Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9030624J02Rik |
T |
A |
7: 118,804,191 (GRCm38) |
|
probably benign |
Het |
Abca4 |
A |
G |
3: 122,170,954 (GRCm38) |
T929A |
probably damaging |
Het |
Adam6b |
G |
A |
12: 113,491,393 (GRCm38) |
R610H |
probably damaging |
Het |
Adamts12 |
T |
A |
15: 11,311,599 (GRCm38) |
M1314K |
probably benign |
Het |
Alg6 |
T |
A |
4: 99,753,054 (GRCm38) |
F152I |
probably damaging |
Het |
Aopep |
A |
G |
13: 63,199,500 (GRCm38) |
|
probably benign |
Het |
Arid5b |
A |
G |
10: 68,128,975 (GRCm38) |
S289P |
probably damaging |
Het |
Axin1 |
T |
C |
17: 26,194,072 (GRCm38) |
F780L |
probably damaging |
Het |
C9 |
C |
T |
15: 6,483,231 (GRCm38) |
S278L |
possibly damaging |
Het |
Calr4 |
A |
T |
4: 109,244,115 (GRCm38) |
I65F |
probably damaging |
Het |
Cdh23 |
A |
G |
10: 60,523,548 (GRCm38) |
V260A |
probably benign |
Het |
Ddx25 |
T |
C |
9: 35,543,595 (GRCm38) |
|
probably benign |
Het |
Dppa4 |
A |
G |
16: 48,291,083 (GRCm38) |
T92A |
possibly damaging |
Het |
Ercc5 |
T |
C |
1: 44,163,898 (GRCm38) |
Y232H |
probably damaging |
Het |
Exoc4 |
A |
G |
6: 33,918,399 (GRCm38) |
|
probably null |
Het |
Fam149a |
A |
G |
8: 45,351,786 (GRCm38) |
V253A |
probably damaging |
Het |
Fam209 |
C |
T |
2: 172,474,182 (GRCm38) |
T159I |
probably damaging |
Het |
Gcfc2 |
A |
T |
6: 81,936,015 (GRCm38) |
N265I |
probably damaging |
Het |
Glud1 |
T |
C |
14: 34,336,130 (GRCm38) |
V366A |
probably benign |
Het |
Hdac10 |
T |
C |
15: 89,128,442 (GRCm38) |
T3A |
probably damaging |
Het |
Ifnar1 |
T |
C |
16: 91,489,782 (GRCm38) |
S54P |
probably damaging |
Het |
Itpr2 |
T |
C |
6: 146,144,185 (GRCm38) |
Y2561C |
probably damaging |
Het |
Klhl30 |
A |
G |
1: 91,354,157 (GRCm38) |
E160G |
possibly damaging |
Het |
Kmt2d |
A |
T |
15: 98,862,333 (GRCm38) |
S1015T |
unknown |
Het |
Lactb2 |
A |
G |
1: 13,660,374 (GRCm38) |
M26T |
probably damaging |
Het |
Lactbl1 |
A |
T |
4: 136,631,051 (GRCm38) |
D111V |
probably damaging |
Het |
Lig4 |
T |
C |
8: 9,972,775 (GRCm38) |
Y335C |
probably damaging |
Het |
Lrrc8e |
T |
A |
8: 4,235,921 (GRCm38) |
D715E |
probably benign |
Het |
Med6 |
A |
T |
12: 81,579,574 (GRCm38) |
V142D |
possibly damaging |
Het |
Men1 |
G |
A |
19: 6,337,207 (GRCm38) |
|
probably null |
Het |
Mettl13 |
A |
G |
1: 162,535,865 (GRCm38) |
V600A |
possibly damaging |
Het |
Mpdz |
A |
T |
4: 81,310,224 (GRCm38) |
C1314* |
probably null |
Het |
Nbeal2 |
A |
G |
9: 110,635,869 (GRCm38) |
V1009A |
probably damaging |
Het |
Nudt2 |
T |
A |
4: 41,480,474 (GRCm38) |
L119Q |
probably damaging |
Het |
Or5b117 |
T |
C |
19: 13,453,840 (GRCm38) |
M226V |
possibly damaging |
Het |
Osbpl3 |
C |
T |
6: 50,323,068 (GRCm38) |
E519K |
probably damaging |
Het |
Pak6 |
A |
T |
2: 118,689,845 (GRCm38) |
T106S |
possibly damaging |
Het |
Pggt1b |
T |
G |
18: 46,280,719 (GRCm38) |
Q34P |
probably benign |
Het |
Phactr4 |
T |
C |
4: 132,370,992 (GRCm38) |
T322A |
possibly damaging |
Het |
Plekhj1 |
T |
C |
10: 80,796,602 (GRCm38) |
|
probably null |
Het |
Pnpt1 |
T |
C |
11: 29,154,217 (GRCm38) |
|
probably null |
Het |
Pramel32 |
A |
G |
4: 88,629,053 (GRCm38) |
I214T |
probably damaging |
Het |
Prr14l |
T |
C |
5: 32,830,676 (GRCm38) |
I492V |
probably benign |
Het |
Ranbp2 |
C |
A |
10: 58,477,256 (GRCm38) |
A1266E |
probably damaging |
Het |
Riok3 |
G |
A |
18: 12,137,020 (GRCm38) |
D140N |
probably damaging |
Het |
Rsph4a |
G |
A |
10: 33,914,343 (GRCm38) |
E643K |
probably damaging |
Het |
Scara3 |
T |
G |
14: 65,933,121 (GRCm38) |
E103A |
probably benign |
Het |
Sgk3 |
T |
C |
1: 9,868,384 (GRCm38) |
V33A |
probably damaging |
Het |
Slc38a4 |
A |
G |
15: 96,999,494 (GRCm38) |
F480S |
probably damaging |
Het |
Slc44a1 |
G |
A |
4: 53,543,571 (GRCm38) |
V372M |
probably damaging |
Het |
Slc9a2 |
A |
G |
1: 40,767,737 (GRCm38) |
Y728C |
probably benign |
Het |
Sox4 |
C |
A |
13: 28,952,973 (GRCm38) |
G17W |
probably damaging |
Het |
Spidr |
A |
T |
16: 15,895,578 (GRCm38) |
L847Q |
probably damaging |
Het |
Sptb |
A |
G |
12: 76,620,753 (GRCm38) |
S857P |
probably benign |
Het |
Syde1 |
A |
G |
10: 78,585,809 (GRCm38) |
V636A |
probably damaging |
Het |
Syna |
A |
G |
5: 134,559,717 (GRCm38) |
L126P |
possibly damaging |
Het |
Taar2 |
A |
G |
10: 23,941,368 (GRCm38) |
T269A |
possibly damaging |
Het |
Tapbp |
C |
T |
17: 33,925,704 (GRCm38) |
T258I |
probably damaging |
Het |
Tcf20 |
T |
A |
15: 82,857,142 (GRCm38) |
Q36L |
possibly damaging |
Het |
Tmem131l |
A |
T |
3: 83,942,500 (GRCm38) |
M260K |
probably damaging |
Het |
Tnc |
T |
A |
4: 64,016,824 (GRCm38) |
|
probably benign |
Het |
Ugp2 |
T |
A |
11: 21,354,345 (GRCm38) |
E27D |
probably benign |
Het |
Wdr27 |
A |
T |
17: 14,928,310 (GRCm38) |
C140* |
probably null |
Het |
Wnt2b |
T |
C |
3: 104,953,133 (GRCm38) |
T153A |
possibly damaging |
Het |
Xirp2 |
A |
T |
2: 67,513,375 (GRCm38) |
T1987S |
probably benign |
Het |
Zfp36l1 |
C |
A |
12: 80,110,464 (GRCm38) |
G48C |
probably damaging |
Het |
Zfp474 |
A |
T |
18: 52,638,493 (GRCm38) |
I73F |
possibly damaging |
Het |
Zfp790 |
T |
A |
7: 29,828,563 (GRCm38) |
F224L |
probably benign |
Het |
|
Other mutations in Nmur2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01591:Nmur2
|
APN |
11 |
56,026,999 (GRCm38) |
missense |
probably benign |
|
IGL01960:Nmur2
|
APN |
11 |
56,040,511 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02108:Nmur2
|
APN |
11 |
56,040,364 (GRCm38) |
missense |
probably benign |
0.33 |
IGL02602:Nmur2
|
APN |
11 |
56,027,063 (GRCm38) |
missense |
probably benign |
0.19 |
PIT4677001:Nmur2
|
UTSW |
11 |
56,033,009 (GRCm38) |
missense |
probably benign |
0.00 |
R0324:Nmur2
|
UTSW |
11 |
56,040,520 (GRCm38) |
missense |
probably damaging |
1.00 |
R0458:Nmur2
|
UTSW |
11 |
56,040,568 (GRCm38) |
missense |
possibly damaging |
0.93 |
R0718:Nmur2
|
UTSW |
11 |
56,029,498 (GRCm38) |
splice site |
probably benign |
|
R1799:Nmur2
|
UTSW |
11 |
56,029,621 (GRCm38) |
missense |
probably damaging |
1.00 |
R2099:Nmur2
|
UTSW |
11 |
56,040,763 (GRCm38) |
missense |
probably benign |
0.00 |
R2263:Nmur2
|
UTSW |
11 |
56,029,561 (GRCm38) |
missense |
probably damaging |
0.97 |
R3701:Nmur2
|
UTSW |
11 |
56,040,777 (GRCm38) |
missense |
probably damaging |
0.99 |
R3705:Nmur2
|
UTSW |
11 |
56,040,474 (GRCm38) |
missense |
probably damaging |
1.00 |
R3951:Nmur2
|
UTSW |
11 |
56,040,225 (GRCm38) |
missense |
probably damaging |
1.00 |
R4083:Nmur2
|
UTSW |
11 |
56,040,225 (GRCm38) |
missense |
probably damaging |
1.00 |
R4744:Nmur2
|
UTSW |
11 |
56,040,835 (GRCm38) |
missense |
probably benign |
0.01 |
R4747:Nmur2
|
UTSW |
11 |
56,040,279 (GRCm38) |
missense |
probably benign |
0.05 |
R5288:Nmur2
|
UTSW |
11 |
56,040,214 (GRCm38) |
missense |
probably damaging |
1.00 |
R5384:Nmur2
|
UTSW |
11 |
56,040,214 (GRCm38) |
missense |
probably damaging |
1.00 |
R5579:Nmur2
|
UTSW |
11 |
56,033,009 (GRCm38) |
missense |
probably benign |
0.00 |
R6329:Nmur2
|
UTSW |
11 |
56,029,585 (GRCm38) |
missense |
probably benign |
0.30 |
R6477:Nmur2
|
UTSW |
11 |
56,029,591 (GRCm38) |
missense |
probably damaging |
1.00 |
R7445:Nmur2
|
UTSW |
11 |
56,032,940 (GRCm38) |
missense |
probably damaging |
0.97 |
R7580:Nmur2
|
UTSW |
11 |
56,026,982 (GRCm38) |
missense |
probably benign |
0.03 |
R7899:Nmur2
|
UTSW |
11 |
56,040,335 (GRCm38) |
missense |
probably benign |
|
R8688:Nmur2
|
UTSW |
11 |
56,040,828 (GRCm38) |
missense |
probably damaging |
1.00 |
R9090:Nmur2
|
UTSW |
11 |
56,040,482 (GRCm38) |
missense |
probably benign |
0.44 |
R9098:Nmur2
|
UTSW |
11 |
56,029,582 (GRCm38) |
missense |
possibly damaging |
0.93 |
R9271:Nmur2
|
UTSW |
11 |
56,040,482 (GRCm38) |
missense |
probably benign |
0.44 |
R9542:Nmur2
|
UTSW |
11 |
56,040,823 (GRCm38) |
missense |
probably damaging |
0.98 |
X0062:Nmur2
|
UTSW |
11 |
56,040,849 (GRCm38) |
missense |
probably benign |
0.01 |
Z1176:Nmur2
|
UTSW |
11 |
56,027,101 (GRCm38) |
missense |
probably benign |
0.12 |
Z1186:Nmur2
|
UTSW |
11 |
56,040,278 (GRCm38) |
missense |
probably benign |
|
Z1187:Nmur2
|
UTSW |
11 |
56,040,278 (GRCm38) |
missense |
probably benign |
|
Z1188:Nmur2
|
UTSW |
11 |
56,040,278 (GRCm38) |
missense |
probably benign |
|
Z1189:Nmur2
|
UTSW |
11 |
56,040,278 (GRCm38) |
missense |
probably benign |
|
Z1190:Nmur2
|
UTSW |
11 |
56,040,278 (GRCm38) |
missense |
probably benign |
|
Z1191:Nmur2
|
UTSW |
11 |
56,040,278 (GRCm38) |
missense |
probably benign |
|
Z1192:Nmur2
|
UTSW |
11 |
56,040,278 (GRCm38) |
missense |
probably benign |
|
|