Incidental Mutation 'IGL02400:Gm5828'
ID291864
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? Probably non essential (E-score: 0.219) question?
Stock #IGL02400
Quality Score
Status
Chromosome1
Chromosomal Location16768279-16770138 bp(-) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) G to T at 16769818 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: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2610028H24Rik A G 10: 76,454,810 I128V possibly damaging Het
Arfgef3 G T 10: 18,646,257 Q674K probably damaging Het
Atp6v0a2 T A 5: 124,721,785 N851K probably benign Het
Chrna7 A G 7: 63,099,322 C471R probably damaging Het
Csgalnact1 C A 8: 68,401,492 G219V probably damaging Het
Egflam T A 15: 7,247,053 K544M probably benign Het
Erbb3 A C 10: 128,579,524 N385K probably benign Het
Fancm A G 12: 65,113,815 R1388G probably damaging Het
Gm10720 C A 9: 3,016,900 probably null Het
Gm20489 A T X: 101,263,338 N328K possibly damaging Het
Gnaq T C 19: 16,316,128 Y145H probably damaging Het
Itgbl1 A G 14: 123,846,526 D148G probably damaging Het
Myc T G 15: 61,989,911 probably benign Het
Olfr1033 A T 2: 86,042,076 I254F probably benign Het
Olfr801 A G 10: 129,669,883 V212A probably damaging Het
Olfr975 A G 9: 39,950,339 V144A probably benign Het
Padi3 T G 4: 140,788,868 K567T probably benign Het
Pi4ka T C 16: 17,293,884 T1576A probably damaging Het
Pikfyve A G 1: 65,252,569 R1316G probably damaging Het
Ryr2 A G 13: 11,605,244 probably benign Het
Sash1 G A 10: 8,733,647 R713* probably null Het
Tmem214 G A 5: 30,872,746 A296T probably benign Het
Tnfsf4 T A 1: 161,395,705 C42S possibly damaging Het
Tpp1 A G 7: 105,747,031 I487T possibly damaging Het
Trim43a T A 9: 88,582,112 N25K probably benign Het
Tuft1 T C 3: 94,635,502 probably benign Het
Usp46 T C 5: 74,037,052 H26R probably benign Het
Zfp560 A T 9: 20,350,600 I85N possibly damaging Het
Other mutations in Gm5828
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01143:Gm5828 APN 1 16769948 exon noncoding transcript
IGL01751:Gm5828 APN 1 16769984 exon noncoding transcript
IGL02275:Gm5828 APN 1 16769118 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