Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930447A16Rik |
C |
A |
15: 37,425,979 (GRCm39) |
|
probably benign |
Het |
Abcb5 |
A |
T |
12: 118,832,461 (GRCm39) |
L1171H |
probably damaging |
Het |
Ace |
A |
T |
11: 105,862,116 (GRCm39) |
|
probably null |
Het |
Adsl |
G |
T |
15: 80,832,734 (GRCm39) |
|
probably benign |
Het |
Cabin1 |
A |
G |
10: 75,585,890 (GRCm39) |
M215T |
probably benign |
Het |
Cabp2 |
A |
T |
19: 4,134,892 (GRCm39) |
R77S |
probably damaging |
Het |
Cast |
A |
T |
13: 74,882,177 (GRCm39) |
H40Q |
possibly damaging |
Het |
Ccar1 |
A |
T |
10: 62,586,358 (GRCm39) |
Y946N |
unknown |
Het |
Ccdc9b |
C |
T |
2: 118,587,702 (GRCm39) |
R544K |
unknown |
Het |
Chst14 |
A |
G |
2: 118,758,010 (GRCm39) |
Y268C |
probably damaging |
Het |
Dennd1a |
T |
C |
2: 37,872,920 (GRCm39) |
|
probably null |
Het |
Dnah1 |
A |
G |
14: 30,990,861 (GRCm39) |
Y3153H |
probably damaging |
Het |
Entpd8 |
T |
C |
2: 24,973,856 (GRCm39) |
V271A |
probably benign |
Het |
Eppk1 |
C |
T |
15: 75,994,319 (GRCm39) |
R854Q |
probably benign |
Het |
Fam234b |
A |
G |
6: 135,210,287 (GRCm39) |
Y561C |
probably damaging |
Het |
Flg |
A |
G |
3: 93,195,448 (GRCm39) |
|
probably benign |
Het |
Galnt5 |
T |
A |
2: 57,907,160 (GRCm39) |
M541K |
probably damaging |
Het |
Gjd3 |
C |
A |
11: 98,873,488 (GRCm39) |
E119* |
probably null |
Het |
Gm266 |
T |
C |
12: 111,451,799 (GRCm39) |
T136A |
possibly damaging |
Het |
Gng11 |
G |
A |
6: 4,008,045 (GRCm39) |
C36Y |
possibly damaging |
Het |
Gse1 |
G |
A |
8: 121,280,391 (GRCm39) |
V36I |
probably damaging |
Het |
Hycc2 |
T |
C |
1: 58,568,981 (GRCm39) |
T477A |
probably benign |
Het |
Invs |
A |
T |
4: 48,397,598 (GRCm39) |
H335L |
probably damaging |
Het |
Kcnc2 |
A |
T |
10: 112,292,101 (GRCm39) |
I28F |
probably damaging |
Het |
Klhl40 |
C |
T |
9: 121,607,892 (GRCm39) |
H351Y |
probably damaging |
Het |
Kremen2 |
A |
G |
17: 23,961,201 (GRCm39) |
L382P |
probably benign |
Het |
Lenep |
A |
T |
3: 89,309,784 (GRCm39) |
C55S |
possibly damaging |
Het |
Lrp12 |
A |
T |
15: 39,741,970 (GRCm39) |
Y248* |
probably null |
Het |
Man2c1 |
A |
G |
9: 57,038,325 (GRCm39) |
|
probably null |
Het |
Map2k2 |
T |
C |
10: 80,955,376 (GRCm39) |
M32T |
possibly damaging |
Het |
Mnt |
A |
G |
11: 74,722,218 (GRCm39) |
R22G |
probably damaging |
Het |
Mroh1 |
G |
T |
15: 76,327,558 (GRCm39) |
E1127* |
probably null |
Het |
Mtmr4 |
A |
G |
11: 87,502,735 (GRCm39) |
R930G |
possibly damaging |
Het |
Nalcn |
A |
G |
14: 123,608,935 (GRCm39) |
V644A |
probably benign |
Het |
Ngf |
G |
T |
3: 102,427,991 (GRCm39) |
V247F |
probably damaging |
Het |
Ninj2 |
A |
G |
6: 120,175,018 (GRCm39) |
Y63C |
probably damaging |
Het |
Or4c121 |
T |
C |
2: 89,024,312 (GRCm39) |
E22G |
possibly damaging |
Het |
Or51g2 |
A |
T |
7: 102,622,938 (GRCm39) |
I87N |
probably damaging |
Het |
Phf12 |
A |
C |
11: 77,918,235 (GRCm39) |
I816L |
probably damaging |
Het |
Pkhd1 |
C |
A |
1: 20,593,199 (GRCm39) |
G1638V |
probably damaging |
Het |
Plce1 |
T |
A |
19: 38,512,903 (GRCm39) |
S67R |
probably benign |
Het |
Plekhf1 |
A |
G |
7: 37,920,768 (GRCm39) |
F267L |
probably damaging |
Het |
Poc1b |
A |
T |
10: 98,960,770 (GRCm39) |
K60* |
probably null |
Het |
Ppic |
G |
A |
18: 53,544,612 (GRCm39) |
T66M |
probably damaging |
Het |
Prep |
G |
T |
10: 45,029,223 (GRCm39) |
G541V |
probably damaging |
Het |
Rasal3 |
C |
T |
17: 32,611,093 (GRCm39) |
V947I |
probably benign |
Het |
Rbl1 |
T |
C |
2: 157,035,124 (GRCm39) |
R319G |
probably damaging |
Het |
Rbm34 |
A |
G |
8: 127,696,821 (GRCm39) |
S94P |
probably benign |
Het |
Repin1 |
G |
T |
6: 48,574,279 (GRCm39) |
E403* |
probably null |
Het |
Sacm1l |
T |
C |
9: 123,406,123 (GRCm39) |
|
probably null |
Het |
Scaf8 |
T |
C |
17: 3,213,295 (GRCm39) |
|
probably benign |
Het |
Sfrp4 |
A |
G |
13: 19,816,336 (GRCm39) |
|
probably null |
Het |
Slc37a3 |
T |
C |
6: 39,321,297 (GRCm39) |
I406V |
possibly damaging |
Het |
Sorbs1 |
G |
C |
19: 40,365,244 (GRCm39) |
R180G |
probably benign |
Het |
Sptbn1 |
C |
A |
11: 30,169,750 (GRCm39) |
|
probably benign |
Het |
St8sia5 |
T |
C |
18: 77,342,114 (GRCm39) |
Y275H |
probably damaging |
Het |
Stab1 |
A |
T |
14: 30,885,008 (GRCm39) |
C137* |
probably null |
Het |
Svep1 |
A |
G |
4: 58,206,025 (GRCm39) |
S118P |
probably benign |
Het |
Tbx6 |
A |
G |
7: 126,380,656 (GRCm39) |
|
probably null |
Het |
Tril |
C |
T |
6: 53,796,295 (GRCm39) |
S309N |
possibly damaging |
Het |
Trmt13 |
A |
G |
3: 116,386,094 (GRCm39) |
|
probably null |
Het |
Trpm1 |
T |
A |
7: 63,874,356 (GRCm39) |
|
probably null |
Het |
Tyr |
T |
C |
7: 87,142,000 (GRCm39) |
T110A |
probably benign |
Het |
Upf1 |
A |
C |
8: 70,789,702 (GRCm39) |
F711C |
probably damaging |
Het |
Usp5 |
A |
T |
6: 124,800,480 (GRCm39) |
V267D |
probably damaging |
Het |
Virma |
C |
A |
4: 11,516,949 (GRCm39) |
D714E |
probably benign |
Het |
Vmn2r115 |
A |
C |
17: 23,564,773 (GRCm39) |
Q220P |
possibly damaging |
Het |
Vmn2r40 |
T |
C |
7: 8,911,191 (GRCm39) |
I701V |
|
Het |
Vwde |
T |
A |
6: 13,187,652 (GRCm39) |
M612L |
probably benign |
Het |
Wwox |
A |
G |
8: 115,215,646 (GRCm39) |
T140A |
probably benign |
Het |
Zbtb17 |
CCCCCACCTCCACAGACCCCA |
CCCCCACCTCCACAGACCCCACCTCCACAGACCCCA |
4: 141,194,139 (GRCm39) |
|
probably benign |
Het |
Zbtb9 |
T |
A |
17: 27,193,448 (GRCm39) |
C284* |
probably null |
Het |
Zdhhc12 |
C |
A |
2: 29,983,486 (GRCm39) |
A39S |
probably benign |
Het |
Zfp532 |
T |
A |
18: 65,758,227 (GRCm39) |
I720K |
possibly damaging |
Het |
Zfp595 |
G |
A |
13: 67,465,244 (GRCm39) |
R340C |
probably damaging |
Het |
|
Other mutations in Scrn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00755:Scrn1
|
APN |
6 |
54,497,694 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL00937:Scrn1
|
APN |
6 |
54,497,718 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01568:Scrn1
|
APN |
6 |
54,499,739 (GRCm39) |
unclassified |
probably benign |
|
IGL02572:Scrn1
|
APN |
6 |
54,489,186 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03251:Scrn1
|
APN |
6 |
54,525,322 (GRCm39) |
nonsense |
probably null |
|
IGL03279:Scrn1
|
APN |
6 |
54,525,322 (GRCm39) |
nonsense |
probably null |
|
IGL03301:Scrn1
|
APN |
6 |
54,525,322 (GRCm39) |
nonsense |
probably null |
|
IGL03307:Scrn1
|
APN |
6 |
54,525,322 (GRCm39) |
nonsense |
probably null |
|
R1583:Scrn1
|
UTSW |
6 |
54,497,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R1658:Scrn1
|
UTSW |
6 |
54,497,791 (GRCm39) |
missense |
probably benign |
|
R1843:Scrn1
|
UTSW |
6 |
54,499,826 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2314:Scrn1
|
UTSW |
6 |
54,502,631 (GRCm39) |
missense |
probably benign |
0.43 |
R4795:Scrn1
|
UTSW |
6 |
54,497,754 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4960:Scrn1
|
UTSW |
6 |
54,511,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R5420:Scrn1
|
UTSW |
6 |
54,489,048 (GRCm39) |
missense |
probably benign |
0.15 |
R8057:Scrn1
|
UTSW |
6 |
54,497,758 (GRCm39) |
missense |
probably benign |
|
R8340:Scrn1
|
UTSW |
6 |
54,511,518 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9465:Scrn1
|
UTSW |
6 |
54,502,649 (GRCm39) |
missense |
probably damaging |
1.00 |
|