Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3100002H09Rik |
T |
G |
4: 124,504,280 (GRCm39) |
M91L |
unknown |
Het |
A2m |
C |
T |
6: 121,653,891 (GRCm39) |
T1408M |
probably damaging |
Het |
Abca16 |
C |
T |
7: 120,143,995 (GRCm39) |
T1671M |
probably damaging |
Het |
Adamts8 |
A |
T |
9: 30,862,632 (GRCm39) |
N279I |
probably damaging |
Het |
Adgre1 |
T |
A |
17: 57,752,034 (GRCm39) |
I594N |
probably damaging |
Het |
Aldh4a1 |
T |
A |
4: 139,369,415 (GRCm39) |
V322E |
probably damaging |
Het |
Atp12a |
A |
T |
14: 56,610,837 (GRCm39) |
Y327F |
probably benign |
Het |
C4b |
T |
C |
17: 34,959,309 (GRCm39) |
T422A |
probably damaging |
Het |
Cacna1c |
A |
T |
6: 118,664,143 (GRCm39) |
S668T |
probably damaging |
Het |
Cchcr1 |
A |
T |
17: 35,837,577 (GRCm39) |
E426D |
probably damaging |
Het |
Ccr3 |
G |
A |
9: 123,828,830 (GRCm39) |
G55D |
probably damaging |
Het |
Cdipt |
T |
A |
7: 126,578,704 (GRCm39) |
|
probably null |
Het |
Cep19 |
A |
G |
16: 31,922,716 (GRCm39) |
|
probably benign |
Het |
Cts6 |
T |
A |
13: 61,349,626 (GRCm39) |
M56L |
probably benign |
Het |
Cyp3a11 |
C |
A |
5: 145,802,787 (GRCm39) |
M235I |
probably benign |
Het |
Dnajc21 |
A |
T |
15: 10,462,363 (GRCm39) |
D87E |
possibly damaging |
Het |
Ell |
A |
C |
8: 70,992,357 (GRCm39) |
M1L |
possibly damaging |
Het |
Esyt3 |
T |
C |
9: 99,240,466 (GRCm39) |
|
probably benign |
Het |
Ets1 |
T |
C |
9: 32,640,094 (GRCm39) |
|
probably benign |
Het |
Fam222b |
T |
A |
11: 78,045,858 (GRCm39) |
M473K |
probably benign |
Het |
Fanca |
T |
C |
8: 124,030,702 (GRCm39) |
|
probably benign |
Het |
Fbrsl1 |
G |
T |
5: 110,529,484 (GRCm39) |
A67D |
probably damaging |
Het |
Fchsd1 |
G |
A |
18: 38,094,380 (GRCm39) |
P622L |
probably damaging |
Het |
Gal3st2c |
T |
G |
1: 93,936,023 (GRCm39) |
|
probably null |
Het |
Gins2 |
T |
G |
8: 121,308,486 (GRCm39) |
H166P |
possibly damaging |
Het |
Gm10118 |
A |
T |
10: 63,762,845 (GRCm39) |
|
probably benign |
Het |
Gm9979 |
A |
T |
13: 40,859,289 (GRCm39) |
|
noncoding transcript |
Het |
Hspbap1 |
A |
G |
16: 35,622,033 (GRCm39) |
Y126C |
probably damaging |
Het |
Hspd1 |
A |
T |
1: 55,123,928 (GRCm39) |
I64N |
probably damaging |
Het |
Igkv3-4 |
A |
T |
6: 70,649,267 (GRCm39) |
S89C |
probably damaging |
Het |
Il10ra |
T |
A |
9: 45,176,924 (GRCm39) |
K134* |
probably null |
Het |
Il12rb1 |
G |
A |
8: 71,266,411 (GRCm39) |
C252Y |
possibly damaging |
Het |
Il24 |
A |
T |
1: 130,810,253 (GRCm39) |
V201E |
possibly damaging |
Het |
Inpp1 |
A |
G |
1: 52,833,820 (GRCm39) |
I92T |
probably damaging |
Het |
Kcnh5 |
T |
C |
12: 75,023,463 (GRCm39) |
D535G |
probably benign |
Het |
Kcnq4 |
T |
A |
4: 120,573,082 (GRCm39) |
I240F |
probably damaging |
Het |
Leo1 |
T |
A |
9: 75,364,423 (GRCm39) |
I521N |
possibly damaging |
Het |
Mdga1 |
A |
G |
17: 30,058,841 (GRCm39) |
L722P |
probably damaging |
Het |
Met |
G |
T |
6: 17,548,781 (GRCm39) |
V942L |
probably benign |
Het |
Mfn1 |
A |
T |
3: 32,617,996 (GRCm39) |
T110S |
probably benign |
Het |
Mrps15 |
T |
C |
4: 125,942,488 (GRCm39) |
I79T |
probably benign |
Het |
Mycbp2 |
A |
C |
14: 103,360,791 (GRCm39) |
M4497R |
probably damaging |
Het |
Mylk |
T |
A |
16: 34,699,722 (GRCm39) |
S362T |
probably benign |
Het |
Mypn |
A |
G |
10: 62,955,827 (GRCm39) |
F1209L |
probably benign |
Het |
Nab2 |
T |
C |
10: 127,500,526 (GRCm39) |
S189G |
probably damaging |
Het |
Naxe |
A |
C |
3: 87,963,840 (GRCm39) |
|
probably null |
Het |
Ncf1 |
A |
G |
5: 134,252,355 (GRCm39) |
V232A |
probably damaging |
Het |
Nell1 |
A |
G |
7: 49,929,359 (GRCm39) |
Y422C |
probably damaging |
Het |
Nmnat2 |
G |
T |
1: 152,969,807 (GRCm39) |
G176V |
probably damaging |
Het |
Npr1 |
A |
G |
3: 90,362,149 (GRCm39) |
S999P |
probably damaging |
Het |
Nuak1 |
T |
C |
10: 84,211,119 (GRCm39) |
D323G |
probably benign |
Het |
Or4d10b |
A |
G |
19: 12,036,642 (GRCm39) |
V158A |
probably benign |
Het |
Or5h23 |
A |
G |
16: 58,906,360 (GRCm39) |
F162S |
probably benign |
Het |
Or8b3b |
T |
A |
9: 38,584,261 (GRCm39) |
T160S |
probably damaging |
Het |
Osbpl8 |
T |
C |
10: 111,108,029 (GRCm39) |
S342P |
probably damaging |
Het |
Pag1 |
A |
T |
3: 9,764,482 (GRCm39) |
Y224N |
probably damaging |
Het |
Pald1 |
T |
A |
10: 61,179,489 (GRCm39) |
H460L |
probably damaging |
Het |
Per2 |
G |
A |
1: 91,355,578 (GRCm39) |
Q727* |
probably null |
Het |
Pex19 |
T |
C |
1: 171,960,779 (GRCm39) |
V134A |
probably benign |
Het |
Phlpp1 |
A |
T |
1: 106,320,657 (GRCm39) |
I1551F |
possibly damaging |
Het |
Ppef2 |
A |
T |
5: 92,386,998 (GRCm39) |
V313D |
probably damaging |
Het |
Prorp |
T |
C |
12: 55,351,257 (GRCm39) |
S189P |
possibly damaging |
Het |
Pzp |
A |
C |
6: 128,500,759 (GRCm39) |
F153C |
probably damaging |
Het |
Rasl11a |
A |
G |
5: 146,782,052 (GRCm39) |
H9R |
probably benign |
Het |
Rfx3 |
A |
T |
19: 27,779,780 (GRCm39) |
|
probably null |
Het |
Rmnd5b |
A |
T |
11: 51,518,789 (GRCm39) |
I68N |
probably damaging |
Het |
Senp5 |
T |
A |
16: 31,808,331 (GRCm39) |
S281C |
probably damaging |
Het |
Sh3rf1 |
G |
A |
8: 61,814,766 (GRCm39) |
E442K |
probably benign |
Het |
Slc12a3 |
G |
A |
8: 95,072,416 (GRCm39) |
V645M |
probably damaging |
Het |
Slc22a16 |
T |
C |
10: 40,457,337 (GRCm39) |
F193L |
possibly damaging |
Het |
Slc35f1 |
A |
T |
10: 52,984,274 (GRCm39) |
T345S |
possibly damaging |
Het |
Slc9a1 |
G |
A |
4: 133,148,874 (GRCm39) |
R704H |
probably damaging |
Het |
Spta1 |
A |
T |
1: 174,003,336 (GRCm39) |
Y89F |
possibly damaging |
Het |
Sspo |
A |
G |
6: 48,451,425 (GRCm39) |
E2741G |
probably damaging |
Het |
Strn4 |
G |
A |
7: 16,567,799 (GRCm39) |
|
probably null |
Het |
Tanc2 |
A |
G |
11: 105,814,132 (GRCm39) |
T1859A |
probably damaging |
Het |
Tbc1d14 |
A |
T |
5: 36,682,389 (GRCm39) |
Y3N |
probably damaging |
Het |
Tdrd9 |
C |
A |
12: 112,018,414 (GRCm39) |
R1278S |
probably benign |
Het |
Tenm4 |
C |
A |
7: 96,446,608 (GRCm39) |
A826E |
possibly damaging |
Het |
Tenm4 |
G |
T |
7: 96,446,607 (GRCm39) |
A826S |
possibly damaging |
Het |
Tet2 |
C |
T |
3: 133,182,241 (GRCm39) |
|
probably null |
Het |
Tfec |
A |
G |
6: 16,834,199 (GRCm39) |
L236P |
probably benign |
Het |
Tjap1 |
A |
G |
17: 46,569,797 (GRCm39) |
S388P |
probably damaging |
Het |
Tle1 |
T |
C |
4: 72,043,208 (GRCm39) |
T554A |
possibly damaging |
Het |
Tmem17 |
G |
A |
11: 22,467,450 (GRCm39) |
V83I |
probably benign |
Het |
Tnrc6b |
C |
T |
15: 80,760,703 (GRCm39) |
H137Y |
probably damaging |
Het |
Tomm5 |
T |
C |
4: 45,106,679 (GRCm39) |
|
probably benign |
Het |
Top3b |
T |
A |
16: 16,709,441 (GRCm39) |
|
probably benign |
Het |
Tph1 |
T |
C |
7: 46,303,216 (GRCm39) |
H254R |
probably damaging |
Het |
Tpte |
T |
C |
8: 22,841,468 (GRCm39) |
Y487H |
probably damaging |
Het |
Trappc13 |
T |
A |
13: 104,284,749 (GRCm39) |
D241V |
probably damaging |
Het |
Trrap |
A |
G |
5: 144,719,075 (GRCm39) |
I193V |
probably benign |
Het |
Tspear |
A |
T |
10: 77,706,199 (GRCm39) |
H323L |
probably benign |
Het |
Ttc39a |
A |
T |
4: 109,290,184 (GRCm39) |
|
probably null |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Tubg1 |
A |
G |
11: 101,014,858 (GRCm39) |
D200G |
probably damaging |
Het |
Ugdh |
C |
A |
5: 65,580,217 (GRCm39) |
|
probably benign |
Het |
Uso1 |
A |
G |
5: 92,328,467 (GRCm39) |
N355D |
probably benign |
Het |
Vamp4 |
T |
C |
1: 162,420,248 (GRCm39) |
|
probably null |
Het |
Vmn2r5 |
T |
C |
3: 64,411,497 (GRCm39) |
D357G |
probably damaging |
Het |
Vps52 |
A |
G |
17: 34,180,195 (GRCm39) |
T300A |
probably benign |
Het |
Wt1 |
A |
T |
2: 104,957,629 (GRCm39) |
H163L |
probably damaging |
Het |
Xirp2 |
T |
C |
2: 67,344,379 (GRCm39) |
S2207P |
probably benign |
Het |
Xpo6 |
A |
T |
7: 125,706,250 (GRCm39) |
I30N |
probably damaging |
Het |
Zfp386 |
T |
A |
12: 116,023,347 (GRCm39) |
I320K |
probably benign |
Het |
|
Other mutations in Kctd17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02079:Kctd17
|
APN |
15 |
78,314,356 (GRCm39) |
splice site |
probably benign |
|
IGL02209:Kctd17
|
APN |
15 |
78,319,792 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03132:Kctd17
|
APN |
15 |
78,319,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R4676:Kctd17
|
UTSW |
15 |
78,319,959 (GRCm39) |
unclassified |
probably benign |
|
R4793:Kctd17
|
UTSW |
15 |
78,317,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R5428:Kctd17
|
UTSW |
15 |
78,312,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R5779:Kctd17
|
UTSW |
15 |
78,321,333 (GRCm39) |
unclassified |
probably benign |
|
R6249:Kctd17
|
UTSW |
15 |
78,314,239 (GRCm39) |
splice site |
probably null |
|
R6911:Kctd17
|
UTSW |
15 |
78,318,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R7266:Kctd17
|
UTSW |
15 |
78,317,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R7324:Kctd17
|
UTSW |
15 |
78,319,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R7706:Kctd17
|
UTSW |
15 |
78,321,113 (GRCm39) |
unclassified |
probably benign |
|
R7707:Kctd17
|
UTSW |
15 |
78,321,113 (GRCm39) |
unclassified |
probably benign |
|
R7967:Kctd17
|
UTSW |
15 |
78,321,113 (GRCm39) |
unclassified |
probably benign |
|
R7968:Kctd17
|
UTSW |
15 |
78,321,113 (GRCm39) |
unclassified |
probably benign |
|
R7970:Kctd17
|
UTSW |
15 |
78,321,113 (GRCm39) |
unclassified |
probably benign |
|
R7972:Kctd17
|
UTSW |
15 |
78,321,113 (GRCm39) |
unclassified |
probably benign |
|
R7973:Kctd17
|
UTSW |
15 |
78,321,113 (GRCm39) |
unclassified |
probably benign |
|
R8097:Kctd17
|
UTSW |
15 |
78,321,113 (GRCm39) |
unclassified |
probably benign |
|
R8098:Kctd17
|
UTSW |
15 |
78,321,113 (GRCm39) |
unclassified |
probably benign |
|
R8099:Kctd17
|
UTSW |
15 |
78,321,113 (GRCm39) |
unclassified |
probably benign |
|
R8100:Kctd17
|
UTSW |
15 |
78,321,113 (GRCm39) |
unclassified |
probably benign |
|
R8333:Kctd17
|
UTSW |
15 |
78,321,113 (GRCm39) |
unclassified |
probably benign |
|
R9025:Kctd17
|
UTSW |
15 |
78,314,282 (GRCm39) |
missense |
probably damaging |
1.00 |
|