Incidental Mutation 'R1681:Atm'
ID 188521
Institutional Source Beutler Lab
Gene Symbol Atm
Ensembl Gene ENSMUSG00000034218
Gene Name ataxia telangiectasia mutated
Synonyms C030026E19Rik
MMRRC Submission 039717-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.928) question?
Stock # R1681 (G1)
Quality Score 225
Status Not validated
Chromosome 9
Chromosomal Location 53439149-53536740 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to C at 53522155 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Serine at position 265 (I265S)
Ref Sequence ENSEMBL: ENSMUSP00000156344 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000118282] [ENSMUST00000232179]
AlphaFold no structure available at present
Predicted Effect possibly damaging
Transcript: ENSMUST00000118282
AA Change: I265S

PolyPhen 2 Score 0.938 (Sensitivity: 0.80; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000113388
Gene: ENSMUSG00000034218
AA Change: I265S

DomainStartEndE-ValueType
TAN 1 166 5.07e-68 SMART
low complexity region 431 445 N/A INTRINSIC
low complexity region 830 846 N/A INTRINSIC
low complexity region 929 940 N/A INTRINSIC
SCOP:d1gw5a_ 1039 1568 2e-4 SMART
coiled coil region 1615 1644 N/A INTRINSIC
low complexity region 1650 1662 N/A INTRINSIC
Pfam:FAT 2102 2499 4.4e-50 PFAM
low complexity region 2587 2599 N/A INTRINSIC
PI3Kc 2723 3026 1.11e-117 SMART
FATC 3034 3066 3.71e-11 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000132403
Predicted Effect possibly damaging
Transcript: ENSMUST00000232179
AA Change: I265S

PolyPhen 2 Score 0.938 (Sensitivity: 0.80; Specificity: 0.94)
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.6%
  • 20x: 93.6%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to the PI3/PI4-kinase family. This protein is an important cell cycle checkpoint kinase that phosphorylates; thus, it functions as a regulator of a wide variety of downstream proteins, including tumor suppressor proteins p53 and BRCA1, checkpoint kinase CHK2, checkpoint proteins RAD17 and RAD9, and DNA repair protein NBS1. This protein and the closely related kinase ATR are thought to be master controllers of cell cycle checkpoint signaling pathways that are required for cell response to DNA damage and for genome stability. Mutations in this gene are associated with ataxia telangiectasia, an autosomal recessive disorder. [provided by RefSeq, Aug 2010]
PHENOTYPE: Homozygotes for null mutations may exhibit locomotor abnormalities, motor learning deficits, growth retardation, sterility due to meiotic arrest, and susceptibility to thymic lymphomas. Mice homozygous for a kinase dead allele exhibit early embryonic lethality associated with genetic instability. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 87 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acaca T A 11: 84,226,185 I247N probably damaging Het
Ankle1 G T 8: 71,407,618 S260I probably benign Het
Aoc2 T C 11: 101,325,192 S34P probably benign Het
Ap1m1 A C 8: 72,256,122 I397L possibly damaging Het
Apba1 C A 19: 23,936,561 D649E probably damaging Het
Aptx C T 4: 40,697,274 V25M probably benign Het
Arhgef18 G A 8: 3,439,645 G326R probably damaging Het
B3galt4 A T 17: 33,951,213 V17E probably benign Het
Bcl7a T A 5: 123,356,023 M86K possibly damaging Het
Cela3a T A 4: 137,402,684 probably null Het
Cep85 T A 4: 134,148,728 K456* probably null Het
Ces1f C A 8: 93,275,414 A29S probably benign Het
Chd9 A T 8: 90,973,135 I598F probably damaging Het
Cntln T C 4: 84,947,635 L176S probably damaging Het
Cntn3 A T 6: 102,170,668 N909K probably damaging Het
Cntnap5b T C 1: 100,076,107 S271P probably damaging Het
Col6a3 T A 1: 90,773,502 H2564L unknown Het
Cyp2b19 C A 7: 26,763,340 probably null Het
Dapk1 G T 13: 60,718,464 probably null Het
Dnah7b T A 1: 46,324,712 Y3497* probably null Het
Duoxa2 T C 2: 122,299,162 probably null Het
Eny2 T C 15: 44,432,478 W42R probably damaging Het
Epha3 A G 16: 63,595,728 V635A probably damaging Het
Fam167b G C 4: 129,578,276 Q34E probably benign Het
Fam26f A G 10: 34,127,900 F4L probably benign Het
Fancm T C 12: 65,105,656 M962T probably benign Het
Gimap8 T A 6: 48,656,411 I388N probably benign Het
Gpaa1 A G 15: 76,331,453 T22A probably benign Het
Hoxc11 T C 15: 102,955,156 S211P possibly damaging Het
Hsd17b12 T C 2: 94,033,561 N312S unknown Het
Idh2 T G 7: 80,099,158 E125A probably damaging Het
Igdcc4 A G 9: 65,128,795 Y712C probably damaging Het
Kank1 T C 19: 25,410,304 V447A possibly damaging Het
Kif1b T A 4: 149,195,501 probably null Het
Klc4 A T 17: 46,636,770 D335E probably damaging Het
Klhl33 T A 14: 50,893,077 D320V probably benign Het
Krt73 A T 15: 101,802,047 M84K possibly damaging Het
Kti12 T A 4: 108,848,858 I323N probably damaging Het
Kynu T C 2: 43,679,825 L373P probably damaging Het
Lats1 T C 10: 7,705,914 M821T probably damaging Het
Lnx1 A T 5: 74,685,410 H126Q probably benign Het
Lonrf2 G A 1: 38,813,276 P165S probably benign Het
Lrrc4b T A 7: 44,461,177 Y158N probably damaging Het
Lrrc74b C A 16: 17,559,753 R87L probably damaging Het
Meig1 T C 2: 3,409,274 D63G probably damaging Het
Mrpl38 G A 11: 116,138,429 probably benign Het
Naip2 C T 13: 100,161,860 G556D probably benign Het
Naip2 T C 13: 100,161,854 E558G probably benign Het
Nlrp1a T A 11: 71,142,358 E3D unknown Het
Nphs2 T A 1: 156,320,898 D110E probably damaging Het
Nxn T A 11: 76,272,464 K244N probably benign Het
Oas3 A T 5: 120,769,908 F322L probably benign Het
Obscn T A 11: 59,103,325 Y1577F probably damaging Het
Olfr1122 G A 2: 87,388,620 R305K possibly damaging Het
Olfr911-ps1 T A 9: 38,524,117 N128K probably benign Het
Olfr914 G A 9: 38,606,948 G161D probably damaging Het
Olfr917 A G 9: 38,665,320 Y175H probably benign Het
Olfr924 T C 9: 38,848,513 M133T probably damaging Het
Panx1 T C 9: 15,007,783 D260G probably benign Het
Pcdhb15 T C 18: 37,473,813 Y33H probably damaging Het
Pik3ap1 C A 19: 41,308,529 V461F probably damaging Het
Plpp3 G A 4: 105,208,805 probably null Het
Prtn3 A T 10: 79,880,541 T61S probably benign Het
Psen1 T A 12: 83,724,620 Y225N probably damaging Het
Rab44 T A 17: 29,140,124 S429T possibly damaging Het
Ralgapa1 T C 12: 55,762,603 I462M probably benign Het
Rbfox3 T C 11: 118,505,669 N105S probably damaging Het
Rbm7 A C 9: 48,489,721 Y236D possibly damaging Het
Samhd1 T C 2: 157,101,732 T621A probably benign Het
Samt3 C A X: 86,046,650 D49E probably benign Het
Sass6 T C 3: 116,603,473 V26A possibly damaging Het
Scn11a C T 9: 119,804,412 M418I possibly damaging Het
Scrib T C 15: 76,064,567 E480G probably damaging Het
Sec24a T G 11: 51,695,189 T1071P probably damaging Het
Siglecg A C 7: 43,408,941 E84A probably benign Het
Slc6a17 C T 3: 107,474,386 V419I probably damaging Het
Soga1 T C 2: 157,030,530 T966A possibly damaging Het
Ssr2 T C 3: 88,581,042 M75T possibly damaging Het
Tbc1d22b A G 17: 29,575,177 T275A possibly damaging Het
Tbx15 T A 3: 99,351,824 probably null Het
Tll1 A C 8: 64,085,551 L353R possibly damaging Het
Tlr4 C T 4: 66,841,105 P712S probably damaging Het
Tmem145 T A 7: 25,314,734 F424L possibly damaging Het
Tnrc18 T C 5: 142,773,817 K755E unknown Het
Trmt44 A G 5: 35,569,977 I298T probably benign Het
Vmn1r69 A G 7: 10,580,252 V184A probably benign Het
Zfp84 T C 7: 29,777,400 C506R probably damaging Het
Other mutations in Atm
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00090:Atm APN 9 53,524,443 (GRCm38) missense probably damaging 1.00
IGL00466:Atm APN 9 53,499,112 (GRCm38) splice site probably benign
IGL00567:Atm APN 9 53,503,116 (GRCm38) nonsense probably null
IGL00702:Atm APN 9 53,511,831 (GRCm38) missense probably benign 0.02
IGL00743:Atm APN 9 53,513,116 (GRCm38) missense probably benign 0.00
IGL00771:Atm APN 9 53,493,054 (GRCm38) missense probably benign 0.01
IGL00773:Atm APN 9 53,522,144 (GRCm38) missense probably benign 0.00
IGL00819:Atm APN 9 53,518,531 (GRCm38) missense probably damaging 1.00
IGL00864:Atm APN 9 53,533,933 (GRCm38) missense probably damaging 0.99
IGL00985:Atm APN 9 53,459,816 (GRCm38) missense probably damaging 0.98
IGL01109:Atm APN 9 53,490,293 (GRCm38) missense probably damaging 1.00
IGL01120:Atm APN 9 53,461,122 (GRCm38) critical splice acceptor site probably null
IGL01369:Atm APN 9 53,515,317 (GRCm38) missense probably benign
IGL01374:Atm APN 9 53,531,724 (GRCm38) missense possibly damaging 0.58
IGL01406:Atm APN 9 53,439,746 (GRCm38) makesense probably null
IGL01409:Atm APN 9 53,499,171 (GRCm38) missense probably benign 0.01
IGL01434:Atm APN 9 53,507,807 (GRCm38) missense probably benign 0.04
IGL01486:Atm APN 9 53,510,213 (GRCm38) missense probably benign
IGL01583:Atm APN 9 53,484,247 (GRCm38) splice site probably benign
IGL01861:Atm APN 9 53,494,612 (GRCm38) missense probably null 0.89
IGL01865:Atm APN 9 53,461,002 (GRCm38) missense probably damaging 1.00
IGL02026:Atm APN 9 53,442,417 (GRCm38) splice site probably null
IGL02072:Atm APN 9 53,459,796 (GRCm38) missense probably benign 0.01
IGL02075:Atm APN 9 53,527,237 (GRCm38) missense probably damaging 1.00
IGL02127:Atm APN 9 53,487,983 (GRCm38) missense probably damaging 1.00
IGL02175:Atm APN 9 53,480,665 (GRCm38) missense probably damaging 0.99
IGL02246:Atm APN 9 53,527,185 (GRCm38) missense probably benign 0.12
IGL02259:Atm APN 9 53,518,494 (GRCm38) splice site probably benign
IGL02351:Atm APN 9 53,522,176 (GRCm38) missense probably benign 0.04
IGL02358:Atm APN 9 53,522,176 (GRCm38) missense probably benign 0.04
IGL02387:Atm APN 9 53,479,766 (GRCm38) splice site probably null
IGL02417:Atm APN 9 53,479,695 (GRCm38) missense probably benign 0.00
IGL02422:Atm APN 9 53,500,792 (GRCm38) missense probably damaging 1.00
IGL02445:Atm APN 9 53,454,330 (GRCm38) missense probably benign 0.00
IGL02492:Atm APN 9 53,455,859 (GRCm38) missense probably damaging 0.99
IGL02513:Atm APN 9 53,497,262 (GRCm38) splice site probably benign
IGL02633:Atm APN 9 53,448,153 (GRCm38) missense probably damaging 1.00
IGL02634:Atm APN 9 53,516,563 (GRCm38) missense probably benign 0.00
IGL02948:Atm APN 9 53,453,440 (GRCm38) splice site probably benign
IGL02959:Atm APN 9 53,471,418 (GRCm38) missense probably damaging 1.00
IGL02965:Atm APN 9 53,453,563 (GRCm38) missense probably damaging 1.00
IGL03085:Atm APN 9 53,484,171 (GRCm38) missense possibly damaging 0.89
antebellum UTSW 9 53,518,559 (GRCm38) nonsense probably null
bull_run UTSW 9 53,487,922 (GRCm38) missense probably benign 0.09
Civil UTSW 9 53,492,268 (GRCm38) missense possibly damaging 0.78
gettysburg UTSW 9 53,455,988 (GRCm38) splice site probably null
Grant UTSW 9 53,511,917 (GRCm38) nonsense probably null
Indicative UTSW 9 53,445,376 (GRCm38) splice site probably null
Marker UTSW 9 53,454,279 (GRCm38) splice site probably benign
maunder UTSW 9 53,499,197 (GRCm38) nonsense probably null
mockingbird UTSW 9 53,516,467 (GRCm38) nonsense probably null
mockingbird2 UTSW 9 53,488,587 (GRCm38) missense probably damaging 1.00
osphere UTSW 9 53,479,673 (GRCm38) missense probably damaging 0.99
shiloh UTSW 9 53,465,298 (GRCm38) missense probably damaging 1.00
Strato UTSW 9 53,503,018 (GRCm38) missense probably damaging 1.00
thrasher UTSW 9 53,445,507 (GRCm38) missense probably benign 0.01
Tropo UTSW 9 53,531,648 (GRCm38) missense probably damaging 1.00
P0019:Atm UTSW 9 53,465,028 (GRCm38) splice site probably benign
PIT4403001:Atm UTSW 9 53,500,982 (GRCm38) missense probably benign
PIT4687001:Atm UTSW 9 53,486,812 (GRCm38) critical splice donor site probably null
R0004:Atm UTSW 9 53,453,528 (GRCm38) splice site probably benign
R0035:Atm UTSW 9 53,513,180 (GRCm38) missense probably benign 0.01
R0098:Atm UTSW 9 53,518,569 (GRCm38) missense probably benign 0.10
R0098:Atm UTSW 9 53,518,569 (GRCm38) missense probably benign 0.10
R0201:Atm UTSW 9 53,454,279 (GRCm38) splice site probably benign
R0304:Atm UTSW 9 53,516,344 (GRCm38) missense probably benign 0.34
R0308:Atm UTSW 9 53,454,473 (GRCm38) splice site probably null
R0362:Atm UTSW 9 53,458,838 (GRCm38) missense possibly damaging 0.90
R0470:Atm UTSW 9 53,460,966 (GRCm38) missense probably damaging 1.00
R0513:Atm UTSW 9 53,503,948 (GRCm38) missense probably benign 0.00
R0589:Atm UTSW 9 53,490,192 (GRCm38) missense possibly damaging 0.51
R0617:Atm UTSW 9 53,458,941 (GRCm38) nonsense probably null
R0630:Atm UTSW 9 53,531,622 (GRCm38) splice site probably benign
R0652:Atm UTSW 9 53,486,014 (GRCm38) missense probably damaging 0.98
R0698:Atm UTSW 9 53,515,239 (GRCm38) missense probably damaging 1.00
R0737:Atm UTSW 9 53,456,566 (GRCm38) missense probably damaging 1.00
R0885:Atm UTSW 9 53,459,823 (GRCm38) missense probably benign
R0947:Atm UTSW 9 53,504,092 (GRCm38) missense probably benign 0.01
R0948:Atm UTSW 9 53,495,958 (GRCm38) missense probably benign
R1144:Atm UTSW 9 53,511,698 (GRCm38) splice site probably benign
R1252:Atm UTSW 9 53,455,840 (GRCm38) missense probably damaging 1.00
R1295:Atm UTSW 9 53,456,530 (GRCm38) missense probably damaging 1.00
R1296:Atm UTSW 9 53,456,530 (GRCm38) missense probably damaging 1.00
R1419:Atm UTSW 9 53,457,489 (GRCm38) missense probably benign 0.00
R1477:Atm UTSW 9 53,464,273 (GRCm38) missense probably benign 0.00
R1596:Atm UTSW 9 53,453,378 (GRCm38) missense probably damaging 1.00
R1630:Atm UTSW 9 53,479,673 (GRCm38) missense probably damaging 0.99
R1667:Atm UTSW 9 53,500,932 (GRCm38) missense probably damaging 1.00
R1703:Atm UTSW 9 53,500,700 (GRCm38) missense probably benign
R1817:Atm UTSW 9 53,492,233 (GRCm38) splice site probably benign
R1840:Atm UTSW 9 53,456,530 (GRCm38) missense probably damaging 1.00
R1848:Atm UTSW 9 53,468,012 (GRCm38) missense probably benign 0.06
R1906:Atm UTSW 9 53,506,568 (GRCm38) missense probably damaging 1.00
R1958:Atm UTSW 9 53,471,418 (GRCm38) missense probably damaging 1.00
R2108:Atm UTSW 9 53,443,997 (GRCm38) missense probably damaging 1.00
R2116:Atm UTSW 9 53,500,969 (GRCm38) missense probably benign 0.36
R2134:Atm UTSW 9 53,467,964 (GRCm38) critical splice donor site probably null
R2137:Atm UTSW 9 53,453,375 (GRCm38) missense probably damaging 1.00
R2291:Atm UTSW 9 53,490,909 (GRCm38) splice site probably null
R2348:Atm UTSW 9 53,492,268 (GRCm38) missense possibly damaging 0.78
R2483:Atm UTSW 9 53,510,266 (GRCm38) missense probably damaging 1.00
R2567:Atm UTSW 9 53,457,470 (GRCm38) missense possibly damaging 0.72
R2897:Atm UTSW 9 53,507,805 (GRCm38) missense probably damaging 0.99
R2939:Atm UTSW 9 53,494,711 (GRCm38) missense probably damaging 1.00
R3008:Atm UTSW 9 53,480,750 (GRCm38) missense probably benign 0.00
R3236:Atm UTSW 9 53,479,748 (GRCm38) missense probably benign 0.15
R3847:Atm UTSW 9 53,503,075 (GRCm38) missense possibly damaging 0.94
R3889:Atm UTSW 9 53,506,636 (GRCm38) splice site probably benign
R3919:Atm UTSW 9 53,492,278 (GRCm38) missense probably benign 0.00
R4125:Atm UTSW 9 53,450,621 (GRCm38) missense probably damaging 1.00
R4222:Atm UTSW 9 53,480,669 (GRCm38) missense probably benign
R4395:Atm UTSW 9 53,465,227 (GRCm38) missense probably benign 0.09
R4466:Atm UTSW 9 53,448,169 (GRCm38) nonsense probably null
R4502:Atm UTSW 9 53,495,946 (GRCm38) missense possibly damaging 0.92
R4514:Atm UTSW 9 53,493,039 (GRCm38) missense probably damaging 0.99
R4528:Atm UTSW 9 53,500,759 (GRCm38) missense probably benign 0.39
R4593:Atm UTSW 9 53,453,594 (GRCm38) missense possibly damaging 0.55
R4627:Atm UTSW 9 53,456,506 (GRCm38) missense possibly damaging 0.79
R4634:Atm UTSW 9 53,531,733 (GRCm38) missense probably benign 0.01
R4665:Atm UTSW 9 53,464,229 (GRCm38) missense probably benign 0.00
R4672:Atm UTSW 9 53,522,201 (GRCm38) missense probably damaging 0.99
R4741:Atm UTSW 9 53,453,607 (GRCm38) missense probably benign 0.10
R4808:Atm UTSW 9 53,445,495 (GRCm38) missense probably damaging 0.99
R4959:Atm UTSW 9 53,515,301 (GRCm38) missense probably benign
R4996:Atm UTSW 9 53,524,507 (GRCm38) missense probably benign 0.09
R5030:Atm UTSW 9 53,520,109 (GRCm38) nonsense probably null
R5214:Atm UTSW 9 53,491,027 (GRCm38) missense probably benign 0.09
R5260:Atm UTSW 9 53,506,611 (GRCm38) missense probably damaging 0.99
R5311:Atm UTSW 9 53,518,623 (GRCm38) missense probably benign 0.00
R5394:Atm UTSW 9 53,507,777 (GRCm38) critical splice donor site probably null
R5400:Atm UTSW 9 53,503,018 (GRCm38) missense probably damaging 1.00
R5436:Atm UTSW 9 53,459,804 (GRCm38) missense probably benign 0.00
R5441:Atm UTSW 9 53,516,467 (GRCm38) nonsense probably null
R5569:Atm UTSW 9 53,516,450 (GRCm38) nonsense probably null
R5856:Atm UTSW 9 53,495,955 (GRCm38) missense possibly damaging 0.64
R5891:Atm UTSW 9 53,497,159 (GRCm38) missense probably benign
R5910:Atm UTSW 9 53,448,080 (GRCm38) missense probably damaging 0.96
R6054:Atm UTSW 9 53,459,873 (GRCm38) missense probably damaging 1.00
R6062:Atm UTSW 9 53,488,587 (GRCm38) missense probably damaging 1.00
R6092:Atm UTSW 9 53,524,414 (GRCm38) missense probably damaging 1.00
R6127:Atm UTSW 9 53,524,509 (GRCm38) missense probably damaging 1.00
R6160:Atm UTSW 9 53,490,959 (GRCm38) missense probably benign 0.04
R6267:Atm UTSW 9 53,444,000 (GRCm38) missense probably damaging 1.00
R6273:Atm UTSW 9 53,487,922 (GRCm38) missense probably benign 0.09
R6284:Atm UTSW 9 53,445,376 (GRCm38) splice site probably null
R6478:Atm UTSW 9 53,490,254 (GRCm38) missense probably damaging 1.00
R6547:Atm UTSW 9 53,440,157 (GRCm38) missense probably damaging 1.00
R6549:Atm UTSW 9 53,493,177 (GRCm38) missense probably benign 0.00
R6704:Atm UTSW 9 53,458,853 (GRCm38) missense probably benign 0.02
R6715:Atm UTSW 9 53,531,648 (GRCm38) missense probably damaging 1.00
R6737:Atm UTSW 9 53,486,051 (GRCm38) missense probably benign 0.30
R6759:Atm UTSW 9 53,518,559 (GRCm38) nonsense probably null
R6766:Atm UTSW 9 53,490,282 (GRCm38) missense probably damaging 0.99
R6813:Atm UTSW 9 53,497,235 (GRCm38) missense probably benign 0.00
R6852:Atm UTSW 9 53,482,430 (GRCm38) missense possibly damaging 0.93
R7064:Atm UTSW 9 53,507,881 (GRCm38) missense probably benign 0.02
R7208:Atm UTSW 9 53,512,008 (GRCm38) splice site probably null
R7211:Atm UTSW 9 53,488,560 (GRCm38) missense probably benign 0.01
R7220:Atm UTSW 9 53,511,917 (GRCm38) nonsense probably null
R7336:Atm UTSW 9 53,462,503 (GRCm38) missense possibly damaging 0.47
R7363:Atm UTSW 9 53,465,298 (GRCm38) missense probably damaging 1.00
R7378:Atm UTSW 9 53,453,437 (GRCm38) critical splice acceptor site probably null
R7472:Atm UTSW 9 53,448,125 (GRCm38) missense possibly damaging 0.81
R7487:Atm UTSW 9 53,524,354 (GRCm38) missense probably benign
R7497:Atm UTSW 9 53,511,891 (GRCm38) missense probably benign 0.00
R7584:Atm UTSW 9 53,513,127 (GRCm38) missense probably damaging 0.99
R7624:Atm UTSW 9 53,454,768 (GRCm38) missense probably damaging 0.99
R7653:Atm UTSW 9 53,490,302 (GRCm38) nonsense probably null
R7660:Atm UTSW 9 53,445,507 (GRCm38) missense probably benign 0.01
R7679:Atm UTSW 9 53,442,497 (GRCm38) missense probably damaging 1.00
R7720:Atm UTSW 9 53,522,239 (GRCm38) missense possibly damaging 0.54
R8221:Atm UTSW 9 53,455,988 (GRCm38) splice site probably null
R8247:Atm UTSW 9 53,450,570 (GRCm38) missense
R8334:Atm UTSW 9 53,522,273 (GRCm38) missense probably benign 0.00
R8503:Atm UTSW 9 53,488,052 (GRCm38) missense probably damaging 0.99
R8552:Atm UTSW 9 53,524,497 (GRCm38) missense probably damaging 1.00
R8749:Atm UTSW 9 53,499,197 (GRCm38) nonsense probably null
R8838:Atm UTSW 9 53,516,551 (GRCm38) missense probably damaging 0.99
R9126:Atm UTSW 9 53,458,834 (GRCm38) missense probably benign 0.01
R9131:Atm UTSW 9 53,533,744 (GRCm38) missense probably benign 0.10
R9191:Atm UTSW 9 53,527,290 (GRCm38) missense probably benign 0.29
R9257:Atm UTSW 9 53,495,850 (GRCm38) critical splice donor site probably null
R9473:Atm UTSW 9 53,498,972 (GRCm38) missense probably benign
R9558:Atm UTSW 9 53,500,781 (GRCm38) missense probably benign 0.00
R9598:Atm UTSW 9 53,520,081 (GRCm38) missense probably benign 0.34
R9717:Atm UTSW 9 53,516,517 (GRCm38) missense probably damaging 1.00
R9794:Atm UTSW 9 53,518,567 (GRCm38) missense probably benign
X0067:Atm UTSW 9 53,479,694 (GRCm38) missense probably benign 0.00
Z1088:Atm UTSW 9 53,531,687 (GRCm38) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- AGAGAATGCATGAAACCCGTCTCAG -3'
(R):5'- CTTAGCCCCAAGTGAGAATCAGTGG -3'

Sequencing Primer
(F):5'- TCATTCCTCTACAGAACACTGATG -3'
(R):5'- TTTATGGAGAGATTTGAACCCAGG -3'
Posted On 2014-05-09