Incidental Mutation 'IGL02653:Gm5900'
ID 302241
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5900
Ensembl Gene ENSMUSG00000094685
Gene Name predicted pseudogene 5900
Synonyms
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.453) question?
Stock # IGL02653
Quality Score
Status
Chromosome 7
Chromosomal Location 104599122-104599496 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to G at 104599340 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000179862
SMART Domains Protein: ENSMUSP00000136999
Gene: ENSMUSG00000094685

DomainStartEndE-ValueType
MAPKK1_Int 3 121 6.65e-63 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc8 T C 7: 45,765,191 (GRCm39) probably benign Het
Alox5 T A 6: 116,392,438 (GRCm39) H361L probably benign Het
Arid2 A G 15: 96,185,583 (GRCm39) N3S probably damaging Het
Atp1a4 T A 1: 172,078,973 (GRCm39) I182F possibly damaging Het
Cby2 T C 14: 75,820,597 (GRCm39) D385G probably damaging Het
Ctnna2 A T 6: 76,957,760 (GRCm39) D496E probably benign Het
Cyp3a25 G T 5: 145,939,920 (GRCm39) S29Y possibly damaging Het
Dglucy G A 12: 100,837,690 (GRCm39) G611D probably benign Het
Efcab5 T C 11: 77,022,848 (GRCm39) K622E probably damaging Het
Esyt1 T A 10: 128,346,877 (GRCm39) I1071L probably benign Het
Fbn2 T C 18: 58,209,777 (GRCm39) K1035E probably benign Het
Frem1 T G 4: 82,877,571 (GRCm39) E1335D probably benign Het
Ikbke T A 1: 131,199,572 (GRCm39) Q283L possibly damaging Het
Lepr A T 4: 101,622,141 (GRCm39) I358F probably benign Het
Lnpk A G 2: 74,378,392 (GRCm39) V123A probably damaging Het
Mis12 A G 11: 70,916,357 (GRCm39) K130R probably damaging Het
Ncapg2 T A 12: 116,389,526 (GRCm39) probably null Het
Npy6r T C 18: 44,409,694 (GRCm39) *372Q probably null Het
Polr3d T C 14: 70,677,557 (GRCm39) D273G probably damaging Het
Ppp2r3d A G 9: 101,088,892 (GRCm39) V477A probably benign Het
Prpf19 T A 19: 10,880,328 (GRCm39) probably benign Het
Ptgr3 T C 18: 84,113,443 (GRCm39) V373A possibly damaging Het
Pwwp2a A G 11: 43,596,862 (GRCm39) T676A possibly damaging Het
Ralgapb T A 2: 158,285,229 (GRCm39) I242N probably damaging Het
Scn3a A T 2: 65,291,531 (GRCm39) S1738R probably damaging Het
Snapc1 C A 12: 74,029,261 (GRCm39) P348Q probably benign Het
Tbc1d7 T C 13: 43,318,874 (GRCm39) I88V probably benign Het
Tnks2 T C 19: 36,849,851 (GRCm39) S220P probably damaging Het
Trim56 A T 5: 137,141,760 (GRCm39) S585R probably damaging Het
Trpm2 T G 10: 77,748,503 (GRCm39) E1389A probably benign Het
Tspear T A 10: 77,542,799 (GRCm39) probably benign Het
Vmn1r180 T C 7: 23,652,500 (GRCm39) I221T probably damaging Het
Vmn1r204 A C 13: 22,740,800 (GRCm39) I144L probably benign Het
Vmn2r20 A T 6: 123,362,324 (GRCm39) I820N probably damaging Het
Vwa3b T A 1: 37,214,646 (GRCm39) probably benign Het
Wnt1 G A 15: 98,690,336 (GRCm39) G222R probably damaging Het
Other mutations in Gm5900
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01584:Gm5900 APN 7 104,599,361 (GRCm39) exon noncoding transcript
IGL02193:Gm5900 APN 7 104,599,231 (GRCm39) exon noncoding transcript
R2509:Gm5900 UTSW 7 104,599,571 (GRCm39) unclassified noncoding transcript
R2510:Gm5900 UTSW 7 104,599,571 (GRCm39) unclassified noncoding transcript
R5129:Gm5900 UTSW 7 104,599,223 (GRCm39) exon noncoding transcript
R5898:Gm5900 UTSW 7 104,599,468 (GRCm39) exon noncoding transcript
Posted On 2015-04-16