Incidental Mutation 'IGL03291:Gm16503'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm16503
Ensembl Gene ENSMUSG00000078160
Gene Namepredicted gene 16503
Accession Numbers
Is this an essential gene? Possibly essential (E-score: 0.509) question?
Stock #IGL03291
Quality Score
Chromosomal Location147540218-147543500 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 147541078 bp
Amino Acid Change Tyrosine to Asparagine at position 10 (Y10N)
Ref Sequence ENSEMBL: ENSMUSP00000100571 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000104964]
Predicted Effect unknown
Transcript: ENSMUST00000104964
AA Change: Y10N
SMART Domains Protein: ENSMUSP00000100571
Gene: ENSMUSG00000078160
AA Change: Y10N

low complexity region 48 63 N/A INTRINSIC
low complexity region 86 97 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ano1 T A 7: 144,621,675 E502V probably damaging Het
Atic T C 1: 71,570,922 V364A probably benign Het
Cfap44 A T 16: 44,407,311 H125L possibly damaging Het
Ctnna2 T A 6: 76,973,712 E227V probably damaging Het
Ctsf A G 19: 4,859,634 I378V probably benign Het
Eya1 C T 1: 14,184,348 probably null Het
Fat2 C T 11: 55,262,595 R3597H probably benign Het
Gdpd5 T C 7: 99,460,121 probably benign Het
Glcci1 T A 6: 8,579,678 I293K probably damaging Het
Gm5930 A T 14: 44,331,448 I239N possibly damaging Het
Grm5 T C 7: 88,130,796 L1148P probably damaging Het
Kmt2e T A 5: 23,499,291 L1161I probably damaging Het
Megf9 C T 4: 70,488,150 V260I probably benign Het
Mme T A 3: 63,346,104 D456E probably benign Het
Mup8 T A 4: 60,221,950 E61V probably damaging Het
Olfml1 A G 7: 107,590,229 D167G probably damaging Het
Olfr615 T A 7: 103,560,912 M145K possibly damaging Het
Piezo2 T C 18: 63,021,308 K2467E probably damaging Het
Plscr1 T A 9: 92,266,870 F254L probably damaging Het
Prol1 A T 5: 88,328,520 K256N unknown Het
Rapgef4 A T 2: 72,195,703 L339F probably damaging Het
Slc27a2 T C 2: 126,564,750 I118T probably benign Het
Smim7 A T 8: 72,569,994 F19L possibly damaging Het
Svil T A 18: 5,056,150 L428* probably null Het
Tcof1 T C 18: 60,829,061 T699A possibly damaging Het
Thsd7b T A 1: 129,760,355 S668T possibly damaging Het
Tmprss7 T C 16: 45,680,748 D230G probably benign Het
Tyw1 A G 5: 130,299,993 D540G probably damaging Het
Zfp763 A G 17: 33,019,886 V95A probably damaging Het
Other mutations in Gm16503
AlleleSourceChrCoordTypePredicted EffectPPH Score
FR4737:Gm16503 UTSW 4 147541253 missense unknown
FR4976:Gm16503 UTSW 4 147541253 missense unknown
R1916:Gm16503 UTSW 4 147541210 missense unknown
R1983:Gm16503 UTSW 4 147541292 missense unknown
R2936:Gm16503 UTSW 4 147541247 missense unknown
R4226:Gm16503 UTSW 4 147541268 missense unknown
R4765:Gm16503 UTSW 4 147541097 missense unknown
R6249:Gm16503 UTSW 4 147541051 start codon destroyed probably null
R8031:Gm16503 UTSW 4 147541310 missense unknown
Z1176:Gm16503 UTSW 4 147541156 missense unknown
Posted On2016-08-02