Incidental Mutation 'R4885:Atosa'
ID 375644
Institutional Source Beutler Lab
Gene Symbol Atosa
Ensembl Gene ENSMUSG00000034858
Gene Name atos homolog A
Synonyms C130047D21Rik, Fam214a, 6330415I01Rik, BC031353
MMRRC Submission 042851-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.451) question?
Stock # R4885 (G1)
Quality Score 225
Status Validated
Chromosome 9
Chromosomal Location 74860166-74939750 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 74913649 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Proline at position 94 (L94P)
Ref Sequence ENSEMBL: ENSMUSP00000149021 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000081746] [ENSMUST00000170846] [ENSMUST00000214755] [ENSMUST00000215370]
AlphaFold Q69ZK7
Predicted Effect probably damaging
Transcript: ENSMUST00000081746
AA Change: L101P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000080442
Gene: ENSMUSG00000034858
AA Change: L101P

DomainStartEndE-ValueType
low complexity region 349 360 N/A INTRINSIC
internal_repeat_1 361 458 7.22e-14 PROSPERO
internal_repeat_1 473 570 7.22e-14 PROSPERO
low complexity region 840 859 N/A INTRINSIC
DUF4210 885 943 8.5e-29 SMART
Pfam:Chromosome_seg 1024 1081 3.5e-22 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000170846
AA Change: L94P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000129319
Gene: ENSMUSG00000034858
AA Change: L94P

DomainStartEndE-ValueType
low complexity region 342 353 N/A INTRINSIC
internal_repeat_1 354 451 8.38e-14 PROSPERO
internal_repeat_1 466 563 8.38e-14 PROSPERO
low complexity region 833 852 N/A INTRINSIC
DUF4210 878 936 8.5e-29 SMART
Pfam:Chromosome_seg 1016 1074 1.8e-22 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000214755
AA Change: L94P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000215370
AA Change: L94P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Meta Mutation Damage Score 0.9356 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.7%
  • 20x: 93.6%
Validation Efficiency 99% (77/78)
Allele List at MGI
Other mutations in this stock
Total: 72 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcf3 A G 16: 20,370,425 (GRCm39) T317A probably benign Het
Adck1 G A 12: 88,407,865 (GRCm39) A199T probably benign Het
Adgrb1 A T 15: 74,444,011 (GRCm39) M1038L probably benign Het
Anapc10 C T 8: 80,455,779 (GRCm39) T76I probably benign Het
Bptf C T 11: 106,965,474 (GRCm39) S1177N probably benign Het
Bsn A T 9: 107,984,726 (GRCm39) Y337* probably null Het
Ccl20 T A 1: 83,095,580 (GRCm39) V48E possibly damaging Het
Ccnl1 C T 3: 65,864,320 (GRCm39) D122N probably damaging Het
Chat C G 14: 32,176,567 (GRCm39) G69A probably damaging Het
Cr2 T A 1: 194,841,039 (GRCm39) I418F possibly damaging Het
Dmxl1 G C 18: 50,011,862 (GRCm39) A1340P probably damaging Het
Eef2k G A 7: 120,491,155 (GRCm39) R547Q probably benign Het
Eml2 G A 7: 18,937,935 (GRCm39) S793N probably benign Het
Enox1 T A 14: 77,958,290 (GRCm39) L632Q probably damaging Het
Fabp9 T C 3: 10,259,738 (GRCm39) K92E probably damaging Het
Fam234a T C 17: 26,432,559 (GRCm39) H530R probably benign Het
Fancm C T 12: 65,149,417 (GRCm39) Q728* probably null Het
Fgd3 G A 13: 49,417,465 (GRCm39) T666M possibly damaging Het
Foxs1 T C 2: 152,774,301 (GRCm39) M251V probably benign Het
Fsip2 A T 2: 82,818,438 (GRCm39) M4724L probably benign Het
Gemin6 G A 17: 80,535,327 (GRCm39) E96K probably damaging Het
Gfi1 C A 5: 107,871,152 (GRCm39) V80F probably damaging Het
H3c13 G T 3: 96,176,277 (GRCm39) V90F possibly damaging Het
Hectd1 A G 12: 51,847,505 (GRCm39) V442A probably damaging Het
Ift80 A G 3: 68,857,829 (GRCm39) I272T probably damaging Het
Impact C G 18: 13,119,430 (GRCm39) A214G probably damaging Het
Insl6 C T 19: 29,302,556 (GRCm39) E54K probably benign Het
Irak3 T A 10: 120,018,586 (GRCm39) D54V probably damaging Het
Itk C T 11: 46,227,171 (GRCm39) probably null Het
Ivl A T 3: 92,479,718 (GRCm39) C116S probably benign Het
Kcnq4 G A 4: 120,570,260 (GRCm39) A361V probably benign Het
L1td1 C T 4: 98,625,548 (GRCm39) P581L probably benign Het
Lrp1b T C 2: 41,358,905 (GRCm39) E656G probably benign Het
Macrod2 A G 2: 140,261,985 (GRCm39) T89A possibly damaging Het
Mettl13 T C 1: 162,364,837 (GRCm39) D514G probably damaging Het
Mfsd13b A T 7: 120,590,711 (GRCm39) I151F possibly damaging Het
Mical3 G A 6: 120,912,214 (GRCm39) P1882S probably damaging Het
Mycbp2 T C 14: 103,383,382 (GRCm39) E394G possibly damaging Het
Myo16 T A 8: 10,488,892 (GRCm39) S688T probably damaging Het
Neb T C 2: 52,176,058 (GRCm39) Y1467C probably damaging Het
Nhsl3 C T 4: 129,118,238 (GRCm39) R214Q probably damaging Het
Nkx6-3 C A 8: 23,643,914 (GRCm39) P105Q possibly damaging Het
Nlrp1b T C 11: 71,108,710 (GRCm39) T264A possibly damaging Het
Nnat G A 2: 157,403,678 (GRCm39) C122Y probably damaging Het
Notch3 G A 17: 32,360,351 (GRCm39) R1527C probably damaging Het
Or2y16 C T 11: 49,335,449 (GRCm39) T257I probably damaging Het
Or5an1c T G 19: 12,218,082 (GRCm39) probably null Het
Or5h18 A G 16: 58,847,518 (GRCm39) Y251H probably damaging Het
Pds5b C T 5: 150,639,927 (GRCm39) T14I probably benign Het
Phf19 A T 2: 34,789,718 (GRCm39) I334N probably damaging Het
Pik3ap1 T C 19: 41,364,365 (GRCm39) D118G probably benign Het
Pkhd1 T A 1: 20,140,712 (GRCm39) E3886V possibly damaging Het
Pkp1 A G 1: 135,846,690 (GRCm39) S21P possibly damaging Het
Pramel32 T A 4: 88,546,219 (GRCm39) L374F possibly damaging Het
Rack1 C A 11: 48,696,463 (GRCm39) A290E probably damaging Het
Rbm15 A G 3: 107,239,570 (GRCm39) V276A probably benign Het
Rnf216 A T 5: 143,076,335 (GRCm39) L183* probably null Het
Sc5d T C 9: 42,166,922 (GRCm39) I206V probably benign Het
Scpep1 A G 11: 88,826,737 (GRCm39) I233T probably benign Het
Sh3pxd2a A G 19: 47,257,132 (GRCm39) Y529H probably damaging Het
Slc1a4 A C 11: 20,254,384 (GRCm39) V494G probably damaging Het
Slc38a7 T C 8: 96,575,230 (GRCm39) T17A probably benign Het
Smg6 T C 11: 74,932,744 (GRCm39) S73P probably damaging Het
Stk32b T C 5: 37,624,141 (GRCm39) Y202C probably damaging Het
Tas2r140 A G 6: 40,468,334 (GRCm39) S55G probably damaging Het
Tcf12 C T 9: 71,766,122 (GRCm39) G504S probably null Het
Ttc3 G C 16: 94,227,690 (GRCm39) probably null Het
Ttc3 T C 16: 94,220,324 (GRCm39) I568T probably damaging Het
Ttc41 T G 10: 86,594,966 (GRCm39) N913K possibly damaging Het
Vrk1 G A 12: 106,024,231 (GRCm39) V236M probably damaging Het
Wscd1 C T 11: 71,650,972 (GRCm39) R100C probably damaging Het
Zc3h18 C T 8: 123,128,445 (GRCm39) probably benign Het
Other mutations in Atosa
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00333:Atosa APN 9 74,933,072 (GRCm39) missense probably benign 0.28
IGL00588:Atosa APN 9 74,916,863 (GRCm39) missense probably damaging 1.00
IGL01887:Atosa APN 9 74,924,339 (GRCm39) missense probably benign 0.39
IGL02828:Atosa APN 9 74,913,714 (GRCm39) missense probably damaging 1.00
IGL03060:Atosa APN 9 74,917,450 (GRCm39) missense probably damaging 0.96
IGL03277:Atosa APN 9 74,916,514 (GRCm39) missense probably damaging 1.00
R0052:Atosa UTSW 9 74,926,265 (GRCm39) splice site probably benign
R0052:Atosa UTSW 9 74,926,265 (GRCm39) splice site probably benign
R0615:Atosa UTSW 9 74,911,570 (GRCm39) missense probably damaging 1.00
R0723:Atosa UTSW 9 74,916,733 (GRCm39) missense probably damaging 1.00
R1428:Atosa UTSW 9 74,913,603 (GRCm39) missense probably benign 0.07
R1448:Atosa UTSW 9 74,917,456 (GRCm39) nonsense probably null
R1656:Atosa UTSW 9 74,916,241 (GRCm39) missense probably benign 0.00
R2024:Atosa UTSW 9 74,917,672 (GRCm39) missense probably damaging 0.98
R3147:Atosa UTSW 9 74,916,120 (GRCm39) missense probably benign 0.25
R3745:Atosa UTSW 9 74,917,144 (GRCm39) missense probably benign 0.00
R4105:Atosa UTSW 9 74,916,058 (GRCm39) missense probably damaging 1.00
R4224:Atosa UTSW 9 74,916,008 (GRCm39) missense probably damaging 1.00
R4496:Atosa UTSW 9 74,938,813 (GRCm39) missense probably damaging 0.99
R4519:Atosa UTSW 9 74,930,929 (GRCm39) missense probably damaging 1.00
R4715:Atosa UTSW 9 74,920,250 (GRCm39) missense probably damaging 1.00
R5009:Atosa UTSW 9 74,916,171 (GRCm39) missense probably damaging 0.98
R5574:Atosa UTSW 9 74,917,672 (GRCm39) missense probably damaging 1.00
R5645:Atosa UTSW 9 74,932,961 (GRCm39) missense probably damaging 1.00
R5696:Atosa UTSW 9 74,917,399 (GRCm39) missense probably benign 0.01
R5891:Atosa UTSW 9 74,911,668 (GRCm39) missense probably damaging 1.00
R5936:Atosa UTSW 9 74,916,586 (GRCm39) missense probably benign 0.00
R6165:Atosa UTSW 9 74,932,954 (GRCm39) missense probably damaging 0.96
R6228:Atosa UTSW 9 74,913,645 (GRCm39) missense possibly damaging 0.94
R6419:Atosa UTSW 9 74,916,619 (GRCm39) missense probably benign 0.20
R6499:Atosa UTSW 9 74,930,930 (GRCm39) missense probably damaging 1.00
R6631:Atosa UTSW 9 74,861,107 (GRCm39) missense possibly damaging 0.71
R6649:Atosa UTSW 9 74,917,432 (GRCm39) missense probably damaging 0.96
R6849:Atosa UTSW 9 74,916,594 (GRCm39) missense probably damaging 0.96
R7189:Atosa UTSW 9 74,911,633 (GRCm39) missense probably damaging 0.99
R7402:Atosa UTSW 9 74,913,668 (GRCm39) nonsense probably null
R8691:Atosa UTSW 9 74,917,335 (GRCm39) missense probably benign 0.09
R8769:Atosa UTSW 9 74,933,107 (GRCm39) missense probably damaging 1.00
R8944:Atosa UTSW 9 74,911,562 (GRCm39) missense probably damaging 1.00
R9323:Atosa UTSW 9 74,883,415 (GRCm39) intron probably benign
R9621:Atosa UTSW 9 74,917,512 (GRCm39) missense possibly damaging 0.62
R9649:Atosa UTSW 9 74,924,349 (GRCm39) missense possibly damaging 0.74
Predicted Primers PCR Primer
(F):5'- CAAGTGCTACTGCGTATGCTG -3'
(R):5'- GTTCAGAGACATGATGCAGTGG -3'

Sequencing Primer
(F):5'- GTGTTCCTTGTGCAGATATCTAC -3'
(R):5'- CAGTGGCAGGGTAAGGTGTAG -3'
Posted On 2016-03-17