Incidental Mutation 'IGL01750:Gm5263'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5263
Ensembl Gene ENSMUSG00000090323
Gene Namepredicted gene 5263
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01750
Quality Score
Chromosomal Location146420436-146421036 bp(+) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) T to G at 146420564 bp
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000163646
SMART Domains Protein: ENSMUSP00000126089
Gene: ENSMUSG00000090323

PDB:2RR6|A 1 111 6e-46 PDB
SCOP:d1a9na_ 20 119 4e-7 SMART
Blast:AAA 23 92 6e-11 BLAST
Predicted Effect noncoding transcript
Transcript: ENSMUST00000186665
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Alpk3 A G 7: 81,092,282 R616G probably damaging Het
BC030867 T C 11: 102,254,951 probably benign Het
Cacna1b G A 2: 24,654,395 P1260S probably damaging Het
Ccz1 A T 5: 144,004,062 Y225N probably damaging Het
Col15a1 C T 4: 47,303,897 P1101S probably damaging Het
Cyp2d22 T A 15: 82,374,369 H97L probably benign Het
Emsy G A 7: 98,619,301 S511F probably damaging Het
Fnbp1l G T 3: 122,544,677 Y351* probably null Het
Hook2 T C 8: 84,993,236 probably null Het
Itgb4 G A 11: 115,988,926 V635I probably damaging Het
Kmt2d G A 15: 98,853,168 probably benign Het
Lpin1 T C 12: 16,577,176 N123S probably benign Het
Man2c1 T C 9: 57,140,780 probably null Het
Obscn T C 11: 59,031,639 E6558G probably damaging Het
Olfr134 G T 17: 38,175,686 V201L probably benign Het
Olfr531 T C 7: 140,400,657 T130A probably benign Het
Olfr912 C T 9: 38,581,513 P79S probably damaging Het
Pcdh7 A G 5: 57,720,422 T440A probably damaging Het
Pitx1 A G 13: 55,826,491 Y176H probably damaging Het
Plec A G 15: 76,173,389 V4116A probably damaging Het
Polrmt A G 10: 79,739,846 V617A possibly damaging Het
Pprc1 T C 19: 46,071,829 probably benign Het
Rbm19 G A 5: 120,118,792 A57T probably benign Het
Rin1 T C 19: 5,052,036 I134T possibly damaging Het
Thumpd2 G A 17: 81,054,386 A137V probably benign Het
Tle4 T C 19: 14,449,789 Y756C probably damaging Het
Tln1 A G 4: 43,545,435 L986P probably damaging Het
Tmem132c C A 5: 127,462,959 Q350K possibly damaging Het
Zfp474 A G 18: 52,639,277 N334S possibly damaging Het
Other mutations in Gm5263
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01749:Gm5263 APN 1 146420564 exon noncoding transcript
IGL01751:Gm5263 APN 1 146420564 exon noncoding transcript
IGL01767:Gm5263 APN 1 146420564 exon noncoding transcript
IGL01810:Gm5263 APN 1 146420554 exon noncoding transcript
Posted On2015-04-16