Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap6 |
A |
T |
12: 52,927,668 (GRCm39) |
T193S |
probably benign |
Het |
Anpep |
T |
C |
7: 79,486,049 (GRCm39) |
T558A |
possibly damaging |
Het |
Asap2 |
A |
G |
12: 21,263,191 (GRCm39) |
I269V |
probably benign |
Het |
B3galnt2 |
T |
C |
13: 14,165,423 (GRCm39) |
V273A |
probably benign |
Het |
Bag3 |
C |
A |
7: 128,143,923 (GRCm39) |
D306E |
possibly damaging |
Het |
Bahcc1 |
C |
T |
11: 120,177,514 (GRCm39) |
P2076S |
probably damaging |
Het |
Btbd7 |
A |
C |
12: 102,761,563 (GRCm39) |
L541V |
probably damaging |
Het |
C6 |
A |
T |
15: 4,820,465 (GRCm39) |
D492V |
probably damaging |
Het |
Cdhr5 |
C |
T |
7: 140,851,615 (GRCm39) |
S563N |
possibly damaging |
Het |
Cnn1 |
C |
G |
9: 22,019,474 (GRCm39) |
L281V |
probably benign |
Het |
Egflam |
G |
A |
15: 7,281,942 (GRCm39) |
T398I |
probably benign |
Het |
Eif4g2 |
T |
G |
7: 110,673,415 (GRCm39) |
D788A |
probably benign |
Het |
Elavl4 |
T |
C |
4: 110,108,546 (GRCm39) |
E66G |
probably damaging |
Het |
Fbxw16 |
T |
A |
9: 109,276,887 (GRCm39) |
D87V |
probably damaging |
Het |
Fsip2 |
A |
T |
2: 82,820,425 (GRCm39) |
D5386V |
probably damaging |
Het |
Ftl1 |
A |
C |
7: 45,108,959 (GRCm39) |
S33A |
probably benign |
Het |
Gm21560 |
T |
C |
14: 6,218,338 (GRCm38) |
R47G |
probably damaging |
Het |
Itpkc |
A |
T |
7: 26,927,429 (GRCm39) |
C162S |
probably benign |
Het |
Katnip |
T |
A |
7: 125,471,926 (GRCm39) |
I1531N |
probably damaging |
Het |
Kremen2 |
C |
T |
17: 23,962,781 (GRCm39) |
A102T |
probably damaging |
Het |
L3mbtl1 |
A |
T |
2: 162,806,972 (GRCm39) |
Q480L |
probably benign |
Het |
Lyst |
T |
C |
13: 13,823,188 (GRCm39) |
C1387R |
probably benign |
Het |
Nmi |
A |
G |
2: 51,846,003 (GRCm39) |
V93A |
probably damaging |
Het |
Ntn1 |
T |
C |
11: 68,117,397 (GRCm39) |
K484R |
possibly damaging |
Het |
Olig1 |
T |
C |
16: 91,066,915 (GRCm39) |
S51P |
probably benign |
Het |
Or6c76 |
A |
T |
10: 129,611,796 (GRCm39) |
R4S |
probably benign |
Het |
Pah |
G |
T |
10: 87,357,888 (GRCm39) |
V4F |
probably benign |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Pramel39-ps |
A |
T |
5: 94,450,952 (GRCm39) |
N391K |
possibly damaging |
Het |
Prox1 |
C |
A |
1: 189,892,905 (GRCm39) |
E513D |
possibly damaging |
Het |
Psd3 |
T |
C |
8: 68,573,539 (GRCm39) |
N214S |
probably benign |
Het |
Rhobtb1 |
A |
G |
10: 69,108,628 (GRCm39) |
S505G |
probably benign |
Het |
Ryr1 |
A |
T |
7: 28,801,277 (GRCm39) |
L829H |
probably damaging |
Het |
Sec16a |
A |
T |
2: 26,304,401 (GRCm39) |
D852E |
|
Het |
Senp2 |
T |
C |
16: 21,847,344 (GRCm39) |
|
probably null |
Het |
Sf3b1 |
A |
G |
1: 55,051,376 (GRCm39) |
V184A |
probably benign |
Het |
Skint5 |
T |
C |
4: 113,392,955 (GRCm39) |
T1226A |
unknown |
Het |
Slc1a6 |
G |
A |
10: 78,637,692 (GRCm39) |
R406H |
probably damaging |
Het |
Slc26a4 |
C |
A |
12: 31,578,659 (GRCm39) |
V665L |
possibly damaging |
Het |
Spef2 |
T |
C |
15: 9,647,611 (GRCm39) |
Y932C |
probably damaging |
Het |
Spidr |
T |
A |
16: 15,936,814 (GRCm39) |
N97I |
probably benign |
Het |
Ttn |
A |
G |
2: 76,748,504 (GRCm39) |
S4182P |
probably damaging |
Het |
Tubb6 |
T |
C |
18: 67,534,514 (GRCm39) |
S138P |
probably damaging |
Het |
Ubr2 |
C |
T |
17: 47,292,285 (GRCm39) |
A393T |
probably benign |
Het |
Utrn |
G |
T |
10: 12,689,229 (GRCm39) |
P19T |
probably benign |
Het |
Vcl |
T |
G |
14: 21,033,515 (GRCm39) |
L157W |
probably damaging |
Het |
Vmn1r22 |
A |
T |
6: 57,877,257 (GRCm39) |
M240K |
possibly damaging |
Het |
Vmn2r14 |
A |
T |
5: 109,369,112 (GRCm39) |
S154T |
probably benign |
Het |
Wbp2 |
T |
C |
11: 115,974,724 (GRCm39) |
N37D |
probably benign |
Het |
Zfc3h1 |
C |
G |
10: 115,221,528 (GRCm39) |
D142E |
unknown |
Het |
Zmym6 |
T |
C |
4: 127,002,500 (GRCm39) |
V577A |
probably benign |
Het |
Zxdc |
C |
A |
6: 90,359,189 (GRCm39) |
T607K |
probably benign |
Het |
|
Other mutations in Vmn1r184 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01396:Vmn1r184
|
APN |
7 |
25,966,862 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01411:Vmn1r184
|
APN |
7 |
25,966,320 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02961:Vmn1r184
|
APN |
7 |
25,967,075 (GRCm39) |
missense |
probably benign |
0.27 |
IGL03271:Vmn1r184
|
APN |
7 |
25,967,034 (GRCm39) |
missense |
probably benign |
|
R0302:Vmn1r184
|
UTSW |
7 |
25,966,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R0384:Vmn1r184
|
UTSW |
7 |
25,967,076 (GRCm39) |
missense |
probably benign |
0.41 |
R0591:Vmn1r184
|
UTSW |
7 |
25,966,500 (GRCm39) |
missense |
probably damaging |
0.98 |
R0620:Vmn1r184
|
UTSW |
7 |
25,966,602 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1644:Vmn1r184
|
UTSW |
7 |
25,966,670 (GRCm39) |
missense |
probably benign |
0.00 |
R2304:Vmn1r184
|
UTSW |
7 |
25,966,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R2329:Vmn1r184
|
UTSW |
7 |
25,966,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R3522:Vmn1r184
|
UTSW |
7 |
25,967,008 (GRCm39) |
nonsense |
probably null |
|
R5020:Vmn1r184
|
UTSW |
7 |
25,966,955 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5030:Vmn1r184
|
UTSW |
7 |
25,966,881 (GRCm39) |
missense |
probably benign |
0.25 |
R5049:Vmn1r184
|
UTSW |
7 |
25,966,793 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5076:Vmn1r184
|
UTSW |
7 |
25,966,346 (GRCm39) |
missense |
probably benign |
0.00 |
R5213:Vmn1r184
|
UTSW |
7 |
25,967,136 (GRCm39) |
missense |
probably damaging |
0.99 |
R5554:Vmn1r184
|
UTSW |
7 |
25,966,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R6146:Vmn1r184
|
UTSW |
7 |
25,966,817 (GRCm39) |
missense |
probably benign |
0.08 |
R6868:Vmn1r184
|
UTSW |
7 |
25,966,727 (GRCm39) |
missense |
probably benign |
0.00 |
R6937:Vmn1r184
|
UTSW |
7 |
25,966,750 (GRCm39) |
missense |
probably benign |
0.08 |
R6943:Vmn1r184
|
UTSW |
7 |
25,966,563 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7190:Vmn1r184
|
UTSW |
7 |
25,967,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R7239:Vmn1r184
|
UTSW |
7 |
25,966,602 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7472:Vmn1r184
|
UTSW |
7 |
25,966,824 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8258:Vmn1r184
|
UTSW |
7 |
25,966,686 (GRCm39) |
missense |
probably benign |
0.44 |
R8259:Vmn1r184
|
UTSW |
7 |
25,966,686 (GRCm39) |
missense |
probably benign |
0.44 |
R8911:Vmn1r184
|
UTSW |
7 |
25,966,310 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9008:Vmn1r184
|
UTSW |
7 |
25,967,177 (GRCm39) |
missense |
probably benign |
|
R9159:Vmn1r184
|
UTSW |
7 |
25,966,545 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9548:Vmn1r184
|
UTSW |
7 |
25,966,734 (GRCm39) |
missense |
probably benign |
0.29 |
R9588:Vmn1r184
|
UTSW |
7 |
25,966,347 (GRCm39) |
missense |
probably null |
0.78 |
Z1177:Vmn1r184
|
UTSW |
7 |
25,966,415 (GRCm39) |
missense |
possibly damaging |
0.95 |
|