Incidental Mutation 'R1757:Rictor'
ID |
195010 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Rictor
|
Ensembl Gene |
ENSMUSG00000050310 |
Gene Name |
RPTOR independent companion of MTOR, complex 2 |
Synonyms |
D530039E11Rik, 4921505C17Rik, 6030405M08Rik |
MMRRC Submission |
039789-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R1757 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
15 |
Chromosomal Location |
6737860-6829882 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 6803343 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Glutamine
at position 485
(R485Q)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000051809
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000061656]
|
AlphaFold |
Q6QI06 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000061656
AA Change: R485Q
PolyPhen 2
Score 0.949 (Sensitivity: 0.79; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000051809 Gene: ENSMUSG00000050310 AA Change: R485Q
Domain | Start | End | E-Value | Type |
RICTOR_N
|
57 |
439 |
4.02e-185 |
SMART |
RICTOR_M
|
523 |
742 |
5.66e-98 |
SMART |
RasGEF_N_2
|
743 |
857 |
1.26e-54 |
SMART |
RICTOR_V
|
920 |
992 |
1.44e-40 |
SMART |
low complexity region
|
1019 |
1043 |
N/A |
INTRINSIC |
RICTOR_phospho
|
1084 |
1189 |
4.06e-58 |
SMART |
low complexity region
|
1221 |
1239 |
N/A |
INTRINSIC |
low complexity region
|
1255 |
1266 |
N/A |
INTRINSIC |
low complexity region
|
1273 |
1287 |
N/A |
INTRINSIC |
low complexity region
|
1404 |
1414 |
N/A |
INTRINSIC |
low complexity region
|
1464 |
1474 |
N/A |
INTRINSIC |
low complexity region
|
1616 |
1628 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000228266
|
Meta Mutation Damage Score |
0.1044 |
Coding Region Coverage |
- 1x: 97.5%
- 3x: 96.9%
- 10x: 95.3%
- 20x: 92.4%
|
Validation Efficiency |
100% (111/111) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] RICTOR and MTOR (FRAP1; MIM 601231) are components of a protein complex that integrates nutrient- and growth factor-derived signals to regulate cell growth (Sarbassov et al., 2004 [PubMed 15268862]).[supplied by OMIM, Mar 2008] PHENOTYPE: Mice homozygous for a null allele exhibit embryonic lethality during organogenesis associated with abnormal placental morphology. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd6 |
A |
T |
14: 8,049,867 (GRCm38) |
I219F |
probably damaging |
Het |
Acvr1b |
A |
G |
15: 101,096,703 (GRCm39) |
I207V |
possibly damaging |
Het |
Adamtsl4 |
T |
C |
3: 95,585,252 (GRCm39) |
T839A |
probably benign |
Het |
Akap1 |
C |
T |
11: 88,736,578 (GRCm39) |
R61H |
probably damaging |
Het |
Akap9 |
A |
G |
5: 4,051,667 (GRCm39) |
D1478G |
probably benign |
Het |
Aloxe3 |
T |
A |
11: 69,026,775 (GRCm39) |
V547E |
possibly damaging |
Het |
Ano6 |
G |
A |
15: 95,860,148 (GRCm39) |
A757T |
probably damaging |
Het |
Armc10 |
A |
G |
5: 21,858,455 (GRCm39) |
T167A |
probably damaging |
Het |
BB019430 |
A |
C |
10: 58,539,869 (GRCm39) |
|
noncoding transcript |
Het |
Brms1 |
C |
T |
19: 5,096,435 (GRCm39) |
R82W |
probably damaging |
Het |
Btnl6 |
G |
A |
17: 34,733,062 (GRCm39) |
T267I |
probably benign |
Het |
Catsper4 |
A |
T |
4: 133,945,212 (GRCm39) |
F215L |
probably benign |
Het |
Ccdc188 |
T |
C |
16: 18,036,552 (GRCm39) |
F197S |
probably damaging |
Het |
Cers5 |
A |
C |
15: 99,634,212 (GRCm39) |
C379G |
probably benign |
Het |
Chchd6 |
A |
G |
6: 89,361,626 (GRCm39) |
L259P |
probably damaging |
Het |
Cntnap2 |
T |
A |
6: 46,736,763 (GRCm39) |
C730S |
probably damaging |
Het |
Coch |
T |
G |
12: 51,649,631 (GRCm39) |
V314G |
probably damaging |
Het |
Cog1 |
T |
A |
11: 113,543,130 (GRCm39) |
S213T |
possibly damaging |
Het |
Crot |
A |
T |
5: 9,037,828 (GRCm39) |
F163I |
probably damaging |
Het |
Cyp4f13 |
A |
T |
17: 33,148,932 (GRCm39) |
I162N |
probably damaging |
Het |
Dab2 |
A |
T |
15: 6,359,933 (GRCm39) |
|
probably benign |
Het |
Depdc1b |
C |
T |
13: 108,460,482 (GRCm39) |
R31W |
probably damaging |
Het |
Dlk1 |
T |
C |
12: 109,425,613 (GRCm39) |
F161S |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,137,965 (GRCm39) |
E913G |
probably damaging |
Het |
Dnajc6 |
A |
G |
4: 101,455,028 (GRCm39) |
Y5C |
probably damaging |
Het |
Dock10 |
T |
C |
1: 80,511,586 (GRCm39) |
T1508A |
probably damaging |
Het |
Dstyk |
A |
G |
1: 132,361,832 (GRCm39) |
|
probably benign |
Het |
Efcc1 |
T |
C |
6: 87,726,265 (GRCm39) |
|
probably benign |
Het |
Entpd1 |
T |
C |
19: 40,727,450 (GRCm39) |
Y533H |
probably benign |
Het |
Epha8 |
A |
T |
4: 136,658,789 (GRCm39) |
|
probably null |
Het |
Erich3 |
C |
T |
3: 154,401,402 (GRCm39) |
T17M |
probably damaging |
Het |
Ethe1 |
T |
C |
7: 24,307,899 (GRCm39) |
|
probably benign |
Het |
Fbxw15 |
A |
T |
9: 109,386,347 (GRCm39) |
M211K |
probably damaging |
Het |
Fhod3 |
G |
A |
18: 25,199,335 (GRCm39) |
V669M |
possibly damaging |
Het |
Fktn |
C |
T |
4: 53,747,003 (GRCm39) |
|
probably benign |
Het |
Foxred1 |
G |
A |
9: 35,122,130 (GRCm39) |
R20C |
probably benign |
Het |
Gbp9 |
A |
G |
5: 105,242,319 (GRCm39) |
L140P |
probably damaging |
Het |
Gga1 |
T |
C |
15: 78,773,230 (GRCm39) |
L286P |
probably damaging |
Het |
Gml |
T |
C |
15: 74,685,462 (GRCm39) |
|
probably benign |
Het |
Gsap |
A |
T |
5: 21,486,035 (GRCm39) |
K628N |
probably damaging |
Het |
Gtf3c4 |
G |
A |
2: 28,720,648 (GRCm39) |
|
probably benign |
Het |
H2-M10.6 |
A |
C |
17: 37,124,043 (GRCm39) |
Y169S |
probably benign |
Het |
Hal |
G |
A |
10: 93,330,490 (GRCm39) |
V245I |
probably benign |
Het |
Hebp2 |
T |
C |
10: 18,420,849 (GRCm39) |
Y72C |
probably damaging |
Het |
Helz2 |
T |
C |
2: 180,878,056 (GRCm39) |
E914G |
probably damaging |
Het |
Herc3 |
T |
C |
6: 58,893,455 (GRCm39) |
Y906H |
probably damaging |
Het |
Hfm1 |
A |
T |
5: 107,028,226 (GRCm39) |
|
probably null |
Het |
Hgs |
C |
T |
11: 120,370,889 (GRCm39) |
P582S |
probably damaging |
Het |
Hoxa10 |
G |
A |
6: 52,211,469 (GRCm39) |
P149L |
probably damaging |
Het |
Inpp5j |
T |
A |
11: 3,454,738 (GRCm39) |
Q4L |
possibly damaging |
Het |
Ints8 |
A |
C |
4: 11,254,109 (GRCm39) |
M1R |
probably null |
Het |
Isg15 |
T |
C |
4: 156,284,447 (GRCm39) |
E27G |
possibly damaging |
Het |
Klf13 |
A |
T |
7: 63,541,513 (GRCm39) |
C205S |
probably damaging |
Het |
Lama1 |
A |
T |
17: 68,070,831 (GRCm39) |
Y830F |
probably benign |
Het |
Lama1 |
G |
A |
17: 68,004,378 (GRCm39) |
V17M |
unknown |
Het |
Lama3 |
A |
G |
18: 12,598,556 (GRCm39) |
N988D |
probably benign |
Het |
Lcat |
CAT |
C |
8: 106,668,446 (GRCm39) |
|
probably null |
Het |
Lct |
G |
T |
1: 128,228,994 (GRCm39) |
P833H |
probably damaging |
Het |
Lmf1 |
A |
T |
17: 25,874,184 (GRCm39) |
R403W |
probably damaging |
Het |
Me3 |
T |
G |
7: 89,282,230 (GRCm39) |
S38A |
probably benign |
Het |
Myg1 |
A |
T |
15: 102,240,264 (GRCm39) |
D30V |
probably benign |
Het |
Nbea |
A |
G |
3: 55,537,610 (GRCm39) |
I2841T |
possibly damaging |
Het |
Nek1 |
T |
A |
8: 61,542,847 (GRCm39) |
|
probably null |
Het |
Obsl1 |
C |
T |
1: 75,470,527 (GRCm39) |
R1043H |
probably benign |
Het |
Or4p23 |
G |
T |
2: 88,576,361 (GRCm39) |
D290E |
probably benign |
Het |
Or5b119 |
A |
C |
19: 13,456,971 (GRCm39) |
V197G |
possibly damaging |
Het |
Or6n2 |
A |
T |
1: 173,897,224 (GRCm39) |
Y120F |
probably damaging |
Het |
Or9m2 |
T |
G |
2: 87,820,926 (GRCm39) |
I157R |
probably damaging |
Het |
Osbpl9 |
A |
G |
4: 108,921,780 (GRCm39) |
Y613H |
probably damaging |
Het |
Per3 |
C |
T |
4: 151,127,249 (GRCm39) |
|
probably null |
Het |
Pex6 |
G |
T |
17: 47,034,424 (GRCm39) |
V758L |
probably damaging |
Het |
Pikfyve |
A |
G |
1: 65,291,707 (GRCm39) |
I1309V |
probably damaging |
Het |
Pimreg |
A |
G |
11: 71,933,985 (GRCm39) |
E37G |
possibly damaging |
Het |
Pjvk |
G |
A |
2: 76,486,232 (GRCm39) |
V211I |
probably benign |
Het |
Plekhg4 |
T |
A |
8: 106,108,293 (GRCm39) |
V1112E |
probably damaging |
Het |
Ptprz1 |
T |
A |
6: 23,044,319 (GRCm39) |
M2106K |
probably damaging |
Het |
Rdh16f2 |
G |
T |
10: 127,712,765 (GRCm39) |
L254F |
probably benign |
Het |
Rnf146 |
G |
A |
10: 29,223,475 (GRCm39) |
T137M |
probably damaging |
Het |
Rrp9 |
T |
A |
9: 106,360,203 (GRCm39) |
C204S |
probably damaging |
Het |
Rxylt1 |
T |
C |
10: 121,924,920 (GRCm39) |
T261A |
probably benign |
Het |
Serpinb9h |
T |
C |
13: 33,583,336 (GRCm39) |
S150P |
probably benign |
Het |
Shkbp1 |
T |
C |
7: 27,041,776 (GRCm39) |
T693A |
probably benign |
Het |
Skint9 |
A |
G |
4: 112,271,159 (GRCm39) |
Y84H |
probably benign |
Het |
Slc22a12 |
A |
T |
19: 6,586,761 (GRCm39) |
|
probably null |
Het |
Slfn4 |
T |
C |
11: 83,076,211 (GRCm39) |
C26R |
possibly damaging |
Het |
Snrnp200 |
T |
C |
2: 127,074,363 (GRCm39) |
L1401P |
probably damaging |
Het |
Specc1 |
T |
A |
11: 62,010,110 (GRCm39) |
|
probably null |
Het |
Spef2 |
A |
T |
15: 9,717,568 (GRCm39) |
M316K |
probably damaging |
Het |
Tbc1d22b |
A |
G |
17: 29,790,647 (GRCm39) |
R204G |
probably damaging |
Het |
Tektl1 |
T |
C |
10: 78,583,058 (GRCm39) |
N442S |
probably benign |
Het |
Tgfbr3l |
C |
A |
8: 4,299,548 (GRCm39) |
D110E |
probably benign |
Het |
Ticrr |
T |
G |
7: 79,325,071 (GRCm39) |
S532R |
probably damaging |
Het |
Ticrr |
C |
A |
7: 79,328,794 (GRCm39) |
Y644* |
probably null |
Het |
Traf3ip1 |
A |
T |
1: 91,450,579 (GRCm39) |
T509S |
probably damaging |
Het |
Trmt10b |
T |
C |
4: 45,307,946 (GRCm39) |
Y209H |
probably damaging |
Het |
Trmt6 |
T |
C |
2: 132,652,157 (GRCm39) |
M172V |
probably damaging |
Het |
Tsc1 |
A |
G |
2: 28,576,125 (GRCm39) |
D978G |
probably benign |
Het |
Tshz2 |
C |
A |
2: 169,725,843 (GRCm39) |
F146L |
probably benign |
Het |
Tspyl4 |
G |
T |
10: 34,173,576 (GRCm39) |
E23* |
probably null |
Het |
Ulk2 |
A |
T |
11: 61,732,165 (GRCm39) |
|
probably benign |
Het |
Umodl1 |
A |
T |
17: 31,227,674 (GRCm39) |
I1336F |
probably damaging |
Het |
Vezt |
T |
C |
10: 93,806,425 (GRCm39) |
D662G |
probably benign |
Het |
Vnn1 |
G |
T |
10: 23,776,727 (GRCm39) |
Q359H |
probably benign |
Het |
Vnn1 |
A |
T |
10: 23,776,726 (GRCm39) |
Q359L |
possibly damaging |
Het |
Zdhhc16 |
A |
G |
19: 41,930,394 (GRCm39) |
N14S |
probably damaging |
Het |
Zfp455 |
T |
C |
13: 67,355,601 (GRCm39) |
S225P |
probably damaging |
Het |
Zfp74 |
T |
A |
7: 29,634,486 (GRCm39) |
E407D |
probably benign |
Het |
Zic2 |
T |
A |
14: 122,716,031 (GRCm39) |
H384Q |
possibly damaging |
Het |
|
Other mutations in Rictor |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00488:Rictor
|
APN |
15 |
6,816,071 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00785:Rictor
|
APN |
15 |
6,806,431 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00801:Rictor
|
APN |
15 |
6,824,015 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01072:Rictor
|
APN |
15 |
6,819,043 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01139:Rictor
|
APN |
15 |
6,807,749 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01303:Rictor
|
APN |
15 |
6,738,119 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01307:Rictor
|
APN |
15 |
6,804,085 (GRCm39) |
splice site |
probably null |
|
IGL01767:Rictor
|
APN |
15 |
6,806,865 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01774:Rictor
|
APN |
15 |
6,799,258 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01800:Rictor
|
APN |
15 |
6,804,182 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02192:Rictor
|
APN |
15 |
6,815,895 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02503:Rictor
|
APN |
15 |
6,815,924 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02652:Rictor
|
APN |
15 |
6,805,668 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02656:Rictor
|
APN |
15 |
6,806,401 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02752:Rictor
|
APN |
15 |
6,816,852 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03000:Rictor
|
APN |
15 |
6,798,721 (GRCm39) |
splice site |
probably benign |
|
IGL03118:Rictor
|
APN |
15 |
6,788,999 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03182:Rictor
|
APN |
15 |
6,819,079 (GRCm39) |
missense |
probably benign |
0.08 |
Tense
|
UTSW |
15 |
6,788,977 (GRCm39) |
missense |
possibly damaging |
0.94 |
Tonus
|
UTSW |
15 |
6,798,815 (GRCm39) |
critical splice donor site |
probably null |
|
Torrid
|
UTSW |
15 |
6,789,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R0149:Rictor
|
UTSW |
15 |
6,813,588 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0288:Rictor
|
UTSW |
15 |
6,816,021 (GRCm39) |
missense |
probably benign |
0.08 |
R0304:Rictor
|
UTSW |
15 |
6,815,852 (GRCm39) |
splice site |
probably null |
|
R0336:Rictor
|
UTSW |
15 |
6,806,234 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0361:Rictor
|
UTSW |
15 |
6,813,588 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0423:Rictor
|
UTSW |
15 |
6,803,381 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0453:Rictor
|
UTSW |
15 |
6,738,123 (GRCm39) |
missense |
probably benign |
0.01 |
R0515:Rictor
|
UTSW |
15 |
6,798,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R0630:Rictor
|
UTSW |
15 |
6,823,973 (GRCm39) |
missense |
probably damaging |
1.00 |
R0730:Rictor
|
UTSW |
15 |
6,803,467 (GRCm39) |
splice site |
probably benign |
|
R0744:Rictor
|
UTSW |
15 |
6,793,759 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0836:Rictor
|
UTSW |
15 |
6,793,759 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0881:Rictor
|
UTSW |
15 |
6,821,151 (GRCm39) |
missense |
probably benign |
|
R1114:Rictor
|
UTSW |
15 |
6,823,486 (GRCm39) |
nonsense |
probably null |
|
R1367:Rictor
|
UTSW |
15 |
6,820,119 (GRCm39) |
splice site |
probably benign |
|
R1655:Rictor
|
UTSW |
15 |
6,801,693 (GRCm39) |
missense |
probably benign |
0.00 |
R1678:Rictor
|
UTSW |
15 |
6,785,952 (GRCm39) |
missense |
probably benign |
0.07 |
R1679:Rictor
|
UTSW |
15 |
6,797,571 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1754:Rictor
|
UTSW |
15 |
6,764,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R1762:Rictor
|
UTSW |
15 |
6,786,054 (GRCm39) |
missense |
probably benign |
0.00 |
R1914:Rictor
|
UTSW |
15 |
6,789,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R1915:Rictor
|
UTSW |
15 |
6,789,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R1994:Rictor
|
UTSW |
15 |
6,805,637 (GRCm39) |
missense |
probably benign |
0.18 |
R2145:Rictor
|
UTSW |
15 |
6,794,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R2182:Rictor
|
UTSW |
15 |
6,801,685 (GRCm39) |
missense |
probably damaging |
0.96 |
R2191:Rictor
|
UTSW |
15 |
6,789,095 (GRCm39) |
missense |
probably benign |
0.04 |
R2357:Rictor
|
UTSW |
15 |
6,813,043 (GRCm39) |
missense |
probably damaging |
0.99 |
R2914:Rictor
|
UTSW |
15 |
6,799,476 (GRCm39) |
critical splice donor site |
probably null |
|
R3082:Rictor
|
UTSW |
15 |
6,804,338 (GRCm39) |
missense |
probably benign |
0.15 |
R3885:Rictor
|
UTSW |
15 |
6,789,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R3900:Rictor
|
UTSW |
15 |
6,818,954 (GRCm39) |
missense |
probably benign |
0.01 |
R4376:Rictor
|
UTSW |
15 |
6,816,448 (GRCm39) |
missense |
probably benign |
0.00 |
R4611:Rictor
|
UTSW |
15 |
6,816,625 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4644:Rictor
|
UTSW |
15 |
6,807,416 (GRCm39) |
nonsense |
probably null |
|
R4718:Rictor
|
UTSW |
15 |
6,812,641 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4822:Rictor
|
UTSW |
15 |
6,821,161 (GRCm39) |
missense |
probably benign |
0.01 |
R4980:Rictor
|
UTSW |
15 |
6,811,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R5034:Rictor
|
UTSW |
15 |
6,797,576 (GRCm39) |
missense |
probably damaging |
0.98 |
R5179:Rictor
|
UTSW |
15 |
6,825,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R5386:Rictor
|
UTSW |
15 |
6,818,985 (GRCm39) |
missense |
probably benign |
0.37 |
R5532:Rictor
|
UTSW |
15 |
6,819,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R5549:Rictor
|
UTSW |
15 |
6,816,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R5715:Rictor
|
UTSW |
15 |
6,780,197 (GRCm39) |
nonsense |
probably null |
|
R5733:Rictor
|
UTSW |
15 |
6,812,585 (GRCm39) |
missense |
probably benign |
|
R5822:Rictor
|
UTSW |
15 |
6,823,487 (GRCm39) |
missense |
probably benign |
0.00 |
R5848:Rictor
|
UTSW |
15 |
6,823,487 (GRCm39) |
missense |
probably benign |
0.00 |
R5849:Rictor
|
UTSW |
15 |
6,823,487 (GRCm39) |
missense |
probably benign |
0.00 |
R5850:Rictor
|
UTSW |
15 |
6,823,487 (GRCm39) |
missense |
probably benign |
0.00 |
R5854:Rictor
|
UTSW |
15 |
6,823,487 (GRCm39) |
missense |
probably benign |
0.00 |
R5855:Rictor
|
UTSW |
15 |
6,823,487 (GRCm39) |
missense |
probably benign |
0.00 |
R5856:Rictor
|
UTSW |
15 |
6,823,487 (GRCm39) |
missense |
probably benign |
0.00 |
R5936:Rictor
|
UTSW |
15 |
6,813,642 (GRCm39) |
missense |
probably damaging |
0.99 |
R6155:Rictor
|
UTSW |
15 |
6,823,458 (GRCm39) |
missense |
probably benign |
0.44 |
R6394:Rictor
|
UTSW |
15 |
6,798,790 (GRCm39) |
missense |
possibly damaging |
0.59 |
R6549:Rictor
|
UTSW |
15 |
6,825,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R6611:Rictor
|
UTSW |
15 |
6,780,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R6657:Rictor
|
UTSW |
15 |
6,788,977 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6705:Rictor
|
UTSW |
15 |
6,823,493 (GRCm39) |
missense |
probably benign |
0.00 |
R6819:Rictor
|
UTSW |
15 |
6,825,517 (GRCm39) |
critical splice donor site |
probably null |
|
R6985:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R6989:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R7016:Rictor
|
UTSW |
15 |
6,804,361 (GRCm39) |
critical splice donor site |
probably null |
|
R7030:Rictor
|
UTSW |
15 |
6,737,934 (GRCm39) |
critical splice donor site |
probably null |
|
R7066:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R7067:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R7216:Rictor
|
UTSW |
15 |
6,798,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R7396:Rictor
|
UTSW |
15 |
6,816,462 (GRCm39) |
missense |
not run |
|
R7449:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R7450:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R7452:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R7616:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R7620:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R7643:Rictor
|
UTSW |
15 |
6,798,750 (GRCm39) |
nonsense |
probably null |
|
R7699:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R7700:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R7749:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R7750:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R7751:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R7753:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R7841:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R7894:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R7897:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R7898:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R7937:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R7944:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R8062:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R8063:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R8094:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R8119:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R8134:Rictor
|
UTSW |
15 |
6,801,635 (GRCm39) |
missense |
probably benign |
0.27 |
R8166:Rictor
|
UTSW |
15 |
6,798,815 (GRCm39) |
critical splice donor site |
probably null |
|
R8324:Rictor
|
UTSW |
15 |
6,775,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R8343:Rictor
|
UTSW |
15 |
6,807,800 (GRCm39) |
critical splice donor site |
probably null |
|
R8691:Rictor
|
UTSW |
15 |
6,816,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R8859:Rictor
|
UTSW |
15 |
6,813,067 (GRCm39) |
missense |
probably damaging |
0.98 |
R8953:Rictor
|
UTSW |
15 |
6,823,928 (GRCm39) |
missense |
probably benign |
0.39 |
R8977:Rictor
|
UTSW |
15 |
6,812,566 (GRCm39) |
missense |
probably benign |
|
R9008:Rictor
|
UTSW |
15 |
6,801,610 (GRCm39) |
splice site |
probably benign |
|
R9369:Rictor
|
UTSW |
15 |
6,773,848 (GRCm39) |
missense |
probably benign |
0.00 |
R9563:Rictor
|
UTSW |
15 |
6,797,562 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9695:Rictor
|
UTSW |
15 |
6,816,010 (GRCm39) |
missense |
probably benign |
0.00 |
X0020:Rictor
|
UTSW |
15 |
6,785,963 (GRCm39) |
missense |
probably benign |
0.32 |
X0060:Rictor
|
UTSW |
15 |
6,816,033 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Predicted Primers |
PCR Primer
(F):5'- CCCCACCAAAATTTGCTTGGTAATCTC -3'
(R):5'- AGTTAGGTCGTCAAAGATCCTCAATGC -3'
Sequencing Primer
(F):5'- CAAAATTTGCTTGGTAATCTCTGTTG -3'
(R):5'- gtggaagagatgtaaggagagtg -3'
|
Posted On |
2014-05-23 |