Incidental Mutation 'R6321:Ank2'
ID 510333
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 044418-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R6321 (G1)
Quality Score 225.009
Status Validated
Chromosome 3
Chromosomal Location 126715261-127292999 bp(-) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) T to C at 126740587 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: ENSMUST00000182025
Predicted Effect probably benign
Transcript: ENSMUST00000182062
Predicted Effect unknown
Transcript: ENSMUST00000182064
AA Change: I1766V
SMART Domains Protein: ENSMUSP00000138620
Gene: ENSMUSG00000032826
AA Change: I1766V

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: I1679V
SMART Domains Protein: ENSMUSP00000138753
Gene: ENSMUSG00000032826
AA Change: I1679V

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 noncoding transcript
Transcript: ENSMUST00000183075
Meta Mutation Damage Score 0.1357 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.3%
  • 20x: 97.8%
Validation Efficiency 100% (52/52)
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: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actbl2 G T 13: 111,391,915 (GRCm39) M83I probably damaging Het
Adgra2 T A 8: 27,604,190 (GRCm39) M460K probably benign Het
Aldh16a1 G A 7: 44,799,189 (GRCm39) A31V probably damaging Het
Arrdc4 C A 7: 68,398,793 (GRCm39) D8Y probably benign Het
Auts2 A G 5: 131,494,953 (GRCm39) Y110H probably damaging Het
Blnk A T 19: 40,922,903 (GRCm39) Y405N probably damaging Het
Capsl T C 15: 9,461,855 (GRCm39) F84L probably damaging Het
Cdcp3 T C 7: 130,858,735 (GRCm39) probably null Het
Cenpl T C 1: 160,902,465 (GRCm39) S46P probably benign Het
Chd1l G A 3: 97,494,483 (GRCm39) A399V probably damaging Het
Chrnd C T 1: 87,119,951 (GRCm39) R90C probably damaging Het
Cyfip2 A T 11: 46,182,347 (GRCm39) M37K probably benign Het
Dnah11 T C 12: 118,106,027 (GRCm39) E625G possibly damaging Het
Dnah5 T G 15: 28,372,557 (GRCm39) V2936G probably damaging Het
Dock9 A G 14: 121,783,433 (GRCm39) M2055T probably damaging Het
Epb41l2 A T 10: 25,344,026 (GRCm39) R274S probably damaging Het
Erich3 A T 3: 154,433,139 (GRCm39) H371L probably damaging Het
Evi5l C A 8: 4,253,080 (GRCm39) P454T probably benign Het
Gm10549 C A 18: 33,597,358 (GRCm39) probably benign Het
Gm11595 G A 11: 99,663,381 (GRCm39) R100C unknown Het
Golgb1 T A 16: 36,738,559 (GRCm39) C2299* probably null Het
Heca G C 10: 17,790,991 (GRCm39) probably null Het
Hecw1 C T 13: 14,697,414 (GRCm39) A9T probably benign Het
Hs3st6 T A 17: 24,977,542 (GRCm39) W341R probably damaging Het
Kidins220 C T 12: 25,107,533 (GRCm39) S1571L probably benign Het
Klk1b9 A G 7: 43,443,732 (GRCm39) E82G probably damaging Het
Ltbp3 C A 19: 5,795,685 (GRCm39) H180Q probably benign Het
Mecom A G 3: 30,034,741 (GRCm39) Y502H probably damaging Het
Mfsd2a A G 4: 122,843,165 (GRCm39) V372A probably benign Het
Mrgprd A G 7: 144,875,879 (GRCm39) D250G probably benign Het
Muc2 A G 7: 141,287,397 (GRCm39) D191G probably benign Het
Myl10 G C 5: 136,726,825 (GRCm39) V70L probably benign Het
Naip6 C A 13: 100,436,909 (GRCm39) S538I probably benign Het
Or4f59 A G 2: 111,873,113 (GRCm39) V88A probably benign Het
Or52w1 A G 7: 105,018,109 (GRCm39) Y192C probably damaging Het
Pnpla6 T C 8: 3,594,015 (GRCm39) V1342A probably benign Het
Ppp1r9a A G 6: 5,115,151 (GRCm39) E789G probably damaging Het
Prkdc A G 16: 15,532,783 (GRCm39) T1471A probably benign Het
Scarb1 T A 5: 125,381,395 (GRCm39) S50C probably damaging Het
Slc4a8 C T 15: 100,687,045 (GRCm39) T283M probably damaging Het
Smc2 C A 4: 52,462,814 (GRCm39) D601E probably benign Het
Snx6 C A 12: 54,798,798 (GRCm39) V221F probably damaging Het
Spag17 A C 3: 99,995,743 (GRCm39) K1794T probably benign Het
Tpo A G 12: 30,153,107 (GRCm39) W416R probably damaging Het
Ttc13 C A 8: 125,409,930 (GRCm39) K427N probably damaging Het
Upf3a A T 8: 13,837,466 (GRCm39) N137I possibly damaging Het
Ush2a C T 1: 188,581,243 (GRCm39) Q3708* probably null Het
Zbtb17 G A 4: 141,190,694 (GRCm39) G171S probably benign Het
Zfp451 A G 1: 33,852,816 (GRCm39) F33L probably damaging Het
Zfp454 A G 11: 50,763,876 (GRCm39) F408L probably damaging Het
Zfp639 T C 3: 32,571,237 (GRCm39) Y40H 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
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'- CACTGGTGTGTGCCTTTCAG -3'
(R):5'- AATAAGGGGAAGGCCACCTC -3'

Sequencing Primer
(F):5'- AAAGGGAAGAGTGTCTTTCTGC -3'
(R):5'- GGCCTGGCGATCAAAAAGCC -3'
Posted On 2018-04-02