Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb5 |
T |
C |
12: 118,896,310 (GRCm39) |
I340V |
probably benign |
Het |
Ano1 |
T |
G |
7: 144,187,390 (GRCm39) |
S459R |
possibly damaging |
Het |
Cop1 |
T |
C |
1: 159,060,417 (GRCm39) |
V67A |
possibly damaging |
Het |
Cop1 |
A |
G |
1: 159,072,242 (GRCm39) |
Y186C |
probably damaging |
Het |
Cst11 |
G |
A |
2: 148,612,346 (GRCm39) |
T97I |
probably benign |
Het |
Ephb2 |
T |
A |
4: 136,387,019 (GRCm39) |
Y736F |
possibly damaging |
Het |
Extl1 |
TGCGTTGCACCGATACCGGG |
TG |
4: 134,084,988 (GRCm39) |
|
probably benign |
Het |
Hmcn2 |
T |
C |
2: 31,225,463 (GRCm39) |
I124T |
probably damaging |
Het |
Hpn |
T |
C |
7: 30,799,323 (GRCm39) |
Y271C |
possibly damaging |
Het |
Kmt2a |
A |
G |
9: 44,759,846 (GRCm39) |
S668P |
probably benign |
Het |
Lgmn |
T |
C |
12: 102,364,536 (GRCm39) |
D311G |
probably damaging |
Het |
Macroh2a1 |
T |
C |
13: 56,231,109 (GRCm39) |
|
probably null |
Het |
Mfsd14b |
T |
C |
13: 65,260,307 (GRCm39) |
|
probably benign |
Het |
Micu1 |
C |
A |
10: 59,592,549 (GRCm39) |
|
probably benign |
Het |
Muc5b |
A |
G |
7: 141,425,532 (GRCm39) |
I4726V |
probably benign |
Het |
Nadk2 |
T |
A |
15: 9,103,080 (GRCm39) |
N310K |
probably damaging |
Het |
Napg |
T |
C |
18: 63,116,431 (GRCm39) |
|
probably benign |
Het |
Nav3 |
G |
A |
10: 109,552,389 (GRCm39) |
R1818W |
probably damaging |
Het |
Ntpcr |
T |
C |
8: 126,464,170 (GRCm39) |
|
probably benign |
Het |
Or1j13 |
T |
C |
2: 36,369,779 (GRCm39) |
D121G |
probably damaging |
Het |
Or51af1 |
T |
A |
7: 103,141,954 (GRCm39) |
I44F |
probably damaging |
Het |
Or5b99 |
A |
G |
19: 12,977,151 (GRCm39) |
D267G |
probably benign |
Het |
Or6c214 |
A |
G |
10: 129,590,866 (GRCm39) |
V151A |
probably benign |
Het |
Pdia2 |
A |
G |
17: 26,417,803 (GRCm39) |
F69L |
probably damaging |
Het |
Pik3r4 |
A |
G |
9: 105,564,404 (GRCm39) |
T1333A |
probably damaging |
Het |
Platr26 |
A |
T |
2: 71,553,631 (GRCm39) |
|
noncoding transcript |
Het |
Proc |
T |
C |
18: 32,266,536 (GRCm39) |
D97G |
probably benign |
Het |
Ptpn23 |
C |
T |
9: 110,217,845 (GRCm39) |
R700H |
probably benign |
Het |
Rragc |
T |
A |
4: 123,818,575 (GRCm39) |
|
probably null |
Het |
Serac1 |
A |
T |
17: 6,111,855 (GRCm39) |
F244I |
probably benign |
Het |
Snrpd3 |
A |
G |
10: 75,368,039 (GRCm39) |
D52G |
probably damaging |
Het |
Thrb |
G |
T |
14: 17,981,837 (GRCm38) |
|
probably benign |
Het |
Ttc6 |
T |
C |
12: 57,735,435 (GRCm39) |
|
probably benign |
Het |
Zfp607b |
T |
A |
7: 27,402,401 (GRCm39) |
C286S |
probably benign |
Het |
|
Other mutations in Krtap4-9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01949:Krtap4-9
|
APN |
11 |
99,676,391 (GRCm39) |
unclassified |
probably benign |
|
IGL02697:Krtap4-9
|
APN |
11 |
99,676,574 (GRCm39) |
missense |
unknown |
|
IGL03176:Krtap4-9
|
APN |
11 |
99,676,106 (GRCm39) |
unclassified |
probably benign |
|
R1773:Krtap4-9
|
UTSW |
11 |
99,676,396 (GRCm39) |
unclassified |
probably benign |
|
R1838:Krtap4-9
|
UTSW |
11 |
99,676,222 (GRCm39) |
unclassified |
probably benign |
|
R2566:Krtap4-9
|
UTSW |
11 |
99,676,492 (GRCm39) |
unclassified |
probably benign |
|
R2888:Krtap4-9
|
UTSW |
11 |
99,676,245 (GRCm39) |
nonsense |
probably null |
|
R3757:Krtap4-9
|
UTSW |
11 |
99,676,444 (GRCm39) |
unclassified |
probably benign |
|
R4633:Krtap4-9
|
UTSW |
11 |
99,676,380 (GRCm39) |
unclassified |
probably benign |
|
R5930:Krtap4-9
|
UTSW |
11 |
99,676,462 (GRCm39) |
unclassified |
probably benign |
|
R6092:Krtap4-9
|
UTSW |
11 |
99,676,481 (GRCm39) |
unclassified |
probably benign |
|
R6501:Krtap4-9
|
UTSW |
11 |
99,676,255 (GRCm39) |
unclassified |
probably benign |
|
R6934:Krtap4-9
|
UTSW |
11 |
99,676,708 (GRCm39) |
nonsense |
probably null |
|
R7131:Krtap4-9
|
UTSW |
11 |
99,676,283 (GRCm39) |
missense |
unknown |
|
R8809:Krtap4-9
|
UTSW |
11 |
99,676,454 (GRCm39) |
missense |
unknown |
|
RF017:Krtap4-9
|
UTSW |
11 |
99,676,225 (GRCm39) |
unclassified |
probably benign |
|
RF023:Krtap4-9
|
UTSW |
11 |
99,676,217 (GRCm39) |
unclassified |
probably benign |
|
|