Incidental Mutation 'R5081:AI593442'
ID 387126
Institutional Source Beutler Lab
Gene Symbol AI593442
Ensembl Gene ENSMUSG00000078307
Gene Name expressed sequence AI593442
Synonyms
MMRRC Submission 042670-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.147) question?
Stock # R5081 (G1)
Quality Score 133
Status Not validated
Chromosome 9
Chromosomal Location 52584342-52591080 bp(-) (GRCm39)
Type of Mutation small deletion (1 aa in frame mutation)
DNA Base Change (assembly) TGAGGAGGAGGAGGAGGA to TGAGGAGGAGGAGGA at 52589114 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000149532 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000098768] [ENSMUST00000213843] [ENSMUST00000213937]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000098768
SMART Domains Protein: ENSMUSP00000096365
Gene: ENSMUSG00000078307

DomainStartEndE-ValueType
low complexity region 23 43 N/A INTRINSIC
transmembrane domain 61 83 N/A INTRINSIC
low complexity region 85 95 N/A INTRINSIC
low complexity region 156 181 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000213681
Predicted Effect probably benign
Transcript: ENSMUST00000213843
Predicted Effect probably benign
Transcript: ENSMUST00000213937
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.4%
  • 10x: 96.5%
  • 20x: 93.2%
Validation Efficiency 93% (65/70)
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Agbl5 G A 5: 31,060,403 (GRCm39) R141Q probably damaging Het
Aig1 A G 10: 13,677,644 (GRCm39) I116T probably benign Het
Alox12 A T 11: 70,146,140 (GRCm39) probably null Het
Ap3s1 T A 18: 46,887,497 (GRCm39) D43E probably benign Het
Arhgap35 A G 7: 16,299,059 (GRCm39) M2T possibly damaging Het
Asah2 T A 19: 31,991,708 (GRCm39) E451V probably benign Het
Ash1l T G 3: 88,892,024 (GRCm39) I1301S probably damaging Het
Ass1 G A 2: 31,378,665 (GRCm39) probably null Het
Ccpg1 A G 9: 72,906,360 (GRCm39) T39A possibly damaging Het
Cd101 T A 3: 100,911,021 (GRCm39) Y879F possibly damaging Het
Cdc23 C A 18: 34,784,742 (GRCm39) V7L unknown Het
Cdh23 T C 10: 60,272,586 (GRCm39) T530A possibly damaging Het
Cep68 G T 11: 20,188,477 (GRCm39) Q643K probably damaging Het
Ces1c A G 8: 93,854,197 (GRCm39) S113P probably damaging Het
Cnga4 T C 7: 105,056,232 (GRCm39) I278T probably benign Het
Col1a1 A G 11: 94,842,402 (GRCm39) D1440G unknown Het
Cspp1 A G 1: 10,117,691 (GRCm39) I48V possibly damaging Het
Ctsj T A 13: 61,151,664 (GRCm39) S85C possibly damaging Het
Cyp39a1 C A 17: 44,057,488 (GRCm39) D442E probably damaging Het
Dock3 A T 9: 106,868,292 (GRCm39) F664Y probably damaging Het
Gpcpd1 A T 2: 132,389,622 (GRCm39) H244Q probably benign Het
Gtf3a T A 5: 146,888,092 (GRCm39) V131E probably benign Het
Gtpbp3 A T 8: 71,943,026 (GRCm39) R147W probably damaging Het
H2-Oa A T 17: 34,313,344 (GRCm39) I132F probably damaging Het
Hsd17b8 G A 17: 34,246,552 (GRCm39) probably benign Het
Idi1 T A 13: 8,937,963 (GRCm39) C91* probably null Het
Itga11 A G 9: 62,662,478 (GRCm39) I484V probably benign Het
Kpna3 C T 14: 61,628,694 (GRCm39) S101N probably damaging Het
Larp4 G A 15: 99,870,898 (GRCm39) probably benign Het
Mink1 T C 11: 70,495,970 (GRCm39) L390P probably damaging Het
Morc1 T G 16: 48,322,715 (GRCm39) S337R probably benign Het
Myo10 A G 15: 25,786,026 (GRCm39) R1236G probably damaging Het
Nkx3-1 T C 14: 69,429,396 (GRCm39) I138T possibly damaging Het
Nnt T C 13: 119,502,936 (GRCm39) N489S probably damaging Het
Nrcam A T 12: 44,617,136 (GRCm39) I711F probably benign Het
Ntrk3 A G 7: 78,227,522 (GRCm39) S4P probably damaging Het
Obsl1 T C 1: 75,464,607 (GRCm39) T1605A possibly damaging Het
Or1j17 A G 2: 36,578,655 (GRCm39) I214V possibly damaging Het
Or7g32 A G 9: 19,408,557 (GRCm39) E171G probably benign Het
Pank1 T C 19: 34,856,316 (GRCm39) H54R probably benign Het
Pgm2l1 A G 7: 99,917,472 (GRCm39) I530V probably benign Het
Psmd2 A G 16: 20,480,405 (GRCm39) T709A probably benign Het
Qsox1 G T 1: 155,688,581 (GRCm39) probably benign Het
Rbm14 A G 19: 4,852,823 (GRCm39) S520P probably benign Het
Rbm15b G A 9: 106,762,120 (GRCm39) R683C probably benign Het
Rhbdd2 T A 5: 135,664,876 (GRCm39) V69D probably damaging Het
Sart1 T C 19: 5,438,576 (GRCm39) E27G possibly damaging Het
Scn4a G A 11: 106,239,553 (GRCm39) P153L probably damaging Het
Serpinb6d A T 13: 33,855,230 (GRCm39) R301S probably benign Het
Sf3a2 C A 10: 80,640,275 (GRCm39) probably benign Het
Syne1 T C 10: 4,997,767 (GRCm39) D400G probably benign Het
Tenm2 T C 11: 35,915,460 (GRCm39) S2025G possibly damaging Het
Ttc16 A T 2: 32,657,988 (GRCm39) D476E probably damaging Het
Ttc9c A T 19: 8,793,396 (GRCm39) C81* probably null Het
Ulk2 G A 11: 61,694,488 (GRCm39) P474L probably damaging Het
Vmn1r66 A G 7: 10,008,722 (GRCm39) C104R probably damaging Het
Vwa2 C T 19: 56,897,752 (GRCm39) H686Y probably damaging Het
Other mutations in AI593442
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02703:AI593442 APN 9 52,589,418 (GRCm39) missense probably damaging 1.00
R1370:AI593442 UTSW 9 52,589,308 (GRCm39) missense probably damaging 1.00
R1977:AI593442 UTSW 9 52,589,492 (GRCm39) missense probably damaging 0.99
R2118:AI593442 UTSW 9 52,588,993 (GRCm39) missense probably benign 0.00
R2248:AI593442 UTSW 9 52,589,114 (GRCm39) small deletion probably benign
R4154:AI593442 UTSW 9 52,589,204 (GRCm39) missense probably benign
X0002:AI593442 UTSW 9 52,589,114 (GRCm39) small deletion probably benign
Z1176:AI593442 UTSW 9 52,589,245 (GRCm39) missense probably damaging 1.00
Z1177:AI593442 UTSW 9 52,589,212 (GRCm39) missense possibly damaging 0.58
Predicted Primers PCR Primer
(F):5'- ACGGTCAAGATGCTGGAGAC -3'
(R):5'- TCCACAAGCGTAGGATGAAG -3'

Sequencing Primer
(F):5'- CTGGAGACGAGGAAAGGGTC -3'
(R):5'- CGGAAGATGCAGAGGGCTC -3'
Posted On 2016-06-06