Incidental Mutation 'IGL01751:Gm5263'
ID 278830
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5263
Ensembl Gene ENSMUSG00000090323
Gene Name predicted gene 5263
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL01751
Quality Score
Status
Chromosome 1
Chromosomal Location 146296174-146296774 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to G at 146296302 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
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: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700018F24Rik A G 5: 144,979,981 (GRCm39) probably null Het
Abtb3 C A 10: 85,490,366 (GRCm39) Q1011K probably damaging Het
Aoc1l2 A T 6: 48,907,522 (GRCm39) H174L possibly damaging Het
Auts2 G T 5: 131,501,198 (GRCm39) Q72K probably damaging Het
Ccdc7b A T 8: 129,863,049 (GRCm39) probably benign Het
Frem3 A G 8: 81,342,372 (GRCm39) E1555G probably benign Het
Gm5828 A G 1: 16,840,208 (GRCm39) noncoding transcript Het
Gm6605 T C 7: 38,147,630 (GRCm39) noncoding transcript Het
Gvin3 T A 7: 106,201,516 (GRCm39) N576I possibly damaging Het
Hps3 T C 3: 20,065,130 (GRCm39) D638G probably damaging Het
Igdcc4 A T 9: 65,039,014 (GRCm39) N887I probably damaging Het
Itpkc G A 7: 26,912,491 (GRCm39) probably benign Het
Mfge8 A G 7: 78,786,403 (GRCm39) probably null Het
Mrc2 G T 11: 105,216,560 (GRCm39) L116F probably benign Het
Necab1 T C 4: 14,978,171 (GRCm39) D226G probably damaging Het
Neurod2 T C 11: 98,218,201 (GRCm39) E321G possibly damaging Het
Obp2b G T 2: 25,627,760 (GRCm39) V59L possibly damaging Het
Olr1 T C 6: 129,465,811 (GRCm39) N65S possibly damaging Het
Or14c39 A T 7: 86,343,997 (GRCm39) Q111L probably benign Het
Or2n1 G T 17: 38,486,577 (GRCm39) V201L probably benign Het
Or5d43 A T 2: 88,104,977 (GRCm39) C139S possibly damaging Het
Or8b48 C T 9: 38,492,809 (GRCm39) P79S probably damaging Het
Rock1 A G 18: 10,079,113 (GRCm39) probably null Het
Scn3a T A 2: 65,291,596 (GRCm39) M1717L possibly damaging Het
Smg7 T C 1: 152,719,812 (GRCm39) D903G possibly damaging Het
Tlr1 A T 5: 65,083,290 (GRCm39) L429* probably null Het
Ttll9 A T 2: 152,825,025 (GRCm39) N68I probably damaging Het
Ttn A G 2: 76,567,943 (GRCm39) V25904A possibly damaging Het
Uaca G A 9: 60,777,139 (GRCm39) V507M probably damaging Het
Vmn1r195 G T 13: 22,463,421 (GRCm39) C297F probably benign Het
Zdhhc2 G A 8: 40,926,042 (GRCm39) A346T probably benign Het
Other mutations in Gm5263
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01749:Gm5263 APN 1 146,296,302 (GRCm39) exon noncoding transcript
IGL01750:Gm5263 APN 1 146,296,302 (GRCm39) exon noncoding transcript
IGL01767:Gm5263 APN 1 146,296,302 (GRCm39) exon noncoding transcript
IGL01810:Gm5263 APN 1 146,296,292 (GRCm39) exon noncoding transcript
Posted On 2015-04-16