Incidental Mutation 'IGL00514:4933409G03Rik'
ID7174
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4933409G03Rik
Ensembl Gene ENSMUSG00000053896
Gene NameRIKEN cDNA 4933409G03 gene
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.084) question?
Stock #IGL00514
Quality Score
Status
Chromosome2
Chromosomal Location68582413-68616463 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 68601797 bp
ZygosityHeterozygous
Amino Acid Change Glutamic Acid to Glycine at position 75 (E75G)
Gene Model predicted gene model for transcript(s): [ENSMUST00000102713]
Predicted Effect unknown
Transcript: ENSMUST00000102713
AA Change: E94G
SMART Domains Protein: ENSMUSP00000099774
Gene: ENSMUSG00000053896
AA Change: E94G

DomainStartEndE-ValueType
low complexity region 74 86 N/A INTRINSIC
low complexity region 89 133 N/A INTRINSIC
low complexity region 194 206 N/A INTRINSIC
low complexity region 220 231 N/A INTRINSIC
low complexity region 260 272 N/A INTRINSIC
low complexity region 293 305 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000137117
AA Change: E75G
SMART Domains Protein: ENSMUSP00000117165
Gene: ENSMUSG00000053896
AA Change: E75G

DomainStartEndE-ValueType
low complexity region 56 68 N/A INTRINSIC
low complexity region 71 115 N/A INTRINSIC
low complexity region 176 188 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ank3 T C 10: 69,982,205 probably benign Het
Aplf A G 6: 87,668,408 probably benign Het
Baz2b A T 2: 59,962,477 F436I probably benign Het
Blmh A G 11: 76,967,013 D327G probably damaging Het
Bmt2 A T 6: 13,628,753 H310Q probably damaging Het
Cfap46 C T 7: 139,660,689 S56N probably damaging Het
Col19a1 T C 1: 24,536,932 K110E unknown Het
Cyp2c68 T C 19: 39,712,495 D293G probably damaging Het
Ears2 T A 7: 122,039,762 K480* probably null Het
Efhc1 C T 1: 20,979,481 Q522* probably null Het
Ehd4 G A 2: 120,091,213 P521S probably damaging Het
Endov G T 11: 119,491,465 probably benign Het
Fgfr2 T G 7: 130,167,711 T648P probably benign Het
Hsf5 A G 11: 87,623,096 Y329C probably damaging Het
Kntc1 T A 5: 123,791,527 S1308T probably benign Het
Mill1 A T 7: 18,264,641 T259S possibly damaging Het
Ms4a4c C T 19: 11,419,036 A111V probably damaging Het
Myh1 G T 11: 67,219,784 R1507M probably damaging Het
Nbeal1 G A 1: 60,217,225 D210N probably benign Het
Neo1 G T 9: 58,921,919 probably benign Het
Nipsnap2 A G 5: 129,754,851 D236G probably damaging Het
Plekhh2 G T 17: 84,596,306 probably null Het
Prox2 A T 12: 85,094,778 M217K probably benign Het
Rgl2 G A 17: 33,933,136 G299E probably benign Het
Rragb T G X: 153,171,298 C370W possibly damaging Het
Scn9a A T 2: 66,563,601 N209K probably damaging Het
Sec61g A T 11: 16,501,817 probably benign Het
Slc38a7 A G 8: 95,840,477 probably benign Het
Smcr8 A T 11: 60,778,367 K114* probably null Het
Stag3 T C 5: 138,300,135 L730P probably damaging Het
Syn3 A G 10: 86,354,416 L183P probably damaging Het
Tbk1 A T 10: 121,552,250 C637S probably benign Het
Tmem30c A T 16: 57,270,074 Y257N probably damaging Het
Trpm3 C T 19: 22,987,659 T1506M probably benign Het
Yes1 A C 5: 32,655,129 K248Q probably benign Het
Zfp638 A T 6: 83,956,698 K811N probably damaging Het
Other mutations in 4933409G03Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00498:4933409G03Rik APN 2 68601898 missense unknown
IGL02173:4933409G03Rik APN 2 68613057 missense unknown
IGL02252:4933409G03Rik APN 2 68614334 splice site probably benign
PIT4812001:4933409G03Rik UTSW 2 68588948 missense probably benign 0.16
R0196:4933409G03Rik UTSW 2 68616247 unclassified probably benign
R1939:4933409G03Rik UTSW 2 68588984 missense possibly damaging 0.83
R2422:4933409G03Rik UTSW 2 68591520 missense probably benign 0.16
R3435:4933409G03Rik UTSW 2 68601845 missense unknown
R4124:4933409G03Rik UTSW 2 68616224 unclassified probably benign
R4243:4933409G03Rik UTSW 2 68593543 intron probably benign
R4424:4933409G03Rik UTSW 2 68615147 unclassified probably benign
R4649:4933409G03Rik UTSW 2 68606215 missense unknown
R4650:4933409G03Rik UTSW 2 68606215 missense unknown
R4651:4933409G03Rik UTSW 2 68606215 missense unknown
R4652:4933409G03Rik UTSW 2 68606215 missense unknown
R4653:4933409G03Rik UTSW 2 68606215 missense unknown
R4732:4933409G03Rik UTSW 2 68614721 unclassified probably benign
R4733:4933409G03Rik UTSW 2 68614721 unclassified probably benign
R5144:4933409G03Rik UTSW 2 68616260 unclassified probably benign
R5499:4933409G03Rik UTSW 2 68601793 missense unknown
R5828:4933409G03Rik UTSW 2 68601800 missense unknown
R5936:4933409G03Rik UTSW 2 68615504 unclassified probably benign
R6323:4933409G03Rik UTSW 2 68606224 missense unknown
Posted On2012-04-20