Incidental Mutation 'IGL01702:Gm9956'
ID 104514
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm9956
Ensembl Gene ENSMUSG00000054758
Gene Name predicted gene 9956
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL01702
Quality Score
Status
Chromosome 10
Chromosomal Location 56621230-56624350 bp(+) (GRCm39)
Type of Mutation start gained
DNA Base Change (assembly) A to G at 56621335 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
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: 77,273,886 (GRCm39) probably null Het
Asb2 C T 12: 103,302,164 (GRCm39) G128E possibly damaging Het
Atp11c A T X: 59,315,263 (GRCm39) S683T probably damaging Het
Brinp3 A G 1: 146,627,735 (GRCm39) probably benign Het
Cpeb3 A T 19: 37,103,782 (GRCm39) M369K possibly damaging Het
Exoc5 A T 14: 49,253,072 (GRCm39) C580* probably null Het
Gzmk C T 13: 113,317,084 (GRCm39) V32I probably damaging Het
Hsf4 T C 8: 105,998,221 (GRCm39) I129T probably damaging Het
Igkv1-115 T A 6: 68,138,516 (GRCm39) W40R probably damaging Het
Iqub A T 6: 24,500,312 (GRCm39) M314K probably benign Het
Krt87 T C 15: 101,389,099 (GRCm39) T78A probably benign Het
Med28 T C 5: 45,682,633 (GRCm39) S100P probably benign Het
Prx G A 7: 27,219,212 (GRCm39) V1238I probably benign Het
Ptprq T C 10: 107,353,727 (GRCm39) N2263S probably benign Het
Rab12 A G 17: 66,826,384 (GRCm39) F61S probably damaging Het
Serpinb9d T C 13: 33,387,006 (GRCm39) F358S probably damaging Het
Slc25a3 A T 10: 90,953,987 (GRCm39) Y242N probably damaging Het
Smtnl1 T C 2: 84,649,034 (GRCm39) I73M possibly damaging Het
Tnp1 C A 1: 73,054,877 (GRCm39) probably benign Het
Trim5 T C 7: 103,928,638 (GRCm39) E101G probably damaging Het
Other mutations in Gm9956
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02411:Gm9956 APN 10 56,621,388 (GRCm39) missense unknown
IGL02898:Gm9956 APN 10 56,621,350 (GRCm39) missense unknown
R0513:Gm9956 UTSW 10 56,621,291 (GRCm39) start gained
R0731:Gm9956 UTSW 10 56,621,639 (GRCm39) nonsense probably null
R0841:Gm9956 UTSW 10 56,621,425 (GRCm39) missense unknown
R0841:Gm9956 UTSW 10 56,621,424 (GRCm39) missense unknown
R1289:Gm9956 UTSW 10 56,621,676 (GRCm39) missense probably damaging 0.99
Posted On 2014-01-21