Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610040J01Rik |
C |
A |
5: 64,055,289 (GRCm39) |
|
probably null |
Het |
Amph |
A |
G |
13: 19,279,007 (GRCm39) |
K161E |
probably benign |
Het |
Aox1 |
A |
T |
1: 58,348,088 (GRCm39) |
H602L |
probably benign |
Het |
Areg |
A |
G |
5: 91,291,492 (GRCm39) |
N145S |
probably damaging |
Het |
Arhgap29 |
C |
T |
3: 121,782,222 (GRCm39) |
T142I |
probably damaging |
Het |
Bcar3 |
C |
T |
3: 122,304,805 (GRCm39) |
|
probably benign |
Het |
Brpf3 |
C |
T |
17: 29,025,248 (GRCm39) |
A107V |
probably benign |
Het |
Btnl2 |
T |
A |
17: 34,587,682 (GRCm39) |
S509T |
possibly damaging |
Het |
Cacna2d2 |
A |
G |
9: 107,402,653 (GRCm39) |
|
probably null |
Het |
Casz1 |
C |
T |
4: 149,028,888 (GRCm39) |
P1111L |
probably damaging |
Het |
Chd9 |
A |
C |
8: 91,767,769 (GRCm39) |
E2422A |
probably damaging |
Het |
Clrn3 |
T |
C |
7: 135,130,133 (GRCm39) |
I34V |
probably benign |
Het |
Cnksr3 |
C |
T |
10: 7,104,467 (GRCm39) |
D79N |
probably damaging |
Het |
Cops8 |
A |
G |
1: 90,539,729 (GRCm39) |
|
probably null |
Het |
Cpa2 |
A |
G |
6: 30,564,345 (GRCm39) |
K392R |
probably benign |
Het |
Dnajc28 |
G |
A |
16: 91,413,795 (GRCm39) |
R150* |
probably null |
Het |
Dnase1l3 |
T |
C |
14: 7,994,299 (GRCm38) |
|
probably benign |
Het |
Gdpd5 |
A |
T |
7: 99,105,689 (GRCm39) |
T502S |
probably benign |
Het |
Gp2 |
A |
T |
7: 119,049,375 (GRCm39) |
D387E |
probably damaging |
Het |
Gpr179 |
A |
G |
11: 97,242,364 (GRCm39) |
L160P |
probably benign |
Het |
Hmcn1 |
G |
A |
1: 150,522,409 (GRCm39) |
T3497M |
probably benign |
Het |
Idh3b |
T |
A |
2: 130,122,420 (GRCm39) |
T322S |
possibly damaging |
Het |
Kit |
A |
T |
5: 75,781,540 (GRCm39) |
N323I |
possibly damaging |
Het |
Kng2 |
T |
C |
16: 22,806,246 (GRCm39) |
S445G |
unknown |
Het |
Lin54 |
A |
G |
5: 100,602,358 (GRCm39) |
V393A |
probably benign |
Het |
Lyst |
T |
A |
13: 13,872,945 (GRCm39) |
W2715R |
probably damaging |
Het |
Mad1l1 |
T |
C |
5: 140,300,813 (GRCm39) |
T28A |
probably benign |
Het |
Med7 |
T |
A |
11: 46,332,073 (GRCm39) |
C223S |
probably benign |
Het |
Megf8 |
T |
A |
7: 25,053,298 (GRCm39) |
L1823Q |
probably damaging |
Het |
Mga |
C |
A |
2: 119,777,719 (GRCm39) |
Q1755K |
probably benign |
Het |
Mgat4b |
A |
T |
11: 50,101,801 (GRCm39) |
N22I |
probably benign |
Het |
Ndufb6 |
C |
T |
4: 40,270,665 (GRCm39) |
|
probably null |
Het |
Neil3 |
A |
G |
8: 54,042,129 (GRCm39) |
L490P |
probably benign |
Het |
Nek9 |
C |
T |
12: 85,350,417 (GRCm39) |
V886I |
probably benign |
Het |
Nol4l |
A |
T |
2: 153,262,473 (GRCm39) |
Y366* |
probably null |
Het |
Nt5dc2 |
A |
G |
14: 30,860,886 (GRCm39) |
T354A |
probably damaging |
Het |
Or1j11 |
T |
A |
2: 36,311,715 (GRCm39) |
Y102N |
probably damaging |
Het |
Pde2a |
G |
A |
7: 101,149,655 (GRCm39) |
|
probably null |
Het |
Phf1 |
T |
C |
17: 27,156,044 (GRCm39) |
F444L |
possibly damaging |
Het |
Plin4 |
G |
A |
17: 56,414,019 (GRCm39) |
T202I |
possibly damaging |
Het |
Plk4 |
G |
C |
3: 40,768,009 (GRCm39) |
V851L |
probably damaging |
Het |
Pp2d1 |
A |
G |
17: 53,822,257 (GRCm39) |
S270P |
probably damaging |
Het |
Ripor1 |
C |
A |
8: 106,347,520 (GRCm39) |
L1028M |
unknown |
Het |
Scn9a |
A |
G |
2: 66,370,874 (GRCm39) |
F569L |
probably damaging |
Het |
Sel1l2 |
T |
A |
2: 140,104,626 (GRCm39) |
L306F |
probably damaging |
Het |
Spic |
A |
T |
10: 88,513,428 (GRCm39) |
S86T |
probably damaging |
Het |
Spmip10 |
T |
A |
18: 56,722,547 (GRCm39) |
|
probably benign |
Het |
Stkld1 |
A |
G |
2: 26,836,668 (GRCm39) |
N278S |
probably benign |
Het |
Taar7d |
T |
A |
10: 23,903,495 (GRCm39) |
F126I |
probably benign |
Het |
Tbc1d31 |
A |
G |
15: 57,824,345 (GRCm39) |
E869G |
possibly damaging |
Het |
Tbcd |
C |
T |
11: 121,384,711 (GRCm39) |
T315M |
probably benign |
Het |
Terf2 |
T |
C |
8: 107,809,656 (GRCm39) |
K221E |
possibly damaging |
Het |
Thsd7a |
T |
A |
6: 12,468,962 (GRCm39) |
T539S |
|
Het |
Tll2 |
A |
G |
19: 41,077,313 (GRCm39) |
F818L |
possibly damaging |
Het |
Tmem87a |
T |
C |
2: 120,200,959 (GRCm39) |
T427A |
possibly damaging |
Het |
Ush2a |
C |
A |
1: 188,183,952 (GRCm39) |
Q1419K |
possibly damaging |
Het |
Vill |
T |
A |
9: 118,895,821 (GRCm39) |
F511Y |
probably damaging |
Het |
Virma |
T |
A |
4: 11,542,128 (GRCm39) |
D1521E |
probably benign |
Het |
Vps13c |
A |
G |
9: 67,766,072 (GRCm39) |
D63G |
probably benign |
Het |
Vrk2 |
A |
G |
11: 26,485,575 (GRCm39) |
F138L |
probably benign |
Het |
Zfp710 |
T |
C |
7: 79,735,775 (GRCm39) |
I514T |
probably damaging |
Het |
Zgrf1 |
T |
A |
3: 127,357,032 (GRCm39) |
F753I |
possibly 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 |
|
IGL00497:Ccdc91
|
APN |
6 |
147,508,485 (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 |
|
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 |
|
|