Incidental Mutation 'IGL01590:Gm5286'
ID91581
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5286
Ensembl Gene ENSMUSG00000090268
Gene Namepredicted gene 5286
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01590
Quality Score
Status
Chromosome3
Chromosomal Location94196714-94199802 bp(+) (GRCm38)
Type of Mutationutr 5 prime
DNA Base Change (assembly) G to A at 94198367 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000125267 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000159524]
Predicted Effect noncoding transcript
Transcript: ENSMUST00000159267
Predicted Effect probably benign
Transcript: ENSMUST00000159524
SMART Domains Protein: ENSMUSP00000125267
Gene: ENSMUSG00000090268

DomainStartEndE-ValueType
MATH 17 126 7.18e-6 SMART
BTB 184 283 8.21e-26 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921504E06Rik T A 2: 19,477,779 probably benign Het
Adgrb2 T G 4: 130,013,813 probably benign Het
Apcs C T 1: 172,894,467 G104D probably damaging Het
Atp10b G A 11: 43,172,721 R161H probably benign Het
Cep250 A T 2: 155,992,317 Q2054L possibly damaging Het
Dennd6a T G 14: 26,619,352 V207G probably benign Het
Ehbp1 C A 11: 22,095,611 D688Y possibly damaging Het
Fam83a C A 15: 58,009,777 S334Y probably damaging Het
Fam83e T A 7: 45,723,936 F242Y probably null Het
Fnip1 A T 11: 54,493,300 D341V probably damaging Het
Gm17359 A C 3: 79,449,340 N150T probably damaging Het
Gpatch3 A G 4: 133,580,717 probably benign Het
Gpc2 C A 5: 138,274,378 V558F probably damaging Het
H2-M10.6 A G 17: 36,812,749 N112D probably benign Het
Hs6st1 A T 1: 36,103,704 D240V probably damaging Het
Inpp5f T A 7: 128,664,307 probably null Het
Itga8 G T 2: 12,160,333 H822N probably damaging Het
Kif20b T A 19: 34,954,726 N1263K possibly damaging Het
Krt28 A G 11: 99,374,394 probably null Het
Muc5ac A T 7: 141,798,893 M706L probably benign Het
Olfr340 A T 2: 36,452,992 M136L probably benign Het
Olfr651 A C 7: 104,553,575 I219L probably benign Het
Prox2 A G 12: 85,088,071 W479R probably damaging Het
Rps19 A T 7: 24,888,456 D152V probably damaging Het
Slc20a1 G A 2: 129,209,226 probably benign Het
Slc7a2 C T 8: 40,914,100 P564S probably damaging Het
Slco1a5 C A 6: 142,250,319 M319I probably benign Het
Tanc1 A G 2: 59,785,473 T275A probably benign Het
Tenm3 A G 8: 48,228,802 S2598P probably damaging Het
Tiparp G A 3: 65,531,976 E56K probably benign Het
Trpm5 G A 7: 143,082,734 R489C probably damaging Het
Vmn2r84 C A 10: 130,386,095 G752V probably damaging Het
Wnt5b T A 6: 119,440,554 T130S possibly damaging Het
Other mutations in Gm5286
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02603:Gm5286 APN 3 94198437 missense possibly damaging 0.53
R7130:Gm5286 UTSW 3 94198527 missense probably damaging 1.00
R7209:Gm5286 UTSW 3 94198705 missense probably benign
R7595:Gm5286 UTSW 3 94198417 missense probably benign 0.15
R7661:Gm5286 UTSW 3 94198402 missense probably damaging 0.98
Posted On2013-12-09