Incidental Mutation 'IGL01101:Gm8362'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm8362
Ensembl Gene ENSMUSG00000090404
Gene Namepredicted gene 8362
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01101
Quality Score
Chromosomal Location6765962-6774411 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 6767109 bp
Amino Acid Change Serine to Threonine at position 204 (S204T)
Ref Sequence ENSEMBL: ENSMUSP00000128839 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000168790] [ENSMUST00000170673]
Predicted Effect probably benign
Transcript: ENSMUST00000168790
AA Change: S204T

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)
SMART Domains Protein: ENSMUSP00000128839
Gene: ENSMUSG00000090404
AA Change: S204T

Pfam:Takusan 48 128 8.3e-21 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000170673
SMART Domains Protein: ENSMUSP00000131018
Gene: ENSMUSG00000090404

Pfam:Takusan 46 129 4.9e-31 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000181787
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
5830411N06Rik A T 7: 140,296,104 Q543L probably benign Het
Adamts20 T A 15: 94,344,042 D695V probably damaging Het
Ahnak T C 19: 9,012,887 probably benign Het
Akap4 T A X: 7,076,184 M242K probably benign Het
Cd207 T C 6: 83,675,857 D97G probably benign Het
Cdc20 A G 4: 118,435,552 V333A possibly damaging Het
Cdhr2 A G 13: 54,718,135 probably benign Het
Cfhr1 T A 1: 139,553,584 Y186F probably benign Het
Cnbd1 T A 4: 18,907,098 I159F probably benign Het
Cyp2j11 A C 4: 96,339,095 M228R probably benign Het
Dach1 C A 14: 97,840,204 S581I possibly damaging Het
Dbnl A G 11: 5,793,722 D71G possibly damaging Het
F8 T A X: 75,287,387 T966S possibly damaging Het
Filip1 T A 9: 79,898,246 L75F probably benign Het
Foxi2 A G 7: 135,412,007 Y322C probably benign Het
Ftsj3 A G 11: 106,255,632 V7A probably benign Het
Ibtk C A 9: 85,732,622 probably benign Het
Marf1 C T 16: 14,146,736 V267I possibly damaging Het
Mmp27 T A 9: 7,573,415 D169E probably damaging Het
Olfr1115 C A 2: 87,252,462 T175K probably damaging Het
Olfr1247 C T 2: 89,609,847 C85Y probably benign Het
Olfr728 A T 14: 50,140,054 M195K probably benign Het
P4ha2 G T 11: 54,119,305 C296F probably damaging Het
Slc38a5 T C X: 8,271,511 probably benign Het
Sorbs2 G T 8: 45,745,423 R36L possibly damaging Het
Tmem207 A C 16: 26,517,877 Y42* probably null Het
Vmn2r115 G A 17: 23,345,997 R286K probably benign Het
Other mutations in Gm8362
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02118:Gm8362 APN 14 6771516 missense probably damaging 1.00
Posted On2013-06-21