Incidental Mutation 'IGL01806:Gm6408'
ID 155673
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm6408
Ensembl Gene ENSMUSG00000096344
Gene Name predicted gene 6408
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.085) question?
Stock # IGL01806
Quality Score
Status
Chromosome 5
Chromosomal Location 146418775-146421514 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 146418892 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Histidine at position 30 (R30H)
Ref Sequence ENSEMBL: ENSMUSP00000136735 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000179032]
AlphaFold J3QNG1
Predicted Effect probably damaging
Transcript: ENSMUST00000179032
AA Change: R30H

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000136735
Gene: ENSMUSG00000096344
AA Change: R30H

DomainStartEndE-ValueType
RasGEFN 66 182 4.47e-3 SMART
low complexity region 270 292 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrg1 T C 8: 95,739,559 (GRCm39) S670P probably damaging Het
Ap5m1 T A 14: 49,317,797 (GRCm39) F351L probably damaging Het
Cacnb2 A G 2: 14,619,079 (GRCm39) Y38C probably damaging Het
Ccdc28a C T 10: 18,095,262 (GRCm39) A151T possibly damaging Het
Cgnl1 T C 9: 71,557,604 (GRCm39) E976G probably damaging Het
Cyp2c39 A G 19: 39,525,264 (GRCm39) Y189C probably damaging Het
Dbt T C 3: 116,326,954 (GRCm39) V101A probably damaging Het
Evc A G 5: 37,477,578 (GRCm39) probably null Het
Fastkd5 A G 2: 130,457,532 (GRCm39) Y353H probably benign Het
Lhx8 A G 3: 154,027,992 (GRCm39) S156P probably damaging Het
Mki67 T C 7: 135,300,686 (GRCm39) I1449M probably damaging Het
Mtrr A T 13: 68,728,719 (GRCm39) V27E possibly damaging Het
Myh14 A G 7: 44,307,363 (GRCm39) V226A probably benign Het
Nek1 T C 8: 61,577,246 (GRCm39) S1076P possibly damaging Het
Or52z14 C T 7: 103,253,548 (GRCm39) A229V probably benign Het
Or6ae1 G T 7: 139,742,841 (GRCm39) N7K probably benign Het
Pcdhb7 A G 18: 37,475,548 (GRCm39) D228G possibly damaging Het
Pias3 T C 3: 96,611,073 (GRCm39) S414P probably benign Het
Plcd4 G A 1: 74,591,192 (GRCm39) V196I probably benign Het
Proca1 A G 11: 78,095,737 (GRCm39) D123G probably damaging Het
Ptpn3 A G 4: 57,254,915 (GRCm39) probably null Het
Ptprq C A 10: 107,535,469 (GRCm39) R432L probably damaging Het
Rasgrp4 A G 7: 28,838,475 (GRCm39) K108E possibly damaging Het
Siglecg A G 7: 43,060,888 (GRCm39) probably null Het
Srpra A G 9: 35,126,201 (GRCm39) T465A possibly damaging Het
Tmpo G A 10: 90,999,104 (GRCm39) R228C probably benign Het
Zeb1 G A 18: 5,767,867 (GRCm39) V793M possibly damaging Het
Other mutations in Gm6408
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01695:Gm6408 APN 5 146,418,939 (GRCm39) splice site probably benign
R0211:Gm6408 UTSW 5 146,419,870 (GRCm39) missense probably benign 0.04
R1763:Gm6408 UTSW 5 146,419,132 (GRCm39) missense probably damaging 1.00
R3745:Gm6408 UTSW 5 146,421,246 (GRCm39) missense probably damaging 1.00
R4393:Gm6408 UTSW 5 146,419,147 (GRCm39) missense probably damaging 1.00
R5586:Gm6408 UTSW 5 146,421,267 (GRCm39) missense possibly damaging 0.71
R5734:Gm6408 UTSW 5 146,419,192 (GRCm39) missense probably benign 0.07
R5999:Gm6408 UTSW 5 146,421,067 (GRCm39) missense possibly damaging 0.86
R6181:Gm6408 UTSW 5 146,420,582 (GRCm39) missense possibly damaging 0.84
R7007:Gm6408 UTSW 5 146,420,647 (GRCm39) missense probably damaging 1.00
R7063:Gm6408 UTSW 5 146,420,594 (GRCm39) missense probably benign 0.01
R7224:Gm6408 UTSW 5 146,421,180 (GRCm39) missense probably benign 0.10
R7734:Gm6408 UTSW 5 146,421,160 (GRCm39) nonsense probably null
R8676:Gm6408 UTSW 5 146,419,237 (GRCm39) missense probably benign 0.02
R8847:Gm6408 UTSW 5 146,420,602 (GRCm39) missense probably benign 0.20
R9758:Gm6408 UTSW 5 146,420,628 (GRCm39) missense probably benign 0.28
Posted On 2014-02-04