Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adpgk |
T |
G |
9: 59,217,600 (GRCm39) |
D204E |
probably damaging |
Het |
Aqr |
C |
A |
2: 113,961,215 (GRCm39) |
V682L |
possibly damaging |
Het |
Bmper |
A |
T |
9: 23,136,113 (GRCm39) |
N65Y |
possibly damaging |
Het |
Calb1 |
T |
C |
4: 15,900,925 (GRCm39) |
L171P |
probably damaging |
Het |
Card11 |
T |
C |
5: 140,892,415 (GRCm39) |
M217V |
probably damaging |
Het |
Col11a2 |
A |
G |
17: 34,265,412 (GRCm39) |
|
probably null |
Het |
Dpm1 |
T |
C |
2: 168,052,472 (GRCm39) |
T255A |
probably benign |
Het |
Efhb |
A |
G |
17: 53,752,803 (GRCm39) |
Y440H |
probably damaging |
Het |
Elp2 |
T |
C |
18: 24,737,170 (GRCm39) |
V40A |
probably damaging |
Het |
Far2 |
A |
T |
6: 148,076,629 (GRCm39) |
N491Y |
possibly damaging |
Het |
Frem1 |
T |
A |
4: 82,868,517 (GRCm39) |
H1488L |
probably benign |
Het |
Frrs1l |
C |
A |
4: 56,990,144 (GRCm39) |
R43L |
unknown |
Het |
Galnt3 |
G |
A |
2: 65,937,432 (GRCm39) |
R93C |
probably benign |
Het |
Gm8225 |
A |
G |
17: 26,762,363 (GRCm39) |
T185A |
possibly damaging |
Het |
Hoxc12 |
T |
G |
15: 102,846,855 (GRCm39) |
L249W |
probably damaging |
Het |
Lrrc75b |
A |
T |
10: 75,393,099 (GRCm39) |
H83Q |
probably damaging |
Het |
Muc4 |
A |
T |
16: 32,576,391 (GRCm39) |
T1964S |
unknown |
Het |
Nob1 |
T |
C |
8: 108,145,049 (GRCm39) |
D142G |
probably benign |
Het |
Or2y1d |
T |
C |
11: 49,321,753 (GRCm39) |
V150A |
probably benign |
Het |
Or4p19 |
A |
T |
2: 88,242,104 (GRCm39) |
H299Q |
probably benign |
Het |
Or4p22 |
A |
T |
2: 88,317,601 (GRCm39) |
Y175F |
possibly damaging |
Het |
Or5b24 |
G |
A |
19: 12,912,641 (GRCm39) |
D180N |
probably damaging |
Het |
Or5d16 |
A |
G |
2: 87,773,571 (GRCm39) |
Y134H |
probably damaging |
Het |
Patj |
A |
T |
4: 98,329,327 (GRCm39) |
N527I |
probably damaging |
Het |
Pik3c2g |
A |
G |
6: 139,805,096 (GRCm39) |
I543V |
|
Het |
Ppp1r2 |
A |
T |
16: 31,077,279 (GRCm39) |
N150K |
probably damaging |
Het |
Prl7d1 |
A |
T |
13: 27,894,161 (GRCm39) |
L135Q |
probably damaging |
Het |
Ralgds |
G |
T |
2: 28,435,226 (GRCm39) |
E461* |
probably null |
Het |
Ramac |
C |
T |
7: 81,417,327 (GRCm39) |
P9L |
possibly damaging |
Het |
Rasa3 |
T |
A |
8: 13,655,887 (GRCm39) |
H116L |
probably benign |
Het |
Sec24d |
C |
T |
3: 123,136,827 (GRCm39) |
P520L |
probably damaging |
Het |
Sfmbt1 |
T |
G |
14: 30,518,283 (GRCm39) |
S376A |
probably benign |
Het |
Sspo |
A |
G |
6: 48,458,173 (GRCm39) |
T3290A |
probably benign |
Het |
Stk25 |
G |
A |
1: 93,552,346 (GRCm39) |
P345S |
probably benign |
Het |
Sycp2l |
A |
G |
13: 41,300,148 (GRCm39) |
E454G |
probably null |
Het |
Tecpr1 |
T |
C |
5: 144,150,885 (GRCm39) |
K308E |
probably damaging |
Het |
Thtpa |
C |
T |
14: 55,332,962 (GRCm39) |
P16S |
probably damaging |
Het |
Trim65 |
T |
A |
11: 116,018,535 (GRCm39) |
I247F |
possibly damaging |
Het |
Trpc6 |
T |
G |
9: 8,610,149 (GRCm39) |
Y206D |
probably benign |
Het |
Ttn |
G |
A |
2: 76,703,307 (GRCm39) |
T9357I |
unknown |
Het |
Ugt2b1 |
C |
A |
5: 87,074,342 (GRCm39) |
A6S |
probably benign |
Het |
Vmn1r175 |
A |
G |
7: 23,508,603 (GRCm39) |
V8A |
possibly damaging |
Het |
Vps13b |
T |
A |
15: 35,878,971 (GRCm39) |
I2990N |
probably damaging |
Het |
Xirp2 |
G |
A |
2: 67,345,826 (GRCm39) |
R2689Q |
possibly damaging |
Het |
Zfp831 |
T |
A |
2: 174,488,516 (GRCm39) |
Y1064N |
possibly damaging |
Het |
|
Other mutations in H2-Q1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01448:H2-Q1
|
APN |
17 |
35,542,437 (GRCm39) |
splice site |
probably benign |
|
IGL01769:H2-Q1
|
APN |
17 |
35,542,505 (GRCm39) |
missense |
probably benign |
0.26 |
PIT4531001:H2-Q1
|
UTSW |
17 |
35,539,892 (GRCm39) |
missense |
probably benign |
0.37 |
R0380:H2-Q1
|
UTSW |
17 |
35,542,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R0570:H2-Q1
|
UTSW |
17 |
35,540,373 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1935:H2-Q1
|
UTSW |
17 |
35,542,469 (GRCm39) |
missense |
probably benign |
0.08 |
R4352:H2-Q1
|
UTSW |
17 |
35,539,919 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4672:H2-Q1
|
UTSW |
17 |
35,539,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R4774:H2-Q1
|
UTSW |
17 |
35,540,242 (GRCm39) |
splice site |
probably benign |
|
R5941:H2-Q1
|
UTSW |
17 |
35,540,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R6825:H2-Q1
|
UTSW |
17 |
35,540,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R7136:H2-Q1
|
UTSW |
17 |
35,539,603 (GRCm39) |
critical splice donor site |
probably null |
|
R7303:H2-Q1
|
UTSW |
17 |
35,540,312 (GRCm39) |
missense |
probably benign |
0.00 |
R7991:H2-Q1
|
UTSW |
17 |
35,540,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R8306:H2-Q1
|
UTSW |
17 |
35,539,997 (GRCm39) |
nonsense |
probably null |
|
R8786:H2-Q1
|
UTSW |
17 |
35,539,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R9381:H2-Q1
|
UTSW |
17 |
35,542,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R9454:H2-Q1
|
UTSW |
17 |
35,540,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R9622:H2-Q1
|
UTSW |
17 |
35,542,532 (GRCm39) |
missense |
probably benign |
0.23 |
|