Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
A |
G |
11: 119,937,746 (GRCm39) |
S11P |
unknown |
Het |
Adrb2 |
T |
C |
18: 62,312,004 (GRCm39) |
T274A |
probably damaging |
Het |
Aph1b |
A |
G |
9: 66,701,503 (GRCm39) |
S45P |
probably damaging |
Het |
Atp9b |
A |
T |
18: 80,887,806 (GRCm39) |
D321E |
|
Het |
C1qbp |
A |
G |
11: 70,869,543 (GRCm39) |
V180A |
possibly damaging |
Het |
C4b |
G |
T |
17: 34,953,513 (GRCm39) |
A990D |
probably damaging |
Het |
Ccdc80 |
T |
A |
16: 44,915,612 (GRCm39) |
S123T |
possibly damaging |
Het |
Cdh18 |
A |
C |
15: 23,474,138 (GRCm39) |
E669D |
possibly damaging |
Het |
Ceacam3 |
T |
A |
7: 16,895,608 (GRCm39) |
V526D |
|
Het |
Cenpf |
C |
T |
1: 189,404,782 (GRCm39) |
C349Y |
probably damaging |
Het |
Dmrt2 |
T |
C |
19: 25,655,379 (GRCm39) |
V326A |
probably damaging |
Het |
Dock9 |
T |
C |
14: 121,783,454 (GRCm39) |
Q2023R |
probably damaging |
Het |
Exd2 |
A |
G |
12: 80,522,771 (GRCm39) |
R77G |
probably benign |
Het |
Exph5 |
A |
T |
9: 53,287,148 (GRCm39) |
K1410* |
probably null |
Het |
Eya2 |
A |
G |
2: 165,608,988 (GRCm39) |
T443A |
probably damaging |
Het |
Fam135a |
G |
A |
1: 24,067,569 (GRCm39) |
T1100M |
probably benign |
Het |
Foxp2 |
G |
T |
6: 15,403,866 (GRCm39) |
R381L |
unknown |
Het |
Grm7 |
T |
G |
6: 111,057,315 (GRCm39) |
V305G |
probably benign |
Het |
Gzma |
G |
A |
13: 113,237,464 (GRCm39) |
R8W |
probably benign |
Het |
H6pd |
T |
C |
4: 150,066,133 (GRCm39) |
E759G |
probably benign |
Het |
Ift27 |
A |
G |
15: 78,048,391 (GRCm39) |
V154A |
probably benign |
Het |
Kif1a |
A |
T |
1: 92,950,141 (GRCm39) |
S1429T |
probably benign |
Het |
Lrrn1 |
T |
A |
6: 107,546,294 (GRCm39) |
D697E |
probably benign |
Het |
Mcrs1 |
A |
T |
15: 99,141,575 (GRCm39) |
I387N |
probably damaging |
Het |
Muc16 |
T |
C |
9: 18,448,807 (GRCm39) |
T7675A |
probably damaging |
Het |
Nid1 |
C |
A |
13: 13,612,416 (GRCm39) |
L44I |
possibly damaging |
Het |
Or2f2 |
A |
T |
6: 42,767,644 (GRCm39) |
T224S |
possibly damaging |
Het |
Or4m1 |
T |
C |
14: 50,558,233 (GRCm39) |
T20A |
probably benign |
Het |
Or5h27 |
A |
G |
16: 59,006,117 (GRCm39) |
I243T |
unknown |
Het |
Or8k1 |
T |
A |
2: 86,047,457 (GRCm39) |
E199V |
probably damaging |
Het |
Pde11a |
C |
T |
2: 75,889,354 (GRCm39) |
D707N |
probably damaging |
Het |
Pigf |
A |
T |
17: 87,327,910 (GRCm39) |
L119* |
probably null |
Het |
Pkd1l1 |
A |
T |
11: 8,820,277 (GRCm39) |
C1679* |
probably null |
Het |
Prnp |
A |
G |
2: 131,778,669 (GRCm39) |
N107S |
probably benign |
Het |
Ptgfr |
C |
T |
3: 151,541,053 (GRCm39) |
V152M |
possibly damaging |
Het |
Rap2b |
A |
G |
3: 61,271,805 (GRCm39) |
|
probably benign |
Het |
Rtn4 |
A |
G |
11: 29,657,300 (GRCm39) |
T485A |
probably damaging |
Het |
Sec23b |
A |
G |
2: 144,401,234 (GRCm39) |
T32A |
probably benign |
Het |
Skint5 |
A |
T |
4: 113,437,679 (GRCm39) |
|
probably null |
Het |
Slc13a5 |
A |
G |
11: 72,148,210 (GRCm39) |
L275P |
probably damaging |
Het |
Slc20a1 |
C |
T |
2: 129,041,784 (GRCm39) |
A49V |
probably damaging |
Het |
Slc35g2 |
A |
G |
9: 100,435,224 (GRCm39) |
I149T |
probably benign |
Het |
Syk |
T |
A |
13: 52,778,763 (GRCm39) |
I283K |
probably benign |
Het |
Taf7l2 |
T |
C |
10: 115,948,440 (GRCm39) |
Y362C |
probably benign |
Het |
Tnfsf13b |
G |
A |
8: 10,056,795 (GRCm39) |
|
probably benign |
Het |
Ubr1 |
A |
G |
2: 120,701,476 (GRCm39) |
V1592A |
probably benign |
Het |
Vopp1 |
T |
C |
6: 57,739,379 (GRCm39) |
*123W |
probably null |
Het |
Xpo4 |
T |
A |
14: 57,841,913 (GRCm39) |
Q467H |
probably damaging |
Het |
Zdhhc22 |
A |
C |
12: 87,035,143 (GRCm39) |
V103G |
possibly damaging |
Het |
Zfp868 |
A |
G |
8: 70,064,160 (GRCm39) |
S392P |
probably damaging |
Het |
|
Other mutations in Naf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00806:Naf1
|
APN |
8 |
67,338,452 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01861:Naf1
|
APN |
8 |
67,317,185 (GRCm39) |
splice site |
probably benign |
|
IGL02817:Naf1
|
APN |
8 |
67,336,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R0016:Naf1
|
UTSW |
8 |
67,341,707 (GRCm39) |
splice site |
probably benign |
|
R0092:Naf1
|
UTSW |
8 |
67,341,760 (GRCm39) |
missense |
probably benign |
0.24 |
R2062:Naf1
|
UTSW |
8 |
67,340,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R2065:Naf1
|
UTSW |
8 |
67,340,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R2066:Naf1
|
UTSW |
8 |
67,340,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R2068:Naf1
|
UTSW |
8 |
67,340,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R2209:Naf1
|
UTSW |
8 |
67,313,188 (GRCm39) |
unclassified |
probably benign |
|
R4296:Naf1
|
UTSW |
8 |
67,342,114 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5186:Naf1
|
UTSW |
8 |
67,332,298 (GRCm39) |
missense |
probably benign |
0.10 |
R5560:Naf1
|
UTSW |
8 |
67,336,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R6122:Naf1
|
UTSW |
8 |
67,336,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R6143:Naf1
|
UTSW |
8 |
67,330,347 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6389:Naf1
|
UTSW |
8 |
67,313,680 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6827:Naf1
|
UTSW |
8 |
67,330,343 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7083:Naf1
|
UTSW |
8 |
67,313,138 (GRCm39) |
unclassified |
probably benign |
|
R7444:Naf1
|
UTSW |
8 |
67,313,200 (GRCm39) |
unclassified |
probably benign |
|
R7727:Naf1
|
UTSW |
8 |
67,313,200 (GRCm39) |
unclassified |
probably benign |
|
R7818:Naf1
|
UTSW |
8 |
67,342,028 (GRCm39) |
missense |
probably damaging |
0.97 |
R7860:Naf1
|
UTSW |
8 |
67,313,165 (GRCm39) |
missense |
unknown |
|
R7923:Naf1
|
UTSW |
8 |
67,313,200 (GRCm39) |
unclassified |
probably benign |
|
R7977:Naf1
|
UTSW |
8 |
67,313,146 (GRCm39) |
unclassified |
probably benign |
|
R8462:Naf1
|
UTSW |
8 |
67,313,200 (GRCm39) |
unclassified |
probably benign |
|
R8815:Naf1
|
UTSW |
8 |
67,317,333 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8989:Naf1
|
UTSW |
8 |
67,313,628 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9138:Naf1
|
UTSW |
8 |
67,317,198 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9231:Naf1
|
UTSW |
8 |
67,313,146 (GRCm39) |
unclassified |
probably benign |
|
R9283:Naf1
|
UTSW |
8 |
67,313,503 (GRCm39) |
missense |
unknown |
|
R9445:Naf1
|
UTSW |
8 |
67,336,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R9454:Naf1
|
UTSW |
8 |
67,313,200 (GRCm39) |
unclassified |
probably benign |
|
R9680:Naf1
|
UTSW |
8 |
67,313,200 (GRCm39) |
unclassified |
probably benign |
|
|