Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam10 |
A |
G |
9: 70,647,357 (GRCm39) |
D19G |
possibly damaging |
Het |
Adhfe1 |
A |
G |
1: 9,633,778 (GRCm39) |
K342R |
probably benign |
Het |
Adk |
A |
G |
14: 21,368,244 (GRCm39) |
N223S |
probably damaging |
Het |
Aff4 |
A |
G |
11: 53,289,212 (GRCm39) |
S454G |
probably benign |
Het |
Ahnak |
T |
A |
19: 8,984,420 (GRCm39) |
N1901K |
probably damaging |
Het |
Camsap1 |
T |
C |
2: 25,819,755 (GRCm39) |
T1578A |
probably benign |
Het |
Ccdc63 |
A |
C |
5: 122,268,350 (GRCm39) |
|
probably null |
Het |
Ceacam1 |
G |
T |
7: 25,176,113 (GRCm39) |
S27Y |
probably benign |
Het |
Cntn4 |
A |
G |
6: 106,414,825 (GRCm39) |
|
probably benign |
Het |
Cyp2d26 |
A |
G |
15: 82,676,928 (GRCm39) |
|
probably benign |
Het |
Cyp3a13 |
A |
T |
5: 137,908,237 (GRCm39) |
V204E |
probably damaging |
Het |
Cyp51 |
G |
A |
5: 4,136,636 (GRCm39) |
|
probably benign |
Het |
Dipk1a |
T |
C |
5: 108,057,886 (GRCm39) |
D179G |
probably damaging |
Het |
Epb41l4b |
T |
G |
4: 57,142,866 (GRCm39) |
E96D |
probably benign |
Het |
Epg5 |
A |
G |
18: 78,067,202 (GRCm39) |
E2221G |
probably damaging |
Het |
Fbxo21 |
T |
A |
5: 118,146,169 (GRCm39) |
N597K |
probably damaging |
Het |
Fpr-rs4 |
CAGGAA |
CA |
17: 18,242,596 (GRCm39) |
|
probably null |
Het |
Fsip1 |
C |
A |
2: 118,072,197 (GRCm39) |
E195D |
probably damaging |
Het |
Gm10152 |
T |
C |
7: 144,317,049 (GRCm39) |
F35L |
unknown |
Het |
Gtpbp6 |
A |
C |
5: 110,254,931 (GRCm39) |
V87G |
probably damaging |
Het |
Hal |
A |
G |
10: 93,327,002 (GRCm39) |
T176A |
probably damaging |
Het |
Il12rb2 |
G |
T |
6: 67,337,529 (GRCm39) |
N117K |
probably benign |
Het |
Kalrn |
A |
G |
16: 34,072,680 (GRCm39) |
V734A |
probably benign |
Het |
Klf7 |
A |
G |
1: 64,117,913 (GRCm39) |
V228A |
possibly damaging |
Het |
Kng1 |
A |
G |
16: 22,877,354 (GRCm39) |
Y54C |
probably damaging |
Het |
Lpcat2 |
T |
G |
8: 93,596,471 (GRCm39) |
N169K |
possibly damaging |
Het |
Magohb |
A |
T |
6: 131,266,385 (GRCm39) |
S40R |
probably damaging |
Het |
Mgam |
A |
G |
6: 40,633,363 (GRCm39) |
D186G |
possibly damaging |
Het |
Mycbp2 |
A |
G |
14: 103,469,960 (GRCm39) |
|
probably null |
Het |
Myh15 |
A |
G |
16: 48,975,928 (GRCm39) |
D1332G |
probably damaging |
Het |
Myh9 |
G |
A |
15: 77,655,332 (GRCm39) |
T1208M |
possibly damaging |
Het |
Ncor2 |
C |
T |
5: 125,161,996 (GRCm39) |
R426H |
unknown |
Het |
Nradd |
T |
C |
9: 110,450,697 (GRCm39) |
E160G |
probably benign |
Het |
Or10u4 |
G |
A |
10: 129,801,861 (GRCm39) |
S230L |
probably damaging |
Het |
Or2a54 |
T |
A |
6: 43,093,312 (GRCm39) |
M212K |
probably benign |
Het |
Otog |
A |
T |
7: 45,937,063 (GRCm39) |
T1591S |
probably damaging |
Het |
Oxsr1 |
A |
G |
9: 119,076,140 (GRCm39) |
S389P |
probably benign |
Het |
Pde3a |
A |
G |
6: 141,434,732 (GRCm39) |
|
probably benign |
Het |
Pi4k2b |
A |
T |
5: 52,905,773 (GRCm39) |
I105L |
probably benign |
Het |
Pilrb1 |
T |
C |
5: 137,853,153 (GRCm39) |
R217G |
possibly damaging |
Het |
Poteg |
A |
T |
8: 27,946,774 (GRCm39) |
I159L |
probably benign |
Het |
Ppargc1a |
A |
G |
5: 51,705,858 (GRCm39) |
F75S |
probably damaging |
Het |
Ptk2b |
T |
G |
14: 66,409,954 (GRCm39) |
D466A |
probably benign |
Het |
Ptpn21 |
A |
G |
12: 98,655,785 (GRCm39) |
V394A |
possibly damaging |
Het |
Rsf1 |
GCG |
GCGACGGCGACG |
7: 97,229,114 (GRCm39) |
|
probably benign |
Het |
Shisa3 |
G |
A |
5: 67,768,651 (GRCm39) |
E184K |
possibly damaging |
Het |
Slc4a2 |
A |
G |
5: 24,636,557 (GRCm39) |
H283R |
probably damaging |
Het |
Slc9a3 |
A |
G |
13: 74,311,860 (GRCm39) |
S603G |
probably damaging |
Het |
Tas2r124 |
A |
G |
6: 132,731,858 (GRCm39) |
I56V |
possibly damaging |
Het |
Tbcd |
G |
T |
11: 121,431,762 (GRCm39) |
C470F |
probably damaging |
Het |
Thsd1 |
A |
G |
8: 22,749,333 (GRCm39) |
R674G |
probably benign |
Het |
Zbtb11 |
T |
A |
16: 55,818,372 (GRCm39) |
C599S |
probably damaging |
Het |
Zfp541 |
A |
G |
7: 15,812,252 (GRCm39) |
R302G |
possibly damaging |
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 |
|
IGL01537:Cit
|
APN |
5 |
116,071,913 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
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 |
|