Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam15 |
A |
G |
3: 89,253,135 (GRCm39) |
Y230H |
probably benign |
Het |
Ano7 |
G |
T |
1: 93,312,641 (GRCm39) |
|
probably null |
Het |
Arap2 |
T |
C |
5: 62,834,506 (GRCm39) |
Y792C |
probably damaging |
Het |
Art3 |
C |
A |
5: 92,560,100 (GRCm39) |
|
probably benign |
Het |
Atad2 |
C |
T |
15: 57,963,250 (GRCm39) |
G1085D |
probably benign |
Het |
Birc6 |
C |
A |
17: 74,953,497 (GRCm39) |
A3253E |
probably damaging |
Het |
C9 |
C |
T |
15: 6,526,607 (GRCm39) |
P547L |
probably benign |
Het |
Cecr2 |
T |
C |
6: 120,739,169 (GRCm39) |
S1271P |
probably damaging |
Het |
Ces1e |
T |
A |
8: 93,948,305 (GRCm39) |
K105* |
probably null |
Het |
Cpsf4 |
A |
G |
5: 145,115,683 (GRCm39) |
N204S |
probably benign |
Het |
Cracd |
A |
G |
5: 77,006,275 (GRCm39) |
T879A |
unknown |
Het |
Dgkz |
T |
C |
2: 91,769,733 (GRCm39) |
D615G |
possibly damaging |
Het |
Disp1 |
G |
T |
1: 182,869,974 (GRCm39) |
N815K |
probably damaging |
Het |
Enah |
A |
G |
1: 181,758,750 (GRCm39) |
|
probably benign |
Het |
Fcgbp |
A |
G |
7: 27,800,919 (GRCm39) |
T1322A |
possibly damaging |
Het |
Frem1 |
A |
G |
4: 82,918,395 (GRCm39) |
F516L |
probably damaging |
Het |
Fry |
G |
A |
5: 150,323,136 (GRCm39) |
A1096T |
probably damaging |
Het |
Fyco1 |
T |
C |
9: 123,660,413 (GRCm39) |
Y190C |
probably damaging |
Het |
Gfra1 |
T |
C |
19: 58,227,687 (GRCm39) |
D417G |
probably benign |
Het |
Gigyf2 |
T |
C |
1: 87,368,485 (GRCm39) |
I1055T |
probably damaging |
Het |
Invs |
A |
G |
4: 48,398,146 (GRCm39) |
E444G |
probably damaging |
Het |
Itga10 |
A |
G |
3: 96,559,901 (GRCm39) |
T519A |
probably benign |
Het |
Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
Kdm2b |
A |
G |
5: 123,009,931 (GRCm39) |
S727P |
probably benign |
Het |
Kidins220 |
A |
T |
12: 25,107,139 (GRCm39) |
K1531* |
probably null |
Het |
Ksr1 |
C |
T |
11: 78,929,024 (GRCm39) |
V266M |
probably damaging |
Het |
Lin9 |
T |
A |
1: 180,496,763 (GRCm39) |
L351I |
probably benign |
Het |
Lipi |
T |
C |
16: 75,370,798 (GRCm39) |
R140G |
possibly damaging |
Het |
Lrrc32 |
T |
C |
7: 98,147,618 (GRCm39) |
S133P |
probably damaging |
Het |
Map3k7 |
T |
A |
4: 31,964,318 (GRCm39) |
I19N |
probably damaging |
Het |
Marf1 |
A |
G |
16: 13,970,449 (GRCm39) |
V90A |
probably benign |
Het |
Mark3 |
T |
C |
12: 111,621,877 (GRCm39) |
L673P |
probably damaging |
Het |
Meis1 |
T |
C |
11: 18,966,229 (GRCm39) |
H48R |
probably benign |
Het |
Mettl26 |
G |
A |
17: 26,094,995 (GRCm39) |
V87M |
probably damaging |
Het |
Mknk2 |
T |
C |
10: 80,511,696 (GRCm39) |
R5G |
probably benign |
Het |
Mtcl3 |
G |
T |
10: 29,026,240 (GRCm39) |
V441F |
probably damaging |
Het |
Mterf1b |
T |
C |
5: 4,246,956 (GRCm39) |
V199A |
possibly damaging |
Het |
Ncs1 |
T |
A |
2: 31,170,666 (GRCm39) |
|
probably null |
Het |
Nek10 |
T |
C |
14: 14,986,704 (GRCm38) |
V1014A |
probably benign |
Het |
Notch2 |
A |
G |
3: 98,042,744 (GRCm39) |
N1370D |
probably benign |
Het |
Nr2e3 |
TCCATCGGAGTGTTCCC |
TC |
9: 59,850,701 (GRCm39) |
|
probably benign |
Het |
Opn5 |
C |
G |
17: 42,903,897 (GRCm39) |
R146T |
probably damaging |
Het |
Or1e16 |
AGCGGTCGTAGGC |
AGC |
11: 73,286,480 (GRCm39) |
|
probably null |
Het |
Or5m3 |
T |
C |
2: 85,838,636 (GRCm39) |
I172T |
probably damaging |
Het |
Or8b55 |
T |
A |
9: 38,726,952 (GRCm39) |
M51K |
probably benign |
Het |
Or8g33 |
A |
G |
9: 39,338,032 (GRCm39) |
C112R |
probably damaging |
Het |
Pcdhb18 |
G |
A |
18: 37,623,537 (GRCm39) |
R289Q |
probably benign |
Het |
Pcyox1l |
C |
T |
18: 61,832,359 (GRCm39) |
|
probably null |
Het |
Plxnb2 |
T |
C |
15: 89,044,962 (GRCm39) |
T1128A |
possibly damaging |
Het |
Prex1 |
T |
C |
2: 166,425,127 (GRCm39) |
T960A |
probably benign |
Het |
Prkaa2 |
A |
C |
4: 104,893,291 (GRCm39) |
*553G |
probably null |
Het |
Rasgrp4 |
A |
G |
7: 28,844,639 (GRCm39) |
D297G |
probably damaging |
Het |
Sdf4 |
G |
A |
4: 156,083,856 (GRCm39) |
V109I |
probably benign |
Het |
Sgsm1 |
A |
T |
5: 113,398,822 (GRCm39) |
I750N |
probably damaging |
Het |
Shtn1 |
T |
A |
19: 59,020,673 (GRCm39) |
K183M |
probably damaging |
Het |
Skic3 |
A |
G |
13: 76,303,852 (GRCm39) |
T1257A |
probably benign |
Het |
Slc22a30 |
T |
C |
19: 8,381,945 (GRCm39) |
T109A |
probably benign |
Het |
Slco1c1 |
A |
G |
6: 141,487,929 (GRCm39) |
D99G |
probably damaging |
Het |
Tcf25 |
T |
A |
8: 124,122,354 (GRCm39) |
|
probably null |
Het |
Tex10 |
A |
G |
4: 48,452,928 (GRCm39) |
V677A |
probably benign |
Het |
Tmem131l |
A |
G |
3: 83,847,879 (GRCm39) |
S329P |
probably benign |
Het |
Trappc10 |
T |
A |
10: 78,058,573 (GRCm39) |
N136I |
probably damaging |
Het |
Trpt1 |
T |
C |
19: 6,975,906 (GRCm39) |
F173L |
probably benign |
Het |
Ube4b |
G |
A |
4: 149,421,925 (GRCm39) |
R955C |
probably damaging |
Het |
Usp34 |
C |
A |
11: 23,371,340 (GRCm39) |
P1840T |
probably benign |
Het |
Vmn1r27 |
A |
T |
6: 58,192,985 (GRCm39) |
N6K |
possibly damaging |
Het |
Wdr25 |
T |
C |
12: 108,993,347 (GRCm39) |
V521A |
possibly damaging |
Het |
Wdr64 |
G |
A |
1: 175,639,623 (GRCm39) |
E1031K |
possibly damaging |
Het |
Wnt10a |
A |
G |
1: 74,839,755 (GRCm39) |
N147S |
probably damaging |
Het |
Zbed5 |
T |
C |
5: 129,931,059 (GRCm39) |
I336T |
possibly damaging |
Het |
Zfp758 |
T |
A |
17: 22,594,796 (GRCm39) |
H427Q |
probably damaging |
Het |
Zfp961 |
C |
A |
8: 72,722,070 (GRCm39) |
H194Q |
probably damaging |
Het |
|
Other mutations in Serpinb3d |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01582:Serpinb3d
|
APN |
1 |
107,007,396 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01917:Serpinb3d
|
APN |
1 |
107,007,411 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02732:Serpinb3d
|
APN |
1 |
107,010,526 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02988:Serpinb3d
|
UTSW |
1 |
107,006,266 (GRCm39) |
missense |
probably benign |
|
R0540:Serpinb3d
|
UTSW |
1 |
107,006,962 (GRCm39) |
missense |
probably benign |
0.01 |
R0594:Serpinb3d
|
UTSW |
1 |
107,007,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R1666:Serpinb3d
|
UTSW |
1 |
107,008,481 (GRCm39) |
missense |
probably benign |
0.18 |
R1668:Serpinb3d
|
UTSW |
1 |
107,008,481 (GRCm39) |
missense |
probably benign |
0.18 |
R1905:Serpinb3d
|
UTSW |
1 |
107,007,014 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1994:Serpinb3d
|
UTSW |
1 |
107,008,518 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2021:Serpinb3d
|
UTSW |
1 |
107,006,182 (GRCm39) |
missense |
probably benign |
0.05 |
R2022:Serpinb3d
|
UTSW |
1 |
107,006,182 (GRCm39) |
missense |
probably benign |
0.05 |
R3760:Serpinb3d
|
UTSW |
1 |
107,009,304 (GRCm39) |
splice site |
probably benign |
|
R4118:Serpinb3d
|
UTSW |
1 |
107,006,960 (GRCm39) |
missense |
possibly damaging |
0.58 |
R4496:Serpinb3d
|
UTSW |
1 |
107,007,022 (GRCm39) |
missense |
probably damaging |
0.98 |
R4770:Serpinb3d
|
UTSW |
1 |
107,006,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R4793:Serpinb3d
|
UTSW |
1 |
107,005,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R5174:Serpinb3d
|
UTSW |
1 |
107,006,228 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5434:Serpinb3d
|
UTSW |
1 |
107,006,263 (GRCm39) |
missense |
probably benign |
0.02 |
R5820:Serpinb3d
|
UTSW |
1 |
107,006,089 (GRCm39) |
missense |
probably damaging |
0.99 |
R5935:Serpinb3d
|
UTSW |
1 |
107,011,105 (GRCm39) |
missense |
probably benign |
0.00 |
R6056:Serpinb3d
|
UTSW |
1 |
107,007,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R6092:Serpinb3d
|
UTSW |
1 |
107,006,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R6188:Serpinb3d
|
UTSW |
1 |
107,006,237 (GRCm39) |
missense |
probably damaging |
0.98 |
R6247:Serpinb3d
|
UTSW |
1 |
107,010,490 (GRCm39) |
missense |
probably benign |
0.01 |
R6369:Serpinb3d
|
UTSW |
1 |
107,008,483 (GRCm39) |
missense |
probably benign |
0.00 |
R6476:Serpinb3d
|
UTSW |
1 |
107,011,071 (GRCm39) |
missense |
probably benign |
0.09 |
R7178:Serpinb3d
|
UTSW |
1 |
107,008,506 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7743:Serpinb3d
|
UTSW |
1 |
107,007,088 (GRCm39) |
missense |
probably damaging |
0.99 |
R7765:Serpinb3d
|
UTSW |
1 |
107,007,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R8371:Serpinb3d
|
UTSW |
1 |
107,008,469 (GRCm39) |
missense |
probably damaging |
1.00 |
|