Incidental Mutation 'IGL02598:Gm4907'
ID299948
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm4907
Ensembl Gene ENSMUSG00000068113
Gene Namepredicted gene 4907
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.053) question?
Stock #IGL02598
Quality Score
Status
ChromosomeX
Chromosomal Location23882553-23907607 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 23907471 bp
ZygosityHeterozygous
Amino Acid Change Threonine to Serine at position 404 (T404S)
Ref Sequence ENSEMBL: ENSMUSP00000136747 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000116614] [ENSMUST00000163718]
Predicted Effect probably benign
Transcript: ENSMUST00000116614
AA Change: T404S

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
SMART Domains Protein: ENSMUSP00000112313
Gene: ENSMUSG00000068113
AA Change: T404S

DomainStartEndE-ValueType
Pfam:PET 88 186 3e-42 PFAM
LIM 225 282 4.38e-11 SMART
LIM 290 342 1.51e-14 SMART
LIM 350 405 3.05e-10 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000163718
AA Change: T404S

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
SMART Domains Protein: ENSMUSP00000136747
Gene: ENSMUSG00000068113
AA Change: T404S

DomainStartEndE-ValueType
Pfam:PET 83 188 8.7e-43 PFAM
LIM 225 282 4.38e-11 SMART
LIM 290 342 1.51e-14 SMART
LIM 350 405 3.05e-10 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933414I15Rik A T 11: 50,943,621 M1K probably null Het
Abca13 C T 11: 9,431,898 T3850I probably damaging Het
Abcc4 A T 14: 118,668,369 L95* probably null Het
Acacb A G 5: 114,246,037 Y2209C probably damaging Het
Acadm A G 3: 153,938,544 probably benign Het
Arid2 G A 15: 96,371,536 V1177M probably damaging Het
Atp8a1 A T 5: 67,682,756 probably null Het
BC048403 G A 10: 121,739,971 probably benign Het
Catsperd A G 17: 56,647,815 probably null Het
Cd28 A G 1: 60,763,339 probably benign Het
Cep164 A G 9: 45,770,704 Y1934H probably damaging Het
Cep350 T C 1: 155,862,967 I2377V probably benign Het
Csmd3 T C 15: 47,669,690 K1581E probably damaging Het
Dab2 A T 15: 6,429,366 N232I probably damaging Het
Dyrk4 G A 6: 126,884,019 probably benign Het
Efcab14 T A 4: 115,740,434 C75* probably null Het
Elovl1 T C 4: 118,431,419 probably null Het
Eps8l2 T G 7: 141,354,936 probably benign Het
Grik1 A T 16: 87,947,984 V460E probably damaging Het
Gtf2f2 A G 14: 76,007,742 S35P probably benign Het
Ifi203 A G 1: 173,935,002 probably benign Het
Ifi209 T C 1: 173,644,715 V374A probably damaging Het
Lars A G 18: 42,227,277 S705P possibly damaging Het
Lcmt1 A G 7: 123,421,648 probably benign Het
Limd1 T A 9: 123,480,171 Y312N probably benign Het
Limd1 T C 9: 123,516,868 S571P probably benign Het
Lin28b A T 10: 45,420,526 D125E possibly damaging Het
Lmtk3 T C 7: 45,793,140 S416P probably damaging Het
Map7d3 T C X: 56,809,786 T446A probably benign Het
Masp1 T A 16: 23,459,631 M523L probably benign Het
Mroh4 C A 15: 74,611,243 probably null Het
Mtmr6 G A 14: 60,300,504 A651T probably damaging Het
Myocd A G 11: 65,183,470 S738P probably benign Het
Olfr1176 A T 2: 88,340,251 I229F possibly damaging Het
Olfr685 A G 7: 105,180,956 V134A probably damaging Het
Olfr714 A T 7: 107,074,716 N296I possibly damaging Het
Olfr803 A T 10: 129,691,273 I256N possibly damaging Het
Olfr984 A T 9: 40,100,565 F308L probably benign Het
Parg G T 14: 32,214,324 V479L probably damaging Het
Pcdhb10 C A 18: 37,413,781 H637N possibly damaging Het
Plekhg2 G A 7: 28,360,475 T1118I possibly damaging Het
Podxl T C 6: 31,524,420 E400G probably damaging Het
Prss54 C A 8: 95,565,709 V81F probably damaging Het
Pzp A G 6: 128,487,457 L1369P probably benign Het
Rfx8 A T 1: 39,695,968 probably benign Het
Rgs6 C T 12: 83,091,797 P302S probably benign Het
Rnf148 A C 6: 23,654,457 I180S probably damaging Het
Sacm1l A G 9: 123,578,996 D350G probably benign Het
Slc33a1 C T 3: 63,943,332 G524S probably benign Het
Slc5a7 A G 17: 54,284,193 V237A probably benign Het
Spink7 T C 18: 62,594,285 D56G probably damaging Het
Syn3 A G 10: 86,467,199 S31P probably damaging Het
Thrb C A 14: 18,008,606 P110Q possibly damaging Het
Vmn2r76 G T 7: 86,228,671 T506K probably benign Het
Vps45 A G 3: 96,031,042 L486P probably benign Het
Zan G A 5: 137,446,211 T1823M unknown Het
Zdhhc6 T A 19: 55,314,527 Q14L probably benign Het
Zfp990 A T 4: 145,536,963 N177I possibly damaging Het
Other mutations in Gm4907
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00766:Gm4907 APN X 23906599 missense probably benign 0.03
R0883:Gm4907 UTSW X 23907051 missense probably benign 0.00
R1758:Gm4907 UTSW X 23906751 missense probably benign
R2049:Gm4907 UTSW X 23907310 missense probably benign 0.31
R2141:Gm4907 UTSW X 23907310 missense probably benign 0.31
R2142:Gm4907 UTSW X 23907310 missense probably benign 0.31
R3891:Gm4907 UTSW X 23906941 missense probably damaging 1.00
R5022:Gm4907 UTSW X 23907241 missense probably damaging 1.00
R5023:Gm4907 UTSW X 23907241 missense probably damaging 1.00
R5057:Gm4907 UTSW X 23907241 missense probably damaging 1.00
X0024:Gm4907 UTSW X 23907052 missense probably damaging 0.96
X0025:Gm4907 UTSW X 23907361 missense probably damaging 1.00
Posted On2015-04-16