Incidental Mutation 'IGL02653:Gm5900'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5900
Ensembl Gene ENSMUSG00000094685
Gene Namepredicted pseudogene 5900
Accession Numbers
Is this an essential gene? Possibly essential (E-score: 0.523) question?
Stock #IGL02653
Quality Score
Chromosomal Location104949176-104950435 bp(-) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) A to G at 104950133 bp
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

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: 46,115,767 probably benign Het
Alox5 T A 6: 116,415,477 H361L probably benign Het
Arid2 A G 15: 96,287,702 N3S probably damaging Het
Atp1a4 T A 1: 172,251,406 I182F possibly damaging Het
Ctnna2 A T 6: 76,980,777 D496E probably benign Het
Cyp3a25 G T 5: 146,003,110 S29Y possibly damaging Het
Dglucy G A 12: 100,871,431 G611D probably benign Het
Efcab5 T C 11: 77,132,022 K622E probably damaging Het
Esyt1 T A 10: 128,511,008 I1071L probably benign Het
Fbn2 T C 18: 58,076,705 K1035E probably benign Het
Frem1 T G 4: 82,959,334 E1335D probably benign Het
Ikbke T A 1: 131,271,835 Q283L possibly damaging Het
Lepr A T 4: 101,764,944 I358F probably benign Het
Lnpk A G 2: 74,548,048 V123A probably damaging Het
Mis12 A G 11: 71,025,531 K130R probably damaging Het
Ncapg2 T A 12: 116,425,906 probably null Het
Npy6r T C 18: 44,276,627 *372Q probably null Het
Polr3d T C 14: 70,440,117 D273G probably damaging Het
Ppp2r3a A G 9: 101,211,693 V477A probably benign Het
Prpf19 T A 19: 10,902,964 probably benign Het
Pwwp2a A G 11: 43,706,035 T676A possibly damaging Het
Ralgapb T A 2: 158,443,309 I242N probably damaging Het
Scn3a A T 2: 65,461,187 S1738R probably damaging Het
Snapc1 C A 12: 73,982,487 P348Q probably benign Het
Spert T C 14: 75,583,157 D385G probably damaging Het
Tbc1d7 T C 13: 43,165,398 I88V probably benign Het
Tnks2 T C 19: 36,872,451 S220P probably damaging Het
Trim56 A T 5: 137,112,906 S585R probably damaging Het
Trpm2 T G 10: 77,912,669 E1389A probably benign Het
Tspear T A 10: 77,706,965 probably benign Het
Vmn1r180 T C 7: 23,953,075 I221T probably damaging Het
Vmn1r204 A C 13: 22,556,630 I144L probably benign Het
Vmn2r20 A T 6: 123,385,365 I820N probably damaging Het
Vwa3b T A 1: 37,175,565 probably benign Het
Wnt1 G A 15: 98,792,455 G222R probably damaging Het
Zadh2 T C 18: 84,095,318 V373A possibly damaging Het
Other mutations in Gm5900
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01584:Gm5900 APN 7 104950154 exon noncoding transcript
IGL02193:Gm5900 APN 7 104950024 exon noncoding transcript
R2509:Gm5900 UTSW 7 104950364 unclassified noncoding transcript
R2510:Gm5900 UTSW 7 104950364 unclassified noncoding transcript
R5129:Gm5900 UTSW 7 104950016 exon noncoding transcript
R5898:Gm5900 UTSW 7 104950261 exon noncoding transcript
Posted On2015-04-16