Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6430550D23Rik |
A |
G |
2: 155,845,731 (GRCm39) |
F9S |
unknown |
Het |
Abhd10 |
A |
G |
16: 45,557,997 (GRCm39) |
F101L |
probably damaging |
Het |
Acp2 |
A |
G |
2: 91,034,651 (GRCm39) |
T93A |
probably benign |
Het |
Adamts9 |
C |
T |
6: 92,837,048 (GRCm39) |
|
probably benign |
Het |
Aknad1 |
T |
A |
3: 108,682,615 (GRCm39) |
|
probably benign |
Het |
Ank3 |
A |
T |
10: 69,822,785 (GRCm39) |
T485S |
probably benign |
Het |
Caly |
G |
A |
7: 139,652,503 (GRCm39) |
R82C |
probably damaging |
Het |
Cfhr2 |
A |
G |
1: 139,786,343 (GRCm39) |
L8P |
probably damaging |
Het |
Cpeb2 |
T |
A |
5: 43,438,775 (GRCm39) |
L869* |
probably null |
Het |
Cxxc1 |
A |
G |
18: 74,350,331 (GRCm39) |
K33E |
possibly damaging |
Het |
Cyp17a1 |
T |
C |
19: 46,659,533 (GRCm39) |
|
probably null |
Het |
Cyp4a30b |
G |
A |
4: 115,309,976 (GRCm39) |
W59* |
probably null |
Het |
Dennd4b |
T |
C |
3: 90,185,172 (GRCm39) |
V1204A |
probably damaging |
Het |
Dpyd |
T |
A |
3: 118,935,565 (GRCm39) |
D663E |
possibly damaging |
Het |
Esrrg |
A |
T |
1: 187,933,205 (GRCm39) |
|
probably benign |
Het |
Exoc2 |
A |
C |
13: 31,090,822 (GRCm39) |
L261V |
probably damaging |
Het |
Exosc9 |
T |
C |
3: 36,609,662 (GRCm39) |
L185S |
probably damaging |
Het |
Gcnt3 |
T |
C |
9: 69,941,728 (GRCm39) |
K280R |
probably benign |
Het |
Ighv1-64 |
A |
T |
12: 115,471,217 (GRCm39) |
M100K |
probably benign |
Het |
Impdh2 |
G |
A |
9: 108,441,978 (GRCm39) |
|
probably null |
Het |
Itsn2 |
T |
A |
12: 4,721,474 (GRCm39) |
I1068K |
probably damaging |
Het |
Kif5c |
T |
C |
2: 49,584,783 (GRCm39) |
C169R |
probably damaging |
Het |
Kndc1 |
A |
G |
7: 139,490,130 (GRCm39) |
S211G |
probably benign |
Het |
Lama2 |
T |
A |
10: 27,066,530 (GRCm39) |
E1117V |
probably damaging |
Het |
Lgals4 |
C |
T |
7: 28,540,921 (GRCm39) |
R282C |
probably damaging |
Het |
Lsg1 |
T |
A |
16: 30,399,865 (GRCm39) |
|
probably null |
Het |
Mab21l4 |
C |
T |
1: 93,082,208 (GRCm39) |
|
probably null |
Het |
Msh3 |
A |
G |
13: 92,411,374 (GRCm39) |
S608P |
possibly damaging |
Het |
Mslnl |
T |
A |
17: 25,964,062 (GRCm39) |
F464I |
probably benign |
Het |
Mycbp2 |
T |
A |
14: 103,460,586 (GRCm39) |
K1493N |
probably damaging |
Het |
Myo15a |
A |
T |
11: 60,401,679 (GRCm39) |
|
probably null |
Het |
Myo1b |
A |
T |
1: 51,794,896 (GRCm39) |
F1065I |
probably benign |
Het |
Nf1 |
A |
G |
11: 79,345,136 (GRCm39) |
|
probably benign |
Het |
Nup153 |
C |
A |
13: 46,881,027 (GRCm39) |
|
probably benign |
Het |
Or4f4-ps1 |
T |
A |
2: 111,330,497 (GRCm39) |
I300K |
probably damaging |
Het |
Or5b97 |
A |
G |
19: 12,878,274 (GRCm39) |
V290A |
possibly damaging |
Het |
Osbpl7 |
A |
G |
11: 96,943,194 (GRCm39) |
T149A |
probably benign |
Het |
Parp1 |
A |
G |
1: 180,396,690 (GRCm39) |
D31G |
probably benign |
Het |
Pcdha6 |
T |
A |
18: 37,101,203 (GRCm39) |
V132E |
possibly damaging |
Het |
Pcdhb8 |
T |
A |
18: 37,489,975 (GRCm39) |
L551Q |
possibly damaging |
Het |
Pcsk9 |
T |
A |
4: 106,311,808 (GRCm39) |
T190S |
probably damaging |
Het |
Pdgfrb |
A |
T |
18: 61,197,049 (GRCm39) |
T162S |
probably benign |
Het |
Pi4ka |
C |
T |
16: 17,136,234 (GRCm39) |
R908Q |
|
Het |
Pnpla8 |
A |
G |
12: 44,330,222 (GRCm39) |
E258G |
probably benign |
Het |
Prrc2c |
A |
T |
1: 162,537,127 (GRCm39) |
S643T |
unknown |
Het |
Rnf20 |
T |
G |
4: 49,655,964 (GRCm39) |
I970S |
possibly damaging |
Het |
Robo2 |
A |
T |
16: 73,755,247 (GRCm39) |
V758D |
probably damaging |
Het |
Robo4 |
G |
A |
9: 37,319,577 (GRCm39) |
S609N |
possibly damaging |
Het |
Rrbp1 |
G |
A |
2: 143,830,920 (GRCm39) |
Q416* |
probably null |
Het |
Rsf1 |
GCG |
GCGACGGCGACG |
7: 97,229,114 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
C |
A |
13: 11,701,833 (GRCm39) |
E2941D |
probably damaging |
Het |
Sh3rf1 |
G |
A |
8: 61,825,687 (GRCm39) |
V561I |
probably benign |
Het |
Slc4a4 |
T |
A |
5: 89,280,301 (GRCm39) |
D366E |
probably damaging |
Het |
Slfn14 |
T |
G |
11: 83,174,715 (GRCm39) |
Q92P |
probably damaging |
Het |
Slfn4 |
A |
T |
11: 83,077,770 (GRCm39) |
Y186F |
probably damaging |
Het |
Smpd4 |
T |
C |
16: 17,453,410 (GRCm39) |
L309P |
possibly damaging |
Het |
Smyd3 |
G |
T |
1: 178,920,482 (GRCm39) |
N217K |
probably benign |
Het |
Spen |
T |
C |
4: 141,197,129 (GRCm39) |
T3547A |
probably benign |
Het |
Suclg1 |
A |
T |
6: 73,253,729 (GRCm39) |
I126F |
unknown |
Het |
Tenm4 |
C |
T |
7: 96,555,148 (GRCm39) |
P2618S |
probably benign |
Het |
Tmprss15 |
A |
T |
16: 78,798,702 (GRCm39) |
I660N |
possibly damaging |
Het |
Trf |
A |
T |
9: 103,087,723 (GRCm39) |
V677D |
probably damaging |
Het |
Trim36 |
T |
C |
18: 46,302,452 (GRCm39) |
N532S |
probably benign |
Het |
Trim37 |
T |
C |
11: 87,037,885 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
C |
2: 76,570,454 (GRCm39) |
N26813S |
probably benign |
Het |
Vmn1r199 |
T |
A |
13: 22,567,537 (GRCm39) |
V277D |
probably damaging |
Het |
Wdfy3 |
T |
C |
5: 102,077,951 (GRCm39) |
D873G |
probably benign |
Het |
Wdr27 |
T |
C |
17: 15,103,929 (GRCm39) |
T726A |
probably damaging |
Het |
Wdr97 |
T |
C |
15: 76,240,775 (GRCm39) |
Y488H |
|
Het |
Wdtc1 |
A |
T |
4: 133,031,511 (GRCm39) |
C236* |
probably null |
Het |
Wnk4 |
A |
C |
11: 101,167,092 (GRCm39) |
S1083R |
unknown |
Het |
Wwc1 |
A |
T |
11: 35,774,234 (GRCm39) |
I342N |
probably damaging |
Het |
Zbtb40 |
A |
G |
4: 136,725,957 (GRCm39) |
L534P |
probably damaging |
Het |
Zfp62 |
T |
C |
11: 49,108,227 (GRCm39) |
C773R |
probably damaging |
Het |
Zfp709 |
T |
A |
8: 72,643,027 (GRCm39) |
I152N |
probably benign |
Het |
Zfp738 |
T |
C |
13: 67,819,550 (GRCm39) |
Y147C |
probably damaging |
Het |
Zscan18 |
A |
C |
7: 12,503,625 (GRCm39) |
S645A |
probably benign |
Het |
Zw10 |
A |
G |
9: 48,988,861 (GRCm39) |
Y709C |
probably damaging |
Het |
|
Other mutations in Scd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00800:Scd2
|
APN |
19 |
44,286,569 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01105:Scd2
|
APN |
19 |
44,286,497 (GRCm39) |
missense |
probably benign |
0.38 |
IGL02201:Scd2
|
APN |
19 |
44,289,779 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02680:Scd2
|
APN |
19 |
44,289,685 (GRCm39) |
missense |
probably benign |
0.00 |
unkinked
|
UTSW |
19 |
44,288,198 (GRCm39) |
nonsense |
probably null |
|
R0012:Scd2
|
UTSW |
19 |
44,289,685 (GRCm39) |
missense |
probably benign |
0.00 |
R0366:Scd2
|
UTSW |
19 |
44,289,685 (GRCm39) |
missense |
probably benign |
0.00 |
R0368:Scd2
|
UTSW |
19 |
44,289,685 (GRCm39) |
missense |
probably benign |
0.00 |
R0373:Scd2
|
UTSW |
19 |
44,291,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R1282:Scd2
|
UTSW |
19 |
44,283,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R1581:Scd2
|
UTSW |
19 |
44,286,538 (GRCm39) |
missense |
probably benign |
0.04 |
R2008:Scd2
|
UTSW |
19 |
44,291,610 (GRCm39) |
missense |
probably benign |
0.23 |
R2329:Scd2
|
UTSW |
19 |
44,286,492 (GRCm39) |
nonsense |
probably null |
|
R4755:Scd2
|
UTSW |
19 |
44,289,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R4812:Scd2
|
UTSW |
19 |
44,289,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R5024:Scd2
|
UTSW |
19 |
44,289,710 (GRCm39) |
missense |
probably benign |
0.02 |
R5568:Scd2
|
UTSW |
19 |
44,288,142 (GRCm39) |
missense |
probably damaging |
0.99 |
R5702:Scd2
|
UTSW |
19 |
44,286,502 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6248:Scd2
|
UTSW |
19 |
44,291,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R6377:Scd2
|
UTSW |
19 |
44,288,198 (GRCm39) |
nonsense |
probably null |
|
R8422:Scd2
|
UTSW |
19 |
44,289,743 (GRCm39) |
missense |
probably benign |
0.00 |
R8424:Scd2
|
UTSW |
19 |
44,289,743 (GRCm39) |
missense |
probably benign |
0.00 |
R9597:Scd2
|
UTSW |
19 |
44,288,246 (GRCm39) |
missense |
probably damaging |
1.00 |
|