Incidental Mutation 'IGL01927:Gm5862'
ID279136
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5862
Ensembl Gene ENSMUSG00000067700
Gene Namepredicted gene 5862
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.144) question?
Stock #IGL01927
Quality Score
Status
Chromosome5
Chromosomal Location26017278-26022916 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to C at 26022771 bp
ZygosityHeterozygous
Amino Acid Change Tryptophan to Glycine at position 41 (W41G)
Ref Sequence ENSEMBL: ENSMUSP00000072133 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000072286]
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: 23 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930402F06Rik A G 2: 35,376,014 Y215H probably damaging Het
Acsm2 T C 7: 119,578,212 F317L possibly damaging Het
Akr1d1 A G 6: 37,564,459 D297G probably benign Het
Atp10b A G 11: 43,259,404 probably benign Het
Atp8b4 T C 2: 126,322,976 Y1140C probably damaging Het
Cap2 T A 13: 46,635,633 S105T probably benign Het
Cspg5 A T 9: 110,262,084 I414F probably damaging Het
Ereg T A 5: 91,086,812 V28E probably damaging Het
Fam69b A G 2: 26,636,115 M354V probably benign Het
Gm10717 C T 9: 3,025,616 S67L probably benign Het
Ift81 G A 5: 122,593,129 T321M probably benign Het
Kcnip2 T A 19: 45,795,605 Q95L probably damaging Het
Meis1 C T 11: 18,881,811 R409H probably benign Het
Opa1 T C 16: 29,586,995 I126T probably benign Het
Osbpl8 T C 10: 111,270,616 Y295H probably benign Het
Ppip5k2 A T 1: 97,713,123 V1005E probably damaging Het
Prdm10 A G 9: 31,335,398 probably benign Het
Rptor T A 11: 119,657,674 V58E probably damaging Het
Togaram1 C T 12: 64,976,702 A687V probably benign Het
Vmn2r1 T C 3: 64,081,684 F15L probably benign Het
Vmn2r82 T C 10: 79,378,072 L164P probably damaging Het
Vmn2r-ps159 C T 4: 156,338,254 noncoding transcript Het
Zfp623 T A 15: 75,947,505 N103K possibly damaging Het
Other mutations in Gm5862
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01606:Gm5862 APN 5 26019516 missense probably benign
IGL01863:Gm5862 APN 5 26022771 missense probably benign
IGL01868:Gm5862 APN 5 26022771 missense probably benign
IGL01873:Gm5862 APN 5 26022771 missense probably benign
IGL01881:Gm5862 APN 5 26022771 missense probably benign
IGL01902:Gm5862 APN 5 26022771 missense probably benign
IGL01905:Gm5862 APN 5 26022771 missense probably benign
IGL01909:Gm5862 APN 5 26022771 missense probably benign
IGL01917:Gm5862 APN 5 26022771 missense probably benign
IGL01924:Gm5862 APN 5 26022771 missense probably benign
IGL01951:Gm5862 APN 5 26022771 missense probably benign
IGL03374:Gm5862 APN 5 26019512 missense probably damaging 0.98
R2475:Gm5862 UTSW 5 26019492 missense probably damaging 1.00
R3828:Gm5862 UTSW 5 26019347 missense probably benign 0.27
R4591:Gm5862 UTSW 5 26019488 missense possibly damaging 0.95
R6916:Gm5862 UTSW 5 26019348 missense probably benign
R8291:Gm5862 UTSW 5 26019446 missense probably benign 0.32
Z1176:Gm5862 UTSW 5 26018487 frame shift probably null
Posted On2015-04-16