Incidental Mutation 'ANU05:Tedc1'
ID 262508
Institutional Source Beutler Lab
Gene Symbol Tedc1
Ensembl Gene ENSMUSG00000037466
Gene Name tubulin epsilon and delta complex 1
Synonyms 4930427A07Rik
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # ANU05
Quality Score 225
Status Not validated
Chromosome 12
Chromosomal Location 113120041-113129668 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) C to T at 113126808 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Stop codon at position 357 (R357*)
Ref Sequence ENSEMBL: ENSMUSP00000035351 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000049271] [ENSMUST00000196755] [ENSMUST00000200522]
AlphaFold Q3UK37
Predicted Effect probably null
Transcript: ENSMUST00000049271
AA Change: R357*
SMART Domains Protein: ENSMUSP00000035351
Gene: ENSMUSG00000037466
AA Change: R357*

DomainStartEndE-ValueType
low complexity region 2 21 N/A INTRINSIC
Pfam:DUF4509 41 221 4.8e-65 PFAM
low complexity region 233 245 N/A INTRINSIC
Pfam:DUF4510 258 418 3.1e-73 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000196755
SMART Domains Protein: ENSMUSP00000143431
Gene: ENSMUSG00000037466

DomainStartEndE-ValueType
low complexity region 1 20 N/A INTRINSIC
Pfam:DUF4509 40 138 4.1e-32 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000198072
Predicted Effect probably benign
Transcript: ENSMUST00000200522
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.3%
  • 10x: 96.5%
  • 20x: 93.3%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110038F14Rik G A 15: 76,834,475 (GRCm39) V124I probably damaging Het
Acaca A G 11: 84,206,678 (GRCm39) K1513E probably damaging Het
Acacb T A 5: 114,363,931 (GRCm39) F1464Y probably benign Het
Adgrg6 G A 10: 14,286,274 (GRCm39) A1114V possibly damaging Het
Agl A G 3: 116,566,438 (GRCm39) I975T possibly damaging Het
Akap7 T C 10: 25,147,451 (GRCm39) H93R probably damaging Het
Arhgef11 T C 3: 87,640,481 (GRCm39) W1213R probably benign Het
Ccar1 T A 10: 62,592,428 (GRCm39) E708V probably damaging Het
Cfap206 C T 4: 34,721,562 (GRCm39) S162N probably damaging Het
Cilp T C 9: 65,186,265 (GRCm39) S787P possibly damaging Het
Col6a3 G A 1: 90,730,014 (GRCm39) T1157I probably damaging Het
D630003M21Rik T C 2: 158,038,308 (GRCm39) Y1046C probably benign Het
Dock3 A G 9: 106,772,862 (GRCm39) S464P probably benign Het
Dusp19 A G 2: 80,454,618 (GRCm39) T113A probably benign Het
Dync1h1 A C 12: 110,615,538 (GRCm39) Y2957S probably benign Het
Epdr1 T C 13: 19,778,814 (GRCm39) Y94C probably damaging Het
Fcho1 A T 8: 72,165,191 (GRCm39) L422Q probably benign Het
Gca T A 2: 62,520,787 (GRCm39) Y210* probably null Het
Gpnmb T C 6: 49,032,615 (GRCm39) V513A probably benign Het
Irx4 A G 13: 73,415,786 (GRCm39) T192A probably damaging Het
Isca1 T C 13: 59,906,785 (GRCm39) T54A probably benign Het
Kif12 GGGGC GGGGCCTCCACCCGGCGGGC 4: 63,089,660 (GRCm39) probably benign Het
L3mbtl1 T C 2: 162,812,100 (GRCm39) V715A probably benign Het
Lama1 G A 17: 68,045,865 (GRCm39) D257N probably damaging Het
Lgr5 T C 10: 115,314,439 (GRCm39) H166R probably damaging Het
M6pr A G 6: 122,289,218 (GRCm39) R9G probably benign Het
Nmt2 T G 2: 3,315,731 (GRCm39) S240R probably benign Het
Npas3 A G 12: 54,114,857 (GRCm39) E593G possibly damaging Het
Or8k30 G A 2: 86,339,513 (GRCm39) A237T possibly damaging Het
Pank4 T C 4: 155,059,103 (GRCm39) M412T probably damaging Het
Psd A G 19: 46,303,186 (GRCm39) V100A possibly damaging Het
Rab11fip3 T C 17: 26,235,087 (GRCm39) T28A probably damaging Het
Rnpepl1 A T 1: 92,847,468 (GRCm39) D685V probably benign Het
Rrad T C 8: 105,357,283 (GRCm39) E88G probably benign Het
Sdk2 T A 11: 113,733,906 (GRCm39) M846L probably benign Het
Sparcl1 A T 5: 104,242,581 (GRCm39) V36E possibly damaging Het
Spmip5 A T 19: 58,777,545 (GRCm39) H80Q probably damaging Het
Srrm4 C T 5: 116,605,628 (GRCm39) E210K unknown Het
Stk25 A T 1: 93,551,145 (GRCm39) probably null Het
Tacr3 A T 3: 134,635,810 (GRCm39) Y338F probably damaging Het
Tap2 A T 17: 34,428,184 (GRCm39) Q286L probably benign Het
Tubgcp5 C A 7: 55,458,277 (GRCm39) A396E possibly damaging Het
Ube2o T C 11: 116,430,960 (GRCm39) D980G probably damaging Het
Vmn1r86 T C 7: 12,836,433 (GRCm39) M98V probably benign Het
Vmn2r58 T A 7: 41,513,935 (GRCm39) H236L probably benign Het
Zfp521 T C 18: 13,950,303 (GRCm39) H1217R probably damaging Het
Zfyve1 A T 12: 83,601,779 (GRCm39) F110I probably benign Het
Other mutations in Tedc1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01066:Tedc1 APN 12 113,126,770 (GRCm39) missense probably damaging 0.97
IGL01074:Tedc1 APN 12 113,126,808 (GRCm39) nonsense probably null
IGL01075:Tedc1 APN 12 113,126,808 (GRCm39) nonsense probably null
IGL01077:Tedc1 APN 12 113,126,808 (GRCm39) nonsense probably null
IGL01084:Tedc1 APN 12 113,126,808 (GRCm39) nonsense probably null
IGL01103:Tedc1 APN 12 113,126,808 (GRCm39) nonsense probably null
IGL01108:Tedc1 APN 12 113,126,808 (GRCm39) nonsense probably null
IGL01137:Tedc1 APN 12 113,126,808 (GRCm39) nonsense probably null
IGL01142:Tedc1 APN 12 113,126,808 (GRCm39) nonsense probably null
IGL01149:Tedc1 APN 12 113,126,808 (GRCm39) nonsense probably null
IGL01150:Tedc1 APN 12 113,126,808 (GRCm39) nonsense probably null
IGL01151:Tedc1 APN 12 113,126,808 (GRCm39) nonsense probably null
IGL02646:Tedc1 APN 12 113,120,921 (GRCm39) missense possibly damaging 0.68
IGL02989:Tedc1 APN 12 113,126,941 (GRCm39) missense probably benign 0.09
ANU22:Tedc1 UTSW 12 113,126,808 (GRCm39) nonsense probably null
R1309:Tedc1 UTSW 12 113,125,400 (GRCm39) missense probably benign
R1555:Tedc1 UTSW 12 113,120,117 (GRCm39) unclassified probably benign
R2092:Tedc1 UTSW 12 113,121,340 (GRCm39) missense probably damaging 1.00
R3053:Tedc1 UTSW 12 113,120,087 (GRCm39) unclassified probably benign
R4130:Tedc1 UTSW 12 113,126,828 (GRCm39) missense probably benign 0.01
R5050:Tedc1 UTSW 12 113,120,325 (GRCm39) missense possibly damaging 0.86
R5386:Tedc1 UTSW 12 113,120,302 (GRCm39) missense probably benign 0.03
R6377:Tedc1 UTSW 12 113,124,975 (GRCm39) missense probably damaging 1.00
R6749:Tedc1 UTSW 12 113,121,702 (GRCm39) missense probably damaging 1.00
R6761:Tedc1 UTSW 12 113,125,334 (GRCm39) missense probably damaging 1.00
R8220:Tedc1 UTSW 12 113,120,375 (GRCm39) critical splice donor site probably null
R9240:Tedc1 UTSW 12 113,121,310 (GRCm39) missense probably benign 0.43
Predicted Primers PCR Primer
(F):5'- CCTTGGCTCAAGAGCATCTGTACC -3'
(R):5'- AAACCTCTCAGGAGGACCAGACTG -3'

Sequencing Primer
(F):5'- AAGAGCATCTGTACCTTCTCTCAC -3'
(R):5'- CTCTGAGATCCTACACAGATGG -3'
Posted On 2015-02-04