Incidental Mutation 'IGL02197:Gm5134'
ID 284107
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5134
Ensembl Gene ENSMUSG00000033255
Gene Name predicted gene 5134
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.097) question?
Stock # IGL02197
Quality Score
Status
Chromosome 10
Chromosomal Location 75790348-75845425 bp(+) (GRCm39)
Type of Mutation critical splice donor site (2 bp from exon)
DNA Base Change (assembly) T to C at 75790536 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000097172 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099577]
AlphaFold E9QAB5
Predicted Effect probably null
Transcript: ENSMUST00000099577
SMART Domains Protein: ENSMUSP00000097172
Gene: ENSMUSG00000033255

DomainStartEndE-ValueType
Pfam:SSF 32 466 2.9e-119 PFAM
transmembrane domain 500 522 N/A INTRINSIC
transmembrane domain 651 670 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgap21 T C 2: 20,885,117 (GRCm39) S526G probably benign Het
Atad2b A T 12: 5,068,056 (GRCm39) N1018I possibly damaging Het
Baz1b A G 5: 135,237,951 (GRCm39) E209G probably benign Het
Bltp1 A G 3: 36,960,884 (GRCm39) T445A probably damaging Het
Capn11 T A 17: 45,950,782 (GRCm39) T264S probably benign Het
Cdh1 A G 8: 107,380,418 (GRCm39) E187G probably benign Het
Cps1 A G 1: 67,196,923 (GRCm39) I325V probably benign Het
Csgalnact1 C A 8: 68,854,144 (GRCm39) G219V probably damaging Het
Dmbt1 A G 7: 130,687,152 (GRCm39) probably benign Het
Dnaaf3 T C 7: 4,530,496 (GRCm39) D203G probably damaging Het
Eif2ak3 A G 6: 70,878,441 (GRCm39) Y1045C probably benign Het
Fam13a T A 6: 58,912,586 (GRCm39) D689V possibly damaging Het
Fnip1 T A 11: 54,384,200 (GRCm39) L342I probably damaging Het
Frk T A 10: 34,360,330 (GRCm39) N110K probably damaging Het
Gm53 T C 11: 96,142,549 (GRCm39) noncoding transcript Het
Gm9312 A T 12: 24,302,163 (GRCm39) noncoding transcript Het
Gm9936 A G 5: 114,995,152 (GRCm39) probably benign Het
Hk3 A G 13: 55,162,281 (GRCm39) F108L probably damaging Het
Homer2 A T 7: 81,260,147 (GRCm39) S296T probably benign Het
Itga2b T A 11: 102,357,145 (GRCm39) H245L probably benign Het
Ky T C 9: 102,414,985 (GRCm39) F299S possibly damaging Het
Lama5 A G 2: 179,849,012 (GRCm39) Y224H possibly damaging Het
Leng9 G T 7: 4,151,723 (GRCm39) L318I probably damaging Het
Lpin1 A G 12: 16,608,408 (GRCm39) probably null Het
Lrp2 T C 2: 69,297,224 (GRCm39) I3246V probably benign Het
Map2k3 A G 11: 60,837,590 (GRCm39) Y230C probably damaging Het
Myef2 T C 2: 124,955,959 (GRCm39) probably null Het
Myh3 A T 11: 66,989,409 (GRCm39) I1510L probably benign Het
Mypn T C 10: 62,959,057 (GRCm39) D1088G possibly damaging Het
Nek9 C A 12: 85,354,704 (GRCm39) V745L probably null Het
Neu1 T A 17: 35,153,641 (GRCm39) V355D possibly damaging Het
Nlrp4a G T 7: 26,148,703 (GRCm39) K103N possibly damaging Het
Or4c107 A G 2: 88,789,028 (GRCm39) T73A probably benign Het
Or6e1 T C 14: 54,519,409 (GRCm39) *314W probably null Het
Papola A T 12: 105,795,442 (GRCm39) N631I possibly damaging Het
Pcnx1 T C 12: 81,965,878 (GRCm39) S682P probably benign Het
Pcnx1 T C 12: 82,039,925 (GRCm39) S2071P possibly damaging Het
Pga5 A G 19: 10,649,277 (GRCm39) probably benign Het
Phlda1 T A 10: 111,343,014 (GRCm39) M250K probably damaging Het
Phox2b A G 5: 67,253,869 (GRCm39) probably benign Het
Pkdrej A G 15: 85,699,994 (GRCm39) Y1981H possibly damaging Het
Pold1 G A 7: 44,191,663 (GRCm39) P108S probably benign Het
Ptprg T G 14: 12,220,613 (GRCm38) F442V probably damaging Het
Rab36 A G 10: 74,887,874 (GRCm39) I248M probably damaging Het
Scnn1b G A 7: 121,502,113 (GRCm39) R257Q probably null Het
Sdc1 A G 12: 8,840,835 (GRCm39) Q200R possibly damaging Het
Slc10a7 A G 8: 79,242,292 (GRCm39) T60A probably damaging Het
Snx13 A G 12: 35,156,800 (GRCm39) D484G probably damaging Het
Tlr1 G A 5: 65,083,797 (GRCm39) T260M probably damaging Het
Tpcn1 A G 5: 120,691,596 (GRCm39) V286A probably damaging Het
Traip T G 9: 107,845,936 (GRCm39) L343R possibly damaging Het
Unc13b A G 4: 43,165,828 (GRCm39) H204R probably damaging Het
Unc80 A G 1: 66,569,224 (GRCm39) S960G probably benign Het
V1ra8 C T 6: 90,180,184 (GRCm39) P129L probably benign Het
Vps13b T A 15: 35,930,202 (GRCm39) F3980I probably benign Het
Vps13d T C 4: 144,854,879 (GRCm39) N2248S probably benign Het
Vps26c G T 16: 94,302,549 (GRCm39) probably benign Het
Wnk4 T C 11: 101,154,783 (GRCm39) L324P probably damaging Het
Other mutations in Gm5134
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00941:Gm5134 APN 10 75,836,255 (GRCm39) missense possibly damaging 0.70
IGL01371:Gm5134 APN 10 75,840,581 (GRCm39) missense probably damaging 0.99
IGL02140:Gm5134 APN 10 75,821,945 (GRCm39) missense probably benign 0.03
IGL02233:Gm5134 APN 10 75,844,334 (GRCm39) critical splice acceptor site probably null
IGL02612:Gm5134 APN 10 75,828,323 (GRCm39) missense probably damaging 1.00
IGL02896:Gm5134 APN 10 75,810,058 (GRCm39) missense possibly damaging 0.82
R0021:Gm5134 UTSW 10 75,829,718 (GRCm39) missense probably damaging 1.00
R0021:Gm5134 UTSW 10 75,829,718 (GRCm39) missense probably damaging 1.00
R0035:Gm5134 UTSW 10 75,829,698 (GRCm39) missense probably benign 0.01
R0035:Gm5134 UTSW 10 75,829,698 (GRCm39) missense probably benign 0.01
R0110:Gm5134 UTSW 10 75,810,079 (GRCm39) missense probably benign 0.03
R0499:Gm5134 UTSW 10 75,828,359 (GRCm39) missense probably benign 0.00
R0510:Gm5134 UTSW 10 75,810,079 (GRCm39) missense probably benign 0.03
R1429:Gm5134 UTSW 10 75,814,215 (GRCm39) missense probably damaging 1.00
R1726:Gm5134 UTSW 10 75,828,361 (GRCm39) missense possibly damaging 0.83
R1918:Gm5134 UTSW 10 75,812,180 (GRCm39) missense possibly damaging 0.70
R1956:Gm5134 UTSW 10 75,840,680 (GRCm39) missense possibly damaging 0.89
R1993:Gm5134 UTSW 10 75,802,227 (GRCm39) missense probably damaging 0.96
R2049:Gm5134 UTSW 10 75,840,718 (GRCm39) missense possibly damaging 0.92
R2188:Gm5134 UTSW 10 75,831,670 (GRCm39) missense probably damaging 1.00
R3551:Gm5134 UTSW 10 75,836,281 (GRCm39) missense probably benign 0.08
R4074:Gm5134 UTSW 10 75,844,365 (GRCm39) missense probably damaging 1.00
R4435:Gm5134 UTSW 10 75,831,658 (GRCm39) missense probably damaging 1.00
R4466:Gm5134 UTSW 10 75,844,409 (GRCm39) missense probably benign 0.00
R5180:Gm5134 UTSW 10 75,812,200 (GRCm39) missense probably damaging 1.00
R5446:Gm5134 UTSW 10 75,831,670 (GRCm39) missense probably damaging 1.00
R5601:Gm5134 UTSW 10 75,821,786 (GRCm39) missense probably damaging 0.98
R5627:Gm5134 UTSW 10 75,821,942 (GRCm39) missense possibly damaging 0.93
R5777:Gm5134 UTSW 10 75,840,594 (GRCm39) missense probably benign 0.00
R5867:Gm5134 UTSW 10 75,844,450 (GRCm39) missense probably benign 0.00
R6145:Gm5134 UTSW 10 75,831,673 (GRCm39) missense probably damaging 0.99
R6232:Gm5134 UTSW 10 75,821,859 (GRCm39) missense possibly damaging 0.95
R6271:Gm5134 UTSW 10 75,831,643 (GRCm39) missense probably benign 0.32
R6329:Gm5134 UTSW 10 75,790,494 (GRCm39) missense possibly damaging 0.68
R6723:Gm5134 UTSW 10 75,844,453 (GRCm39) missense probably benign
R7049:Gm5134 UTSW 10 75,828,292 (GRCm39) missense probably damaging 0.97
R7305:Gm5134 UTSW 10 75,836,233 (GRCm39) missense probably damaging 1.00
R7579:Gm5134 UTSW 10 75,800,271 (GRCm39) missense probably damaging 1.00
R9190:Gm5134 UTSW 10 75,844,645 (GRCm39) missense probably damaging 1.00
R9716:Gm5134 UTSW 10 75,821,943 (GRCm39) missense probably benign 0.27
R9718:Gm5134 UTSW 10 75,828,331 (GRCm39) missense possibly damaging 0.90
X0050:Gm5134 UTSW 10 75,828,344 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16