Incidental Mutation 'R6035:Ankrd31'
ID 479174
Institutional Source Beutler Lab
Gene Symbol Ankrd31
Ensembl Gene ENSMUSG00000109561
Gene Name ankyrin repeat domain 31
Synonyms
MMRRC Submission 044207-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R6035 (G1)
Quality Score 225.009
Status Not validated
Chromosome 13
Chromosomal Location 96884797-97046302 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 96968721 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Proline to Glutamine at position 786 (P786Q)
Ref Sequence ENSEMBL: ENSMUSP00000146720 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000207464] [ENSMUST00000208758]
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000207464
AA Change: P636Q
Predicted Effect probably benign
Transcript: ENSMUST00000208758
AA Change: P786Q

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)
Coding Region Coverage
  • 1x: 99.8%
  • 3x: 98.9%
  • 10x: 91.8%
  • 20x: 70.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 80 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A2m G T 6: 121,615,353 (GRCm39) G76W probably damaging Het
Abca17 A T 17: 24,500,219 (GRCm39) F1324Y possibly damaging Het
Abca8b A T 11: 109,862,686 (GRCm39) probably null Het
Abcc12 A G 8: 87,244,033 (GRCm39) M1040T probably damaging Het
Abtb1 A G 6: 88,818,788 (GRCm39) F7L probably damaging Het
Adcy9 T C 16: 4,122,377 (GRCm39) T558A probably benign Het
Adgrb1 A T 15: 74,412,292 (GRCm39) T424S possibly damaging Het
Afg3l2 G T 18: 67,554,329 (GRCm39) L458M probably damaging Het
Arhgap39 G T 15: 76,621,424 (GRCm39) Y392* probably null Het
Ash1l T C 3: 88,892,326 (GRCm39) Y1402H probably damaging Het
Carmil2 G T 8: 106,419,195 (GRCm39) W749L probably benign Het
Ccar1 A G 10: 62,587,564 (GRCm39) Y867H unknown Het
Cdh13 A G 8: 119,232,437 (GRCm39) D47G probably benign Het
Chst9 T A 18: 15,585,910 (GRCm39) T218S probably benign Het
Clec2i G A 6: 128,870,587 (GRCm39) V67I probably benign Het
Cox7a2 T A 9: 79,667,028 (GRCm39) probably benign Het
Cplx3 A G 9: 57,519,030 (GRCm39) probably null Het
Cpz A G 5: 35,674,929 (GRCm39) C107R probably damaging Het
Dapk1 T A 13: 60,909,013 (GRCm39) C1209S possibly damaging Het
Ddx41 T C 13: 55,681,781 (GRCm39) M307V probably benign Het
Defa24 A G 8: 22,224,565 (GRCm39) I5V probably benign Het
Dgcr8 A T 16: 18,076,178 (GRCm39) N2K probably damaging Het
Ebf2 A G 14: 67,476,423 (GRCm39) D131G probably damaging Het
Fam149b C T 14: 20,427,985 (GRCm39) R424C probably damaging Het
Fbln2 G A 6: 91,240,335 (GRCm39) V714M probably damaging Het
Fgf5 T C 5: 98,423,385 (GRCm39) Y257H probably damaging Het
Fmo3 A C 1: 162,791,605 (GRCm39) V224G probably damaging Het
Gigyf2 T C 1: 87,338,450 (GRCm39) I394T possibly damaging Het
Glmn T A 5: 107,741,746 (GRCm39) probably null Het
Greb1l T C 18: 10,501,025 (GRCm39) I385T possibly damaging Het
Grhl1 C A 12: 24,658,449 (GRCm39) Q365K probably benign Het
Gsdme G A 6: 50,206,306 (GRCm39) T179M probably damaging Het
Gtf2a1l A G 17: 89,018,962 (GRCm39) T349A probably benign Het
Hax1 GTCATCATCATCATCATC GTCATCATCATCATCATCATC 3: 89,905,247 (GRCm39) probably benign Het
Il5ra G A 6: 106,718,226 (GRCm39) T76I probably damaging Het
Itga8 T C 2: 12,196,525 (GRCm39) T631A probably benign Het
Kcnh6 G A 11: 105,909,978 (GRCm39) probably null Het
Krt26 C T 11: 99,224,415 (GRCm39) E368K probably benign Het
Lhx9 T C 1: 138,766,281 (GRCm39) D169G possibly damaging Het
Lmod3 A G 6: 97,224,234 (GRCm39) L529P probably damaging Het
Mroh2a G A 1: 88,158,390 (GRCm39) V146M probably damaging Het
Nup155 A G 15: 8,173,577 (GRCm39) T891A probably benign Het
Or11g24 A G 14: 50,661,984 (GRCm39) T3A probably benign Het
Or1e1 T C 11: 73,244,582 (GRCm39) M1T probably null Het
Or1j13 T A 2: 36,369,996 (GRCm39) I49F probably damaging Het
Or1p4-ps1 T C 11: 74,208,285 (GRCm39) *145R probably null Het
Or8b36 ATTGCTGTTT ATTGCTGTTTGCTGTTT 9: 37,937,836 (GRCm39) probably null Het
Papln G C 12: 83,821,454 (GRCm39) G262A probably damaging Het
Pdcd1lg2 G A 19: 29,423,435 (GRCm39) V160I probably benign Het
Pde8b A G 13: 95,164,105 (GRCm39) probably benign Het
Ppme1 G A 7: 100,004,002 (GRCm39) R68* probably null Het
Ptprn2 A T 12: 117,219,215 (GRCm39) N949Y probably damaging Het
Qser1 C A 2: 104,617,468 (GRCm39) D1115Y probably damaging Het
Rad54l G T 4: 115,954,666 (GRCm39) D674E probably damaging Het
Ripk4 T A 16: 97,545,387 (GRCm39) D420V probably damaging Het
Ros1 G T 10: 51,954,067 (GRCm39) S1857R probably benign Het
Rsf1 ATGGCG ATGGCGACGGTGGCG 7: 97,229,111 (GRCm39) probably benign Het
Rsf1 A G 7: 97,311,316 (GRCm39) E682G probably benign Het
Samd4 G A 14: 47,325,329 (GRCm39) R515H probably damaging Het
Selp T A 1: 163,969,079 (GRCm39) W560R probably benign Het
Shc3 A T 13: 51,615,468 (GRCm39) L163Q probably damaging Het
Shh G A 5: 28,666,397 (GRCm39) A163V probably damaging Het
Slc17a8 T C 10: 89,427,937 (GRCm39) R113G possibly damaging Het
Slc5a6 C A 5: 31,206,168 (GRCm39) probably benign Het
Smarcd2 A G 11: 106,157,715 (GRCm39) probably null Het
Sytl3 A G 17: 6,995,664 (GRCm39) D148G probably damaging Het
Tnks G T 8: 35,385,615 (GRCm39) H297Q possibly damaging Het
Trbv21 A T 6: 41,179,568 (GRCm39) probably benign Het
Ube3c T C 5: 29,806,161 (GRCm39) F268L probably benign Het
Ugt2b5 T C 5: 87,287,541 (GRCm39) I209V probably benign Het
Usp1 A G 4: 98,818,082 (GRCm39) N140S probably damaging Het
Vcam1 T C 3: 115,919,606 (GRCm39) Y226C probably damaging Het
Vmn1r129 T A 7: 21,094,534 (GRCm39) Q228L probably damaging Het
Vmn1r209 T A 13: 22,990,202 (GRCm39) N163Y probably benign Het
Vmn1r85 A G 7: 12,818,854 (GRCm39) S97P probably damaging Het
Vmn2r30 C T 7: 7,337,350 (GRCm39) M95I probably benign Het
Vmn2r74 G A 7: 85,601,098 (GRCm39) R847C probably damaging Het
Wdr70 G A 15: 7,916,830 (GRCm39) T529I possibly damaging Het
Zfp532 T G 18: 65,757,005 (GRCm39) S313A possibly damaging Het
Zhx3 A T 2: 160,621,463 (GRCm39) N901K probably benign Het
Other mutations in Ankrd31
AlleleSourceChrCoordTypePredicted EffectPPH Score
R6001:Ankrd31 UTSW 13 96,962,717 (GRCm39) missense probably damaging 1.00
R6035:Ankrd31 UTSW 13 96,968,721 (GRCm39) missense probably benign 0.00
R6273:Ankrd31 UTSW 13 96,988,181 (GRCm39) missense possibly damaging 0.61
R6291:Ankrd31 UTSW 13 97,014,746 (GRCm39) missense possibly damaging 0.72
R6387:Ankrd31 UTSW 13 96,967,081 (GRCm39) missense probably damaging 0.99
R6608:Ankrd31 UTSW 13 96,969,288 (GRCm39) missense probably damaging 0.99
R6680:Ankrd31 UTSW 13 96,967,117 (GRCm39) critical splice donor site probably null
R6738:Ankrd31 UTSW 13 97,040,635 (GRCm39) missense possibly damaging 0.79
R6860:Ankrd31 UTSW 13 96,968,094 (GRCm39) missense probably benign 0.01
R6988:Ankrd31 UTSW 13 97,014,757 (GRCm39) missense probably damaging 1.00
R7305:Ankrd31 UTSW 13 97,015,479 (GRCm39) missense probably damaging 0.99
R7586:Ankrd31 UTSW 13 96,968,562 (GRCm39) missense possibly damaging 0.92
R7631:Ankrd31 UTSW 13 97,015,462 (GRCm39) missense probably benign 0.04
R7842:Ankrd31 UTSW 13 96,957,966 (GRCm39) critical splice donor site probably null
R7890:Ankrd31 UTSW 13 96,968,379 (GRCm39) missense probably benign 0.27
R7911:Ankrd31 UTSW 13 97,015,608 (GRCm39) missense possibly damaging 0.47
R8052:Ankrd31 UTSW 13 96,969,036 (GRCm39) missense probably benign 0.07
R8133:Ankrd31 UTSW 13 97,003,003 (GRCm39) critical splice donor site probably null
R8430:Ankrd31 UTSW 13 96,988,199 (GRCm39) missense possibly damaging 0.78
R8752:Ankrd31 UTSW 13 96,916,879 (GRCm39) missense probably damaging 0.99
R8767:Ankrd31 UTSW 13 96,969,224 (GRCm39) missense probably damaging 1.00
R8793:Ankrd31 UTSW 13 96,968,221 (GRCm39) missense probably damaging 0.97
R8903:Ankrd31 UTSW 13 96,969,329 (GRCm39) missense probably damaging 1.00
R8917:Ankrd31 UTSW 13 96,969,212 (GRCm39) missense probably damaging 0.98
R8946:Ankrd31 UTSW 13 97,046,037 (GRCm39) makesense probably null
R9006:Ankrd31 UTSW 13 96,967,104 (GRCm39) missense probably benign 0.00
R9022:Ankrd31 UTSW 13 96,962,655 (GRCm39) missense probably benign 0.01
R9045:Ankrd31 UTSW 13 96,968,034 (GRCm39) nonsense probably null
R9098:Ankrd31 UTSW 13 96,916,879 (GRCm39) missense probably damaging 0.97
R9115:Ankrd31 UTSW 13 96,940,773 (GRCm39) critical splice donor site probably null
R9202:Ankrd31 UTSW 13 97,015,383 (GRCm39) nonsense probably null
R9211:Ankrd31 UTSW 13 97,029,551 (GRCm39) missense possibly damaging 0.93
R9297:Ankrd31 UTSW 13 97,015,085 (GRCm39) missense probably benign 0.04
R9318:Ankrd31 UTSW 13 97,015,085 (GRCm39) missense probably benign 0.04
R9377:Ankrd31 UTSW 13 97,014,733 (GRCm39) missense probably benign 0.10
R9454:Ankrd31 UTSW 13 96,916,846 (GRCm39) missense possibly damaging 0.70
R9454:Ankrd31 UTSW 13 96,916,842 (GRCm39) missense probably damaging 0.97
R9538:Ankrd31 UTSW 13 97,009,193 (GRCm39) missense probably benign 0.24
Predicted Primers
Posted On 2017-06-26