Incidental Mutation 'IGL02275:Gm5828'
ID287301
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5828
Ensembl Gene ENSMUSG00000091020
Gene Namepredicted gene 5828
Synonyms
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.271) question?
Stock #IGL02275
Quality Score
Status
Chromosome1
Chromosomal Location16768279-16770138 bp(-) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) T to A at 16769118 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000071842
SMART Domains Protein: ENSMUSP00000136559
Gene: ENSMUSG00000091020

DomainStartEndE-ValueType
low complexity region 60 74 N/A INTRINSIC
low complexity region 143 163 N/A INTRINSIC
low complexity region 174 182 N/A INTRINSIC
low complexity region 207 218 N/A INTRINSIC
HMG 222 292 1.88e-17 SMART
low complexity region 307 339 N/A INTRINSIC
low complexity region 435 481 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 24 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700037C18Rik T A 16: 3,906,282 D130V probably damaging Het
4930596D02Rik T C 14: 35,811,923 T9A probably benign Het
Anapc1 C A 2: 128,659,852 A757S probably benign Het
Bpifa6 A T 2: 153,992,272 D328V probably benign Het
Casc1 T C 6: 145,177,364 Y592C probably damaging Het
Cdh19 T A 1: 110,925,886 K275I probably benign Het
Col18a1 A G 10: 77,059,383 I1148T possibly damaging Het
Commd1 A T 11: 22,900,017 V222D probably damaging Het
Crim1 T A 17: 78,369,998 M876K possibly damaging Het
Dennd1b C A 1: 139,081,254 H232N probably damaging Het
Dhx57 T C 17: 80,274,839 T393A probably benign Het
Gabrb2 G T 11: 42,591,894 R193L probably benign Het
Gm6483 C T 8: 19,691,613 P55S probably damaging Het
Hsp90ab1 T C 17: 45,568,438 Y619C possibly damaging Het
Kctd19 A G 8: 105,396,374 I136T probably damaging Het
Olfr134 G T 17: 38,175,686 V201L probably benign Het
Olfr1361 A C 13: 21,659,000 F108V probably benign Het
Sel1l T C 12: 91,815,015 Y532C probably damaging Het
Sirpb1a A G 3: 15,410,409 probably null Het
Ush2a C T 1: 188,263,269 T79M possibly damaging Het
Usp24 T C 4: 106,387,493 V1215A probably damaging Het
Vdac3-ps1 T C 13: 18,030,794 noncoding transcript Het
Vmn2r75 T C 7: 86,165,140 T382A probably benign Het
Vps53 T C 11: 76,047,123 Y728C probably benign Het
Other mutations in Gm5828
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01143:Gm5828 APN 1 16769948 exon noncoding transcript
IGL01751:Gm5828 APN 1 16769984 exon noncoding transcript
IGL02400:Gm5828 APN 1 16769818 exon noncoding transcript
IGL02480:Gm5828 APN 1 16769542 exon noncoding transcript
R0143:Gm5828 UTSW 1 16768355 exon noncoding transcript
R1245:Gm5828 UTSW 1 16769129 exon noncoding transcript
R1405:Gm5828 UTSW 1 16769544 exon noncoding transcript
R1514:Gm5828 UTSW 1 16769359 exon noncoding transcript
R1644:Gm5828 UTSW 1 16769261 exon noncoding transcript
R2118:Gm5828 UTSW 1 16769975 exon noncoding transcript
R2290:Gm5828 UTSW 1 16768344 exon noncoding transcript
R3428:Gm5828 UTSW 1 16768614 exon noncoding transcript
R3962:Gm5828 UTSW 1 16768644 exon noncoding transcript
R4657:Gm5828 UTSW 1 16769418 exon noncoding transcript
R5067:Gm5828 UTSW 1 16769292 exon noncoding transcript
Posted On2015-04-16