Incidental Mutation 'R5387:Ankhd1'
ID 425377
Institutional Source Beutler Lab
Gene Symbol Ankhd1
Ensembl Gene ENSMUSG00000024483
Gene Name ankyrin repeat and KH domain containing 1
Synonyms
MMRRC Submission 042959-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R5387 (G1)
Quality Score 225
Status Validated
Chromosome 18
Chromosomal Location 36559987-36665917 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) C to A at 36634644 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Histidine to Asparagine at position 1205 (H1205N)
Ref Sequence ENSEMBL: ENSMUSP00000123270 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000006205] [ENSMUST00000142977] [ENSMUST00000155329]
AlphaFold E9PUR0
Predicted Effect probably damaging
Transcript: ENSMUST00000006205
AA Change: H1205N

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000006205
Gene: ENSMUSG00000024483
AA Change: H1205N

DomainStartEndE-ValueType
low complexity region 20 38 N/A INTRINSIC
low complexity region 48 78 N/A INTRINSIC
low complexity region 91 109 N/A INTRINSIC
ANK 207 236 2.11e2 SMART
ANK 240 269 3.31e-1 SMART
ANK 274 303 5.24e-4 SMART
ANK 307 336 7.64e-6 SMART
ANK 340 369 2.7e-6 SMART
ANK 374 403 3.23e-4 SMART
ANK 407 436 1.61e-4 SMART
ANK 440 469 5.16e-3 SMART
ANK 473 502 4.16e-7 SMART
ANK 507 536 1.68e-2 SMART
ANK 537 566 7.02e-5 SMART
ANK 570 599 7.95e-4 SMART
ANK 603 632 4.56e-4 SMART
ANK 637 666 9.64e-3 SMART
ANK 670 699 6.71e-2 SMART
coiled coil region 815 855 N/A INTRINSIC
ANK 1057 1086 2.07e-2 SMART
ANK 1090 1119 2.48e-5 SMART
ANK 1124 1153 3.85e-2 SMART
ANK 1157 1186 1.61e-4 SMART
ANK 1192 1221 1.24e-5 SMART
ANK 1226 1255 1.59e-3 SMART
ANK 1259 1288 3.91e-3 SMART
ANK 1294 1323 5.93e-3 SMART
ANK 1327 1356 9.41e-6 SMART
ANK 1360 1393 3.8e-1 SMART
coiled coil region 1422 1486 N/A INTRINSIC
low complexity region 1509 1526 N/A INTRINSIC
low complexity region 1538 1557 N/A INTRINSIC
low complexity region 1585 1604 N/A INTRINSIC
KH 1693 1763 5.04e-13 SMART
low complexity region 1968 2001 N/A INTRINSIC
low complexity region 2041 2057 N/A INTRINSIC
low complexity region 2064 2081 N/A INTRINSIC
low complexity region 2334 2346 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000130035
SMART Domains Protein: ENSMUSP00000117110
Gene: ENSMUSG00000024483

DomainStartEndE-ValueType
ANK 2 26 5.35e2 SMART
ANK 30 59 9.41e-6 SMART
ANK 63 96 3.8e-1 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000136030
SMART Domains Protein: ENSMUSP00000115837
Gene: ENSMUSG00000024483

DomainStartEndE-ValueType
ANK 94 123 2.07e-2 SMART
ANK 127 156 2.48e-5 SMART
ANK 161 190 3.85e-2 SMART
ANK 194 219 4.23e1 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000142780
Predicted Effect probably damaging
Transcript: ENSMUST00000142977
AA Change: H1205N

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000120290
Gene: ENSMUSG00000024483
AA Change: H1205N

DomainStartEndE-ValueType
low complexity region 20 38 N/A INTRINSIC
low complexity region 48 78 N/A INTRINSIC
low complexity region 91 109 N/A INTRINSIC
ANK 207 236 2.11e2 SMART
ANK 240 269 3.31e-1 SMART
ANK 274 303 5.24e-4 SMART
ANK 307 336 7.64e-6 SMART
ANK 340 369 2.7e-6 SMART
ANK 374 403 3.23e-4 SMART
ANK 407 436 1.61e-4 SMART
ANK 440 469 5.16e-3 SMART
ANK 473 502 4.16e-7 SMART
ANK 507 536 1.68e-2 SMART
ANK 537 566 7.02e-5 SMART
ANK 570 599 7.95e-4 SMART
ANK 603 632 4.56e-4 SMART
ANK 637 666 9.64e-3 SMART
ANK 670 699 6.71e-2 SMART
coiled coil region 815 855 N/A INTRINSIC
ANK 1057 1086 2.07e-2 SMART
ANK 1090 1119 2.48e-5 SMART
ANK 1124 1153 3.85e-2 SMART
ANK 1157 1186 1.61e-4 SMART
ANK 1192 1221 1.24e-5 SMART
ANK 1226 1255 1.59e-3 SMART
ANK 1259 1288 3.91e-3 SMART
ANK 1294 1323 5.93e-3 SMART
ANK 1327 1356 9.41e-6 SMART
ANK 1360 1393 3.8e-1 SMART
coiled coil region 1422 1486 N/A INTRINSIC
low complexity region 1509 1526 N/A INTRINSIC
low complexity region 1538 1557 N/A INTRINSIC
low complexity region 1585 1604 N/A INTRINSIC
KH 1693 1763 5.04e-13 SMART
low complexity region 1968 2001 N/A INTRINSIC
low complexity region 2041 2057 N/A INTRINSIC
low complexity region 2064 2081 N/A INTRINSIC
low complexity region 2334 2346 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000153612
SMART Domains Protein: ENSMUSP00000116462
Gene: ENSMUSG00000024483

DomainStartEndE-ValueType
ANK 10 39 9.41e-6 SMART
ANK 43 76 3.8e-1 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000155329
AA Change: H1205N

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000123270
Gene: ENSMUSG00000024483
AA Change: H1205N

DomainStartEndE-ValueType
low complexity region 20 38 N/A INTRINSIC
low complexity region 48 78 N/A INTRINSIC
low complexity region 91 109 N/A INTRINSIC
ANK 207 236 2.11e2 SMART
ANK 240 269 3.31e-1 SMART
ANK 274 303 5.24e-4 SMART
ANK 307 336 7.64e-6 SMART
ANK 340 369 2.7e-6 SMART
ANK 374 403 3.23e-4 SMART
ANK 407 436 1.61e-4 SMART
ANK 440 469 5.16e-3 SMART
ANK 473 502 4.16e-7 SMART
ANK 507 536 1.68e-2 SMART
ANK 537 566 7.02e-5 SMART
ANK 570 599 7.95e-4 SMART
ANK 603 632 4.56e-4 SMART
ANK 637 666 9.64e-3 SMART
ANK 670 699 6.71e-2 SMART
coiled coil region 815 855 N/A INTRINSIC
ANK 1057 1086 2.07e-2 SMART
ANK 1090 1119 2.48e-5 SMART
ANK 1124 1153 3.85e-2 SMART
ANK 1157 1186 1.61e-4 SMART
ANK 1192 1221 1.24e-5 SMART
ANK 1226 1255 1.59e-3 SMART
ANK 1259 1288 3.91e-3 SMART
ANK 1294 1323 5.93e-3 SMART
ANK 1327 1356 9.41e-6 SMART
ANK 1360 1393 3.8e-1 SMART
coiled coil region 1422 1486 N/A INTRINSIC
low complexity region 1509 1526 N/A INTRINSIC
low complexity region 1538 1557 N/A INTRINSIC
low complexity region 1585 1604 N/A INTRINSIC
KH 1693 1763 5.04e-13 SMART
low complexity region 1968 2001 N/A INTRINSIC
low complexity region 2041 2057 N/A INTRINSIC
low complexity region 2064 2081 N/A INTRINSIC
low complexity region 2342 2362 N/A INTRINSIC
Meta Mutation Damage Score 0.3703 question?
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.8%
  • 10x: 97.6%
  • 20x: 96.0%
Validation Efficiency 99% (80/81)
Allele List at MGI
Other mutations in this stock
Total: 74 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2210408I21Rik T A 13: 77,259,973 (GRCm38) S140T probably benign Het
Ahnak T C 19: 9,003,691 (GRCm38) S780P probably damaging Het
Ano1 T C 7: 144,648,619 (GRCm38) K139R probably benign Het
Anp32b T G 4: 46,468,573 (GRCm38) C114W probably damaging Het
Ascl1 C T 10: 87,492,689 (GRCm38) A134T probably damaging Het
Atl2 C T 17: 79,852,800 (GRCm38) E453K probably benign Het
Aup1 C T 6: 83,055,024 (GRCm38) A84V probably damaging Het
Btbd7 A T 12: 102,837,785 (GRCm38) M332K probably damaging Het
Cacna1d A G 14: 30,100,751 (GRCm38) V1107A probably damaging Het
Cd33 G A 7: 43,532,053 (GRCm38) Q114* probably null Het
Cdhr18 C A 14: 13,914,438 (GRCm38) M1I probably null Het
Col4a4 C T 1: 82,493,591 (GRCm38) G681E unknown Het
Defb22 C A 2: 152,485,906 (GRCm38) A120S unknown Het
Dnah7b A G 1: 46,188,659 (GRCm38) I1347M probably damaging Het
Efcab5 A G 11: 77,134,842 (GRCm38) I549T possibly damaging Het
Esp15 T A 17: 39,644,577 (GRCm38) probably null Het
Fbxo7 A G 10: 86,024,654 (GRCm38) T42A probably benign Het
Filip1 A G 9: 79,818,274 (GRCm38) I1021T probably benign Het
Gad1 C A 2: 70,563,851 (GRCm38) S7* probably null Het
H2ac7 T A 13: 23,574,667 (GRCm38) probably null Het
H2-Q7 C T 17: 35,439,542 (GRCm38) T52M probably damaging Het
H2-T3 C T 17: 36,186,702 (GRCm38) G28R probably benign Het
Idh2 TCCCAGG T 7: 80,098,331 (GRCm38) probably benign Het
Ift81 A G 5: 122,555,535 (GRCm38) Y604H probably damaging Het
Igsf11 A G 16: 39,022,423 (GRCm38) Y154C probably damaging Het
Kif26b G T 1: 178,914,876 (GRCm38) A846S probably benign Het
Lnx2 G A 5: 147,028,154 (GRCm38) P420S probably benign Het
Lrit2 A G 14: 37,072,259 (GRCm38) T427A probably damaging Het
Lrrc43 G T 5: 123,499,671 (GRCm38) probably null Het
Mettl25b A T 3: 87,930,011 (GRCm38) probably benign Het
Mug1 T C 6: 121,884,394 (GRCm38) Y1325H probably damaging Het
Naglu A T 11: 101,076,724 (GRCm38) Y500F probably damaging Het
Npy4r A G 14: 34,146,983 (GRCm38) M116T probably benign Het
Nrdc A G 4: 109,039,762 (GRCm38) Y526C probably damaging Het
Nrp2 T C 1: 62,762,813 (GRCm38) S472P probably benign Het
Or12d2 T A 17: 37,314,292 (GRCm38) T31S probably benign Het
Or12k8 T C 2: 37,085,719 (GRCm38) T10A possibly damaging Het
Otogl T A 10: 107,780,933 (GRCm38) T1828S probably benign Het
Pank2 C T 2: 131,274,262 (GRCm38) T200I probably benign Het
Pbrm1 A G 14: 31,082,610 (GRCm38) Y946C probably damaging Het
Pde12 A T 14: 26,666,453 (GRCm38) S437T probably benign Het
Pikfyve A G 1: 65,265,268 (GRCm38) K1710E possibly damaging Het
Plcd3 A G 11: 103,078,455 (GRCm38) S229P probably damaging Het
Polr3a T C 14: 24,454,941 (GRCm38) I1084V possibly damaging Het
Prkaa2 C A 4: 105,040,177 (GRCm38) D280Y probably damaging Het
Ptprg T A 14: 12,153,873 (GRCm38) S531R probably damaging Het
R3hdm2 T C 10: 127,485,434 (GRCm38) S620P probably damaging Het
Rab33b A G 3: 51,493,455 (GRCm38) T117A probably damaging Het
Rasal2 T C 1: 157,157,765 (GRCm38) D804G possibly damaging Het
Rbp3 A G 14: 33,956,413 (GRCm38) T773A possibly damaging Het
Rspry1 A G 8: 94,638,286 (GRCm38) T185A possibly damaging Het
Sec61a2 G T 2: 5,882,545 (GRCm38) probably benign Het
Setx C T 2: 29,147,594 (GRCm38) R1364C probably benign Het
Shtn1 G T 19: 59,038,369 (GRCm38) L97M probably damaging Het
Slc35f1 T C 10: 53,108,164 (GRCm38) L340P probably damaging Het
Slc45a1 T A 4: 150,643,909 (GRCm38) probably benign Het
Slmap T C 14: 26,459,933 (GRCm38) E386G probably benign Het
Smc2 C T 4: 52,475,096 (GRCm38) A924V probably benign Het
Sp110 C G 1: 85,589,118 (GRCm38) E219D probably damaging Het
Tecta G A 9: 42,375,063 (GRCm38) L766F probably damaging Het
Tle3 C T 9: 61,407,489 (GRCm38) probably null Het
Top3a A G 11: 60,762,490 (GRCm38) F53L probably damaging Het
Trappc2b A T 11: 51,685,974 (GRCm38) D32E probably benign Het
Trem1 T C 17: 48,241,513 (GRCm38) I26T possibly damaging Het
Ttc7b G T 12: 100,446,963 (GRCm38) Q199K possibly damaging Het
Ubap2l T C 3: 90,006,596 (GRCm38) Y975C probably benign Het
Ubxn11 C A 4: 134,123,426 (GRCm38) D196E probably damaging Het
Unc80 A G 1: 66,530,021 (GRCm38) H945R possibly damaging Het
Usp15 A G 10: 123,131,286 (GRCm38) I405T probably damaging Het
Uty C T Y: 1,189,339 (GRCm38) E138K probably damaging Het
Wapl A G 14: 34,677,295 (GRCm38) E107G probably benign Het
Wbp1l T C 19: 46,644,457 (GRCm38) probably null Het
Zfp184 T G 13: 21,949,640 (GRCm38) probably benign Het
Zfp36 A C 7: 28,377,868 (GRCm38) L205R possibly damaging Het
Other mutations in Ankhd1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00088:Ankhd1 APN 18 36,665,459 (GRCm38) unclassified probably benign
IGL00927:Ankhd1 APN 18 36,632,072 (GRCm38) missense probably benign 0.01
IGL01367:Ankhd1 APN 18 36,578,643 (GRCm38) missense probably benign 0.16
IGL01624:Ankhd1 APN 18 36,658,013 (GRCm38) missense probably damaging 1.00
IGL01725:Ankhd1 APN 18 36,648,153 (GRCm38) missense probably benign 0.04
IGL01767:Ankhd1 APN 18 36,648,374 (GRCm38) missense probably damaging 1.00
IGL02005:Ankhd1 APN 18 36,648,426 (GRCm38) missense probably damaging 1.00
IGL02009:Ankhd1 APN 18 36,624,661 (GRCm38) missense probably damaging 1.00
IGL02246:Ankhd1 APN 18 36,656,726 (GRCm38) missense probably damaging 1.00
IGL02336:Ankhd1 APN 18 36,594,814 (GRCm38) missense probably damaging 0.97
IGL02628:Ankhd1 APN 18 36,647,703 (GRCm38) missense probably benign 0.00
IGL02644:Ankhd1 APN 18 36,578,775 (GRCm38) critical splice donor site probably null
IGL02735:Ankhd1 APN 18 36,648,546 (GRCm38) missense probably benign 0.00
IGL02877:Ankhd1 APN 18 36,594,823 (GRCm38) missense probably damaging 1.00
IGL03129:Ankhd1 APN 18 36,658,008 (GRCm38) nonsense probably null
IGL03163:Ankhd1 APN 18 36,647,628 (GRCm38) missense probably damaging 0.97
IGL03182:Ankhd1 APN 18 36,578,774 (GRCm38) missense probably benign 0.06
IGL03184:Ankhd1 APN 18 36,647,777 (GRCm38) missense probably damaging 1.00
IGL03398:Ankhd1 APN 18 36,656,837 (GRCm38) splice site probably benign
FR4304:Ankhd1 UTSW 18 36,560,924 (GRCm38) small insertion probably benign
R0051:Ankhd1 UTSW 18 36,647,188 (GRCm38) unclassified probably benign
R0089:Ankhd1 UTSW 18 36,640,356 (GRCm38) missense probably damaging 0.99
R0105:Ankhd1 UTSW 18 36,646,766 (GRCm38) missense probably damaging 1.00
R0149:Ankhd1 UTSW 18 36,647,214 (GRCm38) missense probably damaging 1.00
R0243:Ankhd1 UTSW 18 36,634,734 (GRCm38) missense probably damaging 1.00
R0322:Ankhd1 UTSW 18 36,658,008 (GRCm38) nonsense probably null
R0361:Ankhd1 UTSW 18 36,647,214 (GRCm38) missense probably damaging 1.00
R0389:Ankhd1 UTSW 18 36,644,599 (GRCm38) missense possibly damaging 0.48
R0418:Ankhd1 UTSW 18 36,634,300 (GRCm38) missense probably damaging 1.00
R0443:Ankhd1 UTSW 18 36,644,599 (GRCm38) missense possibly damaging 0.48
R0540:Ankhd1 UTSW 18 36,640,280 (GRCm38) missense probably damaging 1.00
R0607:Ankhd1 UTSW 18 36,640,280 (GRCm38) missense probably damaging 1.00
R0738:Ankhd1 UTSW 18 36,645,249 (GRCm38) splice site probably benign
R1127:Ankhd1 UTSW 18 36,634,346 (GRCm38) missense probably damaging 1.00
R1434:Ankhd1 UTSW 18 36,625,159 (GRCm38) missense probably benign 0.09
R1742:Ankhd1 UTSW 18 36,625,265 (GRCm38) missense probably damaging 1.00
R1776:Ankhd1 UTSW 18 36,647,308 (GRCm38) missense probably benign 0.17
R1856:Ankhd1 UTSW 18 36,644,527 (GRCm38) missense probably benign 0.00
R1923:Ankhd1 UTSW 18 36,648,030 (GRCm38) missense probably benign 0.08
R2044:Ankhd1 UTSW 18 36,645,113 (GRCm38) missense probably benign 0.31
R2112:Ankhd1 UTSW 18 36,641,626 (GRCm38) missense probably damaging 1.00
R2115:Ankhd1 UTSW 18 36,634,308 (GRCm38) missense probably damaging 1.00
R2136:Ankhd1 UTSW 18 36,647,621 (GRCm38) missense probably benign
R2196:Ankhd1 UTSW 18 36,648,379 (GRCm38) missense probably damaging 1.00
R2291:Ankhd1 UTSW 18 36,644,333 (GRCm38) missense probably benign 0.31
R2305:Ankhd1 UTSW 18 36,642,926 (GRCm38) missense possibly damaging 0.59
R2309:Ankhd1 UTSW 18 36,624,765 (GRCm38) missense probably damaging 1.00
R2519:Ankhd1 UTSW 18 36,578,543 (GRCm38) splice site probably null
R2958:Ankhd1 UTSW 18 36,634,729 (GRCm38) missense probably damaging 1.00
R3978:Ankhd1 UTSW 18 36,647,613 (GRCm38) missense probably damaging 0.96
R3980:Ankhd1 UTSW 18 36,647,613 (GRCm38) missense probably damaging 0.96
R4159:Ankhd1 UTSW 18 36,589,540 (GRCm38) missense possibly damaging 0.91
R4199:Ankhd1 UTSW 18 36,661,048 (GRCm38) unclassified probably benign
R4323:Ankhd1 UTSW 18 36,578,633 (GRCm38) missense probably damaging 1.00
R4356:Ankhd1 UTSW 18 36,643,043 (GRCm38) nonsense probably null
R4496:Ankhd1 UTSW 18 36,560,786 (GRCm38) missense probably damaging 0.98
R4551:Ankhd1 UTSW 18 36,655,507 (GRCm38) splice site probably null
R4590:Ankhd1 UTSW 18 36,583,644 (GRCm38) missense probably damaging 1.00
R4667:Ankhd1 UTSW 18 36,648,021 (GRCm38) missense possibly damaging 0.77
R4889:Ankhd1 UTSW 18 36,578,734 (GRCm38) missense probably null 0.00
R4923:Ankhd1 UTSW 18 36,589,452 (GRCm38) missense probably damaging 1.00
R5091:Ankhd1 UTSW 18 36,625,027 (GRCm38) missense possibly damaging 0.68
R5254:Ankhd1 UTSW 18 36,656,715 (GRCm38) missense probably benign 0.05
R5314:Ankhd1 UTSW 18 36,561,058 (GRCm38) splice site probably null
R5336:Ankhd1 UTSW 18 36,646,716 (GRCm38) missense probably damaging 1.00
R5367:Ankhd1 UTSW 18 36,589,408 (GRCm38) missense probably damaging 1.00
R5384:Ankhd1 UTSW 18 36,591,495 (GRCm38) missense probably damaging 1.00
R5385:Ankhd1 UTSW 18 36,591,495 (GRCm38) missense probably damaging 1.00
R5458:Ankhd1 UTSW 18 36,648,485 (GRCm38) missense probably benign 0.01
R5599:Ankhd1 UTSW 18 36,560,807 (GRCm38) missense probably damaging 0.98
R5659:Ankhd1 UTSW 18 36,561,050 (GRCm38) missense probably damaging 1.00
R5750:Ankhd1 UTSW 18 36,624,902 (GRCm38) missense probably benign 0.00
R5874:Ankhd1 UTSW 18 36,640,269 (GRCm38) missense possibly damaging 0.92
R5894:Ankhd1 UTSW 18 36,647,524 (GRCm38) missense probably damaging 0.99
R5969:Ankhd1 UTSW 18 36,600,834 (GRCm38) missense probably damaging 1.00
R6133:Ankhd1 UTSW 18 36,625,126 (GRCm38) missense possibly damaging 0.77
R6190:Ankhd1 UTSW 18 36,611,809 (GRCm38) missense possibly damaging 0.84
R6247:Ankhd1 UTSW 18 36,654,146 (GRCm38) missense probably benign 0.00
R6512:Ankhd1 UTSW 18 36,591,456 (GRCm38) missense probably damaging 1.00
R6649:Ankhd1 UTSW 18 36,600,783 (GRCm38) splice site probably null
R6653:Ankhd1 UTSW 18 36,600,783 (GRCm38) splice site probably null
R6763:Ankhd1 UTSW 18 36,642,969 (GRCm38) missense probably benign 0.31
R6976:Ankhd1 UTSW 18 36,648,254 (GRCm38) missense probably benign 0.00
R7075:Ankhd1 UTSW 18 36,559,989 (GRCm38) missense
R7208:Ankhd1 UTSW 18 36,625,028 (GRCm38) missense probably benign
R7305:Ankhd1 UTSW 18 36,632,205 (GRCm38) missense
R7615:Ankhd1 UTSW 18 36,656,773 (GRCm38) missense
R7654:Ankhd1 UTSW 18 36,594,101 (GRCm38) missense probably damaging 1.00
R7781:Ankhd1 UTSW 18 36,625,205 (GRCm38) missense probably damaging 1.00
R7842:Ankhd1 UTSW 18 36,647,828 (GRCm38) missense probably benign 0.00
R7965:Ankhd1 UTSW 18 36,658,412 (GRCm38) missense
R8006:Ankhd1 UTSW 18 36,648,719 (GRCm38) missense
R8037:Ankhd1 UTSW 18 36,638,623 (GRCm38) missense probably damaging 0.98
R8123:Ankhd1 UTSW 18 36,575,083 (GRCm38) missense
R8195:Ankhd1 UTSW 18 36,654,177 (GRCm38) missense
R8305:Ankhd1 UTSW 18 36,647,166 (GRCm38) missense possibly damaging 0.79
R8708:Ankhd1 UTSW 18 36,594,291 (GRCm38) missense probably damaging 1.00
R8827:Ankhd1 UTSW 18 36,624,580 (GRCm38) nonsense probably null
R9138:Ankhd1 UTSW 18 36,560,908 (GRCm38) small deletion probably benign
R9139:Ankhd1 UTSW 18 36,578,757 (GRCm38) missense
R9186:Ankhd1 UTSW 18 36,634,330 (GRCm38) missense possibly damaging 0.95
R9245:Ankhd1 UTSW 18 36,655,600 (GRCm38) missense
R9254:Ankhd1 UTSW 18 36,644,627 (GRCm38) missense probably benign 0.03
R9262:Ankhd1 UTSW 18 36,632,746 (GRCm38) missense
R9379:Ankhd1 UTSW 18 36,644,627 (GRCm38) missense probably benign 0.03
R9436:Ankhd1 UTSW 18 36,641,601 (GRCm38) missense probably benign 0.04
R9436:Ankhd1 UTSW 18 36,560,988 (GRCm38) missense probably benign 0.39
R9541:Ankhd1 UTSW 18 36,624,644 (GRCm38) missense
R9584:Ankhd1 UTSW 18 36,665,451 (GRCm38) missense probably benign 0.06
R9664:Ankhd1 UTSW 18 36,647,825 (GRCm38) missense probably benign 0.03
RF001:Ankhd1 UTSW 18 36,560,921 (GRCm38) small insertion probably benign
RF004:Ankhd1 UTSW 18 36,560,910 (GRCm38) small insertion probably benign
RF007:Ankhd1 UTSW 18 36,560,909 (GRCm38) small insertion probably benign
RF008:Ankhd1 UTSW 18 36,560,924 (GRCm38) small insertion probably benign
RF009:Ankhd1 UTSW 18 36,560,922 (GRCm38) small insertion probably benign
RF013:Ankhd1 UTSW 18 36,560,926 (GRCm38) small insertion probably benign
RF016:Ankhd1 UTSW 18 36,560,910 (GRCm38) small insertion probably benign
RF016:Ankhd1 UTSW 18 36,560,909 (GRCm38) small insertion probably benign
RF017:Ankhd1 UTSW 18 36,560,909 (GRCm38) small insertion probably benign
RF018:Ankhd1 UTSW 18 36,560,912 (GRCm38) small insertion probably benign
RF026:Ankhd1 UTSW 18 36,560,912 (GRCm38) small insertion probably benign
RF030:Ankhd1 UTSW 18 36,560,927 (GRCm38) small insertion probably benign
RF030:Ankhd1 UTSW 18 36,560,913 (GRCm38) small insertion probably benign
RF039:Ankhd1 UTSW 18 36,560,918 (GRCm38) small insertion probably benign
RF043:Ankhd1 UTSW 18 36,560,917 (GRCm38) small insertion probably benign
RF046:Ankhd1 UTSW 18 36,560,926 (GRCm38) small insertion probably benign
RF047:Ankhd1 UTSW 18 36,560,923 (GRCm38) small insertion probably benign
RF047:Ankhd1 UTSW 18 36,560,917 (GRCm38) small insertion probably benign
RF049:Ankhd1 UTSW 18 36,560,923 (GRCm38) small insertion probably benign
RF050:Ankhd1 UTSW 18 36,560,927 (GRCm38) small insertion probably benign
RF054:Ankhd1 UTSW 18 36,560,929 (GRCm38) small insertion probably benign
RF057:Ankhd1 UTSW 18 36,560,929 (GRCm38) small insertion probably benign
RF060:Ankhd1 UTSW 18 36,560,922 (GRCm38) small insertion probably benign
RF061:Ankhd1 UTSW 18 36,560,921 (GRCm38) small insertion probably benign
RF062:Ankhd1 UTSW 18 36,560,918 (GRCm38) small insertion probably benign
X0027:Ankhd1 UTSW 18 36,624,832 (GRCm38) missense probably damaging 1.00
X0065:Ankhd1 UTSW 18 36,578,764 (GRCm38) nonsense probably null
X0066:Ankhd1 UTSW 18 36,646,704 (GRCm38) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TACACCACTGAGTCTGGCTG -3'
(R):5'- ATAAAACTCTTACCTTTGCCCTGTG -3'

Sequencing Primer
(F):5'- CTGGCTGCATCTGGAGGATAC -3'
(R):5'- GCCCTGTGTTCAACATTGG -3'
Posted On 2016-08-04