3: 14,481,255 F153L probably benign Het
Smchd1 A T 17: 71,360,191 D1735E probably damaging Het
Stk40 A G 4: 126,123,714 probably null Het
Tas2r124 C T 6: 132,755,534 L269F possibly damaging Het
Tmem260 A C 14: 48,496,293 I216L probably benign Het
Ubr1 C A 2: 120,961,156 A116S possibly damaging Het
Unc13a T C 8: 71,649,549 K991R probably damaging Het
Vmn2r66 T C 7: 85,007,930 Y89C probably benign Het
Vps13b A C 15: 35,875,820 I2784L probably damaging Het
Zbtb26 T A 2: 37,436,600 K141N possibly damaging Het
Zranb1 T A 7: 132,950,397 M259K probably damaging Het
Other mutations in Fgfr1op2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02591:Fgfr1op2 APN 6 146588846 missense probably damaging 0.97
IGL02626:Fgfr1op2 APN 6 146590011 missense probably benign 0.37
R1381:Fgfr1op2 UTSW 6 146588741 missense probably damaging 1.00
R3740:Fgfr1op2 UTSW 6 146595233 missense possibly damaging 0.94
R3934:Fgfr1op2 UTSW 6 146595171 splice site probably benign
R5471:Fgfr1op2 UTSW 6 146597362 unclassified probably null
R6842:Fgfr1op2 UTSW 6 146590038 critical splice donor site probably null
R6988:Fgfr1op2 UTSW 6 146589965 missense probably damaging 0.99
Posted On2016-08-02