Incidental Mutation 'R7468:Ankrd17'
ID 578939
Institutional Source Beutler Lab
Gene Symbol Ankrd17
Ensembl Gene ENSMUSG00000055204
Gene Name ankyrin repeat domain 17
Synonyms Gtar, A130069E23Rik, 4933425K22Rik
MMRRC Submission 045542-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R7468 (G1)
Quality Score 225.009
Status Validated
Chromosome 5
Chromosomal Location 90375025-90514436 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 90390902 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Serine at position 2256 (N2256S)
Ref Sequence ENSEMBL: ENSMUSP00000014421 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000014421] [ENSMUST00000081914] [ENSMUST00000168058] [ENSMUST00000197021]
AlphaFold Q99NH0
Predicted Effect probably benign
Transcript: ENSMUST00000014421
AA Change: N2256S

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000014421
Gene: ENSMUSG00000055204
AA Change: N2256S

DomainStartEndE-ValueType
low complexity region 6 40 N/A INTRINSIC
low complexity region 55 71 N/A INTRINSIC
low complexity region 82 130 N/A INTRINSIC
ANK 229 258 8.62e1 SMART
ANK 262 291 3.31e-1 SMART
ANK 296 325 3.51e-5 SMART
ANK 329 358 1.33e-5 SMART
ANK 362 391 3.46e-4 SMART
ANK 396 425 3.23e-4 SMART
ANK 429 458 1.61e-4 SMART
ANK 462 491 1.46e-2 SMART
ANK 495 524 3.88e-7 SMART
ANK 529 558 4.19e-3 SMART
ANK 559 588 1.76e-5 SMART
ANK 592 621 3.51e-5 SMART
ANK 625 654 5.62e-4 SMART
ANK 659 688 1.29e-3 SMART
ANK 692 721 1.44e-1 SMART
coiled coil region 800 883 N/A INTRINSIC
low complexity region 890 903 N/A INTRINSIC
low complexity region 955 968 N/A INTRINSIC
low complexity region 986 997 N/A INTRINSIC
low complexity region 1046 1060 N/A INTRINSIC
ANK 1078 1107 2.13e-4 SMART
ANK 1111 1140 8.19e-6 SMART
ANK 1145 1174 1.68e-2 SMART
ANK 1178 1207 1.61e-4 SMART
ANK 1213 1242 1.43e-5 SMART
ANK 1247 1276 1.83e-3 SMART
ANK 1280 1309 3.91e-3 SMART
ANK 1315 1344 1.93e-2 SMART
ANK 1348 1377 8.78e-6 SMART
ANK 1381 1410 7.59e-1 SMART
coiled coil region 1454 1522 N/A INTRINSIC
low complexity region 1597 1611 N/A INTRINSIC
low complexity region 1616 1636 N/A INTRINSIC
KH 1720 1790 8.31e-14 SMART
low complexity region 1816 1827 N/A INTRINSIC
low complexity region 1834 1850 N/A INTRINSIC
low complexity region 1946 1989 N/A INTRINSIC
low complexity region 1996 2024 N/A INTRINSIC
low complexity region 2035 2052 N/A INTRINSIC
low complexity region 2068 2077 N/A INTRINSIC
low complexity region 2086 2110 N/A INTRINSIC
low complexity region 2175 2189 N/A INTRINSIC
low complexity region 2348 2365 N/A INTRINSIC
low complexity region 2392 2411 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000081914
AA Change: N2005S

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000080587
Gene: ENSMUSG00000055204
AA Change: N2005S

DomainStartEndE-ValueType
low complexity region 6 40 N/A INTRINSIC
low complexity region 55 71 N/A INTRINSIC
low complexity region 82 130 N/A INTRINSIC
ANK 229 258 8.62e1 SMART
ANK 262 291 3.31e-1 SMART
ANK 296 325 3.51e-5 SMART
ANK 329 358 1.33e-5 SMART
ANK 362 391 3.46e-4 SMART
ANK 396 425 3.23e-4 SMART
ANK 429 458 1.61e-4 SMART
ANK 462 491 1.46e-2 SMART
ANK 495 524 3.88e-7 SMART
ANK 529 558 4.19e-3 SMART
ANK 559 588 1.76e-5 SMART
ANK 592 621 3.51e-5 SMART
ANK 625 654 5.62e-4 SMART
ANK 659 688 1.29e-3 SMART
ANK 692 721 1.44e-1 SMART
low complexity region 795 809 N/A INTRINSIC
ANK 827 856 2.13e-4 SMART
ANK 860 889 8.19e-6 SMART
ANK 894 923 1.68e-2 SMART
ANK 927 956 1.61e-4 SMART
ANK 962 991 1.43e-5 SMART
ANK 996 1025 1.83e-3 SMART
ANK 1029 1058 3.91e-3 SMART
ANK 1064 1093 1.93e-2 SMART
ANK 1097 1126 8.78e-6 SMART
ANK 1130 1159 7.59e-1 SMART
coiled coil region 1203 1271 N/A INTRINSIC
low complexity region 1346 1360 N/A INTRINSIC
low complexity region 1365 1385 N/A INTRINSIC
KH 1469 1539 8.31e-14 SMART
low complexity region 1565 1576 N/A INTRINSIC
low complexity region 1583 1599 N/A INTRINSIC
low complexity region 1695 1738 N/A INTRINSIC
low complexity region 1745 1773 N/A INTRINSIC
low complexity region 1784 1801 N/A INTRINSIC
low complexity region 1817 1826 N/A INTRINSIC
low complexity region 1835 1859 N/A INTRINSIC
low complexity region 1924 1938 N/A INTRINSIC
low complexity region 2097 2114 N/A INTRINSIC
low complexity region 2141 2160 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000168058
AA Change: N2255S
SMART Domains Protein: ENSMUSP00000128960
Gene: ENSMUSG00000055204
AA Change: N2255S

DomainStartEndE-ValueType
low complexity region 6 40 N/A INTRINSIC
low complexity region 55 71 N/A INTRINSIC
low complexity region 82 130 N/A INTRINSIC
ANK 229 258 8.62e1 SMART
ANK 262 291 3.31e-1 SMART
ANK 296 325 3.51e-5 SMART
ANK 329 358 1.33e-5 SMART
ANK 362 391 3.46e-4 SMART
ANK 396 425 3.23e-4 SMART
ANK 429 458 1.61e-4 SMART
ANK 462 491 1.46e-2 SMART
ANK 495 524 3.88e-7 SMART
ANK 529 558 4.19e-3 SMART
ANK 559 588 1.76e-5 SMART
ANK 592 621 3.51e-5 SMART
ANK 625 654 5.62e-4 SMART
ANK 659 688 1.29e-3 SMART
ANK 692 721 1.44e-1 SMART
coiled coil region 800 883 N/A INTRINSIC
low complexity region 890 903 N/A INTRINSIC
low complexity region 955 968 N/A INTRINSIC
low complexity region 986 997 N/A INTRINSIC
low complexity region 1046 1060 N/A INTRINSIC
ANK 1078 1107 2.13e-4 SMART
ANK 1111 1140 8.19e-6 SMART
ANK 1145 1174 1.68e-2 SMART
ANK 1178 1207 1.61e-4 SMART
ANK 1213 1242 1.43e-5 SMART
ANK 1247 1276 1.83e-3 SMART
ANK 1280 1309 3.91e-3 SMART
ANK 1315 1344 1.93e-2 SMART
ANK 1348 1377 8.78e-6 SMART
ANK 1381 1410 7.59e-1 SMART
coiled coil region 1454 1522 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000197021
AA Change: N2147S

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000142575
Gene: ENSMUSG00000055204
AA Change: N2147S

DomainStartEndE-ValueType
ANK 120 149 5.4e-1 SMART
ANK 153 182 2e-3 SMART
ANK 187 216 2.2e-7 SMART
ANK 220 249 8.2e-8 SMART
ANK 253 282 2.2e-6 SMART
ANK 287 316 2.1e-6 SMART
ANK 320 349 9.9e-7 SMART
ANK 353 382 9.5e-5 SMART
ANK 386 415 2.4e-9 SMART
ANK 420 449 2.6e-5 SMART
ANK 450 479 1.1e-7 SMART
ANK 483 512 2.2e-7 SMART
ANK 516 545 3.5e-6 SMART
ANK 550 579 7.9e-6 SMART
ANK 583 612 8.9e-4 SMART
coiled coil region 691 774 N/A INTRINSIC
low complexity region 781 794 N/A INTRINSIC
low complexity region 846 859 N/A INTRINSIC
low complexity region 877 888 N/A INTRINSIC
low complexity region 937 951 N/A INTRINSIC
ANK 969 998 1.4e-6 SMART
ANK 1002 1031 5.3e-8 SMART
ANK 1036 1065 1e-4 SMART
ANK 1069 1098 1e-6 SMART
ANK 1104 1133 9.1e-8 SMART
ANK 1138 1167 1.2e-5 SMART
ANK 1171 1200 2.5e-5 SMART
ANK 1206 1235 1.2e-4 SMART
ANK 1239 1268 5.5e-8 SMART
ANK 1272 1301 4.7e-3 SMART
coiled coil region 1345 1413 N/A INTRINSIC
low complexity region 1488 1502 N/A INTRINSIC
low complexity region 1507 1527 N/A INTRINSIC
KH 1611 1681 5.1e-16 SMART
low complexity region 1707 1718 N/A INTRINSIC
low complexity region 1725 1741 N/A INTRINSIC
low complexity region 1837 1880 N/A INTRINSIC
low complexity region 1887 1915 N/A INTRINSIC
low complexity region 1926 1943 N/A INTRINSIC
low complexity region 1959 1968 N/A INTRINSIC
low complexity region 1977 2001 N/A INTRINSIC
low complexity region 2066 2080 N/A INTRINSIC
low complexity region 2239 2256 N/A INTRINSIC
low complexity region 2283 2302 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 98% (86/88)
MGI Phenotype FUNCTION: This gene encodes a protein with ankyrin repeats, which are associated with protein-protein interactions. Studies suggest that this protein is involved in liver development. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a null mutation display embryonic lethality during organogenesis with hemorrhages, impaired vascular smooth muscle cell development, impaired vascular integrity, and growth retardation. [provided by MGI curators]
Allele List at MGI

All alleles(133) : Targeted(4) Gene trapped(129)
Other mutations in this stock
Total: 88 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abl2 T G 1: 156,450,104 (GRCm39) N90K possibly damaging Het
Acox1 T C 11: 116,069,001 (GRCm39) T415A possibly damaging Het
Acy1 T C 9: 106,314,921 (GRCm39) M1V probably null Het
Akap13 G A 7: 75,380,213 (GRCm39) R462H probably damaging Het
Alpk3 C A 7: 80,750,746 (GRCm39) Y1505* probably null Het
Ankrd22 C A 19: 34,126,692 (GRCm39) C46F possibly damaging Het
Arhgef5 A T 6: 43,257,605 (GRCm39) K1291* probably null Het
Arl9 T A 5: 77,158,276 (GRCm39) Y119* probably null Het
Asb14 T C 14: 26,622,805 (GRCm39) V89A probably benign Het
Banp T G 8: 122,676,588 (GRCm39) probably null Het
Btn2a2 T C 13: 23,666,933 (GRCm39) N224S probably benign Het
C1ra C T 6: 124,499,403 (GRCm39) Q530* probably null Het
C2cd6 A C 1: 59,107,844 (GRCm39) S273A probably benign Het
Cd1d2 A T 3: 86,895,583 (GRCm39) probably null Het
Cdc42bpb T C 12: 111,306,307 (GRCm39) D132G probably damaging Het
Cfap45 C A 1: 172,362,877 (GRCm39) Y289* probably null Het
Chrdl2 T C 7: 99,659,332 (GRCm39) probably null Het
Cilk1 A G 9: 78,065,221 (GRCm39) K377R probably benign Het
Cst5 C T 2: 149,247,496 (GRCm39) L71F probably benign Het
Dcaf11 T C 14: 55,802,966 (GRCm39) F292L possibly damaging Het
Dgcr8 A G 16: 18,077,487 (GRCm39) F641S probably damaging Het
Dnm3 G A 1: 162,149,198 (GRCm39) probably null Het
Efcab3 G T 11: 104,640,526 (GRCm39) S1088I probably benign Het
Eral1 T C 11: 77,966,219 (GRCm39) K320E probably damaging Het
Eva1a A G 6: 82,069,002 (GRCm39) T110A possibly damaging Het
Fbxo42 A G 4: 140,926,917 (GRCm39) D399G possibly damaging Het
Frs2 T C 10: 116,910,007 (GRCm39) T452A possibly damaging Het
Git2 T A 5: 114,871,958 (GRCm39) D542V probably damaging Het
Grk2 T A 19: 4,356,063 (GRCm39) probably benign Het
Gsg1l2 A G 11: 67,676,110 (GRCm39) N158S possibly damaging Het
Hc T C 2: 34,918,063 (GRCm39) N740S probably benign Het
Hectd1 T C 12: 51,791,588 (GRCm39) probably null Het
Hemk1 A G 9: 107,208,288 (GRCm39) probably null Het
Hormad2 G T 11: 4,362,245 (GRCm39) Y126* probably null Het
Hr A G 14: 70,795,652 (GRCm39) E399G possibly damaging Het
Ilf3 C A 9: 21,314,707 (GRCm39) H780N unknown Het
Inpp5e A T 2: 26,298,161 (GRCm39) S147T probably benign Het
Irag2 C A 6: 145,119,427 (GRCm39) probably null Het
Jmjd6 T C 11: 116,733,275 (GRCm39) D134G probably damaging Het
Kif23 G T 9: 61,844,457 (GRCm39) Y120* probably null Het
Klk12 T A 7: 43,422,780 (GRCm39) Y236N probably damaging Het
Kmt5b C A 19: 3,852,799 (GRCm39) Y186* probably null Het
Krtap9-5 A G 11: 99,840,132 (GRCm39) T278A unknown Het
Lca5 T A 9: 83,305,509 (GRCm39) D99V probably damaging Het
Leng9 A G 7: 4,151,800 (GRCm39) V292A probably benign Het
Lime1 A G 2: 181,025,135 (GRCm39) R231G probably benign Het
Mctp2 T A 7: 71,861,438 (GRCm39) E402D probably damaging Het
Mrpl28 T A 17: 26,343,589 (GRCm39) S116R probably damaging Het
Muc15 A T 2: 110,561,862 (GRCm39) R99S probably benign Het
Myh2 G A 11: 67,083,368 (GRCm39) A1444T probably benign Het
Mynn T A 3: 30,657,825 (GRCm39) Y48N probably damaging Het
Myo1b A T 1: 51,836,639 (GRCm39) V274E possibly damaging Het
Nemp1 T A 10: 127,528,923 (GRCm39) M209K possibly damaging Het
Nlrc4 G T 17: 74,752,507 (GRCm39) D625E probably benign Het
Or10al6 C T 17: 38,082,910 (GRCm39) A122V probably damaging Het
Or11a4 T C 17: 37,536,276 (GRCm39) F87L probably benign Het
Or4p4 T C 2: 88,482,622 (GRCm39) L42P probably damaging Het
Otog T C 7: 45,913,543 (GRCm39) V792A probably benign Het
Paqr8 T C 1: 21,005,442 (GRCm39) Y199H probably damaging Het
Popdc3 A G 10: 45,191,117 (GRCm39) D76G probably damaging Het
Ppme1 T C 7: 99,991,069 (GRCm39) N210D probably benign Het
Prdm15 A C 16: 97,636,842 (GRCm39) Y158* probably null Het
Prrg2 A T 7: 44,709,687 (GRCm39) L70Q probably benign Het
Psmg4 C T 13: 34,361,966 (GRCm39) R85W probably damaging Het
Rab11fip4 A T 11: 79,580,478 (GRCm39) T437S probably benign Het
Rap2a T A 14: 120,716,338 (GRCm39) M67K probably damaging Het
Rnf123 A T 9: 107,946,208 (GRCm39) H322Q probably benign Het
Rxfp2 A T 5: 149,990,801 (GRCm39) T521S possibly damaging Het
Scrn2 T G 11: 96,923,992 (GRCm39) V292G possibly damaging Het
Serpina3n C A 12: 104,377,656 (GRCm39) P303H probably benign Het
Spop C T 11: 95,376,727 (GRCm39) T260M probably damaging Het
Surf2 G A 2: 26,809,354 (GRCm39) G224D probably benign Het
Synm T G 7: 67,382,971 (GRCm39) N669T unknown Het
Tmprss13 T C 9: 45,239,721 (GRCm39) S10P unknown Het
Trav9d-1 T A 14: 53,029,970 (GRCm39) S25T probably benign Het
Trpc3 A T 3: 36,678,565 (GRCm39) I840K probably damaging Het
Tsbp1 T A 17: 34,636,539 (GRCm39) probably null Het
Tssc4 C A 7: 142,622,999 (GRCm39) probably benign Het
Ttc39d G T 17: 80,523,579 (GRCm39) R79S possibly damaging Het
Txlnb T A 10: 17,675,082 (GRCm39) S78R probably damaging Het
Vmn1r142 T A 7: 21,862,784 (GRCm39) Q226L possibly damaging Het
Vmn1r230 T C 17: 21,067,146 (GRCm39) S112P probably damaging Het
Wrnip1 T C 13: 33,000,360 (GRCm39) F456L possibly damaging Het
Zc3h8 G T 2: 128,775,215 (GRCm39) H148Q probably benign Het
Zcchc3 A G 2: 152,256,615 (GRCm39) V28A probably benign Het
Zdbf2 T A 1: 63,346,669 (GRCm39) C1683S probably benign Het
Zfp874a T C 13: 67,573,723 (GRCm39) probably null Het
Zmym4 A G 4: 126,776,029 (GRCm39) S1260P probably benign Het
Other mutations in Ankrd17
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00236:Ankrd17 APN 5 90,381,787 (GRCm39) missense probably damaging 0.98
IGL00484:Ankrd17 APN 5 90,416,220 (GRCm39) missense probably damaging 0.99
IGL01320:Ankrd17 APN 5 90,407,988 (GRCm39) missense probably damaging 0.99
IGL01776:Ankrd17 APN 5 90,431,223 (GRCm39) nonsense probably null
IGL02093:Ankrd17 APN 5 90,390,822 (GRCm39) missense possibly damaging 0.93
IGL02292:Ankrd17 APN 5 90,400,718 (GRCm39) unclassified probably benign
IGL02302:Ankrd17 APN 5 90,431,057 (GRCm39) missense probably benign 0.23
IGL02472:Ankrd17 APN 5 90,412,010 (GRCm39) missense probably damaging 1.00
IGL02705:Ankrd17 APN 5 90,430,974 (GRCm39) missense probably benign 0.15
IGL02727:Ankrd17 APN 5 90,392,151 (GRCm39) missense possibly damaging 0.93
IGL02884:Ankrd17 APN 5 90,412,616 (GRCm39) missense probably damaging 1.00
3-1:Ankrd17 UTSW 5 90,391,013 (GRCm39) missense probably damaging 0.99
PIT1430001:Ankrd17 UTSW 5 90,400,832 (GRCm39) missense possibly damaging 0.91
R0025:Ankrd17 UTSW 5 90,398,264 (GRCm39) missense probably damaging 0.99
R0076:Ankrd17 UTSW 5 90,392,265 (GRCm39) nonsense probably null
R0076:Ankrd17 UTSW 5 90,392,265 (GRCm39) nonsense probably null
R0271:Ankrd17 UTSW 5 90,402,658 (GRCm39) missense possibly damaging 0.90
R0684:Ankrd17 UTSW 5 90,411,857 (GRCm39) missense probably damaging 0.99
R1239:Ankrd17 UTSW 5 90,436,535 (GRCm39) missense probably damaging 0.99
R1457:Ankrd17 UTSW 5 90,433,705 (GRCm39) missense possibly damaging 0.92
R1505:Ankrd17 UTSW 5 90,447,885 (GRCm39) missense possibly damaging 0.53
R1766:Ankrd17 UTSW 5 90,412,656 (GRCm39) missense possibly damaging 0.95
R1770:Ankrd17 UTSW 5 90,391,235 (GRCm39) missense possibly damaging 0.84
R1780:Ankrd17 UTSW 5 90,380,274 (GRCm39) missense probably damaging 0.96
R1916:Ankrd17 UTSW 5 90,408,000 (GRCm39) missense probably damaging 1.00
R1926:Ankrd17 UTSW 5 90,392,028 (GRCm39) missense probably damaging 1.00
R2090:Ankrd17 UTSW 5 90,445,905 (GRCm39) missense possibly damaging 0.92
R2153:Ankrd17 UTSW 5 90,381,918 (GRCm39) missense probably damaging 0.98
R2279:Ankrd17 UTSW 5 90,412,576 (GRCm39) missense probably damaging 1.00
R2420:Ankrd17 UTSW 5 90,437,179 (GRCm39) missense possibly damaging 0.94
R3012:Ankrd17 UTSW 5 90,378,727 (GRCm39) missense probably damaging 1.00
R3417:Ankrd17 UTSW 5 90,391,772 (GRCm39) missense possibly damaging 0.86
R3704:Ankrd17 UTSW 5 90,391,828 (GRCm39) missense possibly damaging 0.72
R4581:Ankrd17 UTSW 5 90,430,979 (GRCm39) missense possibly damaging 0.67
R4850:Ankrd17 UTSW 5 90,412,645 (GRCm39) missense probably damaging 1.00
R4926:Ankrd17 UTSW 5 90,447,891 (GRCm39) missense probably damaging 1.00
R5023:Ankrd17 UTSW 5 90,430,727 (GRCm39) missense probably damaging 1.00
R5068:Ankrd17 UTSW 5 90,402,667 (GRCm39) missense probably damaging 0.96
R5109:Ankrd17 UTSW 5 90,391,395 (GRCm39) missense possibly damaging 0.83
R5111:Ankrd17 UTSW 5 90,390,858 (GRCm39) missense possibly damaging 0.85
R5214:Ankrd17 UTSW 5 90,431,319 (GRCm39) missense possibly damaging 0.48
R5362:Ankrd17 UTSW 5 90,413,404 (GRCm39) missense probably damaging 1.00
R5576:Ankrd17 UTSW 5 90,391,083 (GRCm39) missense probably benign 0.00
R5615:Ankrd17 UTSW 5 90,431,295 (GRCm39) missense possibly damaging 0.88
R5874:Ankrd17 UTSW 5 90,416,656 (GRCm39) intron probably benign
R5932:Ankrd17 UTSW 5 90,413,295 (GRCm39) missense probably damaging 1.00
R5944:Ankrd17 UTSW 5 90,433,702 (GRCm39) missense probably damaging 1.00
R5993:Ankrd17 UTSW 5 90,487,531 (GRCm39) intron probably benign
R6052:Ankrd17 UTSW 5 90,401,691 (GRCm39) missense probably benign 0.03
R6088:Ankrd17 UTSW 5 90,401,547 (GRCm39) missense possibly damaging 0.95
R6306:Ankrd17 UTSW 5 90,392,013 (GRCm39) missense probably benign 0.03
R6418:Ankrd17 UTSW 5 90,426,204 (GRCm39) missense possibly damaging 0.89
R6663:Ankrd17 UTSW 5 90,411,923 (GRCm39) missense probably damaging 1.00
R6758:Ankrd17 UTSW 5 90,411,172 (GRCm39) missense probably damaging 1.00
R6782:Ankrd17 UTSW 5 90,402,597 (GRCm39) missense possibly damaging 0.91
R6793:Ankrd17 UTSW 5 90,413,371 (GRCm39) missense probably damaging 1.00
R6929:Ankrd17 UTSW 5 90,433,384 (GRCm39) missense possibly damaging 0.86
R7008:Ankrd17 UTSW 5 90,407,955 (GRCm39) missense possibly damaging 0.93
R7051:Ankrd17 UTSW 5 90,514,310 (GRCm39) unclassified probably benign
R7077:Ankrd17 UTSW 5 90,433,723 (GRCm39) missense possibly damaging 0.92
R7134:Ankrd17 UTSW 5 90,433,382 (GRCm39) missense probably benign 0.03
R7134:Ankrd17 UTSW 5 90,380,173 (GRCm39) missense probably damaging 0.99
R7138:Ankrd17 UTSW 5 90,390,836 (GRCm39) missense probably benign 0.38
R7143:Ankrd17 UTSW 5 90,433,820 (GRCm39) missense possibly damaging 0.85
R7173:Ankrd17 UTSW 5 90,407,976 (GRCm39) missense possibly damaging 0.95
R7176:Ankrd17 UTSW 5 90,416,594 (GRCm39) missense probably damaging 0.99
R7365:Ankrd17 UTSW 5 90,439,010 (GRCm39) missense possibly damaging 0.45
R7390:Ankrd17 UTSW 5 90,430,779 (GRCm39) missense probably benign 0.13
R7430:Ankrd17 UTSW 5 90,443,516 (GRCm39) missense possibly damaging 0.80
R7483:Ankrd17 UTSW 5 90,447,855 (GRCm39) missense probably benign 0.00
R7492:Ankrd17 UTSW 5 90,381,807 (GRCm39) missense possibly damaging 0.85
R7610:Ankrd17 UTSW 5 90,380,222 (GRCm39) missense possibly damaging 0.93
R7636:Ankrd17 UTSW 5 90,380,239 (GRCm39) missense possibly damaging 0.53
R7790:Ankrd17 UTSW 5 90,408,011 (GRCm39) missense possibly damaging 0.61
R7839:Ankrd17 UTSW 5 90,411,213 (GRCm39) missense probably damaging 0.97
R7853:Ankrd17 UTSW 5 90,386,825 (GRCm39) missense possibly damaging 0.91
R7976:Ankrd17 UTSW 5 90,431,451 (GRCm39) nonsense probably null
R8054:Ankrd17 UTSW 5 90,438,914 (GRCm39) missense probably benign 0.43
R8230:Ankrd17 UTSW 5 90,391,835 (GRCm39) missense possibly damaging 0.86
R8274:Ankrd17 UTSW 5 90,430,718 (GRCm39) missense probably benign 0.15
R8365:Ankrd17 UTSW 5 90,398,378 (GRCm39) missense possibly damaging 0.95
R8532:Ankrd17 UTSW 5 90,412,679 (GRCm39) missense probably damaging 1.00
R8729:Ankrd17 UTSW 5 90,443,452 (GRCm39) missense probably benign
R8812:Ankrd17 UTSW 5 90,441,062 (GRCm39) missense probably benign 0.09
R8933:Ankrd17 UTSW 5 90,406,325 (GRCm39) missense probably damaging 0.99
R9051:Ankrd17 UTSW 5 90,411,134 (GRCm39) missense probably damaging 0.99
R9055:Ankrd17 UTSW 5 90,380,168 (GRCm39) missense probably benign 0.33
R9136:Ankrd17 UTSW 5 90,392,278 (GRCm39) missense probably damaging 0.96
R9158:Ankrd17 UTSW 5 90,416,575 (GRCm39) missense probably damaging 1.00
R9201:Ankrd17 UTSW 5 90,378,798 (GRCm39) missense possibly damaging 0.84
R9315:Ankrd17 UTSW 5 90,398,360 (GRCm39) missense probably damaging 0.97
R9364:Ankrd17 UTSW 5 90,416,508 (GRCm39) missense probably damaging 1.00
R9366:Ankrd17 UTSW 5 90,416,508 (GRCm39) missense probably damaging 1.00
R9368:Ankrd17 UTSW 5 90,416,508 (GRCm39) missense probably damaging 1.00
R9368:Ankrd17 UTSW 5 90,391,986 (GRCm39) missense possibly damaging 0.91
R9369:Ankrd17 UTSW 5 90,416,508 (GRCm39) missense probably damaging 1.00
R9381:Ankrd17 UTSW 5 90,416,508 (GRCm39) missense probably damaging 1.00
R9570:Ankrd17 UTSW 5 90,401,536 (GRCm39) missense
X0019:Ankrd17 UTSW 5 90,446,513 (GRCm39) missense probably damaging 1.00
Z1177:Ankrd17 UTSW 5 90,437,184 (GRCm39) missense possibly damaging 0.86
Z1177:Ankrd17 UTSW 5 90,431,364 (GRCm39) missense possibly damaging 0.83
Predicted Primers PCR Primer
(F):5'- ACACTTACCTGAGGGACTTGG -3'
(R):5'- ACAAGACTCCAGCTCCAGTG -3'

Sequencing Primer
(F):5'- CTTACCTGAGGGACTTGGAGCAG -3'
(R):5'- AGCTCCAGTGCAGAGTTCATC -3'
Posted On 2019-10-07