Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2410004B18Rik |
T |
A |
3: 145,644,848 (GRCm39) |
S156T |
probably damaging |
Het |
Adra1a |
T |
A |
14: 66,875,634 (GRCm39) |
M203K |
probably damaging |
Het |
Adtrp |
G |
A |
13: 41,969,636 (GRCm39) |
T89I |
possibly damaging |
Het |
Akt3 |
G |
T |
1: 176,886,955 (GRCm39) |
T298K |
probably damaging |
Het |
Aldh4a1 |
G |
T |
4: 139,350,511 (GRCm39) |
|
probably benign |
Het |
Aplf |
T |
C |
6: 87,640,779 (GRCm39) |
T77A |
possibly damaging |
Het |
Arid4b |
T |
A |
13: 14,355,815 (GRCm39) |
W618R |
probably damaging |
Het |
Asxl3 |
C |
A |
18: 22,585,465 (GRCm39) |
P130Q |
probably damaging |
Het |
Asxl3 |
A |
G |
18: 22,585,471 (GRCm39) |
K132R |
probably damaging |
Het |
Atp11a |
T |
C |
8: 12,878,483 (GRCm39) |
M353T |
probably damaging |
Het |
Atp11b |
A |
G |
3: 35,861,038 (GRCm39) |
D375G |
probably damaging |
Het |
Cage1 |
C |
T |
13: 38,201,338 (GRCm39) |
A656T |
possibly damaging |
Het |
Casz1 |
C |
T |
4: 149,023,497 (GRCm39) |
P801S |
probably damaging |
Het |
Cdc14b |
A |
T |
13: 64,368,758 (GRCm39) |
|
probably benign |
Het |
Cdin1 |
A |
G |
2: 115,607,504 (GRCm39) |
T286A |
probably benign |
Het |
Cox6b2 |
A |
G |
7: 4,755,086 (GRCm39) |
F63L |
probably benign |
Het |
Cramp1 |
A |
C |
17: 25,198,603 (GRCm39) |
V773G |
possibly damaging |
Het |
Cul7 |
A |
G |
17: 46,965,448 (GRCm39) |
E542G |
probably benign |
Het |
Cyp2c55 |
T |
C |
19: 39,019,790 (GRCm39) |
Y243H |
possibly damaging |
Het |
Dnah9 |
C |
A |
11: 65,962,925 (GRCm39) |
D1797Y |
possibly damaging |
Het |
Dpep2 |
C |
A |
8: 106,715,944 (GRCm39) |
A298S |
|
Het |
Dvl3 |
G |
A |
16: 20,342,826 (GRCm39) |
|
probably null |
Het |
Dynlt2a3 |
A |
G |
17: 15,187,942 (GRCm39) |
Y111H |
probably damaging |
Het |
Enpp3 |
T |
C |
10: 24,674,172 (GRCm39) |
D376G |
possibly damaging |
Het |
Ffar4 |
T |
C |
19: 38,102,232 (GRCm39) |
I289T |
possibly damaging |
Het |
Gm5565 |
T |
C |
5: 146,094,849 (GRCm39) |
Y299C |
probably damaging |
Het |
Gm57858 |
A |
G |
3: 36,087,033 (GRCm39) |
I187T |
probably benign |
Het |
Gpat3 |
A |
T |
5: 100,994,788 (GRCm39) |
M39L |
probably benign |
Het |
Gpr153 |
T |
C |
4: 152,364,664 (GRCm39) |
L240P |
probably damaging |
Het |
Gpr182 |
T |
C |
10: 127,586,517 (GRCm39) |
I145V |
probably benign |
Het |
H2-Q4 |
A |
T |
17: 35,598,969 (GRCm39) |
T80S |
possibly damaging |
Het |
Hnf1a |
T |
A |
5: 115,088,882 (GRCm39) |
T545S |
probably benign |
Het |
Kif5b |
A |
C |
18: 6,208,261 (GRCm39) |
F946V |
probably benign |
Het |
Krtap16-1 |
C |
T |
11: 99,877,167 (GRCm39) |
C79Y |
probably damaging |
Het |
Lama2 |
A |
G |
10: 26,882,697 (GRCm39) |
V2622A |
possibly damaging |
Het |
Lrrc37a |
T |
A |
11: 103,391,375 (GRCm39) |
Q1350L |
probably damaging |
Het |
Map2k2 |
G |
A |
10: 80,955,498 (GRCm39) |
V294I |
probably benign |
Het |
Meak7 |
T |
C |
8: 120,489,050 (GRCm39) |
N411S |
probably benign |
Het |
Mtus1 |
G |
A |
8: 41,536,760 (GRCm39) |
H319Y |
possibly damaging |
Het |
Ncdn |
T |
C |
4: 126,644,621 (GRCm39) |
D67G |
possibly damaging |
Het |
Ngef |
G |
A |
1: 87,431,010 (GRCm39) |
P269L |
probably damaging |
Het |
Nlrp9b |
A |
G |
7: 19,757,401 (GRCm39) |
I213V |
possibly damaging |
Het |
Nyap2 |
G |
A |
1: 81,275,803 (GRCm39) |
R649H |
possibly damaging |
Het |
Or14a258 |
A |
G |
7: 86,035,248 (GRCm39) |
S207P |
probably benign |
Het |
Or4a67 |
C |
A |
2: 88,598,299 (GRCm39) |
R120L |
probably damaging |
Het |
Or5d20-ps1 |
T |
G |
2: 87,931,416 (GRCm39) |
D305A |
unknown |
Het |
Pi4kb |
T |
A |
3: 94,900,428 (GRCm39) |
L354Q |
probably damaging |
Het |
Plekhh2 |
T |
C |
17: 84,898,190 (GRCm39) |
S944P |
probably damaging |
Het |
Podn |
C |
T |
4: 107,878,743 (GRCm39) |
V375M |
probably damaging |
Het |
Pramel12 |
C |
A |
4: 143,145,673 (GRCm39) |
Q381K |
possibly damaging |
Het |
Psmb2 |
T |
A |
4: 126,599,895 (GRCm39) |
H110Q |
probably benign |
Het |
Rasip1 |
A |
G |
7: 45,282,066 (GRCm39) |
E523G |
possibly damaging |
Het |
Ripor1 |
T |
G |
8: 106,342,783 (GRCm39) |
C219G |
probably damaging |
Het |
Rps6ka2 |
G |
C |
17: 7,567,678 (GRCm39) |
V714L |
probably damaging |
Het |
Sass6 |
G |
T |
3: 116,407,647 (GRCm39) |
L254F |
probably damaging |
Het |
Scarf2 |
G |
A |
16: 17,624,270 (GRCm39) |
G525E |
probably damaging |
Het |
Sh3d21 |
T |
A |
4: 126,046,131 (GRCm39) |
|
probably benign |
Het |
Sh3tc1 |
C |
A |
5: 35,863,827 (GRCm39) |
A787S |
probably benign |
Het |
Skint5 |
T |
A |
4: 113,512,919 (GRCm39) |
N871I |
unknown |
Het |
Slc48a1 |
T |
G |
15: 97,687,833 (GRCm39) |
D62E |
probably damaging |
Het |
Slc6a21 |
G |
A |
7: 44,936,398 (GRCm39) |
M157I |
|
Het |
Slurp2 |
T |
C |
15: 74,614,961 (GRCm39) |
D60G |
probably benign |
Het |
Sparcl1 |
G |
T |
5: 104,240,979 (GRCm39) |
N148K |
possibly damaging |
Het |
Spata31e4 |
C |
T |
13: 50,856,128 (GRCm39) |
R589* |
probably null |
Het |
Spsb2 |
T |
A |
6: 124,786,976 (GRCm39) |
N236K |
probably benign |
Het |
Sptb |
G |
T |
12: 76,679,308 (GRCm39) |
|
probably benign |
Het |
Ssc4d |
A |
T |
5: 135,990,030 (GRCm39) |
C41S |
probably damaging |
Het |
Tecta |
A |
T |
9: 42,286,375 (GRCm39) |
D760E |
probably benign |
Het |
Tesmin |
G |
T |
19: 3,439,431 (GRCm39) |
|
probably benign |
Het |
Tiam1 |
A |
C |
16: 89,601,776 (GRCm39) |
|
probably benign |
Het |
Tnrc6a |
T |
C |
7: 122,778,946 (GRCm39) |
L1219S |
probably damaging |
Het |
Tram1 |
T |
G |
1: 13,639,830 (GRCm39) |
I306L |
probably benign |
Het |
Trank1 |
A |
C |
9: 111,191,500 (GRCm39) |
D503A |
probably damaging |
Het |
Ttc21b |
T |
C |
2: 66,031,596 (GRCm39) |
H1044R |
|
Het |
Ubac2 |
T |
C |
14: 122,145,626 (GRCm39) |
F95L |
probably benign |
Het |
Vmn2r91 |
A |
T |
17: 18,326,296 (GRCm39) |
M194L |
probably benign |
Het |
Yju2b |
C |
T |
8: 84,990,527 (GRCm39) |
R35Q |
probably damaging |
Het |
Zdhhc1 |
G |
T |
8: 106,205,533 (GRCm39) |
H90Q |
probably damaging |
Het |
Zfp169 |
C |
T |
13: 48,652,292 (GRCm39) |
V42I |
probably damaging |
Het |
Zfp81 |
A |
G |
17: 33,553,387 (GRCm39) |
C476R |
probably damaging |
Het |
|
Other mutations in 4930522L14Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02622:4930522L14Rik
|
APN |
5 |
109,887,101 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0164:4930522L14Rik
|
UTSW |
5 |
109,884,713 (GRCm39) |
missense |
probably damaging |
0.96 |
R0164:4930522L14Rik
|
UTSW |
5 |
109,884,713 (GRCm39) |
missense |
probably damaging |
0.96 |
R0432:4930522L14Rik
|
UTSW |
5 |
109,884,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R0463:4930522L14Rik
|
UTSW |
5 |
109,884,926 (GRCm39) |
unclassified |
probably benign |
|
R0891:4930522L14Rik
|
UTSW |
5 |
109,884,156 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1289:4930522L14Rik
|
UTSW |
5 |
109,884,756 (GRCm39) |
nonsense |
probably null |
|
R1637:4930522L14Rik
|
UTSW |
5 |
109,886,858 (GRCm39) |
missense |
probably benign |
0.01 |
R1764:4930522L14Rik
|
UTSW |
5 |
109,884,655 (GRCm39) |
missense |
probably benign |
0.22 |
R1793:4930522L14Rik
|
UTSW |
5 |
109,884,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R1860:4930522L14Rik
|
UTSW |
5 |
109,884,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R1899:4930522L14Rik
|
UTSW |
5 |
109,884,664 (GRCm39) |
missense |
probably benign |
0.04 |
R2135:4930522L14Rik
|
UTSW |
5 |
109,885,509 (GRCm39) |
missense |
probably benign |
0.00 |
R2143:4930522L14Rik
|
UTSW |
5 |
109,884,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R2877:4930522L14Rik
|
UTSW |
5 |
109,886,811 (GRCm39) |
splice site |
probably benign |
|
R3847:4930522L14Rik
|
UTSW |
5 |
109,884,190 (GRCm39) |
splice site |
probably null |
|
R4431:4930522L14Rik
|
UTSW |
5 |
109,884,440 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4578:4930522L14Rik
|
UTSW |
5 |
109,884,537 (GRCm39) |
nonsense |
probably null |
|
R4611:4930522L14Rik
|
UTSW |
5 |
109,885,259 (GRCm39) |
missense |
probably benign |
0.00 |
R4776:4930522L14Rik
|
UTSW |
5 |
109,884,739 (GRCm39) |
missense |
probably benign |
0.22 |
R4921:4930522L14Rik
|
UTSW |
5 |
109,885,662 (GRCm39) |
missense |
probably benign |
0.25 |
R4937:4930522L14Rik
|
UTSW |
5 |
109,884,067 (GRCm39) |
missense |
probably benign |
0.12 |
R4952:4930522L14Rik
|
UTSW |
5 |
109,887,063 (GRCm39) |
critical splice donor site |
probably null |
|
R4980:4930522L14Rik
|
UTSW |
5 |
109,885,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R5079:4930522L14Rik
|
UTSW |
5 |
109,885,196 (GRCm39) |
missense |
probably benign |
|
R5088:4930522L14Rik
|
UTSW |
5 |
109,883,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R5143:4930522L14Rik
|
UTSW |
5 |
109,887,064 (GRCm39) |
critical splice donor site |
probably null |
|
R5183:4930522L14Rik
|
UTSW |
5 |
109,887,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R5461:4930522L14Rik
|
UTSW |
5 |
109,884,643 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5498:4930522L14Rik
|
UTSW |
5 |
109,885,413 (GRCm39) |
missense |
probably benign |
0.05 |
R5576:4930522L14Rik
|
UTSW |
5 |
109,885,570 (GRCm39) |
missense |
probably benign |
0.00 |
R6081:4930522L14Rik
|
UTSW |
5 |
109,887,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R6387:4930522L14Rik
|
UTSW |
5 |
109,884,881 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6509:4930522L14Rik
|
UTSW |
5 |
109,885,250 (GRCm39) |
nonsense |
probably null |
|
R6585:4930522L14Rik
|
UTSW |
5 |
109,885,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R7309:4930522L14Rik
|
UTSW |
5 |
109,884,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R7740:4930522L14Rik
|
UTSW |
5 |
109,885,370 (GRCm39) |
nonsense |
probably null |
|
R7877:4930522L14Rik
|
UTSW |
5 |
109,884,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R8526:4930522L14Rik
|
UTSW |
5 |
109,885,655 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8884:4930522L14Rik
|
UTSW |
5 |
109,885,354 (GRCm39) |
missense |
probably damaging |
0.98 |
R9432:4930522L14Rik
|
UTSW |
5 |
109,884,917 (GRCm39) |
missense |
unknown |
|
|