Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700029H14Rik |
T |
C |
8: 13,601,842 (GRCm39) |
|
probably benign |
Het |
5730507C01Rik |
A |
T |
12: 18,583,424 (GRCm39) |
R161S |
possibly damaging |
Het |
Adamts5 |
T |
C |
16: 85,663,530 (GRCm39) |
I735V |
probably benign |
Het |
Arid1a |
G |
T |
4: 133,408,435 (GRCm39) |
P2024Q |
unknown |
Het |
Ascc3 |
G |
T |
10: 50,625,022 (GRCm39) |
V1637L |
probably benign |
Het |
B3galt4 |
T |
C |
17: 34,169,764 (GRCm39) |
Y158C |
probably damaging |
Het |
BC049715 |
A |
G |
6: 136,817,143 (GRCm39) |
T128A |
possibly damaging |
Het |
Btaf1 |
T |
A |
19: 36,922,629 (GRCm39) |
I11N |
probably damaging |
Het |
Cfb |
T |
C |
17: 35,077,485 (GRCm39) |
I496V |
probably damaging |
Het |
Chd8 |
A |
T |
14: 52,441,517 (GRCm39) |
H858Q |
probably benign |
Het |
Chrne |
T |
C |
11: 70,506,549 (GRCm39) |
I324V |
probably benign |
Het |
Clec14a |
T |
C |
12: 58,314,451 (GRCm39) |
I390M |
probably damaging |
Het |
Cpsf3 |
A |
G |
12: 21,347,800 (GRCm39) |
Y207C |
probably damaging |
Het |
Cubn |
A |
C |
2: 13,474,574 (GRCm39) |
I410S |
possibly damaging |
Het |
Cubn |
T |
A |
2: 13,474,575 (GRCm39) |
I410F |
possibly damaging |
Het |
Dlc1 |
T |
C |
8: 37,050,740 (GRCm39) |
E997G |
possibly damaging |
Het |
Emilin1 |
G |
T |
5: 31,072,366 (GRCm39) |
V71F |
probably damaging |
Het |
Esrp2 |
T |
C |
8: 106,861,307 (GRCm39) |
E164G |
probably damaging |
Het |
Fars2 |
A |
G |
13: 36,721,285 (GRCm39) |
T410A |
probably benign |
Het |
Fat3 |
A |
G |
9: 15,903,552 (GRCm39) |
V2981A |
probably damaging |
Het |
Fkbp15 |
G |
A |
4: 62,244,373 (GRCm39) |
T472I |
probably benign |
Het |
Gm6871 |
A |
G |
7: 41,222,869 (GRCm39) |
V73A |
probably benign |
Het |
Gnl2 |
T |
G |
4: 124,947,320 (GRCm39) |
S647R |
probably benign |
Het |
Grb10 |
T |
C |
11: 11,884,207 (GRCm39) |
I500V |
possibly damaging |
Het |
Herc1 |
T |
C |
9: 66,353,356 (GRCm39) |
|
probably benign |
Het |
Iqgap2 |
A |
C |
13: 95,826,207 (GRCm39) |
|
probably null |
Het |
Kcnu1 |
A |
T |
8: 26,427,646 (GRCm39) |
N321I |
probably benign |
Het |
Kif23 |
G |
A |
9: 61,833,687 (GRCm39) |
R519* |
probably null |
Het |
Klhl1 |
C |
T |
14: 96,619,225 (GRCm39) |
R224Q |
probably benign |
Het |
Lama1 |
T |
C |
17: 68,098,605 (GRCm39) |
|
probably null |
Het |
Lamp3 |
T |
C |
16: 19,492,302 (GRCm39) |
Y314C |
probably damaging |
Het |
Lamtor5 |
C |
A |
3: 107,189,227 (GRCm39) |
R88S |
probably damaging |
Het |
Nbea |
G |
T |
3: 55,726,715 (GRCm39) |
A2088E |
probably benign |
Het |
Neo1 |
A |
G |
9: 58,897,463 (GRCm39) |
|
probably benign |
Het |
Ntn4 |
A |
T |
10: 93,518,291 (GRCm39) |
R199S |
probably benign |
Het |
Or5ap2 |
A |
T |
2: 85,680,311 (GRCm39) |
R172* |
probably null |
Het |
Plekho2 |
A |
G |
9: 65,464,334 (GRCm39) |
S172P |
possibly damaging |
Het |
Pmp2 |
T |
C |
3: 10,245,823 (GRCm39) |
Y129C |
probably damaging |
Het |
Prss3b |
T |
C |
6: 41,011,281 (GRCm39) |
N34D |
probably benign |
Het |
Ralgapa2 |
A |
T |
2: 146,270,592 (GRCm39) |
M578K |
possibly damaging |
Het |
Ranbp3 |
C |
T |
17: 57,015,219 (GRCm39) |
T307M |
possibly damaging |
Het |
Setdb2 |
A |
T |
14: 59,644,193 (GRCm39) |
|
probably null |
Het |
Sirpb1b |
A |
T |
3: 15,613,656 (GRCm39) |
V75E |
probably damaging |
Het |
Slc13a1 |
A |
T |
6: 24,100,292 (GRCm39) |
L397Q |
probably damaging |
Het |
Slc19a1 |
T |
A |
10: 76,878,742 (GRCm39) |
I355N |
probably damaging |
Het |
Slc51a |
T |
A |
16: 32,295,254 (GRCm39) |
I275F |
possibly damaging |
Het |
Spink14 |
T |
C |
18: 44,164,934 (GRCm39) |
S84P |
probably damaging |
Het |
Stx2 |
A |
G |
5: 129,070,641 (GRCm39) |
|
probably benign |
Het |
Tgfbi |
G |
T |
13: 56,780,006 (GRCm39) |
|
probably benign |
Het |
Tshr |
T |
A |
12: 91,504,643 (GRCm39) |
M527K |
probably damaging |
Het |
Upb1 |
T |
C |
10: 75,248,717 (GRCm39) |
V79A |
probably damaging |
Het |
Zdhhc5 |
A |
T |
2: 84,521,587 (GRCm39) |
|
probably null |
Het |
Zfp11 |
C |
T |
5: 129,735,302 (GRCm39) |
G53E |
possibly damaging |
Het |
Zfp280d |
T |
C |
9: 72,219,519 (GRCm39) |
V32A |
probably benign |
Het |
|
Other mutations in Serpinb11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01487:Serpinb11
|
APN |
1 |
107,307,568 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01893:Serpinb11
|
APN |
1 |
107,305,388 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01893:Serpinb11
|
APN |
1 |
107,305,387 (GRCm39) |
missense |
probably benign |
|
IGL03011:Serpinb11
|
APN |
1 |
107,307,546 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03126:Serpinb11
|
APN |
1 |
107,307,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R0138:Serpinb11
|
UTSW |
1 |
107,305,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R0153:Serpinb11
|
UTSW |
1 |
107,299,933 (GRCm39) |
missense |
probably benign |
0.07 |
R1550:Serpinb11
|
UTSW |
1 |
107,307,418 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1764:Serpinb11
|
UTSW |
1 |
107,304,532 (GRCm39) |
missense |
probably benign |
0.03 |
R1972:Serpinb11
|
UTSW |
1 |
107,297,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R3103:Serpinb11
|
UTSW |
1 |
107,305,338 (GRCm39) |
missense |
probably benign |
0.07 |
R3768:Serpinb11
|
UTSW |
1 |
107,305,392 (GRCm39) |
critical splice donor site |
probably null |
|
R4332:Serpinb11
|
UTSW |
1 |
107,297,294 (GRCm39) |
critical splice donor site |
probably null |
|
R5001:Serpinb11
|
UTSW |
1 |
107,304,598 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5010:Serpinb11
|
UTSW |
1 |
107,307,379 (GRCm39) |
missense |
probably benign |
|
R5043:Serpinb11
|
UTSW |
1 |
107,297,195 (GRCm39) |
missense |
probably damaging |
0.97 |
R5186:Serpinb11
|
UTSW |
1 |
107,307,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R5833:Serpinb11
|
UTSW |
1 |
107,305,392 (GRCm39) |
critical splice donor site |
probably null |
|
R5907:Serpinb11
|
UTSW |
1 |
107,299,919 (GRCm39) |
missense |
probably benign |
0.12 |
R6244:Serpinb11
|
UTSW |
1 |
107,299,972 (GRCm39) |
missense |
probably damaging |
0.99 |
R6395:Serpinb11
|
UTSW |
1 |
107,299,781 (GRCm39) |
splice site |
probably null |
|
R7111:Serpinb11
|
UTSW |
1 |
107,304,614 (GRCm39) |
missense |
probably benign |
0.00 |
R7354:Serpinb11
|
UTSW |
1 |
107,305,263 (GRCm39) |
missense |
probably benign |
0.03 |
R7664:Serpinb11
|
UTSW |
1 |
107,307,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R8075:Serpinb11
|
UTSW |
1 |
107,298,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R8223:Serpinb11
|
UTSW |
1 |
107,305,262 (GRCm39) |
missense |
probably benign |
0.01 |
R9091:Serpinb11
|
UTSW |
1 |
107,304,533 (GRCm39) |
missense |
probably benign |
0.15 |
R9270:Serpinb11
|
UTSW |
1 |
107,304,533 (GRCm39) |
missense |
probably benign |
0.15 |
|