Incidental Mutation 'R0646:Mtor'
ID |
57138 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Mtor
|
Ensembl Gene |
ENSMUSG00000028991 |
Gene Name |
mechanistic target of rapamycin kinase |
Synonyms |
flat, 2610315D21Rik, RAPT1, RAFT1, mechanistic target of rapamycin (serine/threonine kinase), FKBP-rapamycin-associated protein FRAP, Frap1 |
MMRRC Submission |
038831-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R0646 (G1)
|
Quality Score |
207 |
Status
|
Validated
|
Chromosome |
4 |
Chromosomal Location |
148533068-148642140 bp(+) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
T to A
at 148568811 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Stop codon
at position 1110
(Y1110*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000099510
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000103221]
|
AlphaFold |
Q9JLN9 |
Predicted Effect |
probably null
Transcript: ENSMUST00000103221
AA Change: Y1110*
|
SMART Domains |
Protein: ENSMUSP00000099510 Gene: ENSMUSG00000028991 AA Change: Y1110*
Domain | Start | End | E-Value | Type |
low complexity region
|
7 |
21 |
N/A |
INTRINSIC |
low complexity region
|
179 |
191 |
N/A |
INTRINSIC |
low complexity region
|
277 |
288 |
N/A |
INTRINSIC |
low complexity region
|
774 |
790 |
N/A |
INTRINSIC |
DUF3385
|
854 |
1024 |
1.51e-93 |
SMART |
low complexity region
|
1279 |
1300 |
N/A |
INTRINSIC |
Pfam:FAT
|
1513 |
1908 |
2.3e-134 |
PFAM |
Rapamycin_bind
|
2015 |
2114 |
7.94e-61 |
SMART |
PI3Kc
|
2183 |
2484 |
8.84e-121 |
SMART |
FATC
|
2517 |
2549 |
2.11e-15 |
SMART |
|
Meta Mutation Damage Score |
0.9755 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.7%
- 10x: 97.4%
- 20x: 95.7%
|
Validation Efficiency |
95% (123/130) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to a family of phosphatidylinositol kinase-related kinases. These kinases mediate cellular responses to stresses such as DNA damage and nutrient deprivation. This protein acts as the target for the cell-cycle arrest and immunosuppressive effects of the FKBP12-rapamycin complex. The ANGPTL7 gene is located in an intron of this gene. [provided by RefSeq, Sep 2008] PHENOTYPE: Mice homozygous for targeted, gene trap and ENU-induced null alleles exhibit embryonic lethality by E12.5 with abnormal embryogenesis. Mice homozygous for the ENU mutation further exhibit abnormal brain development. [provided by MGI curators]
|
Allele List at MGI |
All alleles(25) : Targeted(12) Gene trapped(12) Chemically induced(1)
|
Other mutations in this stock |
Total: 125 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930432E11Rik |
C |
T |
7: 29,260,710 (GRCm39) |
|
noncoding transcript |
Het |
Abcb11 |
A |
G |
2: 69,115,627 (GRCm39) |
I579T |
probably damaging |
Het |
Abcc9 |
T |
C |
6: 142,627,830 (GRCm39) |
N400S |
probably benign |
Het |
Adarb2 |
T |
C |
13: 8,781,855 (GRCm39) |
L577P |
probably damaging |
Het |
Agt |
A |
C |
8: 125,283,852 (GRCm39) |
N422K |
probably damaging |
Het |
Ahnak |
A |
T |
19: 8,990,766 (GRCm39) |
K4017* |
probably null |
Het |
Akap13 |
C |
A |
7: 75,397,494 (GRCm39) |
Q2575K |
probably damaging |
Het |
Aldh3a2 |
A |
T |
11: 61,144,541 (GRCm39) |
I339K |
probably damaging |
Het |
Alox15 |
G |
T |
11: 70,236,450 (GRCm39) |
Y483* |
probably null |
Het |
Ampd1 |
A |
T |
3: 103,006,913 (GRCm39) |
I713F |
probably damaging |
Het |
Amph |
A |
T |
13: 19,297,286 (GRCm39) |
E344V |
possibly damaging |
Het |
Arhgef18 |
T |
C |
8: 3,436,959 (GRCm39) |
Y250H |
probably damaging |
Het |
Arid5b |
A |
G |
10: 67,932,807 (GRCm39) |
S1032P |
probably damaging |
Het |
Armc8 |
C |
A |
9: 99,387,741 (GRCm39) |
L393F |
probably damaging |
Het |
Bpnt1 |
A |
G |
1: 185,077,623 (GRCm39) |
|
probably null |
Het |
Cachd1 |
G |
A |
4: 100,845,418 (GRCm39) |
R970H |
probably damaging |
Het |
Cd207 |
T |
C |
6: 83,652,738 (GRCm39) |
T131A |
probably benign |
Het |
Cd83 |
G |
A |
13: 43,951,009 (GRCm39) |
V54I |
probably benign |
Het |
Cfap43 |
T |
C |
19: 47,752,115 (GRCm39) |
K1086E |
probably benign |
Het |
Cfap65 |
A |
T |
1: 74,941,328 (GRCm39) |
V1837E |
probably benign |
Het |
Clcnka |
T |
A |
4: 141,123,917 (GRCm39) |
H89L |
probably benign |
Het |
Cnga4 |
T |
C |
7: 105,054,182 (GRCm39) |
I50T |
possibly damaging |
Het |
Cog5 |
A |
G |
12: 31,887,358 (GRCm39) |
|
probably benign |
Het |
Col11a2 |
T |
A |
17: 34,278,322 (GRCm39) |
|
probably null |
Het |
Col28a1 |
T |
G |
6: 8,175,291 (GRCm39) |
I186L |
possibly damaging |
Het |
Col4a2 |
T |
A |
8: 11,481,252 (GRCm39) |
M808K |
probably benign |
Het |
Copb2 |
A |
G |
9: 98,445,528 (GRCm39) |
|
probably benign |
Het |
Dbnl |
G |
A |
11: 5,745,441 (GRCm39) |
|
probably benign |
Het |
Dbx2 |
T |
C |
15: 95,552,493 (GRCm39) |
T51A |
possibly damaging |
Het |
Dcp1a |
A |
T |
14: 30,224,842 (GRCm39) |
M123L |
probably damaging |
Het |
Ddx42 |
T |
A |
11: 106,123,659 (GRCm39) |
F217I |
probably benign |
Het |
Dlc1 |
T |
C |
8: 37,325,205 (GRCm39) |
T367A |
probably benign |
Het |
Dmgdh |
A |
T |
13: 93,888,863 (GRCm39) |
T834S |
probably benign |
Het |
Dnah8 |
T |
C |
17: 30,903,147 (GRCm39) |
S929P |
probably damaging |
Het |
Dnase1l2 |
C |
A |
17: 24,660,056 (GRCm39) |
V271L |
possibly damaging |
Het |
Dsc1 |
T |
C |
18: 20,229,114 (GRCm39) |
Y392C |
probably damaging |
Het |
Edn1 |
T |
C |
13: 42,458,718 (GRCm39) |
|
probably benign |
Het |
Efcab3 |
G |
A |
11: 104,611,327 (GRCm39) |
D390N |
probably benign |
Het |
Eps8l3 |
T |
C |
3: 107,792,126 (GRCm39) |
L351P |
probably damaging |
Het |
F12 |
G |
A |
13: 55,570,296 (GRCm39) |
|
probably benign |
Het |
Fam47e |
T |
C |
5: 92,726,317 (GRCm39) |
|
probably benign |
Het |
Fcrl5 |
C |
A |
3: 87,349,320 (GRCm39) |
Q32K |
probably benign |
Het |
Fndc1 |
C |
T |
17: 7,960,505 (GRCm39) |
V1637I |
possibly damaging |
Het |
Foxg1 |
G |
T |
12: 49,431,350 (GRCm39) |
|
probably benign |
Het |
Frrs1 |
A |
T |
3: 116,696,070 (GRCm39) |
I530F |
possibly damaging |
Het |
Galnt5 |
A |
T |
2: 57,889,097 (GRCm39) |
K232N |
probably benign |
Het |
Ggt5 |
G |
A |
10: 75,438,482 (GRCm39) |
V68M |
probably damaging |
Het |
Gm16519 |
T |
C |
17: 71,236,101 (GRCm39) |
C17R |
probably benign |
Het |
Gm17535 |
A |
G |
9: 3,035,804 (GRCm39) |
Y224C |
probably null |
Het |
Gm9631 |
T |
G |
11: 121,836,455 (GRCm39) |
D28A |
probably damaging |
Het |
Gpx2 |
T |
C |
12: 76,842,087 (GRCm39) |
I21M |
probably benign |
Het |
H2-Q2 |
T |
G |
17: 35,564,661 (GRCm39) |
D354E |
probably damaging |
Het |
Icam2 |
A |
T |
11: 106,271,717 (GRCm39) |
I71K |
probably damaging |
Het |
Il12a |
T |
C |
3: 68,605,223 (GRCm39) |
|
probably benign |
Het |
Insm2 |
C |
G |
12: 55,647,225 (GRCm39) |
A323G |
probably benign |
Het |
Itga1 |
T |
C |
13: 115,104,835 (GRCm39) |
T1064A |
probably benign |
Het |
Itgad |
T |
A |
7: 127,773,176 (GRCm39) |
V11E |
possibly damaging |
Het |
Kctd15 |
C |
T |
7: 34,344,306 (GRCm39) |
S115N |
probably damaging |
Het |
Klra5 |
A |
G |
6: 129,880,527 (GRCm39) |
W124R |
probably damaging |
Het |
Kng2 |
T |
A |
16: 22,806,486 (GRCm39) |
D571V |
probably benign |
Het |
Kpna6 |
A |
T |
4: 129,544,583 (GRCm39) |
F380I |
probably benign |
Het |
Lipo3 |
A |
T |
19: 33,762,169 (GRCm39) |
Y109* |
probably null |
Het |
Lrrc37 |
T |
A |
11: 103,503,986 (GRCm39) |
K485* |
probably null |
Het |
Man2a2 |
T |
C |
7: 80,012,945 (GRCm39) |
H540R |
possibly damaging |
Het |
Map2k4 |
T |
C |
11: 65,603,101 (GRCm39) |
E188G |
probably damaging |
Het |
Mast4 |
T |
C |
13: 102,895,252 (GRCm39) |
|
probably benign |
Het |
Mbtd1 |
A |
G |
11: 93,796,038 (GRCm39) |
D25G |
probably damaging |
Het |
Med13 |
T |
A |
11: 86,221,915 (GRCm39) |
Q238L |
possibly damaging |
Het |
Mmachc |
A |
G |
4: 116,560,851 (GRCm39) |
Y215H |
probably damaging |
Het |
Nek2 |
A |
G |
1: 191,554,331 (GRCm39) |
N57D |
probably damaging |
Het |
Nek7 |
ACCCC |
ACCC |
1: 138,443,431 (GRCm39) |
|
probably null |
Het |
Neo1 |
G |
T |
9: 58,838,317 (GRCm39) |
T489K |
probably damaging |
Het |
Neu1 |
T |
A |
17: 35,153,736 (GRCm39) |
Y387N |
probably damaging |
Het |
Nfasc |
A |
T |
1: 132,536,176 (GRCm39) |
C586* |
probably null |
Het |
Nle1 |
G |
A |
11: 82,795,671 (GRCm39) |
L259F |
probably damaging |
Het |
Nrde2 |
G |
A |
12: 100,110,105 (GRCm39) |
Q309* |
probably null |
Het |
Nufip2 |
C |
T |
11: 77,577,279 (GRCm39) |
H76Y |
probably benign |
Het |
Or10ak16 |
A |
C |
4: 118,750,687 (GRCm39) |
T136P |
probably damaging |
Het |
Or2y13 |
A |
T |
11: 49,415,405 (GRCm39) |
N285I |
probably damaging |
Het |
Or4k6 |
A |
T |
14: 50,476,096 (GRCm39) |
I82N |
probably damaging |
Het |
Or52e18 |
A |
T |
7: 104,609,018 (GRCm39) |
I307N |
probably benign |
Het |
Or52r1c |
T |
C |
7: 102,735,358 (GRCm39) |
F206S |
probably damaging |
Het |
Or9s18 |
A |
T |
13: 65,300,877 (GRCm39) |
I280F |
probably damaging |
Het |
Pcdhb5 |
A |
G |
18: 37,454,675 (GRCm39) |
T352A |
probably benign |
Het |
Pcdhb7 |
A |
T |
18: 37,476,442 (GRCm39) |
D526V |
probably damaging |
Het |
Phkg1 |
A |
T |
5: 129,893,394 (GRCm39) |
|
probably null |
Het |
Plg |
C |
T |
17: 12,637,623 (GRCm39) |
T744M |
probably damaging |
Het |
Plxnd1 |
A |
C |
6: 115,935,660 (GRCm39) |
|
probably benign |
Het |
Poglut1 |
A |
T |
16: 38,349,837 (GRCm39) |
I312N |
probably damaging |
Het |
Ppp1r16a |
C |
T |
15: 76,574,999 (GRCm39) |
|
probably benign |
Het |
Ppt1 |
A |
G |
4: 122,737,892 (GRCm39) |
M77V |
probably benign |
Het |
Pramel26 |
A |
C |
4: 143,539,155 (GRCm39) |
S113A |
possibly damaging |
Het |
Pramel5 |
G |
T |
4: 143,998,190 (GRCm39) |
T351N |
probably damaging |
Het |
Psmb4 |
G |
A |
3: 94,792,275 (GRCm39) |
R216C |
probably benign |
Het |
Ptprd |
T |
C |
4: 76,002,640 (GRCm39) |
T699A |
probably damaging |
Het |
Retreg3 |
A |
T |
11: 100,989,455 (GRCm39) |
|
probably benign |
Het |
Sanbr |
C |
T |
11: 23,525,491 (GRCm39) |
R716H |
probably damaging |
Het |
Scaper |
G |
A |
9: 55,665,340 (GRCm39) |
A389V |
probably damaging |
Het |
Serinc5 |
G |
A |
13: 92,825,245 (GRCm39) |
D225N |
possibly damaging |
Het |
Slco1a1 |
T |
G |
6: 141,871,480 (GRCm39) |
|
probably benign |
Het |
Snapc1 |
C |
T |
12: 74,021,806 (GRCm39) |
R81C |
probably damaging |
Het |
Sod3 |
A |
T |
5: 52,525,421 (GRCm39) |
D40V |
probably benign |
Het |
Sorcs3 |
C |
A |
19: 48,194,734 (GRCm39) |
A39E |
probably benign |
Het |
Spon1 |
A |
T |
7: 113,639,056 (GRCm39) |
T761S |
probably benign |
Het |
Syde2 |
A |
G |
3: 145,720,004 (GRCm39) |
|
probably null |
Het |
Synm |
T |
A |
7: 67,408,916 (GRCm39) |
D154V |
probably benign |
Het |
Synpo2 |
T |
C |
3: 122,908,098 (GRCm39) |
E406G |
probably damaging |
Het |
Tcea3 |
T |
A |
4: 135,975,382 (GRCm39) |
L8* |
probably null |
Het |
Tec |
G |
A |
5: 72,980,840 (GRCm39) |
L33F |
probably damaging |
Het |
Tex15 |
T |
A |
8: 34,072,354 (GRCm39) |
S2634T |
possibly damaging |
Het |
Tg |
T |
A |
15: 66,601,475 (GRCm39) |
Y162N |
probably damaging |
Het |
Tmem8b |
G |
A |
4: 43,690,123 (GRCm39) |
V853I |
probably benign |
Het |
Togaram1 |
A |
G |
12: 65,068,240 (GRCm39) |
K1748E |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,728,822 (GRCm39) |
|
probably benign |
Het |
Usp36 |
C |
T |
11: 118,163,847 (GRCm39) |
D234N |
probably damaging |
Het |
Usp40 |
G |
A |
1: 87,906,244 (GRCm39) |
P664S |
probably benign |
Het |
Vmn1r54 |
T |
A |
6: 90,246,635 (GRCm39) |
L183H |
probably benign |
Het |
Vmn1r58 |
T |
G |
7: 5,413,676 (GRCm39) |
I185L |
probably benign |
Het |
Wnt8a |
A |
T |
18: 34,680,618 (GRCm39) |
R328W |
probably benign |
Het |
Yars1 |
A |
G |
4: 129,107,732 (GRCm39) |
|
probably benign |
Het |
Zbtb49 |
A |
C |
5: 38,358,018 (GRCm39) |
M745R |
probably damaging |
Het |
Zeb1 |
T |
G |
18: 5,759,027 (GRCm39) |
F162V |
probably damaging |
Het |
Zfp369 |
A |
T |
13: 65,445,362 (GRCm39) |
H835L |
probably damaging |
Het |
Zic5 |
A |
G |
14: 122,701,351 (GRCm39) |
V460A |
unknown |
Het |
Zp3 |
A |
G |
5: 136,013,210 (GRCm39) |
N181D |
possibly damaging |
Het |
|
Other mutations in Mtor |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01123:Mtor
|
APN |
4 |
148,537,494 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01447:Mtor
|
APN |
4 |
148,615,214 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL01551:Mtor
|
APN |
4 |
148,556,494 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01661:Mtor
|
APN |
4 |
148,599,308 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL01675:Mtor
|
APN |
4 |
148,569,111 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01743:Mtor
|
APN |
4 |
148,615,070 (GRCm39) |
splice site |
probably benign |
|
IGL02015:Mtor
|
APN |
4 |
148,624,570 (GRCm39) |
nonsense |
probably null |
|
IGL02084:Mtor
|
APN |
4 |
148,555,137 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02095:Mtor
|
APN |
4 |
148,628,998 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02129:Mtor
|
APN |
4 |
148,634,302 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02260:Mtor
|
APN |
4 |
148,622,758 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02329:Mtor
|
APN |
4 |
148,619,396 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02440:Mtor
|
APN |
4 |
148,576,104 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02440:Mtor
|
APN |
4 |
148,630,886 (GRCm39) |
missense |
probably benign |
0.24 |
IGL02449:Mtor
|
APN |
4 |
148,618,378 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02479:Mtor
|
APN |
4 |
148,555,041 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02904:Mtor
|
APN |
4 |
148,576,069 (GRCm39) |
splice site |
probably benign |
|
IGL02904:Mtor
|
APN |
4 |
148,536,851 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02931:Mtor
|
APN |
4 |
148,549,421 (GRCm39) |
missense |
probably benign |
0.22 |
IGL03048:Mtor
|
APN |
4 |
148,630,847 (GRCm39) |
splice site |
probably benign |
|
IGL03133:Mtor
|
APN |
4 |
148,568,776 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03142:Mtor
|
APN |
4 |
148,538,356 (GRCm39) |
missense |
probably benign |
0.00 |
Brushes
|
UTSW |
4 |
148,548,205 (GRCm39) |
missense |
probably benign |
0.00 |
Dynamo
|
UTSW |
4 |
148,547,367 (GRCm39) |
missense |
probably benign |
0.00 |
engine
|
UTSW |
4 |
148,641,312 (GRCm39) |
splice site |
probably null |
|
Erg
|
UTSW |
4 |
148,630,053 (GRCm39) |
missense |
probably damaging |
1.00 |
Lindor
|
UTSW |
4 |
148,539,103 (GRCm39) |
missense |
probably damaging |
1.00 |
motor
|
UTSW |
4 |
148,575,817 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4858_Mtor_211
|
UTSW |
4 |
148,539,273 (GRCm39) |
makesense |
probably null |
|
Vigor
|
UTSW |
4 |
148,623,356 (GRCm39) |
missense |
probably damaging |
1.00 |
Vim
|
UTSW |
4 |
148,610,260 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4519001:Mtor
|
UTSW |
4 |
148,608,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R0045:Mtor
|
UTSW |
4 |
148,549,406 (GRCm39) |
missense |
probably benign |
0.42 |
R0048:Mtor
|
UTSW |
4 |
148,623,338 (GRCm39) |
nonsense |
probably null |
|
R0048:Mtor
|
UTSW |
4 |
148,623,338 (GRCm39) |
nonsense |
probably null |
|
R0103:Mtor
|
UTSW |
4 |
148,618,359 (GRCm39) |
missense |
probably benign |
0.05 |
R0112:Mtor
|
UTSW |
4 |
148,565,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R0137:Mtor
|
UTSW |
4 |
148,555,081 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0184:Mtor
|
UTSW |
4 |
148,549,428 (GRCm39) |
missense |
probably benign |
0.05 |
R0208:Mtor
|
UTSW |
4 |
148,549,432 (GRCm39) |
missense |
probably benign |
0.43 |
R0329:Mtor
|
UTSW |
4 |
148,568,837 (GRCm39) |
missense |
probably benign |
|
R0330:Mtor
|
UTSW |
4 |
148,568,837 (GRCm39) |
missense |
probably benign |
|
R0365:Mtor
|
UTSW |
4 |
148,570,507 (GRCm39) |
missense |
probably benign |
0.01 |
R0537:Mtor
|
UTSW |
4 |
148,622,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R0542:Mtor
|
UTSW |
4 |
148,624,907 (GRCm39) |
missense |
probably benign |
0.02 |
R0556:Mtor
|
UTSW |
4 |
148,553,837 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0613:Mtor
|
UTSW |
4 |
148,610,503 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0710:Mtor
|
UTSW |
4 |
148,548,848 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0791:Mtor
|
UTSW |
4 |
148,547,367 (GRCm39) |
missense |
probably benign |
0.00 |
R0792:Mtor
|
UTSW |
4 |
148,547,367 (GRCm39) |
missense |
probably benign |
0.00 |
R0866:Mtor
|
UTSW |
4 |
148,570,513 (GRCm39) |
missense |
probably benign |
0.04 |
R0973:Mtor
|
UTSW |
4 |
148,634,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R1027:Mtor
|
UTSW |
4 |
148,624,456 (GRCm39) |
missense |
probably benign |
0.03 |
R1028:Mtor
|
UTSW |
4 |
148,623,287 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1289:Mtor
|
UTSW |
4 |
148,554,764 (GRCm39) |
missense |
probably benign |
0.10 |
R1416:Mtor
|
UTSW |
4 |
148,575,871 (GRCm39) |
nonsense |
probably null |
|
R1465:Mtor
|
UTSW |
4 |
148,610,450 (GRCm39) |
splice site |
probably benign |
|
R1506:Mtor
|
UTSW |
4 |
148,620,962 (GRCm39) |
splice site |
probably benign |
|
R1624:Mtor
|
UTSW |
4 |
148,632,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R1695:Mtor
|
UTSW |
4 |
148,623,364 (GRCm39) |
missense |
probably benign |
0.08 |
R1771:Mtor
|
UTSW |
4 |
148,555,081 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1800:Mtor
|
UTSW |
4 |
148,547,349 (GRCm39) |
missense |
probably benign |
0.00 |
R1855:Mtor
|
UTSW |
4 |
148,637,546 (GRCm39) |
missense |
probably benign |
0.02 |
R1857:Mtor
|
UTSW |
4 |
148,565,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R1867:Mtor
|
UTSW |
4 |
148,539,089 (GRCm39) |
missense |
probably damaging |
0.97 |
R1954:Mtor
|
UTSW |
4 |
148,552,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R2054:Mtor
|
UTSW |
4 |
148,550,482 (GRCm39) |
missense |
probably benign |
0.00 |
R2054:Mtor
|
UTSW |
4 |
148,547,309 (GRCm39) |
missense |
probably benign |
0.05 |
R2099:Mtor
|
UTSW |
4 |
148,634,649 (GRCm39) |
nonsense |
probably null |
|
R2148:Mtor
|
UTSW |
4 |
148,540,469 (GRCm39) |
missense |
possibly damaging |
0.56 |
R2214:Mtor
|
UTSW |
4 |
148,623,327 (GRCm39) |
missense |
probably benign |
0.39 |
R2281:Mtor
|
UTSW |
4 |
148,574,012 (GRCm39) |
missense |
probably benign |
0.02 |
R2512:Mtor
|
UTSW |
4 |
148,614,948 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2870:Mtor
|
UTSW |
4 |
148,624,487 (GRCm39) |
missense |
probably benign |
0.00 |
R2870:Mtor
|
UTSW |
4 |
148,624,487 (GRCm39) |
missense |
probably benign |
0.00 |
R2871:Mtor
|
UTSW |
4 |
148,624,487 (GRCm39) |
missense |
probably benign |
0.00 |
R2871:Mtor
|
UTSW |
4 |
148,624,487 (GRCm39) |
missense |
probably benign |
0.00 |
R2872:Mtor
|
UTSW |
4 |
148,624,487 (GRCm39) |
missense |
probably benign |
0.00 |
R2872:Mtor
|
UTSW |
4 |
148,624,487 (GRCm39) |
missense |
probably benign |
0.00 |
R2873:Mtor
|
UTSW |
4 |
148,624,487 (GRCm39) |
missense |
probably benign |
0.00 |
R4032:Mtor
|
UTSW |
4 |
148,621,209 (GRCm39) |
missense |
probably benign |
0.03 |
R4073:Mtor
|
UTSW |
4 |
148,633,832 (GRCm39) |
missense |
probably damaging |
0.99 |
R4273:Mtor
|
UTSW |
4 |
148,634,609 (GRCm39) |
missense |
probably benign |
0.21 |
R4611:Mtor
|
UTSW |
4 |
148,570,576 (GRCm39) |
missense |
probably benign |
0.03 |
R4858:Mtor
|
UTSW |
4 |
148,539,273 (GRCm39) |
makesense |
probably null |
|
R4942:Mtor
|
UTSW |
4 |
148,556,599 (GRCm39) |
missense |
probably benign |
0.03 |
R4967:Mtor
|
UTSW |
4 |
148,575,817 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4995:Mtor
|
UTSW |
4 |
148,610,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R5054:Mtor
|
UTSW |
4 |
148,641,312 (GRCm39) |
splice site |
probably null |
|
R5215:Mtor
|
UTSW |
4 |
148,538,440 (GRCm39) |
missense |
probably benign |
|
R5249:Mtor
|
UTSW |
4 |
148,548,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R5289:Mtor
|
UTSW |
4 |
148,550,549 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5365:Mtor
|
UTSW |
4 |
148,634,587 (GRCm39) |
missense |
probably damaging |
0.99 |
R5498:Mtor
|
UTSW |
4 |
148,624,821 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5514:Mtor
|
UTSW |
4 |
148,630,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R5540:Mtor
|
UTSW |
4 |
148,539,165 (GRCm39) |
missense |
probably benign |
0.01 |
R5600:Mtor
|
UTSW |
4 |
148,575,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R5615:Mtor
|
UTSW |
4 |
148,622,733 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5632:Mtor
|
UTSW |
4 |
148,553,463 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5641:Mtor
|
UTSW |
4 |
148,630,882 (GRCm39) |
missense |
probably damaging |
0.98 |
R5834:Mtor
|
UTSW |
4 |
148,620,993 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5984:Mtor
|
UTSW |
4 |
148,623,284 (GRCm39) |
missense |
probably benign |
0.02 |
R6056:Mtor
|
UTSW |
4 |
148,621,892 (GRCm39) |
missense |
probably benign |
0.00 |
R6225:Mtor
|
UTSW |
4 |
148,605,794 (GRCm39) |
missense |
probably benign |
0.04 |
R6262:Mtor
|
UTSW |
4 |
148,610,552 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6335:Mtor
|
UTSW |
4 |
148,550,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R6479:Mtor
|
UTSW |
4 |
148,635,457 (GRCm39) |
missense |
probably benign |
0.16 |
R6543:Mtor
|
UTSW |
4 |
148,630,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R6711:Mtor
|
UTSW |
4 |
148,536,824 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6715:Mtor
|
UTSW |
4 |
148,623,004 (GRCm39) |
missense |
probably benign |
0.00 |
R6744:Mtor
|
UTSW |
4 |
148,543,112 (GRCm39) |
missense |
probably benign |
0.01 |
R6748:Mtor
|
UTSW |
4 |
148,634,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R6762:Mtor
|
UTSW |
4 |
148,622,938 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6836:Mtor
|
UTSW |
4 |
148,573,955 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6948:Mtor
|
UTSW |
4 |
148,621,209 (GRCm39) |
missense |
probably benign |
0.12 |
R6979:Mtor
|
UTSW |
4 |
148,608,930 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6992:Mtor
|
UTSW |
4 |
148,548,932 (GRCm39) |
missense |
probably benign |
|
R7271:Mtor
|
UTSW |
4 |
148,630,942 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7423:Mtor
|
UTSW |
4 |
148,640,801 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7434:Mtor
|
UTSW |
4 |
148,549,416 (GRCm39) |
missense |
probably benign |
0.39 |
R7619:Mtor
|
UTSW |
4 |
148,547,252 (GRCm39) |
missense |
probably damaging |
0.98 |
R7634:Mtor
|
UTSW |
4 |
148,536,807 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7697:Mtor
|
UTSW |
4 |
148,624,765 (GRCm39) |
nonsense |
probably null |
|
R7737:Mtor
|
UTSW |
4 |
148,623,195 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7791:Mtor
|
UTSW |
4 |
148,547,397 (GRCm39) |
missense |
probably benign |
0.00 |
R7858:Mtor
|
UTSW |
4 |
148,539,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R8035:Mtor
|
UTSW |
4 |
148,630,856 (GRCm39) |
missense |
probably benign |
0.29 |
R8076:Mtor
|
UTSW |
4 |
148,610,260 (GRCm39) |
critical splice donor site |
probably null |
|
R8078:Mtor
|
UTSW |
4 |
148,552,744 (GRCm39) |
missense |
probably benign |
|
R8928:Mtor
|
UTSW |
4 |
148,623,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R9040:Mtor
|
UTSW |
4 |
148,548,205 (GRCm39) |
missense |
probably benign |
0.00 |
R9116:Mtor
|
UTSW |
4 |
148,637,198 (GRCm39) |
missense |
probably benign |
|
R9284:Mtor
|
UTSW |
4 |
148,543,537 (GRCm39) |
missense |
probably benign |
0.03 |
R9310:Mtor
|
UTSW |
4 |
148,553,834 (GRCm39) |
missense |
probably benign |
0.03 |
R9374:Mtor
|
UTSW |
4 |
148,599,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R9417:Mtor
|
UTSW |
4 |
148,622,776 (GRCm39) |
nonsense |
probably null |
|
R9465:Mtor
|
UTSW |
4 |
148,624,839 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9492:Mtor
|
UTSW |
4 |
148,568,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R9499:Mtor
|
UTSW |
4 |
148,599,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R9516:Mtor
|
UTSW |
4 |
148,569,103 (GRCm39) |
missense |
probably benign |
0.23 |
R9600:Mtor
|
UTSW |
4 |
148,632,092 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9622:Mtor
|
UTSW |
4 |
148,568,169 (GRCm39) |
missense |
probably damaging |
0.99 |
X0025:Mtor
|
UTSW |
4 |
148,615,171 (GRCm39) |
missense |
probably benign |
0.09 |
Z1176:Mtor
|
UTSW |
4 |
148,634,587 (GRCm39) |
missense |
possibly damaging |
0.69 |
Z1176:Mtor
|
UTSW |
4 |
148,634,582 (GRCm39) |
missense |
probably benign |
0.08 |
|
Predicted Primers |
PCR Primer
(F):5'- GGCTCTTCAGCATCCCTACAGAAC -3'
(R):5'- ACGAACTATTGGGTGAATGATGCGG -3'
Sequencing Primer
(F):5'- GCATCCCTACAGAACTTTGAGTG -3'
(R):5'- TCCTGTGAGTGACATGAATCC -3'
|
Posted On |
2013-07-11 |