Incidental Mutation 'IGL01700:Ankrd36'
ID 104439
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ankrd36
Ensembl Gene ENSMUSG00000020481
Gene Name ankyrin repeat domain 36
Synonyms GC3, 1700012M14Rik, 1700008J08Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.051) question?
Stock # IGL01700
Quality Score
Status
Chromosome 11
Chromosomal Location 5519684-5639337 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 5582198 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 276 (T276A)
Ref Sequence ENSEMBL: ENSMUSP00000120499 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000109856] [ENSMUST00000118112] [ENSMUST00000137933]
AlphaFold D3Z4K0
Predicted Effect probably benign
Transcript: ENSMUST00000109856
AA Change: T918A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000105482
Gene: ENSMUSG00000020481
AA Change: T918A

DomainStartEndE-ValueType
Blast:ANK 29 62 3e-12 BLAST
ANK 66 95 4.5e-3 SMART
ANK 99 128 1.44e-1 SMART
ANK 132 161 4.6e0 SMART
ANK 165 194 2.48e-5 SMART
ANK 198 227 4.67e-1 SMART
internal_repeat_1 449 555 1.04e-5 PROSPERO
internal_repeat_1 891 981 1.04e-5 PROSPERO
low complexity region 1105 1118 N/A INTRINSIC
coiled coil region 1268 1297 N/A INTRINSIC
coiled coil region 1318 1338 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000118112
AA Change: T951A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000122397
Gene: ENSMUSG00000020481
AA Change: T951A

DomainStartEndE-ValueType
Blast:ANK 29 62 3e-12 BLAST
ANK 66 95 2.9e-5 SMART
ANK 99 128 9.4e-4 SMART
ANK 132 161 2.9e-2 SMART
ANK 165 194 1.5e-7 SMART
ANK 198 227 2.9e-3 SMART
internal_repeat_1 255 352 8.15e-5 PROSPERO
internal_repeat_1 438 538 8.15e-5 PROSPERO
low complexity region 1138 1151 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000120982
Predicted Effect probably benign
Transcript: ENSMUST00000137933
AA Change: T276A

PolyPhen 2 Score 0.048 (Sensitivity: 0.94; Specificity: 0.83)
SMART Domains Protein: ENSMUSP00000120499
Gene: ENSMUSG00000020481
AA Change: T276A

DomainStartEndE-ValueType
low complexity region 463 476 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca12 T A 1: 71,319,549 (GRCm39) M1778L probably benign Het
Aldh6a1 C T 12: 84,486,312 (GRCm39) C202Y probably damaging Het
Ankrd55 T C 13: 112,517,702 (GRCm39) I556T probably benign Het
Aqp4 A G 18: 15,532,922 (GRCm39) I57T probably benign Het
Atp1a1 T C 3: 101,501,574 (GRCm39) D43G possibly damaging Het
Cyld G A 8: 89,433,727 (GRCm39) R172H probably damaging Het
Ear2 A T 14: 44,340,716 (GRCm39) R125* probably null Het
Efcab9 T C 11: 32,477,451 (GRCm39) R24G probably damaging Het
F7 C A 8: 13,078,685 (GRCm39) Q39K probably benign Het
Galntl6 A T 8: 58,411,494 (GRCm39) probably benign Het
Kcnj5 A G 9: 32,233,925 (GRCm39) V130A probably damaging Het
Magee2 A G X: 103,899,574 (GRCm39) I359T possibly damaging Het
Myh1 T G 11: 67,102,238 (GRCm39) I843S probably damaging Het
Nfat5 T A 8: 108,065,762 (GRCm39) M98K probably damaging Het
Nrip3 T A 7: 109,361,074 (GRCm39) N200I possibly damaging Het
Or6c219 A T 10: 129,781,810 (GRCm39) N40K probably damaging Het
Phkb A T 8: 86,744,094 (GRCm39) Q581L probably benign Het
Plxdc2 T C 2: 16,516,926 (GRCm39) V69A probably benign Het
Pou3f1 G T 4: 124,552,650 (GRCm39) W384L probably damaging Het
Prrc2a G A 17: 35,369,643 (GRCm39) S1890L possibly damaging Het
Psmc1 C A 12: 100,079,337 (GRCm39) P27H probably damaging Het
Pvr C A 7: 19,643,157 (GRCm39) A359S probably benign Het
Rasal1 A T 5: 120,814,882 (GRCm39) I711F probably benign Het
Ror1 C T 4: 100,266,968 (GRCm39) A223V probably damaging Het
Slc22a16 A T 10: 40,479,904 (GRCm39) I638L unknown Het
Slfn10-ps C T 11: 82,919,938 (GRCm39) noncoding transcript Het
Sptbn4 A G 7: 27,103,693 (GRCm39) L1176P probably damaging Het
Usp21 A T 1: 171,110,975 (GRCm39) F421I probably damaging Het
Utp25 G A 1: 192,800,573 (GRCm39) P416S probably damaging Het
Vmn1r61 T A 7: 5,614,202 (GRCm39) R37S possibly damaging Het
Vps13a G A 19: 16,722,221 (GRCm39) R364* probably null Het
Vps29 A G 5: 122,500,930 (GRCm39) Y165C probably damaging Het
Wdfy4 T C 14: 32,742,195 (GRCm39) probably benign Het
Wdr24 A G 17: 26,044,802 (GRCm39) D219G probably damaging Het
Xpo1 T C 11: 23,226,422 (GRCm39) probably benign Het
Zfp831 C A 2: 174,486,711 (GRCm39) T462K possibly damaging Het
Zswim5 T C 4: 116,843,658 (GRCm39) probably benign Het
Other mutations in Ankrd36
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00087:Ankrd36 APN 11 5,570,131 (GRCm39) missense probably benign 0.01
IGL01361:Ankrd36 APN 11 5,546,706 (GRCm39) splice site probably benign
IGL01370:Ankrd36 APN 11 5,534,019 (GRCm39) missense probably benign 0.06
IGL01384:Ankrd36 APN 11 5,578,348 (GRCm39) missense probably benign 0.33
IGL01484:Ankrd36 APN 11 5,579,006 (GRCm39) missense possibly damaging 0.90
IGL01524:Ankrd36 APN 11 5,585,092 (GRCm39) missense probably benign
IGL02322:Ankrd36 APN 11 5,564,619 (GRCm39) missense possibly damaging 0.86
IGL02511:Ankrd36 APN 11 5,610,845 (GRCm39) splice site probably null
IGL02824:Ankrd36 APN 11 5,524,246 (GRCm39) missense possibly damaging 0.67
IGL03204:Ankrd36 APN 11 5,534,023 (GRCm39) missense possibly damaging 0.70
PIT4508001:Ankrd36 UTSW 11 5,557,137 (GRCm39) missense possibly damaging 0.53
R0058:Ankrd36 UTSW 11 5,580,691 (GRCm39) splice site probably benign
R0058:Ankrd36 UTSW 11 5,580,691 (GRCm39) splice site probably benign
R0304:Ankrd36 UTSW 11 5,578,981 (GRCm39) missense possibly damaging 0.55
R0504:Ankrd36 UTSW 11 5,579,274 (GRCm39) missense probably damaging 0.99
R0550:Ankrd36 UTSW 11 5,557,429 (GRCm39) critical splice donor site probably null
R0563:Ankrd36 UTSW 11 5,579,322 (GRCm39) missense probably benign 0.33
R0891:Ankrd36 UTSW 11 5,637,316 (GRCm39) missense possibly damaging 0.72
R1018:Ankrd36 UTSW 11 5,596,876 (GRCm39) unclassified probably benign
R1468:Ankrd36 UTSW 11 5,525,752 (GRCm39) missense probably damaging 0.99
R1468:Ankrd36 UTSW 11 5,525,752 (GRCm39) missense probably damaging 0.99
R1558:Ankrd36 UTSW 11 5,585,329 (GRCm39) missense probably damaging 0.99
R1663:Ankrd36 UTSW 11 5,570,126 (GRCm39) missense possibly damaging 0.70
R1682:Ankrd36 UTSW 11 5,557,143 (GRCm39) missense possibly damaging 0.84
R1898:Ankrd36 UTSW 11 5,525,683 (GRCm39) missense probably benign 0.33
R2019:Ankrd36 UTSW 11 5,639,140 (GRCm39) missense probably benign
R2032:Ankrd36 UTSW 11 5,578,616 (GRCm39) missense possibly damaging 0.86
R2084:Ankrd36 UTSW 11 5,612,378 (GRCm39) nonsense probably null
R4097:Ankrd36 UTSW 11 5,578,703 (GRCm39) missense possibly damaging 0.85
R4572:Ankrd36 UTSW 11 5,639,340 (GRCm39) splice site probably null
R4601:Ankrd36 UTSW 11 5,520,102 (GRCm39) missense probably benign 0.04
R4770:Ankrd36 UTSW 11 5,540,870 (GRCm39) missense possibly damaging 0.73
R4777:Ankrd36 UTSW 11 5,557,120 (GRCm39) missense probably benign
R4894:Ankrd36 UTSW 11 5,585,332 (GRCm39) missense probably damaging 0.98
R5288:Ankrd36 UTSW 11 5,639,340 (GRCm39) unclassified probably benign
R5366:Ankrd36 UTSW 11 5,542,841 (GRCm39) nonsense probably null
R5384:Ankrd36 UTSW 11 5,639,340 (GRCm39) unclassified probably benign
R5385:Ankrd36 UTSW 11 5,639,340 (GRCm39) unclassified probably benign
R6109:Ankrd36 UTSW 11 5,578,941 (GRCm39) missense probably damaging 0.98
R6155:Ankrd36 UTSW 11 5,637,442 (GRCm39) missense probably benign 0.00
R6186:Ankrd36 UTSW 11 5,593,812 (GRCm39) missense possibly damaging 0.81
R6289:Ankrd36 UTSW 11 5,578,837 (GRCm39) missense probably damaging 0.96
R6476:Ankrd36 UTSW 11 5,578,753 (GRCm39) missense probably benign 0.05
R6816:Ankrd36 UTSW 11 5,593,765 (GRCm39) missense possibly damaging 0.66
R6880:Ankrd36 UTSW 11 5,578,748 (GRCm39) missense probably damaging 0.99
R6919:Ankrd36 UTSW 11 5,579,299 (GRCm39) missense probably benign
R7007:Ankrd36 UTSW 11 5,639,168 (GRCm39) missense probably benign 0.00
R7515:Ankrd36 UTSW 11 5,578,905 (GRCm39) missense possibly damaging 0.94
R7617:Ankrd36 UTSW 11 5,637,348 (GRCm39) missense probably benign 0.33
R7684:Ankrd36 UTSW 11 5,520,113 (GRCm39) missense possibly damaging 0.49
R7746:Ankrd36 UTSW 11 5,637,451 (GRCm39) missense possibly damaging 0.96
R7783:Ankrd36 UTSW 11 5,585,359 (GRCm39) missense probably damaging 0.99
R7790:Ankrd36 UTSW 11 5,585,176 (GRCm39) missense possibly damaging 0.80
R8221:Ankrd36 UTSW 11 5,534,016 (GRCm39) missense possibly damaging 0.53
R8671:Ankrd36 UTSW 11 5,579,312 (GRCm39) missense probably benign 0.05
R8732:Ankrd36 UTSW 11 5,578,906 (GRCm39) missense possibly damaging 0.90
R8768:Ankrd36 UTSW 11 5,593,763 (GRCm39) missense probably benign 0.00
R9026:Ankrd36 UTSW 11 5,610,696 (GRCm39) missense probably benign
R9093:Ankrd36 UTSW 11 5,589,132 (GRCm39) missense probably benign
R9211:Ankrd36 UTSW 11 5,612,370 (GRCm39) missense possibly damaging 0.85
R9300:Ankrd36 UTSW 11 5,519,979 (GRCm39) missense possibly damaging 0.84
R9644:Ankrd36 UTSW 11 5,593,835 (GRCm39) missense possibly damaging 0.90
RF004:Ankrd36 UTSW 11 5,612,411 (GRCm39) missense possibly damaging 0.53
U24488:Ankrd36 UTSW 11 5,580,772 (GRCm39) missense probably damaging 0.99
Z1176:Ankrd36 UTSW 11 5,565,538 (GRCm39) missense probably benign
Z1177:Ankrd36 UTSW 11 5,593,738 (GRCm39) missense probably damaging 0.96
Z1177:Ankrd36 UTSW 11 5,579,345 (GRCm39) missense probably benign 0.01
Z1177:Ankrd36 UTSW 11 5,521,117 (GRCm39) missense probably damaging 0.97
Posted On 2014-01-21