Other mutations in this stock |
Total: 117 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aars2 |
T |
A |
17: 45,827,847 (GRCm39) |
D555E |
probably damaging |
Het |
Adgre1 |
C |
A |
17: 57,757,073 (GRCm39) |
Q777K |
possibly damaging |
Het |
Agpat4 |
G |
A |
17: 12,429,264 (GRCm39) |
|
probably null |
Het |
Ak7 |
G |
A |
12: 105,679,834 (GRCm39) |
V123M |
probably benign |
Het |
Ankle1 |
AT |
A |
8: 71,859,851 (GRCm39) |
|
probably benign |
Het |
Ankrd44 |
T |
G |
1: 54,805,907 (GRCm39) |
|
probably benign |
Het |
Aprt |
A |
T |
8: 123,302,154 (GRCm39) |
|
probably null |
Het |
Aptx |
T |
C |
4: 40,702,766 (GRCm39) |
|
probably null |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
AY358078 |
T |
A |
14: 52,063,532 (GRCm39) |
C393S |
possibly damaging |
Het |
Bbip1 |
T |
C |
19: 53,920,606 (GRCm39) |
M1V |
probably null |
Het |
Cacng7 |
T |
A |
7: 3,385,207 (GRCm39) |
M36K |
probably benign |
Het |
Camta1 |
A |
G |
4: 151,169,284 (GRCm39) |
W156R |
probably damaging |
Het |
Casd1 |
G |
A |
6: 4,631,165 (GRCm39) |
|
probably null |
Het |
Casz1 |
T |
A |
4: 149,017,724 (GRCm39) |
Y338N |
probably damaging |
Het |
Ccdc66 |
T |
C |
14: 27,222,377 (GRCm39) |
N122S |
probably damaging |
Het |
Celf2 |
G |
T |
2: 6,590,831 (GRCm39) |
N279K |
possibly damaging |
Het |
Cfap96 |
A |
T |
8: 46,423,505 (GRCm39) |
I69N |
probably damaging |
Het |
Cit |
A |
G |
5: 116,132,146 (GRCm39) |
T1801A |
probably benign |
Het |
Cnot2 |
A |
G |
10: 116,335,323 (GRCm39) |
I275T |
probably damaging |
Het |
Ddx4 |
T |
C |
13: 112,748,594 (GRCm39) |
K435E |
probably damaging |
Het |
Dnajc6 |
T |
C |
4: 101,468,461 (GRCm39) |
F166L |
probably damaging |
Het |
Dst |
T |
C |
1: 34,208,937 (GRCm39) |
L820P |
probably damaging |
Het |
Dusp11 |
T |
A |
6: 85,927,037 (GRCm39) |
N193Y |
probably damaging |
Het |
Eif1ad7 |
T |
C |
12: 88,238,544 (GRCm39) |
N72S |
probably benign |
Het |
Eif3m |
A |
T |
2: 104,843,633 (GRCm39) |
N116K |
probably benign |
Het |
Epb41l1 |
A |
T |
2: 156,351,181 (GRCm39) |
E418D |
possibly damaging |
Het |
Esyt2 |
T |
G |
12: 116,282,510 (GRCm39) |
N153K |
probably damaging |
Het |
Exoc6b |
T |
G |
6: 84,980,141 (GRCm39) |
|
probably benign |
Het |
Ezr |
C |
T |
17: 7,007,121 (GRCm39) |
E502K |
possibly damaging |
Het |
Fbxw11 |
T |
A |
11: 32,661,859 (GRCm39) |
Y66N |
possibly damaging |
Het |
Frem2 |
A |
G |
3: 53,455,228 (GRCm39) |
L2116S |
possibly damaging |
Het |
Fry |
T |
C |
5: 150,309,569 (GRCm39) |
L671P |
probably damaging |
Het |
Galnt7 |
A |
G |
8: 57,998,803 (GRCm39) |
I262T |
probably damaging |
Het |
Glp1r |
T |
C |
17: 31,150,221 (GRCm39) |
F381S |
probably benign |
Het |
Gm3867 |
T |
C |
9: 36,168,567 (GRCm39) |
|
noncoding transcript |
Het |
Gm8741 |
G |
T |
17: 35,555,062 (GRCm39) |
|
noncoding transcript |
Het |
Golgb1 |
A |
G |
16: 36,738,987 (GRCm39) |
D2442G |
probably damaging |
Het |
Gp1bb |
A |
T |
16: 18,439,893 (GRCm39) |
L67Q |
probably damaging |
Het |
Gstm7 |
G |
A |
3: 107,834,235 (GRCm39) |
T206I |
possibly damaging |
Het |
H2bc7 |
A |
T |
13: 23,758,231 (GRCm39) |
V45E |
possibly damaging |
Het |
Hs3st5 |
A |
T |
10: 36,704,802 (GRCm39) |
D35V |
probably benign |
Het |
Hspa13 |
T |
C |
16: 75,558,190 (GRCm39) |
H125R |
probably benign |
Het |
Hspa1a |
T |
G |
17: 35,190,156 (GRCm39) |
H249P |
probably damaging |
Het |
Igkv10-95 |
A |
T |
6: 68,657,562 (GRCm39) |
Q6L |
probably damaging |
Het |
Il1rap |
T |
A |
16: 26,533,526 (GRCm39) |
L474H |
probably benign |
Het |
Ipo11 |
T |
A |
13: 107,016,245 (GRCm39) |
Y489F |
probably benign |
Het |
Itga5 |
A |
G |
15: 103,259,259 (GRCm39) |
Y723H |
probably damaging |
Het |
Itih2 |
T |
C |
2: 10,109,971 (GRCm39) |
N594S |
probably damaging |
Het |
Itk |
T |
A |
11: 46,227,342 (GRCm39) |
Q427L |
probably benign |
Het |
Kif26b |
A |
G |
1: 178,506,920 (GRCm39) |
Y332C |
probably damaging |
Het |
Kmt2c |
G |
A |
5: 25,559,382 (GRCm39) |
R1086W |
probably damaging |
Het |
Ktn1 |
T |
A |
14: 47,963,636 (GRCm39) |
|
probably benign |
Het |
Lars2 |
T |
A |
9: 123,247,758 (GRCm39) |
I305N |
probably damaging |
Het |
Lgmn |
G |
T |
12: 102,366,383 (GRCm39) |
|
probably benign |
Het |
Ltbp4 |
C |
T |
7: 27,006,125 (GRCm39) |
E1453K |
probably damaging |
Het |
Lypd8 |
G |
A |
11: 58,277,675 (GRCm39) |
M152I |
probably benign |
Het |
Man2a1 |
T |
A |
17: 65,019,454 (GRCm39) |
S773T |
probably benign |
Het |
Map2k6 |
T |
G |
11: 110,390,300 (GRCm39) |
L278R |
probably damaging |
Het |
Mbtps1 |
A |
T |
8: 120,262,086 (GRCm39) |
D354E |
probably damaging |
Het |
Mcpt9 |
C |
T |
14: 56,266,049 (GRCm39) |
V60M |
probably damaging |
Het |
Mical3 |
C |
A |
6: 120,911,799 (GRCm39) |
E1083* |
probably null |
Het |
Mms19 |
A |
G |
19: 41,933,935 (GRCm39) |
V811A |
possibly damaging |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Mslnl |
G |
A |
17: 25,961,908 (GRCm39) |
V128M |
probably damaging |
Het |
Mtcl1 |
T |
A |
17: 66,684,882 (GRCm39) |
H520L |
probably benign |
Het |
Mymk |
A |
T |
2: 26,952,719 (GRCm39) |
F130I |
probably damaging |
Het |
Myo1f |
C |
T |
17: 33,801,306 (GRCm39) |
R333C |
probably damaging |
Het |
Myo9a |
T |
A |
9: 59,779,165 (GRCm39) |
H1640Q |
probably benign |
Het |
Nav1 |
A |
G |
1: 135,520,186 (GRCm39) |
|
probably benign |
Het |
Ncbp3 |
G |
T |
11: 72,969,844 (GRCm39) |
G564C |
probably damaging |
Het |
Ncoa4 |
A |
T |
14: 31,898,682 (GRCm39) |
I501L |
probably benign |
Het |
Ngp |
T |
A |
9: 110,249,883 (GRCm39) |
N60K |
possibly damaging |
Het |
Npc1l1 |
G |
T |
11: 6,178,215 (GRCm39) |
D398E |
probably damaging |
Het |
Nphs2 |
T |
A |
1: 156,153,701 (GRCm39) |
M264K |
probably damaging |
Het |
Or4s2b |
G |
A |
2: 88,508,240 (GRCm39) |
V14I |
probably benign |
Het |
Or4s2b |
T |
G |
2: 88,508,523 (GRCm39) |
V101G |
probably benign |
Het |
Or7e165 |
T |
A |
9: 19,694,442 (GRCm39) |
Y4* |
probably null |
Het |
Or8b8 |
T |
A |
9: 37,809,622 (GRCm39) |
S307R |
probably benign |
Het |
Patz1 |
A |
G |
11: 3,256,241 (GRCm39) |
Y509C |
probably damaging |
Het |
Pax8 |
G |
A |
2: 24,311,595 (GRCm39) |
P447S |
probably damaging |
Het |
Pde11a |
A |
G |
2: 75,988,677 (GRCm39) |
V488A |
probably benign |
Het |
Pex11g |
C |
T |
8: 3,515,899 (GRCm39) |
V45M |
probably benign |
Het |
Pik3ip1 |
T |
A |
11: 3,283,327 (GRCm39) |
S142R |
probably damaging |
Het |
Pitpnm2 |
C |
G |
5: 124,263,434 (GRCm39) |
A819P |
probably damaging |
Het |
Pla2g4e |
T |
G |
2: 120,016,863 (GRCm39) |
H226P |
possibly damaging |
Het |
Plin4 |
T |
A |
17: 56,412,418 (GRCm39) |
M538L |
probably benign |
Het |
Ppp3cb |
T |
C |
14: 20,570,714 (GRCm39) |
N339S |
possibly damaging |
Het |
Rev1 |
T |
C |
1: 38,092,730 (GRCm39) |
E1202G |
probably damaging |
Het |
Rngtt |
T |
A |
4: 33,339,133 (GRCm39) |
|
probably benign |
Het |
Serpinb12 |
T |
A |
1: 106,876,883 (GRCm39) |
D66E |
probably benign |
Het |
Sgsm1 |
A |
T |
5: 113,403,173 (GRCm39) |
F958Y |
probably damaging |
Het |
Slc35e2 |
T |
C |
4: 155,702,106 (GRCm39) |
F290S |
probably benign |
Het |
Sorl1 |
C |
T |
9: 41,943,210 (GRCm39) |
V889M |
possibly damaging |
Het |
Sptlc3 |
G |
A |
2: 139,478,600 (GRCm39) |
V520I |
probably benign |
Het |
Stam |
A |
T |
2: 14,120,669 (GRCm39) |
H53L |
probably damaging |
Het |
Tarbp1 |
A |
G |
8: 127,201,069 (GRCm39) |
Y246H |
probably damaging |
Het |
Tbx15 |
A |
G |
3: 99,259,683 (GRCm39) |
Y518C |
probably damaging |
Het |
Tdrd5 |
T |
A |
1: 156,111,944 (GRCm39) |
T479S |
probably benign |
Het |
Tescl |
T |
C |
7: 24,032,683 (GRCm39) |
E214G |
probably damaging |
Het |
Tex10 |
T |
C |
4: 48,452,946 (GRCm39) |
D671G |
probably benign |
Het |
Tmem132d |
A |
G |
5: 128,061,360 (GRCm39) |
V414A |
probably benign |
Het |
Tmem41b |
T |
A |
7: 109,573,941 (GRCm39) |
|
probably benign |
Het |
Tnfrsf18 |
A |
G |
4: 156,106,337 (GRCm39) |
|
probably benign |
Het |
Tulp4 |
T |
A |
17: 6,249,108 (GRCm39) |
D42E |
probably damaging |
Het |
Ubtd1 |
A |
G |
19: 42,022,103 (GRCm39) |
N125S |
probably damaging |
Het |
Ubxn4 |
T |
A |
1: 128,183,186 (GRCm39) |
F68I |
probably benign |
Het |
Urb1 |
A |
G |
16: 90,573,159 (GRCm39) |
S958P |
probably benign |
Het |
Vash2 |
T |
C |
1: 190,692,498 (GRCm39) |
S226G |
probably benign |
Het |
Vmn2r120 |
C |
T |
17: 57,816,120 (GRCm39) |
G745E |
probably damaging |
Het |
Vmn2r58 |
T |
A |
7: 41,487,117 (GRCm39) |
I593F |
probably benign |
Het |
Zfp398 |
T |
C |
6: 47,817,361 (GRCm39) |
L67P |
probably damaging |
Het |
Zfp607b |
T |
A |
7: 27,403,120 (GRCm39) |
H525Q |
probably damaging |
Het |
Zfp629 |
T |
C |
7: 127,211,492 (GRCm39) |
T106A |
probably benign |
Het |
Zfp980 |
G |
A |
4: 145,428,653 (GRCm39) |
G461S |
probably benign |
Het |
Zic5 |
T |
A |
14: 122,702,212 (GRCm39) |
D173V |
probably damaging |
Het |
Zranb2 |
G |
A |
3: 157,247,521 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Stox2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02234:Stox2
|
APN |
8 |
47,646,647 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02331:Stox2
|
APN |
8 |
47,644,979 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02399:Stox2
|
APN |
8 |
47,639,573 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03091:Stox2
|
APN |
8 |
47,646,222 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL03143:Stox2
|
APN |
8 |
47,646,839 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL03307:Stox2
|
APN |
8 |
47,647,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R0082:Stox2
|
UTSW |
8 |
47,656,317 (GRCm39) |
splice site |
probably benign |
|
R0313:Stox2
|
UTSW |
8 |
47,645,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R0382:Stox2
|
UTSW |
8 |
47,656,319 (GRCm39) |
splice site |
probably benign |
|
R0513:Stox2
|
UTSW |
8 |
47,646,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R0539:Stox2
|
UTSW |
8 |
47,647,070 (GRCm39) |
missense |
probably damaging |
0.97 |
R0920:Stox2
|
UTSW |
8 |
47,646,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R1764:Stox2
|
UTSW |
8 |
47,647,051 (GRCm39) |
nonsense |
probably null |
|
R1923:Stox2
|
UTSW |
8 |
47,646,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R2311:Stox2
|
UTSW |
8 |
47,645,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R3196:Stox2
|
UTSW |
8 |
47,645,865 (GRCm39) |
missense |
probably damaging |
0.99 |
R3715:Stox2
|
UTSW |
8 |
47,866,187 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4300:Stox2
|
UTSW |
8 |
47,647,027 (GRCm39) |
nonsense |
probably null |
|
R4534:Stox2
|
UTSW |
8 |
47,646,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R4600:Stox2
|
UTSW |
8 |
47,645,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R4601:Stox2
|
UTSW |
8 |
47,645,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R4602:Stox2
|
UTSW |
8 |
47,645,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R4603:Stox2
|
UTSW |
8 |
47,645,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R4624:Stox2
|
UTSW |
8 |
47,646,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R4672:Stox2
|
UTSW |
8 |
47,645,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R4888:Stox2
|
UTSW |
8 |
47,656,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R4944:Stox2
|
UTSW |
8 |
47,866,300 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5331:Stox2
|
UTSW |
8 |
47,866,662 (GRCm39) |
utr 5 prime |
probably benign |
|
R5349:Stox2
|
UTSW |
8 |
47,740,951 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5367:Stox2
|
UTSW |
8 |
47,656,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R5471:Stox2
|
UTSW |
8 |
47,646,548 (GRCm39) |
missense |
probably damaging |
0.96 |
R5561:Stox2
|
UTSW |
8 |
47,646,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R5630:Stox2
|
UTSW |
8 |
47,644,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R5719:Stox2
|
UTSW |
8 |
47,866,172 (GRCm39) |
nonsense |
probably null |
|
R5733:Stox2
|
UTSW |
8 |
47,866,172 (GRCm39) |
nonsense |
probably null |
|
R5996:Stox2
|
UTSW |
8 |
47,656,182 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6170:Stox2
|
UTSW |
8 |
47,645,055 (GRCm39) |
missense |
probably benign |
0.02 |
R6458:Stox2
|
UTSW |
8 |
47,645,079 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6786:Stox2
|
UTSW |
8 |
47,639,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R6815:Stox2
|
UTSW |
8 |
47,646,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R6951:Stox2
|
UTSW |
8 |
47,656,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R7193:Stox2
|
UTSW |
8 |
47,639,489 (GRCm39) |
missense |
probably benign |
|
R7330:Stox2
|
UTSW |
8 |
47,645,271 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7552:Stox2
|
UTSW |
8 |
47,656,154 (GRCm39) |
critical splice donor site |
probably null |
|
R8001:Stox2
|
UTSW |
8 |
47,639,512 (GRCm39) |
missense |
probably benign |
0.06 |
R8266:Stox2
|
UTSW |
8 |
47,645,060 (GRCm39) |
missense |
probably damaging |
0.99 |
R8506:Stox2
|
UTSW |
8 |
47,645,108 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8935:Stox2
|
UTSW |
8 |
47,645,895 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9261:Stox2
|
UTSW |
8 |
47,645,441 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9325:Stox2
|
UTSW |
8 |
47,647,095 (GRCm39) |
missense |
probably benign |
0.45 |
R9505:Stox2
|
UTSW |
8 |
47,645,304 (GRCm39) |
missense |
probably benign |
0.28 |
X0027:Stox2
|
UTSW |
8 |
47,646,875 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1177:Stox2
|
UTSW |
8 |
47,647,085 (GRCm39) |
missense |
probably damaging |
1.00 |
|