Incidental Mutation 'R4579:Ank2'
ID 343478
Institutional Source Beutler Lab
Gene Symbol Ank2
Ensembl Gene ENSMUSG00000032826
Gene Name ankyrin 2, brain
Synonyms Gm4392, Ank-2, ankyrin B, Ankyrin-B, Ankyrin-2
MMRRC Submission 041801-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R4579 (G1)
Quality Score 225
Status Validated
Chromosome 3
Chromosomal Location 126715261-127292999 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 126752612 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Aspartic acid at position 368 (V368D)
Ref Sequence ENSEMBL: ENSMUSP00000043765 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000044443] [ENSMUST00000182064] [ENSMUST00000182078] [ENSMUST00000182711] [ENSMUST00000182959]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000044443
AA Change: V368D

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000043765
Gene: ENSMUSG00000032826
AA Change: V368D

DomainStartEndE-ValueType
low complexity region 9 22 N/A INTRINSIC
low complexity region 57 69 N/A INTRINSIC
ZU5 128 232 4.13e-61 SMART
Pfam:ZU5 289 374 2.8e-8 PFAM
low complexity region 587 597 N/A INTRINSIC
DEATH 603 697 1.52e-27 SMART
low complexity region 732 748 N/A INTRINSIC
low complexity region 860 873 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000182025
Predicted Effect probably benign
Transcript: ENSMUST00000182062
Predicted Effect unknown
Transcript: ENSMUST00000182064
AA Change: V1239D
SMART Domains Protein: ENSMUSP00000138620
Gene: ENSMUSG00000032826
AA Change: V1239D

DomainStartEndE-ValueType
ANK 9 38 1e1 SMART
ANK 42 71 8.9e-7 SMART
ANK 75 104 4.4e-9 SMART
ANK 108 137 2.8e-9 SMART
ANK 141 169 5.3e-1 SMART
ANK 170 199 7.3e-1 SMART
ANK 211 240 1.1e-7 SMART
ANK 244 273 4.4e-9 SMART
ANK 277 306 9.3e-8 SMART
ANK 310 339 2.1e-8 SMART
ANK 343 372 1.3e-7 SMART
ANK 376 405 6.2e-9 SMART
ANK 409 438 1.1e-7 SMART
ANK 442 471 2.9e-8 SMART
ANK 475 504 1.1e-5 SMART
ANK 508 537 6.5e-6 SMART
ANK 541 570 2.3e-7 SMART
ANK 574 603 2.4e-7 SMART
ANK 607 636 3.2e-9 SMART
ANK 640 669 5.5e-5 SMART
ANK 673 702 1.9e-8 SMART
ANK 706 735 3.3e-9 SMART
low complexity region 755 775 N/A INTRINSIC
low complexity region 793 806 N/A INTRINSIC
low complexity region 841 853 N/A INTRINSIC
ZU5 912 1016 2e-63 SMART
low complexity region 1371 1381 N/A INTRINSIC
low complexity region 1448 1463 N/A INTRINSIC
low complexity region 1490 1503 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000182078
AA Change: V1152D
SMART Domains Protein: ENSMUSP00000138753
Gene: ENSMUSG00000032826
AA Change: V1152D

DomainStartEndE-ValueType
low complexity region 7 18 N/A INTRINSIC
low complexity region 114 125 N/A INTRINSIC
low complexity region 191 209 N/A INTRINSIC
low complexity region 304 312 N/A INTRINSIC
low complexity region 478 493 N/A INTRINSIC
low complexity region 527 544 N/A INTRINSIC
DEATH 591 685 1e-29 SMART
low complexity region 720 736 N/A INTRINSIC
low complexity region 848 861 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000182711
SMART Domains Protein: ENSMUSP00000138781
Gene: ENSMUSG00000032826

DomainStartEndE-ValueType
ANK 26 55 1e1 SMART
ANK 59 88 8.9e-7 SMART
ANK 92 121 4.4e-9 SMART
ANK 125 154 2.8e-9 SMART
ANK 158 186 5.3e-1 SMART
ANK 187 216 7.3e-1 SMART
ANK 228 257 1.1e-7 SMART
ANK 261 290 4.4e-9 SMART
ANK 294 323 9.3e-8 SMART
ANK 327 356 2.1e-8 SMART
ANK 360 389 1.3e-7 SMART
ANK 393 422 6.2e-9 SMART
ANK 426 455 1.1e-7 SMART
ANK 459 488 2.9e-8 SMART
ANK 492 521 1.1e-5 SMART
ANK 525 554 6.5e-6 SMART
ANK 558 587 2.3e-7 SMART
ANK 591 620 5.3e-7 SMART
ANK 624 653 2.4e-7 SMART
ANK 657 686 3.2e-9 SMART
ANK 690 719 5.5e-5 SMART
ANK 723 752 1.9e-8 SMART
ANK 756 785 3.3e-9 SMART
low complexity region 805 825 N/A INTRINSIC
low complexity region 843 856 N/A INTRINSIC
ZU5 961 1098 1.1e-50 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000183075
Predicted Effect probably benign
Transcript: ENSMUST00000182959
SMART Domains Protein: ENSMUSP00000138251
Gene: ENSMUSG00000032826

DomainStartEndE-ValueType
ANK 9 38 1.63e3 SMART
ANK 42 71 1.4e-4 SMART
ANK 75 104 6.76e-7 SMART
ANK 108 137 4.46e-7 SMART
ANK 141 169 8.36e1 SMART
ANK 170 199 1.17e2 SMART
ANK 211 240 1.76e-5 SMART
ANK 244 273 6.76e-7 SMART
ANK 277 306 1.43e-5 SMART
ANK 310 339 3.33e-6 SMART
ANK 343 372 2.02e-5 SMART
ANK 376 405 9.55e-7 SMART
ANK 409 438 1.76e-5 SMART
ANK 442 471 4.71e-6 SMART
ANK 475 504 1.7e-3 SMART
ANK 508 537 1.05e-3 SMART
ANK 541 570 3.51e-5 SMART
ANK 574 603 8.65e-5 SMART
ANK 607 636 3.76e-5 SMART
ANK 640 669 5.12e-7 SMART
ANK 673 702 8.39e-3 SMART
ANK 706 735 2.9e-6 SMART
ANK 739 768 5.12e-7 SMART
low complexity region 788 808 N/A INTRINSIC
low complexity region 826 839 N/A INTRINSIC
low complexity region 874 886 N/A INTRINSIC
Pfam:ZU5 945 1028 1.5e-30 PFAM
Pfam:ZU5 1021 1082 4.4e-21 PFAM
Meta Mutation Damage Score 0.4651 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.3%
Validation Efficiency 97% (88/91)
MGI Phenotype PHENOTYPE: Homozygous mutation of this gene results in death by postnatal day 8, although some animals survive to P20. Mutant animals display reduced body size, impaired balance and locomotion, brain structure dysmorphologies, abnormal lens, and optic nerve degeneration. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 79 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A930004D18Rik A G 2: 18,031,848 (GRCm39) I90T probably damaging Het
Acox3 A G 5: 35,761,987 (GRCm39) N444D probably damaging Het
Adamts16 A G 13: 70,927,743 (GRCm39) Y499H probably damaging Het
Ajm1 T A 2: 25,469,661 (GRCm39) R83S possibly damaging Het
Atad5 T C 11: 79,986,017 (GRCm39) V368A probably damaging Het
Atp13a5 T C 16: 29,067,090 (GRCm39) probably null Het
Bdh1 A T 16: 31,254,954 (GRCm39) probably benign Het
Bmp6 A T 13: 38,653,701 (GRCm39) Y256F probably damaging Het
Bub1b C A 2: 118,453,657 (GRCm39) S496* probably null Het
Capn15 C T 17: 26,178,811 (GRCm39) R1128H probably damaging Het
Ccnf T A 17: 24,450,303 (GRCm39) R461* probably null Het
Col6a1 C T 10: 76,547,191 (GRCm39) V725I unknown Het
Cp T C 3: 20,011,599 (GRCm39) probably null Het
Cul2 T C 18: 3,430,957 (GRCm39) V577A probably benign Het
Cux2 A T 5: 121,998,716 (GRCm39) I1408K probably benign Het
Cyp2c69 T A 19: 39,869,630 (GRCm39) T130S possibly damaging Het
Cyp3a57 A G 5: 145,311,074 (GRCm39) T278A probably benign Het
Dchs1 T G 7: 105,403,972 (GRCm39) T2857P probably damaging Het
Dchs1 A G 7: 105,408,180 (GRCm39) M1884T probably benign Het
Dnah3 T C 7: 119,608,554 (GRCm39) S1802G probably damaging Het
Dner T C 1: 84,361,537 (GRCm39) S691G probably damaging Het
Dzip1l A T 9: 99,529,267 (GRCm39) Q332L probably damaging Het
Eprs1 A G 1: 185,133,804 (GRCm39) Y827C probably damaging Het
Ermp1 A T 19: 29,594,051 (GRCm39) N706K probably damaging Het
F830045P16Rik A G 2: 129,305,423 (GRCm39) L317S probably damaging Het
Fam120c G T X: 150,219,179 (GRCm39) G696W probably damaging Het
Fance T A 17: 28,536,125 (GRCm39) probably null Het
Fancl G T 11: 26,418,423 (GRCm39) probably null Het
Fbxo30 T A 10: 11,165,293 (GRCm39) V5E probably benign Het
Foxn4 A T 5: 114,394,886 (GRCm39) I347N possibly damaging Het
Galr2 A T 11: 116,172,325 (GRCm39) D5V probably benign Het
Gm4845 T G 1: 141,184,865 (GRCm39) noncoding transcript Het
Gnao1 A T 8: 94,693,532 (GRCm39) Q73L probably damaging Het
Gnpat T A 8: 125,605,241 (GRCm39) probably null Het
H2-T5 C T 17: 36,472,649 (GRCm39) probably benign Het
Hectd1 A G 12: 51,791,356 (GRCm39) M2594T probably damaging Het
Hint3 T C 10: 30,486,428 (GRCm39) H117R probably damaging Het
Hsd3b6 A G 3: 98,713,541 (GRCm39) F253L probably damaging Het
Itgal A G 7: 126,904,466 (GRCm39) D313G possibly damaging Het
Kbtbd2 A T 6: 56,755,893 (GRCm39) D614E probably damaging Het
Ksr2 A T 5: 117,894,335 (GRCm39) I825F probably damaging Het
L3mbtl4 A T 17: 69,071,635 (GRCm39) S521C probably benign Het
Lamc1 T C 1: 153,123,015 (GRCm39) N725S probably damaging Het
Med1 T G 11: 98,049,248 (GRCm39) E516A possibly damaging Het
Mical3 A T 6: 120,935,660 (GRCm39) V1622E probably benign Het
Miip G A 4: 147,945,518 (GRCm39) P373S probably damaging Het
Myo7a C A 7: 97,722,400 (GRCm39) S1175I probably damaging Het
Ndst3 A T 3: 123,340,474 (GRCm39) D781E probably benign Het
Nf1 T A 11: 79,359,583 (GRCm39) V1407E probably damaging Het
Opalin A G 19: 41,056,196 (GRCm39) L33P probably damaging Het
Or2f2 A T 6: 42,767,458 (GRCm39) I162F probably benign Het
Or2n1b G C 17: 38,460,296 (GRCm39) K272N probably damaging Het
Or4c111 T C 2: 88,843,488 (GRCm39) I307V probably benign Het
Or8b12i G T 9: 20,082,410 (GRCm39) S152R probably damaging Het
Or8k28 T C 2: 86,285,859 (GRCm39) Y252C probably damaging Het
Or8s10 A T 15: 98,335,560 (GRCm39) D70V probably damaging Het
Pcdhb2 T A 18: 37,429,168 (GRCm39) N23K probably damaging Het
Pdap1 A G 5: 145,073,691 (GRCm39) probably benign Het
Pds5b A G 5: 150,670,197 (GRCm39) E395G probably damaging Het
Pex1 C A 5: 3,668,880 (GRCm39) R624S probably benign Het
Pitrm1 G A 13: 6,608,261 (GRCm39) V329I probably benign Het
Pop1 G A 15: 34,515,970 (GRCm39) probably benign Het
Prkaa1 A G 15: 5,190,082 (GRCm39) probably null Het
Slc38a6 G T 12: 73,335,298 (GRCm39) probably null Het
Slc5a9 T A 4: 111,750,384 (GRCm39) Y158F probably damaging Het
Spata3 T A 1: 85,954,175 (GRCm39) V114E probably damaging Het
Tbcb T A 7: 29,931,019 (GRCm39) I34F possibly damaging Het
Tek T A 4: 94,751,903 (GRCm39) Y1014* probably null Het
Togaram1 G T 12: 65,014,681 (GRCm39) C644F probably damaging Het
Trim56 A C 5: 137,142,918 (GRCm39) D199E possibly damaging Het
Tssk3 A T 4: 129,383,110 (GRCm39) D187E probably benign Het
Ttn G A 2: 76,727,147 (GRCm39) probably benign Het
Twf2 G A 9: 106,090,025 (GRCm39) R126Q probably benign Het
Ugt1a10 T C 1: 87,983,838 (GRCm39) M212T probably benign Het
Vmn1r177 A T 7: 23,565,772 (GRCm39) F35I possibly damaging Het
Vmn1r44 T A 6: 89,870,915 (GRCm39) H77Q possibly damaging Het
Zfp1004 T A 2: 150,034,143 (GRCm39) Y186N probably damaging Het
Zfp524 G A 7: 5,021,347 (GRCm39) V292I probably benign Het
Zfp788 T G 7: 41,297,018 (GRCm39) I56S probably benign Het
Other mutations in Ank2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01298:Ank2 APN 3 126,753,369 (GRCm39) missense possibly damaging 0.80
IGL01652:Ank2 APN 3 126,726,690 (GRCm39) missense probably benign 0.00
IGL01969:Ank2 APN 3 126,746,872 (GRCm39) missense possibly damaging 0.47
IGL02122:Ank2 APN 3 126,731,523 (GRCm39) splice site probably benign
IGL02537:Ank2 APN 3 126,749,565 (GRCm39) missense probably damaging 1.00
IGL02858:Ank2 APN 3 126,749,519 (GRCm39) missense probably damaging 1.00
IGL02981:Ank2 APN 3 126,728,211 (GRCm39) missense possibly damaging 0.58
IGL02981:Ank2 APN 3 126,749,519 (GRCm39) missense probably damaging 1.00
IGL03024:Ank2 APN 3 126,749,519 (GRCm39) missense probably damaging 1.00
IGL03074:Ank2 APN 3 126,749,519 (GRCm39) missense probably damaging 1.00
IGL03111:Ank2 APN 3 126,749,519 (GRCm39) missense probably damaging 1.00
IGL03129:Ank2 APN 3 126,749,519 (GRCm39) missense probably damaging 1.00
IGL03174:Ank2 APN 3 126,733,744 (GRCm39) missense probably damaging 0.98
IGL03177:Ank2 APN 3 126,749,519 (GRCm39) missense probably damaging 1.00
IGL03185:Ank2 APN 3 126,749,519 (GRCm39) missense probably damaging 1.00
IGL03188:Ank2 APN 3 126,749,519 (GRCm39) missense probably damaging 1.00
IGL03242:Ank2 APN 3 126,722,454 (GRCm39) missense possibly damaging 0.90
IGL03244:Ank2 APN 3 126,749,519 (GRCm39) missense probably damaging 1.00
IGL03248:Ank2 APN 3 126,749,519 (GRCm39) missense probably damaging 1.00
IGL03285:Ank2 APN 3 126,749,519 (GRCm39) missense probably damaging 1.00
IGL03304:Ank2 APN 3 126,749,519 (GRCm39) missense probably damaging 1.00
IGL03358:Ank2 APN 3 126,749,519 (GRCm39) missense probably damaging 1.00
IGL03380:Ank2 APN 3 126,749,519 (GRCm39) missense probably damaging 1.00
IGL03389:Ank2 APN 3 126,749,519 (GRCm39) missense probably damaging 1.00
IGL03400:Ank2 APN 3 126,749,519 (GRCm39) missense probably damaging 1.00
IGL03409:Ank2 APN 3 126,749,519 (GRCm39) missense probably damaging 1.00
ballast UTSW 3 126,736,782 (GRCm39) missense unknown
Chain UTSW 3 126,740,587 (GRCm39) intron probably benign
Deadman UTSW 3 126,723,471 (GRCm39) missense probably benign 0.19
drag UTSW 3 126,797,631 (GRCm39) missense probably damaging 1.00
mooring UTSW 3 126,728,226 (GRCm39) missense possibly damaging 0.73
Treasure UTSW 3 126,740,398 (GRCm39) missense unknown
Windlass UTSW 3 126,739,798 (GRCm39) missense probably benign
R0033:Ank2 UTSW 3 126,898,397 (GRCm39) splice site probably benign
R0042:Ank2 UTSW 3 126,730,280 (GRCm39) missense probably damaging 0.99
R0042:Ank2 UTSW 3 126,730,280 (GRCm39) missense probably damaging 0.99
R0079:Ank2 UTSW 3 126,728,264 (GRCm39) missense probably benign 0.01
R0423:Ank2 UTSW 3 126,723,509 (GRCm39) nonsense probably null
R0699:Ank2 UTSW 3 126,723,478 (GRCm39) missense probably benign 0.00
R0724:Ank2 UTSW 3 126,755,986 (GRCm39) missense probably damaging 1.00
R0990:Ank2 UTSW 3 126,728,315 (GRCm39) missense possibly damaging 0.64
R1450:Ank2 UTSW 3 126,750,951 (GRCm39) missense possibly damaging 0.94
R1500:Ank2 UTSW 3 126,726,631 (GRCm39) missense probably benign
R1702:Ank2 UTSW 3 126,749,548 (GRCm39) missense probably benign 0.00
R1703:Ank2 UTSW 3 126,723,415 (GRCm39) missense probably damaging 1.00
R1710:Ank2 UTSW 3 126,726,709 (GRCm39) nonsense probably null
R1743:Ank2 UTSW 3 126,722,324 (GRCm39) missense probably damaging 0.99
R1775:Ank2 UTSW 3 126,728,196 (GRCm39) missense probably benign 0.00
R1852:Ank2 UTSW 3 126,791,500 (GRCm39) critical splice donor site probably null
R2198:Ank2 UTSW 3 126,728,226 (GRCm39) missense possibly damaging 0.73
R2892:Ank2 UTSW 3 127,041,892 (GRCm39) splice site probably null
R2893:Ank2 UTSW 3 127,041,892 (GRCm39) splice site probably null
R2894:Ank2 UTSW 3 127,041,892 (GRCm39) splice site probably null
R3148:Ank2 UTSW 3 126,726,724 (GRCm39) missense probably benign 0.00
R3776:Ank2 UTSW 3 126,735,911 (GRCm39) intron probably benign
R3784:Ank2 UTSW 3 126,746,842 (GRCm39) missense probably damaging 1.00
R3856:Ank2 UTSW 3 126,723,493 (GRCm39) missense probably benign 0.00
R3906:Ank2 UTSW 3 126,810,547 (GRCm39) missense probably damaging 1.00
R3907:Ank2 UTSW 3 126,810,547 (GRCm39) missense probably damaging 1.00
R3953:Ank2 UTSW 3 126,781,809 (GRCm39) missense probably damaging 1.00
R3963:Ank2 UTSW 3 126,728,245 (GRCm39) missense probably benign
R4367:Ank2 UTSW 3 126,739,798 (GRCm39) missense probably benign
R4414:Ank2 UTSW 3 127,019,411 (GRCm39) critical splice donor site probably null
R4432:Ank2 UTSW 3 126,741,455 (GRCm39) intron probably benign
R4433:Ank2 UTSW 3 126,741,455 (GRCm39) intron probably benign
R4597:Ank2 UTSW 3 126,781,800 (GRCm39) missense probably damaging 1.00
R4603:Ank2 UTSW 3 126,825,665 (GRCm39) missense probably benign 0.00
R4729:Ank2 UTSW 3 126,770,545 (GRCm39) nonsense probably null
R4815:Ank2 UTSW 3 126,730,410 (GRCm39) missense probably benign
R4826:Ank2 UTSW 3 126,749,650 (GRCm39) missense probably benign 0.35
R4871:Ank2 UTSW 3 126,753,444 (GRCm39) missense probably damaging 1.00
R4880:Ank2 UTSW 3 126,840,475 (GRCm39) splice site probably null
R4915:Ank2 UTSW 3 126,736,320 (GRCm39) intron probably benign
R4935:Ank2 UTSW 3 126,749,713 (GRCm39) missense probably damaging 1.00
R4936:Ank2 UTSW 3 126,748,688 (GRCm39) missense possibly damaging 0.94
R4937:Ank2 UTSW 3 126,756,050 (GRCm39) missense probably damaging 1.00
R4946:Ank2 UTSW 3 126,735,589 (GRCm39) intron probably benign
R4963:Ank2 UTSW 3 126,825,745 (GRCm39) missense probably benign 0.01
R4989:Ank2 UTSW 3 126,757,094 (GRCm39) missense possibly damaging 0.94
R5023:Ank2 UTSW 3 126,735,520 (GRCm39) intron probably benign
R5060:Ank2 UTSW 3 126,739,570 (GRCm39) intron probably benign
R5078:Ank2 UTSW 3 126,736,002 (GRCm39) intron probably benign
R5086:Ank2 UTSW 3 126,740,997 (GRCm39) intron probably benign
R5134:Ank2 UTSW 3 126,757,094 (GRCm39) missense possibly damaging 0.94
R5148:Ank2 UTSW 3 126,819,285 (GRCm39) splice site probably null
R5175:Ank2 UTSW 3 126,797,673 (GRCm39) missense probably damaging 1.00
R5275:Ank2 UTSW 3 126,825,832 (GRCm39) missense probably damaging 1.00
R5295:Ank2 UTSW 3 126,825,832 (GRCm39) missense probably damaging 1.00
R5303:Ank2 UTSW 3 126,739,453 (GRCm39) intron probably benign
R5309:Ank2 UTSW 3 126,753,417 (GRCm39) missense probably damaging 0.99
R5312:Ank2 UTSW 3 126,753,417 (GRCm39) missense probably damaging 0.99
R5352:Ank2 UTSW 3 127,292,640 (GRCm39) utr 5 prime probably benign
R5355:Ank2 UTSW 3 126,737,698 (GRCm39) intron probably benign
R5386:Ank2 UTSW 3 126,775,582 (GRCm39) missense probably benign 0.01
R5396:Ank2 UTSW 3 126,746,875 (GRCm39) missense probably damaging 1.00
R5518:Ank2 UTSW 3 126,753,348 (GRCm39) missense probably damaging 0.98
R5534:Ank2 UTSW 3 126,740,947 (GRCm39) intron probably benign
R5554:Ank2 UTSW 3 126,792,622 (GRCm39) missense possibly damaging 0.78
R5582:Ank2 UTSW 3 126,739,954 (GRCm39) intron probably benign
R5747:Ank2 UTSW 3 126,735,400 (GRCm39) intron probably benign
R5794:Ank2 UTSW 3 126,723,669 (GRCm39) missense probably benign 0.00
R5831:Ank2 UTSW 3 127,132,808 (GRCm39) start gained probably benign
R5925:Ank2 UTSW 3 126,726,612 (GRCm39) missense probably benign 0.18
R5954:Ank2 UTSW 3 126,791,510 (GRCm39) missense probably benign 0.34
R5956:Ank2 UTSW 3 126,736,337 (GRCm39) intron probably benign
R5986:Ank2 UTSW 3 126,806,335 (GRCm39) missense possibly damaging 0.94
R5992:Ank2 UTSW 3 126,753,300 (GRCm39) critical splice donor site probably null
R6020:Ank2 UTSW 3 126,740,470 (GRCm39) intron probably benign
R6027:Ank2 UTSW 3 126,791,528 (GRCm39) missense possibly damaging 0.92
R6049:Ank2 UTSW 3 126,736,669 (GRCm39) missense possibly damaging 0.95
R6060:Ank2 UTSW 3 126,749,601 (GRCm39) missense probably damaging 1.00
R6114:Ank2 UTSW 3 126,804,700 (GRCm39) missense probably damaging 1.00
R6124:Ank2 UTSW 3 127,041,800 (GRCm39) missense probably benign 0.31
R6156:Ank2 UTSW 3 126,737,886 (GRCm39) missense probably damaging 1.00
R6173:Ank2 UTSW 3 126,846,395 (GRCm39) missense probably damaging 1.00
R6176:Ank2 UTSW 3 126,739,120 (GRCm39) missense probably benign 0.05
R6184:Ank2 UTSW 3 126,756,047 (GRCm39) missense probably damaging 1.00
R6199:Ank2 UTSW 3 126,797,655 (GRCm39) missense probably damaging 1.00
R6241:Ank2 UTSW 3 126,846,397 (GRCm39) missense probably damaging 1.00
R6254:Ank2 UTSW 3 126,735,453 (GRCm39) intron probably benign
R6259:Ank2 UTSW 3 126,810,635 (GRCm39) missense probably benign 0.28
R6260:Ank2 UTSW 3 126,737,206 (GRCm39) missense probably benign
R6321:Ank2 UTSW 3 126,740,587 (GRCm39) intron probably benign
R6393:Ank2 UTSW 3 126,723,406 (GRCm39) missense probably damaging 1.00
R6406:Ank2 UTSW 3 126,825,874 (GRCm39) missense probably damaging 1.00
R6544:Ank2 UTSW 3 126,726,871 (GRCm39) missense probably damaging 0.99
R6583:Ank2 UTSW 3 126,810,613 (GRCm39) missense probably damaging 1.00
R6739:Ank2 UTSW 3 126,873,643 (GRCm39) missense probably damaging 1.00
R6754:Ank2 UTSW 3 126,890,488 (GRCm39) intron probably benign
R6786:Ank2 UTSW 3 126,752,581 (GRCm39) missense probably damaging 0.99
R6798:Ank2 UTSW 3 126,737,913 (GRCm39) intron probably benign
R6882:Ank2 UTSW 3 126,739,406 (GRCm39) intron probably benign
R6940:Ank2 UTSW 3 126,735,621 (GRCm39) intron probably benign
R6949:Ank2 UTSW 3 126,804,533 (GRCm39) missense probably benign 0.00
R7001:Ank2 UTSW 3 126,871,230 (GRCm39) missense probably damaging 1.00
R7033:Ank2 UTSW 3 126,738,499 (GRCm39) nonsense probably null
R7036:Ank2 UTSW 3 126,740,041 (GRCm39) intron probably benign
R7045:Ank2 UTSW 3 126,806,393 (GRCm39) missense probably damaging 1.00
R7048:Ank2 UTSW 3 126,819,267 (GRCm39) missense probably benign 0.03
R7054:Ank2 UTSW 3 126,736,952 (GRCm39) intron probably benign
R7069:Ank2 UTSW 3 126,739,947 (GRCm39) intron probably benign
R7091:Ank2 UTSW 3 126,817,000 (GRCm39) missense probably damaging 0.98
R7107:Ank2 UTSW 3 126,797,631 (GRCm39) missense probably damaging 1.00
R7175:Ank2 UTSW 3 126,740,590 (GRCm39) missense unknown
R7191:Ank2 UTSW 3 126,740,041 (GRCm39) missense unknown
R7272:Ank2 UTSW 3 126,736,782 (GRCm39) missense unknown
R7381:Ank2 UTSW 3 126,730,277 (GRCm39) missense possibly damaging 0.46
R7394:Ank2 UTSW 3 126,730,302 (GRCm39) missense possibly damaging 0.77
R7462:Ank2 UTSW 3 126,736,683 (GRCm39) missense unknown
R7490:Ank2 UTSW 3 126,752,538 (GRCm39) missense probably damaging 0.99
R7514:Ank2 UTSW 3 126,819,252 (GRCm39) missense probably benign 0.06
R7534:Ank2 UTSW 3 126,727,982 (GRCm39) splice site probably null
R7540:Ank2 UTSW 3 126,781,808 (GRCm39) missense possibly damaging 0.94
R7547:Ank2 UTSW 3 126,738,852 (GRCm39) missense unknown
R7579:Ank2 UTSW 3 126,740,047 (GRCm39) missense unknown
R7584:Ank2 UTSW 3 126,739,777 (GRCm39) nonsense probably null
R7625:Ank2 UTSW 3 126,846,449 (GRCm39) missense probably damaging 1.00
R7698:Ank2 UTSW 3 126,825,860 (GRCm39) missense probably benign 0.35
R7716:Ank2 UTSW 3 126,736,815 (GRCm39) missense unknown
R7718:Ank2 UTSW 3 126,758,662 (GRCm39) missense possibly damaging 0.88
R7722:Ank2 UTSW 3 126,822,951 (GRCm39) missense probably benign 0.01
R7738:Ank2 UTSW 3 126,741,271 (GRCm39) missense
R7977:Ank2 UTSW 3 126,739,356 (GRCm39) missense unknown
R7987:Ank2 UTSW 3 126,739,356 (GRCm39) missense unknown
R8007:Ank2 UTSW 3 126,730,096 (GRCm39) intron probably benign
R8150:Ank2 UTSW 3 126,741,162 (GRCm39) missense
R8161:Ank2 UTSW 3 126,825,778 (GRCm39) missense
R8196:Ank2 UTSW 3 126,723,532 (GRCm39) missense probably damaging 0.99
R8248:Ank2 UTSW 3 126,731,434 (GRCm39) missense possibly damaging 0.78
R8255:Ank2 UTSW 3 126,740,398 (GRCm39) missense unknown
R8279:Ank2 UTSW 3 126,726,820 (GRCm39) missense probably benign 0.04
R8300:Ank2 UTSW 3 126,804,555 (GRCm39) missense
R8716:Ank2 UTSW 3 126,736,488 (GRCm39) nonsense probably null
R8724:Ank2 UTSW 3 126,737,405 (GRCm39) missense unknown
R8765:Ank2 UTSW 3 126,850,731 (GRCm39) missense possibly damaging 0.94
R8779:Ank2 UTSW 3 126,758,751 (GRCm39) missense probably damaging 0.99
R8783:Ank2 UTSW 3 126,846,455 (GRCm39) missense probably damaging 1.00
R8785:Ank2 UTSW 3 126,791,570 (GRCm39) missense probably damaging 1.00
R8826:Ank2 UTSW 3 126,740,951 (GRCm39) missense unknown
R8872:Ank2 UTSW 3 126,791,525 (GRCm39) missense possibly damaging 0.88
R8903:Ank2 UTSW 3 126,840,431 (GRCm39) missense probably damaging 1.00
R8906:Ank2 UTSW 3 126,726,720 (GRCm39) missense probably benign 0.00
R8918:Ank2 UTSW 3 126,737,380 (GRCm39) missense unknown
R8947:Ank2 UTSW 3 126,736,396 (GRCm39) intron probably benign
R8977:Ank2 UTSW 3 126,738,575 (GRCm39) missense unknown
R8990:Ank2 UTSW 3 126,841,829 (GRCm39) critical splice donor site probably null
R8994:Ank2 UTSW 3 126,723,471 (GRCm39) missense probably benign 0.19
R9009:Ank2 UTSW 3 126,728,025 (GRCm39) unclassified probably benign
R9123:Ank2 UTSW 3 126,733,744 (GRCm39) missense probably damaging 1.00
R9125:Ank2 UTSW 3 126,733,744 (GRCm39) missense probably damaging 1.00
R9130:Ank2 UTSW 3 126,810,565 (GRCm39) missense
R9175:Ank2 UTSW 3 126,722,402 (GRCm39) missense possibly damaging 0.52
R9220:Ank2 UTSW 3 126,737,086 (GRCm39) missense unknown
R9225:Ank2 UTSW 3 126,736,111 (GRCm39) missense unknown
R9286:Ank2 UTSW 3 126,846,381 (GRCm39) missense probably damaging 0.99
R9325:Ank2 UTSW 3 126,775,504 (GRCm39) missense probably damaging 0.98
R9367:Ank2 UTSW 3 126,738,678 (GRCm39) missense unknown
R9385:Ank2 UTSW 3 126,753,366 (GRCm39) missense probably benign 0.00
R9391:Ank2 UTSW 3 126,731,394 (GRCm39) missense probably damaging 0.99
R9422:Ank2 UTSW 3 126,890,505 (GRCm39) missense unknown
R9536:Ank2 UTSW 3 126,736,031 (GRCm39) missense unknown
R9647:Ank2 UTSW 3 126,792,623 (GRCm39) missense possibly damaging 0.93
R9650:Ank2 UTSW 3 126,735,829 (GRCm39) missense unknown
R9666:Ank2 UTSW 3 126,726,838 (GRCm39) nonsense probably null
R9686:Ank2 UTSW 3 126,740,550 (GRCm39) missense unknown
R9730:Ank2 UTSW 3 127,019,493 (GRCm39) missense
R9738:Ank2 UTSW 3 126,737,121 (GRCm39) missense unknown
R9743:Ank2 UTSW 3 126,733,794 (GRCm39) missense possibly damaging 0.81
R9747:Ank2 UTSW 3 126,752,667 (GRCm39) missense probably damaging 1.00
R9800:Ank2 UTSW 3 126,740,149 (GRCm39) missense unknown
R9803:Ank2 UTSW 3 126,752,726 (GRCm39) missense possibly damaging 0.64
RF020:Ank2 UTSW 3 126,739,125 (GRCm39) missense unknown
Z1088:Ank2 UTSW 3 126,823,158 (GRCm39) missense possibly damaging 0.45
Z1177:Ank2 UTSW 3 126,738,006 (GRCm39) missense unknown
Z1187:Ank2 UTSW 3 126,749,601 (GRCm39) missense probably damaging 1.00
Z1190:Ank2 UTSW 3 126,749,601 (GRCm39) missense probably damaging 1.00
Z1192:Ank2 UTSW 3 126,749,601 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CAGCTACCTATAGTAAATGTAACGTAG -3'
(R):5'- CCACCAAACTCATTTGTGAGAG -3'

Sequencing Primer
(F):5'- CCTGTTATGCTGCACAGTA -3'
(R):5'- CCAAACTCATTTGTGAGAGAAAAAGC -3'
Posted On 2015-09-24