Other mutations in this stock |
Total: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700006A11Rik |
T |
C |
3: 124,200,102 (GRCm39) |
I497V |
probably benign |
Het |
4930571K23Rik |
C |
A |
7: 124,968,311 (GRCm39) |
|
noncoding transcript |
Het |
Abca17 |
G |
T |
17: 24,508,587 (GRCm39) |
|
probably benign |
Het |
Ablim1 |
C |
T |
19: 57,140,791 (GRCm39) |
R196Q |
probably damaging |
Het |
Acot11 |
T |
C |
4: 106,612,516 (GRCm39) |
I379V |
possibly damaging |
Het |
Acot4 |
G |
A |
12: 84,088,647 (GRCm39) |
G165D |
probably damaging |
Het |
Agrn |
A |
T |
4: 156,250,881 (GRCm39) |
|
probably null |
Het |
Ahctf1 |
T |
C |
1: 179,598,258 (GRCm39) |
S945G |
possibly damaging |
Het |
Akr1c13 |
C |
T |
13: 4,248,583 (GRCm39) |
R263C |
probably damaging |
Het |
Arfgap1 |
T |
A |
2: 180,615,846 (GRCm39) |
|
probably benign |
Het |
Arhgef3 |
A |
G |
14: 27,101,633 (GRCm39) |
K103R |
probably damaging |
Het |
Cabp1 |
A |
T |
5: 115,310,843 (GRCm39) |
N211K |
probably damaging |
Het |
Cacna1c |
T |
A |
6: 118,711,943 (GRCm39) |
D261V |
probably damaging |
Het |
Car11 |
G |
A |
7: 45,350,783 (GRCm39) |
G93E |
probably damaging |
Het |
Card10 |
A |
G |
15: 78,664,473 (GRCm39) |
I821T |
probably benign |
Het |
Cast |
T |
C |
13: 74,885,735 (GRCm39) |
I277V |
probably benign |
Het |
Cenpj |
T |
C |
14: 56,769,694 (GRCm39) |
K1165R |
probably null |
Het |
Cenpk |
A |
G |
13: 104,370,675 (GRCm39) |
|
probably null |
Het |
Cfap251 |
A |
G |
5: 123,394,169 (GRCm39) |
K353E |
probably benign |
Het |
Cmya5 |
T |
C |
13: 93,230,066 (GRCm39) |
Q1674R |
probably benign |
Het |
Cnnm1 |
T |
A |
19: 43,430,325 (GRCm39) |
V481D |
probably damaging |
Het |
Cracdl |
T |
C |
1: 37,664,381 (GRCm39) |
M506V |
probably benign |
Het |
Csmd3 |
CCTTTGCGCTT |
CCTT |
15: 47,604,632 (GRCm39) |
|
probably null |
Het |
Cyp2c50 |
G |
A |
19: 40,079,013 (GRCm39) |
V119I |
probably benign |
Het |
Dnah7b |
A |
G |
1: 46,234,447 (GRCm39) |
T1460A |
probably damaging |
Het |
Dnah8 |
G |
A |
17: 30,994,019 (GRCm39) |
D3379N |
probably benign |
Het |
Dnajc4 |
C |
T |
19: 6,968,111 (GRCm39) |
R55H |
probably damaging |
Het |
Ebf4 |
C |
T |
2: 130,148,482 (GRCm39) |
R98* |
probably null |
Het |
Epha4 |
G |
A |
1: 77,488,339 (GRCm39) |
A47V |
possibly damaging |
Het |
Ercc8 |
T |
C |
13: 108,320,251 (GRCm39) |
|
probably benign |
Het |
Exo1 |
T |
C |
1: 175,733,399 (GRCm39) |
F75S |
probably damaging |
Het |
Fam168a |
G |
T |
7: 100,483,391 (GRCm39) |
|
probably null |
Het |
Fat3 |
G |
A |
9: 15,836,310 (GRCm39) |
R4065W |
possibly damaging |
Het |
Gm5431 |
T |
A |
11: 48,779,536 (GRCm39) |
N740I |
probably benign |
Het |
Gm5900 |
T |
A |
7: 104,599,571 (GRCm39) |
|
noncoding transcript |
Het |
Gpi1 |
A |
G |
7: 33,905,348 (GRCm39) |
S359P |
probably damaging |
Het |
Gpr156 |
A |
G |
16: 37,768,149 (GRCm39) |
R22G |
probably benign |
Het |
Greb1 |
A |
G |
12: 16,774,923 (GRCm39) |
V158A |
probably damaging |
Het |
Grin2c |
T |
A |
11: 115,141,894 (GRCm39) |
K842* |
probably null |
Het |
Gsta5 |
T |
A |
9: 78,202,089 (GRCm39) |
M1K |
probably null |
Het |
Hnf4a |
T |
A |
2: 163,408,161 (GRCm39) |
L329Q |
probably damaging |
Het |
Hsp90ab1 |
A |
G |
17: 45,880,267 (GRCm39) |
L92P |
probably damaging |
Het |
Ido1 |
T |
A |
8: 25,074,501 (GRCm39) |
R290* |
probably null |
Het |
Ifnlr1 |
G |
T |
4: 135,432,559 (GRCm39) |
D332Y |
probably damaging |
Het |
Ift172 |
T |
C |
5: 31,420,312 (GRCm39) |
N1108S |
probably benign |
Het |
Igkv3-9 |
T |
A |
6: 70,565,728 (GRCm39) |
M109K |
probably benign |
Het |
Igsf10 |
T |
C |
3: 59,239,287 (GRCm39) |
D298G |
probably damaging |
Het |
Iqck |
T |
G |
7: 118,475,505 (GRCm39) |
M98R |
probably benign |
Het |
Klk1b1 |
T |
C |
7: 43,618,803 (GRCm39) |
V60A |
probably damaging |
Het |
Krtap1-3 |
C |
T |
11: 99,481,653 (GRCm39) |
E165K |
unknown |
Het |
Lair1 |
A |
G |
7: 4,013,782 (GRCm39) |
L155P |
probably damaging |
Het |
Maco1 |
A |
G |
4: 134,531,699 (GRCm39) |
S657P |
probably damaging |
Het |
Mast4 |
G |
T |
13: 102,990,350 (GRCm39) |
S57Y |
probably damaging |
Het |
Mical3 |
T |
C |
6: 121,011,118 (GRCm39) |
H360R |
probably damaging |
Het |
Muc5b |
A |
T |
7: 141,412,798 (GRCm39) |
N1915Y |
unknown |
Het |
Myh1 |
A |
G |
11: 67,096,423 (GRCm39) |
I301V |
probably benign |
Het |
Nck2 |
T |
A |
1: 43,593,393 (GRCm39) |
V200E |
probably damaging |
Het |
Odad4 |
T |
G |
11: 100,444,361 (GRCm39) |
L222R |
probably damaging |
Het |
Or2y1b |
T |
G |
11: 49,209,048 (GRCm39) |
L225R |
probably damaging |
Het |
Or4b12 |
T |
C |
2: 90,096,030 (GRCm39) |
Y248C |
possibly damaging |
Het |
Or4c109 |
T |
G |
2: 88,817,775 (GRCm39) |
Y257S |
probably damaging |
Het |
Or4f60 |
T |
A |
2: 111,902,837 (GRCm39) |
L30F |
probably benign |
Het |
Or4k38 |
C |
T |
2: 111,166,076 (GRCm39) |
V116I |
probably damaging |
Het |
Or5b101 |
T |
A |
19: 13,005,058 (GRCm39) |
I212F |
probably damaging |
Het |
Or8b12i |
A |
G |
9: 20,082,525 (GRCm39) |
L114P |
probably damaging |
Het |
Otoa |
C |
T |
7: 120,759,695 (GRCm39) |
T1099I |
probably benign |
Het |
Pask |
T |
A |
1: 93,258,485 (GRCm39) |
I288F |
possibly damaging |
Het |
Pcnx4 |
T |
C |
12: 72,613,746 (GRCm39) |
W564R |
probably damaging |
Het |
Pip4p1 |
A |
T |
14: 51,167,115 (GRCm39) |
Y129* |
probably null |
Het |
Pitpnm2 |
T |
C |
5: 124,274,389 (GRCm39) |
E240G |
probably damaging |
Het |
Ppp1r16b |
A |
G |
2: 158,603,383 (GRCm39) |
Y436C |
possibly damaging |
Het |
Pramel27 |
G |
A |
4: 143,578,561 (GRCm39) |
V274I |
probably benign |
Het |
Prkca |
T |
C |
11: 107,870,032 (GRCm39) |
Y37C |
probably damaging |
Het |
Rad18 |
T |
G |
6: 112,652,883 (GRCm39) |
H238P |
possibly damaging |
Het |
Rap1b |
T |
A |
10: 117,654,444 (GRCm39) |
Q1L |
probably damaging |
Het |
Rgs9 |
T |
C |
11: 109,159,798 (GRCm39) |
Y178C |
probably benign |
Het |
Rpl3l |
A |
T |
17: 24,951,360 (GRCm39) |
D87V |
possibly damaging |
Het |
Scrn2 |
T |
C |
11: 96,923,992 (GRCm39) |
V292A |
possibly damaging |
Het |
Sdad1 |
A |
G |
5: 92,453,684 (GRCm39) |
Y35H |
probably benign |
Het |
Sez6l2 |
T |
C |
7: 126,552,944 (GRCm39) |
S177P |
probably benign |
Het |
Sh3bp1 |
C |
T |
15: 78,795,706 (GRCm39) |
P612S |
probably damaging |
Het |
Shank1 |
T |
C |
7: 44,001,148 (GRCm39) |
S956P |
unknown |
Het |
Shank1 |
G |
A |
7: 44,001,547 (GRCm39) |
A1089T |
unknown |
Het |
Shprh |
G |
A |
10: 11,042,468 (GRCm39) |
C817Y |
probably damaging |
Het |
Spata22 |
C |
T |
11: 73,236,593 (GRCm39) |
P300S |
probably damaging |
Het |
Sstr2 |
A |
T |
11: 113,515,749 (GRCm39) |
I223F |
probably damaging |
Het |
Stom |
C |
T |
2: 35,210,354 (GRCm39) |
A217T |
probably damaging |
Het |
Stpg1 |
T |
C |
4: 135,263,960 (GRCm39) |
V341A |
probably benign |
Het |
Tagap |
A |
G |
17: 8,147,586 (GRCm39) |
T99A |
probably benign |
Het |
Tas1r2 |
A |
G |
4: 139,387,162 (GRCm39) |
N207S |
probably damaging |
Het |
Thbs2 |
A |
G |
17: 14,906,105 (GRCm39) |
V265A |
probably benign |
Het |
Thyn1 |
A |
G |
9: 26,911,316 (GRCm39) |
R3G |
possibly damaging |
Het |
Tia1 |
T |
A |
6: 86,401,312 (GRCm39) |
|
probably null |
Het |
Tktl2 |
A |
G |
8: 66,965,504 (GRCm39) |
E354G |
probably benign |
Het |
Tmc8 |
A |
G |
11: 117,683,511 (GRCm39) |
T689A |
possibly damaging |
Het |
Tmem11 |
A |
T |
11: 60,755,807 (GRCm39) |
|
probably null |
Het |
Tnik |
T |
C |
3: 28,722,064 (GRCm39) |
V1310A |
probably damaging |
Het |
Trappc10 |
A |
G |
10: 78,047,357 (GRCm39) |
S380P |
possibly damaging |
Het |
Trim8 |
C |
T |
19: 46,503,734 (GRCm39) |
P429S |
probably benign |
Het |
Ttn |
C |
A |
2: 76,687,756 (GRCm39) |
|
probably benign |
Het |
Ulk2 |
T |
C |
11: 61,678,340 (GRCm39) |
Y793C |
probably benign |
Het |
Vill |
G |
A |
9: 118,899,370 (GRCm39) |
V337M |
possibly damaging |
Het |
Vps53 |
C |
A |
11: 75,957,661 (GRCm39) |
V364F |
possibly damaging |
Het |
Zan |
A |
T |
5: 137,454,848 (GRCm39) |
I1396N |
unknown |
Het |
Zfa-ps |
A |
C |
10: 52,420,339 (GRCm39) |
|
noncoding transcript |
Het |
Zfp426 |
T |
C |
9: 20,381,977 (GRCm39) |
T337A |
possibly damaging |
Het |
Zfp536 |
T |
C |
7: 37,267,403 (GRCm39) |
E671G |
possibly damaging |
Het |
Zfp985 |
A |
G |
4: 147,667,443 (GRCm39) |
T104A |
possibly damaging |
Het |
|
Other mutations in Or52n2c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01664:Or52n2c
|
APN |
7 |
104,574,311 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02250:Or52n2c
|
APN |
7 |
104,574,222 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02743:Or52n2c
|
APN |
7 |
104,574,075 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03105:Or52n2c
|
APN |
7 |
104,574,971 (GRCm39) |
unclassified |
probably benign |
|
IGL03252:Or52n2c
|
APN |
7 |
104,574,594 (GRCm39) |
missense |
probably benign |
0.16 |
IGL03387:Or52n2c
|
APN |
7 |
104,574,580 (GRCm39) |
missense |
probably benign |
0.01 |
R1534:Or52n2c
|
UTSW |
7 |
104,574,621 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2510:Or52n2c
|
UTSW |
7 |
104,574,894 (GRCm39) |
missense |
probably benign |
0.40 |
R4739:Or52n2c
|
UTSW |
7 |
104,574,017 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4995:Or52n2c
|
UTSW |
7 |
104,574,942 (GRCm39) |
missense |
probably benign |
0.01 |
R5071:Or52n2c
|
UTSW |
7 |
104,574,700 (GRCm39) |
missense |
probably benign |
|
R5074:Or52n2c
|
UTSW |
7 |
104,574,700 (GRCm39) |
missense |
probably benign |
|
R5208:Or52n2c
|
UTSW |
7 |
104,574,933 (GRCm39) |
missense |
probably benign |
|
R5293:Or52n2c
|
UTSW |
7 |
104,574,486 (GRCm39) |
missense |
probably benign |
0.00 |
R6061:Or52n2c
|
UTSW |
7 |
104,574,599 (GRCm39) |
missense |
probably benign |
0.28 |
R6063:Or52n2c
|
UTSW |
7 |
104,574,599 (GRCm39) |
missense |
probably benign |
0.28 |
R6064:Or52n2c
|
UTSW |
7 |
104,574,599 (GRCm39) |
missense |
probably benign |
0.28 |
R6172:Or52n2c
|
UTSW |
7 |
104,574,503 (GRCm39) |
missense |
probably benign |
0.40 |
R6492:Or52n2c
|
UTSW |
7 |
104,574,852 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6933:Or52n2c
|
UTSW |
7 |
104,574,330 (GRCm39) |
missense |
probably benign |
0.21 |
R7040:Or52n2c
|
UTSW |
7 |
104,574,717 (GRCm39) |
missense |
probably benign |
0.02 |
R7587:Or52n2c
|
UTSW |
7 |
104,574,263 (GRCm39) |
missense |
probably benign |
0.28 |
R7841:Or52n2c
|
UTSW |
7 |
104,574,066 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7869:Or52n2c
|
UTSW |
7 |
104,574,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R7902:Or52n2c
|
UTSW |
7 |
104,574,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R8296:Or52n2c
|
UTSW |
7 |
104,574,828 (GRCm39) |
missense |
probably benign |
0.00 |
R8670:Or52n2c
|
UTSW |
7 |
104,574,419 (GRCm39) |
missense |
probably damaging |
0.98 |
R8680:Or52n2c
|
UTSW |
7 |
104,574,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R8695:Or52n2c
|
UTSW |
7 |
104,574,146 (GRCm39) |
missense |
probably benign |
0.30 |
R9158:Or52n2c
|
UTSW |
7 |
104,574,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R9261:Or52n2c
|
UTSW |
7 |
104,574,305 (GRCm39) |
missense |
probably benign |
0.04 |
R9681:Or52n2c
|
UTSW |
7 |
104,574,075 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Or52n2c
|
UTSW |
7 |
104,574,200 (GRCm39) |
missense |
probably damaging |
1.00 |
|