Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930111J21Rik1 |
T |
A |
11: 48,838,496 (GRCm39) |
E697V |
probably damaging |
Het |
Actn4 |
T |
C |
7: 28,594,864 (GRCm39) |
D805G |
probably benign |
Het |
Adam2 |
C |
T |
14: 66,275,071 (GRCm39) |
S554N |
probably benign |
Het |
Adra2b |
A |
G |
2: 127,206,283 (GRCm39) |
T267A |
probably benign |
Het |
Apobec4 |
A |
T |
1: 152,632,415 (GRCm39) |
T148S |
probably damaging |
Het |
Bok |
C |
A |
1: 93,616,947 (GRCm39) |
Q98K |
probably benign |
Het |
Cacnb4 |
A |
T |
2: 52,327,016 (GRCm39) |
L394Q |
probably damaging |
Het |
Ccar2 |
T |
C |
14: 70,381,105 (GRCm39) |
K287E |
probably benign |
Het |
Cdyl2 |
T |
A |
8: 117,350,669 (GRCm39) |
E154V |
probably benign |
Het |
Cenpn |
T |
G |
8: 117,660,149 (GRCm39) |
Y160D |
probably damaging |
Het |
Cfap20 |
T |
C |
8: 96,149,514 (GRCm39) |
Y58C |
probably benign |
Het |
Creb5 |
T |
A |
6: 53,658,039 (GRCm39) |
L123Q |
unknown |
Het |
Cspg4 |
G |
A |
9: 56,797,342 (GRCm39) |
V1269M |
probably damaging |
Het |
Cyp2b19 |
G |
T |
7: 26,466,353 (GRCm39) |
K385N |
probably null |
Het |
Cyp2b19 |
A |
T |
7: 26,466,352 (GRCm39) |
K385M |
probably damaging |
Het |
Ercc2 |
C |
A |
7: 19,124,060 (GRCm39) |
D422E |
probably benign |
Het |
Fbxl12 |
A |
G |
9: 20,550,109 (GRCm39) |
V129A |
possibly damaging |
Het |
Fbxo11 |
T |
C |
17: 88,321,951 (GRCm39) |
E84G |
|
Het |
Fmn1 |
T |
C |
2: 113,425,402 (GRCm39) |
L1192S |
probably damaging |
Het |
Galk2 |
T |
C |
2: 125,824,979 (GRCm39) |
F392L |
probably benign |
Het |
Gas2l3 |
G |
A |
10: 89,258,135 (GRCm39) |
H153Y |
probably damaging |
Het |
Gcn1 |
A |
T |
5: 115,713,341 (GRCm39) |
K101N |
possibly damaging |
Het |
Gmfg |
C |
T |
7: 28,145,359 (GRCm39) |
Q101* |
probably null |
Het |
Gpr108 |
C |
T |
17: 57,545,039 (GRCm39) |
C309Y |
probably damaging |
Het |
H3c8 |
T |
C |
13: 23,719,761 (GRCm39) |
L49P |
probably damaging |
Het |
Hscb |
A |
T |
5: 110,982,595 (GRCm39) |
I164N |
probably damaging |
Het |
Kifc2 |
T |
C |
15: 76,546,397 (GRCm39) |
W260R |
probably damaging |
Het |
Lrp6 |
T |
A |
6: 134,447,662 (GRCm39) |
D995V |
possibly damaging |
Het |
Lrrc1 |
T |
A |
9: 77,358,708 (GRCm39) |
I308F |
probably damaging |
Het |
Map7 |
C |
T |
10: 20,153,966 (GRCm39) |
A694V |
unknown |
Het |
Mapre2 |
A |
G |
18: 23,965,993 (GRCm39) |
D68G |
probably benign |
Het |
Mertk |
A |
T |
2: 128,593,880 (GRCm39) |
I295F |
probably benign |
Het |
Mst1 |
T |
A |
9: 107,962,053 (GRCm39) |
C690* |
probably null |
Het |
Nde1 |
A |
G |
16: 13,988,345 (GRCm39) |
E76G |
probably damaging |
Het |
Nek5 |
T |
C |
8: 22,564,040 (GRCm39) |
T597A |
probably benign |
Het |
Nup210l |
T |
C |
3: 90,117,693 (GRCm39) |
F1800L |
probably benign |
Het |
Or5c1 |
A |
G |
2: 37,222,148 (GRCm39) |
I130V |
possibly damaging |
Het |
Pdpn |
T |
A |
4: 142,997,101 (GRCm39) |
D131V |
probably benign |
Het |
Pgap6 |
T |
C |
17: 26,337,861 (GRCm39) |
V415A |
probably damaging |
Het |
Pot1a |
T |
C |
6: 25,775,718 (GRCm39) |
T118A |
possibly damaging |
Het |
Prom1 |
A |
G |
5: 44,158,179 (GRCm39) |
I843T |
probably benign |
Het |
Prrt3 |
T |
C |
6: 113,474,587 (GRCm39) |
T212A |
probably benign |
Het |
Rabgap1 |
A |
G |
2: 37,433,246 (GRCm39) |
|
probably null |
Het |
Rarb |
A |
T |
14: 16,574,858 (GRCm38) |
S53T |
probably damaging |
Het |
Rnft2 |
A |
G |
5: 118,375,330 (GRCm39) |
S140P |
probably benign |
Het |
Rxfp1 |
T |
C |
3: 79,563,581 (GRCm39) |
M362V |
probably benign |
Het |
Sall2 |
G |
A |
14: 52,551,617 (GRCm39) |
T526M |
probably damaging |
Het |
Scube1 |
T |
C |
15: 83,501,000 (GRCm39) |
D598G |
|
Het |
Sema3f |
T |
A |
9: 107,566,972 (GRCm39) |
I186F |
possibly damaging |
Het |
Shank2 |
A |
G |
7: 143,622,462 (GRCm39) |
T199A |
possibly damaging |
Het |
Sipa1l2 |
T |
A |
8: 126,169,453 (GRCm39) |
M1427L |
probably benign |
Het |
Sis |
C |
T |
3: 72,828,490 (GRCm39) |
G1195D |
probably benign |
Het |
Slc25a39 |
A |
T |
11: 102,295,390 (GRCm39) |
H193Q |
probably benign |
Het |
Sprr2b |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
3: 92,224,826 (GRCm39) |
|
probably benign |
Het |
Srgn |
A |
C |
10: 62,343,444 (GRCm39) |
L17R |
probably damaging |
Het |
Stard5 |
A |
G |
7: 83,281,944 (GRCm39) |
N34D |
probably benign |
Het |
Syt8 |
A |
T |
7: 141,993,203 (GRCm39) |
D220V |
probably damaging |
Het |
Tex15 |
A |
G |
8: 34,064,509 (GRCm39) |
E1313G |
probably benign |
Het |
Tmem131l |
T |
C |
3: 83,868,911 (GRCm39) |
R155G |
probably damaging |
Het |
Tmem220 |
T |
C |
11: 66,916,093 (GRCm39) |
V30A |
probably damaging |
Het |
Tollip |
A |
G |
7: 141,445,731 (GRCm39) |
I119T |
probably damaging |
Het |
Treml4 |
G |
A |
17: 48,571,672 (GRCm39) |
G25D |
probably damaging |
Het |
Trim7 |
T |
C |
11: 48,728,460 (GRCm39) |
F36S |
probably damaging |
Het |
Txnrd3 |
T |
A |
6: 89,640,166 (GRCm39) |
C293* |
probably null |
Het |
Utp14b |
A |
G |
1: 78,643,482 (GRCm39) |
D460G |
probably benign |
Het |
Vmn2r41 |
T |
A |
7: 8,153,329 (GRCm39) |
N397Y |
probably benign |
Het |
Vmn2r67 |
T |
C |
7: 84,786,017 (GRCm39) |
I663V |
probably benign |
Het |
Zfp292 |
T |
A |
4: 34,839,460 (GRCm39) |
H135L |
probably damaging |
Het |
Zfp420 |
C |
T |
7: 29,575,480 (GRCm39) |
R567* |
probably null |
Het |
Zfp518b |
C |
T |
5: 38,830,773 (GRCm39) |
V411M |
probably benign |
Het |
Zfp638 |
T |
A |
6: 83,956,680 (GRCm39) |
D1762E |
probably damaging |
Het |
Zfp691 |
T |
A |
4: 119,028,230 (GRCm39) |
M1L |
possibly damaging |
Het |
|
Other mutations in B4galt1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01795:B4galt1
|
APN |
4 |
40,807,760 (GRCm39) |
missense |
probably damaging |
1.00 |
periwinkle
|
UTSW |
4 |
40,807,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R1589:B4galt1
|
UTSW |
4 |
40,823,575 (GRCm39) |
missense |
probably benign |
0.28 |
R3797:B4galt1
|
UTSW |
4 |
40,807,258 (GRCm39) |
missense |
probably benign |
0.12 |
R4419:B4galt1
|
UTSW |
4 |
40,853,537 (GRCm39) |
missense |
probably benign |
|
R4703:B4galt1
|
UTSW |
4 |
40,823,569 (GRCm39) |
missense |
probably benign |
0.14 |
R4727:B4galt1
|
UTSW |
4 |
40,807,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R5706:B4galt1
|
UTSW |
4 |
40,807,268 (GRCm39) |
missense |
probably damaging |
0.97 |
R5903:B4galt1
|
UTSW |
4 |
40,807,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R6860:B4galt1
|
UTSW |
4 |
40,807,796 (GRCm39) |
missense |
probably benign |
0.00 |
R6878:B4galt1
|
UTSW |
4 |
40,809,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R6943:B4galt1
|
UTSW |
4 |
40,812,860 (GRCm39) |
missense |
probably benign |
0.00 |
R7239:B4galt1
|
UTSW |
4 |
40,812,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R7479:B4galt1
|
UTSW |
4 |
40,823,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R7792:B4galt1
|
UTSW |
4 |
40,809,373 (GRCm39) |
missense |
probably benign |
0.00 |
R7887:B4galt1
|
UTSW |
4 |
40,823,501 (GRCm39) |
missense |
probably benign |
0.08 |
R7923:B4galt1
|
UTSW |
4 |
40,809,373 (GRCm39) |
missense |
probably benign |
0.00 |
R8330:B4galt1
|
UTSW |
4 |
40,812,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R8968:B4galt1
|
UTSW |
4 |
40,807,243 (GRCm39) |
missense |
probably benign |
|
R9450:B4galt1
|
UTSW |
4 |
40,853,804 (GRCm39) |
start codon destroyed |
probably null |
0.98 |
R9705:B4galt1
|
UTSW |
4 |
40,853,474 (GRCm39) |
missense |
probably benign |
0.03 |
|