Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017N19Rik |
A |
T |
10: 100,451,106 (GRCm39) |
R446S |
probably damaging |
Het |
2900092C05Rik |
A |
T |
7: 12,288,664 (GRCm39) |
H159L |
probably benign |
Het |
4933405O20Rik |
G |
A |
7: 50,249,838 (GRCm39) |
V291I |
probably damaging |
Het |
A2ml1 |
A |
G |
6: 128,558,085 (GRCm39) |
Y24H |
probably damaging |
Het |
Adgrv1 |
C |
T |
13: 81,583,678 (GRCm39) |
|
probably null |
Het |
Ankrd52 |
C |
T |
10: 128,218,566 (GRCm39) |
H351Y |
probably damaging |
Het |
Anks6 |
C |
A |
4: 47,035,748 (GRCm39) |
A588S |
probably benign |
Het |
Arl15 |
T |
G |
13: 114,070,645 (GRCm39) |
V80G |
probably damaging |
Het |
Atp8a1 |
A |
G |
5: 67,904,628 (GRCm39) |
I532T |
possibly damaging |
Het |
Birc6 |
T |
C |
17: 74,910,031 (GRCm39) |
C1475R |
probably damaging |
Het |
Carmil1 |
C |
T |
13: 24,253,719 (GRCm39) |
R394Q |
probably damaging |
Het |
Cbfa2t2 |
T |
C |
2: 154,359,697 (GRCm39) |
I254T |
probably damaging |
Het |
Cemip2 |
A |
G |
19: 21,803,447 (GRCm39) |
T827A |
probably benign |
Het |
Col6a3 |
A |
G |
1: 90,749,571 (GRCm39) |
V421A |
possibly damaging |
Het |
Cped1 |
T |
C |
6: 22,254,607 (GRCm39) |
V1000A |
probably damaging |
Het |
Cr1l |
A |
T |
1: 194,797,076 (GRCm39) |
Y282* |
probably null |
Het |
Cryl1 |
G |
T |
14: 57,620,236 (GRCm39) |
T43K |
probably benign |
Het |
Csmd2 |
C |
T |
4: 127,952,827 (GRCm39) |
P92L |
probably damaging |
Het |
Ddx60 |
G |
A |
8: 62,474,444 (GRCm39) |
|
probably null |
Het |
Dhrs7b |
C |
T |
11: 60,743,328 (GRCm39) |
R187* |
probably null |
Het |
Dmtf1 |
T |
C |
5: 9,190,451 (GRCm39) |
T88A |
probably damaging |
Het |
Dnah2 |
T |
C |
11: 69,411,707 (GRCm39) |
E305G |
possibly damaging |
Het |
Dscaml1 |
A |
C |
9: 45,632,596 (GRCm39) |
N1154T |
probably benign |
Het |
Efhc1 |
A |
G |
1: 21,030,442 (GRCm39) |
Y125C |
probably damaging |
Het |
Egflam |
T |
A |
15: 7,347,726 (GRCm39) |
Y68F |
possibly damaging |
Het |
Gm18358 |
A |
G |
7: 84,739,756 (GRCm39) |
|
noncoding transcript |
Het |
Gm3443 |
T |
G |
19: 21,534,960 (GRCm39) |
I75S |
probably benign |
Het |
Gpr182 |
C |
A |
10: 127,586,748 (GRCm39) |
V68F |
possibly damaging |
Het |
Herc1 |
T |
A |
9: 66,340,604 (GRCm39) |
M1651K |
possibly damaging |
Het |
Hey1 |
A |
T |
3: 8,731,418 (GRCm39) |
|
probably null |
Het |
Ighv1-43 |
A |
C |
12: 114,909,829 (GRCm39) |
V31G |
probably benign |
Het |
Il17rc |
T |
C |
6: 113,459,692 (GRCm39) |
V450A |
probably damaging |
Het |
Kbtbd4 |
T |
G |
2: 90,736,487 (GRCm39) |
V166G |
probably benign |
Het |
Marveld2 |
T |
C |
13: 100,748,197 (GRCm39) |
N294S |
possibly damaging |
Het |
Mtdh |
A |
G |
15: 34,099,720 (GRCm39) |
K61E |
probably damaging |
Het |
Muc5ac |
T |
C |
7: 141,350,104 (GRCm39) |
S616P |
possibly damaging |
Het |
Myh15 |
T |
C |
16: 48,973,866 (GRCm39) |
L1292P |
probably damaging |
Het |
Nek8 |
C |
T |
11: 78,058,651 (GRCm39) |
V550M |
probably benign |
Het |
Nup155 |
T |
A |
15: 8,159,721 (GRCm39) |
|
probably null |
Het |
Or2y17 |
G |
A |
11: 49,231,592 (GRCm39) |
V78M |
probably damaging |
Het |
Or7c70 |
A |
T |
10: 78,683,572 (GRCm39) |
M59K |
possibly damaging |
Het |
Or8b36 |
ATTGCTGTTT |
ATTGCTGTTTGCTGTTT |
9: 37,937,836 (GRCm39) |
|
probably null |
Het |
Papln |
G |
A |
12: 83,831,143 (GRCm39) |
W1099* |
probably null |
Het |
Pcdhb17 |
A |
G |
18: 37,618,720 (GRCm39) |
Y170C |
probably damaging |
Het |
Pramel12 |
T |
C |
4: 143,144,229 (GRCm39) |
Y192H |
probably benign |
Het |
Prss39 |
T |
G |
1: 34,541,783 (GRCm39) |
C287G |
probably damaging |
Het |
Pyroxd2 |
A |
G |
19: 42,723,911 (GRCm39) |
V338A |
probably damaging |
Het |
Rab19 |
T |
A |
6: 39,360,860 (GRCm39) |
F3I |
probably benign |
Het |
Relt |
A |
G |
7: 100,512,355 (GRCm39) |
|
probably benign |
Het |
Sbf2 |
T |
A |
7: 109,977,193 (GRCm39) |
H647L |
probably benign |
Het |
Scube1 |
C |
T |
15: 83,513,689 (GRCm39) |
C327Y |
probably damaging |
Het |
Sec14l4 |
A |
C |
11: 3,990,055 (GRCm39) |
Q118P |
possibly damaging |
Het |
Shisa9 |
C |
G |
16: 12,085,292 (GRCm39) |
D300E |
probably benign |
Het |
Smg1 |
A |
G |
7: 117,740,580 (GRCm39) |
|
probably benign |
Het |
Sncaip |
A |
G |
18: 53,002,393 (GRCm39) |
T305A |
probably benign |
Het |
Sorcs3 |
T |
C |
19: 48,784,889 (GRCm39) |
V1104A |
probably damaging |
Het |
Ugt1a6b |
C |
T |
1: 88,143,982 (GRCm39) |
R201C |
probably damaging |
Het |
Unc119b |
A |
G |
5: 115,268,612 (GRCm39) |
V91A |
probably benign |
Het |
Uvssa |
A |
G |
5: 33,547,204 (GRCm39) |
K257E |
probably damaging |
Het |
Vmn1r199 |
A |
C |
13: 22,567,416 (GRCm39) |
M237L |
probably benign |
Het |
Vmn1r69 |
G |
A |
7: 10,314,417 (GRCm39) |
R26W |
probably damaging |
Het |
Vmn2r54 |
A |
G |
7: 12,366,143 (GRCm39) |
F264L |
probably damaging |
Het |
Vmn2r7 |
C |
T |
3: 64,623,464 (GRCm39) |
W285* |
probably null |
Het |
Vmn2r78 |
T |
A |
7: 86,569,541 (GRCm39) |
S145T |
possibly damaging |
Het |
Vmn2r78 |
T |
A |
7: 86,604,115 (GRCm39) |
N764K |
probably benign |
Het |
Wdr5b |
T |
G |
16: 35,862,374 (GRCm39) |
H164Q |
probably damaging |
Het |
Zcchc7 |
G |
A |
4: 44,894,982 (GRCm39) |
V236I |
possibly damaging |
Het |
Zfp729b |
G |
A |
13: 67,739,740 (GRCm39) |
R842C |
probably benign |
Het |
|
Other mutations in Gcm2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01312:Gcm2
|
APN |
13 |
41,256,607 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01476:Gcm2
|
APN |
13 |
41,259,217 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02034:Gcm2
|
APN |
13 |
41,259,269 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02186:Gcm2
|
APN |
13 |
41,258,125 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02456:Gcm2
|
APN |
13 |
41,256,477 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03142:Gcm2
|
APN |
13 |
41,256,711 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03184:Gcm2
|
APN |
13 |
41,258,888 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4403001:Gcm2
|
UTSW |
13 |
41,256,315 (GRCm39) |
missense |
probably benign |
0.01 |
R0227:Gcm2
|
UTSW |
13 |
41,259,332 (GRCm39) |
missense |
probably damaging |
0.99 |
R1061:Gcm2
|
UTSW |
13 |
41,259,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R1813:Gcm2
|
UTSW |
13 |
41,259,367 (GRCm39) |
missense |
probably benign |
0.19 |
R2057:Gcm2
|
UTSW |
13 |
41,263,430 (GRCm39) |
start codon destroyed |
probably null |
0.28 |
R2058:Gcm2
|
UTSW |
13 |
41,263,430 (GRCm39) |
start codon destroyed |
probably null |
0.28 |
R2059:Gcm2
|
UTSW |
13 |
41,263,430 (GRCm39) |
start codon destroyed |
probably null |
0.28 |
R2351:Gcm2
|
UTSW |
13 |
41,257,094 (GRCm39) |
missense |
probably benign |
0.02 |
R4653:Gcm2
|
UTSW |
13 |
41,256,317 (GRCm39) |
missense |
probably benign |
0.21 |
R4782:Gcm2
|
UTSW |
13 |
41,256,970 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4799:Gcm2
|
UTSW |
13 |
41,256,970 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5135:Gcm2
|
UTSW |
13 |
41,256,435 (GRCm39) |
missense |
probably benign |
|
R5162:Gcm2
|
UTSW |
13 |
41,257,131 (GRCm39) |
missense |
probably benign |
0.01 |
R5665:Gcm2
|
UTSW |
13 |
41,263,387 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5756:Gcm2
|
UTSW |
13 |
41,263,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R5771:Gcm2
|
UTSW |
13 |
41,256,991 (GRCm39) |
missense |
probably benign |
0.40 |
R5928:Gcm2
|
UTSW |
13 |
41,256,874 (GRCm39) |
missense |
probably benign |
0.00 |
R6394:Gcm2
|
UTSW |
13 |
41,263,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R6578:Gcm2
|
UTSW |
13 |
41,259,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R6798:Gcm2
|
UTSW |
13 |
41,259,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R7088:Gcm2
|
UTSW |
13 |
41,256,840 (GRCm39) |
missense |
probably damaging |
0.98 |
R7413:Gcm2
|
UTSW |
13 |
41,259,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R7456:Gcm2
|
UTSW |
13 |
41,256,751 (GRCm39) |
missense |
probably benign |
0.02 |
R8293:Gcm2
|
UTSW |
13 |
41,256,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R8738:Gcm2
|
UTSW |
13 |
41,258,096 (GRCm39) |
missense |
probably benign |
0.41 |
R9087:Gcm2
|
UTSW |
13 |
41,263,406 (GRCm39) |
missense |
|
|
R9316:Gcm2
|
UTSW |
13 |
41,259,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R9799:Gcm2
|
UTSW |
13 |
41,258,924 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Gcm2
|
UTSW |
13 |
41,256,268 (GRCm39) |
missense |
probably damaging |
1.00 |
|