Incidental Mutation 'R5994:Ttll10'
ID 482120
Institutional Source Beutler Lab
Gene Symbol Ttll10
Ensembl Gene ENSMUSG00000029074
Gene Name tubulin tyrosine ligase-like family, member 10
Synonyms 4833412E22Rik, 4930595O22Rik, Ttll5
MMRRC Submission 044173-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R5994 (G1)
Quality Score 106.008
Status Not validated
Chromosome 4
Chromosomal Location 156119292-156135274 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 156133189 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000139077 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000051509] [ENSMUST00000184348] [ENSMUST00000184348] [ENSMUST00000184684]
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000030951
SMART Domains Protein: ENSMUSP00000030951
Gene: ENSMUSG00000029074

DomainStartEndE-ValueType
low complexity region 15 29 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000051509
SMART Domains Protein: ENSMUSP00000055671
Gene: ENSMUSG00000029074

DomainStartEndE-ValueType
low complexity region 14 29 N/A INTRINSIC
low complexity region 63 73 N/A INTRINSIC
low complexity region 104 118 N/A INTRINSIC
Pfam:TTL 189 507 1.8e-48 PFAM
low complexity region 541 583 N/A INTRINSIC
low complexity region 587 600 N/A INTRINSIC
low complexity region 622 638 N/A INTRINSIC
low complexity region 652 671 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000097731
SMART Domains Protein: ENSMUSP00000095337
Gene: ENSMUSG00000029074

DomainStartEndE-ValueType
low complexity region 92 102 N/A INTRINSIC
low complexity region 267 282 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000138361
Predicted Effect noncoding transcript
Transcript: ENSMUST00000153649
SMART Domains Protein: ENSMUSP00000116933
Gene: ENSMUSG00000029074

DomainStartEndE-ValueType
low complexity region 15 29 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000183563
Predicted Effect probably null
Transcript: ENSMUST00000184348
SMART Domains Protein: ENSMUSP00000139316
Gene: ENSMUSG00000029074

DomainStartEndE-ValueType
low complexity region 92 102 N/A INTRINSIC
low complexity region 133 147 N/A INTRINSIC
Pfam:TTL 218 536 7.9e-48 PFAM
low complexity region 570 612 N/A INTRINSIC
low complexity region 616 629 N/A INTRINSIC
low complexity region 651 667 N/A INTRINSIC
low complexity region 681 700 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000184348
SMART Domains Protein: ENSMUSP00000139316
Gene: ENSMUSG00000029074

DomainStartEndE-ValueType
low complexity region 92 102 N/A INTRINSIC
low complexity region 133 147 N/A INTRINSIC
Pfam:TTL 218 536 7.9e-48 PFAM
low complexity region 570 612 N/A INTRINSIC
low complexity region 616 629 N/A INTRINSIC
low complexity region 651 667 N/A INTRINSIC
low complexity region 681 700 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000184684
SMART Domains Protein: ENSMUSP00000139077
Gene: ENSMUSG00000029074

DomainStartEndE-ValueType
low complexity region 15 29 N/A INTRINSIC
Pfam:TTL 100 418 2.5e-48 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000184750
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.5%
  • 10x: 97.4%
  • 20x: 91.7%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A2m A T 6: 121,647,862 (GRCm39) H1118L probably benign Het
Abca8b A G 11: 109,840,592 (GRCm39) probably null Het
Abcb5 A T 12: 118,928,995 (GRCm39) probably null Het
Adcy6 A T 15: 98,491,545 (GRCm39) I1016N probably damaging Het
Afg3l2 A T 18: 67,562,140 (GRCm39) C312S probably damaging Het
Ano8 C T 8: 71,937,478 (GRCm39) V89M probably damaging Het
Arhgap21 C T 2: 20,886,187 (GRCm39) G330D possibly damaging Het
Caskin1 T C 17: 24,715,935 (GRCm39) L195P probably damaging Het
Cfap54 A G 10: 92,874,943 (GRCm39) I514T probably damaging Het
Ctdsp2 G A 10: 126,831,689 (GRCm39) probably benign Het
Cyp4x1 T C 4: 114,979,142 (GRCm39) I152V probably benign Het
Dglucy G A 12: 100,808,959 (GRCm39) R219Q probably benign Het
Disp3 G T 4: 148,338,741 (GRCm39) A810E possibly damaging Het
Dtx4 T C 19: 12,478,517 (GRCm39) Y22C probably damaging Het
Edaradd A T 13: 12,493,377 (GRCm39) I105N probably damaging Het
Eepd1 C T 9: 25,514,749 (GRCm39) P519S probably damaging Het
Fscn3 A T 6: 28,430,294 (GRCm39) S155C probably benign Het
Gm10134 A T 2: 28,396,258 (GRCm39) E51V probably damaging Het
Gm7247 C T 14: 51,601,805 (GRCm39) S26F probably benign Het
Golga7 T C 8: 23,740,281 (GRCm39) E83G probably benign Het
Gpr12 T C 5: 146,520,241 (GRCm39) H227R probably damaging Het
Hoxa2 T G 6: 52,141,372 (GRCm39) S85R possibly damaging Het
Hrnr T C 3: 93,239,607 (GRCm39) S3282P unknown Het
Ift74 C A 4: 94,579,961 (GRCm39) T543K possibly damaging Het
Klf10 C A 15: 38,296,285 (GRCm39) R420L probably damaging Het
Krt77 T A 15: 101,771,290 (GRCm39) I338F probably damaging Het
Limch1 A T 5: 67,131,965 (GRCm39) S152C probably damaging Het
Mgat4e T A 1: 134,469,234 (GRCm39) H270L probably benign Het
Myrf A T 19: 10,196,481 (GRCm39) L504Q probably null Het
Nckipsd A G 9: 108,691,176 (GRCm39) Q366R probably benign Het
Npy5r A T 8: 67,134,751 (GRCm39) V14D probably benign Het
Nrap T A 19: 56,340,031 (GRCm39) R830* probably null Het
Ogfrl1 A T 1: 23,418,070 (GRCm39) Y103N probably damaging Het
Or10g7 A T 9: 39,905,519 (GRCm39) R138* probably null Het
P2rx4 T A 5: 122,863,142 (GRCm39) L232H probably damaging Het
Pabpc2 A T 18: 39,906,947 (GRCm39) T71S probably benign Het
Paip2b C A 6: 83,785,867 (GRCm39) S121I probably damaging Het
Pofut1 C T 2: 153,103,149 (GRCm39) T261I possibly damaging Het
Ppp6c G T 2: 39,101,004 (GRCm39) T46K possibly damaging Het
Prkd2 C A 7: 16,584,261 (GRCm39) H371Q probably benign Het
Prrc2c A T 1: 162,501,725 (GRCm39) probably null Het
Psd3 C T 8: 68,172,620 (GRCm39) A894T probably damaging Het
Pygm A T 19: 6,448,073 (GRCm39) probably null Het
Pzp A T 6: 128,468,560 (GRCm39) M989K probably damaging Het
Ralgapa2 A T 2: 146,203,373 (GRCm39) S1159T probably benign Het
Rapgefl1 T C 11: 98,740,986 (GRCm39) F575L probably benign Het
Rassf6 A G 5: 90,765,627 (GRCm39) L28S probably damaging Het
Rbp3 G T 14: 33,676,857 (GRCm39) K268N probably damaging Het
Rela C T 19: 5,697,092 (GRCm39) T433M possibly damaging Het
Rnf103 T A 6: 71,473,894 (GRCm39) S102R probably damaging Het
Scarf2 A G 16: 17,624,243 (GRCm39) N516S probably damaging Het
Sdcbp2 T C 2: 151,429,403 (GRCm39) I241T probably damaging Het
Septin7 T C 9: 25,199,494 (GRCm39) I131T possibly damaging Het
Sh3pxd2b T C 11: 32,357,570 (GRCm39) F191L probably damaging Het
Siglec15 C A 18: 78,090,590 (GRCm39) C236F probably damaging Het
Slc11a2 T C 15: 100,295,562 (GRCm39) T520A probably benign Het
Slc26a11 C A 11: 119,270,738 (GRCm39) F553L probably benign Het
Smchd1 G A 17: 71,672,404 (GRCm39) P1596S possibly damaging Het
Taar7b A G 10: 23,876,246 (GRCm39) H137R probably damaging Het
Thap12 T A 7: 98,365,237 (GRCm39) C468* probably null Het
Timp4 C T 6: 115,224,315 (GRCm39) G118D probably damaging Het
Tnnt3 A G 7: 142,065,003 (GRCm39) K48E probably damaging Het
Trmt10a T A 3: 137,862,475 (GRCm39) I255N probably damaging Het
Tut7 T G 13: 59,937,023 (GRCm39) Y806S probably damaging Het
Ube4b A G 4: 149,457,389 (GRCm39) Y283H probably damaging Het
Ucp1 G T 8: 84,020,567 (GRCm39) V126L possibly damaging Het
Unc13b T A 4: 43,172,596 (GRCm39) probably benign Het
Vps13b T C 15: 35,875,918 (GRCm39) S2768P probably damaging Het
Zfp101 T A 17: 33,599,936 (GRCm39) M607L probably benign Het
Zfp292 C T 4: 34,805,464 (GRCm39) V2527M possibly damaging Het
Zfp503 T A 14: 22,035,630 (GRCm39) T429S possibly damaging Het
Other mutations in Ttll10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01629:Ttll10 APN 4 156,131,351 (GRCm39) missense probably benign 0.09
IGL02109:Ttll10 APN 4 156,131,937 (GRCm39) missense probably benign
IGL02121:Ttll10 APN 4 156,132,890 (GRCm39) missense probably benign 0.04
F6893:Ttll10 UTSW 4 156,132,775 (GRCm39) missense probably benign 0.00
R0366:Ttll10 UTSW 4 156,119,612 (GRCm39) missense probably damaging 0.97
R0502:Ttll10 UTSW 4 156,132,005 (GRCm39) splice site probably benign
R0503:Ttll10 UTSW 4 156,132,005 (GRCm39) splice site probably benign
R0523:Ttll10 UTSW 4 156,129,818 (GRCm39) nonsense probably null
R0865:Ttll10 UTSW 4 156,128,135 (GRCm39) missense probably damaging 1.00
R0907:Ttll10 UTSW 4 156,120,621 (GRCm39) nonsense probably null
R1125:Ttll10 UTSW 4 156,119,495 (GRCm39) missense possibly damaging 0.73
R1555:Ttll10 UTSW 4 156,119,596 (GRCm39) missense probably benign 0.00
R1797:Ttll10 UTSW 4 156,132,024 (GRCm39) missense probably damaging 0.96
R3899:Ttll10 UTSW 4 156,120,257 (GRCm39) missense probably damaging 1.00
R4426:Ttll10 UTSW 4 156,133,018 (GRCm39) missense possibly damaging 0.55
R5715:Ttll10 UTSW 4 156,129,848 (GRCm39) missense probably damaging 1.00
R5762:Ttll10 UTSW 4 156,119,438 (GRCm39) missense possibly damaging 0.93
R5814:Ttll10 UTSW 4 156,132,084 (GRCm39) missense possibly damaging 0.51
R5958:Ttll10 UTSW 4 156,120,523 (GRCm39) splice site probably null
R6084:Ttll10 UTSW 4 156,129,814 (GRCm39) missense probably benign 0.34
R7027:Ttll10 UTSW 4 156,120,258 (GRCm39) missense possibly damaging 0.70
R7719:Ttll10 UTSW 4 156,131,665 (GRCm39) splice site probably null
R8010:Ttll10 UTSW 4 156,131,618 (GRCm39) missense probably damaging 1.00
R8118:Ttll10 UTSW 4 156,129,219 (GRCm39) missense probably benign 0.05
R8167:Ttll10 UTSW 4 156,129,213 (GRCm39) missense probably null 0.01
R8213:Ttll10 UTSW 4 156,120,691 (GRCm39) missense probably benign 0.15
R8835:Ttll10 UTSW 4 156,133,055 (GRCm39) missense probably benign 0.00
R9487:Ttll10 UTSW 4 156,127,616 (GRCm39) missense probably benign 0.00
R9639:Ttll10 UTSW 4 156,119,503 (GRCm39) missense probably benign 0.07
Z1176:Ttll10 UTSW 4 156,132,974 (GRCm39) missense probably benign
Z1177:Ttll10 UTSW 4 156,131,895 (GRCm39) missense possibly damaging 0.57
Predicted Primers
Posted On 2017-06-27