Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
C |
A |
5: 8,949,677 (GRCm39) |
T79K |
probably damaging |
Het |
Ackr3 |
G |
T |
1: 90,142,558 (GRCm39) |
G339V |
probably damaging |
Het |
Agpat4 |
G |
T |
17: 12,429,186 (GRCm39) |
R146L |
probably damaging |
Het |
Ampd1 |
C |
T |
3: 102,998,936 (GRCm39) |
R364C |
probably damaging |
Het |
Atrnl1 |
A |
G |
19: 57,645,660 (GRCm39) |
T507A |
probably benign |
Het |
Cand2 |
C |
G |
6: 115,768,923 (GRCm39) |
R578G |
probably benign |
Het |
Capg |
C |
T |
6: 72,532,869 (GRCm39) |
P111L |
probably damaging |
Het |
Carm1 |
C |
T |
9: 21,494,350 (GRCm39) |
T289I |
probably damaging |
Het |
Ccr6 |
A |
G |
17: 8,474,965 (GRCm39) |
I57V |
probably benign |
Het |
Cdk5rap2 |
T |
C |
4: 70,255,583 (GRCm39) |
I434V |
possibly damaging |
Het |
Chrdl2 |
C |
T |
7: 99,655,743 (GRCm39) |
|
probably benign |
Het |
Cntnap5a |
A |
G |
1: 116,220,109 (GRCm39) |
T640A |
probably benign |
Het |
Ctsd |
T |
C |
7: 141,937,280 (GRCm39) |
|
probably null |
Het |
D17H6S53E |
G |
T |
17: 35,346,536 (GRCm39) |
R149L |
possibly damaging |
Het |
Dync1i1 |
A |
G |
6: 5,769,706 (GRCm39) |
T77A |
probably benign |
Het |
Emc2 |
T |
C |
15: 43,358,639 (GRCm39) |
M100T |
probably benign |
Het |
Esrra |
A |
G |
19: 6,889,863 (GRCm39) |
V290A |
probably benign |
Het |
Fbl |
T |
C |
7: 27,876,620 (GRCm39) |
I207T |
probably benign |
Het |
Fktn |
G |
A |
4: 53,734,854 (GRCm39) |
G125D |
probably benign |
Het |
Gcc1 |
T |
A |
6: 28,420,375 (GRCm39) |
N314I |
possibly damaging |
Het |
Gzmm |
A |
T |
10: 79,530,354 (GRCm39) |
D175V |
probably damaging |
Het |
Heatr1 |
G |
A |
13: 12,448,806 (GRCm39) |
M1840I |
probably benign |
Het |
Helz |
T |
C |
11: 107,523,153 (GRCm39) |
L779P |
probably damaging |
Het |
Impg1 |
T |
A |
9: 80,289,064 (GRCm39) |
N331I |
probably damaging |
Het |
Inmt |
C |
T |
6: 55,150,270 (GRCm39) |
|
probably null |
Het |
Inpp5a |
C |
T |
7: 139,061,634 (GRCm39) |
T102M |
probably damaging |
Het |
Lamc3 |
A |
G |
2: 31,788,323 (GRCm39) |
Y161C |
probably benign |
Het |
Lpin2 |
A |
G |
17: 71,553,966 (GRCm39) |
*932W |
probably null |
Het |
Lrp3 |
C |
T |
7: 34,901,934 (GRCm39) |
R649H |
probably benign |
Het |
Madd |
G |
A |
2: 90,973,949 (GRCm39) |
T1464I |
probably damaging |
Het |
Nceh1 |
C |
A |
3: 27,293,777 (GRCm39) |
Y178* |
probably null |
Het |
Or5ae2 |
A |
T |
7: 84,506,086 (GRCm39) |
K172* |
probably null |
Het |
Or5b96 |
T |
A |
19: 12,867,989 (GRCm39) |
|
probably benign |
Het |
Pramel39-ps |
G |
T |
5: 94,451,001 (GRCm39) |
P375H |
probably damaging |
Het |
Ptchd4 |
A |
T |
17: 42,627,604 (GRCm39) |
R22* |
probably null |
Het |
Ptpru |
C |
T |
4: 131,530,341 (GRCm39) |
G560S |
probably damaging |
Het |
Ralgapb |
G |
T |
2: 158,277,386 (GRCm39) |
R250L |
probably benign |
Het |
Rcor1 |
T |
A |
12: 111,076,228 (GRCm39) |
Y395* |
probably null |
Het |
Slc40a1 |
A |
G |
1: 45,950,129 (GRCm39) |
V441A |
probably benign |
Het |
Slc6a13 |
T |
A |
6: 121,295,228 (GRCm39) |
F77Y |
probably damaging |
Het |
Slc6a15 |
T |
A |
10: 103,229,406 (GRCm39) |
C148* |
probably null |
Het |
Sox10 |
T |
C |
15: 79,040,640 (GRCm39) |
Y300C |
probably damaging |
Het |
Tomm70a |
T |
A |
16: 56,958,383 (GRCm39) |
|
probably benign |
Het |
Tor4a |
A |
G |
2: 25,085,537 (GRCm39) |
V122A |
probably benign |
Het |
Tpi1 |
T |
C |
6: 124,791,138 (GRCm39) |
Q33R |
probably benign |
Het |
Unk |
T |
C |
11: 115,940,184 (GRCm39) |
V179A |
probably benign |
Het |
Ush2a |
G |
T |
1: 188,365,787 (GRCm39) |
G2214C |
probably damaging |
Het |
Vmn1r159 |
T |
A |
7: 22,542,912 (GRCm39) |
Y40F |
probably benign |
Het |
Wbp2nl |
T |
C |
15: 82,192,748 (GRCm39) |
V144A |
probably benign |
Het |
Wdpcp |
A |
G |
11: 21,835,040 (GRCm39) |
E681G |
probably benign |
Het |
|
Other mutations in Slc35f6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R4596:Slc35f6
|
UTSW |
5 |
30,805,406 (GRCm39) |
missense |
probably damaging |
0.99 |
R4665:Slc35f6
|
UTSW |
5 |
30,812,957 (GRCm39) |
missense |
probably damaging |
0.99 |
R4666:Slc35f6
|
UTSW |
5 |
30,812,957 (GRCm39) |
missense |
probably damaging |
0.99 |
R4994:Slc35f6
|
UTSW |
5 |
30,805,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R6500:Slc35f6
|
UTSW |
5 |
30,814,164 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6682:Slc35f6
|
UTSW |
5 |
30,814,764 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7107:Slc35f6
|
UTSW |
5 |
30,814,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R7117:Slc35f6
|
UTSW |
5 |
30,815,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R7219:Slc35f6
|
UTSW |
5 |
30,814,796 (GRCm39) |
missense |
probably benign |
0.02 |
R7852:Slc35f6
|
UTSW |
5 |
30,814,159 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8292:Slc35f6
|
UTSW |
5 |
30,813,375 (GRCm39) |
missense |
probably benign |
0.25 |
R9571:Slc35f6
|
UTSW |
5 |
30,815,180 (GRCm39) |
missense |
possibly damaging |
0.88 |
Z1176:Slc35f6
|
UTSW |
5 |
30,815,039 (GRCm39) |
missense |
probably damaging |
1.00 |
|