Incidental Mutation 'IGL01751:Gm5828'
ID153139
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: 0.291) question?
Stock #IGL01751
Quality Score
Status
Chromosome1
Chromosomal Location16768279-16770138 bp(-) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) A to G at 16769984 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: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1600015I10Rik A T 6: 48,930,588 H174L possibly damaging Het
1700018F24Rik A G 5: 145,043,171 probably null Het
Auts2 G T 5: 131,472,360 Q72K probably damaging Het
Btbd11 C A 10: 85,654,502 Q1011K probably damaging Het
Ccdc7b A T 8: 129,136,568 probably benign Het
Frem3 A G 8: 80,615,743 E1555G probably benign Het
Gm1966 T A 7: 106,602,309 N576I possibly damaging Het
Gm5263 T G 1: 146,420,564 noncoding transcript Het
Gm6605 T C 7: 38,448,206 noncoding transcript Het
Hps3 T C 3: 20,010,966 D638G probably damaging Het
Igdcc4 A T 9: 65,131,732 N887I probably damaging Het
Itpkc G A 7: 27,213,066 probably benign Het
Mfge8 A G 7: 79,136,655 probably null Het
Mrc2 G T 11: 105,325,734 L116F probably benign Het
Necab1 T C 4: 14,978,171 D226G probably damaging Het
Neurod2 T C 11: 98,327,375 E321G possibly damaging Het
Obp2b G T 2: 25,737,748 V59L possibly damaging Het
Olfr1173 A T 2: 88,274,633 C139S possibly damaging Het
Olfr134 G T 17: 38,175,686 V201L probably benign Het
Olfr292 A T 7: 86,694,789 Q111L probably benign Het
Olfr912 C T 9: 38,581,513 P79S probably damaging Het
Olr1 T C 6: 129,488,848 N65S possibly damaging Het
Rock1 A G 18: 10,079,113 probably null Het
Scn3a T A 2: 65,461,252 M1717L possibly damaging Het
Smg7 T C 1: 152,844,061 D903G possibly damaging Het
Tlr1 A T 5: 64,925,947 L429* probably null Het
Ttll9 A T 2: 152,983,105 N68I probably damaging Het
Ttn A G 2: 76,737,599 V25904A possibly damaging Het
Uaca G A 9: 60,869,857 V507M probably damaging Het
Vmn1r195 G T 13: 22,279,251 C297F probably benign Het
Zdhhc2 G A 8: 40,473,001 A346T probably benign Het
Other mutations in Gm5828
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01143:Gm5828 APN 1 16769948 exon noncoding transcript
IGL02275:Gm5828 APN 1 16769118 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 On2014-02-04