Incidental Mutation 'IGL01750:Gm5263'
ID278821
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5263
Ensembl Gene ENSMUSG00000090323
Gene Namepredicted gene 5263
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01750
Quality Score
Status
Chromosome1
Chromosomal Location146420436-146421036 bp(+) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) T to G at 146420564 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000163646
SMART Domains Protein: ENSMUSP00000126089
Gene: ENSMUSG00000090323

DomainStartEndE-ValueType
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