Incidental Mutation 'R9009:Ank2'
ID 711097
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 068839-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R9009 (G1)
Quality Score 90.0077
Status Validated
Chromosome 3
Chromosomal Location 126715261-127292999 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 126728025 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000044443] [ENSMUST00000182064] [ENSMUST00000182078]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000044443
SMART Domains Protein: ENSMUSP00000043765
Gene: ENSMUSG00000032826

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: ENSMUST00000182062
Predicted Effect probably benign
Transcript: ENSMUST00000182064
SMART Domains Protein: ENSMUSP00000138620
Gene: ENSMUSG00000032826

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 probably benign
Transcript: ENSMUST00000182078
SMART Domains Protein: ENSMUSP00000138753
Gene: ENSMUSG00000032826

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: ENSMUST00000182118
Predicted Effect probably benign
Transcript: ENSMUST00000182571
Meta Mutation Damage Score 0.0846 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency 94% (58/62)
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: 65 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
6430548M08Rik T A 8: 120,878,279 (GRCm39) probably benign Het
Ahctf1 C T 1: 179,581,171 (GRCm39) S1677N probably benign Het
Arid3c A T 4: 41,729,925 (GRCm39) I90N probably benign Het
Asb1 C A 1: 91,480,205 (GRCm39) D301E unknown Het
Asb1 T G 1: 91,480,206 (GRCm39) *302G probably null Het
Birc2 A T 9: 7,833,937 (GRCm39) F181L probably benign Het
Bnip1 T A 17: 27,001,590 (GRCm39) probably benign Het
Card6 TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG 15: 5,128,173 (GRCm39) probably benign Het
Cd2ap T C 17: 43,116,135 (GRCm39) D575G possibly damaging Het
Cdca7 T A 2: 72,314,273 (GRCm39) H248Q probably damaging Het
Chd2 T C 7: 73,143,192 (GRCm39) D567G probably benign Het
Chd2 T C 7: 73,140,402 (GRCm39) I609V probably benign Het
Cnmd T A 14: 79,894,085 (GRCm39) T101S probably damaging Het
Col6a4 T C 9: 105,954,404 (GRCm39) T312A probably benign Het
Cript C A 17: 87,338,475 (GRCm39) T41N probably damaging Het
Cts6 T C 13: 61,344,261 (GRCm39) I264V probably benign Het
Cyp4a32 C T 4: 115,467,802 (GRCm39) T262I probably null Het
D430041D05Rik T A 2: 104,240,521 (GRCm39) probably benign Het
Dctd C T 8: 48,564,712 (GRCm39) P5S probably benign Het
Det1 T C 7: 78,492,984 (GRCm39) N340S probably benign Het
Dnah7b A G 1: 46,262,232 (GRCm39) N2032D probably benign Het
Dscam T A 16: 96,840,116 (GRCm39) T164S probably benign Het
Emcn T C 3: 137,124,775 (GRCm39) V196A possibly damaging Het
Fbxo32 A G 15: 58,046,358 (GRCm39) I284T possibly damaging Het
Gimap3 C A 6: 48,742,094 (GRCm39) D279Y possibly damaging Het
Gm43302 C T 5: 105,427,974 (GRCm39) D196N probably benign Het
Gpc6 C A 14: 117,424,217 (GRCm39) H102N possibly damaging Het
Gpr158 A T 2: 21,581,760 (GRCm39) D413V probably damaging Het
Ifi207 T C 1: 173,555,382 (GRCm39) R767G probably damaging Het
Kcnip2 T C 19: 45,800,634 (GRCm39) probably benign Het
Kifap3 A C 1: 163,696,291 (GRCm39) D640A probably damaging Het
Lmbrd2 A T 15: 9,157,311 (GRCm39) Q183L possibly damaging Het
Malt1 A G 18: 65,577,911 (GRCm39) I135V probably benign Het
Mfhas1 T C 8: 36,057,109 (GRCm39) V528A probably damaging Het
Mllt10 T C 2: 18,167,163 (GRCm39) S363P probably damaging Het
Mrnip A G 11: 50,073,323 (GRCm39) Y44C probably damaging Het
Mstn C T 1: 53,103,131 (GRCm39) Q156* probably null Het
Mtmr7 T C 8: 41,008,904 (GRCm39) D469G possibly damaging Het
Muc6 A G 7: 141,217,018 (GRCm39) S2552P possibly damaging Het
Myo1f C A 17: 33,823,662 (GRCm39) N1063K probably benign Het
Or52k2 T A 7: 102,253,642 (GRCm39) I27N probably benign Het
Or5af1 A T 11: 58,722,280 (GRCm39) Y100F probably benign Het
Or6z5 G A 7: 6,477,399 (GRCm39) V97M probably benign Het
Orai2 A G 5: 136,179,430 (GRCm39) V201A possibly damaging Het
Pcdhga6 A T 18: 37,841,878 (GRCm39) T533S possibly damaging Het
Pkd1l1 T A 11: 8,881,552 (GRCm39) K907N Het
Plaat5 G T 19: 7,614,823 (GRCm39) M228I probably benign Het
Ppp1r15a A T 7: 45,174,049 (GRCm39) V253E probably benign Het
Ppp1r9b A G 11: 94,887,467 (GRCm39) E493G probably benign Het
Prdm1 T C 10: 44,322,997 (GRCm39) N151S probably benign Het
Prkcd C T 14: 30,329,297 (GRCm39) A163T probably damaging Het
Prl7a2 T A 13: 27,849,994 (GRCm39) E26V probably damaging Het
Ptprm A T 17: 66,996,354 (GRCm39) N1278K probably damaging Het
Ptprz1 T A 6: 23,001,653 (GRCm39) S1248T possibly damaging Het
Scn9a T C 2: 66,338,927 (GRCm39) I1186M probably damaging Het
Sv2a T C 3: 96,094,409 (GRCm39) F248S probably benign Het
Tas2r116 T A 6: 132,832,963 (GRCm39) I188K probably damaging Het
Tcf21 T C 10: 22,693,671 (GRCm39) T169A probably benign Het
Tecrl C A 5: 83,432,121 (GRCm39) C258F probably damaging Het
Tet2 T A 3: 133,193,360 (GRCm39) E358V possibly damaging Het
Thada A T 17: 84,759,203 (GRCm39) S219T possibly damaging Het
Tpgs2 T A 18: 25,301,777 (GRCm39) probably benign Het
Ttc6 A T 12: 57,744,219 (GRCm39) I1284F probably damaging Het
Vmn1r160 T C 7: 22,571,127 (GRCm39) V160A possibly damaging Het
Vmn1r44 T C 6: 89,870,671 (GRCm39) L139P probably damaging 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
R4579:Ank2 UTSW 3 126,752,612 (GRCm39) missense probably damaging 1.00
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
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'- CCCGTAAGTCATGACTGTGCTC -3'
(R):5'- TCTCAGGGAAAACGCAAGAC -3'

Sequencing Primer
(F):5'- TCATGACTGTGCTCAGGAAG -3'
(R):5'- GACCAGCAGGAATATTAGTGAGTTTC -3'
Posted On 2022-04-20