Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
C |
T |
14: 32,384,039 (GRCm39) |
R642Q |
possibly damaging |
Het |
Aadacl2fm3 |
A |
G |
3: 59,772,639 (GRCm39) |
T48A |
probably benign |
Het |
Aadacl4fm1 |
A |
G |
4: 144,255,194 (GRCm39) |
T205A |
probably benign |
Het |
Aadacl4fm4 |
T |
C |
4: 144,396,845 (GRCm39) |
S296G |
probably benign |
Het |
Anxa10 |
C |
T |
8: 62,514,038 (GRCm39) |
|
probably null |
Het |
Bcl11a |
A |
T |
11: 24,113,928 (GRCm39) |
M424L |
probably damaging |
Het |
Bhlhe41 |
A |
G |
6: 145,809,456 (GRCm39) |
S119P |
probably damaging |
Het |
C2cd3 |
A |
G |
7: 100,071,888 (GRCm39) |
D1033G |
probably benign |
Het |
Ccdc174 |
T |
C |
6: 91,876,561 (GRCm39) |
V466A |
probably benign |
Het |
Dnaaf11 |
T |
A |
15: 66,310,264 (GRCm39) |
T335S |
possibly damaging |
Het |
Drd2 |
T |
C |
9: 49,306,940 (GRCm39) |
Y9H |
probably damaging |
Het |
Fbxw14 |
T |
A |
9: 109,105,236 (GRCm39) |
I310F |
possibly damaging |
Het |
Grm3 |
C |
T |
5: 9,620,297 (GRCm39) |
V316I |
probably benign |
Het |
Gys2 |
A |
G |
6: 142,391,739 (GRCm39) |
Y508H |
probably damaging |
Het |
Lrp1b |
T |
A |
2: 40,765,063 (GRCm39) |
D2921V |
probably damaging |
Het |
Macrod2 |
A |
G |
2: 140,294,547 (GRCm39) |
K71R |
probably damaging |
Het |
Myh7 |
A |
T |
14: 55,211,327 (GRCm39) |
V1614E |
possibly damaging |
Het |
Or8k23 |
T |
A |
2: 86,186,239 (GRCm39) |
K162N |
probably damaging |
Het |
Pirb |
T |
A |
7: 3,722,731 (GRCm39) |
N87I |
probably benign |
Het |
Pmfbp1 |
A |
G |
8: 110,257,115 (GRCm39) |
|
probably null |
Het |
Rasa4 |
A |
G |
5: 136,134,510 (GRCm39) |
N627S |
probably benign |
Het |
Spata31d1b |
A |
C |
13: 59,864,468 (GRCm39) |
M539L |
probably benign |
Het |
Tbc1d23 |
A |
T |
16: 57,034,525 (GRCm39) |
|
probably null |
Het |
Tnfrsf1b |
A |
T |
4: 144,950,926 (GRCm39) |
L229Q |
probably benign |
Het |
Trip12 |
A |
T |
1: 84,714,758 (GRCm39) |
V443E |
probably damaging |
Het |
Ush2a |
G |
T |
1: 188,485,733 (GRCm39) |
V2948L |
probably damaging |
Het |
Vmn1r204 |
A |
T |
13: 22,741,209 (GRCm39) |
Y280F |
possibly damaging |
Het |
Vmn2r115 |
ATCTTCT |
ATCT |
17: 23,578,962 (GRCm39) |
|
probably benign |
Het |
Vmn2r93 |
G |
T |
17: 18,518,710 (GRCm39) |
K56N |
probably benign |
Het |
Xrn1 |
A |
G |
9: 95,885,918 (GRCm39) |
I880V |
probably benign |
Het |
Zfp106 |
C |
T |
2: 120,365,195 (GRCm39) |
G404E |
probably benign |
Het |
|
Other mutations in Nckap1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00496:Nckap1
|
APN |
2 |
80,336,546 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL00896:Nckap1
|
APN |
2 |
80,411,297 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL01343:Nckap1
|
APN |
2 |
80,350,186 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL01593:Nckap1
|
APN |
2 |
80,350,914 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01677:Nckap1
|
APN |
2 |
80,360,641 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01873:Nckap1
|
APN |
2 |
80,383,729 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01874:Nckap1
|
APN |
2 |
80,355,980 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01947:Nckap1
|
APN |
2 |
80,339,097 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02268:Nckap1
|
APN |
2 |
80,358,962 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02348:Nckap1
|
APN |
2 |
80,348,326 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03349:Nckap1
|
APN |
2 |
80,355,904 (GRCm39) |
missense |
probably benign |
0.07 |
PIT4151001:Nckap1
|
UTSW |
2 |
80,350,714 (GRCm39) |
critical splice donor site |
probably null |
|
R0326:Nckap1
|
UTSW |
2 |
80,383,714 (GRCm39) |
missense |
probably benign |
0.41 |
R0345:Nckap1
|
UTSW |
2 |
80,375,321 (GRCm39) |
splice site |
probably benign |
|
R0520:Nckap1
|
UTSW |
2 |
80,371,874 (GRCm39) |
splice site |
probably benign |
|
R0603:Nckap1
|
UTSW |
2 |
80,343,073 (GRCm39) |
missense |
probably benign |
0.19 |
R0924:Nckap1
|
UTSW |
2 |
80,384,593 (GRCm39) |
missense |
probably benign |
0.34 |
R0930:Nckap1
|
UTSW |
2 |
80,384,593 (GRCm39) |
missense |
probably benign |
0.34 |
R0964:Nckap1
|
UTSW |
2 |
80,378,243 (GRCm39) |
critical splice donor site |
probably null |
|
R1122:Nckap1
|
UTSW |
2 |
80,348,286 (GRCm39) |
missense |
probably benign |
0.12 |
R1123:Nckap1
|
UTSW |
2 |
80,348,286 (GRCm39) |
missense |
probably benign |
0.12 |
R1125:Nckap1
|
UTSW |
2 |
80,348,286 (GRCm39) |
missense |
probably benign |
0.12 |
R1127:Nckap1
|
UTSW |
2 |
80,348,286 (GRCm39) |
missense |
probably benign |
0.12 |
R1182:Nckap1
|
UTSW |
2 |
80,348,286 (GRCm39) |
missense |
probably benign |
0.12 |
R1234:Nckap1
|
UTSW |
2 |
80,348,286 (GRCm39) |
missense |
probably benign |
0.12 |
R1236:Nckap1
|
UTSW |
2 |
80,348,286 (GRCm39) |
missense |
probably benign |
0.12 |
R1384:Nckap1
|
UTSW |
2 |
80,364,014 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1402:Nckap1
|
UTSW |
2 |
80,348,286 (GRCm39) |
missense |
probably benign |
0.12 |
R1402:Nckap1
|
UTSW |
2 |
80,348,286 (GRCm39) |
missense |
probably benign |
0.12 |
R1511:Nckap1
|
UTSW |
2 |
80,383,759 (GRCm39) |
missense |
probably damaging |
0.99 |
R1677:Nckap1
|
UTSW |
2 |
80,348,286 (GRCm39) |
missense |
probably benign |
0.12 |
R1686:Nckap1
|
UTSW |
2 |
80,348,286 (GRCm39) |
missense |
probably benign |
0.12 |
R1687:Nckap1
|
UTSW |
2 |
80,350,929 (GRCm39) |
missense |
probably damaging |
0.96 |
R1717:Nckap1
|
UTSW |
2 |
80,343,014 (GRCm39) |
splice site |
probably benign |
|
R1789:Nckap1
|
UTSW |
2 |
80,350,900 (GRCm39) |
missense |
probably benign |
0.44 |
R1822:Nckap1
|
UTSW |
2 |
80,348,242 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1840:Nckap1
|
UTSW |
2 |
80,332,594 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1926:Nckap1
|
UTSW |
2 |
80,337,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R1968:Nckap1
|
UTSW |
2 |
80,348,286 (GRCm39) |
missense |
probably benign |
0.12 |
R1970:Nckap1
|
UTSW |
2 |
80,348,286 (GRCm39) |
missense |
probably benign |
0.12 |
R2027:Nckap1
|
UTSW |
2 |
80,365,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R2063:Nckap1
|
UTSW |
2 |
80,400,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R2504:Nckap1
|
UTSW |
2 |
80,360,562 (GRCm39) |
missense |
probably benign |
0.40 |
R3824:Nckap1
|
UTSW |
2 |
80,370,904 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4784:Nckap1
|
UTSW |
2 |
80,337,278 (GRCm39) |
missense |
probably benign |
0.15 |
R4908:Nckap1
|
UTSW |
2 |
80,353,718 (GRCm39) |
critical splice donor site |
probably null |
|
R5077:Nckap1
|
UTSW |
2 |
80,379,277 (GRCm39) |
missense |
probably damaging |
0.99 |
R5311:Nckap1
|
UTSW |
2 |
80,370,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R5439:Nckap1
|
UTSW |
2 |
80,343,034 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6141:Nckap1
|
UTSW |
2 |
80,360,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R6209:Nckap1
|
UTSW |
2 |
80,355,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R6226:Nckap1
|
UTSW |
2 |
80,339,125 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6294:Nckap1
|
UTSW |
2 |
80,371,858 (GRCm39) |
missense |
probably benign |
0.03 |
R6458:Nckap1
|
UTSW |
2 |
80,342,893 (GRCm39) |
splice site |
probably null |
|
R6937:Nckap1
|
UTSW |
2 |
80,339,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R6986:Nckap1
|
UTSW |
2 |
80,350,911 (GRCm39) |
missense |
probably benign |
0.03 |
R7180:Nckap1
|
UTSW |
2 |
80,337,236 (GRCm39) |
missense |
probably benign |
0.01 |
R7208:Nckap1
|
UTSW |
2 |
80,370,542 (GRCm39) |
missense |
probably benign |
0.24 |
R7363:Nckap1
|
UTSW |
2 |
80,370,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R7448:Nckap1
|
UTSW |
2 |
80,354,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R7513:Nckap1
|
UTSW |
2 |
80,332,635 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7806:Nckap1
|
UTSW |
2 |
80,371,843 (GRCm39) |
missense |
probably damaging |
0.98 |
R8143:Nckap1
|
UTSW |
2 |
80,336,530 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8270:Nckap1
|
UTSW |
2 |
80,355,008 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8775:Nckap1
|
UTSW |
2 |
80,375,410 (GRCm39) |
missense |
probably benign |
0.00 |
R8775-TAIL:Nckap1
|
UTSW |
2 |
80,375,410 (GRCm39) |
missense |
probably benign |
0.00 |
R8886:Nckap1
|
UTSW |
2 |
80,339,055 (GRCm39) |
critical splice donor site |
probably null |
|
R8913:Nckap1
|
UTSW |
2 |
80,401,564 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9080:Nckap1
|
UTSW |
2 |
80,350,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R9287:Nckap1
|
UTSW |
2 |
80,383,750 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9722:Nckap1
|
UTSW |
2 |
80,401,568 (GRCm39) |
nonsense |
probably null |
|
R9749:Nckap1
|
UTSW |
2 |
80,401,568 (GRCm39) |
nonsense |
probably null |
|
Z1176:Nckap1
|
UTSW |
2 |
80,370,852 (GRCm39) |
critical splice donor site |
probably null |
|
|