Incidental Mutation 'IGL01902:Gm5862'
ID 279053
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5862
Ensembl Gene ENSMUSG00000067700
Gene Name predicted gene 5862
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.196) question?
Stock # IGL01902
Quality Score
Status
Chromosome 5
Chromosomal Location 26223419-26227889 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 26227769 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tryptophan to Glycine at position 41 (W41G)
Ref Sequence ENSEMBL: ENSMUSP00000072133 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000072286]
AlphaFold K7N5V5
Predicted Effect probably benign
Transcript: ENSMUST00000072286
AA Change: W41G

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000072133
Gene: ENSMUSG00000067700
AA Change: W41G

DomainStartEndE-ValueType
Pfam:Takusan 50 134 1.6e-25 PFAM
low complexity region 154 168 N/A INTRINSIC
low complexity region 235 259 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4931406B18Rik A G 7: 43,147,267 (GRCm39) S228P probably damaging Het
Adamtsl2 A T 2: 26,977,264 (GRCm39) I242F probably damaging Het
Bicdl1 A G 5: 115,789,933 (GRCm39) L284P probably damaging Het
Bnc2 A G 4: 84,309,181 (GRCm39) I138T probably damaging Het
Cep350 A G 1: 155,737,731 (GRCm39) L2704S probably damaging Het
Col7a1 C A 9: 108,806,895 (GRCm39) P2442T unknown Het
Cpne6 A T 14: 55,750,207 (GRCm39) T113S possibly damaging Het
Crnkl1 T C 2: 145,766,632 (GRCm39) probably null Het
Cyp2c67 T A 19: 39,637,470 (GRCm39) D2V probably damaging Het
Frzb T A 2: 80,243,711 (GRCm39) S323C probably damaging Het
Gm21738 G A 14: 19,416,979 (GRCm38) S144L probably benign Het
Ins2 C T 7: 142,233,179 (GRCm39) C31Y probably damaging Het
Lipf A T 19: 33,948,179 (GRCm39) N234Y probably benign Het
Mtf1 T C 4: 124,698,720 (GRCm39) F73L probably damaging Het
Nrxn1 A G 17: 91,395,919 (GRCm39) probably null Het
Pcnx1 A G 12: 82,025,868 (GRCm39) T1538A probably damaging Het
Polr1a T A 6: 71,940,732 (GRCm39) V47D probably damaging Het
Prune2 A G 19: 17,096,002 (GRCm39) E502G probably benign Het
Ralgapa2 C T 2: 146,156,934 (GRCm39) V1886M probably damaging Het
Rapgef3 T A 15: 97,648,181 (GRCm39) H676L probably benign Het
Rbm20 A T 19: 53,829,422 (GRCm39) N607Y probably damaging Het
Smc5 G A 19: 23,237,132 (GRCm39) T233I possibly damaging Het
Snx13 A T 12: 35,183,306 (GRCm39) probably null Het
Suz12 T A 11: 79,916,776 (GRCm39) C510S probably benign Het
Tab2 A T 10: 7,795,756 (GRCm39) M242K probably benign Het
Tep1 A G 14: 51,103,548 (GRCm39) probably benign Het
Vmn2r129 C T 4: 156,690,549 (GRCm39) noncoding transcript Het
Other mutations in Gm5862
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01606:Gm5862 APN 5 26,224,514 (GRCm39) missense probably benign
IGL01863:Gm5862 APN 5 26,227,769 (GRCm39) missense probably benign
IGL01868:Gm5862 APN 5 26,227,769 (GRCm39) missense probably benign
IGL01873:Gm5862 APN 5 26,227,769 (GRCm39) missense probably benign
IGL01881:Gm5862 APN 5 26,227,769 (GRCm39) missense probably benign
IGL01905:Gm5862 APN 5 26,227,769 (GRCm39) missense probably benign
IGL01909:Gm5862 APN 5 26,227,769 (GRCm39) missense probably benign
IGL01917:Gm5862 APN 5 26,227,769 (GRCm39) missense probably benign
IGL01924:Gm5862 APN 5 26,227,769 (GRCm39) missense probably benign
IGL01927:Gm5862 APN 5 26,227,769 (GRCm39) missense probably benign
IGL01951:Gm5862 APN 5 26,227,769 (GRCm39) missense probably benign
IGL03374:Gm5862 APN 5 26,224,510 (GRCm39) missense probably damaging 0.98
R2475:Gm5862 UTSW 5 26,224,490 (GRCm39) missense probably damaging 1.00
R3828:Gm5862 UTSW 5 26,224,345 (GRCm39) missense probably benign 0.27
R4591:Gm5862 UTSW 5 26,224,486 (GRCm39) missense possibly damaging 0.95
R6916:Gm5862 UTSW 5 26,224,346 (GRCm39) missense probably benign
R8291:Gm5862 UTSW 5 26,224,444 (GRCm39) missense probably benign 0.32
R8927:Gm5862 UTSW 5 26,226,678 (GRCm39) missense probably damaging 0.98
R8928:Gm5862 UTSW 5 26,226,678 (GRCm39) missense probably damaging 0.98
R9074:Gm5862 UTSW 5 26,226,624 (GRCm39) missense probably damaging 0.98
Z1176:Gm5862 UTSW 5 26,223,485 (GRCm39) frame shift probably null
Posted On 2015-04-16