Incidental Mutation 'R7586:Ttll3'
| ID |
587135 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ttll3
|
| Ensembl Gene |
ENSMUSG00000030276 |
| Gene Name |
tubulin tyrosine ligase-like family, member 3 |
| Synonyms |
4833441J24Rik |
| MMRRC Submission |
045668-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R7586 (G1)
|
| Quality Score |
217.468 |
|
Status
|
Validated
|
| Chromosome |
6 |
| Chromosomal Location |
113366221-113391548 bp(+) (GRCm39) |
| Type of Mutation |
frame shift |
| DNA Base Change (assembly) |
CAAAGTAA to CAAAGTAAAGTAA
at 113376118 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000145049
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000032414]
[ENSMUST00000038889]
[ENSMUST00000204026]
[ENSMUST00000205017]
|
| AlphaFold |
A4Q9E5 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000032414
|
| SMART Domains |
Protein: ENSMUSP00000032414
Gene: ENSMUSG00000030276
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
3 |
20 |
N/A |
INTRINSIC |
|
low complexity region
|
214 |
231 |
N/A |
INTRINSIC |
|
low complexity region
|
234 |
248 |
N/A |
INTRINSIC |
|
Pfam:TTL
|
404 |
698 |
7.7e-84 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000038889
|
| SMART Domains |
Protein: ENSMUSP00000037870
Gene: ENSMUSG00000030276
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
3 |
20 |
N/A |
INTRINSIC |
|
low complexity region
|
214 |
231 |
N/A |
INTRINSIC |
|
low complexity region
|
234 |
248 |
N/A |
INTRINSIC |
|
Pfam:TTL
|
404 |
699 |
9e-85 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000203524
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000204026
|
| SMART Domains |
Protein: ENSMUSP00000145049
Gene: ENSMUSG00000030276
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
66 |
83 |
N/A |
INTRINSIC |
|
low complexity region
|
86 |
100 |
N/A |
INTRINSIC |
|
low complexity region
|
248 |
259 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000205017
|
| Meta Mutation Damage Score |
0.9756 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.9%
|
| Validation Efficiency |
100% (67/67) |
| MGI Phenotype |
PHENOTYPE: Mice homozygous for a knock-out allele exhibit a reduced number of primary cilia in colon epithelia accompanied by an increased rate of cell division which is compensated by faster tissue turnover in the colon. Mice exhibit increased incidence of colon tumors by chemical induction. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 65 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Ankdd1a |
C |
T |
9: 65,409,466 (GRCm39) |
|
probably null |
Het |
| Ankrd31 |
A |
G |
13: 96,968,562 (GRCm39) |
E733G |
possibly damaging |
Het |
| Cars2 |
C |
T |
8: 11,580,321 (GRCm39) |
W239* |
probably null |
Het |
| Catsperz |
A |
T |
19: 6,899,929 (GRCm39) |
L192* |
probably null |
Het |
| Ccdc168 |
G |
A |
1: 44,099,173 (GRCm39) |
R642W |
probably benign |
Het |
| Cdh3 |
T |
C |
8: 107,237,975 (GRCm39) |
|
probably null |
Het |
| Cfh |
C |
T |
1: 140,075,459 (GRCm39) |
V260M |
probably damaging |
Het |
| Clcn4 |
T |
A |
7: 7,296,958 (GRCm39) |
S227C |
probably benign |
Het |
| Cntn3 |
A |
T |
6: 102,397,388 (GRCm39) |
W62R |
probably damaging |
Het |
| Col27a1 |
C |
A |
4: 63,143,278 (GRCm39) |
A322D |
probably damaging |
Het |
| Egflam |
C |
T |
15: 7,238,082 (GRCm39) |
G934S |
probably damaging |
Het |
| Eloa |
A |
G |
4: 135,734,510 (GRCm39) |
V665A |
probably damaging |
Het |
| Epg5 |
A |
G |
18: 78,073,275 (GRCm39) |
T2433A |
probably benign |
Het |
| Ercc5 |
A |
G |
1: 44,215,011 (GRCm39) |
N848S |
possibly damaging |
Het |
| Fbrsl1 |
A |
C |
5: 110,526,020 (GRCm39) |
F61V |
probably damaging |
Het |
| Fry |
T |
C |
5: 150,349,683 (GRCm39) |
Y1595H |
probably damaging |
Het |
| Fstl4 |
A |
G |
11: 52,963,256 (GRCm39) |
N213D |
probably benign |
Het |
| Gab2 |
C |
T |
7: 96,950,645 (GRCm39) |
P446L |
probably damaging |
Het |
| Ganab |
A |
T |
19: 8,888,716 (GRCm39) |
Y552F |
possibly damaging |
Het |
| Gfy |
C |
T |
7: 44,826,962 (GRCm39) |
R378Q |
probably damaging |
Het |
| Gm3285 |
T |
C |
10: 77,697,875 (GRCm39) |
V8A |
unknown |
Het |
| Grip1 |
A |
T |
10: 119,913,043 (GRCm39) |
|
probably null |
Het |
| Gtf3c3 |
A |
G |
1: 54,442,752 (GRCm39) |
L764P |
probably damaging |
Het |
| Igfbp2 |
A |
T |
1: 72,888,307 (GRCm39) |
M150L |
probably benign |
Het |
| Jakmip2 |
C |
T |
18: 43,673,676 (GRCm39) |
R796Q |
probably damaging |
Het |
| Jpt1 |
T |
A |
11: 115,389,021 (GRCm39) |
R141W |
probably damaging |
Het |
| Junb |
T |
C |
8: 85,704,802 (GRCm39) |
E86G |
probably damaging |
Het |
| Klhl41 |
A |
T |
2: 69,505,068 (GRCm39) |
D457V |
probably benign |
Het |
| Lama2 |
T |
C |
10: 26,977,389 (GRCm39) |
Y1930C |
probably benign |
Het |
| Med13 |
A |
T |
11: 86,161,828 (GRCm39) |
I2167N |
probably damaging |
Het |
| Msh3 |
A |
G |
13: 92,485,840 (GRCm39) |
|
probably benign |
Het |
| Myo1b |
A |
C |
1: 51,817,483 (GRCm39) |
I593S |
probably damaging |
Het |
| Myo1c |
A |
T |
11: 75,548,345 (GRCm39) |
T16S |
possibly damaging |
Het |
| Ndufaf4 |
C |
T |
4: 24,901,829 (GRCm39) |
L126F |
probably damaging |
Het |
| Nlrp9a |
A |
T |
7: 26,256,721 (GRCm39) |
N113I |
possibly damaging |
Het |
| Or5d43 |
T |
A |
2: 88,104,794 (GRCm39) |
I200F |
probably damaging |
Het |
| Or5g23 |
G |
C |
2: 85,438,528 (GRCm39) |
S242C |
probably damaging |
Het |
| Or5p6 |
T |
A |
7: 107,631,128 (GRCm39) |
T141S |
probably benign |
Het |
| Pabpc6 |
A |
T |
17: 9,887,611 (GRCm39) |
D313E |
probably damaging |
Het |
| Pcdhb2 |
G |
T |
18: 37,428,857 (GRCm39) |
G277* |
probably null |
Het |
| Phkb |
T |
G |
8: 86,756,226 (GRCm39) |
V840G |
probably damaging |
Het |
| Pip4k2c |
A |
G |
10: 127,034,955 (GRCm39) |
F415S |
probably damaging |
Het |
| Ptprb |
A |
G |
10: 116,179,779 (GRCm39) |
E1112G |
probably damaging |
Het |
| Pum2 |
A |
G |
12: 8,797,206 (GRCm39) |
D847G |
probably damaging |
Het |
| Qrich2 |
C |
T |
11: 116,346,450 (GRCm39) |
R1458H |
probably benign |
Het |
| Rdh11 |
T |
C |
12: 79,231,957 (GRCm39) |
Y199C |
probably damaging |
Het |
| Resf1 |
A |
T |
6: 149,228,291 (GRCm39) |
N446Y |
possibly damaging |
Het |
| Scamp3 |
A |
G |
3: 89,087,673 (GRCm39) |
Y171C |
probably damaging |
Het |
| Serpinb9b |
T |
C |
13: 33,223,743 (GRCm39) |
S312P |
probably damaging |
Het |
| Slain2 |
G |
A |
5: 73,123,165 (GRCm39) |
S461N |
probably benign |
Het |
| Slc23a1 |
G |
A |
18: 35,758,891 (GRCm39) |
T100I |
probably damaging |
Het |
| Spata31d1b |
T |
A |
13: 59,866,194 (GRCm39) |
I1114N |
probably damaging |
Het |
| Spinkl |
A |
G |
18: 44,307,656 (GRCm39) |
S2P |
probably damaging |
Het |
| Srrt |
T |
C |
5: 137,300,457 (GRCm39) |
N173S |
probably damaging |
Het |
| Stk24 |
C |
T |
14: 121,539,699 (GRCm39) |
A166T |
probably damaging |
Het |
| Supt16 |
A |
T |
14: 52,411,013 (GRCm39) |
V697E |
probably damaging |
Het |
| Taf6l |
C |
T |
19: 8,761,210 (GRCm39) |
E53K |
probably damaging |
Het |
| Tmem81 |
A |
T |
1: 132,435,511 (GRCm39) |
I106F |
probably damaging |
Het |
| Tnxb |
C |
A |
17: 34,935,382 (GRCm39) |
L2561I |
probably damaging |
Het |
| Top3b |
G |
A |
16: 16,709,232 (GRCm39) |
R640H |
probably benign |
Het |
| Trpm7 |
A |
T |
2: 126,652,085 (GRCm39) |
S1463T |
probably benign |
Het |
| Tubal3 |
A |
C |
13: 3,978,198 (GRCm39) |
D38A |
possibly damaging |
Het |
| Vps13a |
T |
A |
19: 16,624,962 (GRCm39) |
I2766F |
probably benign |
Het |
| Wwc1 |
A |
T |
11: 35,735,022 (GRCm39) |
V951E |
possibly damaging |
Het |
| Zfp777 |
A |
T |
6: 48,006,152 (GRCm39) |
M414K |
probably benign |
Het |
|
| Other mutations in Ttll3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01338:Ttll3
|
APN |
6 |
113,371,690 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01677:Ttll3
|
APN |
6 |
113,389,945 (GRCm39) |
missense |
probably benign |
|
|
IGL01697:Ttll3
|
APN |
6 |
113,376,690 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01944:Ttll3
|
APN |
6 |
113,391,076 (GRCm39) |
missense |
probably benign |
|
|
IGL02688:Ttll3
|
APN |
6 |
113,376,700 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03068:Ttll3
|
APN |
6 |
113,386,158 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0373:Ttll3
|
UTSW |
6 |
113,375,738 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0472:Ttll3
|
UTSW |
6 |
113,386,300 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0625:Ttll3
|
UTSW |
6 |
113,385,864 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R1868:Ttll3
|
UTSW |
6 |
113,369,725 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R2026:Ttll3
|
UTSW |
6 |
113,375,731 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2061:Ttll3
|
UTSW |
6 |
113,386,003 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R2128:Ttll3
|
UTSW |
6 |
113,389,895 (GRCm39) |
missense |
probably benign |
0.31 |
|
R2896:Ttll3
|
UTSW |
6 |
113,369,683 (GRCm39) |
missense |
probably benign |
0.15 |
|
R2903:Ttll3
|
UTSW |
6 |
113,384,284 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2906:Ttll3
|
UTSW |
6 |
113,369,471 (GRCm39) |
unclassified |
probably benign |
|
|
R4659:Ttll3
|
UTSW |
6 |
113,391,102 (GRCm39) |
missense |
probably benign |
|
|
R4746:Ttll3
|
UTSW |
6 |
113,384,353 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4984:Ttll3
|
UTSW |
6 |
113,389,901 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5358:Ttll3
|
UTSW |
6 |
113,378,292 (GRCm39) |
missense |
probably benign |
0.26 |
|
R5372:Ttll3
|
UTSW |
6 |
113,378,382 (GRCm39) |
nonsense |
probably null |
|
|
R5525:Ttll3
|
UTSW |
6 |
113,389,939 (GRCm39) |
missense |
probably benign |
|
|
R5548:Ttll3
|
UTSW |
6 |
113,370,078 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5694:Ttll3
|
UTSW |
6 |
113,376,669 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5993:Ttll3
|
UTSW |
6 |
113,374,992 (GRCm39) |
nonsense |
probably null |
|
|
R6119:Ttll3
|
UTSW |
6 |
113,371,702 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6268:Ttll3
|
UTSW |
6 |
113,369,524 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6719:Ttll3
|
UTSW |
6 |
113,375,993 (GRCm39) |
intron |
probably benign |
|
|
R6852:Ttll3
|
UTSW |
6 |
113,376,120 (GRCm39) |
frame shift |
probably null |
|
|
R6852:Ttll3
|
UTSW |
6 |
113,376,116 (GRCm39) |
frame shift |
probably null |
|
|
R6852:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
|
R6853:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
|
R6854:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
|
R7170:Ttll3
|
UTSW |
6 |
113,390,839 (GRCm39) |
missense |
probably benign |
0.41 |
|
R7239:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
|
R7302:Ttll3
|
UTSW |
6 |
113,386,246 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7330:Ttll3
|
UTSW |
6 |
113,376,125 (GRCm39) |
frame shift |
probably null |
|
|
R7330:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
|
R7587:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
|
R7701:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
|
R7702:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
|
R7776:Ttll3
|
UTSW |
6 |
113,376,120 (GRCm39) |
frame shift |
probably null |
|
|
R7793:Ttll3
|
UTSW |
6 |
113,376,120 (GRCm39) |
frame shift |
probably null |
|
|
R7797:Ttll3
|
UTSW |
6 |
113,371,738 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R7824:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
|
R7825:Ttll3
|
UTSW |
6 |
113,376,120 (GRCm39) |
frame shift |
probably null |
|
|
R7825:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
|
R7826:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
|
R7827:Ttll3
|
UTSW |
6 |
113,376,123 (GRCm39) |
frame shift |
probably null |
|
|
R7827:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
|
R7831:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
|
R7832:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
|
R7833:Ttll3
|
UTSW |
6 |
113,386,298 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7966:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
|
R8344:Ttll3
|
UTSW |
6 |
113,371,959 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8418:Ttll3
|
UTSW |
6 |
113,371,734 (GRCm39) |
missense |
probably benign |
0.04 |
|
R8768:Ttll3
|
UTSW |
6 |
113,385,949 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9017:Ttll3
|
UTSW |
6 |
113,389,850 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9036:Ttll3
|
UTSW |
6 |
113,376,657 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R9090:Ttll3
|
UTSW |
6 |
113,369,596 (GRCm39) |
missense |
probably benign |
|
|
R9271:Ttll3
|
UTSW |
6 |
113,369,596 (GRCm39) |
missense |
probably benign |
|
|
R9329:Ttll3
|
UTSW |
6 |
113,369,635 (GRCm39) |
missense |
probably benign |
|
|
R9532:Ttll3
|
UTSW |
6 |
113,385,970 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R9535:Ttll3
|
UTSW |
6 |
113,389,834 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9725:Ttll3
|
UTSW |
6 |
113,386,114 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- AAAGAGCAAGCCTCCCCTTG -3'
(R):5'- TGTGACCAGCCTGCCTTTAG -3'
Sequencing Primer
(F):5'- TGTGGCCTCTGTAACCCCAG -3'
(R):5'- GCTGCCTTGGAACTCACTATGAAG -3'
|
| Posted On |
2019-10-24 |
Incidental Mutation