Incidental Mutation 'IGL01682:Gm10228'
ID103845
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm10228
Ensembl Gene ENSMUSG00000068074
Gene Namepredicted gene 10228
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01682
Quality Score
Status
Chromosome16
Chromosomal Location89040923-89041472 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 89041185 bp
ZygosityHeterozygous
Amino Acid Change Tyrosine to Phenylalanine at position 77 (Y77F)
Ref Sequence ENSEMBL: ENSMUSP00000086506 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000089105]
Predicted Effect unknown
Transcript: ENSMUST00000089105
AA Change: Y77F
SMART Domains Protein: ENSMUSP00000086506
Gene: ENSMUSG00000068074
AA Change: Y77F

DomainStartEndE-ValueType
Pfam:KRTAP 1 62 2.4e-8 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Agmo T C 12: 37,357,627 probably benign Het
Atp2c1 C T 9: 105,452,842 G93D probably damaging Het
C2cd6 T G 1: 59,062,501 Y333S probably damaging Het
Cacna1a A G 8: 84,536,438 E414G possibly damaging Het
Capn10 C A 1: 92,940,384 T191K probably benign Het
Cd226 A T 18: 89,269,063 R328S probably damaging Het
Cdk10 A G 8: 123,227,658 probably null Het
Cyp4a31 T A 4: 115,578,031 V486D probably damaging Het
Dgke A T 11: 89,052,441 L241I probably damaging Het
Dnah6 G T 6: 73,075,802 A2965E probably damaging Het
Fbn2 A T 18: 58,072,671 C1112S probably damaging Het
Gng3 T C 19: 8,838,580 I25V probably benign Het
Gramd2 A G 9: 59,712,110 I61M possibly damaging Het
Hcar2 T C 5: 123,864,519 N307S probably benign Het
Iars G A 13: 49,709,658 E529K probably damaging Het
Ilvbl C T 10: 78,577,107 probably benign Het
Lrp1 T C 10: 127,574,978 K1447R probably benign Het
Mmp20 A G 9: 7,671,375 D426G probably benign Het
Muc4 G A 16: 32,754,086 G1321R probably benign Het
Olfr1289 G A 2: 111,483,843 G138S probably damaging Het
Olfr568 C T 7: 102,877,233 L38F probably benign Het
Pip4k2a A G 2: 18,997,968 S10P probably benign Het
Pth1r A T 9: 110,723,706 probably null Het
Rprd1b T C 2: 158,050,160 I201T probably damaging Het
Rsbn1 A G 3: 103,962,380 N719S probably benign Het
Sorcs1 C T 19: 50,181,506 G939E probably benign Het
Ssfa2 A G 2: 79,635,637 Q33R probably damaging Het
St8sia5 A G 18: 77,248,500 K210E probably damaging Het
Trav3-1 G A 14: 52,581,192 V108M probably benign Het
Washc4 T C 10: 83,580,306 I820T possibly damaging Het
Other mutations in Gm10228
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1946:Gm10228 UTSW 16 89041353 missense unknown
R7431:Gm10228 UTSW 16 89041213 missense unknown
R7763:Gm10228 UTSW 16 89041299 missense unknown
Posted On2014-01-21