Incidental Mutation 'R0542:Ankrd11'
ID 49985
Institutional Source Beutler Lab
Gene Symbol Ankrd11
Ensembl Gene ENSMUSG00000035569
Gene Name ankyrin repeat domain 11
Synonyms Yod, 3010027A04Rik, 2410104C19Rik, 9530048I21Rik
MMRRC Submission 038734-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R0542 (G1)
Quality Score 225
Status Validated
Chromosome 8
Chromosomal Location 123610561-123769016 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 123622509 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Glycine at position 448 (R448G)
Ref Sequence ENSEMBL: ENSMUSP00000095938 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000098333] [ENSMUST00000098334] [ENSMUST00000127664] [ENSMUST00000172906]
AlphaFold E9Q4F7
Predicted Effect probably damaging
Transcript: ENSMUST00000098333
AA Change: R448G

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000095938
Gene: ENSMUSG00000035569
AA Change: R448G

DomainStartEndE-ValueType
ANK 188 217 2.58e-3 SMART
ANK 221 250 1.31e-4 SMART
ANK 254 283 5.04e-6 SMART
low complexity region 311 324 N/A INTRINSIC
low complexity region 366 377 N/A INTRINSIC
low complexity region 429 440 N/A INTRINSIC
low complexity region 470 487 N/A INTRINSIC
low complexity region 499 521 N/A INTRINSIC
low complexity region 534 549 N/A INTRINSIC
low complexity region 596 609 N/A INTRINSIC
low complexity region 649 669 N/A INTRINSIC
coiled coil region 786 826 N/A INTRINSIC
low complexity region 867 877 N/A INTRINSIC
low complexity region 965 984 N/A INTRINSIC
low complexity region 1040 1055 N/A INTRINSIC
low complexity region 1058 1082 N/A INTRINSIC
low complexity region 1187 1200 N/A INTRINSIC
low complexity region 1204 1227 N/A INTRINSIC
low complexity region 1268 1289 N/A INTRINSIC
low complexity region 1294 1306 N/A INTRINSIC
coiled coil region 1374 1406 N/A INTRINSIC
low complexity region 1476 1496 N/A INTRINSIC
low complexity region 1508 1523 N/A INTRINSIC
low complexity region 1526 1547 N/A INTRINSIC
coiled coil region 1598 1625 N/A INTRINSIC
low complexity region 1770 1781 N/A INTRINSIC
low complexity region 1874 1885 N/A INTRINSIC
low complexity region 1913 1922 N/A INTRINSIC
low complexity region 1969 1979 N/A INTRINSIC
low complexity region 2035 2045 N/A INTRINSIC
low complexity region 2057 2071 N/A INTRINSIC
low complexity region 2162 2179 N/A INTRINSIC
low complexity region 2191 2209 N/A INTRINSIC
low complexity region 2224 2236 N/A INTRINSIC
low complexity region 2250 2263 N/A INTRINSIC
low complexity region 2294 2305 N/A INTRINSIC
low complexity region 2391 2409 N/A INTRINSIC
low complexity region 2445 2455 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000098334
AA Change: R427G

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000095939
Gene: ENSMUSG00000035569
AA Change: R427G

DomainStartEndE-ValueType
ANK 167 196 2.58e-3 SMART
ANK 200 229 1.31e-4 SMART
ANK 233 262 5.04e-6 SMART
low complexity region 290 303 N/A INTRINSIC
low complexity region 345 356 N/A INTRINSIC
low complexity region 408 419 N/A INTRINSIC
low complexity region 449 466 N/A INTRINSIC
low complexity region 478 500 N/A INTRINSIC
low complexity region 513 528 N/A INTRINSIC
low complexity region 575 588 N/A INTRINSIC
low complexity region 628 648 N/A INTRINSIC
coiled coil region 765 805 N/A INTRINSIC
low complexity region 846 856 N/A INTRINSIC
low complexity region 944 963 N/A INTRINSIC
low complexity region 1019 1034 N/A INTRINSIC
low complexity region 1037 1061 N/A INTRINSIC
low complexity region 1166 1179 N/A INTRINSIC
low complexity region 1183 1206 N/A INTRINSIC
low complexity region 1247 1268 N/A INTRINSIC
low complexity region 1273 1285 N/A INTRINSIC
coiled coil region 1353 1385 N/A INTRINSIC
low complexity region 1455 1475 N/A INTRINSIC
low complexity region 1487 1502 N/A INTRINSIC
low complexity region 1505 1526 N/A INTRINSIC
coiled coil region 1577 1604 N/A INTRINSIC
low complexity region 1749 1760 N/A INTRINSIC
low complexity region 1853 1864 N/A INTRINSIC
low complexity region 1892 1901 N/A INTRINSIC
low complexity region 1948 1958 N/A INTRINSIC
low complexity region 2014 2024 N/A INTRINSIC
low complexity region 2036 2050 N/A INTRINSIC
low complexity region 2141 2158 N/A INTRINSIC
low complexity region 2170 2188 N/A INTRINSIC
low complexity region 2203 2215 N/A INTRINSIC
low complexity region 2229 2242 N/A INTRINSIC
low complexity region 2273 2284 N/A INTRINSIC
low complexity region 2370 2388 N/A INTRINSIC
low complexity region 2424 2434 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000127664
SMART Domains Protein: ENSMUSP00000118564
Gene: ENSMUSG00000092329

DomainStartEndE-ValueType
Pfam:Glycos_transf_2 104 287 7.4e-31 PFAM
Pfam:Glyco_transf_7C 261 331 4.9e-8 PFAM
RICIN 406 531 9.28e-27 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000172906
Predicted Effect noncoding transcript
Transcript: ENSMUST00000211940
Predicted Effect probably benign
Transcript: ENSMUST00000212050
Predicted Effect noncoding transcript
Transcript: ENSMUST00000212337
Predicted Effect noncoding transcript
Transcript: ENSMUST00000212728
Meta Mutation Damage Score 0.3385 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 97.1%
  • 20x: 95.0%
Validation Efficiency 99% (70/71)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This locus encodes an ankryin repeat domain-containing protein. The encoded protein inhibits ligand-dependent activation of transcription. Mutations in this gene have been associated with KBG syndrome, which is characterized by macrodontia, distinctive craniofacial features, short stature, skeletal anomalies, global developmental delay, seizures and intellectual disability. Alternatively spliced transcript variants have been described. Related pseudogenes exist on chromosomes 2 and X. [provided by RefSeq, Jan 2012]
PHENOTYPE: Mice homozygous for a spontaneous allele die by E9.5, are small and fail to turn. Mice heterozygous for a spontaneous allele exhibit craniofacial abnormalities, decreased weight, osteoporosis and osteopenia. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 69 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abhd12b C A 12: 70,210,269 (GRCm39) N71K possibly damaging Het
Adgrl2 A G 3: 148,564,854 (GRCm39) I242T probably damaging Het
Adgrv1 A G 13: 81,721,437 (GRCm39) S714P probably damaging Het
Agap3 G A 5: 24,705,184 (GRCm39) R704Q possibly damaging Het
Anks1b T C 10: 89,909,829 (GRCm39) probably benign Het
Caml A T 13: 55,770,974 (GRCm39) Q24L possibly damaging Het
Cdc14b G A 13: 64,391,497 (GRCm39) T124I probably benign Het
Clca3a2 A G 3: 144,781,571 (GRCm39) probably benign Het
Col12a1 A G 9: 79,512,610 (GRCm39) probably null Het
Crispld1 T C 1: 17,816,992 (GRCm39) V183A possibly damaging Het
Cstdc1 A G 2: 148,624,092 (GRCm39) N22S probably benign Het
Dhx40 C T 11: 86,695,082 (GRCm39) probably null Het
Dmxl1 T A 18: 50,026,761 (GRCm39) D1956E probably benign Het
Dsc2 A G 18: 20,184,283 (GRCm39) V35A probably damaging Het
Dync2i2 A G 2: 29,921,837 (GRCm39) V508A probably damaging Het
Elovl2 A G 13: 41,345,452 (GRCm39) probably benign Het
Gapvd1 T C 2: 34,615,048 (GRCm39) probably benign Het
Gnaq T A 19: 16,196,982 (GRCm39) I56N probably damaging Het
Gpr139 T C 7: 118,744,306 (GRCm39) D93G probably benign Het
Hars1 C T 18: 36,904,234 (GRCm39) R215H probably benign Het
Helz2 C A 2: 180,873,882 (GRCm39) W2204L probably damaging Het
Ift70b A G 2: 75,767,055 (GRCm39) V566A probably damaging Het
Itgb6 A T 2: 60,435,480 (GRCm39) C757S possibly damaging Het
Kpnb1 G A 11: 97,078,398 (GRCm39) T5I probably benign Het
Krt82 T C 15: 101,454,035 (GRCm39) probably benign Het
Lgals9 T A 11: 78,860,546 (GRCm39) K175N possibly damaging Het
Lrp2 A G 2: 69,258,998 (GRCm39) I4564T probably benign Het
Mblac1 A G 5: 138,192,798 (GRCm39) T47A possibly damaging Het
Med12l G A 3: 58,949,822 (GRCm39) D182N probably damaging Het
Megf9 A G 4: 70,353,585 (GRCm39) I407T probably benign Het
Mtmr6 A T 14: 60,529,578 (GRCm39) probably null Het
Mtor A G 4: 148,624,907 (GRCm39) T2173A probably benign Het
Mzt1 A T 14: 99,277,938 (GRCm39) probably benign Het
Narf T C 11: 121,143,690 (GRCm39) L444P probably damaging Het
Nsd1 A T 13: 55,408,271 (GRCm39) Q1305L possibly damaging Het
Ntsr1 A G 2: 180,184,374 (GRCm39) Y359C probably damaging Het
Olfm1 A G 2: 28,104,640 (GRCm39) D159G possibly damaging Het
Or2l13b A T 16: 19,348,732 (GRCm39) *313R probably null Het
Pcdh1 C T 18: 38,322,975 (GRCm39) V953I probably damaging Het
Pcdhb11 A T 18: 37,556,887 (GRCm39) D739V probably damaging Het
Pdgfd A G 9: 6,359,769 (GRCm39) N280S probably damaging Het
Per2 A T 1: 91,366,054 (GRCm39) probably null Het
Pfkp G T 13: 6,672,028 (GRCm39) C122* probably null Het
Plxna4 G A 6: 32,169,232 (GRCm39) R1322W probably damaging Het
Ppox A G 1: 171,106,818 (GRCm39) L202P probably damaging Het
Ppp1r3e G A 14: 55,114,588 (GRCm39) P58L probably benign Het
Prr23a2 A C 9: 98,739,086 (GRCm39) N148T probably benign Het
Psd T C 19: 46,302,649 (GRCm39) T842A probably damaging Het
Ranbp2 C T 10: 58,314,236 (GRCm39) A1652V probably benign Het
Rragd G A 4: 33,007,103 (GRCm39) V144M probably damaging Het
Sema6a T G 18: 47,381,643 (GRCm39) D968A probably damaging Het
Slc30a5 A T 13: 100,945,793 (GRCm39) probably null Het
Snx17 G T 5: 31,353,895 (GRCm39) probably null Het
Styxl2 A T 1: 165,928,853 (GRCm39) M253K possibly damaging Het
Syt14 G T 1: 192,613,111 (GRCm39) T563K probably damaging Het
Tada3 T C 6: 113,352,175 (GRCm39) K85E probably damaging Het
Tspear T C 10: 77,716,921 (GRCm39) V532A probably benign Het
Ttn A T 2: 76,723,453 (GRCm39) C6426S possibly damaging Het
Unc79 T C 12: 103,060,437 (GRCm39) probably benign Het
Usp19 A G 9: 108,371,584 (GRCm39) probably null Het
Vav3 G A 3: 109,434,746 (GRCm39) D426N probably damaging Het
Vezt T C 10: 93,842,958 (GRCm39) probably null Het
Vldlr G T 19: 27,213,655 (GRCm39) R114L probably benign Het
Wwc2 C T 8: 48,321,414 (GRCm39) V567I unknown Het
Zfp423 T C 8: 88,507,237 (GRCm39) T911A probably damaging Het
Zfp719 A G 7: 43,238,677 (GRCm39) probably null Het
Zkscan16 A T 4: 58,956,597 (GRCm39) H293L possibly damaging Het
Zkscan6 A C 11: 65,719,525 (GRCm39) N515T possibly damaging Het
Znfx1 A G 2: 166,897,575 (GRCm39) S450P probably damaging Het
Other mutations in Ankrd11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00949:Ankrd11 APN 8 123,635,467 (GRCm39) missense possibly damaging 0.59
IGL00971:Ankrd11 APN 8 123,622,092 (GRCm39) missense probably damaging 1.00
IGL01017:Ankrd11 APN 8 123,621,467 (GRCm39) missense probably damaging 1.00
IGL01137:Ankrd11 APN 8 123,611,075 (GRCm39) missense probably damaging 0.99
IGL01659:Ankrd11 APN 8 123,622,110 (GRCm39) missense probably damaging 1.00
IGL01920:Ankrd11 APN 8 123,642,636 (GRCm39) splice site probably benign
IGL01964:Ankrd11 APN 8 123,616,475 (GRCm39) missense probably damaging 0.97
IGL02131:Ankrd11 APN 8 123,621,149 (GRCm39) missense probably damaging 1.00
IGL02226:Ankrd11 APN 8 123,618,984 (GRCm39) missense probably damaging 1.00
IGL02549:Ankrd11 APN 8 123,618,032 (GRCm39) missense probably damaging 1.00
IGL02642:Ankrd11 APN 8 123,617,390 (GRCm39) missense probably damaging 1.00
IGL02643:Ankrd11 APN 8 123,619,061 (GRCm39) missense probably damaging 0.98
IGL02861:Ankrd11 APN 8 123,622,566 (GRCm39) missense probably damaging 0.99
IGL03086:Ankrd11 APN 8 123,621,249 (GRCm39) missense probably damaging 1.00
IGL03336:Ankrd11 APN 8 123,618,582 (GRCm39) missense probably benign 0.00
anchors UTSW 8 123,622,509 (GRCm39) missense probably damaging 0.99
away UTSW 8 123,618,692 (GRCm39) missense probably damaging 1.00
bluebell UTSW 8 123,618,524 (GRCm39) missense probably damaging 0.97
Navy UTSW 8 123,635,473 (GRCm39) nonsense probably null
BB001:Ankrd11 UTSW 8 123,622,641 (GRCm39) missense possibly damaging 0.95
BB011:Ankrd11 UTSW 8 123,622,641 (GRCm39) missense possibly damaging 0.95
R0051:Ankrd11 UTSW 8 123,616,481 (GRCm39) missense probably damaging 1.00
R0051:Ankrd11 UTSW 8 123,616,481 (GRCm39) missense probably damaging 1.00
R0110:Ankrd11 UTSW 8 123,618,914 (GRCm39) missense possibly damaging 0.95
R0281:Ankrd11 UTSW 8 123,622,307 (GRCm39) missense probably benign 0.01
R0450:Ankrd11 UTSW 8 123,618,914 (GRCm39) missense possibly damaging 0.95
R0481:Ankrd11 UTSW 8 123,626,775 (GRCm39) missense probably damaging 1.00
R0606:Ankrd11 UTSW 8 123,619,571 (GRCm39) missense probably benign 0.04
R0702:Ankrd11 UTSW 8 123,616,505 (GRCm39) missense probably damaging 1.00
R0730:Ankrd11 UTSW 8 123,618,692 (GRCm39) missense probably damaging 1.00
R0737:Ankrd11 UTSW 8 123,622,575 (GRCm39) missense probably damaging 0.99
R1401:Ankrd11 UTSW 8 123,619,789 (GRCm39) missense probably benign 0.23
R1464:Ankrd11 UTSW 8 123,619,463 (GRCm39) missense probably damaging 1.00
R1464:Ankrd11 UTSW 8 123,619,463 (GRCm39) missense probably damaging 1.00
R1470:Ankrd11 UTSW 8 123,626,463 (GRCm39) missense probably damaging 0.98
R1470:Ankrd11 UTSW 8 123,626,463 (GRCm39) missense probably damaging 0.98
R1641:Ankrd11 UTSW 8 123,618,485 (GRCm39) missense probably benign 0.03
R1950:Ankrd11 UTSW 8 123,616,608 (GRCm39) missense probably damaging 1.00
R2004:Ankrd11 UTSW 8 123,629,161 (GRCm39) critical splice donor site probably null
R2401:Ankrd11 UTSW 8 123,635,473 (GRCm39) nonsense probably null
R2425:Ankrd11 UTSW 8 123,619,902 (GRCm39) missense possibly damaging 0.86
R2830:Ankrd11 UTSW 8 123,618,935 (GRCm39) missense probably damaging 1.00
R2910:Ankrd11 UTSW 8 123,635,537 (GRCm39) missense probably damaging 1.00
R2911:Ankrd11 UTSW 8 123,635,537 (GRCm39) missense probably damaging 1.00
R3736:Ankrd11 UTSW 8 123,618,524 (GRCm39) missense probably damaging 0.97
R3738:Ankrd11 UTSW 8 123,623,454 (GRCm39) unclassified probably benign
R3739:Ankrd11 UTSW 8 123,623,454 (GRCm39) unclassified probably benign
R3813:Ankrd11 UTSW 8 123,618,117 (GRCm39) missense probably benign
R4012:Ankrd11 UTSW 8 123,619,156 (GRCm39) missense probably damaging 0.98
R4183:Ankrd11 UTSW 8 123,626,415 (GRCm39) missense possibly damaging 0.88
R4213:Ankrd11 UTSW 8 123,617,765 (GRCm39) missense probably benign 0.00
R4469:Ankrd11 UTSW 8 123,623,326 (GRCm39) missense probably damaging 1.00
R4482:Ankrd11 UTSW 8 123,620,228 (GRCm39) missense probably damaging 1.00
R4935:Ankrd11 UTSW 8 123,626,922 (GRCm39) missense probably benign 0.02
R4940:Ankrd11 UTSW 8 123,616,560 (GRCm39) missense probably damaging 1.00
R5145:Ankrd11 UTSW 8 123,617,943 (GRCm39) utr 3 prime probably benign
R5154:Ankrd11 UTSW 8 123,619,878 (GRCm39) missense probably damaging 1.00
R5230:Ankrd11 UTSW 8 123,617,216 (GRCm39) missense probably benign 0.11
R5283:Ankrd11 UTSW 8 123,610,921 (GRCm39) missense probably damaging 1.00
R5377:Ankrd11 UTSW 8 123,620,453 (GRCm39) splice site probably null
R5513:Ankrd11 UTSW 8 123,619,259 (GRCm39) missense probably benign 0.38
R5518:Ankrd11 UTSW 8 123,617,733 (GRCm39) missense possibly damaging 0.93
R5549:Ankrd11 UTSW 8 123,617,117 (GRCm39) missense probably benign 0.02
R5579:Ankrd11 UTSW 8 123,610,970 (GRCm39) missense probably damaging 0.97
R5595:Ankrd11 UTSW 8 123,621,043 (GRCm39) nonsense probably null
R5650:Ankrd11 UTSW 8 123,614,136 (GRCm39) missense probably damaging 0.99
R5717:Ankrd11 UTSW 8 123,619,377 (GRCm39) missense possibly damaging 0.92
R5753:Ankrd11 UTSW 8 123,622,043 (GRCm39) missense possibly damaging 0.90
R5782:Ankrd11 UTSW 8 123,626,756 (GRCm39) missense probably damaging 1.00
R5812:Ankrd11 UTSW 8 123,620,544 (GRCm39) splice site probably null
R5823:Ankrd11 UTSW 8 123,622,529 (GRCm39) missense probably benign 0.12
R5900:Ankrd11 UTSW 8 123,617,805 (GRCm39) missense probably benign 0.00
R5975:Ankrd11 UTSW 8 123,616,488 (GRCm39) missense possibly damaging 0.93
R5979:Ankrd11 UTSW 8 123,619,139 (GRCm39) missense probably damaging 1.00
R6000:Ankrd11 UTSW 8 123,617,934 (GRCm39) missense possibly damaging 0.73
R6145:Ankrd11 UTSW 8 123,619,400 (GRCm39) missense probably damaging 1.00
R6252:Ankrd11 UTSW 8 123,620,561 (GRCm39) missense possibly damaging 0.87
R6302:Ankrd11 UTSW 8 123,616,728 (GRCm39) missense probably benign
R6457:Ankrd11 UTSW 8 123,635,503 (GRCm39) missense probably damaging 1.00
R6513:Ankrd11 UTSW 8 123,616,919 (GRCm39) missense probably benign 0.02
R6582:Ankrd11 UTSW 8 123,618,368 (GRCm39) missense probably benign 0.00
R6738:Ankrd11 UTSW 8 123,618,660 (GRCm39) missense probably damaging 0.99
R6865:Ankrd11 UTSW 8 123,621,683 (GRCm39) missense probably benign 0.41
R6913:Ankrd11 UTSW 8 123,621,650 (GRCm39) missense probably benign 0.01
R7101:Ankrd11 UTSW 8 123,622,194 (GRCm39) missense probably benign 0.35
R7116:Ankrd11 UTSW 8 123,622,869 (GRCm39) missense probably damaging 1.00
R7477:Ankrd11 UTSW 8 123,621,124 (GRCm39) missense possibly damaging 0.91
R7534:Ankrd11 UTSW 8 123,621,149 (GRCm39) missense probably damaging 1.00
R7555:Ankrd11 UTSW 8 123,614,145 (GRCm39) missense probably damaging 0.99
R7627:Ankrd11 UTSW 8 123,617,690 (GRCm39) missense possibly damaging 0.63
R7658:Ankrd11 UTSW 8 123,620,403 (GRCm39) missense probably benign
R7721:Ankrd11 UTSW 8 123,621,498 (GRCm39) missense probably damaging 1.00
R7731:Ankrd11 UTSW 8 123,622,172 (GRCm39) missense probably benign 0.12
R7792:Ankrd11 UTSW 8 123,610,970 (GRCm39) missense probably damaging 0.97
R7924:Ankrd11 UTSW 8 123,622,641 (GRCm39) missense possibly damaging 0.95
R7939:Ankrd11 UTSW 8 123,617,812 (GRCm39) missense probably damaging 1.00
R8022:Ankrd11 UTSW 8 123,614,332 (GRCm39) missense probably damaging 1.00
R8222:Ankrd11 UTSW 8 123,622,347 (GRCm39) missense probably damaging 0.98
R8362:Ankrd11 UTSW 8 123,618,797 (GRCm39) missense probably damaging 0.96
R8430:Ankrd11 UTSW 8 123,620,105 (GRCm39) missense probably benign 0.01
R8511:Ankrd11 UTSW 8 123,626,468 (GRCm39) missense
R8726:Ankrd11 UTSW 8 123,620,765 (GRCm39) missense possibly damaging 0.90
R8888:Ankrd11 UTSW 8 123,621,014 (GRCm39) missense possibly damaging 0.87
R8895:Ankrd11 UTSW 8 123,621,014 (GRCm39) missense possibly damaging 0.87
R8928:Ankrd11 UTSW 8 123,622,718 (GRCm39) missense probably damaging 0.99
R8930:Ankrd11 UTSW 8 123,622,718 (GRCm39) missense probably damaging 0.99
R8931:Ankrd11 UTSW 8 123,622,718 (GRCm39) missense probably damaging 0.99
R8936:Ankrd11 UTSW 8 123,621,840 (GRCm39) missense possibly damaging 0.69
R9018:Ankrd11 UTSW 8 123,622,251 (GRCm39) missense probably damaging 1.00
R9113:Ankrd11 UTSW 8 123,614,072 (GRCm39) missense possibly damaging 0.60
R9399:Ankrd11 UTSW 8 123,618,179 (GRCm39) missense probably benign
R9644:Ankrd11 UTSW 8 123,617,682 (GRCm39) missense probably benign 0.00
R9645:Ankrd11 UTSW 8 123,617,682 (GRCm39) missense probably benign 0.00
R9647:Ankrd11 UTSW 8 123,617,682 (GRCm39) missense probably benign 0.00
R9683:Ankrd11 UTSW 8 123,617,682 (GRCm39) missense probably benign 0.00
RF019:Ankrd11 UTSW 8 123,623,373 (GRCm39) missense probably damaging 1.00
Z1176:Ankrd11 UTSW 8 123,622,542 (GRCm39) missense possibly damaging 0.68
Z1177:Ankrd11 UTSW 8 123,626,881 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- ATTGTCAGTGCGCCAGTGCTTC -3'
(R):5'- GGCCAACAGCTTCATTTCCATACCC -3'

Sequencing Primer
(F):5'- TCGCTCTCTGAGGACTCAC -3'
(R):5'- TTCCATACCCAAGATGGAAGTG -3'
Posted On 2013-06-12