Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310003L06Rik |
A |
T |
5: 87,971,933 (GRCm38) |
D183V |
probably damaging |
Het |
Ambra1 |
T |
A |
2: 91,885,719 (GRCm38) |
D858E |
probably damaging |
Het |
Amdhd2 |
T |
C |
17: 24,156,604 (GRCm38) |
T370A |
probably benign |
Het |
Amy1 |
A |
G |
3: 113,558,094 (GRCm38) |
W449R |
probably benign |
Het |
Aox3 |
A |
T |
1: 58,186,280 (GRCm38) |
I1179F |
probably benign |
Het |
Atp10a |
C |
A |
7: 58,824,327 (GRCm38) |
Q1121K |
probably damaging |
Het |
Btaf1 |
C |
T |
19: 36,951,148 (GRCm38) |
A123V |
probably benign |
Het |
Car6 |
T |
C |
4: 150,198,141 (GRCm38) |
K16E |
probably benign |
Het |
Cgnl1 |
C |
T |
9: 71,656,096 (GRCm38) |
D779N |
probably benign |
Het |
Cyp2a4 |
G |
A |
7: 26,308,537 (GRCm38) |
R123Q |
possibly damaging |
Het |
D430041D05Rik |
C |
T |
2: 104,156,816 (GRCm38) |
R1895Q |
probably damaging |
Het |
D5Ertd579e |
T |
A |
5: 36,616,206 (GRCm38) |
T282S |
probably benign |
Het |
Dsel |
T |
C |
1: 111,859,962 (GRCm38) |
T948A |
probably benign |
Het |
Ednrb |
A |
T |
14: 103,843,100 (GRCm38) |
I126N |
probably damaging |
Het |
Egln1 |
A |
G |
8: 124,948,306 (GRCm38) |
M250T |
probably benign |
Het |
Epb41l3 |
A |
T |
17: 69,253,468 (GRCm38) |
I337L |
possibly damaging |
Het |
Epg5 |
T |
C |
18: 77,948,745 (GRCm38) |
I219T |
probably benign |
Het |
Gm13030 |
T |
C |
4: 138,873,419 (GRCm38) |
|
probably benign |
Het |
Gm1527 |
T |
A |
3: 28,926,661 (GRCm38) |
C637S |
probably benign |
Het |
Hist1h1a |
A |
G |
13: 23,763,949 (GRCm38) |
N78S |
possibly damaging |
Het |
Insrr |
T |
C |
3: 87,814,291 (GRCm38) |
I1168T |
possibly damaging |
Het |
Ireb2 |
T |
C |
9: 54,896,552 (GRCm38) |
V509A |
possibly damaging |
Het |
Kmt2c |
T |
C |
5: 25,354,717 (GRCm38) |
D981G |
probably damaging |
Het |
Ktn1 |
A |
G |
14: 47,725,960 (GRCm38) |
E1164G |
probably damaging |
Het |
L3hypdh |
A |
T |
12: 72,079,527 (GRCm38) |
V213E |
probably damaging |
Het |
Masp1 |
T |
G |
16: 23,491,959 (GRCm38) |
D241A |
probably damaging |
Het |
Mfsd13b |
A |
G |
7: 120,991,824 (GRCm38) |
I1V |
probably null |
Het |
Muc5b |
T |
C |
7: 141,869,754 (GRCm38) |
V4531A |
probably benign |
Het |
Myh2 |
A |
T |
11: 67,174,941 (GRCm38) |
|
probably null |
Het |
Naip5 |
A |
G |
13: 100,221,533 (GRCm38) |
L1065P |
probably damaging |
Het |
Necab1 |
T |
C |
4: 15,140,219 (GRCm38) |
|
probably benign |
Het |
Nemf |
A |
G |
12: 69,353,786 (GRCm38) |
|
probably benign |
Het |
Nfil3 |
A |
T |
13: 52,968,033 (GRCm38) |
D278E |
possibly damaging |
Het |
Nup98 |
T |
C |
7: 102,180,424 (GRCm38) |
N393S |
probably damaging |
Het |
Ogdh |
T |
A |
11: 6,349,393 (GRCm38) |
M753K |
probably benign |
Het |
Olfr11 |
A |
T |
13: 21,639,436 (GRCm38) |
V29E |
probably damaging |
Het |
Olfr1297 |
C |
T |
2: 111,621,739 (GRCm38) |
V112M |
probably benign |
Het |
Olfr273 |
T |
C |
4: 52,855,568 (GRCm38) |
Y315C |
probably benign |
Het |
Olfr561 |
T |
C |
7: 102,775,243 (GRCm38) |
F240L |
probably benign |
Het |
Olfr901 |
T |
A |
9: 38,431,082 (GRCm38) |
S267T |
probably benign |
Het |
Pkd2 |
A |
G |
5: 104,477,123 (GRCm38) |
K262E |
probably benign |
Het |
Plce1 |
C |
T |
19: 38,727,013 (GRCm38) |
|
probably benign |
Het |
Ppm1f |
T |
A |
16: 16,923,880 (GRCm38) |
M406K |
possibly damaging |
Het |
Ptgs1 |
C |
T |
2: 36,242,847 (GRCm38) |
Q286* |
probably null |
Het |
Scube2 |
T |
C |
7: 109,808,505 (GRCm38) |
T743A |
possibly damaging |
Het |
Tipin |
T |
A |
9: 64,290,376 (GRCm38) |
L69* |
probably null |
Het |
Tlk1 |
T |
A |
2: 70,738,445 (GRCm38) |
K404N |
probably damaging |
Het |
Tmem59 |
C |
A |
4: 107,178,774 (GRCm38) |
L16I |
probably damaging |
Het |
Utrn |
T |
C |
10: 12,737,082 (GRCm38) |
E426G |
probably benign |
Het |
Yjefn3 |
T |
C |
8: 69,889,487 (GRCm38) |
N28D |
probably damaging |
Het |
Zfp598 |
A |
C |
17: 24,679,667 (GRCm38) |
D480A |
probably damaging |
Het |
|
Other mutations in Xdh |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00493:Xdh
|
APN |
17 |
73,923,106 (GRCm38) |
missense |
possibly damaging |
0.58 |
IGL00556:Xdh
|
APN |
17 |
73,884,435 (GRCm38) |
makesense |
probably null |
|
IGL01524:Xdh
|
APN |
17 |
73,923,137 (GRCm38) |
critical splice acceptor site |
probably null |
|
IGL01604:Xdh
|
APN |
17 |
73,909,337 (GRCm38) |
missense |
probably benign |
0.02 |
IGL01625:Xdh
|
APN |
17 |
73,916,786 (GRCm38) |
critical splice donor site |
probably null |
|
IGL01778:Xdh
|
APN |
17 |
73,900,280 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01804:Xdh
|
APN |
17 |
73,892,759 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01825:Xdh
|
APN |
17 |
73,891,245 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01929:Xdh
|
APN |
17 |
73,934,855 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02068:Xdh
|
APN |
17 |
73,913,950 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02079:Xdh
|
APN |
17 |
73,891,277 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02210:Xdh
|
APN |
17 |
73,943,895 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02261:Xdh
|
APN |
17 |
73,913,965 (GRCm38) |
missense |
possibly damaging |
0.81 |
IGL02365:Xdh
|
APN |
17 |
73,943,890 (GRCm38) |
missense |
probably benign |
0.14 |
IGL02424:Xdh
|
APN |
17 |
73,926,570 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02491:Xdh
|
APN |
17 |
73,886,464 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02525:Xdh
|
APN |
17 |
73,924,995 (GRCm38) |
missense |
possibly damaging |
0.91 |
IGL02578:Xdh
|
APN |
17 |
73,906,246 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02793:Xdh
|
APN |
17 |
73,900,581 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02939:Xdh
|
APN |
17 |
73,943,845 (GRCm38) |
critical splice donor site |
probably null |
|
IGL03327:Xdh
|
APN |
17 |
73,916,792 (GRCm38) |
missense |
probably benign |
|
IGL03345:Xdh
|
APN |
17 |
73,906,032 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL03353:Xdh
|
APN |
17 |
73,895,786 (GRCm38) |
missense |
possibly damaging |
0.65 |
inky
|
UTSW |
17 |
73,921,351 (GRCm38) |
missense |
probably damaging |
1.00 |
nucleus
|
UTSW |
17 |
73,899,012 (GRCm38) |
nonsense |
probably null |
|
squidgame
|
UTSW |
17 |
73,939,836 (GRCm38) |
missense |
probably benign |
|
R0018:Xdh
|
UTSW |
17 |
73,925,025 (GRCm38) |
missense |
probably benign |
0.00 |
R0018:Xdh
|
UTSW |
17 |
73,925,025 (GRCm38) |
missense |
probably benign |
0.00 |
R0033:Xdh
|
UTSW |
17 |
73,907,632 (GRCm38) |
missense |
probably benign |
0.06 |
R0079:Xdh
|
UTSW |
17 |
73,891,218 (GRCm38) |
missense |
probably damaging |
1.00 |
R0086:Xdh
|
UTSW |
17 |
73,884,438 (GRCm38) |
missense |
probably benign |
|
R0319:Xdh
|
UTSW |
17 |
73,906,101 (GRCm38) |
splice site |
probably benign |
|
R0336:Xdh
|
UTSW |
17 |
73,922,463 (GRCm38) |
missense |
possibly damaging |
0.91 |
R0389:Xdh
|
UTSW |
17 |
73,898,362 (GRCm38) |
missense |
probably damaging |
1.00 |
R0684:Xdh
|
UTSW |
17 |
73,943,891 (GRCm38) |
missense |
probably damaging |
0.97 |
R0930:Xdh
|
UTSW |
17 |
73,923,082 (GRCm38) |
missense |
probably benign |
0.00 |
R1073:Xdh
|
UTSW |
17 |
73,939,836 (GRCm38) |
missense |
probably benign |
|
R1114:Xdh
|
UTSW |
17 |
73,941,149 (GRCm38) |
splice site |
probably benign |
|
R1201:Xdh
|
UTSW |
17 |
73,918,418 (GRCm38) |
missense |
probably benign |
0.05 |
R1230:Xdh
|
UTSW |
17 |
73,891,256 (GRCm38) |
missense |
probably damaging |
1.00 |
R1351:Xdh
|
UTSW |
17 |
73,923,078 (GRCm38) |
missense |
probably benign |
0.02 |
R1470:Xdh
|
UTSW |
17 |
73,891,112 (GRCm38) |
missense |
probably damaging |
1.00 |
R1470:Xdh
|
UTSW |
17 |
73,891,112 (GRCm38) |
missense |
probably damaging |
1.00 |
R1485:Xdh
|
UTSW |
17 |
73,914,019 (GRCm38) |
nonsense |
probably null |
|
R1548:Xdh
|
UTSW |
17 |
73,913,901 (GRCm38) |
missense |
probably damaging |
0.98 |
R1637:Xdh
|
UTSW |
17 |
73,900,578 (GRCm38) |
missense |
probably benign |
|
R1641:Xdh
|
UTSW |
17 |
73,926,552 (GRCm38) |
missense |
probably benign |
|
R1758:Xdh
|
UTSW |
17 |
73,910,209 (GRCm38) |
missense |
probably damaging |
1.00 |
R1951:Xdh
|
UTSW |
17 |
73,907,658 (GRCm38) |
missense |
probably damaging |
1.00 |
R1969:Xdh
|
UTSW |
17 |
73,892,751 (GRCm38) |
missense |
possibly damaging |
0.55 |
R2024:Xdh
|
UTSW |
17 |
73,921,305 (GRCm38) |
missense |
possibly damaging |
0.92 |
R2157:Xdh
|
UTSW |
17 |
73,922,537 (GRCm38) |
missense |
probably damaging |
1.00 |
R2300:Xdh
|
UTSW |
17 |
73,891,265 (GRCm38) |
missense |
probably damaging |
1.00 |
R3783:Xdh
|
UTSW |
17 |
73,893,595 (GRCm38) |
splice site |
probably benign |
|
R3796:Xdh
|
UTSW |
17 |
73,907,658 (GRCm38) |
missense |
probably damaging |
1.00 |
R3797:Xdh
|
UTSW |
17 |
73,907,658 (GRCm38) |
missense |
probably damaging |
1.00 |
R3798:Xdh
|
UTSW |
17 |
73,907,658 (GRCm38) |
missense |
probably damaging |
1.00 |
R3799:Xdh
|
UTSW |
17 |
73,907,658 (GRCm38) |
missense |
probably damaging |
1.00 |
R3819:Xdh
|
UTSW |
17 |
73,906,725 (GRCm38) |
missense |
probably benign |
0.35 |
R4085:Xdh
|
UTSW |
17 |
73,916,879 (GRCm38) |
missense |
probably benign |
0.35 |
R4240:Xdh
|
UTSW |
17 |
73,895,795 (GRCm38) |
missense |
possibly damaging |
0.72 |
R4356:Xdh
|
UTSW |
17 |
73,915,690 (GRCm38) |
missense |
probably benign |
0.01 |
R4522:Xdh
|
UTSW |
17 |
73,898,344 (GRCm38) |
missense |
probably damaging |
1.00 |
R4523:Xdh
|
UTSW |
17 |
73,898,344 (GRCm38) |
missense |
probably damaging |
1.00 |
R4524:Xdh
|
UTSW |
17 |
73,898,344 (GRCm38) |
missense |
probably damaging |
1.00 |
R4600:Xdh
|
UTSW |
17 |
73,910,200 (GRCm38) |
missense |
probably benign |
0.19 |
R4617:Xdh
|
UTSW |
17 |
73,918,394 (GRCm38) |
missense |
probably damaging |
0.99 |
R4756:Xdh
|
UTSW |
17 |
73,886,386 (GRCm38) |
missense |
probably benign |
0.24 |
R4761:Xdh
|
UTSW |
17 |
73,910,267 (GRCm38) |
missense |
possibly damaging |
0.91 |
R4815:Xdh
|
UTSW |
17 |
73,906,215 (GRCm38) |
missense |
probably damaging |
1.00 |
R4850:Xdh
|
UTSW |
17 |
73,898,335 (GRCm38) |
missense |
probably damaging |
1.00 |
R4896:Xdh
|
UTSW |
17 |
73,910,243 (GRCm38) |
missense |
probably damaging |
0.96 |
R4897:Xdh
|
UTSW |
17 |
73,900,708 (GRCm38) |
missense |
probably benign |
|
R4923:Xdh
|
UTSW |
17 |
73,924,936 (GRCm38) |
missense |
possibly damaging |
0.72 |
R4977:Xdh
|
UTSW |
17 |
73,898,970 (GRCm38) |
missense |
probably benign |
0.05 |
R5030:Xdh
|
UTSW |
17 |
73,891,293 (GRCm38) |
missense |
probably damaging |
1.00 |
R5185:Xdh
|
UTSW |
17 |
73,925,011 (GRCm38) |
missense |
probably damaging |
1.00 |
R5347:Xdh
|
UTSW |
17 |
73,925,032 (GRCm38) |
missense |
probably benign |
|
R5556:Xdh
|
UTSW |
17 |
73,897,764 (GRCm38) |
missense |
probably benign |
0.21 |
R5566:Xdh
|
UTSW |
17 |
73,893,622 (GRCm38) |
missense |
probably damaging |
1.00 |
R5568:Xdh
|
UTSW |
17 |
73,943,885 (GRCm38) |
missense |
possibly damaging |
0.90 |
R5635:Xdh
|
UTSW |
17 |
73,913,875 (GRCm38) |
missense |
possibly damaging |
0.92 |
R5662:Xdh
|
UTSW |
17 |
73,941,115 (GRCm38) |
missense |
probably damaging |
0.99 |
R5955:Xdh
|
UTSW |
17 |
73,898,320 (GRCm38) |
missense |
probably damaging |
1.00 |
R6058:Xdh
|
UTSW |
17 |
73,906,269 (GRCm38) |
missense |
probably damaging |
1.00 |
R6061:Xdh
|
UTSW |
17 |
73,921,347 (GRCm38) |
missense |
probably damaging |
1.00 |
R6412:Xdh
|
UTSW |
17 |
73,935,907 (GRCm38) |
missense |
probably benign |
0.09 |
R6526:Xdh
|
UTSW |
17 |
73,900,551 (GRCm38) |
missense |
probably damaging |
0.97 |
R6558:Xdh
|
UTSW |
17 |
73,893,713 (GRCm38) |
missense |
possibly damaging |
0.95 |
R6843:Xdh
|
UTSW |
17 |
73,923,130 (GRCm38) |
missense |
probably damaging |
1.00 |
R6932:Xdh
|
UTSW |
17 |
73,922,562 (GRCm38) |
missense |
probably damaging |
0.99 |
R7028:Xdh
|
UTSW |
17 |
73,943,873 (GRCm38) |
missense |
probably damaging |
0.99 |
R7418:Xdh
|
UTSW |
17 |
73,913,965 (GRCm38) |
missense |
possibly damaging |
0.81 |
R7503:Xdh
|
UTSW |
17 |
73,926,210 (GRCm38) |
missense |
probably damaging |
1.00 |
R7653:Xdh
|
UTSW |
17 |
73,897,045 (GRCm38) |
missense |
probably benign |
0.10 |
R7763:Xdh
|
UTSW |
17 |
73,934,834 (GRCm38) |
missense |
possibly damaging |
0.69 |
R7768:Xdh
|
UTSW |
17 |
73,939,836 (GRCm38) |
missense |
probably benign |
|
R7904:Xdh
|
UTSW |
17 |
73,922,472 (GRCm38) |
missense |
probably benign |
0.09 |
R8010:Xdh
|
UTSW |
17 |
73,909,317 (GRCm38) |
nonsense |
probably null |
|
R8067:Xdh
|
UTSW |
17 |
73,900,657 (GRCm38) |
missense |
probably benign |
0.01 |
R8238:Xdh
|
UTSW |
17 |
73,886,417 (GRCm38) |
missense |
probably benign |
|
R8253:Xdh
|
UTSW |
17 |
73,918,382 (GRCm38) |
missense |
possibly damaging |
0.94 |
R8346:Xdh
|
UTSW |
17 |
73,913,943 (GRCm38) |
missense |
probably damaging |
1.00 |
R8350:Xdh
|
UTSW |
17 |
73,934,842 (GRCm38) |
missense |
probably damaging |
1.00 |
R8381:Xdh
|
UTSW |
17 |
73,912,461 (GRCm38) |
missense |
probably benign |
|
R8427:Xdh
|
UTSW |
17 |
73,935,931 (GRCm38) |
missense |
probably damaging |
1.00 |
R8465:Xdh
|
UTSW |
17 |
73,899,012 (GRCm38) |
nonsense |
probably null |
|
R8478:Xdh
|
UTSW |
17 |
73,906,058 (GRCm38) |
missense |
probably benign |
0.00 |
R8680:Xdh
|
UTSW |
17 |
73,922,505 (GRCm38) |
missense |
probably benign |
|
R8802:Xdh
|
UTSW |
17 |
73,918,410 (GRCm38) |
missense |
probably benign |
0.00 |
R8984:Xdh
|
UTSW |
17 |
73,921,351 (GRCm38) |
missense |
probably damaging |
1.00 |
R8985:Xdh
|
UTSW |
17 |
73,921,351 (GRCm38) |
missense |
probably damaging |
1.00 |
R8995:Xdh
|
UTSW |
17 |
73,898,374 (GRCm38) |
missense |
probably damaging |
1.00 |
R9035:Xdh
|
UTSW |
17 |
73,910,227 (GRCm38) |
missense |
probably benign |
|
R9149:Xdh
|
UTSW |
17 |
73,915,693 (GRCm38) |
missense |
probably benign |
|
R9181:Xdh
|
UTSW |
17 |
73,925,011 (GRCm38) |
missense |
probably damaging |
1.00 |
R9357:Xdh
|
UTSW |
17 |
73,926,546 (GRCm38) |
critical splice donor site |
probably null |
|
R9357:Xdh
|
UTSW |
17 |
73,907,716 (GRCm38) |
missense |
probably damaging |
0.97 |
R9609:Xdh
|
UTSW |
17 |
73,924,995 (GRCm38) |
missense |
possibly damaging |
0.91 |
R9803:Xdh
|
UTSW |
17 |
73,922,460 (GRCm38) |
missense |
probably benign |
|
X0019:Xdh
|
UTSW |
17 |
73,918,454 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1088:Xdh
|
UTSW |
17 |
73,886,428 (GRCm38) |
missense |
probably benign |
|
Z1176:Xdh
|
UTSW |
17 |
73,923,042 (GRCm38) |
critical splice donor site |
probably null |
|
Z1177:Xdh
|
UTSW |
17 |
73,897,695 (GRCm38) |
missense |
probably damaging |
1.00 |
|