Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg5 |
G |
A |
17: 84,976,425 (GRCm39) |
H471Y |
probably damaging |
Het |
Ank2 |
T |
A |
3: 126,733,744 (GRCm39) |
D622V |
probably damaging |
Het |
Apoe |
T |
A |
7: 19,432,375 (GRCm39) |
|
probably benign |
Het |
Asz1 |
T |
C |
6: 18,054,561 (GRCm39) |
E414G |
probably benign |
Het |
Atp2a2 |
A |
T |
5: 122,604,918 (GRCm39) |
C420* |
probably null |
Het |
Cd84 |
A |
T |
1: 171,712,153 (GRCm39) |
|
probably null |
Het |
Cdca2 |
T |
A |
14: 67,917,762 (GRCm39) |
R545S |
probably benign |
Het |
Cep250 |
C |
T |
2: 155,812,042 (GRCm39) |
A446V |
unknown |
Het |
Cib1 |
T |
C |
7: 79,877,751 (GRCm39) |
D182G |
probably damaging |
Het |
Cpsf2 |
A |
G |
12: 101,963,555 (GRCm39) |
D428G |
probably damaging |
Het |
Cspg4b |
C |
T |
13: 113,505,374 (GRCm39) |
P2168S |
|
Het |
Dap3 |
T |
A |
3: 88,837,861 (GRCm39) |
T130S |
probably benign |
Het |
Ddb2 |
T |
A |
2: 91,064,593 (GRCm39) |
K106* |
probably null |
Het |
Ehd2 |
G |
A |
7: 15,684,626 (GRCm39) |
A391V |
probably damaging |
Het |
Evpl |
A |
T |
11: 116,115,008 (GRCm39) |
I894N |
possibly damaging |
Het |
Gabrb2 |
A |
G |
11: 42,482,693 (GRCm39) |
T184A |
probably damaging |
Het |
Gfpt1 |
G |
A |
6: 87,053,248 (GRCm39) |
V403I |
probably benign |
Het |
Gli1 |
A |
G |
10: 127,167,202 (GRCm39) |
S684P |
possibly damaging |
Het |
Gm7276 |
A |
G |
18: 77,273,147 (GRCm39) |
S196P |
unknown |
Het |
Hoxc10 |
C |
T |
15: 102,875,810 (GRCm39) |
P173L |
probably benign |
Het |
Kif2c |
A |
T |
4: 117,024,291 (GRCm39) |
S359T |
probably benign |
Het |
Lmln |
T |
G |
16: 32,930,202 (GRCm39) |
L553R |
probably benign |
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Mettl1 |
T |
A |
10: 126,880,911 (GRCm39) |
V191D |
possibly damaging |
Het |
Mical2 |
A |
C |
7: 111,870,589 (GRCm39) |
K26T |
possibly damaging |
Het |
Myl1 |
A |
T |
1: 66,973,675 (GRCm39) |
|
probably null |
Het |
Nfat5 |
A |
G |
8: 108,078,141 (GRCm39) |
T427A |
probably damaging |
Het |
Noa1 |
T |
C |
5: 77,457,038 (GRCm39) |
Y289C |
possibly damaging |
Het |
Or5d14 |
C |
T |
2: 87,880,294 (GRCm39) |
V225M |
probably damaging |
Het |
Or8b49 |
T |
A |
9: 38,506,108 (GRCm39) |
I197K |
probably damaging |
Het |
Piezo2 |
A |
G |
18: 63,178,589 (GRCm39) |
I1776T |
probably benign |
Het |
Ppp1r7 |
A |
G |
1: 93,285,497 (GRCm39) |
I246V |
probably benign |
Het |
Ppp4c |
T |
A |
7: 126,386,739 (GRCm39) |
E116V |
probably damaging |
Het |
Psme2 |
T |
A |
14: 55,828,302 (GRCm39) |
K15N |
possibly damaging |
Het |
Retreg1 |
C |
T |
15: 25,968,618 (GRCm39) |
R125C |
probably damaging |
Het |
Rnf145 |
G |
T |
11: 44,450,819 (GRCm39) |
R381L |
probably damaging |
Het |
Rsf1 |
G |
GACGGCGGCA |
7: 97,229,116 (GRCm39) |
|
probably benign |
Het |
Ryr1 |
G |
A |
7: 28,771,229 (GRCm39) |
T2604I |
probably damaging |
Het |
Sag |
T |
C |
1: 87,751,043 (GRCm39) |
S170P |
probably damaging |
Het |
Sema3b |
T |
A |
9: 107,478,173 (GRCm39) |
N404I |
possibly damaging |
Het |
Serpina1b |
A |
T |
12: 103,696,566 (GRCm39) |
L281Q |
probably damaging |
Het |
Slc22a1 |
T |
A |
17: 12,878,598 (GRCm39) |
T372S |
probably benign |
Het |
Slco6d1 |
A |
T |
1: 98,423,919 (GRCm39) |
N524Y |
probably damaging |
Het |
Smarca2 |
T |
A |
19: 26,693,583 (GRCm39) |
D1262E |
possibly damaging |
Het |
Syne2 |
A |
T |
12: 76,040,838 (GRCm39) |
H3832L |
probably damaging |
Het |
Tarbp1 |
G |
T |
8: 127,174,202 (GRCm39) |
T868K |
possibly damaging |
Het |
Trp63 |
C |
T |
16: 25,639,247 (GRCm39) |
A145V |
probably damaging |
Het |
Tsc2 |
C |
T |
17: 24,823,802 (GRCm39) |
R1001K |
probably null |
Het |
Ttc39b |
T |
C |
4: 83,189,444 (GRCm39) |
D30G |
probably damaging |
Het |
Usf3 |
A |
G |
16: 44,041,030 (GRCm39) |
T1837A |
probably benign |
Het |
Usp25 |
T |
A |
16: 76,911,969 (GRCm39) |
|
probably null |
Het |
Vmn1r27 |
G |
A |
6: 58,192,416 (GRCm39) |
T196I |
probably benign |
Het |
Vrk3 |
C |
T |
7: 44,407,254 (GRCm39) |
S75F |
possibly damaging |
Het |
Washc5 |
T |
C |
15: 59,209,134 (GRCm39) |
Y1030C |
probably damaging |
Het |
Wdr47 |
T |
C |
3: 108,526,106 (GRCm39) |
F210L |
probably damaging |
Het |
Zfp853 |
G |
A |
5: 143,274,496 (GRCm39) |
Q390* |
probably null |
Het |
Zfyve9 |
A |
T |
4: 108,575,760 (GRCm39) |
D440E |
probably benign |
Het |
|
Other mutations in Hrnr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00848:Hrnr
|
APN |
3 |
93,230,204 (GRCm39) |
missense |
unknown |
|
IGL02326:Hrnr
|
APN |
3 |
93,231,052 (GRCm39) |
missense |
unknown |
|
IGL03030:Hrnr
|
APN |
3 |
93,227,908 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL03281:Hrnr
|
APN |
3 |
93,230,158 (GRCm39) |
missense |
probably benign |
0.04 |
R0140:Hrnr
|
UTSW |
3 |
93,238,800 (GRCm39) |
nonsense |
probably null |
|
R0709:Hrnr
|
UTSW |
3 |
93,239,815 (GRCm39) |
missense |
unknown |
|
R1179:Hrnr
|
UTSW |
3 |
93,239,850 (GRCm39) |
missense |
unknown |
|
R1528:Hrnr
|
UTSW |
3 |
93,230,101 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1640:Hrnr
|
UTSW |
3 |
93,239,823 (GRCm39) |
missense |
unknown |
|
R1987:Hrnr
|
UTSW |
3 |
93,239,911 (GRCm39) |
missense |
unknown |
|
R1988:Hrnr
|
UTSW |
3 |
93,239,911 (GRCm39) |
missense |
unknown |
|
R3846:Hrnr
|
UTSW |
3 |
93,239,464 (GRCm39) |
missense |
unknown |
|
R3871:Hrnr
|
UTSW |
3 |
93,239,181 (GRCm39) |
missense |
unknown |
|
R3938:Hrnr
|
UTSW |
3 |
93,230,162 (GRCm39) |
missense |
probably benign |
0.35 |
R4569:Hrnr
|
UTSW |
3 |
93,230,875 (GRCm39) |
missense |
unknown |
|
R4690:Hrnr
|
UTSW |
3 |
93,230,959 (GRCm39) |
missense |
unknown |
|
R4761:Hrnr
|
UTSW |
3 |
93,230,062 (GRCm39) |
missense |
probably damaging |
0.96 |
R5182:Hrnr
|
UTSW |
3 |
93,239,450 (GRCm39) |
missense |
unknown |
|
R5292:Hrnr
|
UTSW |
3 |
93,239,199 (GRCm39) |
missense |
unknown |
|
R5739:Hrnr
|
UTSW |
3 |
93,230,436 (GRCm39) |
missense |
unknown |
|
R5845:Hrnr
|
UTSW |
3 |
93,239,944 (GRCm39) |
missense |
unknown |
|
R5994:Hrnr
|
UTSW |
3 |
93,239,607 (GRCm39) |
missense |
unknown |
|
R6169:Hrnr
|
UTSW |
3 |
93,233,062 (GRCm39) |
nonsense |
probably null |
|
R6216:Hrnr
|
UTSW |
3 |
93,239,469 (GRCm39) |
missense |
unknown |
|
R6256:Hrnr
|
UTSW |
3 |
93,229,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R6670:Hrnr
|
UTSW |
3 |
93,239,192 (GRCm39) |
missense |
unknown |
|
R6790:Hrnr
|
UTSW |
3 |
93,236,382 (GRCm39) |
missense |
unknown |
|
R6936:Hrnr
|
UTSW |
3 |
93,239,667 (GRCm39) |
missense |
unknown |
|
R7049:Hrnr
|
UTSW |
3 |
93,230,461 (GRCm39) |
nonsense |
probably null |
|
R7358:Hrnr
|
UTSW |
3 |
93,230,448 (GRCm39) |
nonsense |
probably null |
|
R7383:Hrnr
|
UTSW |
3 |
93,239,098 (GRCm39) |
missense |
unknown |
|
R7724:Hrnr
|
UTSW |
3 |
93,230,323 (GRCm39) |
missense |
unknown |
|
R7762:Hrnr
|
UTSW |
3 |
93,239,506 (GRCm39) |
missense |
unknown |
|
R7945:Hrnr
|
UTSW |
3 |
93,239,506 (GRCm39) |
missense |
unknown |
|
R8086:Hrnr
|
UTSW |
3 |
93,230,728 (GRCm39) |
missense |
unknown |
|
R8115:Hrnr
|
UTSW |
3 |
93,231,039 (GRCm39) |
missense |
unknown |
|
R8383:Hrnr
|
UTSW |
3 |
93,239,653 (GRCm39) |
missense |
unknown |
|
R8685:Hrnr
|
UTSW |
3 |
93,230,205 (GRCm39) |
missense |
unknown |
|
R8809:Hrnr
|
UTSW |
3 |
93,239,443 (GRCm39) |
missense |
unknown |
|
R9125:Hrnr
|
UTSW |
3 |
93,238,863 (GRCm39) |
missense |
unknown |
|
R9129:Hrnr
|
UTSW |
3 |
93,231,277 (GRCm39) |
missense |
unknown |
|
R9572:Hrnr
|
UTSW |
3 |
93,239,467 (GRCm39) |
missense |
unknown |
|
R9627:Hrnr
|
UTSW |
3 |
93,233,235 (GRCm39) |
missense |
unknown |
|
R9698:Hrnr
|
UTSW |
3 |
93,233,094 (GRCm39) |
missense |
unknown |
|
R9717:Hrnr
|
UTSW |
3 |
93,227,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R9749:Hrnr
|
UTSW |
3 |
93,231,384 (GRCm39) |
missense |
unknown |
|
R9781:Hrnr
|
UTSW |
3 |
93,239,696 (GRCm39) |
missense |
unknown |
|
R9785:Hrnr
|
UTSW |
3 |
93,238,861 (GRCm39) |
missense |
unknown |
|
|