Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afap1l1 |
A |
G |
18: 61,866,860 (GRCm39) |
L733P |
probably benign |
Het |
Aqr |
G |
A |
2: 113,949,261 (GRCm39) |
A979V |
possibly damaging |
Het |
Axin1 |
A |
G |
17: 26,407,153 (GRCm39) |
E582G |
probably benign |
Het |
Catsper1 |
T |
C |
19: 5,386,264 (GRCm39) |
S166P |
possibly damaging |
Het |
Cd248 |
G |
T |
19: 5,120,201 (GRCm39) |
G683V |
probably damaging |
Het |
Celsr1 |
G |
T |
15: 85,915,427 (GRCm39) |
Q849K |
possibly damaging |
Het |
Ctnnal1 |
C |
A |
4: 56,835,306 (GRCm39) |
V324F |
probably benign |
Het |
Ctrc |
C |
A |
4: 141,571,028 (GRCm39) |
V71L |
possibly damaging |
Het |
Exoc3l |
C |
A |
8: 106,019,070 (GRCm39) |
D465Y |
probably damaging |
Het |
Flna |
T |
C |
X: 73,284,888 (GRCm39) |
E417G |
probably benign |
Het |
Grm6 |
T |
A |
11: 50,750,766 (GRCm39) |
V643D |
probably damaging |
Het |
Inpp4b |
A |
G |
8: 82,759,800 (GRCm39) |
Y615C |
probably benign |
Het |
Itga3 |
T |
C |
11: 94,959,597 (GRCm39) |
Y92C |
probably damaging |
Het |
Jak3 |
T |
C |
8: 72,138,763 (GRCm39) |
|
probably null |
Het |
Kcnh6 |
T |
A |
11: 105,918,460 (GRCm39) |
I823N |
possibly damaging |
Het |
Klhl38 |
A |
T |
15: 58,186,417 (GRCm39) |
V104D |
probably damaging |
Het |
Lpo |
C |
T |
11: 87,697,732 (GRCm39) |
V692M |
possibly damaging |
Het |
Mnd1 |
T |
C |
3: 84,023,786 (GRCm39) |
H100R |
probably benign |
Het |
Mterf4 |
A |
G |
1: 93,230,526 (GRCm39) |
F207L |
probably damaging |
Het |
Oog3 |
C |
A |
4: 143,884,721 (GRCm39) |
W405L |
probably benign |
Het |
Or2t26 |
T |
C |
11: 49,039,384 (GRCm39) |
L100P |
probably damaging |
Het |
Ptpn3 |
A |
G |
4: 57,205,020 (GRCm39) |
Y714H |
probably damaging |
Het |
Spata31f3 |
T |
C |
4: 42,868,549 (GRCm39) |
D358G |
probably damaging |
Het |
Steap3 |
T |
C |
1: 120,169,502 (GRCm39) |
Y265C |
probably damaging |
Het |
Tcl1 |
C |
A |
12: 105,185,082 (GRCm39) |
E43* |
probably null |
Het |
Terb1 |
A |
G |
8: 105,221,500 (GRCm39) |
|
probably null |
Het |
Tmprss11a |
T |
A |
5: 86,570,507 (GRCm39) |
I151F |
possibly damaging |
Het |
Trappc10 |
T |
C |
10: 78,046,610 (GRCm39) |
R430G |
probably damaging |
Het |
Usp17le |
T |
C |
7: 104,418,933 (GRCm39) |
N70D |
probably benign |
Het |
Vmn1r45 |
T |
C |
6: 89,910,503 (GRCm39) |
S36G |
possibly damaging |
Het |
Vsig8 |
A |
C |
1: 172,387,943 (GRCm39) |
Y11S |
probably damaging |
Het |
Vwa5b2 |
T |
A |
16: 20,416,851 (GRCm39) |
L516Q |
probably damaging |
Het |
|
Other mutations in Abcc5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00917:Abcc5
|
APN |
16 |
20,241,107 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00928:Abcc5
|
APN |
16 |
20,217,720 (GRCm39) |
unclassified |
probably benign |
|
IGL01350:Abcc5
|
APN |
16 |
20,187,208 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01774:Abcc5
|
APN |
16 |
20,197,207 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01934:Abcc5
|
APN |
16 |
20,241,191 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02426:Abcc5
|
APN |
16 |
20,157,675 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02797:Abcc5
|
APN |
16 |
20,187,214 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02938:Abcc5
|
APN |
16 |
20,180,979 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL03367:Abcc5
|
APN |
16 |
20,211,561 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL03411:Abcc5
|
APN |
16 |
20,218,310 (GRCm39) |
missense |
probably damaging |
0.97 |
PIT4508001:Abcc5
|
UTSW |
16 |
20,176,128 (GRCm39) |
missense |
probably damaging |
0.97 |
R0021:Abcc5
|
UTSW |
16 |
20,197,411 (GRCm39) |
nonsense |
probably null |
|
R0021:Abcc5
|
UTSW |
16 |
20,197,411 (GRCm39) |
nonsense |
probably null |
|
R0220:Abcc5
|
UTSW |
16 |
20,187,852 (GRCm39) |
missense |
probably benign |
|
R0281:Abcc5
|
UTSW |
16 |
20,241,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R0401:Abcc5
|
UTSW |
16 |
20,195,308 (GRCm39) |
missense |
probably benign |
0.09 |
R0448:Abcc5
|
UTSW |
16 |
20,218,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R0477:Abcc5
|
UTSW |
16 |
20,217,635 (GRCm39) |
missense |
probably damaging |
0.96 |
R0477:Abcc5
|
UTSW |
16 |
20,187,319 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0601:Abcc5
|
UTSW |
16 |
20,223,309 (GRCm39) |
splice site |
probably benign |
|
R0648:Abcc5
|
UTSW |
16 |
20,184,632 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0709:Abcc5
|
UTSW |
16 |
20,195,342 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1144:Abcc5
|
UTSW |
16 |
20,241,188 (GRCm39) |
utr 5 prime |
probably benign |
|
R1552:Abcc5
|
UTSW |
16 |
20,217,617 (GRCm39) |
missense |
probably damaging |
0.99 |
R1625:Abcc5
|
UTSW |
16 |
20,184,567 (GRCm39) |
missense |
probably damaging |
0.99 |
R1748:Abcc5
|
UTSW |
16 |
20,152,338 (GRCm39) |
missense |
probably benign |
0.01 |
R1789:Abcc5
|
UTSW |
16 |
20,184,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R1801:Abcc5
|
UTSW |
16 |
20,157,637 (GRCm39) |
missense |
probably benign |
0.43 |
R1909:Abcc5
|
UTSW |
16 |
20,195,259 (GRCm39) |
critical splice donor site |
probably null |
|
R2046:Abcc5
|
UTSW |
16 |
20,218,567 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2203:Abcc5
|
UTSW |
16 |
20,224,632 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3031:Abcc5
|
UTSW |
16 |
20,193,863 (GRCm39) |
missense |
probably damaging |
0.99 |
R3417:Abcc5
|
UTSW |
16 |
20,224,302 (GRCm39) |
splice site |
probably benign |
|
R3708:Abcc5
|
UTSW |
16 |
20,190,930 (GRCm39) |
missense |
probably benign |
0.30 |
R3731:Abcc5
|
UTSW |
16 |
20,217,684 (GRCm39) |
nonsense |
probably null |
|
R3829:Abcc5
|
UTSW |
16 |
20,184,615 (GRCm39) |
missense |
probably benign |
0.00 |
R3847:Abcc5
|
UTSW |
16 |
20,190,906 (GRCm39) |
missense |
probably benign |
0.12 |
R3850:Abcc5
|
UTSW |
16 |
20,190,906 (GRCm39) |
missense |
probably benign |
0.12 |
R3955:Abcc5
|
UTSW |
16 |
20,224,293 (GRCm39) |
missense |
probably damaging |
0.97 |
R4072:Abcc5
|
UTSW |
16 |
20,152,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R4432:Abcc5
|
UTSW |
16 |
20,186,937 (GRCm39) |
splice site |
probably null |
|
R4433:Abcc5
|
UTSW |
16 |
20,186,937 (GRCm39) |
splice site |
probably null |
|
R4505:Abcc5
|
UTSW |
16 |
20,152,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R4506:Abcc5
|
UTSW |
16 |
20,152,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R4715:Abcc5
|
UTSW |
16 |
20,217,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R4739:Abcc5
|
UTSW |
16 |
20,218,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R4866:Abcc5
|
UTSW |
16 |
20,241,182 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R4905:Abcc5
|
UTSW |
16 |
20,218,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R4907:Abcc5
|
UTSW |
16 |
20,195,296 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5088:Abcc5
|
UTSW |
16 |
20,195,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R5232:Abcc5
|
UTSW |
16 |
20,157,672 (GRCm39) |
missense |
probably damaging |
0.96 |
R5559:Abcc5
|
UTSW |
16 |
20,157,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R5647:Abcc5
|
UTSW |
16 |
20,218,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R5861:Abcc5
|
UTSW |
16 |
20,218,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R6190:Abcc5
|
UTSW |
16 |
20,211,529 (GRCm39) |
missense |
probably benign |
0.02 |
R6213:Abcc5
|
UTSW |
16 |
20,218,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R6511:Abcc5
|
UTSW |
16 |
20,195,344 (GRCm39) |
missense |
probably damaging |
0.99 |
R6732:Abcc5
|
UTSW |
16 |
20,223,434 (GRCm39) |
missense |
probably benign |
0.01 |
R6815:Abcc5
|
UTSW |
16 |
20,152,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R6913:Abcc5
|
UTSW |
16 |
20,197,494 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6945:Abcc5
|
UTSW |
16 |
20,218,759 (GRCm39) |
missense |
probably benign |
|
R7167:Abcc5
|
UTSW |
16 |
20,224,251 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7276:Abcc5
|
UTSW |
16 |
20,195,258 (GRCm39) |
splice site |
probably null |
|
R7318:Abcc5
|
UTSW |
16 |
20,211,293 (GRCm39) |
missense |
probably benign |
0.01 |
R7380:Abcc5
|
UTSW |
16 |
20,215,784 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7419:Abcc5
|
UTSW |
16 |
20,241,173 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7451:Abcc5
|
UTSW |
16 |
20,193,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R7475:Abcc5
|
UTSW |
16 |
20,218,739 (GRCm39) |
missense |
probably benign |
0.04 |
R7567:Abcc5
|
UTSW |
16 |
20,224,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R7601:Abcc5
|
UTSW |
16 |
20,193,882 (GRCm39) |
nonsense |
probably null |
|
R7623:Abcc5
|
UTSW |
16 |
20,163,446 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7682:Abcc5
|
UTSW |
16 |
20,186,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R8128:Abcc5
|
UTSW |
16 |
20,184,473 (GRCm39) |
missense |
probably damaging |
0.98 |
R8327:Abcc5
|
UTSW |
16 |
20,241,068 (GRCm39) |
missense |
probably benign |
0.00 |
R8518:Abcc5
|
UTSW |
16 |
20,223,398 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8678:Abcc5
|
UTSW |
16 |
20,184,685 (GRCm39) |
missense |
probably benign |
0.31 |
R8679:Abcc5
|
UTSW |
16 |
20,152,479 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9206:Abcc5
|
UTSW |
16 |
20,208,139 (GRCm39) |
missense |
probably benign |
0.00 |
R9254:Abcc5
|
UTSW |
16 |
20,152,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R9379:Abcc5
|
UTSW |
16 |
20,152,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R9501:Abcc5
|
UTSW |
16 |
20,214,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R9647:Abcc5
|
UTSW |
16 |
20,195,310 (GRCm39) |
missense |
probably benign |
0.01 |
X0022:Abcc5
|
UTSW |
16 |
20,211,337 (GRCm39) |
missense |
probably damaging |
1.00 |
X0053:Abcc5
|
UTSW |
16 |
20,182,792 (GRCm39) |
missense |
probably damaging |
0.98 |
|