Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atxn1l |
T |
C |
8: 110,459,312 (GRCm39) |
R317G |
probably benign |
Het |
B130006D01Rik |
T |
A |
11: 95,616,992 (GRCm39) |
|
probably benign |
Het |
Brinp2 |
T |
C |
1: 158,074,379 (GRCm39) |
T581A |
probably damaging |
Het |
Cacna1b |
A |
T |
2: 24,548,540 (GRCm39) |
I1179N |
probably damaging |
Het |
Cacnb3 |
A |
G |
15: 98,541,301 (GRCm39) |
D434G |
probably damaging |
Het |
Cdh19 |
T |
C |
1: 110,847,341 (GRCm39) |
T423A |
possibly damaging |
Het |
Chkb |
C |
T |
15: 89,311,986 (GRCm39) |
|
probably benign |
Het |
Clstn3 |
G |
A |
6: 124,408,559 (GRCm39) |
R918C |
possibly damaging |
Het |
Dnah2 |
T |
A |
11: 69,406,906 (GRCm39) |
M200L |
probably benign |
Het |
Dnah9 |
T |
A |
11: 65,838,506 (GRCm39) |
H3097L |
probably benign |
Het |
Dst |
T |
A |
1: 34,314,401 (GRCm39) |
L4217H |
probably damaging |
Het |
Fam107b |
T |
A |
2: 3,779,565 (GRCm39) |
L80Q |
probably damaging |
Het |
Fgfr1 |
T |
A |
8: 26,045,595 (GRCm39) |
C55S |
probably damaging |
Het |
Igkv4-71 |
C |
A |
6: 69,220,264 (GRCm39) |
G78* |
probably null |
Het |
Igsf10 |
A |
G |
3: 59,237,452 (GRCm39) |
S910P |
probably benign |
Het |
Ikzf3 |
T |
C |
11: 98,407,718 (GRCm39) |
D41G |
probably damaging |
Het |
Larp1 |
T |
A |
11: 57,933,648 (GRCm39) |
I358N |
possibly damaging |
Het |
Marchf5 |
C |
T |
19: 37,188,067 (GRCm39) |
|
probably benign |
Het |
Mpdz |
T |
C |
4: 81,287,895 (GRCm39) |
T455A |
probably damaging |
Het |
Myo1b |
A |
G |
1: 51,815,510 (GRCm39) |
V612A |
possibly damaging |
Het |
Nipbl |
T |
C |
15: 8,380,023 (GRCm39) |
D923G |
probably benign |
Het |
Nlrp4b |
T |
C |
7: 10,448,918 (GRCm39) |
F7L |
probably damaging |
Het |
Npas4 |
T |
C |
19: 5,037,355 (GRCm39) |
N313S |
possibly damaging |
Het |
Nynrin |
T |
A |
14: 56,109,502 (GRCm39) |
N1536K |
possibly damaging |
Het |
Or10d5 |
T |
A |
9: 39,861,921 (GRCm39) |
T49S |
probably benign |
Het |
Or13a22 |
A |
G |
7: 140,072,751 (GRCm39) |
N67D |
probably damaging |
Het |
Or4c107 |
T |
C |
2: 88,788,885 (GRCm39) |
V25A |
probably benign |
Het |
Pclo |
T |
C |
5: 14,589,647 (GRCm39) |
V649A |
unknown |
Het |
Pom121 |
A |
G |
5: 135,421,389 (GRCm39) |
|
probably benign |
Het |
Ptcd2 |
A |
T |
13: 99,466,521 (GRCm39) |
I224N |
possibly damaging |
Het |
Rsrp1 |
C |
T |
4: 134,651,290 (GRCm39) |
P18L |
unknown |
Het |
Sash1 |
A |
T |
10: 8,605,422 (GRCm39) |
N989K |
probably damaging |
Het |
Scn2a |
T |
A |
2: 65,546,219 (GRCm39) |
H927Q |
probably benign |
Het |
Selenoi |
G |
T |
5: 30,461,222 (GRCm39) |
V128F |
probably damaging |
Het |
Slc25a42 |
T |
C |
8: 70,642,092 (GRCm39) |
I117V |
probably benign |
Het |
Spata1 |
A |
G |
3: 146,195,558 (GRCm39) |
|
probably benign |
Het |
Sptlc3 |
A |
T |
2: 139,431,615 (GRCm39) |
Y379F |
possibly damaging |
Het |
Tent4a |
A |
T |
13: 69,648,678 (GRCm39) |
S693T |
probably benign |
Het |
Tinag |
C |
T |
9: 76,952,885 (GRCm39) |
R33K |
probably benign |
Het |
Trappc8 |
T |
C |
18: 20,968,061 (GRCm39) |
D1092G |
probably benign |
Het |
Xntrpc |
A |
G |
7: 101,722,401 (GRCm39) |
E22G |
probably damaging |
Het |
Zbtb7b |
A |
G |
3: 89,287,278 (GRCm39) |
M397T |
possibly damaging |
Het |
Zgpat |
A |
G |
2: 181,020,682 (GRCm39) |
D285G |
probably benign |
Het |
|
Other mutations in Cit |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00321:Cit
|
APN |
5 |
115,984,524 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00482:Cit
|
APN |
5 |
116,076,814 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01317:Cit
|
APN |
5 |
116,046,775 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01335:Cit
|
APN |
5 |
116,046,889 (GRCm39) |
splice site |
probably benign |
|
IGL01415:Cit
|
APN |
5 |
116,079,962 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL01447:Cit
|
APN |
5 |
116,011,902 (GRCm39) |
splice site |
probably benign |
|
IGL01621:Cit
|
APN |
5 |
116,130,662 (GRCm39) |
splice site |
probably benign |
|
IGL02010:Cit
|
APN |
5 |
116,014,006 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02538:Cit
|
APN |
5 |
116,125,048 (GRCm39) |
nonsense |
probably null |
|
IGL02607:Cit
|
APN |
5 |
115,997,268 (GRCm39) |
missense |
probably benign |
|
IGL02720:Cit
|
APN |
5 |
116,133,511 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02725:Cit
|
APN |
5 |
116,123,532 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02967:Cit
|
APN |
5 |
116,083,896 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02973:Cit
|
APN |
5 |
116,144,058 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL03383:Cit
|
APN |
5 |
116,011,904 (GRCm39) |
splice site |
probably benign |
|
PIT4514001:Cit
|
UTSW |
5 |
116,135,913 (GRCm39) |
critical splice donor site |
probably null |
|
R0206:Cit
|
UTSW |
5 |
116,132,089 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0206:Cit
|
UTSW |
5 |
116,132,089 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0226:Cit
|
UTSW |
5 |
116,122,899 (GRCm39) |
missense |
probably damaging |
0.99 |
R0320:Cit
|
UTSW |
5 |
116,117,504 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0401:Cit
|
UTSW |
5 |
116,123,538 (GRCm39) |
missense |
probably benign |
0.06 |
R0480:Cit
|
UTSW |
5 |
116,071,452 (GRCm39) |
splice site |
probably benign |
|
R0609:Cit
|
UTSW |
5 |
116,012,002 (GRCm39) |
missense |
probably damaging |
0.98 |
R0737:Cit
|
UTSW |
5 |
116,084,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R1238:Cit
|
UTSW |
5 |
115,989,280 (GRCm39) |
missense |
probably benign |
0.30 |
R1503:Cit
|
UTSW |
5 |
116,011,959 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1551:Cit
|
UTSW |
5 |
116,083,901 (GRCm39) |
missense |
probably benign |
0.00 |
R1602:Cit
|
UTSW |
5 |
116,135,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R1720:Cit
|
UTSW |
5 |
116,105,956 (GRCm39) |
missense |
probably damaging |
0.98 |
R1854:Cit
|
UTSW |
5 |
116,011,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R1886:Cit
|
UTSW |
5 |
116,071,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R2024:Cit
|
UTSW |
5 |
116,143,899 (GRCm39) |
missense |
probably damaging |
0.97 |
R2024:Cit
|
UTSW |
5 |
116,085,983 (GRCm39) |
missense |
probably damaging |
0.97 |
R2048:Cit
|
UTSW |
5 |
116,024,872 (GRCm39) |
splice site |
probably null |
|
R2128:Cit
|
UTSW |
5 |
116,123,566 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2192:Cit
|
UTSW |
5 |
116,106,068 (GRCm39) |
missense |
probably benign |
0.00 |
R2244:Cit
|
UTSW |
5 |
116,064,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R2518:Cit
|
UTSW |
5 |
116,125,105 (GRCm39) |
missense |
probably damaging |
0.99 |
R2679:Cit
|
UTSW |
5 |
116,107,174 (GRCm39) |
missense |
probably benign |
0.00 |
R2898:Cit
|
UTSW |
5 |
116,012,037 (GRCm39) |
splice site |
probably null |
|
R2908:Cit
|
UTSW |
5 |
116,119,735 (GRCm39) |
missense |
probably benign |
0.00 |
R3079:Cit
|
UTSW |
5 |
116,063,545 (GRCm39) |
missense |
probably damaging |
0.97 |
R3779:Cit
|
UTSW |
5 |
115,997,400 (GRCm39) |
missense |
probably benign |
0.01 |
R4081:Cit
|
UTSW |
5 |
116,086,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R4494:Cit
|
UTSW |
5 |
116,012,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R4610:Cit
|
UTSW |
5 |
116,132,146 (GRCm39) |
missense |
probably benign |
0.01 |
R4757:Cit
|
UTSW |
5 |
116,135,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R4788:Cit
|
UTSW |
5 |
116,071,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R4816:Cit
|
UTSW |
5 |
116,046,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R4890:Cit
|
UTSW |
5 |
116,126,182 (GRCm39) |
intron |
probably benign |
|
R4899:Cit
|
UTSW |
5 |
116,001,087 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4928:Cit
|
UTSW |
5 |
116,123,856 (GRCm39) |
missense |
probably benign |
0.00 |
R5073:Cit
|
UTSW |
5 |
116,084,902 (GRCm39) |
missense |
probably benign |
0.24 |
R5151:Cit
|
UTSW |
5 |
116,117,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R5154:Cit
|
UTSW |
5 |
116,126,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R5222:Cit
|
UTSW |
5 |
116,090,602 (GRCm39) |
missense |
probably benign |
0.03 |
R5814:Cit
|
UTSW |
5 |
116,117,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R5935:Cit
|
UTSW |
5 |
116,063,598 (GRCm39) |
intron |
probably benign |
|
R5946:Cit
|
UTSW |
5 |
116,135,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R6051:Cit
|
UTSW |
5 |
115,984,464 (GRCm39) |
missense |
probably benign |
|
R6289:Cit
|
UTSW |
5 |
116,144,385 (GRCm39) |
makesense |
probably null |
|
R6298:Cit
|
UTSW |
5 |
116,086,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R6362:Cit
|
UTSW |
5 |
116,024,735 (GRCm39) |
missense |
probably benign |
0.01 |
R6545:Cit
|
UTSW |
5 |
115,984,493 (GRCm39) |
missense |
probably null |
0.00 |
R6761:Cit
|
UTSW |
5 |
116,046,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R6798:Cit
|
UTSW |
5 |
116,064,585 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6814:Cit
|
UTSW |
5 |
116,023,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R6825:Cit
|
UTSW |
5 |
116,119,833 (GRCm39) |
missense |
probably damaging |
0.99 |
R6845:Cit
|
UTSW |
5 |
116,122,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R6983:Cit
|
UTSW |
5 |
116,132,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R7164:Cit
|
UTSW |
5 |
116,123,846 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7359:Cit
|
UTSW |
5 |
116,064,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R7597:Cit
|
UTSW |
5 |
116,024,740 (GRCm39) |
nonsense |
probably null |
|
R7729:Cit
|
UTSW |
5 |
116,122,881 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7763:Cit
|
UTSW |
5 |
116,125,060 (GRCm39) |
missense |
probably benign |
0.01 |
R7786:Cit
|
UTSW |
5 |
116,001,077 (GRCm39) |
missense |
probably benign |
0.00 |
R7799:Cit
|
UTSW |
5 |
116,001,027 (GRCm39) |
missense |
probably benign |
0.00 |
R8060:Cit
|
UTSW |
5 |
116,046,786 (GRCm39) |
missense |
probably benign |
0.00 |
R8068:Cit
|
UTSW |
5 |
116,120,294 (GRCm39) |
missense |
probably benign |
0.03 |
R8068:Cit
|
UTSW |
5 |
116,090,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R8122:Cit
|
UTSW |
5 |
116,107,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R8177:Cit
|
UTSW |
5 |
116,126,218 (GRCm39) |
missense |
probably benign |
0.18 |
R8178:Cit
|
UTSW |
5 |
116,107,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R8265:Cit
|
UTSW |
5 |
116,126,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R8359:Cit
|
UTSW |
5 |
116,122,603 (GRCm39) |
splice site |
probably null |
|
R8397:Cit
|
UTSW |
5 |
116,024,856 (GRCm39) |
missense |
probably benign |
|
R8489:Cit
|
UTSW |
5 |
116,083,962 (GRCm39) |
critical splice donor site |
probably null |
|
R8784:Cit
|
UTSW |
5 |
115,984,442 (GRCm39) |
nonsense |
probably null |
|
R8798:Cit
|
UTSW |
5 |
116,107,102 (GRCm39) |
missense |
probably damaging |
0.99 |
R8882:Cit
|
UTSW |
5 |
116,001,089 (GRCm39) |
missense |
probably benign |
0.04 |
R8984:Cit
|
UTSW |
5 |
116,064,534 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9091:Cit
|
UTSW |
5 |
115,984,161 (GRCm39) |
intron |
probably benign |
|
R9127:Cit
|
UTSW |
5 |
116,074,896 (GRCm39) |
nonsense |
probably null |
|
R9204:Cit
|
UTSW |
5 |
116,126,498 (GRCm39) |
missense |
probably damaging |
0.99 |
R9212:Cit
|
UTSW |
5 |
116,013,952 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9279:Cit
|
UTSW |
5 |
116,065,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R9288:Cit
|
UTSW |
5 |
116,123,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R9377:Cit
|
UTSW |
5 |
116,084,914 (GRCm39) |
missense |
probably benign |
0.04 |
R9520:Cit
|
UTSW |
5 |
116,079,954 (GRCm39) |
nonsense |
probably null |
|
Z1088:Cit
|
UTSW |
5 |
116,123,592 (GRCm39) |
missense |
possibly damaging |
0.62 |
Z1176:Cit
|
UTSW |
5 |
116,124,662 (GRCm39) |
missense |
probably damaging |
1.00 |
|