Incidental Mutation 'R5944:Ankrd17'
ID 460469
Institutional Source Beutler Lab
Gene Symbol Ankrd17
Ensembl Gene ENSMUSG00000055204
Gene Name ankyrin repeat domain 17
Synonyms Gtar, A130069E23Rik, 4933425K22Rik
MMRRC Submission 044136-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R5944 (G1)
Quality Score 122
Status Validated
Chromosome 5
Chromosomal Location 90375025-90514436 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 90433702 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Histidine at position 689 (R689H)
Ref Sequence ENSEMBL: ENSMUSP00000151446 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000014421] [ENSMUST00000081914] [ENSMUST00000168058] [ENSMUST00000197021] [ENSMUST00000218526]
AlphaFold Q99NH0
Predicted Effect probably benign
Transcript: ENSMUST00000014421
AA Change: R689H

PolyPhen 2 Score 0.063 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000014421
Gene: ENSMUSG00000055204
AA Change: R689H

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 possibly damaging
Transcript: ENSMUST00000081914
AA Change: R689H

PolyPhen 2 Score 0.954 (Sensitivity: 0.79; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000080587
Gene: ENSMUSG00000055204
AA Change: R689H

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: R689H
SMART Domains Protein: ENSMUSP00000128960
Gene: ENSMUSG00000055204
AA Change: R689H

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 unknown
Transcript: ENSMUST00000197021
AA Change: R580H
SMART Domains Protein: ENSMUSP00000142575
Gene: ENSMUSG00000055204
AA Change: R580H

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 noncoding transcript
Transcript: ENSMUST00000200012
Predicted Effect probably damaging
Transcript: ENSMUST00000218526
AA Change: R689H

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
Meta Mutation Damage Score 0.1275 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 97.9%
  • 20x: 93.8%
Validation Efficiency 86% (51/59)
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: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acacb G T 5: 114,384,041 (GRCm39) R2190L probably damaging Het
Apol7b A T 15: 77,307,967 (GRCm39) V176E probably damaging Het
Arsg T C 11: 109,426,137 (GRCm39) F319S probably damaging Het
Bcar3 T A 3: 122,316,932 (GRCm39) D634E probably benign Het
Bend7 T C 2: 4,749,167 (GRCm39) W95R probably damaging Het
Cenpj A G 14: 56,791,115 (GRCm39) probably null Het
Cfap91 G T 16: 38,148,672 (GRCm39) T252N probably damaging Het
Clasrp A T 7: 19,328,431 (GRCm39) Y116N probably damaging Het
Cldn17 T C 16: 88,303,597 (GRCm39) E44G probably damaging Het
Cyfip1 G A 7: 55,521,878 (GRCm39) E61K probably damaging Het
Dcaf13 A C 15: 39,010,072 (GRCm39) M419L probably benign Het
Eml4 A G 17: 83,753,472 (GRCm39) D269G possibly damaging Het
Fap T C 2: 62,372,605 (GRCm39) Y258C probably damaging Het
Fdxr T A 11: 115,160,672 (GRCm39) T288S probably benign Het
Frs3 T C 17: 48,003,233 (GRCm39) probably benign Het
Gm5581 T A 6: 131,145,363 (GRCm39) noncoding transcript Het
Gm7964 A G 7: 83,405,743 (GRCm39) D187G probably benign Het
Gpc5 T C 14: 115,607,250 (GRCm39) V284A probably benign Het
Hspa9 T C 18: 35,082,076 (GRCm39) T177A possibly damaging Het
Ifi202b T A 1: 173,791,365 (GRCm39) M438L probably benign Het
Ighv1-3 T C 12: 114,445,239 (GRCm39) probably benign Het
Krt36 G T 11: 99,996,139 (GRCm39) A95E probably benign Het
Krt9 C T 11: 100,079,265 (GRCm39) S709N unknown Het
Lmntd1 A T 6: 145,373,042 (GRCm39) S164T probably damaging Het
Or14c41 T A 7: 86,234,486 (GRCm39) M1K probably null Het
Or2ag1b A T 7: 106,288,853 (GRCm39) C28* probably null Het
Or52n4b G A 7: 108,144,484 (GRCm39) A249T possibly damaging Het
Or5b94 C T 19: 12,652,283 (GRCm39) T238I probably damaging Het
Or7a41 A T 10: 78,871,223 (GRCm39) M198L probably benign Het
Papola T A 12: 105,778,644 (GRCm39) F341I possibly damaging Het
Phf3 A G 1: 30,859,785 (GRCm39) L914P probably damaging Het
Sec24d T C 3: 123,087,230 (GRCm39) V132A probably benign Het
Serpini1 G A 3: 75,547,606 (GRCm39) D373N probably damaging Het
Sigirr T C 7: 140,671,300 (GRCm39) Y394C probably damaging Het
Slc29a4 G A 5: 142,704,573 (GRCm39) E372K probably damaging Het
Slc7a4 C T 16: 17,392,220 (GRCm39) V405I possibly damaging Het
Spatc1 T C 15: 76,168,138 (GRCm39) L199P probably damaging Het
Srgap3 T C 6: 112,772,775 (GRCm39) M149V possibly damaging Het
Srsf11 C T 3: 157,728,981 (GRCm39) probably benign Het
Stat3 C T 11: 100,785,931 (GRCm39) A449T probably damaging Het
Stat4 A G 1: 52,113,898 (GRCm39) N203D probably damaging Het
Tanc1 T C 2: 59,667,564 (GRCm39) probably null Het
Trav3-1 T C 14: 52,818,449 (GRCm39) I41T probably benign Het
Usp34 T A 11: 23,313,089 (GRCm39) D525E probably damaging Het
Vars1 T C 17: 35,232,620 (GRCm39) V848A probably damaging Het
Vmn2r101 A T 17: 19,809,769 (GRCm39) D185V probably benign Het
Wiz A G 17: 32,576,671 (GRCm39) S628P probably benign Het
Zfp647 G A 15: 76,796,285 (GRCm39) P125L 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
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
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'- AGCAGTTAGGTCTCAGATACACTTA -3'
(R):5'- GCCTTTGGTATAACACAACCTTTTAT -3'

Sequencing Primer
(F):5'- CAGGACAGTTGTTTTTGC -3'
(R):5'- CTGTAACTATAGCTCCAGTGGGTAC -3'
Posted On 2017-02-28