Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930579G24Rik |
G |
A |
3: 79,538,598 (GRCm39) |
|
probably benign |
Het |
Aatk |
C |
T |
11: 119,901,012 (GRCm39) |
R1128Q |
probably benign |
Het |
Acot6 |
C |
T |
12: 84,156,212 (GRCm39) |
R387C |
probably damaging |
Het |
Adam11 |
A |
G |
11: 102,660,973 (GRCm39) |
E118G |
probably damaging |
Het |
Adcyap1r1 |
G |
A |
6: 55,449,264 (GRCm39) |
V73I |
probably damaging |
Het |
Apol8 |
T |
C |
15: 77,634,214 (GRCm39) |
T121A |
probably damaging |
Het |
Bltp2 |
A |
G |
11: 78,163,759 (GRCm39) |
N1076D |
probably damaging |
Het |
Ccdc91 |
C |
A |
6: 147,508,485 (GRCm39) |
Q404K |
unknown |
Het |
Cpt1b |
T |
C |
15: 89,306,496 (GRCm39) |
K294R |
probably benign |
Het |
Dnah6 |
A |
C |
6: 73,172,744 (GRCm39) |
V238G |
probably damaging |
Het |
Dscaml1 |
T |
C |
9: 45,663,536 (GRCm39) |
S1920P |
probably damaging |
Het |
Gcfc2 |
A |
T |
6: 81,934,951 (GRCm39) |
I737L |
probably benign |
Het |
Gmeb1 |
A |
G |
4: 131,955,296 (GRCm39) |
V293A |
probably benign |
Het |
Gpi-ps |
T |
C |
8: 5,690,563 (GRCm39) |
|
noncoding transcript |
Het |
Hibch |
A |
G |
1: 52,924,349 (GRCm39) |
|
probably benign |
Het |
Ifnab |
A |
G |
4: 88,609,419 (GRCm39) |
Y16H |
probably benign |
Het |
Il17rc |
T |
C |
6: 113,451,132 (GRCm39) |
V155A |
probably damaging |
Het |
Lrr1 |
A |
G |
12: 69,221,356 (GRCm39) |
H166R |
probably benign |
Het |
Map4k5 |
G |
T |
12: 69,892,506 (GRCm39) |
A141E |
probably damaging |
Het |
Mettl17 |
A |
T |
14: 52,126,292 (GRCm39) |
K233N |
probably damaging |
Het |
Mon2 |
A |
G |
10: 122,862,204 (GRCm39) |
L740S |
probably damaging |
Het |
Mpdz |
A |
C |
4: 81,253,979 (GRCm39) |
I1051S |
probably benign |
Het |
Mroh8 |
A |
G |
2: 157,058,834 (GRCm39) |
F944S |
probably damaging |
Het |
Myh13 |
A |
G |
11: 67,233,314 (GRCm39) |
Y611C |
probably damaging |
Het |
Npat |
A |
G |
9: 53,478,100 (GRCm39) |
N951D |
possibly damaging |
Het |
Parp14 |
T |
C |
16: 35,655,206 (GRCm39) |
Y1755C |
probably damaging |
Het |
Phf14 |
T |
C |
6: 11,941,423 (GRCm39) |
|
probably benign |
Het |
Prex2 |
T |
A |
1: 11,256,876 (GRCm39) |
M1196K |
possibly damaging |
Het |
Prkd1 |
A |
T |
12: 50,430,264 (GRCm39) |
D614E |
probably damaging |
Het |
Ptprm |
A |
G |
17: 67,124,967 (GRCm39) |
L794P |
probably damaging |
Het |
Rb1 |
C |
T |
14: 73,502,038 (GRCm39) |
R449H |
probably damaging |
Het |
Scfd1 |
A |
G |
12: 51,474,652 (GRCm39) |
D469G |
probably benign |
Het |
Serpinb1c |
T |
C |
13: 33,067,958 (GRCm39) |
K213E |
probably damaging |
Het |
Sgo1 |
A |
G |
17: 53,984,130 (GRCm39) |
|
probably benign |
Het |
Slc11a1 |
A |
G |
1: 74,421,057 (GRCm39) |
|
probably null |
Het |
Snw1 |
A |
G |
12: 87,499,350 (GRCm39) |
|
probably null |
Het |
Stac3 |
T |
C |
10: 127,339,533 (GRCm39) |
I143T |
probably damaging |
Het |
Tcta |
A |
T |
9: 108,183,115 (GRCm39) |
L10Q |
probably damaging |
Het |
Tha1 |
T |
C |
11: 117,761,831 (GRCm39) |
|
probably benign |
Het |
Trmt1 |
T |
C |
8: 85,422,138 (GRCm39) |
M254T |
possibly damaging |
Het |
Trps1 |
T |
A |
15: 50,524,703 (GRCm39) |
M887L |
possibly damaging |
Het |
Zfyve28 |
A |
G |
5: 34,400,539 (GRCm39) |
V53A |
probably damaging |
Het |
|
Other mutations in Osmr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00163:Osmr
|
APN |
15 |
6,873,926 (GRCm39) |
nonsense |
probably null |
|
IGL00335:Osmr
|
APN |
15 |
6,866,504 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00510:Osmr
|
APN |
15 |
6,853,112 (GRCm39) |
nonsense |
probably null |
|
IGL00811:Osmr
|
APN |
15 |
6,845,147 (GRCm39) |
missense |
probably benign |
0.28 |
IGL00959:Osmr
|
APN |
15 |
6,854,086 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01115:Osmr
|
APN |
15 |
6,876,682 (GRCm39) |
splice site |
probably benign |
|
IGL01307:Osmr
|
APN |
15 |
6,873,908 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01330:Osmr
|
APN |
15 |
6,871,509 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01633:Osmr
|
APN |
15 |
6,854,085 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01780:Osmr
|
APN |
15 |
6,858,144 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02164:Osmr
|
APN |
15 |
6,871,529 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02207:Osmr
|
APN |
15 |
6,876,628 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02338:Osmr
|
APN |
15 |
6,867,210 (GRCm39) |
nonsense |
probably null |
|
IGL02350:Osmr
|
APN |
15 |
6,858,144 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02357:Osmr
|
APN |
15 |
6,858,144 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02545:Osmr
|
APN |
15 |
6,853,060 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02619:Osmr
|
APN |
15 |
6,871,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02685:Osmr
|
APN |
15 |
6,845,054 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02959:Osmr
|
APN |
15 |
6,845,378 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03303:Osmr
|
APN |
15 |
6,872,289 (GRCm39) |
missense |
probably benign |
0.03 |
FR4548:Osmr
|
UTSW |
15 |
6,867,184 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Osmr
|
UTSW |
15 |
6,867,187 (GRCm39) |
nonsense |
probably null |
|
R0149:Osmr
|
UTSW |
15 |
6,871,432 (GRCm39) |
critical splice donor site |
probably null |
|
R0361:Osmr
|
UTSW |
15 |
6,871,432 (GRCm39) |
critical splice donor site |
probably null |
|
R0492:Osmr
|
UTSW |
15 |
6,853,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R0538:Osmr
|
UTSW |
15 |
6,871,419 (GRCm39) |
splice site |
probably benign |
|
R0585:Osmr
|
UTSW |
15 |
6,867,274 (GRCm39) |
missense |
probably benign |
|
R0980:Osmr
|
UTSW |
15 |
6,881,921 (GRCm39) |
missense |
probably benign |
0.00 |
R1221:Osmr
|
UTSW |
15 |
6,853,042 (GRCm39) |
nonsense |
probably null |
|
R1922:Osmr
|
UTSW |
15 |
6,873,848 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2067:Osmr
|
UTSW |
15 |
6,844,896 (GRCm39) |
missense |
probably benign |
0.00 |
R2136:Osmr
|
UTSW |
15 |
6,881,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R2156:Osmr
|
UTSW |
15 |
6,873,891 (GRCm39) |
missense |
probably benign |
0.04 |
R3683:Osmr
|
UTSW |
15 |
6,866,534 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3735:Osmr
|
UTSW |
15 |
6,851,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R3736:Osmr
|
UTSW |
15 |
6,851,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R4011:Osmr
|
UTSW |
15 |
6,854,014 (GRCm39) |
missense |
probably benign |
0.01 |
R4175:Osmr
|
UTSW |
15 |
6,882,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R4555:Osmr
|
UTSW |
15 |
6,845,201 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4581:Osmr
|
UTSW |
15 |
6,872,375 (GRCm39) |
missense |
probably benign |
0.00 |
R4751:Osmr
|
UTSW |
15 |
6,872,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R4758:Osmr
|
UTSW |
15 |
6,882,036 (GRCm39) |
missense |
probably benign |
0.23 |
R4986:Osmr
|
UTSW |
15 |
6,846,061 (GRCm39) |
critical splice donor site |
probably null |
|
R4997:Osmr
|
UTSW |
15 |
6,845,120 (GRCm39) |
missense |
probably benign |
0.25 |
R5077:Osmr
|
UTSW |
15 |
6,873,874 (GRCm39) |
nonsense |
probably null |
|
R5093:Osmr
|
UTSW |
15 |
6,850,560 (GRCm39) |
missense |
probably damaging |
0.96 |
R5120:Osmr
|
UTSW |
15 |
6,856,756 (GRCm39) |
missense |
probably benign |
0.16 |
R5331:Osmr
|
UTSW |
15 |
6,872,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R5812:Osmr
|
UTSW |
15 |
6,866,540 (GRCm39) |
missense |
probably damaging |
0.99 |
R5819:Osmr
|
UTSW |
15 |
6,845,268 (GRCm39) |
missense |
probably benign |
0.00 |
R5876:Osmr
|
UTSW |
15 |
6,850,528 (GRCm39) |
missense |
probably benign |
0.07 |
R5986:Osmr
|
UTSW |
15 |
6,873,934 (GRCm39) |
missense |
probably benign |
0.36 |
R6018:Osmr
|
UTSW |
15 |
6,845,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R6164:Osmr
|
UTSW |
15 |
6,889,833 (GRCm39) |
missense |
probably benign |
0.00 |
R6217:Osmr
|
UTSW |
15 |
6,853,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R6312:Osmr
|
UTSW |
15 |
6,853,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R6349:Osmr
|
UTSW |
15 |
6,850,544 (GRCm39) |
missense |
probably benign |
0.00 |
R6898:Osmr
|
UTSW |
15 |
6,845,364 (GRCm39) |
missense |
probably damaging |
0.97 |
R7139:Osmr
|
UTSW |
15 |
6,850,569 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7412:Osmr
|
UTSW |
15 |
6,853,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R7527:Osmr
|
UTSW |
15 |
6,856,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R7630:Osmr
|
UTSW |
15 |
6,846,452 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7730:Osmr
|
UTSW |
15 |
6,853,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R7990:Osmr
|
UTSW |
15 |
6,881,948 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8094:Osmr
|
UTSW |
15 |
6,845,102 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8187:Osmr
|
UTSW |
15 |
6,850,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R8260:Osmr
|
UTSW |
15 |
6,844,897 (GRCm39) |
missense |
probably benign |
0.41 |
R8366:Osmr
|
UTSW |
15 |
6,850,435 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9051:Osmr
|
UTSW |
15 |
6,882,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R9137:Osmr
|
UTSW |
15 |
6,856,709 (GRCm39) |
missense |
probably benign |
0.13 |
R9182:Osmr
|
UTSW |
15 |
6,850,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R9238:Osmr
|
UTSW |
15 |
6,846,086 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9260:Osmr
|
UTSW |
15 |
6,882,033 (GRCm39) |
missense |
probably benign |
|
R9559:Osmr
|
UTSW |
15 |
6,882,027 (GRCm39) |
missense |
probably damaging |
1.00 |
RF040:Osmr
|
UTSW |
15 |
6,867,182 (GRCm39) |
small insertion |
probably benign |
|
RF055:Osmr
|
UTSW |
15 |
6,867,181 (GRCm39) |
small insertion |
probably benign |
|
|