Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5830454E08Rik |
T |
A |
9: 120,406,693 (GRCm39) |
|
probably benign |
Het |
Ada |
G |
A |
2: 163,572,406 (GRCm39) |
R225C |
probably benign |
Het |
Adamts9 |
T |
C |
6: 92,867,254 (GRCm39) |
K625R |
probably benign |
Het |
Ano1 |
T |
C |
7: 144,210,820 (GRCm39) |
I182V |
possibly damaging |
Het |
Aoc1l2 |
A |
T |
6: 48,908,292 (GRCm39) |
M431L |
probably benign |
Het |
Aox4 |
T |
C |
1: 58,285,445 (GRCm39) |
V643A |
possibly damaging |
Het |
Arcn1 |
T |
C |
9: 44,671,441 (GRCm39) |
I29V |
probably benign |
Het |
Arhgap15 |
A |
G |
2: 43,670,630 (GRCm39) |
T5A |
probably benign |
Het |
Asb10 |
A |
T |
5: 24,745,740 (GRCm39) |
L62Q |
probably damaging |
Het |
Atp23 |
T |
A |
10: 126,723,403 (GRCm39) |
H233L |
possibly damaging |
Het |
Bglap2 |
C |
T |
3: 88,289,432 (GRCm39) |
|
probably benign |
Het |
Carnmt1 |
T |
C |
19: 18,655,098 (GRCm39) |
S84P |
probably damaging |
Het |
Ccdc152 |
A |
G |
15: 3,312,319 (GRCm39) |
I180T |
probably damaging |
Het |
Cdr2l |
T |
C |
11: 115,284,186 (GRCm39) |
F174S |
probably damaging |
Het |
Celsr2 |
C |
T |
3: 108,301,312 (GRCm39) |
V2695I |
probably benign |
Het |
Chd1 |
C |
A |
17: 15,948,460 (GRCm39) |
S127R |
probably benign |
Het |
Chmp4c |
T |
A |
3: 10,450,646 (GRCm39) |
F75L |
probably benign |
Het |
Col13a1 |
A |
C |
10: 61,725,880 (GRCm39) |
V260G |
possibly damaging |
Het |
Col5a1 |
A |
G |
2: 27,915,664 (GRCm39) |
N183D |
probably damaging |
Het |
Cpn1 |
C |
T |
19: 43,974,634 (GRCm39) |
V32M |
probably damaging |
Het |
Cxcl1 |
A |
G |
5: 91,039,373 (GRCm39) |
M39V |
probably benign |
Het |
Dpep2 |
T |
A |
8: 106,712,825 (GRCm39) |
D455V |
probably damaging |
Het |
Dpp7 |
G |
A |
2: 25,242,749 (GRCm39) |
T441I |
possibly damaging |
Het |
Dst |
C |
A |
1: 34,241,640 (GRCm39) |
H4001N |
probably damaging |
Het |
Epg5 |
G |
A |
18: 78,038,828 (GRCm39) |
A1519T |
probably benign |
Het |
Esrp2 |
C |
T |
8: 106,858,820 (GRCm39) |
V606I |
probably benign |
Het |
Fbxo40 |
T |
C |
16: 36,789,236 (GRCm39) |
K625E |
probably damaging |
Het |
Gbp2b |
A |
T |
3: 142,303,946 (GRCm39) |
I14F |
probably damaging |
Het |
Gpr37l1 |
G |
T |
1: 135,094,676 (GRCm39) |
F189L |
probably damaging |
Het |
Heatr5a |
G |
A |
12: 52,003,020 (GRCm39) |
Q161* |
probably null |
Het |
Hspa4l |
T |
C |
3: 40,700,197 (GRCm39) |
Y30H |
possibly damaging |
Het |
Hspg2 |
G |
A |
4: 137,239,237 (GRCm39) |
C388Y |
probably damaging |
Het |
Kcna1 |
A |
G |
6: 126,619,330 (GRCm39) |
I330T |
probably damaging |
Het |
Klhl3 |
T |
A |
13: 58,166,781 (GRCm39) |
Y350F |
probably benign |
Het |
Kntc1 |
T |
C |
5: 123,919,118 (GRCm39) |
|
probably null |
Het |
Krtap10-4 |
A |
T |
10: 77,662,520 (GRCm39) |
C109* |
probably null |
Het |
Lrch4 |
T |
C |
5: 137,636,179 (GRCm39) |
S377P |
probably benign |
Het |
Lrrc8c |
C |
A |
5: 105,755,349 (GRCm39) |
H375N |
probably damaging |
Het |
Lsg1 |
T |
C |
16: 30,380,538 (GRCm39) |
E633G |
probably damaging |
Het |
Mcoln1 |
T |
C |
8: 3,560,697 (GRCm39) |
|
probably benign |
Het |
Med12l |
C |
A |
3: 59,167,109 (GRCm39) |
T1523K |
possibly damaging |
Het |
Mrps27 |
A |
T |
13: 99,547,973 (GRCm39) |
|
probably benign |
Het |
Mzb1 |
T |
A |
18: 35,780,717 (GRCm39) |
Y158F |
probably benign |
Het |
Nat8l |
T |
A |
5: 34,155,823 (GRCm39) |
C160S |
probably damaging |
Het |
Ncf4 |
T |
C |
15: 78,146,593 (GRCm39) |
|
probably benign |
Het |
Or1b1 |
A |
T |
2: 36,994,814 (GRCm39) |
Y283N |
probably damaging |
Het |
Or1o3 |
T |
C |
17: 37,573,730 (GRCm39) |
Y275C |
probably damaging |
Het |
Pak2 |
T |
A |
16: 31,861,936 (GRCm39) |
|
probably benign |
Het |
Pcdhga12 |
T |
C |
18: 37,901,160 (GRCm39) |
I664T |
probably benign |
Het |
Pcnx2 |
A |
C |
8: 126,564,749 (GRCm39) |
L1048R |
possibly damaging |
Het |
Pcsk5 |
T |
C |
19: 17,652,949 (GRCm39) |
M246V |
probably damaging |
Het |
Pkd2l2 |
T |
A |
18: 34,566,355 (GRCm39) |
V522D |
probably benign |
Het |
Plekhh1 |
A |
T |
12: 79,115,880 (GRCm39) |
M808L |
probably benign |
Het |
Plpp2 |
C |
A |
10: 79,362,973 (GRCm39) |
R157L |
probably benign |
Het |
Plrg1 |
T |
A |
3: 82,978,558 (GRCm39) |
H441Q |
probably benign |
Het |
Pnpla6 |
T |
C |
8: 3,572,613 (GRCm39) |
V300A |
probably damaging |
Het |
Ptprb |
A |
T |
10: 116,184,088 (GRCm39) |
K1633N |
possibly damaging |
Het |
Ralgapa1 |
A |
G |
12: 55,659,508 (GRCm39) |
V2004A |
possibly damaging |
Het |
Rasd1 |
G |
T |
11: 59,854,933 (GRCm39) |
S182R |
possibly damaging |
Het |
Rc3h2 |
A |
T |
2: 37,288,373 (GRCm39) |
|
probably null |
Het |
Rrp1b |
T |
A |
17: 32,255,445 (GRCm39) |
|
probably benign |
Het |
Ruvbl1 |
T |
C |
6: 88,474,272 (GRCm39) |
I425T |
probably benign |
Het |
Shisal1 |
T |
C |
15: 84,301,427 (GRCm39) |
D72G |
probably damaging |
Het |
Sipa1l1 |
C |
T |
12: 82,487,682 (GRCm39) |
A1652V |
probably benign |
Het |
Slc14a2 |
C |
A |
18: 78,238,963 (GRCm39) |
V219L |
possibly damaging |
Het |
Smc1b |
G |
T |
15: 84,949,185 (GRCm39) |
P1242Q |
probably damaging |
Het |
Smim33 |
A |
G |
18: 35,861,894 (GRCm39) |
Y126C |
probably damaging |
Het |
Snx27 |
T |
A |
3: 94,431,551 (GRCm39) |
D281V |
probably damaging |
Het |
Spem2 |
C |
T |
11: 69,707,973 (GRCm39) |
V331I |
probably benign |
Het |
Sptb |
C |
A |
12: 76,656,052 (GRCm39) |
K1343N |
probably damaging |
Het |
Sult2a8 |
T |
C |
7: 14,147,584 (GRCm39) |
I236V |
probably benign |
Het |
Syk |
A |
G |
13: 52,765,071 (GRCm39) |
E66G |
probably damaging |
Het |
Synm |
T |
A |
7: 67,385,406 (GRCm39) |
E310V |
probably damaging |
Het |
Tas2r118 |
G |
A |
6: 23,969,209 (GRCm39) |
A284V |
probably benign |
Het |
Thoc2l |
T |
A |
5: 104,667,742 (GRCm39) |
F755I |
probably damaging |
Het |
Tlr11 |
A |
G |
14: 50,600,578 (GRCm39) |
N855D |
possibly damaging |
Het |
Tmem230 |
G |
T |
2: 132,087,871 (GRCm39) |
|
probably benign |
Het |
Trappc8 |
G |
A |
18: 20,977,237 (GRCm39) |
T844I |
probably benign |
Het |
Trmt44 |
T |
C |
5: 35,722,812 (GRCm39) |
S419G |
possibly damaging |
Het |
Trpv1 |
T |
A |
11: 73,132,574 (GRCm39) |
V396E |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Tubgcp2 |
A |
G |
7: 139,587,354 (GRCm39) |
I337T |
possibly damaging |
Het |
Ubr4 |
T |
C |
4: 139,137,934 (GRCm39) |
I1097T |
probably damaging |
Het |
Vmn2r61 |
T |
C |
7: 41,949,953 (GRCm39) |
F791S |
possibly damaging |
Het |
Zdhhc2 |
T |
A |
8: 40,898,825 (GRCm39) |
M45K |
probably benign |
Het |
Zfp383 |
T |
A |
7: 29,614,166 (GRCm39) |
D140E |
probably damaging |
Het |
Zfp712 |
C |
A |
13: 67,189,425 (GRCm39) |
K367N |
probably damaging |
Het |
Zfp763 |
C |
T |
17: 33,237,949 (GRCm39) |
A399T |
probably damaging |
Het |
|
Other mutations in Slc12a2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00491:Slc12a2
|
APN |
18 |
58,069,477 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01099:Slc12a2
|
APN |
18 |
58,039,092 (GRCm39) |
nonsense |
probably null |
|
IGL01896:Slc12a2
|
APN |
18 |
58,029,380 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02266:Slc12a2
|
APN |
18 |
58,045,092 (GRCm39) |
splice site |
probably benign |
|
IGL02489:Slc12a2
|
APN |
18 |
58,045,074 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02681:Slc12a2
|
APN |
18 |
58,012,471 (GRCm39) |
missense |
probably benign |
0.25 |
IGL03068:Slc12a2
|
APN |
18 |
58,037,407 (GRCm39) |
splice site |
probably benign |
|
IGL03076:Slc12a2
|
APN |
18 |
58,059,469 (GRCm39) |
splice site |
probably benign |
|
IGL03086:Slc12a2
|
APN |
18 |
58,054,856 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03238:Slc12a2
|
APN |
18 |
58,047,306 (GRCm39) |
missense |
possibly damaging |
0.85 |
frankie
|
UTSW |
18 |
58,068,035 (GRCm39) |
missense |
possibly damaging |
0.48 |
honeylamb
|
UTSW |
18 |
58,063,238 (GRCm39) |
missense |
probably damaging |
1.00 |
sugar
|
UTSW |
18 |
58,032,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R0048:Slc12a2
|
UTSW |
18 |
58,048,594 (GRCm39) |
splice site |
probably benign |
|
R0194:Slc12a2
|
UTSW |
18 |
58,063,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R0530:Slc12a2
|
UTSW |
18 |
58,052,608 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0959:Slc12a2
|
UTSW |
18 |
58,037,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R1014:Slc12a2
|
UTSW |
18 |
58,054,882 (GRCm39) |
missense |
probably benign |
0.00 |
R1112:Slc12a2
|
UTSW |
18 |
58,070,824 (GRCm39) |
missense |
probably benign |
0.01 |
R1544:Slc12a2
|
UTSW |
18 |
58,012,374 (GRCm39) |
missense |
probably benign |
0.00 |
R1669:Slc12a2
|
UTSW |
18 |
58,037,307 (GRCm39) |
missense |
probably damaging |
0.99 |
R1935:Slc12a2
|
UTSW |
18 |
58,037,425 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1951:Slc12a2
|
UTSW |
18 |
58,012,467 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1990:Slc12a2
|
UTSW |
18 |
58,043,358 (GRCm39) |
missense |
possibly damaging |
0.61 |
R2340:Slc12a2
|
UTSW |
18 |
58,033,122 (GRCm39) |
missense |
probably benign |
0.03 |
R3971:Slc12a2
|
UTSW |
18 |
58,063,268 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4120:Slc12a2
|
UTSW |
18 |
58,032,427 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4223:Slc12a2
|
UTSW |
18 |
58,043,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R4541:Slc12a2
|
UTSW |
18 |
58,046,037 (GRCm39) |
splice site |
probably null |
|
R4678:Slc12a2
|
UTSW |
18 |
58,039,032 (GRCm39) |
nonsense |
probably null |
|
R4931:Slc12a2
|
UTSW |
18 |
58,068,035 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5226:Slc12a2
|
UTSW |
18 |
58,012,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R5648:Slc12a2
|
UTSW |
18 |
58,029,382 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5726:Slc12a2
|
UTSW |
18 |
58,029,426 (GRCm39) |
missense |
probably benign |
0.01 |
R5789:Slc12a2
|
UTSW |
18 |
58,045,091 (GRCm39) |
splice site |
probably null |
|
R5868:Slc12a2
|
UTSW |
18 |
58,077,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R5921:Slc12a2
|
UTSW |
18 |
58,065,595 (GRCm39) |
missense |
probably benign |
0.06 |
R6126:Slc12a2
|
UTSW |
18 |
58,077,116 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6310:Slc12a2
|
UTSW |
18 |
58,048,578 (GRCm39) |
missense |
probably damaging |
0.99 |
R6598:Slc12a2
|
UTSW |
18 |
58,031,145 (GRCm39) |
missense |
probably benign |
0.01 |
R6615:Slc12a2
|
UTSW |
18 |
58,031,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R6911:Slc12a2
|
UTSW |
18 |
58,052,541 (GRCm39) |
missense |
probably benign |
0.05 |
R6957:Slc12a2
|
UTSW |
18 |
58,043,344 (GRCm39) |
nonsense |
probably null |
|
R7411:Slc12a2
|
UTSW |
18 |
58,074,085 (GRCm39) |
missense |
probably benign |
0.01 |
R7508:Slc12a2
|
UTSW |
18 |
58,037,465 (GRCm39) |
missense |
probably benign |
0.01 |
R7645:Slc12a2
|
UTSW |
18 |
58,029,450 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7658:Slc12a2
|
UTSW |
18 |
58,065,596 (GRCm39) |
missense |
probably benign |
0.02 |
R8054:Slc12a2
|
UTSW |
18 |
58,054,944 (GRCm39) |
nonsense |
probably null |
|
R8093:Slc12a2
|
UTSW |
18 |
58,012,423 (GRCm39) |
missense |
probably benign |
0.17 |
R8099:Slc12a2
|
UTSW |
18 |
58,032,464 (GRCm39) |
missense |
probably damaging |
0.99 |
R8121:Slc12a2
|
UTSW |
18 |
58,032,403 (GRCm39) |
missense |
probably benign |
0.44 |
R8214:Slc12a2
|
UTSW |
18 |
58,070,791 (GRCm39) |
missense |
probably benign |
0.29 |
R8273:Slc12a2
|
UTSW |
18 |
58,047,338 (GRCm39) |
splice site |
probably benign |
|
R8341:Slc12a2
|
UTSW |
18 |
58,012,281 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8485:Slc12a2
|
UTSW |
18 |
58,074,218 (GRCm39) |
critical splice donor site |
probably null |
|
R8797:Slc12a2
|
UTSW |
18 |
58,012,455 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9049:Slc12a2
|
UTSW |
18 |
58,054,863 (GRCm39) |
nonsense |
probably null |
|
R9180:Slc12a2
|
UTSW |
18 |
58,069,469 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9256:Slc12a2
|
UTSW |
18 |
58,074,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R9337:Slc12a2
|
UTSW |
18 |
58,063,238 (GRCm39) |
missense |
probably damaging |
1.00 |
|