Incidental Mutation 'R8947:Zfp292'
| ID |
681358 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Zfp292
|
| Ensembl Gene |
ENSMUSG00000039967 |
| Gene Name |
zinc finger protein 292 |
| Synonyms |
Zfp-15, 9430062L07Rik, Zn-16, Zfp15, Zn-15, 5730450D02Rik, Krox-10 |
| MMRRC Submission |
068785-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.861)
|
| Stock # |
R8947 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
4 |
| Chromosomal Location |
34803113-34882960 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 34811835 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Cysteine
at position 403
(Y403C)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000095766
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000047950]
[ENSMUST00000098163]
|
| AlphaFold |
Q9Z2U2 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000047950
AA Change: Y408C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000037233
Gene: ENSMUSG00000039967
AA Change: Y408C
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
19 |
39 |
N/A |
INTRINSIC |
|
low complexity region
|
101 |
120 |
N/A |
INTRINSIC |
|
low complexity region
|
512 |
523 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
540 |
561 |
5.12e1 |
SMART |
|
ZnF_C2H2
|
567 |
589 |
4.72e-2 |
SMART |
|
low complexity region
|
649 |
664 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
681 |
705 |
3.52e-1 |
SMART |
|
ZnF_C2H2
|
722 |
744 |
1.53e-1 |
SMART |
|
ZnF_C2H2
|
750 |
774 |
1.62e0 |
SMART |
|
ZnF_C2H2
|
779 |
803 |
1.08e1 |
SMART |
|
ZnF_C2H2
|
807 |
831 |
1.95e-3 |
SMART |
|
low complexity region
|
1062 |
1078 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
1085 |
1110 |
7.67e-2 |
SMART |
|
ZnF_C2H2
|
1361 |
1381 |
1.93e2 |
SMART |
|
low complexity region
|
1606 |
1618 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
1879 |
1904 |
4.4e-2 |
SMART |
|
ZnF_C2H2
|
1924 |
1949 |
5.42e-2 |
SMART |
|
low complexity region
|
2004 |
2014 |
N/A |
INTRINSIC |
|
low complexity region
|
2024 |
2037 |
N/A |
INTRINSIC |
|
coiled coil region
|
2050 |
2072 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
2091 |
2116 |
4.45e0 |
SMART |
|
low complexity region
|
2121 |
2143 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
2149 |
2174 |
1.64e-1 |
SMART |
|
ZnF_C2H2
|
2193 |
2218 |
3.24e0 |
SMART |
|
ZnF_C2H2
|
2233 |
2258 |
1.18e-2 |
SMART |
|
low complexity region
|
2301 |
2314 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
2362 |
2386 |
2.86e-1 |
SMART |
|
low complexity region
|
2589 |
2605 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000098163
AA Change: Y403C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000095766
Gene: ENSMUSG00000039967
AA Change: Y403C
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
19 |
39 |
N/A |
INTRINSIC |
|
low complexity region
|
101 |
120 |
N/A |
INTRINSIC |
|
low complexity region
|
507 |
518 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
535 |
556 |
5.12e1 |
SMART |
|
ZnF_C2H2
|
562 |
584 |
4.72e-2 |
SMART |
|
low complexity region
|
644 |
659 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
676 |
700 |
3.52e-1 |
SMART |
|
ZnF_C2H2
|
717 |
739 |
1.53e-1 |
SMART |
|
ZnF_C2H2
|
745 |
769 |
1.62e0 |
SMART |
|
ZnF_C2H2
|
774 |
798 |
1.08e1 |
SMART |
|
ZnF_C2H2
|
802 |
826 |
1.95e-3 |
SMART |
|
low complexity region
|
1057 |
1073 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
1080 |
1105 |
7.67e-2 |
SMART |
|
ZnF_C2H2
|
1356 |
1376 |
1.93e2 |
SMART |
|
low complexity region
|
1601 |
1613 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
1874 |
1899 |
4.4e-2 |
SMART |
|
ZnF_C2H2
|
1919 |
1944 |
5.42e-2 |
SMART |
|
low complexity region
|
1999 |
2009 |
N/A |
INTRINSIC |
|
low complexity region
|
2019 |
2032 |
N/A |
INTRINSIC |
|
coiled coil region
|
2045 |
2067 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
2086 |
2111 |
4.45e0 |
SMART |
|
low complexity region
|
2116 |
2138 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
2144 |
2169 |
1.64e-1 |
SMART |
|
ZnF_C2H2
|
2188 |
2213 |
3.24e0 |
SMART |
|
ZnF_C2H2
|
2228 |
2253 |
1.18e-2 |
SMART |
|
low complexity region
|
2296 |
2309 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
2357 |
2381 |
2.86e-1 |
SMART |
|
low complexity region
|
2584 |
2600 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.8%
|
| Validation Efficiency |
99% (93/94) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 97 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930562C15Rik |
T |
A |
16: 4,665,292 (GRCm39) |
F141L |
unknown |
Het |
| A2ml1 |
G |
T |
6: 128,529,219 (GRCm39) |
N974K |
probably damaging |
Het |
| Abcg8 |
T |
C |
17: 84,999,246 (GRCm39) |
L114P |
probably damaging |
Het |
| Akt3 |
A |
T |
1: 176,958,645 (GRCm39) |
W22R |
probably damaging |
Het |
| Ank2 |
C |
T |
3: 126,736,396 (GRCm39) |
|
probably benign |
Het |
| Ap1g1 |
C |
T |
8: 110,589,964 (GRCm39) |
|
probably benign |
Het |
| Arhgef19 |
T |
A |
4: 140,973,618 (GRCm39) |
V35E |
possibly damaging |
Het |
| Baz2b |
T |
C |
2: 59,778,583 (GRCm39) |
D759G |
probably benign |
Het |
| BC051665 |
C |
A |
13: 60,930,004 (GRCm39) |
G320W |
probably damaging |
Het |
| Bche |
T |
A |
3: 73,608,761 (GRCm39) |
T222S |
probably damaging |
Het |
| C8a |
T |
C |
4: 104,679,326 (GRCm39) |
D444G |
probably damaging |
Het |
| Cacna1e |
A |
T |
1: 154,277,896 (GRCm39) |
S2019T |
probably benign |
Het |
| Carm1 |
T |
C |
9: 21,497,749 (GRCm39) |
I373T |
probably damaging |
Het |
| Ccdc39 |
T |
C |
3: 33,869,609 (GRCm39) |
|
probably benign |
Het |
| Clic5 |
A |
T |
17: 44,553,148 (GRCm39) |
|
probably benign |
Het |
| Cntn3 |
A |
G |
6: 102,414,864 (GRCm39) |
F28L |
probably damaging |
Het |
| Col6a5 |
C |
T |
9: 105,822,833 (GRCm39) |
E175K |
unknown |
Het |
| Cpb2 |
T |
C |
14: 75,515,627 (GRCm39) |
Y352H |
probably damaging |
Het |
| Cpeb3 |
A |
T |
19: 37,152,366 (GRCm39) |
D3E |
probably damaging |
Het |
| Ctsl |
T |
C |
13: 64,514,840 (GRCm39) |
T155A |
probably damaging |
Het |
| Cygb |
C |
T |
11: 116,540,645 (GRCm39) |
A114T |
probably damaging |
Het |
| Cyp11a1 |
T |
C |
9: 57,924,738 (GRCm39) |
V17A |
probably benign |
Het |
| Dhcr7 |
T |
G |
7: 143,400,959 (GRCm39) |
I374S |
probably damaging |
Het |
| Dhx36 |
T |
C |
3: 62,380,387 (GRCm39) |
R807G |
probably benign |
Het |
| Diaph1 |
A |
T |
18: 37,986,754 (GRCm39) |
V1077E |
probably damaging |
Het |
| Ehmt2 |
A |
G |
17: 35,127,280 (GRCm39) |
E131G |
possibly damaging |
Het |
| Evpl |
A |
G |
11: 116,112,164 (GRCm39) |
I1842T |
probably damaging |
Het |
| Fastk |
C |
A |
5: 24,646,649 (GRCm39) |
C294F |
probably damaging |
Het |
| Fndc5 |
T |
C |
4: 129,030,929 (GRCm39) |
C20R |
probably benign |
Het |
| Gm7298 |
C |
A |
6: 121,757,553 (GRCm39) |
Q1053K |
possibly damaging |
Het |
| Gm8362 |
A |
G |
14: 18,151,405 (GRCm39) |
|
probably null |
Het |
| Gmps |
T |
A |
3: 63,906,098 (GRCm39) |
I465N |
probably damaging |
Het |
| Heatr4 |
T |
G |
12: 84,001,431 (GRCm39) |
M904L |
probably benign |
Het |
| Hhip |
T |
A |
8: 80,771,785 (GRCm39) |
D175V |
probably damaging |
Het |
| Hmcn2 |
G |
A |
2: 31,278,220 (GRCm39) |
V1641M |
probably damaging |
Het |
| Hoxa5 |
T |
G |
6: 52,179,776 (GRCm39) |
T200P |
probably damaging |
Het |
| Ift122 |
C |
A |
6: 115,901,368 (GRCm39) |
A1050D |
probably benign |
Het |
| Igf2bp2 |
C |
A |
16: 21,897,473 (GRCm39) |
E247* |
probably null |
Het |
| Irak1bp1 |
T |
A |
9: 82,728,846 (GRCm39) |
L259H |
probably damaging |
Het |
| Irgm1 |
G |
A |
11: 48,759,575 (GRCm39) |
|
probably benign |
Het |
| Itih1 |
A |
T |
14: 30,657,866 (GRCm39) |
|
probably benign |
Het |
| Itpk1 |
A |
T |
12: 102,536,582 (GRCm39) |
C355S |
probably benign |
Het |
| Kcng4 |
T |
C |
8: 120,352,452 (GRCm39) |
E486G |
possibly damaging |
Het |
| Kif20b |
T |
C |
19: 34,918,629 (GRCm39) |
V671A |
possibly damaging |
Het |
| Kif28 |
T |
G |
1: 179,544,320 (GRCm39) |
I345L |
possibly damaging |
Het |
| Klri2 |
C |
G |
6: 129,710,742 (GRCm39) |
|
probably null |
Het |
| Kntc1 |
T |
C |
5: 123,925,041 (GRCm39) |
V1118A |
probably benign |
Het |
| Lpin2 |
T |
A |
17: 71,511,871 (GRCm39) |
I34N |
probably benign |
Het |
| Lrch3 |
T |
A |
16: 32,802,199 (GRCm39) |
V264D |
possibly damaging |
Het |
| Lrrk2 |
C |
T |
15: 91,586,473 (GRCm39) |
Q430* |
probably null |
Het |
| Map10 |
T |
G |
8: 126,397,839 (GRCm39) |
S411A |
probably benign |
Het |
| Map1a |
A |
T |
2: 121,135,450 (GRCm39) |
I2089F |
probably benign |
Het |
| Med12l |
T |
A |
3: 58,984,443 (GRCm39) |
|
probably benign |
Het |
| Mypn |
T |
A |
10: 63,005,156 (GRCm39) |
Q317L |
probably damaging |
Het |
| Ncan |
T |
A |
8: 70,555,171 (GRCm39) |
I999F |
probably damaging |
Het |
| Nmrk2 |
C |
A |
10: 81,035,539 (GRCm39) |
R134L |
probably damaging |
Het |
| Or4k42 |
C |
T |
2: 111,320,042 (GRCm39) |
V154I |
probably benign |
Het |
| Or51f1d |
T |
A |
7: 102,701,315 (GRCm39) |
V270E |
probably damaging |
Het |
| Or5k17 |
T |
C |
16: 58,746,433 (GRCm39) |
N167S |
probably benign |
Het |
| Or6z7 |
A |
G |
7: 6,483,246 (GRCm39) |
V303A |
probably benign |
Het |
| Or8b1c |
T |
A |
9: 38,384,685 (GRCm39) |
I214N |
probably damaging |
Het |
| Osbpl1a |
A |
G |
18: 12,899,858 (GRCm39) |
|
probably null |
Het |
| Pcdh1 |
T |
C |
18: 38,332,073 (GRCm39) |
D310G |
possibly damaging |
Het |
| Pkn2 |
C |
T |
3: 142,517,674 (GRCm39) |
|
probably null |
Het |
| Plch1 |
T |
A |
3: 63,691,547 (GRCm39) |
M31L |
probably damaging |
Het |
| Polg2 |
A |
G |
11: 106,659,170 (GRCm39) |
F448L |
probably damaging |
Het |
| Ppp4r3b |
A |
G |
11: 29,150,758 (GRCm39) |
T475A |
possibly damaging |
Het |
| Prdm13 |
C |
T |
4: 21,678,817 (GRCm39) |
E558K |
probably damaging |
Het |
| Prdm9 |
T |
A |
17: 15,764,270 (GRCm39) |
I837F |
possibly damaging |
Het |
| R3hdm1 |
T |
A |
1: 128,102,694 (GRCm39) |
M125K |
possibly damaging |
Het |
| Rbm39 |
A |
T |
2: 155,990,276 (GRCm39) |
V468E |
probably damaging |
Het |
| Rnasel |
T |
A |
1: 153,630,777 (GRCm39) |
V431E |
probably damaging |
Het |
| Rps2 |
T |
A |
17: 24,940,227 (GRCm39) |
D220E |
probably benign |
Het |
| Rsf1 |
T |
C |
7: 97,331,059 (GRCm39) |
|
probably benign |
Het |
| Rsph10b |
G |
T |
5: 143,913,952 (GRCm39) |
A710S |
probably benign |
Het |
| Sez6 |
A |
T |
11: 77,844,353 (GRCm39) |
T59S |
probably damaging |
Het |
| Sf3b1 |
A |
T |
1: 55,039,444 (GRCm39) |
V727E |
probably damaging |
Het |
| Slit2 |
T |
G |
5: 48,407,140 (GRCm39) |
L857R |
probably damaging |
Het |
| Spata31g1 |
T |
A |
4: 42,972,097 (GRCm39) |
S477T |
probably benign |
Het |
| Sspo |
T |
G |
6: 48,425,504 (GRCm39) |
C42G |
probably damaging |
Het |
| Strc |
C |
T |
2: 121,201,470 (GRCm39) |
D1245N |
probably benign |
Het |
| Supv3l1 |
T |
A |
10: 62,268,118 (GRCm39) |
T576S |
probably benign |
Het |
| Tecrl |
C |
T |
5: 83,461,154 (GRCm39) |
R101Q |
probably benign |
Het |
| Tmeff2 |
A |
G |
1: 51,220,952 (GRCm39) |
Y309C |
probably damaging |
Het |
| Tmem43 |
T |
A |
6: 91,462,362 (GRCm39) |
W316R |
probably damaging |
Het |
| Tmigd3 |
T |
C |
3: 105,821,554 (GRCm39) |
V141A |
probably benign |
Het |
| Trav9-1 |
T |
C |
14: 53,725,584 (GRCm39) |
F8L |
probably benign |
Het |
| Trbv5 |
T |
G |
6: 41,039,641 (GRCm39) |
F82C |
probably damaging |
Het |
| Ubtf |
T |
C |
11: 102,205,802 (GRCm39) |
N41S |
possibly damaging |
Het |
| Uggt1 |
T |
C |
1: 36,197,229 (GRCm39) |
T1225A |
probably benign |
Het |
| Vmn1r72 |
T |
C |
7: 11,403,807 (GRCm39) |
R214G |
possibly damaging |
Het |
| Vmn2r12 |
T |
G |
5: 109,234,522 (GRCm39) |
K563N |
possibly damaging |
Het |
| Vmn2r83 |
T |
C |
10: 79,304,873 (GRCm39) |
S28P |
probably benign |
Het |
| Vwa8 |
T |
G |
14: 79,438,552 (GRCm39) |
L1875R |
probably damaging |
Het |
| Xrcc6 |
T |
A |
15: 81,913,866 (GRCm39) |
V64E |
probably damaging |
Het |
| Zfp955a |
A |
T |
17: 33,460,955 (GRCm39) |
H392Q |
probably damaging |
Het |
| Zfyve19 |
T |
C |
2: 119,041,290 (GRCm39) |
S69P |
probably damaging |
Het |
|
| Other mutations in Zfp292 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00401:Zfp292
|
APN |
4 |
34,808,683 (GRCm39) |
missense |
probably benign |
0.15 |
|
IGL00502:Zfp292
|
APN |
4 |
34,809,775 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
IGL00539:Zfp292
|
APN |
4 |
34,808,790 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL00676:Zfp292
|
APN |
4 |
34,807,827 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01068:Zfp292
|
APN |
4 |
34,806,763 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01311:Zfp292
|
APN |
4 |
34,807,961 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01639:Zfp292
|
APN |
4 |
34,809,048 (GRCm39) |
missense |
probably benign |
0.04 |
|
IGL01688:Zfp292
|
APN |
4 |
34,807,855 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
IGL02345:Zfp292
|
APN |
4 |
34,809,244 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
IGL02444:Zfp292
|
APN |
4 |
34,808,810 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
IGL02548:Zfp292
|
APN |
4 |
34,805,416 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02551:Zfp292
|
APN |
4 |
34,806,462 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
IGL02702:Zfp292
|
APN |
4 |
34,809,415 (GRCm39) |
missense |
probably benign |
0.14 |
|
IGL02715:Zfp292
|
APN |
4 |
34,819,542 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03273:Zfp292
|
APN |
4 |
34,806,163 (GRCm39) |
missense |
probably benign |
0.00 |
|
F5770:Zfp292
|
UTSW |
4 |
34,806,783 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
PIT4362001:Zfp292
|
UTSW |
4 |
34,807,524 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0153:Zfp292
|
UTSW |
4 |
34,811,185 (GRCm39) |
missense |
probably benign |
0.26 |
|
R0184:Zfp292
|
UTSW |
4 |
34,819,563 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0295:Zfp292
|
UTSW |
4 |
34,806,281 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0367:Zfp292
|
UTSW |
4 |
34,808,227 (GRCm39) |
missense |
probably benign |
0.25 |
|
R0433:Zfp292
|
UTSW |
4 |
34,839,959 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0481:Zfp292
|
UTSW |
4 |
34,810,059 (GRCm39) |
missense |
probably benign |
0.28 |
|
R0555:Zfp292
|
UTSW |
4 |
34,807,194 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0597:Zfp292
|
UTSW |
4 |
34,807,399 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0748:Zfp292
|
UTSW |
4 |
34,816,424 (GRCm39) |
splice site |
probably benign |
|
|
R0782:Zfp292
|
UTSW |
4 |
34,839,382 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R0834:Zfp292
|
UTSW |
4 |
34,809,114 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0879:Zfp292
|
UTSW |
4 |
34,811,218 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1083:Zfp292
|
UTSW |
4 |
34,807,569 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1343:Zfp292
|
UTSW |
4 |
34,805,238 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1498:Zfp292
|
UTSW |
4 |
34,805,397 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R1714:Zfp292
|
UTSW |
4 |
34,808,935 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1724:Zfp292
|
UTSW |
4 |
34,811,237 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1755:Zfp292
|
UTSW |
4 |
34,811,043 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1837:Zfp292
|
UTSW |
4 |
34,810,264 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1914:Zfp292
|
UTSW |
4 |
34,805,100 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R1915:Zfp292
|
UTSW |
4 |
34,805,100 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R1936:Zfp292
|
UTSW |
4 |
34,807,452 (GRCm39) |
missense |
probably benign |
0.22 |
|
R2107:Zfp292
|
UTSW |
4 |
34,808,593 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R2108:Zfp292
|
UTSW |
4 |
34,808,593 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R2136:Zfp292
|
UTSW |
4 |
34,810,266 (GRCm39) |
missense |
probably benign |
0.13 |
|
R2182:Zfp292
|
UTSW |
4 |
34,807,417 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2186:Zfp292
|
UTSW |
4 |
34,807,962 (GRCm39) |
missense |
probably benign |
0.07 |
|
R2306:Zfp292
|
UTSW |
4 |
34,809,468 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R2350:Zfp292
|
UTSW |
4 |
34,811,281 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2382:Zfp292
|
UTSW |
4 |
34,806,426 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R2872:Zfp292
|
UTSW |
4 |
34,808,595 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2872:Zfp292
|
UTSW |
4 |
34,808,595 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3018:Zfp292
|
UTSW |
4 |
34,808,814 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3812:Zfp292
|
UTSW |
4 |
34,810,326 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4006:Zfp292
|
UTSW |
4 |
34,807,744 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4006:Zfp292
|
UTSW |
4 |
34,809,611 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R4060:Zfp292
|
UTSW |
4 |
34,810,863 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4062:Zfp292
|
UTSW |
4 |
34,810,863 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4063:Zfp292
|
UTSW |
4 |
34,810,863 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4064:Zfp292
|
UTSW |
4 |
34,810,863 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4207:Zfp292
|
UTSW |
4 |
34,806,079 (GRCm39) |
missense |
probably benign |
0.04 |
|
R4641:Zfp292
|
UTSW |
4 |
34,807,828 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4684:Zfp292
|
UTSW |
4 |
34,807,078 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4718:Zfp292
|
UTSW |
4 |
34,819,521 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R4865:Zfp292
|
UTSW |
4 |
34,819,563 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4870:Zfp292
|
UTSW |
4 |
34,808,917 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5097:Zfp292
|
UTSW |
4 |
34,839,878 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R5233:Zfp292
|
UTSW |
4 |
34,809,755 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5246:Zfp292
|
UTSW |
4 |
34,805,842 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R5369:Zfp292
|
UTSW |
4 |
34,807,491 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R5527:Zfp292
|
UTSW |
4 |
34,806,261 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5621:Zfp292
|
UTSW |
4 |
34,811,703 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5770:Zfp292
|
UTSW |
4 |
34,806,747 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5900:Zfp292
|
UTSW |
4 |
34,805,125 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5905:Zfp292
|
UTSW |
4 |
34,819,549 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5994:Zfp292
|
UTSW |
4 |
34,805,464 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R6028:Zfp292
|
UTSW |
4 |
34,819,549 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6056:Zfp292
|
UTSW |
4 |
34,809,784 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6093:Zfp292
|
UTSW |
4 |
34,811,902 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6126:Zfp292
|
UTSW |
4 |
34,808,497 (GRCm39) |
missense |
probably benign |
0.13 |
|
R6209:Zfp292
|
UTSW |
4 |
34,809,442 (GRCm39) |
missense |
probably benign |
0.14 |
|
R6275:Zfp292
|
UTSW |
4 |
34,808,883 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6523:Zfp292
|
UTSW |
4 |
34,816,301 (GRCm39) |
missense |
probably benign |
0.21 |
|
R6747:Zfp292
|
UTSW |
4 |
34,806,894 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6752:Zfp292
|
UTSW |
4 |
34,808,593 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R6967:Zfp292
|
UTSW |
4 |
34,807,812 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7038:Zfp292
|
UTSW |
4 |
34,816,357 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7056:Zfp292
|
UTSW |
4 |
34,809,784 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7088:Zfp292
|
UTSW |
4 |
34,806,796 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7158:Zfp292
|
UTSW |
4 |
34,808,679 (GRCm39) |
missense |
probably benign |
|
|
R7254:Zfp292
|
UTSW |
4 |
34,819,476 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7350:Zfp292
|
UTSW |
4 |
34,806,839 (GRCm39) |
missense |
probably benign |
|
|
R7378:Zfp292
|
UTSW |
4 |
34,808,384 (GRCm39) |
missense |
probably benign |
0.26 |
|
R7535:Zfp292
|
UTSW |
4 |
34,811,487 (GRCm39) |
missense |
probably benign |
0.28 |
|
R7589:Zfp292
|
UTSW |
4 |
34,806,777 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7816:Zfp292
|
UTSW |
4 |
34,809,865 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7979:Zfp292
|
UTSW |
4 |
34,809,198 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7997:Zfp292
|
UTSW |
4 |
34,808,688 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8129:Zfp292
|
UTSW |
4 |
34,807,386 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8211:Zfp292
|
UTSW |
4 |
34,806,163 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8302:Zfp292
|
UTSW |
4 |
34,810,893 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R8500:Zfp292
|
UTSW |
4 |
34,826,691 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8709:Zfp292
|
UTSW |
4 |
34,805,982 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9099:Zfp292
|
UTSW |
4 |
34,809,228 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R9190:Zfp292
|
UTSW |
4 |
34,819,563 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9256:Zfp292
|
UTSW |
4 |
34,839,899 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9371:Zfp292
|
UTSW |
4 |
34,810,800 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9492:Zfp292
|
UTSW |
4 |
34,810,794 (GRCm39) |
missense |
probably benign |
0.12 |
|
R9574:Zfp292
|
UTSW |
4 |
34,839,460 (GRCm39) |
missense |
probably damaging |
1.00 |
|
V7580:Zfp292
|
UTSW |
4 |
34,806,783 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
V7581:Zfp292
|
UTSW |
4 |
34,806,783 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
V7582:Zfp292
|
UTSW |
4 |
34,806,783 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
V7583:Zfp292
|
UTSW |
4 |
34,806,783 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
Z1177:Zfp292
|
UTSW |
4 |
34,811,058 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- AATTGAGGACACAATAGACGCCTC -3'
(R):5'- TGTTTCACAGACTGAAGGGG -3'
Sequencing Primer
(F):5'- AATAGACGCCTCTTCTCCCATGAG -3'
(R):5'- GGACTCGCTACCTGCATAGAATTATG -3'
|
| Posted On |
2021-08-31 |
Incidental Mutation