Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaca |
A |
G |
11: 84,181,112 (GRCm39) |
|
probably null |
Het |
Acsbg3 |
T |
A |
17: 57,192,169 (GRCm39) |
Y577* |
probably null |
Het |
Acsm5 |
T |
C |
7: 119,135,023 (GRCm39) |
V327A |
possibly damaging |
Het |
Agt |
C |
A |
8: 125,283,839 (GRCm39) |
E427* |
probably null |
Het |
Akr1c14 |
T |
C |
13: 4,131,016 (GRCm39) |
L236S |
probably damaging |
Het |
Ammecr1l |
C |
T |
18: 31,904,954 (GRCm39) |
S65L |
probably benign |
Het |
Ankrd33b |
T |
C |
15: 31,367,432 (GRCm39) |
D36G |
probably damaging |
Het |
Ano8 |
A |
T |
8: 71,931,902 (GRCm39) |
C766S |
probably benign |
Het |
Arhgef16 |
G |
T |
4: 154,375,491 (GRCm39) |
P168T |
probably damaging |
Het |
Asic1 |
C |
T |
15: 99,596,700 (GRCm39) |
R499C |
probably damaging |
Het |
Atpsckmt |
T |
G |
15: 31,606,103 (GRCm39) |
S20R |
probably benign |
Het |
Bank1 |
C |
T |
3: 135,919,703 (GRCm39) |
C364Y |
probably damaging |
Het |
Bmerb1 |
T |
A |
16: 13,804,676 (GRCm39) |
S8T |
possibly damaging |
Het |
Cacna1s |
C |
A |
1: 136,004,597 (GRCm39) |
D132E |
probably benign |
Het |
Capn5 |
C |
T |
7: 97,782,089 (GRCm39) |
R217Q |
probably damaging |
Het |
Clasrp |
A |
G |
7: 19,322,528 (GRCm39) |
I284T |
probably benign |
Het |
Coa3 |
T |
A |
11: 101,169,716 (GRCm39) |
K13M |
probably damaging |
Het |
Col13a1 |
A |
T |
10: 61,698,525 (GRCm39) |
M512K |
unknown |
Het |
Colgalt2 |
G |
T |
1: 152,384,312 (GRCm39) |
A551S |
possibly damaging |
Het |
Cryba2 |
T |
C |
1: 74,929,284 (GRCm39) |
Y153C |
possibly damaging |
Het |
Cryzl2 |
T |
C |
1: 157,292,000 (GRCm39) |
V93A |
probably damaging |
Het |
Ctsl |
G |
A |
13: 64,513,032 (GRCm39) |
L297F |
possibly damaging |
Het |
Cyp2r1 |
T |
G |
7: 114,152,135 (GRCm39) |
H274P |
probably benign |
Het |
Ddx4 |
A |
T |
13: 112,761,313 (GRCm39) |
|
probably null |
Het |
Dnai4 |
A |
C |
4: 102,921,727 (GRCm39) |
Y464* |
probably null |
Het |
Dnd1 |
A |
G |
18: 36,897,096 (GRCm39) |
V350A |
possibly damaging |
Het |
Dsg1b |
A |
T |
18: 20,521,221 (GRCm39) |
Q26L |
probably benign |
Het |
Fam20b |
C |
A |
1: 156,515,026 (GRCm39) |
V280F |
possibly damaging |
Het |
Foxb2 |
G |
T |
19: 16,849,820 (GRCm39) |
C395* |
probably null |
Het |
Glb1 |
ACCC |
ACC |
9: 114,250,812 (GRCm39) |
|
probably null |
Het |
Gm9930 |
A |
T |
10: 9,410,547 (GRCm39) |
|
noncoding transcript |
Het |
Hdac7 |
G |
A |
15: 97,704,380 (GRCm39) |
Q497* |
probably null |
Het |
Hk3 |
C |
T |
13: 55,162,239 (GRCm39) |
|
probably null |
Het |
Hsd3b7 |
A |
G |
7: 127,402,251 (GRCm39) |
T330A |
probably benign |
Het |
Il20ra |
A |
T |
10: 19,635,388 (GRCm39) |
Q543L |
probably damaging |
Het |
Itk |
T |
A |
11: 46,251,115 (GRCm39) |
D163V |
probably damaging |
Het |
Kcnu1 |
T |
G |
8: 26,400,916 (GRCm39) |
L688R |
probably damaging |
Het |
Kng1 |
G |
A |
16: 22,879,232 (GRCm39) |
A45T |
possibly damaging |
Het |
Kti12 |
T |
A |
4: 108,705,776 (GRCm39) |
V230E |
possibly damaging |
Het |
Lhfpl7 |
T |
A |
5: 113,383,873 (GRCm39) |
L97* |
probably null |
Het |
Mgat5 |
T |
A |
1: 127,312,584 (GRCm39) |
I241N |
probably damaging |
Het |
Mkln1 |
A |
G |
6: 31,445,067 (GRCm39) |
N321S |
probably benign |
Het |
Mllt10 |
T |
G |
2: 18,076,017 (GRCm39) |
|
probably null |
Het |
Ms4a1 |
C |
A |
19: 11,236,043 (GRCm39) |
|
probably null |
Het |
Ngly1 |
C |
T |
14: 16,290,774 (GRCm38) |
Q419* |
probably null |
Het |
Nipsnap3b |
T |
A |
4: 53,021,343 (GRCm39) |
F243I |
probably damaging |
Het |
Ogfod1 |
T |
A |
8: 94,781,876 (GRCm39) |
|
probably null |
Het |
Or10a2 |
T |
A |
7: 106,673,965 (GRCm39) |
L310Q |
possibly damaging |
Het |
Or2y11 |
C |
T |
11: 49,443,291 (GRCm39) |
T239M |
probably damaging |
Het |
Or51v8 |
T |
A |
7: 103,319,696 (GRCm39) |
I181F |
possibly damaging |
Het |
Or8c20 |
A |
C |
9: 38,260,499 (GRCm39) |
N40T |
probably damaging |
Het |
P2ry14 |
T |
A |
3: 59,022,625 (GRCm39) |
E287D |
probably damaging |
Het |
Pank4 |
A |
T |
4: 155,061,082 (GRCm39) |
R510S |
possibly damaging |
Het |
Pcsk6 |
T |
A |
7: 65,629,915 (GRCm39) |
V347E |
possibly damaging |
Het |
Peg3 |
T |
C |
7: 6,714,427 (GRCm39) |
E265G |
probably damaging |
Het |
Pik3c2b |
C |
A |
1: 133,033,730 (GRCm39) |
P1578H |
probably damaging |
Het |
Pkd1 |
A |
G |
17: 24,814,193 (GRCm39) |
S4188G |
probably benign |
Het |
Ppp1r26 |
A |
G |
2: 28,342,314 (GRCm39) |
D648G |
probably damaging |
Het |
Ptprs |
A |
G |
17: 56,726,621 (GRCm39) |
|
probably null |
Het |
Rab24 |
A |
T |
13: 55,468,738 (GRCm39) |
|
probably null |
Het |
Rap1gap2 |
A |
T |
11: 74,332,592 (GRCm39) |
M71K |
probably damaging |
Het |
Rergl |
T |
G |
6: 139,473,524 (GRCm39) |
K42T |
probably damaging |
Het |
Rigi |
C |
T |
4: 40,216,354 (GRCm39) |
|
probably null |
Het |
Septin5 |
T |
C |
16: 18,443,647 (GRCm39) |
T92A |
probably benign |
Het |
Ski |
A |
G |
4: 155,243,743 (GRCm39) |
|
probably null |
Het |
Slc17a8 |
A |
G |
10: 89,412,192 (GRCm39) |
S414P |
probably benign |
Het |
Slc25a36 |
A |
T |
9: 96,979,228 (GRCm39) |
I71N |
probably damaging |
Het |
Syne2 |
A |
C |
12: 76,155,636 (GRCm39) |
|
probably null |
Het |
Tdrd5 |
C |
A |
1: 156,090,511 (GRCm39) |
W845L |
probably damaging |
Het |
Tfb2m |
T |
C |
1: 179,365,389 (GRCm39) |
I192V |
possibly damaging |
Het |
Tll1 |
T |
G |
8: 64,551,505 (GRCm39) |
D292A |
probably damaging |
Het |
Trank1 |
A |
C |
9: 111,162,876 (GRCm39) |
D45A |
probably damaging |
Het |
Trim17 |
T |
A |
11: 58,859,320 (GRCm39) |
V178E |
probably damaging |
Het |
Trim9 |
A |
T |
12: 70,393,359 (GRCm39) |
L195Q |
probably damaging |
Het |
Ttc27 |
A |
T |
17: 75,163,544 (GRCm39) |
R717S |
possibly damaging |
Het |
Upk2 |
G |
T |
9: 44,365,418 (GRCm39) |
P50Q |
probably damaging |
Het |
Usp9y |
A |
T |
Y: 1,307,880 (GRCm39) |
C2319S |
probably benign |
Het |
Vmn1r4 |
G |
T |
6: 56,933,883 (GRCm39) |
C129F |
probably benign |
Het |
Vmn2r100 |
A |
T |
17: 19,742,178 (GRCm39) |
D184V |
probably damaging |
Het |
Xpnpep3 |
T |
G |
15: 81,311,693 (GRCm39) |
I133S |
possibly damaging |
Het |
Zfp628 |
A |
T |
7: 4,922,939 (GRCm39) |
Q387L |
probably damaging |
Het |
Zic2 |
CCCACCACCACCATCACCACCACCACC |
CCCACCATCACCACCACCACC |
14: 122,713,776 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Crhbp |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01591:Crhbp
|
APN |
13 |
95,580,295 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03058:Crhbp
|
APN |
13 |
95,580,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R0521:Crhbp
|
UTSW |
13 |
95,580,403 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1120:Crhbp
|
UTSW |
13 |
95,578,593 (GRCm39) |
missense |
probably benign |
0.01 |
R4417:Crhbp
|
UTSW |
13 |
95,580,385 (GRCm39) |
missense |
probably benign |
0.02 |
R4925:Crhbp
|
UTSW |
13 |
95,580,318 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4999:Crhbp
|
UTSW |
13 |
95,578,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R5332:Crhbp
|
UTSW |
13 |
95,572,963 (GRCm39) |
missense |
probably damaging |
0.99 |
R5568:Crhbp
|
UTSW |
13 |
95,578,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R5857:Crhbp
|
UTSW |
13 |
95,578,740 (GRCm39) |
missense |
probably benign |
0.01 |
R5861:Crhbp
|
UTSW |
13 |
95,580,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R5875:Crhbp
|
UTSW |
13 |
95,580,304 (GRCm39) |
missense |
probably benign |
0.00 |
R5911:Crhbp
|
UTSW |
13 |
95,568,564 (GRCm39) |
missense |
probably benign |
0.00 |
R6235:Crhbp
|
UTSW |
13 |
95,580,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R7038:Crhbp
|
UTSW |
13 |
95,580,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R7885:Crhbp
|
UTSW |
13 |
95,568,515 (GRCm39) |
missense |
probably damaging |
0.96 |
R8479:Crhbp
|
UTSW |
13 |
95,578,632 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9269:Crhbp
|
UTSW |
13 |
95,573,024 (GRCm39) |
missense |
probably benign |
|
R9676:Crhbp
|
UTSW |
13 |
95,578,711 (GRCm39) |
missense |
probably damaging |
1.00 |
X0052:Crhbp
|
UTSW |
13 |
95,568,501 (GRCm39) |
missense |
probably damaging |
1.00 |
|