Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Accsl |
A |
T |
2: 93,696,589 (GRCm39) |
|
probably benign |
Het |
Adam7 |
T |
G |
14: 68,752,370 (GRCm39) |
K371N |
probably damaging |
Het |
Adgrv1 |
A |
T |
13: 81,705,182 (GRCm39) |
S1543T |
probably damaging |
Het |
Agbl4 |
A |
T |
4: 111,513,515 (GRCm39) |
|
probably benign |
Het |
Arid1b |
T |
A |
17: 5,389,575 (GRCm39) |
I1707N |
probably damaging |
Het |
Atp10a |
T |
C |
7: 58,453,514 (GRCm39) |
V864A |
probably benign |
Het |
Bivm |
A |
G |
1: 44,165,942 (GRCm39) |
T131A |
probably benign |
Het |
Bst1 |
A |
G |
5: 43,982,750 (GRCm39) |
|
probably null |
Het |
C9orf72 |
C |
A |
4: 35,218,630 (GRCm39) |
E76D |
probably damaging |
Het |
Cblb |
T |
C |
16: 52,006,603 (GRCm39) |
|
probably benign |
Het |
Ccdc28b |
T |
C |
4: 129,514,682 (GRCm39) |
|
probably benign |
Het |
Cmas |
G |
T |
6: 142,702,604 (GRCm39) |
G36C |
probably benign |
Het |
Eml6 |
A |
G |
11: 29,699,824 (GRCm39) |
S1771P |
possibly damaging |
Het |
Epc1 |
A |
C |
18: 6,490,525 (GRCm39) |
Y31D |
probably damaging |
Het |
Fbn1 |
A |
T |
2: 125,236,607 (GRCm39) |
C358S |
probably benign |
Het |
Fbxl13 |
A |
T |
5: 21,825,602 (GRCm39) |
|
probably benign |
Het |
Fermt2 |
T |
C |
14: 45,697,425 (GRCm39) |
D642G |
possibly damaging |
Het |
Fmnl2 |
A |
T |
2: 52,962,286 (GRCm39) |
N257I |
probably damaging |
Het |
Fry |
G |
A |
5: 150,404,959 (GRCm39) |
W793* |
probably null |
Het |
Fsd2 |
T |
C |
7: 81,209,518 (GRCm39) |
D108G |
probably benign |
Het |
Glipr1l2 |
C |
A |
10: 111,919,371 (GRCm39) |
L31I |
possibly damaging |
Het |
Gm10608 |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
9: 118,989,784 (GRCm39) |
|
probably null |
Het |
Gm10801 |
C |
T |
2: 98,494,252 (GRCm39) |
|
probably benign |
Het |
Gm21718 |
T |
C |
14: 51,553,348 (GRCm39) |
|
noncoding transcript |
Het |
Gpld1 |
A |
G |
13: 25,141,549 (GRCm39) |
|
probably null |
Het |
Gtf3c2 |
A |
T |
5: 31,325,419 (GRCm39) |
Y500N |
probably damaging |
Het |
Hbs1l |
A |
G |
10: 21,180,537 (GRCm39) |
D73G |
probably damaging |
Het |
Idh1 |
G |
T |
1: 65,200,319 (GRCm39) |
N348K |
probably benign |
Het |
Kank4 |
T |
C |
4: 98,653,806 (GRCm39) |
Y874C |
probably damaging |
Het |
Lamc2 |
A |
T |
1: 153,042,033 (GRCm39) |
S34T |
probably damaging |
Het |
Laptm4a |
T |
C |
12: 8,986,716 (GRCm39) |
V258A |
probably damaging |
Het |
Lrrc19 |
A |
T |
4: 94,526,626 (GRCm39) |
Y310* |
probably null |
Het |
Map3k5 |
G |
A |
10: 19,932,394 (GRCm39) |
|
probably benign |
Het |
Map7 |
G |
A |
10: 20,121,045 (GRCm39) |
E92K |
probably damaging |
Het |
Mettl24 |
G |
A |
10: 40,613,704 (GRCm39) |
A148T |
probably benign |
Het |
Mosmo |
A |
G |
7: 120,329,745 (GRCm39) |
Y122C |
probably benign |
Het |
Nkx3-1 |
T |
C |
14: 69,429,434 (GRCm39) |
S151P |
probably damaging |
Het |
Npm2 |
T |
A |
14: 70,889,661 (GRCm39) |
K54* |
probably null |
Het |
Npr1 |
T |
A |
3: 90,368,689 (GRCm39) |
D457V |
probably benign |
Het |
Nudt21 |
T |
C |
8: 94,757,757 (GRCm39) |
|
probably benign |
Het |
Pcnt |
A |
T |
10: 76,228,878 (GRCm39) |
|
probably null |
Het |
Pik3r4 |
G |
T |
9: 105,540,373 (GRCm39) |
G754C |
probably damaging |
Het |
Rftn2 |
A |
G |
1: 55,250,376 (GRCm39) |
V123A |
probably damaging |
Het |
Rpa1 |
A |
T |
11: 75,203,219 (GRCm39) |
V392D |
probably damaging |
Het |
Rxfp2 |
T |
C |
5: 149,975,021 (GRCm39) |
V210A |
probably benign |
Het |
Slc45a4 |
C |
T |
15: 73,477,278 (GRCm39) |
|
probably benign |
Het |
Syndig1l |
T |
A |
12: 84,725,942 (GRCm39) |
|
probably null |
Het |
Tctn1 |
G |
A |
5: 122,389,752 (GRCm39) |
R257* |
probably null |
Het |
Tenm4 |
A |
T |
7: 96,497,251 (GRCm39) |
E1179V |
probably damaging |
Het |
Txlnb |
A |
G |
10: 17,718,504 (GRCm39) |
N445S |
probably benign |
Het |
Tyrp1 |
C |
T |
4: 80,763,105 (GRCm39) |
Q331* |
probably null |
Het |
Ubap2l |
A |
T |
3: 89,930,807 (GRCm39) |
S413T |
probably benign |
Het |
Vdr |
A |
T |
15: 97,767,214 (GRCm39) |
Y185N |
probably benign |
Het |
Vmn2r66 |
G |
T |
7: 84,654,799 (GRCm39) |
D503E |
probably benign |
Het |
Vmn2r72 |
T |
A |
7: 85,401,152 (GRCm39) |
E89V |
probably damaging |
Het |
Vmn2r87 |
T |
C |
10: 130,313,453 (GRCm39) |
T438A |
probably benign |
Het |
Xrcc6 |
A |
G |
15: 81,915,364 (GRCm39) |
D94G |
probably damaging |
Het |
Ywhaq |
T |
C |
12: 21,445,024 (GRCm39) |
N207S |
probably benign |
Het |
Zfp185 |
A |
T |
X: 72,042,929 (GRCm39) |
E138D |
possibly damaging |
Het |
Zfp981 |
G |
A |
4: 146,622,221 (GRCm39) |
S382N |
probably benign |
Het |
|
Other mutations in Ncr1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00832:Ncr1
|
APN |
7 |
4,344,287 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01994:Ncr1
|
APN |
7 |
4,344,253 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02163:Ncr1
|
APN |
7 |
4,344,262 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02610:Ncr1
|
APN |
7 |
4,341,132 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02885:Ncr1
|
APN |
7 |
4,341,225 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03082:Ncr1
|
APN |
7 |
4,344,241 (GRCm39) |
splice site |
probably benign |
|
R0196:Ncr1
|
UTSW |
7 |
4,343,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R1758:Ncr1
|
UTSW |
7 |
4,343,807 (GRCm39) |
missense |
probably benign |
0.40 |
R2065:Ncr1
|
UTSW |
7 |
4,341,206 (GRCm39) |
missense |
probably benign |
0.00 |
R2135:Ncr1
|
UTSW |
7 |
4,343,756 (GRCm39) |
splice site |
probably benign |
|
R2397:Ncr1
|
UTSW |
7 |
4,341,260 (GRCm39) |
missense |
probably benign |
0.22 |
R5389:Ncr1
|
UTSW |
7 |
4,343,932 (GRCm39) |
missense |
probably benign |
0.01 |
R5648:Ncr1
|
UTSW |
7 |
4,347,519 (GRCm39) |
missense |
probably damaging |
0.97 |
R5690:Ncr1
|
UTSW |
7 |
4,341,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R5817:Ncr1
|
UTSW |
7 |
4,343,894 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5847:Ncr1
|
UTSW |
7 |
4,347,573 (GRCm39) |
missense |
probably benign |
0.04 |
R7033:Ncr1
|
UTSW |
7 |
4,341,144 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7391:Ncr1
|
UTSW |
7 |
4,347,470 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7395:Ncr1
|
UTSW |
7 |
4,341,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R7680:Ncr1
|
UTSW |
7 |
4,341,123 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8163:Ncr1
|
UTSW |
7 |
4,343,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R8472:Ncr1
|
UTSW |
7 |
4,341,120 (GRCm39) |
missense |
probably benign |
0.19 |
R8782:Ncr1
|
UTSW |
7 |
4,340,763 (GRCm39) |
missense |
probably benign |
0.01 |
R8880:Ncr1
|
UTSW |
7 |
4,341,336 (GRCm39) |
missense |
probably benign |
0.00 |
R9066:Ncr1
|
UTSW |
7 |
4,347,552 (GRCm39) |
missense |
probably benign |
0.13 |
R9789:Ncr1
|
UTSW |
7 |
4,344,300 (GRCm39) |
critical splice donor site |
probably null |
|
|