Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930503B20Rik |
A |
G |
3: 146,352,179 (GRCm39) |
L228S |
probably damaging |
Het |
Abca13 |
A |
T |
11: 9,278,136 (GRCm39) |
K3105N |
probably damaging |
Het |
Abca3 |
T |
A |
17: 24,595,700 (GRCm39) |
L351Q |
possibly damaging |
Het |
Acadm |
A |
G |
3: 153,638,680 (GRCm39) |
I231T |
possibly damaging |
Het |
Adamts4 |
A |
T |
1: 171,083,798 (GRCm39) |
Q456L |
probably damaging |
Het |
Adgra3 |
C |
T |
5: 50,159,222 (GRCm39) |
V343I |
probably benign |
Het |
Ajuba |
C |
A |
14: 54,814,645 (GRCm39) |
G26V |
probably damaging |
Het |
Aldh1a1 |
A |
G |
19: 20,597,455 (GRCm39) |
I145M |
possibly damaging |
Het |
Ankrd42 |
G |
A |
7: 92,274,981 (GRCm39) |
Q110* |
probably null |
Het |
Ano3 |
T |
A |
2: 110,513,104 (GRCm39) |
E630D |
probably benign |
Het |
Ap3d1 |
T |
C |
10: 80,549,832 (GRCm39) |
D771G |
probably damaging |
Het |
Arhgap30 |
A |
G |
1: 171,216,896 (GRCm39) |
D21G |
probably damaging |
Het |
Atg13 |
T |
C |
2: 91,509,770 (GRCm39) |
N374S |
probably benign |
Het |
Ccdc168 |
T |
A |
1: 44,095,620 (GRCm39) |
H1826L |
possibly damaging |
Het |
Ccser1 |
A |
T |
6: 61,547,799 (GRCm39) |
M49L |
probably damaging |
Het |
Cpd |
T |
C |
11: 76,688,627 (GRCm39) |
K882E |
probably benign |
Het |
Crtac1 |
G |
A |
19: 42,272,006 (GRCm39) |
L646F |
unknown |
Het |
Cyp27b1 |
T |
G |
10: 126,884,163 (GRCm39) |
V5G |
probably damaging |
Het |
Dcaf11 |
G |
T |
14: 55,806,828 (GRCm39) |
*550Y |
probably null |
Het |
Dhx58 |
A |
G |
11: 100,588,980 (GRCm39) |
|
probably null |
Het |
Dlg2 |
T |
A |
7: 92,087,249 (GRCm39) |
I881N |
probably damaging |
Het |
Ece1 |
C |
T |
4: 137,673,673 (GRCm39) |
T407M |
possibly damaging |
Het |
Ecsit |
C |
T |
9: 21,987,836 (GRCm39) |
V68I |
possibly damaging |
Het |
Egln1 |
T |
C |
8: 125,675,153 (GRCm39) |
D214G |
probably benign |
Het |
Espn |
T |
C |
4: 152,220,002 (GRCm39) |
T47A |
possibly damaging |
Het |
F5 |
A |
G |
1: 164,023,289 (GRCm39) |
I1616V |
possibly damaging |
Het |
Fam43b |
G |
C |
4: 138,122,409 (GRCm39) |
R304G |
probably benign |
Het |
Flnc |
G |
A |
6: 29,438,665 (GRCm39) |
W186* |
probably null |
Het |
Fryl |
T |
C |
5: 73,198,707 (GRCm39) |
D2640G |
possibly damaging |
Het |
Gabrg2 |
T |
C |
11: 41,867,463 (GRCm39) |
K52R |
possibly damaging |
Het |
Ganab |
T |
C |
19: 8,886,832 (GRCm39) |
V306A |
probably damaging |
Het |
Glod4 |
A |
T |
11: 76,128,635 (GRCm39) |
I70N |
possibly damaging |
Het |
Gsn |
T |
A |
2: 35,173,930 (GRCm39) |
V2E |
probably benign |
Het |
H1f2 |
A |
G |
13: 23,922,907 (GRCm39) |
K26E |
probably benign |
Het |
Hrg |
C |
T |
16: 22,780,059 (GRCm39) |
|
probably benign |
Het |
Kctd19 |
T |
C |
8: 106,113,898 (GRCm39) |
T592A |
probably benign |
Het |
Kdm3b |
A |
G |
18: 34,941,472 (GRCm39) |
D521G |
probably damaging |
Het |
Lrba |
A |
G |
3: 86,683,410 (GRCm39) |
H2744R |
possibly damaging |
Het |
Lsr |
C |
T |
7: 30,657,770 (GRCm39) |
A397T |
probably damaging |
Het |
Methig1 |
A |
T |
15: 100,251,241 (GRCm39) |
M51L |
possibly damaging |
Het |
Mga |
A |
G |
2: 119,734,204 (GRCm39) |
I351V |
probably benign |
Het |
Mlf1 |
G |
A |
3: 67,307,084 (GRCm39) |
V250I |
possibly damaging |
Het |
Mreg |
A |
T |
1: 72,231,223 (GRCm39) |
N78K |
probably damaging |
Het |
Mtor |
A |
G |
4: 148,574,012 (GRCm39) |
D1294G |
probably benign |
Het |
Nfkb1 |
T |
C |
3: 135,307,282 (GRCm39) |
I548V |
probably damaging |
Het |
Nlrp3 |
T |
C |
11: 59,439,962 (GRCm39) |
F513S |
possibly damaging |
Het |
Nphp4 |
A |
G |
4: 152,641,500 (GRCm39) |
K1094E |
possibly damaging |
Het |
Nr3c2 |
C |
A |
8: 77,636,536 (GRCm39) |
H546N |
probably damaging |
Het |
Nr4a2 |
T |
A |
2: 57,002,211 (GRCm39) |
M18L |
probably benign |
Het |
Or2y1f |
A |
C |
11: 49,184,459 (GRCm39) |
T104P |
probably benign |
Het |
Or4c109 |
G |
A |
2: 88,817,814 (GRCm39) |
T244I |
probably benign |
Het |
Pclo |
A |
G |
5: 14,590,346 (GRCm39) |
N882S |
unknown |
Het |
Pde6a |
T |
C |
18: 61,395,505 (GRCm39) |
Y583H |
probably damaging |
Het |
Pip5k1b |
T |
A |
19: 24,356,311 (GRCm39) |
Y209F |
probably damaging |
Het |
Plch2 |
A |
T |
4: 155,068,766 (GRCm39) |
S1182T |
probably damaging |
Het |
Ptger2 |
G |
T |
14: 45,227,107 (GRCm39) |
R229L |
probably damaging |
Het |
Ptpru |
C |
A |
4: 131,535,810 (GRCm39) |
G389V |
probably damaging |
Het |
Ric8a |
A |
G |
7: 140,441,851 (GRCm39) |
N249S |
probably benign |
Het |
Slc26a5 |
A |
G |
5: 22,036,508 (GRCm39) |
I266T |
possibly damaging |
Het |
Smyd1 |
T |
C |
6: 71,215,660 (GRCm39) |
N100D |
probably damaging |
Het |
Spmap2l |
T |
C |
5: 77,207,214 (GRCm39) |
I324T |
probably damaging |
Het |
Stag3 |
T |
C |
5: 138,296,546 (GRCm39) |
F468S |
probably damaging |
Het |
Stk31 |
C |
T |
6: 49,394,184 (GRCm39) |
T182I |
probably damaging |
Het |
Svep1 |
G |
T |
4: 58,082,677 (GRCm39) |
N1982K |
possibly damaging |
Het |
Tinagl1 |
A |
G |
4: 130,060,786 (GRCm39) |
Y344H |
probably damaging |
Het |
Tmem216 |
T |
A |
19: 10,529,237 (GRCm39) |
T104S |
probably damaging |
Het |
Tmem231 |
T |
C |
8: 112,645,563 (GRCm39) |
D112G |
probably damaging |
Het |
Ube4b |
A |
G |
4: 149,429,029 (GRCm39) |
I870T |
probably damaging |
Het |
Vwa8 |
T |
A |
14: 79,302,436 (GRCm39) |
L1035Q |
possibly damaging |
Het |
Wdr35 |
A |
G |
12: 9,028,628 (GRCm39) |
Q82R |
probably benign |
Het |
Wnk1 |
A |
T |
6: 119,940,601 (GRCm39) |
|
probably null |
Het |
Zc3h7a |
T |
C |
16: 10,976,458 (GRCm39) |
|
probably benign |
Het |
Zfp532 |
T |
C |
18: 65,757,783 (GRCm39) |
V572A |
probably damaging |
Het |
|
Other mutations in Cdh5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01459:Cdh5
|
APN |
8 |
104,864,449 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02506:Cdh5
|
APN |
8 |
104,864,454 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02737:Cdh5
|
APN |
8 |
104,869,560 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03287:Cdh5
|
APN |
8 |
104,854,747 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03297:Cdh5
|
APN |
8 |
104,854,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0015:Cdh5
|
UTSW |
8 |
104,867,559 (GRCm39) |
missense |
probably benign |
|
R0015:Cdh5
|
UTSW |
8 |
104,867,559 (GRCm39) |
missense |
probably benign |
|
R0126:Cdh5
|
UTSW |
8 |
104,867,314 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0167:Cdh5
|
UTSW |
8 |
104,863,367 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0592:Cdh5
|
UTSW |
8 |
104,857,534 (GRCm39) |
splice site |
probably null |
|
R1760:Cdh5
|
UTSW |
8 |
104,854,801 (GRCm39) |
missense |
probably benign |
|
R1826:Cdh5
|
UTSW |
8 |
104,857,723 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1827:Cdh5
|
UTSW |
8 |
104,839,541 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1840:Cdh5
|
UTSW |
8 |
104,853,248 (GRCm39) |
nonsense |
probably null |
|
R1993:Cdh5
|
UTSW |
8 |
104,864,447 (GRCm39) |
missense |
probably damaging |
0.97 |
R2219:Cdh5
|
UTSW |
8 |
104,869,538 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2239:Cdh5
|
UTSW |
8 |
104,852,304 (GRCm39) |
missense |
possibly damaging |
0.54 |
R2380:Cdh5
|
UTSW |
8 |
104,852,304 (GRCm39) |
missense |
possibly damaging |
0.54 |
R3418:Cdh5
|
UTSW |
8 |
104,856,002 (GRCm39) |
missense |
probably damaging |
0.98 |
R3419:Cdh5
|
UTSW |
8 |
104,856,002 (GRCm39) |
missense |
probably damaging |
0.98 |
R3429:Cdh5
|
UTSW |
8 |
104,857,600 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4491:Cdh5
|
UTSW |
8 |
104,839,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R4823:Cdh5
|
UTSW |
8 |
104,869,301 (GRCm39) |
missense |
probably benign |
0.00 |
R5071:Cdh5
|
UTSW |
8 |
104,867,334 (GRCm39) |
missense |
probably damaging |
0.99 |
R5265:Cdh5
|
UTSW |
8 |
104,869,371 (GRCm39) |
missense |
probably benign |
0.00 |
R5383:Cdh5
|
UTSW |
8 |
104,864,479 (GRCm39) |
missense |
probably benign |
0.17 |
R5447:Cdh5
|
UTSW |
8 |
104,855,994 (GRCm39) |
missense |
probably damaging |
0.99 |
R5580:Cdh5
|
UTSW |
8 |
104,852,126 (GRCm39) |
nonsense |
probably null |
|
R5876:Cdh5
|
UTSW |
8 |
104,869,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R5934:Cdh5
|
UTSW |
8 |
104,864,900 (GRCm39) |
missense |
probably benign |
0.00 |
R6378:Cdh5
|
UTSW |
8 |
104,853,168 (GRCm39) |
splice site |
probably null |
|
R7110:Cdh5
|
UTSW |
8 |
104,867,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R7141:Cdh5
|
UTSW |
8 |
104,839,633 (GRCm39) |
missense |
probably benign |
0.20 |
R7324:Cdh5
|
UTSW |
8 |
104,869,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R7658:Cdh5
|
UTSW |
8 |
104,856,033 (GRCm39) |
critical splice donor site |
probably null |
|
R7806:Cdh5
|
UTSW |
8 |
104,867,448 (GRCm39) |
missense |
probably damaging |
0.98 |
R7811:Cdh5
|
UTSW |
8 |
104,852,235 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7958:Cdh5
|
UTSW |
8 |
104,839,649 (GRCm39) |
missense |
probably benign |
0.01 |
R8270:Cdh5
|
UTSW |
8 |
104,839,672 (GRCm39) |
missense |
probably benign |
0.11 |
R8424:Cdh5
|
UTSW |
8 |
104,856,003 (GRCm39) |
missense |
probably benign |
0.00 |
R8432:Cdh5
|
UTSW |
8 |
104,839,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R8888:Cdh5
|
UTSW |
8 |
104,852,092 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9190:Cdh5
|
UTSW |
8 |
104,867,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R9738:Cdh5
|
UTSW |
8 |
104,863,329 (GRCm39) |
missense |
probably damaging |
0.99 |
X0067:Cdh5
|
UTSW |
8 |
104,869,169 (GRCm39) |
missense |
probably damaging |
0.96 |
|