Other mutations in this stock |
Total: 113 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700001O22Rik |
A |
T |
2: 30,686,566 (GRCm39) |
I242N |
probably benign |
Het |
2510009E07Rik |
G |
T |
16: 21,472,048 (GRCm39) |
Y217* |
probably null |
Het |
4931429L15Rik |
C |
T |
9: 46,220,086 (GRCm39) |
V149M |
probably benign |
Het |
Abcg8 |
G |
T |
17: 85,002,587 (GRCm39) |
|
probably benign |
Het |
Acox1 |
A |
G |
11: 116,089,087 (GRCm39) |
F77S |
probably benign |
Het |
Adgrb3 |
G |
T |
1: 25,586,525 (GRCm39) |
H389Q |
probably benign |
Het |
Ak7 |
A |
G |
12: 105,692,504 (GRCm39) |
N186S |
probably damaging |
Het |
Apobr |
A |
G |
7: 126,185,397 (GRCm39) |
T303A |
probably benign |
Het |
Arnt |
C |
T |
3: 95,355,704 (GRCm39) |
S16L |
possibly damaging |
Het |
Bcl9l |
T |
C |
9: 44,419,996 (GRCm39) |
|
probably null |
Het |
Bco2 |
T |
C |
9: 50,457,284 (GRCm39) |
D86G |
probably damaging |
Het |
Bmpr1b |
T |
A |
3: 141,563,333 (GRCm39) |
I204F |
probably damaging |
Het |
Bpifb5 |
C |
A |
2: 154,072,264 (GRCm39) |
Q324K |
probably benign |
Het |
Cacna2d2 |
G |
A |
9: 107,389,205 (GRCm39) |
V223I |
probably damaging |
Het |
Capn3 |
A |
G |
2: 120,311,228 (GRCm39) |
D105G |
possibly damaging |
Het |
Ccdc40 |
G |
T |
11: 119,153,901 (GRCm39) |
|
probably null |
Het |
Ccdc83 |
T |
A |
7: 89,893,362 (GRCm39) |
S132C |
probably damaging |
Het |
Ckap2l |
A |
G |
2: 129,127,342 (GRCm39) |
S279P |
possibly damaging |
Het |
Cldn12 |
C |
A |
5: 5,558,137 (GRCm39) |
A97S |
probably benign |
Het |
Clec2l |
T |
G |
6: 38,640,309 (GRCm39) |
S47A |
probably benign |
Het |
Csnk1d |
C |
A |
11: 120,863,274 (GRCm39) |
R222M |
possibly damaging |
Het |
Ctnna1 |
T |
A |
18: 35,287,580 (GRCm39) |
D96E |
probably benign |
Het |
D630045J12Rik |
T |
C |
6: 38,145,078 (GRCm39) |
D1316G |
probably damaging |
Het |
Ddx4 |
C |
T |
13: 112,736,547 (GRCm39) |
V608I |
probably damaging |
Het |
Dmtf1 |
T |
C |
5: 9,198,989 (GRCm39) |
E48G |
probably benign |
Het |
Dnah17 |
G |
C |
11: 117,995,361 (GRCm39) |
Q996E |
probably benign |
Het |
Dnah9 |
G |
C |
11: 65,739,197 (GRCm39) |
N4180K |
probably damaging |
Het |
Dpf3 |
T |
A |
12: 83,371,809 (GRCm39) |
|
probably null |
Het |
Drd2 |
T |
C |
9: 49,318,359 (GRCm39) |
F434L |
probably damaging |
Het |
En1 |
A |
G |
1: 120,534,742 (GRCm39) |
T344A |
unknown |
Het |
Eri3 |
A |
G |
4: 117,421,964 (GRCm39) |
T81A |
probably benign |
Het |
Fam20a |
T |
C |
11: 109,576,237 (GRCm39) |
Y174C |
probably damaging |
Het |
Fam234a |
G |
C |
17: 26,435,629 (GRCm39) |
|
probably null |
Het |
Fam76a |
A |
T |
4: 132,631,294 (GRCm39) |
I217N |
probably damaging |
Het |
Fancm |
T |
A |
12: 65,148,466 (GRCm39) |
S694T |
probably benign |
Het |
Fcgbpl1 |
C |
A |
7: 27,830,937 (GRCm39) |
A50E |
possibly damaging |
Het |
Foxo3 |
A |
G |
10: 42,073,258 (GRCm39) |
S420P |
probably benign |
Het |
Foxp4 |
C |
T |
17: 48,186,796 (GRCm39) |
R378Q |
unknown |
Het |
Gm136 |
T |
G |
4: 34,755,986 (GRCm39) |
D9A |
probably benign |
Het |
Gstt2 |
G |
T |
10: 75,668,499 (GRCm39) |
T116N |
probably benign |
Het |
Hs3st6 |
A |
G |
17: 24,972,267 (GRCm39) |
T70A |
probably benign |
Het |
Hspa14 |
A |
G |
2: 3,490,804 (GRCm39) |
V461A |
possibly damaging |
Het |
Itih5 |
A |
T |
2: 10,243,379 (GRCm39) |
D372V |
probably damaging |
Het |
Kcna2 |
A |
T |
3: 107,012,140 (GRCm39) |
R240S |
probably damaging |
Het |
Kctd18 |
T |
C |
1: 58,006,779 (GRCm39) |
I24V |
probably benign |
Het |
Lap3 |
T |
C |
5: 45,663,508 (GRCm39) |
|
probably benign |
Het |
Lcp1 |
T |
C |
14: 75,437,946 (GRCm39) |
S119P |
probably damaging |
Het |
Lig3 |
G |
C |
11: 82,686,544 (GRCm39) |
D642H |
probably benign |
Het |
Lpin1 |
A |
T |
12: 16,630,724 (GRCm39) |
L58H |
probably damaging |
Het |
Map4k5 |
G |
T |
12: 69,873,102 (GRCm39) |
P468Q |
possibly damaging |
Het |
Med31 |
G |
A |
11: 72,106,244 (GRCm39) |
|
probably benign |
Het |
Mki67 |
A |
T |
7: 135,315,688 (GRCm39) |
|
probably null |
Het |
Mrc1 |
G |
A |
2: 14,249,103 (GRCm39) |
|
probably null |
Het |
Msh3 |
A |
G |
13: 92,359,784 (GRCm39) |
I16T |
probably damaging |
Het |
Msh3 |
T |
A |
13: 92,386,328 (GRCm39) |
|
probably benign |
Het |
Myb |
A |
C |
10: 21,016,555 (GRCm39) |
S652A |
probably benign |
Het |
Myh2 |
G |
T |
11: 67,080,004 (GRCm39) |
S1099I |
possibly damaging |
Het |
Myl6b |
A |
G |
10: 128,330,512 (GRCm39) |
V181A |
probably damaging |
Het |
Myt1l |
A |
T |
12: 29,877,091 (GRCm39) |
K247N |
unknown |
Het |
Nanos2 |
G |
T |
7: 18,721,629 (GRCm39) |
V34L |
probably benign |
Het |
Nav1 |
T |
C |
1: 135,460,091 (GRCm39) |
T411A |
probably benign |
Het |
Nedd9 |
T |
A |
13: 41,492,424 (GRCm39) |
I23F |
probably damaging |
Het |
Nes |
G |
A |
3: 87,885,634 (GRCm39) |
V1254I |
possibly damaging |
Het |
Nol6 |
A |
G |
4: 41,119,542 (GRCm39) |
F588S |
probably damaging |
Het |
Numa1 |
C |
T |
7: 101,658,529 (GRCm39) |
A1605V |
probably damaging |
Het |
Ofd1 |
T |
C |
X: 165,210,210 (GRCm39) |
Y205C |
probably benign |
Het |
Olr1 |
T |
C |
6: 129,470,498 (GRCm39) |
E223G |
probably benign |
Het |
Or1e30 |
T |
A |
11: 73,678,616 (GRCm39) |
M284K |
probably damaging |
Het |
Or2ag12 |
T |
A |
7: 106,276,877 (GRCm39) |
N272I |
probably damaging |
Het |
Or4c118 |
A |
T |
2: 88,975,078 (GRCm39) |
C96* |
probably null |
Het |
Or51k2 |
A |
T |
7: 103,596,150 (GRCm39) |
I126F |
probably damaging |
Het |
Or51l4 |
C |
T |
7: 103,404,527 (GRCm39) |
W88* |
probably null |
Het |
Pate6 |
T |
A |
9: 35,700,309 (GRCm39) |
H92L |
probably benign |
Het |
Pclo |
A |
G |
5: 14,763,487 (GRCm39) |
T3987A |
unknown |
Het |
Pik3cg |
A |
T |
12: 32,242,152 (GRCm39) |
V986D |
probably damaging |
Het |
Pitpnm1 |
T |
A |
19: 4,162,450 (GRCm39) |
D1093E |
probably damaging |
Het |
Ppp1r12b |
T |
C |
1: 134,793,651 (GRCm39) |
D571G |
probably benign |
Het |
Rfx1 |
A |
G |
8: 84,822,126 (GRCm39) |
E875G |
probably damaging |
Het |
Rnf145 |
T |
A |
11: 44,439,642 (GRCm39) |
I146N |
probably damaging |
Het |
Rttn |
G |
A |
18: 89,108,557 (GRCm39) |
R1587H |
probably benign |
Het |
Safb |
A |
G |
17: 56,912,821 (GRCm39) |
H883R |
probably benign |
Het |
Sdhb |
A |
G |
4: 140,700,260 (GRCm39) |
D120G |
possibly damaging |
Het |
Serpine3 |
A |
G |
14: 62,902,533 (GRCm39) |
N48S |
probably damaging |
Het |
Sgms1 |
T |
A |
19: 32,137,357 (GRCm39) |
I70L |
probably benign |
Het |
Slc1a7 |
G |
T |
4: 107,825,782 (GRCm39) |
D14Y |
probably benign |
Het |
Smtnl2 |
C |
T |
11: 72,302,183 (GRCm39) |
A93T |
probably benign |
Het |
Srpra |
T |
C |
9: 35,124,834 (GRCm39) |
|
probably null |
Het |
Taf6l |
A |
G |
19: 8,752,866 (GRCm39) |
|
probably null |
Het |
Tbc1d10b |
A |
T |
7: 126,807,036 (GRCm39) |
V167E |
probably benign |
Het |
Tbc1d9 |
G |
A |
8: 83,976,139 (GRCm39) |
R566H |
probably damaging |
Het |
Tenm3 |
A |
G |
8: 48,689,348 (GRCm39) |
Y2080H |
probably damaging |
Het |
Tex14 |
A |
G |
11: 87,402,431 (GRCm39) |
N506S |
probably damaging |
Het |
Thada |
G |
T |
17: 84,617,470 (GRCm39) |
P1349T |
probably damaging |
Het |
Tjp1 |
G |
T |
7: 64,973,826 (GRCm39) |
T476K |
probably damaging |
Het |
Tlr11 |
A |
T |
14: 50,598,691 (GRCm39) |
T226S |
probably benign |
Het |
Tmem131 |
G |
A |
1: 36,843,680 (GRCm39) |
Q1394* |
probably null |
Het |
Tmem161a |
C |
T |
8: 70,629,559 (GRCm39) |
R58W |
probably damaging |
Het |
Tmem219 |
T |
C |
7: 126,496,422 (GRCm39) |
S13G |
probably benign |
Het |
Trp53bp1 |
T |
C |
2: 121,035,517 (GRCm39) |
Y47C |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,731,922 (GRCm39) |
|
probably benign |
Het |
Ush1g |
A |
G |
11: 115,209,280 (GRCm39) |
S305P |
probably damaging |
Het |
Usp37 |
A |
T |
1: 74,479,127 (GRCm39) |
Y948* |
probably null |
Het |
Vav1 |
A |
T |
17: 57,634,697 (GRCm39) |
Y805F |
probably damaging |
Het |
Vmn1r59 |
A |
T |
7: 5,457,038 (GRCm39) |
Y241N |
probably damaging |
Het |
Vmn2r2 |
T |
A |
3: 64,034,121 (GRCm39) |
Y467F |
probably damaging |
Het |
Vps35l |
A |
C |
7: 118,374,557 (GRCm39) |
R352S |
probably damaging |
Het |
Vps54 |
C |
A |
11: 21,242,051 (GRCm39) |
L389I |
probably damaging |
Het |
Vwa8 |
G |
T |
14: 79,162,694 (GRCm39) |
|
probably benign |
Het |
Wdr19 |
G |
T |
5: 65,398,503 (GRCm39) |
|
probably benign |
Het |
Wnt2b |
A |
T |
3: 104,861,933 (GRCm39) |
|
probably benign |
Het |
Xirp2 |
A |
G |
2: 67,342,039 (GRCm39) |
R1427G |
possibly damaging |
Het |
Ylpm1 |
T |
C |
12: 85,087,560 (GRCm39) |
S1115P |
probably damaging |
Het |
Zfp946 |
T |
A |
17: 22,674,406 (GRCm39) |
C387S |
probably damaging |
Het |
|
Other mutations in Mst1r |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00429:Mst1r
|
APN |
9 |
107,790,449 (GRCm39) |
splice site |
probably benign |
|
IGL01327:Mst1r
|
APN |
9 |
107,785,043 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01572:Mst1r
|
APN |
9 |
107,788,791 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01968:Mst1r
|
APN |
9 |
107,794,005 (GRCm39) |
splice site |
probably null |
|
IGL01983:Mst1r
|
APN |
9 |
107,794,475 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02096:Mst1r
|
APN |
9 |
107,794,478 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02203:Mst1r
|
APN |
9 |
107,785,068 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02203:Mst1r
|
APN |
9 |
107,790,348 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02332:Mst1r
|
APN |
9 |
107,785,025 (GRCm39) |
nonsense |
probably null |
|
IGL02402:Mst1r
|
APN |
9 |
107,794,026 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02404:Mst1r
|
APN |
9 |
107,790,266 (GRCm39) |
splice site |
probably benign |
|
IGL02942:Mst1r
|
APN |
9 |
107,790,352 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02951:Mst1r
|
APN |
9 |
107,785,403 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02975:Mst1r
|
APN |
9 |
107,790,379 (GRCm39) |
missense |
probably benign |
0.20 |
IGL03005:Mst1r
|
APN |
9 |
107,791,748 (GRCm39) |
nonsense |
probably null |
|
IGL03304:Mst1r
|
APN |
9 |
107,785,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R0386:Mst1r
|
UTSW |
9 |
107,794,003 (GRCm39) |
splice site |
probably null |
|
R0833:Mst1r
|
UTSW |
9 |
107,791,975 (GRCm39) |
missense |
probably benign |
0.00 |
R0833:Mst1r
|
UTSW |
9 |
107,790,366 (GRCm39) |
missense |
probably benign |
|
R1139:Mst1r
|
UTSW |
9 |
107,797,168 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1371:Mst1r
|
UTSW |
9 |
107,794,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R1477:Mst1r
|
UTSW |
9 |
107,785,523 (GRCm39) |
missense |
probably benign |
|
R1479:Mst1r
|
UTSW |
9 |
107,790,544 (GRCm39) |
splice site |
probably benign |
|
R1541:Mst1r
|
UTSW |
9 |
107,794,562 (GRCm39) |
missense |
probably damaging |
0.99 |
R1698:Mst1r
|
UTSW |
9 |
107,797,179 (GRCm39) |
missense |
probably benign |
0.06 |
R1891:Mst1r
|
UTSW |
9 |
107,790,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R1974:Mst1r
|
UTSW |
9 |
107,793,132 (GRCm39) |
critical splice donor site |
probably null |
|
R1974:Mst1r
|
UTSW |
9 |
107,791,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R2144:Mst1r
|
UTSW |
9 |
107,790,367 (GRCm39) |
missense |
probably benign |
|
R2221:Mst1r
|
UTSW |
9 |
107,785,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R2356:Mst1r
|
UTSW |
9 |
107,795,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R3913:Mst1r
|
UTSW |
9 |
107,791,945 (GRCm39) |
missense |
probably benign |
|
R4768:Mst1r
|
UTSW |
9 |
107,788,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R4793:Mst1r
|
UTSW |
9 |
107,797,124 (GRCm39) |
missense |
probably damaging |
0.96 |
R5141:Mst1r
|
UTSW |
9 |
107,789,440 (GRCm39) |
missense |
probably damaging |
0.99 |
R5191:Mst1r
|
UTSW |
9 |
107,788,750 (GRCm39) |
missense |
probably damaging |
0.98 |
R5238:Mst1r
|
UTSW |
9 |
107,784,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R6024:Mst1r
|
UTSW |
9 |
107,785,350 (GRCm39) |
missense |
probably benign |
0.00 |
R6220:Mst1r
|
UTSW |
9 |
107,784,547 (GRCm39) |
missense |
probably benign |
0.11 |
R6256:Mst1r
|
UTSW |
9 |
107,794,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R6361:Mst1r
|
UTSW |
9 |
107,793,052 (GRCm39) |
missense |
probably benign |
|
R6522:Mst1r
|
UTSW |
9 |
107,790,438 (GRCm39) |
missense |
probably benign |
0.00 |
R6559:Mst1r
|
UTSW |
9 |
107,785,470 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6863:Mst1r
|
UTSW |
9 |
107,797,225 (GRCm39) |
missense |
probably benign |
|
R6868:Mst1r
|
UTSW |
9 |
107,793,132 (GRCm39) |
critical splice donor site |
probably null |
|
R6873:Mst1r
|
UTSW |
9 |
107,788,843 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6978:Mst1r
|
UTSW |
9 |
107,789,793 (GRCm39) |
missense |
probably benign |
0.23 |
R7168:Mst1r
|
UTSW |
9 |
107,785,392 (GRCm39) |
missense |
probably benign |
0.01 |
R7299:Mst1r
|
UTSW |
9 |
107,791,989 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7301:Mst1r
|
UTSW |
9 |
107,791,989 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7405:Mst1r
|
UTSW |
9 |
107,792,321 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7615:Mst1r
|
UTSW |
9 |
107,797,211 (GRCm39) |
missense |
probably benign |
0.05 |
R7684:Mst1r
|
UTSW |
9 |
107,788,762 (GRCm39) |
missense |
probably benign |
0.01 |
R7741:Mst1r
|
UTSW |
9 |
107,784,319 (GRCm39) |
start gained |
probably benign |
|
R7916:Mst1r
|
UTSW |
9 |
107,784,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R7987:Mst1r
|
UTSW |
9 |
107,789,997 (GRCm39) |
splice site |
probably null |
|
R8177:Mst1r
|
UTSW |
9 |
107,784,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R8356:Mst1r
|
UTSW |
9 |
107,794,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R8494:Mst1r
|
UTSW |
9 |
107,791,718 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8692:Mst1r
|
UTSW |
9 |
107,792,050 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8979:Mst1r
|
UTSW |
9 |
107,792,478 (GRCm39) |
missense |
probably damaging |
0.98 |
R9012:Mst1r
|
UTSW |
9 |
107,791,960 (GRCm39) |
missense |
probably benign |
0.01 |
X0026:Mst1r
|
UTSW |
9 |
107,790,402 (GRCm39) |
missense |
probably damaging |
0.97 |
|