Incidental Mutation 'R5445:A430105I19Rik'
ID427379
Institutional Source Beutler Lab
Gene Symbol A430105I19Rik
Ensembl Gene ENSMUSG00000045838
Gene NameRIKEN cDNA A430105I19 gene
Synonyms
MMRRC Submission 043010-MU
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #R5445 (G1)
Quality Score225
Status Not validated
Chromosome2
Chromosomal Location118754158-118762661 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 118759586 bp
ZygosityHeterozygous
Amino Acid Change Aspartic acid to Glycine at position 259 (D259G)
Ref Sequence ENSEMBL: ENSMUSP00000051853 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000059997]
Predicted Effect probably damaging
Transcript: ENSMUST00000059997
AA Change: D259G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000051853
Gene: ENSMUSG00000045838
AA Change: D259G

DomainStartEndE-ValueType
coiled coil region 52 100 N/A INTRINSIC
low complexity region 142 154 N/A INTRINSIC
Pfam:DUF4594 185 361 1.2e-64 PFAM
low complexity region 515 529 N/A INTRINSIC
low complexity region 535 544 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000151270
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.9%
  • 20x: 94.3%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcg5 A T 17: 84,671,129 D300E probably damaging Het
Apbb1ip T C 2: 22,835,948 V244A possibly damaging Het
Arhgap32 T C 9: 32,248,382 S232P probably benign Het
Atf7ip G A 6: 136,587,257 V833M probably damaging Het
Casp7 A G 19: 56,433,338 probably null Het
Celsr2 T A 3: 108,392,658 E2911D probably benign Het
Cep350 T C 1: 155,894,723 D1807G probably benign Het
Chrd A G 16: 20,738,910 T753A possibly damaging Het
Clasp2 A G 9: 113,903,946 D971G probably damaging Het
Cnnm2 A G 19: 46,877,288 T772A possibly damaging Het
Cntn1 A T 15: 92,295,077 N687Y probably damaging Het
Col6a3 G A 1: 90,782,039 R1812* probably null Het
Dsc2 T C 18: 20,035,303 I700V possibly damaging Het
Fam71d G A 12: 78,715,116 E185K probably damaging Het
Flt3 G A 5: 147,355,095 Q540* probably null Het
Fmo4 T A 1: 162,805,273 I170F probably benign Het
Fra10ac1 T A 19: 38,219,462 D72V possibly damaging Het
Gemin6 T G 17: 80,227,749 V46G probably damaging Het
Gm13023 T A 4: 143,795,137 V441E possibly damaging Het
Gm2381 T G 7: 42,820,001 H233P probably damaging Het
Gm5148 T A 3: 37,714,846 Q75L probably damaging Het
Gm8369 T C 19: 11,504,806 V27A possibly damaging Het
Gpr157 T C 4: 150,102,368 S318P probably benign Het
Hectd4 G A 5: 121,266,274 V405M probably benign Het
Hemgn T C 4: 46,400,738 R41G probably benign Het
Hhipl1 T A 12: 108,328,208 L791Q probably damaging Het
Hjurp T G 1: 88,266,316 K290T probably benign Het
Ifi207 T C 1: 173,727,797 E773G probably damaging Het
Kcnh6 T C 11: 106,023,859 Y697H probably damaging Het
Lonrf2 T C 1: 38,807,153 T313A probably benign Het
Lrba G T 3: 86,368,595 V1757L probably benign Het
Lrrc24 T C 15: 76,716,106 T278A probably benign Het
Ltbp2 T C 12: 84,809,654 I679V probably null Het
Mapk4 G T 18: 73,931,002 T383K probably benign Het
Mdn1 C T 4: 32,723,690 P2542L probably damaging Het
Mia3 A G 1: 183,336,022 V208A probably benign Het
Myo15 C A 11: 60,520,777 C3234* probably null Het
Nlrp1b G T 11: 71,217,875 Q267K probably benign Het
Nphp3 A G 9: 104,004,723 K37E probably damaging Het
Nwd2 T C 5: 63,805,338 M755T probably damaging Het
Olfr482 A G 7: 108,094,742 V276A possibly damaging Het
Olfr655 A G 7: 104,596,821 F120S probably damaging Het
Olfr819 T A 10: 129,966,289 H137L probably benign Het
Pdlim5 C T 3: 142,352,734 R83K probably null Het
Plekha5 A T 6: 140,552,733 R173* probably null Het
Rbms3 T A 9: 117,251,785 D6V possibly damaging Het
Rhoq A T 17: 86,964,327 Y57F probably benign Het
Rrm1 A T 7: 102,451,023 T204S possibly damaging Het
Slf1 A T 13: 77,091,204 I447N probably benign Het
Smarcc2 T A 10: 128,488,074 probably benign Het
Spdye4c C T 2: 128,596,564 Q281* probably null Het
Tert T A 13: 73,644,284 M890K probably benign Het
Tln1 C A 4: 43,543,905 R1198L probably benign Het
Tmco4 A G 4: 139,020,867 M253V probably damaging Het
Usp19 G T 9: 108,497,920 V782F possibly damaging Het
Usp33 T A 3: 152,374,623 S464T probably damaging Het
Usp47 A T 7: 112,074,721 Y397F probably damaging Het
Vmn1r12 A G 6: 57,159,481 T144A probably benign Het
Vmn2r90 A T 17: 17,734,124 H850L probably benign Het
Wdr66 C T 5: 123,287,177 T294M probably damaging Het
Zfhx3 A T 8: 108,956,210 Q3427L unknown Het
Zfp236 G T 18: 82,682,156 Q63K probably benign Het
Zfp7 T A 15: 76,890,854 C365* probably null Het
Zfp786 T C 6: 47,819,685 E773G probably damaging Het
Other mutations in A430105I19Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00469:A430105I19Rik APN 2 118759689 missense possibly damaging 0.94
IGL03327:A430105I19Rik APN 2 118761670 missense probably damaging 1.00
R1269:A430105I19Rik UTSW 2 118761390 missense possibly damaging 0.65
R1453:A430105I19Rik UTSW 2 118757422 missense possibly damaging 0.91
R1495:A430105I19Rik UTSW 2 118760532 missense probably damaging 1.00
R1529:A430105I19Rik UTSW 2 118761760 critical splice acceptor site probably null
R1765:A430105I19Rik UTSW 2 118760647 missense probably benign 0.02
R4766:A430105I19Rik UTSW 2 118759577 missense probably damaging 1.00
R5891:A430105I19Rik UTSW 2 118761383 missense probably damaging 1.00
R5895:A430105I19Rik UTSW 2 118759617 missense probably benign 0.02
R7271:A430105I19Rik UTSW 2 118760683 critical splice acceptor site probably null
Predicted Primers PCR Primer
(F):5'- TGTGGTCCCAAGAAAGAGGC -3'
(R):5'- AGGAGCTCCATTCAAATCTTCTC -3'

Sequencing Primer
(F):5'- TGGGACCAGGGTCTGAC -3'
(R):5'- GAGCTCCATTCAAATCTTCTCTCTAC -3'
Posted On2016-09-01