Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
T |
11: 9,328,460 (GRCm39) |
E3511V |
probably null |
Het |
Abca13 |
A |
G |
11: 9,535,502 (GRCm39) |
T4709A |
probably benign |
Het |
Aff1 |
G |
T |
5: 103,958,956 (GRCm39) |
V342F |
probably damaging |
Het |
Ahnak2 |
T |
A |
12: 112,745,756 (GRCm39) |
Q1698L |
|
Het |
Ajap1 |
G |
T |
4: 153,516,813 (GRCm39) |
T176K |
probably damaging |
Het |
Alkal2 |
G |
T |
12: 30,934,850 (GRCm39) |
G23V |
probably damaging |
Het |
Cct3 |
A |
G |
3: 88,220,564 (GRCm39) |
T259A |
probably benign |
Het |
Cdk8 |
C |
T |
5: 146,205,061 (GRCm39) |
L21F |
probably damaging |
Het |
Cimip4 |
T |
C |
15: 78,262,686 (GRCm39) |
R262G |
probably benign |
Het |
Csf2rb |
G |
A |
15: 78,231,581 (GRCm39) |
G494D |
possibly damaging |
Het |
Cstf3 |
G |
T |
2: 104,420,926 (GRCm39) |
|
probably benign |
Het |
Dcp2 |
T |
C |
18: 44,529,071 (GRCm39) |
I62T |
probably benign |
Het |
Dnaaf9 |
ATCCTCCTCCTCCTCCTCC |
ATCCTCCTCCTCCTCC |
2: 130,612,655 (GRCm39) |
|
probably benign |
Het |
Dpp8 |
T |
C |
9: 64,988,133 (GRCm39) |
*893Q |
probably null |
Het |
Dpyd |
A |
T |
3: 119,108,534 (GRCm39) |
H859L |
probably benign |
Het |
Dst |
T |
C |
1: 34,323,501 (GRCm39) |
|
probably null |
Het |
Dynlt2a2 |
A |
G |
17: 15,190,717 (GRCm39) |
Y81H |
probably damaging |
Het |
Egfr |
A |
G |
11: 16,825,027 (GRCm39) |
I456V |
probably benign |
Het |
Elf3 |
A |
G |
1: 135,184,314 (GRCm39) |
F185L |
probably benign |
Het |
Emx1 |
A |
G |
6: 85,171,088 (GRCm39) |
T164A |
possibly damaging |
Het |
Fras1 |
G |
A |
5: 96,891,041 (GRCm39) |
V2857M |
probably damaging |
Het |
Gba2 |
AAAGAACCGTGTATACCGCCTGGGATGGAAAGAA |
AAA |
4: 43,569,937 (GRCm39) |
|
probably null |
Het |
Gda |
T |
A |
19: 21,394,435 (GRCm39) |
T215S |
probably benign |
Het |
Gm14443 |
C |
T |
2: 175,013,640 (GRCm39) |
|
probably null |
Het |
Gpr152 |
C |
T |
19: 4,193,469 (GRCm39) |
P337S |
probably damaging |
Het |
H2-T10 |
A |
G |
17: 36,429,905 (GRCm39) |
I296T |
probably benign |
Het |
Hoxd11 |
G |
A |
2: 74,513,466 (GRCm39) |
E244K |
probably benign |
Het |
Inka1 |
C |
A |
9: 107,861,506 (GRCm39) |
S270I |
probably damaging |
Het |
Kazn |
C |
T |
4: 141,869,002 (GRCm39) |
D325N |
|
Het |
Lama2 |
T |
C |
10: 27,298,655 (GRCm39) |
N147S |
probably damaging |
Het |
Lamc1 |
A |
T |
1: 153,119,167 (GRCm39) |
N817K |
probably benign |
Het |
Met |
T |
C |
6: 17,533,956 (GRCm39) |
S636P |
probably damaging |
Het |
Mrgpra3 |
A |
T |
7: 47,251,051 (GRCm39) |
M1K |
probably null |
Het |
Myh15 |
C |
A |
16: 48,940,381 (GRCm39) |
T777N |
probably damaging |
Het |
Or10ag2 |
C |
A |
2: 87,248,995 (GRCm39) |
A201D |
probably damaging |
Het |
Or6c209 |
G |
A |
10: 129,483,522 (GRCm39) |
C175Y |
probably benign |
Het |
Or8c13 |
T |
C |
9: 38,091,505 (GRCm39) |
T205A |
probably benign |
Het |
Pbx2 |
A |
G |
17: 34,811,707 (GRCm39) |
I60M |
probably damaging |
Het |
Phf8-ps |
C |
A |
17: 33,286,038 (GRCm39) |
A255S |
probably benign |
Het |
Pla2g4a |
T |
C |
1: 149,761,965 (GRCm39) |
N164S |
probably benign |
Het |
Poln |
A |
G |
5: 34,266,717 (GRCm39) |
M480T |
probably benign |
Het |
Ppp2r2a |
T |
C |
14: 67,261,177 (GRCm39) |
N181S |
probably damaging |
Het |
Ppp3r2 |
A |
C |
4: 49,681,705 (GRCm39) |
F82V |
probably damaging |
Het |
Prox2 |
A |
G |
12: 85,142,182 (GRCm39) |
V7A |
probably benign |
Het |
Ptpn3 |
A |
T |
4: 57,270,063 (GRCm39) |
I33K |
possibly damaging |
Het |
Rad21l |
A |
T |
2: 151,497,160 (GRCm39) |
M318K |
probably benign |
Het |
Rftn1 |
A |
G |
17: 50,309,665 (GRCm39) |
S445P |
possibly damaging |
Het |
Rsf1 |
CGGCGGCGG |
CGGCGGCGGGGGCGGCGG |
7: 97,229,130 (GRCm39) |
|
probably benign |
Het |
Rtp4 |
C |
T |
16: 23,431,998 (GRCm39) |
P177S |
possibly damaging |
Het |
Saa4 |
T |
A |
7: 46,379,052 (GRCm39) |
N96I |
possibly damaging |
Het |
Shb |
A |
G |
4: 45,489,079 (GRCm39) |
Y266H |
probably damaging |
Het |
Slc45a4 |
T |
G |
15: 73,461,405 (GRCm39) |
Y88S |
probably damaging |
Het |
Tbccd1 |
A |
G |
16: 22,641,564 (GRCm39) |
M312T |
probably damaging |
Het |
Tecta |
C |
T |
9: 42,299,121 (GRCm39) |
|
probably null |
Het |
Tle1 |
A |
T |
4: 72,044,428 (GRCm39) |
C526* |
probably null |
Het |
Tmem87a |
C |
T |
2: 120,234,441 (GRCm39) |
G34D |
probably damaging |
Het |
Trav13d-1 |
C |
A |
14: 53,089,059 (GRCm39) |
Q23K |
probably benign |
Het |
Txndc11 |
G |
T |
16: 10,893,465 (GRCm39) |
T755N |
possibly damaging |
Het |
Vmn1r223 |
A |
G |
13: 23,434,339 (GRCm39) |
D311G |
probably damaging |
Het |
Vmn2r66 |
T |
A |
7: 84,643,932 (GRCm39) |
Y826F |
possibly damaging |
Het |
Wdr90 |
A |
T |
17: 26,064,399 (GRCm39) |
M1824K |
probably benign |
Het |
Zfp523 |
G |
A |
17: 28,421,562 (GRCm39) |
G440D |
possibly damaging |
Het |
|
Other mutations in Cyp4f39 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00789:Cyp4f39
|
APN |
17 |
32,689,886 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00822:Cyp4f39
|
APN |
17 |
32,689,806 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00857:Cyp4f39
|
APN |
17 |
32,708,631 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01380:Cyp4f39
|
APN |
17 |
32,700,832 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01532:Cyp4f39
|
APN |
17 |
32,689,928 (GRCm39) |
splice site |
probably benign |
|
IGL01756:Cyp4f39
|
APN |
17 |
32,702,415 (GRCm39) |
nonsense |
probably null |
|
IGL02090:Cyp4f39
|
APN |
17 |
32,689,932 (GRCm39) |
splice site |
probably benign |
|
IGL02477:Cyp4f39
|
APN |
17 |
32,708,619 (GRCm39) |
missense |
probably benign |
0.40 |
IGL02824:Cyp4f39
|
APN |
17 |
32,687,659 (GRCm39) |
critical splice donor site |
probably null |
|
N/A:Cyp4f39
|
UTSW |
17 |
32,687,655 (GRCm39) |
missense |
probably benign |
0.03 |
R0145:Cyp4f39
|
UTSW |
17 |
32,705,934 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0288:Cyp4f39
|
UTSW |
17 |
32,711,410 (GRCm39) |
missense |
probably benign |
0.01 |
R1676:Cyp4f39
|
UTSW |
17 |
32,701,176 (GRCm39) |
missense |
probably benign |
0.41 |
R1677:Cyp4f39
|
UTSW |
17 |
32,711,304 (GRCm39) |
missense |
probably benign |
0.30 |
R1874:Cyp4f39
|
UTSW |
17 |
32,702,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R1920:Cyp4f39
|
UTSW |
17 |
32,702,265 (GRCm39) |
missense |
probably benign |
0.00 |
R2049:Cyp4f39
|
UTSW |
17 |
32,701,112 (GRCm39) |
missense |
probably benign |
0.41 |
R2139:Cyp4f39
|
UTSW |
17 |
32,710,163 (GRCm39) |
missense |
probably benign |
0.01 |
R2212:Cyp4f39
|
UTSW |
17 |
32,706,037 (GRCm39) |
missense |
possibly damaging |
0.62 |
R3416:Cyp4f39
|
UTSW |
17 |
32,708,716 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3417:Cyp4f39
|
UTSW |
17 |
32,708,716 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4486:Cyp4f39
|
UTSW |
17 |
32,702,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R5023:Cyp4f39
|
UTSW |
17 |
32,700,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R5523:Cyp4f39
|
UTSW |
17 |
32,689,807 (GRCm39) |
missense |
probably benign |
0.10 |
R5714:Cyp4f39
|
UTSW |
17 |
32,700,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R6010:Cyp4f39
|
UTSW |
17 |
32,701,160 (GRCm39) |
missense |
probably damaging |
0.99 |
R6312:Cyp4f39
|
UTSW |
17 |
32,702,268 (GRCm39) |
missense |
probably benign |
0.00 |
R6477:Cyp4f39
|
UTSW |
17 |
32,700,791 (GRCm39) |
missense |
probably damaging |
0.99 |
R6950:Cyp4f39
|
UTSW |
17 |
32,711,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R7228:Cyp4f39
|
UTSW |
17 |
32,710,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R7311:Cyp4f39
|
UTSW |
17 |
32,708,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R7341:Cyp4f39
|
UTSW |
17 |
32,705,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R7345:Cyp4f39
|
UTSW |
17 |
32,705,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R7405:Cyp4f39
|
UTSW |
17 |
32,700,789 (GRCm39) |
missense |
probably benign |
0.01 |
R7522:Cyp4f39
|
UTSW |
17 |
32,705,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R7842:Cyp4f39
|
UTSW |
17 |
32,702,291 (GRCm39) |
missense |
probably benign |
0.01 |
R8223:Cyp4f39
|
UTSW |
17 |
32,689,839 (GRCm39) |
missense |
probably benign |
0.10 |
R8469:Cyp4f39
|
UTSW |
17 |
32,711,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R8789:Cyp4f39
|
UTSW |
17 |
32,710,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R8865:Cyp4f39
|
UTSW |
17 |
32,702,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R9049:Cyp4f39
|
UTSW |
17 |
32,705,965 (GRCm39) |
missense |
probably damaging |
0.99 |
R9115:Cyp4f39
|
UTSW |
17 |
32,711,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R9402:Cyp4f39
|
UTSW |
17 |
32,710,183 (GRCm39) |
critical splice donor site |
probably null |
|
R9571:Cyp4f39
|
UTSW |
17 |
32,702,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R9600:Cyp4f39
|
UTSW |
17 |
32,705,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R9641:Cyp4f39
|
UTSW |
17 |
32,705,982 (GRCm39) |
missense |
probably damaging |
0.99 |
|