Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930579F01Rik |
T |
C |
3: 137,889,534 (GRCm39) |
I28V |
possibly damaging |
Het |
Adamts2 |
A |
T |
11: 50,627,991 (GRCm39) |
|
probably null |
Het |
Adgrg1 |
T |
C |
8: 95,729,126 (GRCm39) |
F17L |
probably benign |
Het |
Aldob |
A |
G |
4: 49,539,789 (GRCm39) |
L183P |
probably damaging |
Het |
Alg5 |
T |
C |
3: 54,656,063 (GRCm39) |
C270R |
probably benign |
Het |
Anxa4 |
T |
A |
6: 86,720,160 (GRCm39) |
|
probably null |
Het |
Armc2 |
C |
A |
10: 41,869,225 (GRCm39) |
|
probably null |
Het |
Atrnl1 |
A |
G |
19: 58,030,800 (GRCm39) |
N1314S |
probably benign |
Het |
Bbs7 |
T |
A |
3: 36,652,460 (GRCm39) |
E331V |
probably benign |
Het |
Bmper |
T |
A |
9: 23,285,225 (GRCm39) |
V258E |
probably benign |
Het |
Catspere2 |
A |
T |
1: 177,939,139 (GRCm39) |
I671F |
possibly damaging |
Het |
Cd101 |
A |
G |
3: 100,920,376 (GRCm39) |
S508P |
probably damaging |
Het |
Cd177 |
C |
T |
7: 24,444,499 (GRCm39) |
R694H |
probably benign |
Het |
Cnrip1 |
A |
G |
11: 17,004,705 (GRCm39) |
Y85C |
probably damaging |
Het |
Dclk2 |
A |
T |
3: 86,739,070 (GRCm39) |
F310I |
probably benign |
Het |
Dmxl1 |
A |
G |
18: 49,984,562 (GRCm39) |
K186R |
probably null |
Het |
Dmxl1 |
C |
A |
18: 49,996,124 (GRCm39) |
Q417K |
possibly damaging |
Het |
Eloa |
T |
C |
4: 135,740,220 (GRCm39) |
D67G |
possibly damaging |
Het |
Elovl4 |
T |
C |
9: 83,665,278 (GRCm39) |
I103V |
probably benign |
Het |
Gabpa |
C |
G |
16: 84,657,361 (GRCm39) |
A412G |
probably benign |
Het |
Gldn |
T |
A |
9: 54,242,158 (GRCm39) |
|
probably null |
Het |
Ino80d |
A |
T |
1: 63,104,993 (GRCm39) |
I361N |
probably damaging |
Het |
Kalrn |
G |
A |
16: 33,796,073 (GRCm39) |
T1234M |
probably damaging |
Het |
Kcnk13 |
T |
A |
12: 100,028,026 (GRCm39) |
M367K |
probably benign |
Het |
Klrd1 |
G |
A |
6: 129,570,468 (GRCm39) |
R8Q |
possibly damaging |
Het |
Kmt2a |
T |
C |
9: 44,758,942 (GRCm39) |
N969S |
probably benign |
Het |
Lgi4 |
A |
G |
7: 30,768,315 (GRCm39) |
D438G |
probably benign |
Het |
Lig1 |
T |
C |
7: 13,039,840 (GRCm39) |
L684P |
probably damaging |
Het |
Lrp2 |
T |
C |
2: 69,340,846 (GRCm39) |
M1010V |
probably benign |
Het |
Magi3 |
C |
A |
3: 103,996,873 (GRCm39) |
R224I |
probably damaging |
Het |
Mier2 |
T |
C |
10: 79,380,573 (GRCm39) |
N277S |
probably damaging |
Het |
Morn1 |
A |
G |
4: 155,171,112 (GRCm39) |
H17R |
probably benign |
Het |
Nf2 |
A |
T |
11: 4,749,878 (GRCm39) |
S265T |
probably damaging |
Het |
Or5m11b |
A |
G |
2: 85,805,700 (GRCm39) |
T38A |
possibly damaging |
Het |
Or8k24 |
G |
A |
2: 86,216,024 (GRCm39) |
T246I |
possibly damaging |
Het |
Palb2 |
A |
G |
7: 121,726,270 (GRCm39) |
|
probably null |
Het |
Pdzd2 |
C |
T |
15: 12,385,951 (GRCm39) |
V940M |
probably damaging |
Het |
Phldb2 |
T |
C |
16: 45,598,138 (GRCm39) |
K850E |
probably damaging |
Het |
Pitx1 |
G |
A |
13: 55,976,335 (GRCm39) |
T108M |
probably damaging |
Het |
Polr2a |
C |
T |
11: 69,626,787 (GRCm39) |
A1516T |
probably benign |
Het |
Pomp |
T |
A |
5: 147,812,313 (GRCm39) |
M133K |
possibly damaging |
Het |
Prex1 |
T |
C |
2: 166,423,913 (GRCm39) |
E993G |
probably damaging |
Het |
Prrc2c |
C |
A |
1: 162,533,075 (GRCm39) |
|
probably benign |
Het |
Pwp2 |
C |
A |
10: 78,007,917 (GRCm39) |
Q879H |
probably damaging |
Het |
Rab26 |
G |
A |
17: 24,748,766 (GRCm39) |
T245I |
probably damaging |
Het |
Rapgef1 |
A |
G |
2: 29,592,514 (GRCm39) |
D502G |
probably damaging |
Het |
Rsf1 |
GGCG |
GGCGACGGCCGCG |
7: 97,229,113 (GRCm39) |
|
probably benign |
Het |
Sema5a |
T |
A |
15: 32,550,421 (GRCm39) |
D153E |
probably benign |
Het |
Sez6 |
C |
G |
11: 77,844,385 (GRCm39) |
H69Q |
probably damaging |
Het |
Sgsm3 |
A |
T |
15: 80,893,095 (GRCm39) |
T391S |
probably benign |
Het |
Sh3rf2 |
T |
C |
18: 42,234,670 (GRCm39) |
V151A |
possibly damaging |
Het |
Socs1 |
G |
T |
16: 10,602,266 (GRCm39) |
A157E |
probably benign |
Het |
Spmip4 |
T |
A |
6: 50,566,145 (GRCm39) |
Q110L |
possibly damaging |
Het |
Sptbn4 |
C |
A |
7: 27,071,375 (GRCm39) |
V346L |
possibly damaging |
Het |
Srgap1 |
T |
A |
10: 121,621,523 (GRCm39) |
H990L |
probably damaging |
Het |
Tbc1d9 |
G |
T |
8: 83,892,809 (GRCm39) |
G36W |
probably damaging |
Het |
Tbk1 |
T |
C |
10: 121,395,782 (GRCm39) |
E437G |
probably benign |
Het |
Tns3 |
A |
G |
11: 8,481,743 (GRCm39) |
L203P |
probably damaging |
Het |
Tspoap1 |
A |
T |
11: 87,656,638 (GRCm39) |
K283M |
probably damaging |
Het |
Ttyh1 |
C |
T |
7: 4,127,649 (GRCm39) |
|
probably benign |
Het |
Ufd1 |
T |
A |
16: 18,645,850 (GRCm39) |
I254N |
probably benign |
Het |
Ugdh |
T |
G |
5: 65,584,776 (GRCm39) |
T49P |
probably benign |
Het |
Vav3 |
T |
C |
3: 109,434,810 (GRCm39) |
L447P |
probably damaging |
Het |
Vmn1r216 |
A |
T |
13: 23,283,445 (GRCm39) |
K43* |
probably null |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Vmn2r13 |
A |
G |
5: 109,306,015 (GRCm39) |
I521T |
possibly damaging |
Het |
Wdfy3 |
T |
C |
5: 101,991,932 (GRCm39) |
T3470A |
probably benign |
Het |
Wdhd1 |
T |
A |
14: 47,485,587 (GRCm39) |
K791N |
probably damaging |
Het |
Xirp2 |
A |
G |
2: 67,338,911 (GRCm39) |
D384G |
probably damaging |
Het |
Zfp512b |
C |
T |
2: 181,232,273 (GRCm39) |
R86Q |
probably damaging |
Het |
Zfp735 |
A |
C |
11: 73,601,880 (GRCm39) |
I275L |
probably benign |
Het |
Zfp957 |
A |
T |
14: 79,451,344 (GRCm39) |
S152T |
probably damaging |
Het |
|
Other mutations in Clptm1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01614:Clptm1
|
APN |
7 |
19,371,625 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01909:Clptm1
|
APN |
7 |
19,389,701 (GRCm39) |
missense |
probably benign |
0.37 |
IGL03089:Clptm1
|
APN |
7 |
19,371,072 (GRCm39) |
missense |
probably damaging |
1.00 |
H8786:Clptm1
|
UTSW |
7 |
19,369,629 (GRCm39) |
missense |
possibly damaging |
0.54 |
R0128:Clptm1
|
UTSW |
7 |
19,368,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R0835:Clptm1
|
UTSW |
7 |
19,369,599 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1167:Clptm1
|
UTSW |
7 |
19,368,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R1370:Clptm1
|
UTSW |
7 |
19,367,797 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1655:Clptm1
|
UTSW |
7 |
19,379,792 (GRCm39) |
missense |
probably benign |
0.00 |
R1855:Clptm1
|
UTSW |
7 |
19,372,134 (GRCm39) |
missense |
probably benign |
0.05 |
R2004:Clptm1
|
UTSW |
7 |
19,380,762 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2189:Clptm1
|
UTSW |
7 |
19,371,070 (GRCm39) |
nonsense |
probably null |
|
R2203:Clptm1
|
UTSW |
7 |
19,367,817 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3237:Clptm1
|
UTSW |
7 |
19,369,271 (GRCm39) |
missense |
probably damaging |
0.99 |
R3963:Clptm1
|
UTSW |
7 |
19,372,121 (GRCm39) |
nonsense |
probably null |
|
R5416:Clptm1
|
UTSW |
7 |
19,367,741 (GRCm39) |
unclassified |
probably benign |
|
R6110:Clptm1
|
UTSW |
7 |
19,367,731 (GRCm39) |
unclassified |
probably benign |
|
R6474:Clptm1
|
UTSW |
7 |
19,369,762 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6737:Clptm1
|
UTSW |
7 |
19,371,001 (GRCm39) |
critical splice donor site |
probably null |
|
R8144:Clptm1
|
UTSW |
7 |
19,367,827 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8244:Clptm1
|
UTSW |
7 |
19,372,916 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8374:Clptm1
|
UTSW |
7 |
19,372,081 (GRCm39) |
missense |
probably benign |
0.13 |
R8438:Clptm1
|
UTSW |
7 |
19,379,776 (GRCm39) |
missense |
probably benign |
0.00 |
R8885:Clptm1
|
UTSW |
7 |
19,372,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R9399:Clptm1
|
UTSW |
7 |
19,367,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R9467:Clptm1
|
UTSW |
7 |
19,371,449 (GRCm39) |
missense |
probably benign |
0.04 |
R9529:Clptm1
|
UTSW |
7 |
19,371,600 (GRCm39) |
missense |
probably benign |
0.17 |
R9601:Clptm1
|
UTSW |
7 |
19,369,763 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Clptm1
|
UTSW |
7 |
19,371,393 (GRCm39) |
critical splice donor site |
probably null |
|
|