Incidental Mutation 'IGL00323:Gm4553'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm4553
Ensembl Gene ENSMUSG00000090471
Gene Namepredicted gene 4553
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL00323
Quality Score
Chromosomal Location142164696-142165739 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 142165227 bp
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

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: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ap5m1 T C 14: 49,073,790 Y106H probably damaging Het
Atrnl1 C A 19: 57,691,817 N716K probably benign Het
Cdk13 A T 13: 17,721,098 N1075K possibly damaging Het
Daam1 G A 12: 71,958,743 probably benign Het
Exd2 T C 12: 80,476,166 V133A probably damaging Het
Fam58b A G 11: 78,750,956 V236A probably benign Het
Glrb T C 3: 80,861,955 D155G probably damaging Het
Gm13941 T A 2: 111,104,853 M11L unknown Het
Inpp5d G T 1: 87,683,815 V329F probably benign Het
Lilr4b A T 10: 51,481,251 D61V probably benign Het
Malt1 T A 18: 65,448,963 C299* probably null Het
Olfr1306 A T 2: 111,912,036 M298K possibly damaging Het
Olfr1408 G A 1: 173,130,411 Q269* probably null Het
Pigk C A 3: 152,747,632 S282* probably null Het
Pik3r1 T A 13: 101,690,536 M1L probably benign Het
Pnpla1 A G 17: 28,877,442 Y165C probably damaging Het
Rfx7 A G 9: 72,617,420 N631D probably damaging Het
Rp1 T A 1: 4,346,746 D1381V probably damaging Het
Rrp8 T C 7: 105,733,016 probably benign Het
Scn4a A T 11: 106,319,919 D1757E probably benign Het
Sec62 T C 3: 30,810,442 probably benign Het
Smarca5 G A 8: 80,714,041 T598M probably benign Het
Sptbn5 T C 2: 120,054,467 probably benign Het
Srcap T C 7: 127,542,713 probably benign Het
Stab1 T A 14: 31,139,306 E71D probably benign Het
Trhde A T 10: 114,486,747 S716R possibly damaging Het
Ttn T C 2: 76,896,515 probably benign Het
Wscd2 A C 5: 113,551,175 T81P possibly damaging Het
Zfp335 G A 2: 164,892,382 T1295I probably damaging Het
Other mutations in Gm4553
AlleleSourceChrCoordTypePredicted EffectPPH Score
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
IGL00339: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
Posted On2015-08-05