Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam25 |
T |
A |
8: 41,208,239 (GRCm39) |
Y502N |
probably damaging |
Het |
Adam6a |
T |
A |
12: 113,509,484 (GRCm39) |
L619* |
probably null |
Het |
Akap9 |
A |
T |
5: 4,011,587 (GRCm39) |
R763S |
probably benign |
Het |
Akt3 |
G |
A |
1: 176,958,639 (GRCm39) |
P24S |
probably damaging |
Het |
Ano2 |
A |
T |
6: 125,857,382 (GRCm39) |
|
probably null |
Het |
Bahcc1 |
A |
G |
11: 120,163,286 (GRCm39) |
D528G |
possibly damaging |
Het |
Camk1g |
G |
T |
1: 193,030,483 (GRCm39) |
Q409K |
probably benign |
Het |
Cdh3 |
T |
A |
8: 107,274,396 (GRCm39) |
N638K |
probably benign |
Het |
Cgnl1 |
T |
A |
9: 71,562,632 (GRCm39) |
E882D |
possibly damaging |
Het |
Cplane1 |
A |
G |
15: 8,231,785 (GRCm39) |
N1077S |
possibly damaging |
Het |
Cpxm2 |
C |
T |
7: 131,661,651 (GRCm39) |
E379K |
probably damaging |
Het |
Cyp3a16 |
A |
G |
5: 145,389,690 (GRCm39) |
L225P |
probably damaging |
Het |
Dchs1 |
T |
C |
7: 105,411,625 (GRCm39) |
E1497G |
probably damaging |
Het |
Denr |
T |
A |
5: 124,065,117 (GRCm39) |
S157T |
possibly damaging |
Het |
Disp3 |
A |
G |
4: 148,356,101 (GRCm39) |
I253T |
probably damaging |
Het |
Dlgap2 |
C |
T |
8: 14,896,653 (GRCm39) |
T1043M |
probably damaging |
Het |
Epb41l5 |
T |
C |
1: 119,535,804 (GRCm39) |
T355A |
probably damaging |
Het |
Etv6 |
G |
A |
6: 134,013,062 (GRCm39) |
|
probably benign |
Het |
Fbn1 |
T |
C |
2: 125,310,484 (GRCm39) |
I141V |
probably benign |
Het |
Fsip2 |
T |
G |
2: 82,819,272 (GRCm39) |
S5002A |
probably benign |
Het |
Gbf1 |
T |
G |
19: 46,271,837 (GRCm39) |
V1576G |
probably damaging |
Het |
Gmfg |
T |
A |
7: 28,140,733 (GRCm39) |
|
probably null |
Het |
Gsdmc4 |
T |
C |
15: 63,774,706 (GRCm39) |
E25G |
possibly damaging |
Het |
Igkv6-23 |
A |
T |
6: 70,237,884 (GRCm39) |
L12M |
possibly damaging |
Het |
Kank1 |
G |
A |
19: 25,388,138 (GRCm39) |
V604M |
probably damaging |
Het |
Kctd1 |
A |
G |
18: 15,140,822 (GRCm39) |
V40A |
probably damaging |
Het |
Krt222 |
T |
C |
11: 99,127,065 (GRCm39) |
K185R |
possibly damaging |
Het |
Ldc1 |
A |
G |
4: 130,115,527 (GRCm39) |
V7A |
probably benign |
Het |
Lipm |
T |
C |
19: 34,089,494 (GRCm39) |
F151L |
probably damaging |
Het |
Lrrc2 |
A |
T |
9: 110,791,710 (GRCm39) |
N154I |
probably damaging |
Het |
Map1a |
T |
A |
2: 121,132,865 (GRCm39) |
M1227K |
probably damaging |
Het |
Med1 |
T |
C |
11: 98,071,114 (GRCm39) |
T78A |
probably damaging |
Het |
Mrm1 |
A |
G |
11: 84,710,144 (GRCm39) |
S19P |
possibly damaging |
Het |
Naf1 |
GCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAACTGGGATGCGGGCGGAAGACCACCACCGCCGCCAGCCCCGAACTCGGATCCCGGCGGAAGACC |
GCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAACTGGGATGCGGGCGGAAGACCACCACCGCCGCCAGCCCCGAACTCGGATCCCGGCGGAAGACC |
8: 67,313,200 (GRCm39) |
|
probably benign |
Het |
Nap1l1 |
A |
G |
10: 111,330,657 (GRCm39) |
Y354C |
probably damaging |
Het |
Npr1 |
A |
G |
3: 90,368,448 (GRCm39) |
V474A |
probably benign |
Het |
Nyap1 |
A |
T |
5: 137,733,840 (GRCm39) |
S398T |
probably damaging |
Het |
Obox7 |
C |
T |
7: 14,398,067 (GRCm39) |
Q36* |
probably null |
Het |
Or5aq6 |
A |
T |
2: 86,923,390 (GRCm39) |
M117K |
possibly damaging |
Het |
Or6c8 |
A |
T |
10: 128,915,358 (GRCm39) |
I158N |
probably benign |
Het |
P3h1 |
T |
A |
4: 119,090,428 (GRCm39) |
L92H |
probably benign |
Het |
Pappa2 |
T |
C |
1: 158,609,818 (GRCm39) |
T1548A |
possibly damaging |
Het |
Pnisr |
A |
G |
4: 21,873,586 (GRCm39) |
E443G |
probably damaging |
Het |
Prdm2 |
A |
G |
4: 142,859,079 (GRCm39) |
S1404P |
possibly damaging |
Het |
Prom1 |
A |
T |
5: 44,190,284 (GRCm39) |
|
probably null |
Het |
Rbm27 |
A |
T |
18: 42,455,186 (GRCm39) |
Q646H |
probably damaging |
Het |
Scamp3 |
C |
T |
3: 89,087,561 (GRCm39) |
R134* |
probably null |
Het |
Scrt2 |
T |
C |
2: 151,924,018 (GRCm39) |
C17R |
probably benign |
Het |
Setbp1 |
A |
G |
18: 78,902,498 (GRCm39) |
S390P |
probably benign |
Het |
Shank2 |
A |
T |
7: 143,964,837 (GRCm39) |
D815V |
probably damaging |
Het |
Sirt7 |
G |
A |
11: 120,511,296 (GRCm39) |
T285M |
|
Het |
Sis |
T |
G |
3: 72,863,621 (GRCm39) |
S206R |
probably benign |
Het |
Slc24a4 |
T |
G |
12: 102,193,334 (GRCm39) |
D206E |
possibly damaging |
Het |
Slc26a4 |
C |
A |
12: 31,585,292 (GRCm39) |
G501C |
probably damaging |
Het |
Sptb |
T |
C |
12: 76,677,489 (GRCm39) |
N115S |
probably damaging |
Het |
Srprb |
T |
C |
9: 103,074,807 (GRCm39) |
T112A |
possibly damaging |
Het |
Tbk1 |
G |
T |
10: 121,389,841 (GRCm39) |
A537E |
probably benign |
Het |
Tbx19 |
T |
A |
1: 164,970,067 (GRCm39) |
H274L |
probably damaging |
Het |
Tmem130 |
A |
G |
5: 144,674,233 (GRCm39) |
S394P |
probably damaging |
Het |
Tmem40 |
A |
G |
6: 115,718,517 (GRCm39) |
S104P |
possibly damaging |
Het |
Tmprss2 |
T |
A |
16: 97,379,826 (GRCm39) |
Q158L |
probably damaging |
Het |
Tnip1 |
A |
T |
11: 54,828,876 (GRCm39) |
V97D |
possibly damaging |
Het |
Tpr |
T |
A |
1: 150,314,887 (GRCm39) |
S1985T |
probably benign |
Het |
Traf7 |
CA |
CAA |
17: 24,746,737 (GRCm39) |
|
probably benign |
Het |
Trio |
G |
T |
15: 27,744,158 (GRCm39) |
N2591K |
possibly damaging |
Het |
Ushbp1 |
A |
T |
8: 71,838,573 (GRCm39) |
C618S |
possibly damaging |
Het |
Usp34 |
A |
G |
11: 23,317,385 (GRCm39) |
S834G |
possibly damaging |
Het |
Vmn2r103 |
C |
A |
17: 20,019,525 (GRCm39) |
C536* |
probably null |
Het |
Vmn2r124 |
T |
A |
17: 18,293,758 (GRCm39) |
V615D |
probably damaging |
Het |
Zbtb38 |
G |
A |
9: 96,570,397 (GRCm39) |
T229I |
probably benign |
Het |
Zfhx4 |
T |
A |
3: 5,465,656 (GRCm39) |
V1963E |
probably damaging |
Het |
Zfp142 |
G |
A |
1: 74,610,933 (GRCm39) |
T954M |
probably benign |
Het |
Zgrf1 |
A |
G |
3: 127,409,216 (GRCm39) |
Y1730C |
probably benign |
Het |
|
Other mutations in B4galnt4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01598:B4galnt4
|
APN |
7 |
140,650,428 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02055:B4galnt4
|
APN |
7 |
140,650,731 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02248:B4galnt4
|
APN |
7 |
140,647,721 (GRCm39) |
unclassified |
probably benign |
|
IGL02955:B4galnt4
|
APN |
7 |
140,644,591 (GRCm39) |
missense |
probably null |
0.08 |
IGL03334:B4galnt4
|
APN |
7 |
140,647,354 (GRCm39) |
splice site |
probably null |
|
H8786:B4galnt4
|
UTSW |
7 |
140,651,235 (GRCm39) |
missense |
probably damaging |
0.99 |
R0520:B4galnt4
|
UTSW |
7 |
140,647,286 (GRCm39) |
nonsense |
probably null |
|
R0735:B4galnt4
|
UTSW |
7 |
140,644,236 (GRCm39) |
missense |
probably benign |
0.24 |
R1355:B4galnt4
|
UTSW |
7 |
140,645,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R1864:B4galnt4
|
UTSW |
7 |
140,650,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R1874:B4galnt4
|
UTSW |
7 |
140,650,439 (GRCm39) |
missense |
probably damaging |
1.00 |
R1928:B4galnt4
|
UTSW |
7 |
140,648,061 (GRCm39) |
nonsense |
probably null |
|
R1969:B4galnt4
|
UTSW |
7 |
140,644,761 (GRCm39) |
missense |
probably benign |
0.01 |
R3429:B4galnt4
|
UTSW |
7 |
140,650,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R4239:B4galnt4
|
UTSW |
7 |
140,641,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R4382:B4galnt4
|
UTSW |
7 |
140,650,449 (GRCm39) |
missense |
probably damaging |
0.99 |
R4517:B4galnt4
|
UTSW |
7 |
140,647,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R4748:B4galnt4
|
UTSW |
7 |
140,651,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R4827:B4galnt4
|
UTSW |
7 |
140,648,392 (GRCm39) |
missense |
probably benign |
0.00 |
R4831:B4galnt4
|
UTSW |
7 |
140,644,470 (GRCm39) |
critical splice donor site |
probably null |
|
R4831:B4galnt4
|
UTSW |
7 |
140,647,634 (GRCm39) |
missense |
probably damaging |
0.99 |
R4898:B4galnt4
|
UTSW |
7 |
140,648,173 (GRCm39) |
missense |
probably benign |
0.11 |
R5028:B4galnt4
|
UTSW |
7 |
140,647,975 (GRCm39) |
missense |
probably benign |
0.40 |
R5249:B4galnt4
|
UTSW |
7 |
140,644,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R5267:B4galnt4
|
UTSW |
7 |
140,650,524 (GRCm39) |
missense |
probably damaging |
0.99 |
R5728:B4galnt4
|
UTSW |
7 |
140,650,488 (GRCm39) |
missense |
probably benign |
0.00 |
R5924:B4galnt4
|
UTSW |
7 |
140,650,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R6063:B4galnt4
|
UTSW |
7 |
140,644,643 (GRCm39) |
missense |
probably benign |
0.08 |
R6311:B4galnt4
|
UTSW |
7 |
140,648,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R6376:B4galnt4
|
UTSW |
7 |
140,647,335 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6689:B4galnt4
|
UTSW |
7 |
140,647,897 (GRCm39) |
missense |
probably benign |
0.25 |
R6954:B4galnt4
|
UTSW |
7 |
140,647,145 (GRCm39) |
missense |
probably benign |
0.01 |
R6974:B4galnt4
|
UTSW |
7 |
140,647,449 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7041:B4galnt4
|
UTSW |
7 |
140,650,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R7092:B4galnt4
|
UTSW |
7 |
140,648,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R7359:B4galnt4
|
UTSW |
7 |
140,651,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R7367:B4galnt4
|
UTSW |
7 |
140,644,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R7409:B4galnt4
|
UTSW |
7 |
140,646,916 (GRCm39) |
splice site |
probably null |
|
R7519:B4galnt4
|
UTSW |
7 |
140,644,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R7664:B4galnt4
|
UTSW |
7 |
140,647,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R7679:B4galnt4
|
UTSW |
7 |
140,647,678 (GRCm39) |
missense |
probably benign |
0.28 |
R7782:B4galnt4
|
UTSW |
7 |
140,644,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R8103:B4galnt4
|
UTSW |
7 |
140,644,564 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8783:B4galnt4
|
UTSW |
7 |
140,643,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R8796:B4galnt4
|
UTSW |
7 |
140,647,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R8855:B4galnt4
|
UTSW |
7 |
140,648,488 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9545:B4galnt4
|
UTSW |
7 |
140,644,804 (GRCm39) |
missense |
probably benign |
0.04 |
R9629:B4galnt4
|
UTSW |
7 |
140,648,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R9708:B4galnt4
|
UTSW |
7 |
140,647,657 (GRCm39) |
missense |
probably benign |
|
RF007:B4galnt4
|
UTSW |
7 |
140,650,609 (GRCm39) |
critical splice donor site |
probably null |
|
YA93:B4galnt4
|
UTSW |
7 |
140,647,324 (GRCm39) |
missense |
possibly damaging |
0.77 |
|