Incidental Mutation 'R7134:Ankrd17'
ID 552901
Institutional Source Beutler Lab
Gene Symbol Ankrd17
Ensembl Gene ENSMUSG00000055204
Gene Name ankyrin repeat domain 17
Synonyms Gtar, A130069E23Rik, 4933425K22Rik
MMRRC Submission 045219-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R7134 (G1)
Quality Score 225.009
Status Validated
Chromosome 5
Chromosomal Location 90375025-90514436 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 90380173 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Isoleucine at position 2505 (T2505I)
Ref Sequence ENSEMBL: ENSMUSP00000014421 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000014421] [ENSMUST00000081914] [ENSMUST00000168058] [ENSMUST00000197021]
AlphaFold Q99NH0
Predicted Effect probably damaging
Transcript: ENSMUST00000014421
AA Change: T2505I

PolyPhen 2 Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000014421
Gene: ENSMUSG00000055204
AA Change: T2505I

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: T2254I

PolyPhen 2 Score 0.030 (Sensitivity: 0.95; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000080587
Gene: ENSMUSG00000055204
AA Change: T2254I

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: T2504I
SMART Domains Protein: ENSMUSP00000128960
Gene: ENSMUSG00000055204
AA Change: T2504I

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 possibly damaging
Transcript: ENSMUST00000197021
AA Change: T2396I

PolyPhen 2 Score 0.861 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000142575
Gene: ENSMUSG00000055204
AA Change: T2396I

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: 99.9%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 99% (84/85)
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: 85 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcf1 A G 17: 36,270,144 (GRCm39) F638S possibly damaging Het
Actl6b T A 5: 137,562,762 (GRCm39) N159K probably damaging Het
Adam6a T G 12: 113,508,655 (GRCm39) S343A probably benign Het
Asap2 G T 12: 21,315,964 (GRCm39) E919* probably null Het
Atp10b A T 11: 43,136,291 (GRCm39) I1140F probably damaging Het
Cep126 A T 9: 8,103,383 (GRCm39) V209E probably damaging Het
Cfap65 C T 1: 74,965,792 (GRCm39) R406Q probably benign Het
Cldn1 T C 16: 26,190,376 (GRCm39) M1V probably null Het
Cryl1 C T 14: 57,512,956 (GRCm39) D304N probably benign Het
D3Ertd751e T C 3: 41,708,212 (GRCm39) probably null Het
D630044L22Rik A T 17: 26,181,090 (GRCm39) M156L probably benign Het
Ddx21 T C 10: 62,427,634 (GRCm39) D423G possibly damaging Het
Dock2 T A 11: 34,260,363 (GRCm39) M993L probably benign Het
Dusp29 A T 14: 21,727,129 (GRCm39) I173N probably damaging Het
Eif4g1 C T 16: 20,500,252 (GRCm39) A675V probably damaging Het
Eml1 C T 12: 108,472,810 (GRCm39) S206L probably benign Het
Farp2 A C 1: 93,531,181 (GRCm39) I560L probably benign Het
Fbn1 A T 2: 125,223,969 (GRCm39) D593E probably benign Het
Fetub A G 16: 22,748,007 (GRCm39) D61G possibly damaging Het
Fpgs T C 2: 32,576,641 (GRCm39) K329E probably benign Het
Fpgt T C 3: 154,797,120 (GRCm39) Y45C probably damaging Het
Gas2l1 A T 11: 5,011,106 (GRCm39) C574* probably null Het
Gm9747 G T 1: 82,211,837 (GRCm39) C12F unknown Het
H2-T23 T C 17: 36,342,709 (GRCm39) Y143C probably damaging Het
Hhip A T 8: 80,719,142 (GRCm39) S462T probably benign Het
Hnf1a C T 5: 115,091,446 (GRCm39) G416R probably damaging Het
Hoxa5 C T 6: 52,181,023 (GRCm39) C103Y probably damaging Het
Kansl3 G T 1: 36,390,848 (GRCm39) D395E possibly damaging Het
Marchf10 A G 11: 105,299,502 (GRCm39) S116P probably benign Het
Med12l C T 3: 59,001,180 (GRCm39) Q748* probably null Het
Mroh7 T A 4: 106,577,791 (GRCm39) N296Y probably damaging Het
Mtbp T G 15: 55,421,961 (GRCm39) D61E probably benign Het
Muc5b A T 7: 141,411,391 (GRCm39) I1446L unknown Het
Myh15 T C 16: 48,901,705 (GRCm39) V266A possibly damaging Het
Nap1l1 G A 10: 111,330,655 (GRCm39) probably null Het
Napsa A G 7: 44,235,159 (GRCm39) T315A probably benign Het
Nlrc5 A T 8: 95,206,350 (GRCm39) I734F probably damaging Het
Nnt A G 13: 119,531,198 (GRCm39) V183A probably damaging Het
Nploc4 A T 11: 120,276,614 (GRCm39) D477E probably benign Het
Nrip3 A G 7: 109,364,695 (GRCm39) S144P probably damaging Het
Ntng1 A T 3: 109,842,445 (GRCm39) F109L probably benign Het
Or5p61 A G 7: 107,758,883 (GRCm39) Y66H probably damaging Het
Or5v1 T A 17: 37,809,776 (GRCm39) V78D probably damaging Het
Or6aa1 G A 7: 86,044,752 (GRCm39) probably benign Het
Or8b36 A G 9: 37,937,795 (GRCm39) E231G probably benign Het
Pacsin1 G A 17: 27,921,707 (GRCm39) D30N probably damaging Het
Pbld2 A T 10: 62,860,368 (GRCm39) probably benign Het
Pcnx4 C T 12: 72,613,750 (GRCm39) T565I probably damaging Het
Pdzk1 A T 3: 96,763,246 (GRCm39) T225S probably benign Het
Phyhip T G 14: 70,704,639 (GRCm39) I286S probably benign Het
Pkd1 T A 17: 24,813,086 (GRCm39) Y3903N probably damaging Het
Plcb3 A T 19: 6,942,698 (GRCm39) L222Q probably damaging Het
Plcd4 T A 1: 74,593,662 (GRCm39) H262Q probably benign Het
Plekhh1 C T 12: 79,109,390 (GRCm39) A474V probably benign Het
Plppr3 T C 10: 79,701,537 (GRCm39) E435G probably damaging Het
Poln T A 5: 34,276,340 (GRCm39) N305I possibly damaging Het
Pou3f2 T C 4: 22,486,874 (GRCm39) T420A probably benign Het
Ppdpf T C 2: 180,829,523 (GRCm39) Y17H probably damaging Het
Prrx2 C A 2: 30,768,485 (GRCm39) T104K probably damaging Het
Ptprj A T 2: 90,294,822 (GRCm39) L462H probably benign Het
Radil T C 5: 142,471,304 (GRCm39) T991A probably damaging Het
Rbsn T C 6: 92,178,608 (GRCm39) E147G probably damaging Het
Ror2 C T 13: 53,300,742 (GRCm39) V35M probably benign Het
Rps6ka1 T C 4: 133,599,373 (GRCm39) Q18R probably benign Het
Setbp1 T A 18: 78,902,734 (GRCm39) D311V possibly damaging Het
Setd2 C T 9: 110,377,865 (GRCm39) S560L possibly damaging Het
Slc12a5 A T 2: 164,816,878 (GRCm39) I134F probably damaging Het
Speer1h C T 5: 11,647,706 (GRCm39) T148I possibly damaging Het
Svil A G 18: 5,116,080 (GRCm39) D2035G probably damaging Het
Syngap1 T C 17: 27,178,985 (GRCm39) Y665H probably damaging Het
Tbc1d9b T C 11: 50,043,519 (GRCm39) Y547H possibly damaging Het
Tgm2 A G 2: 157,980,812 (GRCm39) V83A probably benign Het
Tmem233 T C 5: 116,189,429 (GRCm39) I117V probably benign Het
Tsen34 A G 7: 3,703,640 (GRCm39) T293A probably damaging Het
Ttn A G 2: 76,709,023 (GRCm39) V8752A unknown Het
Ubac1 A G 2: 25,904,974 (GRCm39) V88A probably benign Het
Uchl4 T C 9: 64,142,621 (GRCm39) V34A probably damaging Het
Ugt2a2 C T 5: 87,608,435 (GRCm39) R468H probably benign Het
Vmn2r102 A T 17: 19,897,749 (GRCm39) T255S probably benign Het
Wdr6 T A 9: 108,450,564 (GRCm39) N988I probably damaging Het
Wnk1 A T 6: 119,903,389 (GRCm39) I2359N unknown Het
Ybey A G 10: 76,304,025 (GRCm39) V59A probably benign Het
Zfp268 T A 4: 145,349,375 (GRCm39) C271S possibly damaging Het
Zfp397 A G 18: 24,090,122 (GRCm39) N142S probably benign Het
Zfy1 A T Y: 725,788 (GRCm39) V659E 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
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
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'- CACAGCTTATGCACTTGGAAATG -3'
(R):5'- CACTAAGCAACATGGATATACTGCTG -3'

Sequencing Primer
(F):5'- GCTTATGCACTTGGAAATGAAAGATG -3'
(R):5'- GCAACATGGATATACTGCTGTAAAC -3'
Posted On 2019-05-15