Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsbg3 |
A |
G |
17: 57,192,098 (GRCm39) |
S554G |
possibly damaging |
Het |
Adcy7 |
G |
T |
8: 89,042,378 (GRCm39) |
R415L |
probably damaging |
Het |
Aox1 |
A |
T |
1: 58,141,759 (GRCm39) |
I1182F |
probably damaging |
Het |
Ccdc7b |
T |
A |
8: 129,811,730 (GRCm39) |
Y147N |
probably benign |
Het |
Clcnka |
A |
G |
4: 141,118,691 (GRCm39) |
I398T |
probably damaging |
Het |
Cst8 |
T |
A |
2: 148,641,796 (GRCm39) |
|
probably null |
Het |
Dcxr |
T |
C |
11: 120,617,841 (GRCm39) |
D45G |
possibly damaging |
Het |
Dhx38 |
A |
T |
8: 110,283,617 (GRCm39) |
M510K |
possibly damaging |
Het |
Dync2i1 |
T |
C |
12: 116,218,061 (GRCm39) |
I182M |
probably benign |
Het |
Ebf1 |
T |
A |
11: 44,882,338 (GRCm39) |
H431Q |
probably damaging |
Het |
Eml4 |
T |
C |
17: 83,768,999 (GRCm39) |
I681T |
probably damaging |
Het |
Etf1 |
T |
C |
18: 35,043,219 (GRCm39) |
N164S |
probably benign |
Het |
Fmo2 |
A |
G |
1: 162,708,226 (GRCm39) |
V303A |
probably damaging |
Het |
Foxl2 |
T |
A |
9: 98,837,715 (GRCm39) |
M1K |
probably null |
Het |
Gm3404 |
A |
T |
5: 146,462,969 (GRCm39) |
E50D |
probably benign |
Het |
Gpr61 |
G |
A |
3: 108,058,647 (GRCm39) |
P5S |
possibly damaging |
Het |
Hcrtr1 |
A |
G |
4: 130,024,653 (GRCm39) |
|
probably benign |
Het |
Ier3ip1 |
T |
A |
18: 77,017,828 (GRCm39) |
F3I |
possibly damaging |
Het |
Ifi206 |
G |
A |
1: 173,308,808 (GRCm39) |
P396L |
|
Het |
Ifi209 |
G |
A |
1: 173,470,236 (GRCm39) |
V275I |
probably benign |
Het |
Ighv1-69 |
T |
C |
12: 115,586,909 (GRCm39) |
S75G |
probably benign |
Het |
Kcnj3 |
A |
T |
2: 55,484,877 (GRCm39) |
H325L |
possibly damaging |
Het |
Klrk1 |
A |
T |
6: 129,593,734 (GRCm39) |
S50T |
possibly damaging |
Het |
Mfsd4b4 |
T |
A |
10: 39,768,514 (GRCm39) |
Y193F |
probably damaging |
Het |
Nlrp5 |
A |
G |
7: 23,116,905 (GRCm39) |
I210V |
possibly damaging |
Het |
Or4p20 |
T |
A |
2: 88,253,746 (GRCm39) |
I208F |
possibly damaging |
Het |
Or5w12 |
A |
T |
2: 87,501,935 (GRCm39) |
Y259N |
possibly damaging |
Het |
Or8b3 |
G |
T |
9: 38,314,196 (GRCm39) |
G6C |
probably damaging |
Het |
Or8d23 |
A |
G |
9: 38,841,622 (GRCm39) |
S52G |
possibly damaging |
Het |
Pax6 |
A |
T |
2: 105,526,718 (GRCm39) |
H208L |
probably benign |
Het |
Pgc |
C |
A |
17: 48,044,745 (GRCm39) |
Q331K |
probably benign |
Het |
Phldb1 |
A |
G |
9: 44,605,721 (GRCm39) |
S370P |
probably damaging |
Het |
Pi4k2a |
T |
C |
19: 42,093,337 (GRCm39) |
I226T |
probably benign |
Het |
Pick1 |
T |
C |
15: 79,132,965 (GRCm39) |
S342P |
probably damaging |
Het |
Plscr1 |
A |
G |
9: 92,153,588 (GRCm39) |
M312V |
probably damaging |
Het |
Ppp3cc |
T |
G |
14: 70,462,468 (GRCm39) |
K399Q |
probably benign |
Het |
Qpctl |
T |
C |
7: 18,880,943 (GRCm39) |
H163R |
probably benign |
Het |
Rab11fip5 |
A |
G |
6: 85,351,110 (GRCm39) |
V134A |
possibly damaging |
Het |
Rasal1 |
T |
A |
5: 120,802,025 (GRCm39) |
|
probably null |
Het |
Rem2 |
T |
A |
14: 54,715,548 (GRCm39) |
I171N |
probably damaging |
Het |
Sec22a |
T |
A |
16: 35,149,885 (GRCm39) |
I214L |
probably benign |
Het |
Slc27a2 |
C |
T |
2: 126,409,700 (GRCm39) |
A294V |
probably damaging |
Het |
Slfn14 |
T |
A |
11: 83,167,430 (GRCm39) |
D695V |
probably damaging |
Het |
Smc6 |
T |
A |
12: 11,359,301 (GRCm39) |
I975K |
probably damaging |
Het |
Spice1 |
T |
C |
16: 44,206,043 (GRCm39) |
F835L |
probably benign |
Het |
Tars2 |
A |
T |
3: 95,658,057 (GRCm39) |
H222Q |
probably benign |
Het |
Tmtc2 |
A |
T |
10: 105,206,477 (GRCm39) |
F273I |
probably damaging |
Het |
Ttc39d |
C |
A |
17: 80,523,891 (GRCm39) |
D183E |
probably benign |
Het |
Vasp |
A |
G |
7: 18,995,946 (GRCm39) |
S128P |
probably benign |
Het |
Vcpip1 |
A |
G |
1: 9,818,378 (GRCm39) |
S2P |
unknown |
Het |
Vmn2r98 |
T |
C |
17: 19,301,184 (GRCm39) |
Y729H |
probably benign |
Het |
Wdr18 |
A |
T |
10: 79,801,944 (GRCm39) |
D243V |
probably benign |
Het |
Xirp2 |
T |
C |
2: 67,343,633 (GRCm39) |
V1958A |
probably benign |
Het |
Zfp451 |
A |
T |
1: 33,816,474 (GRCm39) |
M492K |
probably damaging |
Het |
Zfp804b |
A |
G |
5: 6,820,042 (GRCm39) |
I1007T |
probably benign |
Het |
|
Other mutations in Setbp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00582:Setbp1
|
APN |
18 |
78,798,894 (GRCm39) |
nonsense |
probably null |
0.00 |
IGL00668:Setbp1
|
APN |
18 |
78,900,985 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01628:Setbp1
|
APN |
18 |
78,899,992 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02084:Setbp1
|
APN |
18 |
78,900,625 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02405:Setbp1
|
APN |
18 |
78,900,514 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02427:Setbp1
|
APN |
18 |
78,900,688 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02612:Setbp1
|
APN |
18 |
78,798,925 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02725:Setbp1
|
APN |
18 |
78,900,589 (GRCm39) |
nonsense |
probably null |
|
IGL03005:Setbp1
|
APN |
18 |
78,902,340 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL03123:Setbp1
|
APN |
18 |
78,900,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R1083:Setbp1
|
UTSW |
18 |
78,900,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R1110:Setbp1
|
UTSW |
18 |
78,901,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R1167:Setbp1
|
UTSW |
18 |
78,900,451 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1221:Setbp1
|
UTSW |
18 |
78,899,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R1225:Setbp1
|
UTSW |
18 |
78,901,423 (GRCm39) |
missense |
probably damaging |
0.99 |
R1327:Setbp1
|
UTSW |
18 |
78,826,573 (GRCm39) |
missense |
probably benign |
0.00 |
R1481:Setbp1
|
UTSW |
18 |
78,826,516 (GRCm39) |
missense |
probably benign |
0.01 |
R1482:Setbp1
|
UTSW |
18 |
79,130,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R1496:Setbp1
|
UTSW |
18 |
78,903,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R1550:Setbp1
|
UTSW |
18 |
78,901,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R1708:Setbp1
|
UTSW |
18 |
78,901,682 (GRCm39) |
missense |
probably damaging |
0.99 |
R1751:Setbp1
|
UTSW |
18 |
78,900,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R1922:Setbp1
|
UTSW |
18 |
78,901,577 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1986:Setbp1
|
UTSW |
18 |
78,901,759 (GRCm39) |
missense |
probably damaging |
0.99 |
R2090:Setbp1
|
UTSW |
18 |
78,899,935 (GRCm39) |
missense |
probably benign |
0.00 |
R2851:Setbp1
|
UTSW |
18 |
78,967,211 (GRCm39) |
missense |
probably benign |
0.11 |
R2853:Setbp1
|
UTSW |
18 |
78,967,211 (GRCm39) |
missense |
probably benign |
0.11 |
R2941:Setbp1
|
UTSW |
18 |
78,901,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R3151:Setbp1
|
UTSW |
18 |
78,900,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R3156:Setbp1
|
UTSW |
18 |
78,902,518 (GRCm39) |
missense |
probably benign |
0.00 |
R3807:Setbp1
|
UTSW |
18 |
78,826,537 (GRCm39) |
missense |
probably benign |
0.01 |
R4133:Setbp1
|
UTSW |
18 |
78,900,206 (GRCm39) |
missense |
probably benign |
0.05 |
R4287:Setbp1
|
UTSW |
18 |
78,902,276 (GRCm39) |
missense |
probably benign |
0.03 |
R4345:Setbp1
|
UTSW |
18 |
79,129,794 (GRCm39) |
missense |
probably damaging |
0.99 |
R4374:Setbp1
|
UTSW |
18 |
78,903,137 (GRCm39) |
missense |
probably damaging |
0.97 |
R4377:Setbp1
|
UTSW |
18 |
78,903,137 (GRCm39) |
missense |
probably damaging |
0.97 |
R4378:Setbp1
|
UTSW |
18 |
78,899,833 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4379:Setbp1
|
UTSW |
18 |
79,129,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R4585:Setbp1
|
UTSW |
18 |
79,130,164 (GRCm39) |
missense |
probably benign |
0.00 |
R4595:Setbp1
|
UTSW |
18 |
78,900,731 (GRCm39) |
missense |
probably benign |
0.00 |
R4817:Setbp1
|
UTSW |
18 |
78,902,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R4971:Setbp1
|
UTSW |
18 |
78,901,382 (GRCm39) |
missense |
probably benign |
0.07 |
R4976:Setbp1
|
UTSW |
18 |
79,129,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R5017:Setbp1
|
UTSW |
18 |
78,899,809 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5066:Setbp1
|
UTSW |
18 |
78,900,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R5133:Setbp1
|
UTSW |
18 |
78,900,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R5151:Setbp1
|
UTSW |
18 |
78,901,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R5237:Setbp1
|
UTSW |
18 |
78,900,190 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5480:Setbp1
|
UTSW |
18 |
78,901,278 (GRCm39) |
missense |
probably damaging |
0.99 |
R5507:Setbp1
|
UTSW |
18 |
79,129,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R5529:Setbp1
|
UTSW |
18 |
79,129,867 (GRCm39) |
missense |
probably damaging |
0.99 |
R5622:Setbp1
|
UTSW |
18 |
78,900,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R5722:Setbp1
|
UTSW |
18 |
78,899,860 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5806:Setbp1
|
UTSW |
18 |
78,899,697 (GRCm39) |
splice site |
probably null |
|
R5940:Setbp1
|
UTSW |
18 |
78,798,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R6025:Setbp1
|
UTSW |
18 |
78,902,455 (GRCm39) |
missense |
probably damaging |
0.98 |
R6030:Setbp1
|
UTSW |
18 |
78,900,926 (GRCm39) |
missense |
probably benign |
0.02 |
R6030:Setbp1
|
UTSW |
18 |
78,900,926 (GRCm39) |
missense |
probably benign |
0.02 |
R6250:Setbp1
|
UTSW |
18 |
78,901,217 (GRCm39) |
missense |
probably benign |
0.00 |
R6256:Setbp1
|
UTSW |
18 |
78,900,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R6332:Setbp1
|
UTSW |
18 |
78,826,584 (GRCm39) |
missense |
probably benign |
0.21 |
R6522:Setbp1
|
UTSW |
18 |
78,900,605 (GRCm39) |
missense |
probably damaging |
0.98 |
R6873:Setbp1
|
UTSW |
18 |
78,902,774 (GRCm39) |
missense |
probably benign |
0.00 |
R6886:Setbp1
|
UTSW |
18 |
78,900,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R6986:Setbp1
|
UTSW |
18 |
78,901,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R7131:Setbp1
|
UTSW |
18 |
79,130,175 (GRCm39) |
missense |
probably benign |
0.08 |
R7134:Setbp1
|
UTSW |
18 |
78,902,734 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7215:Setbp1
|
UTSW |
18 |
78,900,052 (GRCm39) |
missense |
probably damaging |
0.97 |
R7219:Setbp1
|
UTSW |
18 |
78,798,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R7378:Setbp1
|
UTSW |
18 |
78,900,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R7461:Setbp1
|
UTSW |
18 |
78,899,707 (GRCm39) |
missense |
probably benign |
0.06 |
R7589:Setbp1
|
UTSW |
18 |
78,899,707 (GRCm39) |
missense |
probably benign |
0.01 |
R7840:Setbp1
|
UTSW |
18 |
78,826,639 (GRCm39) |
missense |
probably benign |
0.03 |
R7849:Setbp1
|
UTSW |
18 |
78,900,068 (GRCm39) |
missense |
probably benign |
0.00 |
R8147:Setbp1
|
UTSW |
18 |
78,900,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R8354:Setbp1
|
UTSW |
18 |
78,900,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R8446:Setbp1
|
UTSW |
18 |
78,900,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R8524:Setbp1
|
UTSW |
18 |
78,901,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R8534:Setbp1
|
UTSW |
18 |
78,826,542 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8694:Setbp1
|
UTSW |
18 |
78,901,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R8931:Setbp1
|
UTSW |
18 |
78,899,723 (GRCm39) |
missense |
probably benign |
0.00 |
R8983:Setbp1
|
UTSW |
18 |
78,902,459 (GRCm39) |
missense |
probably benign |
0.37 |
R9062:Setbp1
|
UTSW |
18 |
78,900,266 (GRCm39) |
missense |
probably benign |
0.01 |
R9113:Setbp1
|
UTSW |
18 |
78,900,948 (GRCm39) |
missense |
probably damaging |
0.99 |
R9364:Setbp1
|
UTSW |
18 |
78,826,599 (GRCm39) |
missense |
probably benign |
0.00 |
R9513:Setbp1
|
UTSW |
18 |
78,899,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R9517:Setbp1
|
UTSW |
18 |
78,901,322 (GRCm39) |
missense |
probably damaging |
0.99 |
R9549:Setbp1
|
UTSW |
18 |
78,902,629 (GRCm39) |
missense |
probably benign |
0.07 |
R9554:Setbp1
|
UTSW |
18 |
78,826,599 (GRCm39) |
missense |
probably benign |
0.00 |
R9680:Setbp1
|
UTSW |
18 |
78,902,498 (GRCm39) |
missense |
probably benign |
|
R9711:Setbp1
|
UTSW |
18 |
78,900,142 (GRCm39) |
missense |
probably benign |
0.30 |
Z1088:Setbp1
|
UTSW |
18 |
78,902,809 (GRCm39) |
missense |
probably damaging |
0.98 |
|