Other mutations in this stock |
Total: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900092C05Rik |
A |
G |
7: 12,246,629 (GRCm39) |
|
probably null |
Het |
4930433I11Rik |
T |
A |
7: 40,643,037 (GRCm39) |
D326E |
probably benign |
Het |
Abca8a |
T |
C |
11: 109,960,212 (GRCm39) |
D676G |
probably damaging |
Het |
Abcb7 |
T |
C |
X: 103,349,005 (GRCm39) |
M153V |
probably benign |
Het |
Ablim3 |
G |
A |
18: 61,982,466 (GRCm39) |
H160Y |
probably benign |
Het |
Acsl6 |
T |
C |
11: 54,251,902 (GRCm39) |
I683T |
probably damaging |
Het |
Adgrg5 |
A |
T |
8: 95,664,428 (GRCm39) |
Y345F |
probably damaging |
Het |
Alg6 |
T |
G |
4: 99,634,599 (GRCm39) |
F114V |
probably benign |
Het |
Ank2 |
A |
C |
3: 126,791,500 (GRCm39) |
|
probably null |
Het |
Ankrd24 |
A |
T |
10: 81,478,775 (GRCm39) |
|
probably benign |
Het |
Ano8 |
T |
C |
8: 71,936,131 (GRCm39) |
K222E |
probably damaging |
Het |
Arhgef5 |
T |
C |
6: 43,252,119 (GRCm39) |
S957P |
probably benign |
Het |
Bltp2 |
A |
G |
11: 78,159,299 (GRCm39) |
D499G |
probably damaging |
Het |
Bmpr1b |
A |
T |
3: 141,563,163 (GRCm39) |
|
probably null |
Het |
C3 |
A |
G |
17: 57,529,823 (GRCm39) |
V2A |
probably damaging |
Het |
Capn1 |
A |
G |
19: 6,059,133 (GRCm39) |
V276A |
possibly damaging |
Het |
Ccdc57 |
T |
C |
11: 120,812,499 (GRCm39) |
E85G |
probably damaging |
Het |
Chil3 |
C |
T |
3: 106,056,117 (GRCm39) |
|
probably null |
Het |
Chl1 |
A |
T |
6: 103,676,120 (GRCm39) |
|
probably null |
Het |
Chodl |
C |
T |
16: 78,738,146 (GRCm39) |
P38L |
probably benign |
Het |
Clec4a2 |
G |
T |
6: 123,116,084 (GRCm39) |
E124* |
probably null |
Het |
Cmtr1 |
T |
C |
17: 29,921,229 (GRCm39) |
V825A |
probably benign |
Het |
Cnksr3 |
T |
C |
10: 7,070,539 (GRCm39) |
I232V |
probably benign |
Het |
Cntn1 |
C |
T |
15: 92,203,021 (GRCm39) |
R768C |
probably damaging |
Het |
Col15a1 |
G |
T |
4: 47,299,278 (GRCm39) |
|
probably null |
Het |
Col6a3 |
T |
A |
1: 90,735,256 (GRCm39) |
I798F |
possibly damaging |
Het |
Cpxcr1 |
T |
A |
X: 115,387,758 (GRCm39) |
L223* |
probably null |
Het |
Cul1 |
A |
G |
6: 47,497,764 (GRCm39) |
N615S |
probably damaging |
Het |
Cxcr2 |
A |
G |
1: 74,198,438 (GRCm39) |
I311V |
probably benign |
Het |
Cyp2c67 |
C |
T |
19: 39,605,811 (GRCm39) |
G362S |
probably benign |
Het |
D930048N14Rik |
T |
A |
11: 51,544,692 (GRCm39) |
|
probably benign |
Het |
Ddx49 |
T |
C |
8: 70,753,633 (GRCm39) |
T79A |
probably damaging |
Het |
Defb46 |
T |
A |
8: 19,289,991 (GRCm39) |
|
probably null |
Het |
Dnah17 |
T |
A |
11: 118,012,742 (GRCm39) |
I145F |
probably damaging |
Het |
Dock8 |
A |
T |
19: 25,104,492 (GRCm39) |
I725F |
probably benign |
Het |
Dppa4 |
G |
A |
16: 48,108,247 (GRCm39) |
A11T |
probably damaging |
Het |
Enam |
T |
A |
5: 88,652,324 (GRCm39) |
S1278T |
possibly damaging |
Het |
Fndc3a |
A |
G |
14: 72,794,283 (GRCm39) |
V829A |
probably damaging |
Het |
Gatb |
T |
G |
3: 85,526,184 (GRCm39) |
L354R |
probably damaging |
Het |
Gm10787 |
A |
T |
10: 76,857,711 (GRCm39) |
|
noncoding transcript |
Het |
Gsap |
T |
A |
5: 21,495,543 (GRCm39) |
|
probably null |
Het |
Gtf2ird1 |
T |
C |
5: 134,411,434 (GRCm39) |
|
probably null |
Het |
Has3 |
A |
T |
8: 107,600,711 (GRCm39) |
I58F |
probably damaging |
Het |
Haus5 |
A |
T |
7: 30,357,926 (GRCm39) |
|
probably null |
Het |
Hip1r |
T |
C |
5: 124,129,568 (GRCm39) |
V169A |
probably benign |
Het |
Hnf1a |
T |
A |
5: 115,108,770 (GRCm39) |
D45V |
probably damaging |
Het |
Il20ra |
T |
A |
10: 19,618,767 (GRCm39) |
Y72N |
probably damaging |
Het |
Ipo11 |
A |
T |
13: 106,948,765 (GRCm39) |
V914E |
possibly damaging |
Het |
Itpr1 |
T |
C |
6: 108,363,667 (GRCm39) |
L763P |
probably damaging |
Het |
Katnal2 |
C |
A |
18: 77,103,719 (GRCm39) |
R104L |
probably benign |
Het |
Kcng4 |
G |
T |
8: 120,352,947 (GRCm39) |
P321Q |
probably benign |
Het |
Larp4b |
T |
C |
13: 9,187,339 (GRCm39) |
|
probably null |
Het |
Lars1 |
T |
C |
18: 42,345,673 (GRCm39) |
N1001S |
probably benign |
Het |
Lhcgr |
T |
A |
17: 89,072,604 (GRCm39) |
I148F |
probably damaging |
Het |
Lsm10 |
T |
A |
4: 125,991,756 (GRCm39) |
S37R |
possibly damaging |
Het |
Mfsd13a |
A |
G |
19: 46,360,619 (GRCm39) |
|
probably null |
Het |
Mipep |
T |
A |
14: 61,080,689 (GRCm39) |
C560* |
probably null |
Het |
Mme |
G |
A |
3: 63,235,467 (GRCm39) |
D172N |
probably benign |
Het |
Mme |
A |
G |
3: 63,235,404 (GRCm39) |
S97G |
probably benign |
Het |
Mtrex |
A |
T |
13: 113,009,461 (GRCm39) |
H979Q |
probably benign |
Het |
Mx1 |
A |
T |
16: 97,249,403 (GRCm39) |
L608Q |
probably damaging |
Het |
Myt1l |
T |
C |
12: 29,901,660 (GRCm39) |
M208T |
probably benign |
Het |
Neb |
T |
C |
2: 52,118,554 (GRCm39) |
I3987V |
probably damaging |
Het |
Neto1 |
T |
C |
18: 86,414,009 (GRCm39) |
M1T |
probably null |
Het |
Nom1 |
T |
C |
5: 29,651,876 (GRCm39) |
F738S |
possibly damaging |
Het |
Or10v1 |
C |
A |
19: 11,874,249 (GRCm39) |
P288H |
probably damaging |
Het |
Or4f61 |
C |
A |
2: 111,922,192 (GRCm39) |
V285L |
probably benign |
Het |
Or51h5 |
C |
T |
7: 102,577,648 (GRCm39) |
S271L |
probably damaging |
Het |
Or5b123 |
C |
T |
19: 13,596,967 (GRCm39) |
S147F |
probably damaging |
Het |
Or5w14 |
T |
C |
2: 87,541,317 (GRCm39) |
|
probably null |
Het |
Or6c203 |
T |
C |
10: 129,010,197 (GRCm39) |
K231R |
probably benign |
Het |
Or6f2 |
T |
A |
7: 139,756,474 (GRCm39) |
L147* |
probably null |
Het |
Or9m1b |
T |
G |
2: 87,836,865 (GRCm39) |
I86L |
probably damaging |
Het |
Pak1ip1 |
A |
G |
13: 41,164,708 (GRCm39) |
T264A |
possibly damaging |
Het |
Palb2 |
G |
T |
7: 121,713,537 (GRCm39) |
D915E |
possibly damaging |
Het |
Pank4 |
T |
C |
4: 155,060,816 (GRCm39) |
L491P |
probably damaging |
Het |
Paqr7 |
T |
C |
4: 134,234,980 (GRCm39) |
V279A |
probably benign |
Het |
Pcif1 |
G |
A |
2: 164,730,386 (GRCm39) |
R373Q |
probably damaging |
Het |
Pdgfa |
T |
A |
5: 138,964,927 (GRCm39) |
N185I |
probably benign |
Het |
Plcd4 |
T |
C |
1: 74,588,520 (GRCm39) |
V123A |
possibly damaging |
Het |
Pramel26 |
T |
C |
4: 143,539,396 (GRCm39) |
I32M |
probably benign |
Het |
Prune2 |
A |
G |
19: 17,176,503 (GRCm39) |
I154V |
probably damaging |
Het |
Rac3 |
T |
G |
11: 120,614,320 (GRCm39) |
L148R |
possibly damaging |
Het |
Rapgef6 |
T |
A |
11: 54,533,637 (GRCm39) |
D362E |
probably benign |
Het |
Rbl1 |
A |
G |
2: 157,016,823 (GRCm39) |
I592T |
probably benign |
Het |
Rbl2 |
A |
C |
8: 91,822,191 (GRCm39) |
D408A |
possibly damaging |
Het |
Retreg2 |
A |
G |
1: 75,123,319 (GRCm39) |
K416E |
probably benign |
Het |
Rorb |
A |
T |
19: 18,939,447 (GRCm39) |
L234H |
probably damaging |
Het |
Rpp40 |
T |
G |
13: 36,080,897 (GRCm39) |
D279A |
probably benign |
Het |
Siglec1 |
C |
A |
2: 130,923,420 (GRCm39) |
V442L |
probably damaging |
Het |
Sik3 |
C |
G |
9: 46,132,387 (GRCm39) |
H1276Q |
probably benign |
Het |
Slc25a34 |
G |
A |
4: 141,349,579 (GRCm39) |
T192I |
probably benign |
Het |
Sp140l1 |
G |
A |
1: 85,062,852 (GRCm39) |
|
probably benign |
Het |
Sptbn5 |
T |
C |
2: 119,902,125 (GRCm39) |
I126M |
possibly damaging |
Het |
Strada |
A |
G |
11: 106,062,047 (GRCm39) |
V94A |
possibly damaging |
Het |
Stxbp5 |
C |
A |
10: 9,688,042 (GRCm39) |
V420F |
possibly damaging |
Het |
Tgm1 |
T |
C |
14: 55,942,398 (GRCm39) |
Y651C |
probably damaging |
Het |
Tmem200c |
T |
A |
17: 69,147,612 (GRCm39) |
V65E |
probably damaging |
Het |
Tmem74 |
A |
T |
15: 43,730,559 (GRCm39) |
D161E |
probably benign |
Het |
Trgc3 |
A |
T |
13: 19,445,261 (GRCm39) |
M70L |
probably damaging |
Het |
Vcan |
T |
G |
13: 89,853,511 (GRCm39) |
E483A |
probably damaging |
Het |
Vmn2r124 |
A |
G |
17: 18,283,436 (GRCm39) |
T377A |
probably benign |
Het |
Vmn2r3 |
A |
C |
3: 64,166,815 (GRCm39) |
I772S |
probably damaging |
Het |
Wdfy3 |
A |
G |
5: 102,063,242 (GRCm39) |
V1342A |
probably benign |
Het |
Zfp507 |
T |
C |
7: 35,487,176 (GRCm39) |
H764R |
probably damaging |
Het |
Znrf3 |
A |
G |
11: 5,237,455 (GRCm39) |
I218T |
possibly damaging |
Het |
|
Other mutations in Nelfcd |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01999:Nelfcd
|
APN |
2 |
174,265,308 (GRCm39) |
splice site |
probably benign |
|
IGL02175:Nelfcd
|
APN |
2 |
174,262,175 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02955:Nelfcd
|
APN |
2 |
174,264,391 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03193:Nelfcd
|
APN |
2 |
174,268,625 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03194:Nelfcd
|
APN |
2 |
174,268,625 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03203:Nelfcd
|
APN |
2 |
174,268,625 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03217:Nelfcd
|
APN |
2 |
174,268,625 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03237:Nelfcd
|
APN |
2 |
174,268,625 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03273:Nelfcd
|
APN |
2 |
174,268,625 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03278:Nelfcd
|
APN |
2 |
174,268,625 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03289:Nelfcd
|
APN |
2 |
174,268,625 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03365:Nelfcd
|
APN |
2 |
174,268,625 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03398:Nelfcd
|
APN |
2 |
174,268,625 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03405:Nelfcd
|
APN |
2 |
174,268,625 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03407:Nelfcd
|
APN |
2 |
174,268,625 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0593:Nelfcd
|
UTSW |
2 |
174,265,223 (GRCm39) |
missense |
probably benign |
0.00 |
R0751:Nelfcd
|
UTSW |
2 |
174,264,807 (GRCm39) |
missense |
probably benign |
0.03 |
R2040:Nelfcd
|
UTSW |
2 |
174,261,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R3606:Nelfcd
|
UTSW |
2 |
174,268,337 (GRCm39) |
missense |
probably benign |
0.10 |
R3716:Nelfcd
|
UTSW |
2 |
174,264,798 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4235:Nelfcd
|
UTSW |
2 |
174,268,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R4607:Nelfcd
|
UTSW |
2 |
174,264,955 (GRCm39) |
missense |
probably benign |
0.01 |
R4775:Nelfcd
|
UTSW |
2 |
174,268,369 (GRCm39) |
missense |
probably damaging |
0.96 |
R5104:Nelfcd
|
UTSW |
2 |
174,268,159 (GRCm39) |
missense |
probably benign |
0.10 |
R5859:Nelfcd
|
UTSW |
2 |
174,268,856 (GRCm39) |
makesense |
probably null |
|
R6025:Nelfcd
|
UTSW |
2 |
174,268,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R6104:Nelfcd
|
UTSW |
2 |
174,265,250 (GRCm39) |
missense |
probably damaging |
0.99 |
R6280:Nelfcd
|
UTSW |
2 |
174,257,739 (GRCm39) |
missense |
probably benign |
|
R7249:Nelfcd
|
UTSW |
2 |
174,264,999 (GRCm39) |
critical splice donor site |
probably null |
|
R7382:Nelfcd
|
UTSW |
2 |
174,265,176 (GRCm39) |
missense |
probably benign |
0.00 |
R7532:Nelfcd
|
UTSW |
2 |
174,268,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R7545:Nelfcd
|
UTSW |
2 |
174,265,771 (GRCm39) |
splice site |
probably null |
|
R7766:Nelfcd
|
UTSW |
2 |
174,268,625 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9011:Nelfcd
|
UTSW |
2 |
174,268,717 (GRCm39) |
missense |
probably benign |
0.15 |
R9094:Nelfcd
|
UTSW |
2 |
174,265,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R9332:Nelfcd
|
UTSW |
2 |
174,264,978 (GRCm39) |
missense |
probably benign |
0.02 |
R9486:Nelfcd
|
UTSW |
2 |
174,268,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R9695:Nelfcd
|
UTSW |
2 |
174,266,923 (GRCm39) |
missense |
probably benign |
0.34 |
Z1088:Nelfcd
|
UTSW |
2 |
174,268,287 (GRCm39) |
frame shift |
probably null |
|
|