Incidental Mutation 'IGL01702:Gm9956'
ID104514
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm9956
Ensembl Gene ENSMUSG00000054758
Gene Namepredicted gene 9956
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01702
Quality Score
Status
Chromosome10
Chromosomal Location56745134-56748254 bp(+) (GRCm38)
Type of Mutationstart gained
DNA Base Change (assembly) A to G at 56745239 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect
SMART Domains Protein: ENSMUSP00000071080
Gene: ENSMUSG00000054758

DomainStartEndE-ValueType
transmembrane domain 94 116 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 20 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Apol7a T C 15: 77,389,686 probably null Het
Asb2 C T 12: 103,335,905 G128E possibly damaging Het
Atp11c A T X: 60,269,903 S683T probably damaging Het
Brinp3 A G 1: 146,751,997 probably benign Het
Cpeb3 A T 19: 37,126,382 M369K possibly damaging Het
Exoc5 A T 14: 49,015,615 C580* probably null Het
Gzmk C T 13: 113,180,550 V32I probably damaging Het
Hsf4 T C 8: 105,271,589 I129T probably damaging Het
Igkv1-115 T A 6: 68,161,532 W40R probably damaging Het
Iqub A T 6: 24,500,313 M314K probably benign Het
Krt83 T C 15: 101,491,218 T78A probably benign Het
Med28 T C 5: 45,525,291 S100P probably benign Het
Prx G A 7: 27,519,787 V1238I probably benign Het
Ptprq T C 10: 107,517,866 N2263S probably benign Het
Rab12 A G 17: 66,519,389 F61S probably damaging Het
Serpinb9d T C 13: 33,203,023 F358S probably damaging Het
Slc25a3 A T 10: 91,118,125 Y242N probably damaging Het
Smtnl1 T C 2: 84,818,690 I73M possibly damaging Het
Tnp1 C A 1: 73,015,718 probably benign Het
Trim5 T C 7: 104,279,431 E101G probably damaging Het
Other mutations in Gm9956
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02411:Gm9956 APN 10 56745292 missense unknown
IGL02898:Gm9956 APN 10 56745254 missense unknown
R0513:Gm9956 UTSW 10 56745195 start gained
R0731:Gm9956 UTSW 10 56745543 nonsense probably null
R0841:Gm9956 UTSW 10 56745328 missense unknown
R0841:Gm9956 UTSW 10 56745329 missense unknown
R1289:Gm9956 UTSW 10 56745580 missense probably damaging 0.99
Posted On2014-01-21