Incidental Mutation 'IGL01912:Gm3633'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm3633
Ensembl Gene ENSMUSG00000095113
Gene Namepredicted gene 3633
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01912
Quality Score
Chromosomal Location42636467-42641917 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) T to C at 42640786 bp
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000126330 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000163102]
Predicted Effect probably benign
Transcript: ENSMUST00000100697
SMART Domains Protein: ENSMUSP00000098262
Gene: ENSMUSG00000095113

Pfam:Takusan 57 137 2.9e-26 PFAM
coiled coil region 164 186 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000163102
SMART Domains Protein: ENSMUSP00000126330
Gene: ENSMUSG00000095113

Pfam:Takusan 1 32 6.1e-9 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc8 A T 7: 46,120,510 D860E probably damaging Het
Actl11 C A 9: 107,929,645 P389Q probably damaging Het
Bsg G T 10: 79,710,140 G103W probably null Het
Camk2d T A 3: 126,810,632 probably null Het
Clcn7 T C 17: 25,153,009 probably benign Het
Dctd C T 8: 48,111,662 probably benign Het
Dpy19l1 C T 9: 24,485,069 R117Q probably damaging Het
Esyt2 T C 12: 116,339,609 I289T probably damaging Het
Exoc6b A C 6: 84,625,174 C753G probably damaging Het
Gm10718 A T 9: 3,025,118 Y194F probably benign Het
Gm21738 G A 14: 19,416,979 S144L probably benign Het
Hrh3 A T 2: 180,101,376 V153D probably damaging Het
Krt77 T A 15: 101,863,851 probably benign Het
Nat3 T A 8: 67,547,746 C92* probably null Het
Nckap1l T A 15: 103,474,146 L525M probably benign Het
Nrp2 T A 1: 62,771,737 C646S probably damaging Het
Olfr512 T C 7: 108,714,258 Y290H possibly damaging Het
Olfr659 T C 7: 104,671,233 I177T possibly damaging Het
Olfr698 T A 7: 106,752,992 Y132F probably damaging Het
Orc1 T C 4: 108,590,744 Y63H probably damaging Het
Otud4 T C 8: 79,673,837 V1059A probably benign Het
Ptprm A G 17: 67,046,118 V235A probably benign Het
Rab3ip G T 10: 116,907,092 Q443K probably benign Het
Tnc C A 4: 64,008,740 D850Y probably damaging Het
Ubxn2b T A 4: 6,203,767 probably null Het
Vmn1r233 T A 17: 20,994,205 Y161F probably benign Het
Vmn1r54 T C 6: 90,269,460 S119P probably damaging Het
Other mutations in Gm3633
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01335:Gm3633 APN 14 42640638 unclassified probably benign
IGL01640:Gm3633 APN 14 42638367 nonsense probably null
IGL01875:Gm3633 APN 14 42639277 missense probably damaging 1.00
R5039:Gm3633 UTSW 14 42639204 missense possibly damaging 0.78
R6866:Gm3633 UTSW 14 42640622 unclassified probably benign
R8298:Gm3633 UTSW 14 42640718 missense
R8687:Gm3633 UTSW 14 42640691 missense
Posted On2014-05-07