Incidental Mutation 'R8933:Ankrd17'
ID 680430
Institutional Source Beutler Lab
Gene Symbol Ankrd17
Ensembl Gene ENSMUSG00000055204
Gene Name ankyrin repeat domain 17
Synonyms Gtar, A130069E23Rik, 4933425K22Rik
MMRRC Submission 068709-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R8933 (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 90406325 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Glycine at position 1453 (S1453G)
Ref Sequence ENSEMBL: ENSMUSP00000151446 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000014421] [ENSMUST00000081914] [ENSMUST00000168058] [ENSMUST00000197021] [ENSMUST00000218526]
AlphaFold Q99NH0
Predicted Effect possibly damaging
Transcript: ENSMUST00000014421
AA Change: S1453G

PolyPhen 2 Score 0.942 (Sensitivity: 0.80; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000014421
Gene: ENSMUSG00000055204
AA Change: S1453G

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: S1202G

PolyPhen 2 Score 0.044 (Sensitivity: 0.94; Specificity: 0.83)
SMART Domains Protein: ENSMUSP00000080587
Gene: ENSMUSG00000055204
AA Change: S1202G

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
SMART Domains Protein: ENSMUSP00000128960
Gene: ENSMUSG00000055204
AA Change: S1452G

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: S1344G

PolyPhen 2 Score 0.177 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000142575
Gene: ENSMUSG00000055204
AA Change: S1344G

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
Predicted Effect probably damaging
Transcript: ENSMUST00000218526
AA Change: S1453G

PolyPhen 2 Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.8%
  • 20x: 99.2%
Validation Efficiency 100% (86/86)
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: 86 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca4 T A 3: 121,921,786 (GRCm39) I1114N probably damaging Het
Ache C A 5: 137,288,449 (GRCm39) R52S possibly damaging Het
AI182371 A T 2: 34,975,714 (GRCm39) probably null Het
Arvcf A G 16: 18,218,845 (GRCm39) N508S probably damaging Het
Aurkc A C 7: 7,005,796 (GRCm39) D136A possibly damaging Het
Bfsp2 A G 9: 103,325,848 (GRCm39) M265T probably benign Het
Bmpr1b T C 3: 141,562,369 (GRCm39) T273A probably damaging Het
Cacnb1 T C 11: 97,896,578 (GRCm39) K406R probably damaging Het
Calcoco2 C T 11: 95,998,252 (GRCm39) probably benign Het
Capza1 T C 3: 104,748,209 (GRCm39) probably null Het
Ccdc63 T A 5: 122,251,265 (GRCm39) I382F probably damaging Het
Cep350 A T 1: 155,739,161 (GRCm39) N2227K probably benign Het
Chia1 T A 3: 106,036,333 (GRCm39) Y304* probably null Het
Col5a2 G A 1: 45,461,123 (GRCm39) P258L Het
Cyp21a1 A G 17: 35,023,285 (GRCm39) L30P probably damaging Het
Dennd4b T A 3: 90,186,523 (GRCm39) H1351Q probably benign Het
Dnah9 T A 11: 65,746,078 (GRCm39) I4012F possibly damaging Het
Drd1 A G 13: 54,207,290 (GRCm39) I301T possibly damaging Het
Dzip1 T A 14: 119,144,326 (GRCm39) H369L probably damaging Het
Fgfrl1 T A 5: 108,851,257 (GRCm39) M58K probably damaging Het
Ftsj3 G T 11: 106,141,660 (GRCm39) D529E probably benign Het
Fut9 A T 4: 25,619,861 (GRCm39) W318R probably damaging Het
Gabrg3 A G 7: 56,634,706 (GRCm39) I159T probably damaging Het
Gabrr1 A T 4: 33,146,972 (GRCm39) D53V probably benign Het
Ggps1 A G 13: 14,228,928 (GRCm39) V85A probably benign Het
Gm5141 C T 13: 62,924,854 (GRCm39) W18* probably null Het
Grik5 T A 7: 24,722,743 (GRCm39) T518S probably benign Het
Hapln3 A T 7: 78,767,378 (GRCm39) probably benign Het
Hbs1l C T 10: 21,243,584 (GRCm39) Q646* probably null Het
Hmox1 T C 8: 75,823,644 (GRCm39) I104T probably benign Het
Ifit1bl1 T C 19: 34,571,413 (GRCm39) Y348C probably damaging Het
Igf2r A T 17: 12,920,131 (GRCm39) S1403T probably damaging Het
Igf2r G A 17: 12,923,524 (GRCm39) T1186M probably damaging Het
Igfbp1 T C 11: 7,148,333 (GRCm39) probably null Het
Ikbip C A 10: 90,919,092 (GRCm39) A35E probably benign Het
Isca1 C T 13: 59,917,497 (GRCm39) A8T probably damaging Het
Itgb2 T C 10: 77,401,022 (GRCm39) L754P probably damaging Het
Itgb6 C T 2: 60,458,247 (GRCm39) C502Y probably damaging Het
Kdm3a A G 6: 71,577,092 (GRCm39) V741A probably benign Het
Kdsr T C 1: 106,680,949 (GRCm39) D83G possibly damaging Het
Kiz T A 2: 146,784,037 (GRCm39) N523K Het
Kmt2a T C 9: 44,733,802 (GRCm39) probably benign Het
Krt25 T C 11: 99,212,064 (GRCm39) E191G probably benign Het
Lipn A G 19: 34,046,880 (GRCm39) I61V probably damaging Het
Lmbr1l T A 15: 98,807,150 (GRCm39) probably null Het
Lrrc4c A G 2: 97,459,826 (GRCm39) K151E probably benign Het
Mab21l3 T C 3: 101,730,774 (GRCm39) Q155R probably benign Het
Mtfr2 G A 10: 20,233,274 (GRCm39) R281H possibly damaging Het
Muc5ac A G 7: 141,343,493 (GRCm39) Y35C possibly damaging Het
Myadm C T 7: 3,345,433 (GRCm39) T65I probably benign Het
Nap1l1 T C 10: 111,328,710 (GRCm39) V213A probably benign Het
Nav2 A G 7: 49,111,705 (GRCm39) D737G probably damaging Het
Ndst4 T A 3: 125,405,155 (GRCm39) V470D probably damaging Het
Nek5 T A 8: 22,601,226 (GRCm39) Y165F probably damaging Het
Nek5 A T 8: 22,610,859 (GRCm39) V48E probably damaging Het
Nr6a1 T C 2: 38,650,400 (GRCm39) I77V probably damaging Het
Nvl A T 1: 180,966,638 (GRCm39) D93E probably benign Het
Or11a4 C A 17: 37,536,346 (GRCm39) T110K possibly damaging Het
Or2q1 A G 6: 42,794,950 (GRCm39) T182A probably benign Het
Or52e5 A G 7: 104,718,599 (GRCm39) probably benign Het
Or52k2 A T 7: 102,253,637 (GRCm39) L25F probably damaging Het
Or52p1 A T 7: 104,266,873 (GRCm39) T4S probably benign Het
Or6c68 A T 10: 129,158,259 (GRCm39) I256F probably damaging Het
Pla2g4c G A 7: 13,073,627 (GRCm39) V225I probably benign Het
Plppr4 T A 3: 117,116,690 (GRCm39) N331I probably damaging Het
Ptpn13 A G 5: 103,727,671 (GRCm39) R2051G probably benign Het
Rbm45 T C 2: 76,209,068 (GRCm39) S346P probably damaging Het
Samd14 A C 11: 94,912,027 (GRCm39) D168A probably damaging Het
Slc15a1 C T 14: 121,724,091 (GRCm39) G172R probably benign Het
Slco3a1 G T 7: 73,934,248 (GRCm39) Y641* probably null Het
Srcap G A 7: 127,151,566 (GRCm39) R2027H probably damaging Het
Stra8 A T 6: 34,904,624 (GRCm39) probably benign Het
Syt11 T C 3: 88,655,011 (GRCm39) Y430C probably damaging Het
Tanc1 T G 2: 59,615,800 (GRCm39) V269G possibly damaging Het
Tead1 A G 7: 112,497,818 (GRCm39) N342S probably benign Het
Tenm3 C T 8: 48,732,095 (GRCm39) A1254T possibly damaging Het
Txlnb A T 10: 17,682,546 (GRCm39) N156I probably damaging Het
Ufl1 A T 4: 25,262,258 (GRCm39) S409R possibly damaging Het
Usp17la A G 7: 104,510,307 (GRCm39) H304R probably benign Het
Vmn1r203 T A 13: 22,708,691 (GRCm39) H157Q possibly damaging Het
Vmn1r37 C T 6: 66,709,231 (GRCm39) R249* probably null Het
Vmn2r96 A G 17: 18,804,241 (GRCm39) Q497R probably benign Het
Vps39 A G 2: 120,169,066 (GRCm39) S292P probably benign Het
Wnk1 A G 6: 120,013,959 (GRCm39) V212A probably damaging Het
Xbp1 T C 11: 5,474,741 (GRCm39) V161A probably benign Het
Zfp113 T C 5: 138,143,092 (GRCm39) Q386R probably damaging 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
R7468:Ankrd17 UTSW 5 90,390,902 (GRCm39) missense probably benign
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
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'- ATATTGCTCCAGTGCTATGATACACAG -3'
(R):5'- GATGTTTTGAGATTACTCTGCCTACC -3'

Sequencing Primer
(F):5'- CCAGTGCTATGATACACAGTCTAAG -3'
(R):5'- GAGATTACTCTGCCTACCCCCAG -3'
Posted On 2021-08-31