Incidental Mutation 'R5330:Ttll13'
ID423148
Institutional Source Beutler Lab
Gene Symbol Ttll13
Ensembl Gene ENSMUSG00000045467
Gene Nametubulin tyrosine ligase-like family, member 13
Synonyms1700111A04Rik
MMRRC Submission 042912-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.173) question?
Stock #R5330 (G1)
Quality Score225
Status Validated
Chromosome7
Chromosomal Location80246376-80260821 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 80260509 bp
ZygosityHeterozygous
Amino Acid Change Valine to Alanine at position 800 (V800A)
Ref Sequence ENSEMBL: ENSMUSP00000062795 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000058266] [ENSMUST00000117989] [ENSMUST00000205270]
Predicted Effect probably benign
Transcript: ENSMUST00000058266
AA Change: V800A

PolyPhen 2 Score 0.326 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000062795
Gene: ENSMUSG00000045467
AA Change: V800A

DomainStartEndE-ValueType
low complexity region 9 30 N/A INTRINSIC
low complexity region 78 86 N/A INTRINSIC
Pfam:TTL 131 427 3.4e-90 PFAM
coiled coil region 504 528 N/A INTRINSIC
low complexity region 589 603 N/A INTRINSIC
low complexity region 646 657 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000107381
SMART Domains Protein: ENSMUSP00000103004
Gene: ENSMUSG00000045467

DomainStartEndE-ValueType
low complexity region 9 30 N/A INTRINSIC
low complexity region 78 86 N/A INTRINSIC
Pfam:TTL 131 427 3.5e-90 PFAM
coiled coil region 504 528 N/A INTRINSIC
low complexity region 589 603 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000117989
SMART Domains Protein: ENSMUSP00000113444
Gene: ENSMUSG00000047084

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
coiled coil region 46 70 N/A INTRINSIC
Pfam:Neugrin 73 293 1.2e-99 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000138005
Predicted Effect probably benign
Transcript: ENSMUST00000205270
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.7%
  • 10x: 97.5%
  • 20x: 95.8%
Validation Efficiency 99% (95/96)
Allele List at MGI
Other mutations in this stock
Total: 88 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700017D01Rik A G 19: 11,091,858 probably benign Het
4930505A04Rik C T 11: 30,426,349 V173M probably damaging Het
A2m A G 6: 121,638,416 D83G probably benign Het
Abca16 T A 7: 120,503,377 I833N probably benign Het
Adam6b C A 12: 113,490,580 P339H possibly damaging Het
Adgrb2 A T 4: 130,022,202 H1505L possibly damaging Het
Aktip A T 8: 91,126,724 F122I probably damaging Het
Ankrd27 T A 7: 35,615,926 L500* probably null Het
Blm T C 7: 80,458,936 E55G possibly damaging Het
Carmil1 A T 13: 24,025,946 probably null Het
Cdca7 T C 2: 72,484,698 C311R probably damaging Het
Cds1 T C 5: 101,798,495 S187P probably damaging Het
Chuk A T 19: 44,078,955 V587E probably damaging Het
Commd10 T C 18: 46,960,430 V19A probably damaging Het
Ctnnd2 C T 15: 30,332,115 T48I probably damaging Het
Cyp2b10 T A 7: 25,913,989 Y203* probably null Het
Dchs1 A T 7: 105,754,602 V2911E probably damaging Het
Dnah12 G A 14: 26,773,830 E1472K probably damaging Het
Dnah3 T C 7: 119,943,648 T3514A probably benign Het
Dnah6 T A 6: 73,074,590 I3074F probably damaging Het
Dnase1l1 C T X: 74,277,038 probably null Het
Fam131c A T 4: 141,382,830 T180S probably benign Het
Fbxo41 T C 6: 85,479,906 E427G probably benign Het
Gabrr2 A G 4: 33,082,583 K236E possibly damaging Het
Gm10152 A T 7: 144,763,546 noncoding transcript Het
Gm10313 T A 8: 46,255,453 noncoding transcript Het
Gm5414 C A 15: 101,624,664 V443F probably damaging Het
Gm7334 T C 17: 50,699,132 S149P possibly damaging Het
Grik2 G A 10: 49,132,771 T740M probably damaging Het
Hdac5 T C 11: 102,197,354 Y930C probably damaging Het
Hepacam2 T C 6: 3,483,377 T211A probably benign Het
Herc4 G T 10: 63,307,799 E703* probably null Het
Hivep2 A G 10: 14,131,420 K1254R probably damaging Het
Hras T C 7: 141,192,940 M1V probably null Het
Ikbkap T C 4: 56,800,001 T42A probably benign Het
Il23r T G 6: 67,423,495 Q617P probably damaging Het
Kank1 A G 19: 25,411,329 T789A probably damaging Het
Kcnj12 A G 11: 61,070,186 K437E probably benign Het
Lct A T 1: 128,298,529 D1374E probably benign Het
Luc7l C A 17: 26,275,733 C104* probably null Het
Lurap1 G A 4: 116,144,404 L31F probably damaging Het
Mark4 G A 7: 19,436,983 P321S probably damaging Het
Med18 A G 4: 132,463,066 probably benign Het
Mia2 A G 12: 59,095,812 S5G probably benign Het
Mrgprb3 T C 7: 48,642,934 T290A possibly damaging Het
Negr1 A T 3: 157,069,276 K210* probably null Het
Nktr T C 9: 121,752,768 probably benign Het
Nob1 T G 8: 107,416,249 T267P probably damaging Het
Nos3 A G 5: 24,369,904 E307G probably damaging Het
Nrxn2 A G 19: 6,490,081 T796A probably damaging Het
Nwd2 C A 5: 63,806,516 L1148I probably benign Het
Pcdh17 T A 14: 84,533,046 V988E probably damaging Het
Pcdha4 G A 18: 36,954,702 R646H probably benign Het
Per3 G T 4: 151,041,302 L187I probably damaging Het
Phlpp2 A G 8: 109,934,035 D774G probably damaging Het
Pibf1 T C 14: 99,140,646 Y403H probably damaging Het
Plcl2 G A 17: 50,509,848 A81T probably benign Het
Polr2a T C 11: 69,747,275 N123D probably benign Het
Psma5 T G 3: 108,268,070 V146G possibly damaging Het
Ptprk A T 10: 28,587,080 D189V probably damaging Het
Relb C T 7: 19,606,705 G509S possibly damaging Het
Rgs11 A T 17: 26,202,973 M1L probably benign Het
Rhbg T A 3: 88,245,468 T313S probably benign Het
Ripply2 T A 9: 87,015,638 probably benign Het
Scap T C 9: 110,381,633 V1011A probably benign Het
Scarf1 G A 11: 75,515,580 G230D probably damaging Het
Sel1l3 A T 5: 53,186,009 Y314N possibly damaging Het
Slc17a8 A G 10: 89,589,494 probably null Het
Slc22a14 A T 9: 119,230,596 L153Q probably damaging Het
Slc22a27 A G 19: 7,879,455 I406T probably benign Het
Slc30a6 A G 17: 74,423,195 D355G probably benign Het
Snta1 C A 2: 154,378,020 E403* probably null Het
Socs7 A G 11: 97,378,026 D382G possibly damaging Het
Spata31d1a A T 13: 59,700,403 C1304S possibly damaging Het
Srebf2 T A 15: 82,196,208 I834N possibly damaging Het
Steap1 G T 5: 5,740,422 H175Q probably damaging Het
Sult2a8 T C 7: 14,413,754 E204G possibly damaging Het
Tacc2 T C 7: 130,733,528 S524P probably damaging Het
Tbc1d9b C T 11: 50,146,313 A263V probably benign Het
Tecta A C 9: 42,337,856 D1903E probably damaging Het
Tmem222 A C 4: 133,277,624 M34R possibly damaging Het
Tnik A G 3: 28,542,018 T187A probably damaging Het
Trpv4 A G 5: 114,635,543 Y253H probably damaging Het
Trpv5 G A 6: 41,660,332 R358C probably benign Het
Ush2a G A 1: 188,728,381 G2613E probably benign Het
Vmn2r58 G A 7: 41,863,960 Q420* probably null Het
Zranb3 G A 1: 127,959,720 P990L probably damaging Het
Zswim9 T A 7: 13,259,985 D748V probably damaging Het
Other mutations in Ttll13
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00808:Ttll13 APN 7 80259549 missense possibly damaging 0.73
IGL01289:Ttll13 APN 7 80260439 missense probably benign
IGL02026:Ttll13 APN 7 80260379 missense probably benign 0.03
IGL02816:Ttll13 APN 7 80253094 missense possibly damaging 0.91
R0345:Ttll13 UTSW 7 80247336 missense probably benign 0.00
R0347:Ttll13 UTSW 7 80260505 missense possibly damaging 0.73
R0491:Ttll13 UTSW 7 80260350 missense probably benign
R1779:Ttll13 UTSW 7 80260508 missense probably benign 0.33
R1983:Ttll13 UTSW 7 80253616 missense possibly damaging 0.70
R2218:Ttll13 UTSW 7 80252502 missense probably damaging 1.00
R2520:Ttll13 UTSW 7 80250216 missense probably damaging 1.00
R4496:Ttll13 UTSW 7 80256919 missense probably benign 0.08
R4736:Ttll13 UTSW 7 80248276 intron probably null
R5930:Ttll13 UTSW 7 80253166 missense probably damaging 1.00
R5985:Ttll13 UTSW 7 80254638 missense probably damaging 1.00
R6060:Ttll13 UTSW 7 80258743 missense probably damaging 1.00
R6182:Ttll13 UTSW 7 80260233 missense probably benign 0.18
R6256:Ttll13 UTSW 7 80258304 missense probably benign 0.00
R6501:Ttll13 UTSW 7 80250176 missense possibly damaging 0.89
R6901:Ttll13 UTSW 7 80250182 missense probably damaging 1.00
R7064:Ttll13 UTSW 7 80257030 missense probably null 0.53
R7127:Ttll13 UTSW 7 80253658 missense possibly damaging 0.53
R7217:Ttll13 UTSW 7 80254163 missense probably damaging 1.00
R7241:Ttll13 UTSW 7 80254163 missense probably damaging 1.00
R7243:Ttll13 UTSW 7 80254163 missense probably damaging 1.00
R7244:Ttll13 UTSW 7 80254163 missense probably damaging 1.00
R7246:Ttll13 UTSW 7 80254163 missense probably damaging 1.00
R7317:Ttll13 UTSW 7 80254163 missense probably damaging 1.00
R7340:Ttll13 UTSW 7 80257024 missense probably damaging 0.98
R7453:Ttll13 UTSW 7 80260434 missense probably benign
R7579:Ttll13 UTSW 7 80258233 missense probably benign 0.00
R7810:Ttll13 UTSW 7 80253127 missense probably damaging 1.00
R7855:Ttll13 UTSW 7 80254097 missense probably damaging 1.00
R7860:Ttll13 UTSW 7 80255387 missense probably benign 0.02
R7938:Ttll13 UTSW 7 80254097 missense probably damaging 1.00
R7943:Ttll13 UTSW 7 80255387 missense probably benign 0.02
Predicted Primers PCR Primer
(F):5'- CACCAGTACTGCAGCATTCCAG -3'
(R):5'- ACCGTAGTCGCTTTTGACTC -3'

Sequencing Primer
(F):5'- TGCAGCATTCCAGCCCAC -3'
(R):5'- TTGACTCCTCCGGGAAAGGAATTC -3'
Posted On2016-08-04