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 |
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 |
Osmr |
T |
C |
15: 6,876,547 (GRCm39) |
S126G |
probably benign |
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 Ccdc91 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00428:Ccdc91
|
APN |
6 |
147,508,452 (GRCm39) |
missense |
unknown |
|
IGL00795:Ccdc91
|
APN |
6 |
147,409,305 (GRCm39) |
missense |
probably damaging |
0.99 |
R1495:Ccdc91
|
UTSW |
6 |
147,435,670 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1725:Ccdc91
|
UTSW |
6 |
147,493,541 (GRCm39) |
missense |
unknown |
|
R3761:Ccdc91
|
UTSW |
6 |
147,464,200 (GRCm39) |
missense |
unknown |
|
R4246:Ccdc91
|
UTSW |
6 |
147,493,646 (GRCm39) |
missense |
unknown |
|
R4591:Ccdc91
|
UTSW |
6 |
147,491,963 (GRCm39) |
missense |
unknown |
|
R4797:Ccdc91
|
UTSW |
6 |
147,493,641 (GRCm39) |
missense |
unknown |
|
R5719:Ccdc91
|
UTSW |
6 |
147,477,001 (GRCm39) |
missense |
unknown |
|
R5721:Ccdc91
|
UTSW |
6 |
147,477,001 (GRCm39) |
missense |
unknown |
|
R6092:Ccdc91
|
UTSW |
6 |
147,437,114 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7156:Ccdc91
|
UTSW |
6 |
147,435,676 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7393:Ccdc91
|
UTSW |
6 |
147,435,527 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7411:Ccdc91
|
UTSW |
6 |
147,493,696 (GRCm39) |
nonsense |
probably null |
|
R7576:Ccdc91
|
UTSW |
6 |
147,491,957 (GRCm39) |
missense |
unknown |
|
R8165:Ccdc91
|
UTSW |
6 |
147,533,086 (GRCm39) |
missense |
unknown |
|
R8311:Ccdc91
|
UTSW |
6 |
147,437,114 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8406:Ccdc91
|
UTSW |
6 |
147,438,920 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8748:Ccdc91
|
UTSW |
6 |
147,464,194 (GRCm39) |
missense |
unknown |
|
R8922:Ccdc91
|
UTSW |
6 |
147,412,358 (GRCm39) |
nonsense |
probably null |
|
R9210:Ccdc91
|
UTSW |
6 |
147,508,398 (GRCm39) |
missense |
unknown |
|
R9212:Ccdc91
|
UTSW |
6 |
147,508,398 (GRCm39) |
missense |
unknown |
|
X0027:Ccdc91
|
UTSW |
6 |
147,492,137 (GRCm39) |
critical splice donor site |
probably null |
|
|