Incidental Mutation 'IGL02718:Gm9602'
ID304830
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm9602
Ensembl Gene ENSMUSG00000090539
Gene Namepredicted gene 9602
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.059) question?
Stock #IGL02718
Quality Score
Status
Chromosome14
Chromosomal Location4776337-4785002 bp(+) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) A to T at 4776474 bp
ZygosityHeterozygous
Amino Acid Change Arginine to Stop codon at position 21 (R21*)
Ref Sequence ENSEMBL: ENSMUSP00000137206 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000163325] [ENSMUST00000177973]
Predicted Effect probably null
Transcript: ENSMUST00000163325
AA Change: R20*
SMART Domains Protein: ENSMUSP00000126151
Gene: ENSMUSG00000090539
AA Change: R20*

DomainStartEndE-ValueType
Pfam:Takusan 48 128 1.9e-26 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000177973
AA Change: R21*
SMART Domains Protein: ENSMUSP00000137206
Gene: ENSMUSG00000090539
AA Change: R21*

DomainStartEndE-ValueType
Pfam:Takusan 47 130 1.9e-36 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2200002J24Rik A G 7: 30,699,904 D41G probably damaging Het
2210408I21Rik T A 13: 77,174,872 Y7N probably damaging Het
4921507P07Rik G T 6: 50,584,387 T184K probably damaging Het
Atf1 C A 15: 100,254,219 Q151K probably damaging Het
Brdt T C 5: 107,350,068 probably benign Het
Cep295 T C 9: 15,325,753 probably null Het
Ctnnd2 A G 15: 31,027,616 S1229G probably damaging Het
Dcaf15 T A 8: 84,098,376 I476L possibly damaging Het
Dlec1 A G 9: 119,137,286 I1108V probably benign Het
Dnah9 T A 11: 65,886,640 H3694L probably damaging Het
Dock10 A T 1: 80,523,818 D1838E probably benign Het
Dusp12 A T 1: 170,880,657 Y164N probably damaging Het
Ephx1 A G 1: 180,999,786 F101L probably damaging Het
Fbn1 C A 2: 125,369,886 C864F probably damaging Het
Fbxw24 T C 9: 109,624,790 E96G possibly damaging Het
Glt1d1 C A 5: 127,650,699 F78L probably damaging Het
Grip1 T A 10: 120,075,515 *713K probably null Het
Hecw1 T C 13: 14,306,935 probably null Het
Il31ra G A 13: 112,530,369 R392* probably null Het
L3hypdh T G 12: 72,084,856 S101R probably damaging Het
Lpar5 T A 6: 125,082,244 D309E probably damaging Het
Masp1 T C 16: 23,476,293 Y406C probably damaging Het
Mpdz T C 4: 81,385,202 I166M probably damaging Het
Nbea A T 3: 55,632,062 Y2759* probably null Het
Ncf1 A T 5: 134,227,448 probably null Het
Nek5 T G 8: 22,097,463 R314S probably benign Het
Nifk A C 1: 118,327,632 N38T probably damaging Het
Obscn C T 11: 59,077,858 V2772M probably damaging Het
Olfr1367 T C 13: 21,347,384 L152P probably damaging Het
Olfr181 T C 16: 58,926,096 I158M possibly damaging Het
Olfr419 G T 1: 174,250,707 Y73* probably null Het
Olfr584 C A 7: 103,085,583 L22I probably benign Het
Olfr707 A T 7: 106,891,329 M260K probably damaging Het
Olfr979 A T 9: 40,000,886 Y114N probably damaging Het
Pbxip1 A G 3: 89,448,004 E610G probably damaging Het
Pfas G T 11: 69,000,145 probably benign Het
Plk4 T C 3: 40,815,021 S102P probably damaging Het
Ptprz1 C T 6: 23,001,349 T1146I possibly damaging Het
Pum2 T A 12: 8,733,344 S598T probably benign Het
Ric1 T A 19: 29,533,240 W74R probably damaging Het
Riok3 C A 18: 12,152,996 S427* probably null Het
Ros1 A T 10: 52,118,232 D1317E probably damaging Het
Sfmbt2 A G 2: 10,402,031 D47G possibly damaging Het
Slc12a1 C T 2: 125,161,079 R177* probably null Het
Snai3 C A 8: 122,456,122 probably null Het
Snx19 A G 9: 30,432,260 N572S possibly damaging Het
Soat1 A T 1: 156,441,429 S151T probably benign Het
Stbd1 A G 5: 92,603,218 E37G possibly damaging Het
Syt10 A G 15: 89,814,079 I354T probably damaging Het
Trip11 A C 12: 101,886,025 S593R probably benign Het
Ubr1 T C 2: 120,914,883 E908G probably damaging Het
Yy1 T C 12: 108,815,479 F357L probably damaging Het
Other mutations in Gm9602
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1317:Gm9602 UTSW 14 4776499 missense probably damaging 1.00
R3811:Gm9602 UTSW 14 4776499 missense probably damaging 1.00
R7172:Gm9602 UTSW 14 4777282 missense possibly damaging 0.62
R8418:Gm9602 UTSW 14 4779201 splice site probably benign
Posted On2015-04-16