Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adat3 |
T |
C |
10: 80,442,654 (GRCm39) |
L164P |
probably damaging |
Het |
Aldh16a1 |
A |
T |
7: 44,795,649 (GRCm39) |
L388Q |
probably damaging |
Het |
Angpt1 |
T |
C |
15: 42,539,664 (GRCm39) |
N65S |
probably damaging |
Het |
Ankrd54 |
G |
A |
15: 78,938,250 (GRCm39) |
T287I |
probably damaging |
Het |
Bltp1 |
CCAGATTCATGTAGCA |
CCA |
3: 37,019,081 (GRCm39) |
|
probably null |
Het |
Cc2d2b |
T |
A |
19: 40,753,801 (GRCm39) |
V108E |
possibly damaging |
Het |
Cd200l1 |
A |
T |
16: 45,262,917 (GRCm39) |
I187N |
probably damaging |
Het |
Cntnap5c |
A |
T |
17: 58,469,245 (GRCm39) |
D609V |
probably damaging |
Het |
Col6a4 |
G |
T |
9: 105,952,589 (GRCm39) |
D436E |
probably damaging |
Het |
Cul9 |
A |
T |
17: 46,851,237 (GRCm39) |
D394E |
probably benign |
Het |
Cyfip1 |
A |
G |
7: 55,523,210 (GRCm39) |
E75G |
probably damaging |
Het |
Efr3a |
G |
A |
15: 65,701,679 (GRCm39) |
V198I |
probably benign |
Het |
Eif2ak2 |
C |
T |
17: 79,173,832 (GRCm39) |
G249S |
probably damaging |
Het |
Erich4 |
A |
T |
7: 25,315,149 (GRCm39) |
M42K |
probably benign |
Het |
Fig4 |
A |
C |
10: 41,132,462 (GRCm39) |
V448G |
probably benign |
Het |
Gas1 |
T |
C |
13: 60,323,848 (GRCm39) |
D303G |
probably damaging |
Het |
Golgb1 |
T |
G |
16: 36,719,083 (GRCm39) |
Y330D |
possibly damaging |
Het |
Gpr146 |
C |
T |
5: 139,378,357 (GRCm39) |
A53V |
probably benign |
Het |
Klk1b27 |
A |
C |
7: 43,705,150 (GRCm39) |
M106L |
probably benign |
Het |
Lipc |
T |
C |
9: 70,720,183 (GRCm39) |
T190A |
probably damaging |
Het |
Lrrc4b |
A |
G |
7: 44,111,231 (GRCm39) |
I368V |
possibly damaging |
Het |
Mmp10 |
A |
T |
9: 7,507,284 (GRCm39) |
Q368L |
probably benign |
Het |
Myo10 |
T |
A |
15: 25,738,057 (GRCm39) |
Y501* |
probably null |
Het |
Neb |
T |
A |
2: 52,055,201 (GRCm39) |
H6445L |
probably benign |
Het |
Numa1 |
T |
A |
7: 101,648,492 (GRCm39) |
M741K |
probably benign |
Het |
Nxn |
T |
A |
11: 76,164,819 (GRCm39) |
I231F |
probably damaging |
Het |
Or1j13 |
A |
G |
2: 36,369,392 (GRCm39) |
L250P |
probably damaging |
Het |
Or5b116 |
T |
C |
19: 13,422,985 (GRCm39) |
L203S |
probably benign |
Het |
Osbp2 |
A |
G |
11: 3,813,414 (GRCm39) |
S152P |
probably benign |
Het |
P3h4 |
T |
C |
11: 100,304,869 (GRCm39) |
T173A |
probably damaging |
Het |
Pcdh15 |
C |
A |
10: 74,221,733 (GRCm39) |
R678S |
probably damaging |
Het |
Pcdhb6 |
C |
A |
18: 37,469,365 (GRCm39) |
T762K |
probably benign |
Het |
Pnrc1 |
G |
A |
4: 33,248,057 (GRCm39) |
P114L |
probably damaging |
Het |
Ppp3ca |
T |
A |
3: 136,574,481 (GRCm39) |
S126R |
probably damaging |
Het |
Prl3d2 |
C |
T |
13: 27,310,000 (GRCm39) |
T155I |
probably benign |
Het |
Prune2 |
C |
A |
19: 17,100,038 (GRCm39) |
N1847K |
probably benign |
Het |
Psg21 |
A |
T |
7: 18,381,223 (GRCm39) |
V440E |
probably damaging |
Het |
Rag1 |
A |
G |
2: 101,472,404 (GRCm39) |
S913P |
probably damaging |
Het |
Rmc1 |
A |
G |
18: 12,301,928 (GRCm39) |
N24S |
probably benign |
Het |
Ros1 |
T |
A |
10: 52,031,030 (GRCm39) |
H525L |
probably damaging |
Het |
Scarb1 |
T |
C |
5: 125,364,447 (GRCm39) |
Y94C |
probably damaging |
Het |
Serpinb6a |
T |
G |
13: 34,114,030 (GRCm39) |
D120A |
probably benign |
Het |
Sik3 |
ACAGCAGCAGCAGCAGCAGCAGCAGCA |
ACAGCAGCAGCAGCAGCAGCAGCA |
9: 46,123,355 (GRCm39) |
|
probably benign |
Het |
Slc39a14 |
T |
C |
14: 70,547,566 (GRCm39) |
D299G |
probably benign |
Het |
Sox1 |
G |
A |
8: 12,446,955 (GRCm39) |
A199T |
probably damaging |
Het |
Strc |
T |
A |
2: 121,205,530 (GRCm39) |
I867F |
probably damaging |
Het |
Tfrc |
A |
G |
16: 32,437,985 (GRCm39) |
K346R |
probably benign |
Het |
Usf3 |
C |
T |
16: 44,040,142 (GRCm39) |
Q1541* |
probably null |
Het |
Wrn |
G |
A |
8: 33,759,082 (GRCm39) |
L716F |
probably damaging |
Het |
Zfp354b |
A |
T |
11: 50,814,136 (GRCm39) |
I263K |
probably benign |
Het |
Zfp804b |
T |
A |
5: 6,821,124 (GRCm39) |
E646D |
probably benign |
Het |
Zfp970 |
G |
T |
2: 177,167,338 (GRCm39) |
C304F |
probably damaging |
Het |
|
Other mutations in Zfp141 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00593:Zfp141
|
APN |
7 |
42,124,731 (GRCm39) |
nonsense |
probably null |
|
IGL00595:Zfp141
|
APN |
7 |
42,126,079 (GRCm39) |
missense |
probably benign |
0.08 |
R0577:Zfp141
|
UTSW |
7 |
42,125,938 (GRCm39) |
missense |
probably benign |
0.14 |
R0883:Zfp141
|
UTSW |
7 |
42,125,480 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1701:Zfp141
|
UTSW |
7 |
42,125,470 (GRCm39) |
missense |
probably benign |
0.35 |
R2290:Zfp141
|
UTSW |
7 |
42,124,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R4176:Zfp141
|
UTSW |
7 |
42,125,705 (GRCm39) |
missense |
probably benign |
0.04 |
R4719:Zfp141
|
UTSW |
7 |
42,126,111 (GRCm39) |
splice site |
probably null |
|
R4897:Zfp141
|
UTSW |
7 |
42,125,629 (GRCm39) |
missense |
probably benign |
0.24 |
R5372:Zfp141
|
UTSW |
7 |
42,126,620 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5438:Zfp141
|
UTSW |
7 |
42,138,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R5447:Zfp141
|
UTSW |
7 |
42,124,983 (GRCm39) |
nonsense |
probably null |
|
R5743:Zfp141
|
UTSW |
7 |
42,125,855 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5969:Zfp141
|
UTSW |
7 |
42,138,912 (GRCm39) |
missense |
probably damaging |
0.98 |
R6731:Zfp141
|
UTSW |
7 |
42,138,924 (GRCm39) |
missense |
probably damaging |
0.99 |
R7127:Zfp141
|
UTSW |
7 |
42,124,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R7474:Zfp141
|
UTSW |
7 |
42,125,678 (GRCm39) |
nonsense |
probably null |
|
R7572:Zfp141
|
UTSW |
7 |
42,124,856 (GRCm39) |
missense |
probably benign |
0.03 |
R7890:Zfp141
|
UTSW |
7 |
42,125,903 (GRCm39) |
missense |
probably damaging |
0.99 |
R8133:Zfp141
|
UTSW |
7 |
42,124,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R8833:Zfp141
|
UTSW |
7 |
42,125,687 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9238:Zfp141
|
UTSW |
7 |
42,125,111 (GRCm39) |
nonsense |
probably null |
|
R9245:Zfp141
|
UTSW |
7 |
42,124,821 (GRCm39) |
nonsense |
probably null |
|
R9339:Zfp141
|
UTSW |
7 |
42,125,639 (GRCm39) |
missense |
probably damaging |
0.98 |
R9348:Zfp141
|
UTSW |
7 |
42,124,814 (GRCm39) |
nonsense |
probably null |
|
R9498:Zfp141
|
UTSW |
7 |
42,125,770 (GRCm39) |
missense |
probably benign |
0.07 |
|