Incidental Mutation 'IGL01909:Gm5862'
ID 279081
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 # IGL01909
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: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700111E14Rik A T 6: 36,914,152 (GRCm39) probably benign Het
Actn2 A T 13: 12,324,479 (GRCm39) probably null Het
Apom C T 17: 35,350,208 (GRCm39) A78T probably benign Het
Bambi A G 18: 3,508,229 (GRCm39) Y7C possibly damaging Het
Cdc42bpb T C 12: 111,289,576 (GRCm39) M418V probably benign Het
Clptm1 T C 7: 19,389,701 (GRCm39) N43D probably benign Het
Cspp1 T C 1: 10,136,886 (GRCm39) V241A probably benign Het
Ctnna3 T A 10: 63,339,910 (GRCm39) I32N probably benign Het
Elp2 A G 18: 24,752,576 (GRCm39) probably benign Het
Frmd4a A G 2: 4,608,844 (GRCm39) D893G probably benign Het
Gm10718 A T 9: 3,025,118 (GRCm39) Y194F probably benign Het
Gm21738 G A 14: 19,416,979 (GRCm38) S144L probably benign Het
H2-M10.1 C A 17: 36,635,971 (GRCm39) G154* probably null Het
Igdcc3 C T 9: 65,051,819 (GRCm39) R141W probably damaging Het
Igkv14-130 A G 6: 67,768,323 (GRCm39) K60E possibly damaging Het
Kcnmb2 A G 3: 32,252,512 (GRCm39) probably benign Het
Lrp4 T C 2: 91,324,529 (GRCm39) L1288P possibly damaging Het
Mavs T A 2: 131,087,441 (GRCm39) M313K probably benign Het
Mia2 A G 12: 59,154,731 (GRCm39) E148G possibly damaging Het
Or6c76b A T 10: 129,692,950 (GRCm39) T188S probably damaging Het
Or8b12b T A 9: 37,684,159 (GRCm39) I68K possibly damaging Het
Or8d1 T A 9: 38,767,013 (GRCm39) Y218* probably null Het
Plekha3 C T 2: 76,517,047 (GRCm39) T133M probably damaging Het
Plxna1 A T 6: 89,309,066 (GRCm39) probably null Het
Septin2 A G 1: 93,426,823 (GRCm39) N144S probably damaging Het
Slc9a4 T C 1: 40,651,451 (GRCm39) probably benign Het
Slco1b2 T A 6: 141,594,312 (GRCm39) I59K probably damaging Het
Sp140l2 A G 1: 85,231,907 (GRCm39) probably benign Het
Tnrc6b A G 15: 80,786,184 (GRCm39) S1243G possibly damaging Het
Unc13a T A 8: 72,091,854 (GRCm39) probably benign Het
Vmn2r105 T C 17: 20,444,918 (GRCm39) R525G probably damaging Het
Vmn2r129 C T 4: 156,690,549 (GRCm39) noncoding transcript Het
Vmn2r37 T A 7: 9,219,032 (GRCm39) K451* probably null Het
Vmn2r71 C T 7: 85,270,001 (GRCm39) T504I probably benign Het
Zfp668 A T 7: 127,465,994 (GRCm39) C397S probably damaging 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
IGL01902:Gm5862 APN 5 26,227,769 (GRCm39) missense probably benign
IGL01905: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