Incidental Mutation 'IGL00339:Gm4553'
ID332334
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm4553
Ensembl Gene ENSMUSG00000090471
Gene Namepredicted gene 4553
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL00339
Quality Score
Status
Chromosome7
Chromosomal Location142164696-142165739 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 142165227 bp
ZygosityHeterozygous
Amino Acid Change Serine to Glycine at position 155 (S155G)
Ref Sequence ENSEMBL: ENSMUSP00000147863 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000168049] [ENSMUST00000210925]
Predicted Effect unknown
Transcript: ENSMUST00000168049
AA Change: S171G
SMART Domains Protein: ENSMUSP00000131778
Gene: ENSMUSG00000090471
AA Change: S171G

DomainStartEndE-ValueType
low complexity region 18 238 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000210925
AA Change: S155G
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700049A03Rik A G 12: 71,167,119 M707V probably benign Het
Amz2 A T 11: 109,434,021 I244F probably damaging Het
Atp4a T C 7: 30,713,204 C112R possibly damaging Het
Axin2 A G 11: 108,923,990 T235A probably benign Het
Barhl2 C T 5: 106,455,499 A265T possibly damaging Het
Brd8 C A 18: 34,609,883 G310* probably null Het
Capn11 A T 17: 45,643,767 I148N probably damaging Het
Caskin2 A G 11: 115,803,599 L392P probably benign Het
Cep72 C T 13: 74,062,268 probably benign Het
Chst11 A G 10: 83,191,633 Y298C possibly damaging Het
Cyp21a1 C T 17: 34,804,134 probably null Het
F830045P16Rik T C 2: 129,460,529 D381G probably damaging Het
Fnip2 T G 3: 79,515,155 H106P probably benign Het
Fosl1 T A 19: 5,450,302 I83K probably damaging Het
Foxk2 C T 11: 121,299,734 T567M probably damaging Het
Frmd4a A G 2: 4,594,714 N208S probably benign Het
Heatr5a A T 12: 51,888,901 I1634N probably damaging Het
Hspg2 C T 4: 137,539,195 T1889M probably damaging Het
Kcnh6 C T 11: 106,019,019 P457S probably damaging Het
Kcnk18 G T 19: 59,235,070 A216S probably benign Het
Klhl42 A G 6: 147,101,733 Y335C probably damaging Het
Lrguk C T 6: 34,043,429 P36L probably damaging Het
Mmp1b T A 9: 7,368,304 R443S probably benign Het
Ncapd3 T C 9: 27,052,353 S501P probably benign Het
Neurl4 C T 11: 69,904,587 R422W probably damaging Het
Nol4 T C 18: 22,823,412 S311G probably benign Het
Oaf T C 9: 43,224,016 D155G probably damaging Het
Oas1g T A 5: 120,886,046 K67* probably null Het
Olfr365 T C 2: 37,201,597 S119P probably damaging Het
Olfr434 T G 6: 43,217,848 L312V probably benign Het
Rims2 C A 15: 39,459,615 T735K probably benign Het
Sema4f T C 6: 82,937,174 T68A probably benign Het
Snx19 T G 9: 30,429,084 V506G possibly damaging Het
Sp140 T A 1: 85,641,822 C107* probably null Het
Sspo G A 6: 48,483,746 probably benign Het
Syce1l T G 8: 113,649,502 L28R probably damaging Het
Tgm3 G A 2: 130,038,413 V380M probably damaging Het
Unc5a T A 13: 54,995,815 V104D possibly damaging Het
Other mutations in Gm4553
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00323:Gm4553 APN 7 142165227 missense unknown
IGL00324:Gm4553 APN 7 142165227 missense unknown
IGL00325:Gm4553 APN 7 142165227 missense unknown
IGL00329:Gm4553 APN 7 142165227 missense unknown
IGL00332:Gm4553 APN 7 142165227 missense unknown
IGL00336:Gm4553 APN 7 142165227 missense unknown
IGL00337:Gm4553 APN 7 142165227 missense unknown
IGL00338:Gm4553 APN 7 142165227 missense unknown
IGL00340:Gm4553 APN 7 142165227 missense unknown
IGL01348:Gm4553 APN 7 142165172 missense unknown
R0468:Gm4553 UTSW 7 142165625 missense unknown
R0568:Gm4553 UTSW 7 142165620 missense unknown
R0932:Gm4553 UTSW 7 142165686 missense unknown
R4988:Gm4553 UTSW 7 142164992 unclassified probably benign
R5050:Gm4553 UTSW 7 142165036 missense unknown
R7317:Gm4553 UTSW 7 142165420 small deletion probably benign
R7372:Gm4553 UTSW 7 142165420 small deletion probably benign
R7709:Gm4553 UTSW 7 142165647 missense unknown
R7901:Gm4553 UTSW 7 142164865 small deletion probably benign
R8179:Gm4553 UTSW 7 142164857 missense unknown
R8296:Gm4553 UTSW 7 142165721 missense unknown
Posted On2015-08-05