Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alox5 |
T |
A |
6: 116,431,278 (GRCm39) |
|
probably null |
Het |
Apol9b |
A |
G |
15: 77,619,840 (GRCm39) |
N212S |
probably damaging |
Het |
Ash1l |
T |
A |
3: 88,971,085 (GRCm39) |
|
probably null |
Het |
Bltp1 |
G |
A |
3: 37,050,607 (GRCm39) |
S2981N |
probably benign |
Het |
Ccdc180 |
A |
T |
4: 45,900,041 (GRCm39) |
K200* |
probably null |
Het |
Ccser2 |
A |
T |
14: 36,662,149 (GRCm39) |
M345K |
probably benign |
Het |
Cdcp2 |
A |
T |
4: 106,954,873 (GRCm39) |
|
probably null |
Het |
Clca3a1 |
T |
C |
3: 144,454,155 (GRCm39) |
|
probably benign |
Het |
Cntn3 |
G |
A |
6: 102,246,051 (GRCm39) |
|
probably benign |
Het |
Col28a1 |
T |
A |
6: 8,075,326 (GRCm39) |
|
probably benign |
Het |
Dock2 |
A |
G |
11: 34,244,325 (GRCm39) |
F1035S |
probably damaging |
Het |
Dsg1a |
A |
T |
18: 20,473,920 (GRCm39) |
S998C |
probably damaging |
Het |
Ecrg4 |
C |
A |
1: 43,781,449 (GRCm39) |
N110K |
possibly damaging |
Het |
Enox1 |
T |
C |
14: 77,744,399 (GRCm39) |
|
probably benign |
Het |
Fgfr3 |
A |
G |
5: 33,887,054 (GRCm39) |
M1V |
probably null |
Het |
Fuca2 |
T |
A |
10: 13,378,870 (GRCm39) |
Y5N |
probably damaging |
Het |
Git2 |
G |
T |
5: 114,883,592 (GRCm39) |
H42Q |
probably damaging |
Het |
Gm7964 |
G |
A |
7: 83,405,602 (GRCm39) |
|
noncoding transcript |
Het |
Hars2 |
G |
A |
18: 36,922,477 (GRCm39) |
E337K |
probably damaging |
Het |
Hells |
A |
G |
19: 38,956,194 (GRCm39) |
R797G |
probably benign |
Het |
Hnf1a |
G |
A |
5: 115,088,803 (GRCm39) |
S571L |
probably benign |
Het |
Hoxa5 |
T |
C |
6: 52,181,320 (GRCm39) |
Y4C |
probably damaging |
Het |
Inpp4a |
G |
A |
1: 37,408,573 (GRCm39) |
|
probably benign |
Het |
Ints6 |
T |
C |
14: 62,934,060 (GRCm39) |
I816V |
probably damaging |
Het |
Itpr1 |
T |
C |
6: 108,492,709 (GRCm39) |
|
probably benign |
Het |
Itprid2 |
T |
A |
2: 79,474,850 (GRCm39) |
S270T |
possibly damaging |
Het |
Kcnt2 |
C |
A |
1: 140,537,352 (GRCm39) |
P1037T |
probably damaging |
Het |
Lyg2 |
T |
A |
1: 37,950,188 (GRCm39) |
M47L |
possibly damaging |
Het |
Macf1 |
G |
T |
4: 123,270,171 (GRCm39) |
A4648D |
probably damaging |
Het |
Mcf2l |
T |
C |
8: 13,046,728 (GRCm39) |
|
probably null |
Het |
Mcm9 |
C |
T |
10: 53,417,694 (GRCm39) |
R3H |
probably damaging |
Het |
Met |
T |
A |
6: 17,491,969 (GRCm39) |
Y244N |
probably damaging |
Het |
Mettl14 |
A |
T |
3: 123,168,411 (GRCm39) |
C210S |
possibly damaging |
Het |
Mrgpra4 |
T |
C |
7: 47,631,058 (GRCm39) |
Y181C |
probably benign |
Het |
Mtch2 |
T |
C |
2: 90,680,026 (GRCm39) |
V86A |
possibly damaging |
Het |
Mttp |
A |
T |
3: 137,817,457 (GRCm39) |
I446N |
possibly damaging |
Het |
Muc4 |
T |
A |
16: 32,577,120 (GRCm39) |
S2207T |
unknown |
Het |
Muc5b |
A |
G |
7: 141,405,522 (GRCm39) |
T944A |
unknown |
Het |
Myo15a |
A |
T |
11: 60,369,877 (GRCm39) |
H879L |
probably benign |
Het |
Nherf4 |
A |
C |
9: 44,160,231 (GRCm39) |
H324Q |
probably damaging |
Het |
Nkiras2 |
G |
A |
11: 100,515,018 (GRCm39) |
|
probably benign |
Het |
Nostrin |
T |
G |
2: 69,019,475 (GRCm39) |
*507E |
probably null |
Het |
Nup205 |
T |
C |
6: 35,175,904 (GRCm39) |
V589A |
probably benign |
Het |
Or12j3 |
A |
G |
7: 139,953,307 (GRCm39) |
I72T |
probably benign |
Het |
Or5b21 |
G |
T |
19: 12,839,252 (GRCm39) |
V38F |
probably benign |
Het |
Or5w17 |
C |
A |
2: 87,583,994 (GRCm39) |
L114F |
probably damaging |
Het |
Oxct2b |
T |
A |
4: 123,010,782 (GRCm39) |
M234K |
possibly damaging |
Het |
Pcdha1 |
A |
T |
18: 37,318,121 (GRCm39) |
I945F |
probably damaging |
Het |
Pik3ca |
G |
A |
3: 32,504,410 (GRCm39) |
|
probably null |
Het |
Pkhd1l1 |
A |
G |
15: 44,386,887 (GRCm39) |
|
probably null |
Het |
Plscr1 |
A |
T |
9: 92,140,099 (GRCm39) |
|
probably null |
Het |
Prkn |
G |
A |
17: 11,286,066 (GRCm39) |
D20N |
probably damaging |
Het |
Psd |
T |
C |
19: 46,307,956 (GRCm39) |
E684G |
possibly damaging |
Het |
Rab11fip3 |
T |
C |
17: 26,213,199 (GRCm39) |
E870G |
probably damaging |
Het |
Rpl22l1 |
C |
A |
3: 28,861,423 (GRCm39) |
Y103* |
probably null |
Het |
Semp2l2b |
T |
C |
10: 21,942,823 (GRCm39) |
S386G |
possibly damaging |
Het |
Slc38a4 |
A |
T |
15: 96,914,720 (GRCm39) |
N44K |
possibly damaging |
Het |
Slco6c1 |
T |
A |
1: 97,055,623 (GRCm39) |
I93F |
probably damaging |
Het |
Strip1 |
G |
A |
3: 107,534,091 (GRCm39) |
T181M |
possibly damaging |
Het |
Stxbp5l |
G |
A |
16: 37,028,458 (GRCm39) |
A535V |
probably damaging |
Het |
Tg |
A |
T |
15: 66,601,446 (GRCm39) |
Q152L |
probably benign |
Het |
Thada |
T |
C |
17: 84,730,591 (GRCm39) |
T1036A |
probably damaging |
Het |
Tnfrsf21 |
C |
T |
17: 43,349,104 (GRCm39) |
H239Y |
probably benign |
Het |
Tns1 |
T |
A |
1: 73,991,856 (GRCm39) |
T941S |
probably benign |
Het |
Tppp3 |
T |
C |
8: 106,194,840 (GRCm39) |
D97G |
probably benign |
Het |
Trp53bp1 |
C |
A |
2: 121,082,349 (GRCm39) |
A317S |
probably null |
Het |
Trpm7 |
T |
C |
2: 126,690,449 (GRCm39) |
I210V |
probably damaging |
Het |
Ubr1 |
A |
G |
2: 120,711,574 (GRCm39) |
L1440P |
probably damaging |
Het |
Utp18 |
A |
T |
11: 93,766,661 (GRCm39) |
Y317N |
probably damaging |
Het |
Zfp719 |
A |
G |
7: 43,238,677 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Zdhhc5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01669:Zdhhc5
|
APN |
2 |
84,521,538 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01795:Zdhhc5
|
APN |
2 |
84,520,390 (GRCm39) |
missense |
probably benign |
|
IGL01862:Zdhhc5
|
APN |
2 |
84,520,836 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4449001:Zdhhc5
|
UTSW |
2 |
84,520,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R0270:Zdhhc5
|
UTSW |
2 |
84,520,459 (GRCm39) |
missense |
probably benign |
0.06 |
R0419:Zdhhc5
|
UTSW |
2 |
84,521,587 (GRCm39) |
splice site |
probably null |
|
R1171:Zdhhc5
|
UTSW |
2 |
84,522,685 (GRCm39) |
missense |
probably benign |
0.00 |
R1450:Zdhhc5
|
UTSW |
2 |
84,532,733 (GRCm39) |
missense |
probably damaging |
0.99 |
R1922:Zdhhc5
|
UTSW |
2 |
84,523,771 (GRCm39) |
missense |
probably damaging |
0.99 |
R2229:Zdhhc5
|
UTSW |
2 |
84,520,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R4799:Zdhhc5
|
UTSW |
2 |
84,523,775 (GRCm39) |
missense |
probably damaging |
0.97 |
R5473:Zdhhc5
|
UTSW |
2 |
84,520,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R5968:Zdhhc5
|
UTSW |
2 |
84,524,719 (GRCm39) |
splice site |
probably null |
|
R6299:Zdhhc5
|
UTSW |
2 |
84,520,825 (GRCm39) |
missense |
probably benign |
0.06 |
R6550:Zdhhc5
|
UTSW |
2 |
84,526,685 (GRCm39) |
missense |
probably benign |
0.03 |
R7069:Zdhhc5
|
UTSW |
2 |
84,545,355 (GRCm39) |
start gained |
probably benign |
|
R7169:Zdhhc5
|
UTSW |
2 |
84,532,675 (GRCm39) |
critical splice donor site |
probably null |
|
R7383:Zdhhc5
|
UTSW |
2 |
84,524,748 (GRCm39) |
missense |
probably benign |
0.44 |
R8703:Zdhhc5
|
UTSW |
2 |
84,520,596 (GRCm39) |
missense |
probably benign |
0.06 |
R9647:Zdhhc5
|
UTSW |
2 |
84,524,750 (GRCm39) |
missense |
probably benign |
0.01 |
R9789:Zdhhc5
|
UTSW |
2 |
84,524,662 (GRCm39) |
missense |
probably damaging |
1.00 |
|