Incidental Mutation 'R0555:Zfp292'
| ID |
45447 |
| 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 |
038747-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.861)
|
| Stock # |
R0555 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
4 |
| Chromosomal Location |
34803113-34882960 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 34807194 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamic Acid to Glycine
at position 1950
(E1950G)
|
| 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: E1955G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000037233
Gene: ENSMUSG00000039967
AA Change: E1955G
| 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: E1950G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000095766
Gene: ENSMUSG00000039967
AA Change: E1950G
| 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 |
|
| Meta Mutation Damage Score |
0.3068 |
| Coding Region Coverage |
- 1x: 99.6%
- 3x: 98.8%
- 10x: 96.9%
- 20x: 93.8%
|
| Validation Efficiency |
100% (98/98) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 96 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam10 |
T |
A |
9: 70,661,516 (GRCm39) |
I363N |
probably damaging |
Het |
| Ahcyl2 |
T |
C |
6: 29,890,670 (GRCm39) |
|
probably benign |
Het |
| Asap1 |
A |
G |
15: 63,966,213 (GRCm39) |
L941P |
probably damaging |
Het |
| Aurka |
G |
A |
2: 172,209,067 (GRCm39) |
R23C |
probably benign |
Het |
| Cacna1c |
C |
T |
6: 118,589,586 (GRCm39) |
R1446H |
probably damaging |
Het |
| Casp8ap2 |
T |
A |
4: 32,640,381 (GRCm39) |
H478Q |
probably damaging |
Het |
| Clcn4 |
C |
T |
7: 7,293,503 (GRCm39) |
A418T |
possibly damaging |
Het |
| Cplx3 |
T |
C |
9: 57,521,384 (GRCm39) |
T193A |
probably benign |
Het |
| Cpxm2 |
A |
T |
7: 131,645,772 (GRCm39) |
Y715* |
probably null |
Het |
| Csmd1 |
T |
C |
8: 16,235,287 (GRCm39) |
M1179V |
probably benign |
Het |
| Ddx21 |
A |
T |
10: 62,423,307 (GRCm39) |
F632I |
probably damaging |
Het |
| Dnai1 |
C |
A |
4: 41,625,335 (GRCm39) |
T433K |
possibly damaging |
Het |
| Dpyd |
G |
A |
3: 119,225,191 (GRCm39) |
G988D |
probably damaging |
Het |
| Dync1i2 |
AAAAGAAGAGGAAAGAAGAGGAAAG |
AAAAGAAGAGGAAAG |
2: 71,044,862 (GRCm39) |
|
probably null |
Het |
| Dync1li2 |
A |
T |
8: 105,147,297 (GRCm39) |
S466T |
probably benign |
Het |
| Ears2 |
T |
C |
7: 121,647,667 (GRCm39) |
T206A |
probably benign |
Het |
| Elmod1 |
A |
T |
9: 53,838,876 (GRCm39) |
|
probably benign |
Het |
| Eps8l3 |
C |
A |
3: 107,799,661 (GRCm39) |
D590E |
probably benign |
Het |
| Etfdh |
A |
T |
3: 79,513,112 (GRCm39) |
H370Q |
probably benign |
Het |
| Fam83g |
C |
A |
11: 61,598,489 (GRCm39) |
A792E |
probably benign |
Het |
| Ffar3 |
G |
T |
7: 30,554,962 (GRCm39) |
Y119* |
probably null |
Het |
| Fosb |
G |
T |
7: 19,041,138 (GRCm39) |
S118R |
possibly damaging |
Het |
| Foxn4 |
G |
A |
5: 114,401,175 (GRCm39) |
L3F |
probably damaging |
Het |
| Foxo4 |
A |
G |
X: 100,298,784 (GRCm39) |
K65E |
probably damaging |
Het |
| Frem2 |
A |
G |
3: 53,424,281 (GRCm39) |
L3052P |
probably damaging |
Het |
| Fubp3 |
G |
A |
2: 31,498,149 (GRCm39) |
R101H |
probably damaging |
Het |
| Gba2 |
C |
A |
4: 43,569,927 (GRCm39) |
G429C |
probably damaging |
Het |
| Gimap1 |
T |
C |
6: 48,718,363 (GRCm39) |
|
probably benign |
Het |
| Gnas |
A |
G |
2: 174,140,304 (GRCm39) |
T158A |
possibly damaging |
Het |
| Gpc5 |
T |
C |
14: 115,789,740 (GRCm39) |
V538A |
probably damaging |
Het |
| Greb1l |
T |
C |
18: 10,458,781 (GRCm39) |
|
probably benign |
Het |
| H2-M10.5 |
G |
A |
17: 37,085,620 (GRCm39) |
G260R |
probably damaging |
Het |
| Hbs1l |
A |
C |
10: 21,225,222 (GRCm39) |
Q412H |
probably benign |
Het |
| Hecw1 |
G |
T |
13: 14,411,526 (GRCm39) |
T1058N |
probably damaging |
Het |
| Heph |
A |
T |
X: 95,601,690 (GRCm39) |
T1027S |
probably damaging |
Het |
| Hoga1 |
A |
C |
19: 42,034,514 (GRCm39) |
E53A |
possibly damaging |
Het |
| Insrr |
T |
G |
3: 87,721,744 (GRCm39) |
|
probably benign |
Het |
| Ipo11 |
A |
T |
13: 107,028,969 (GRCm39) |
V328D |
probably damaging |
Het |
| Jakmip1 |
T |
C |
5: 37,276,217 (GRCm39) |
V509A |
probably damaging |
Het |
| Jmjd1c |
T |
C |
10: 67,061,568 (GRCm39) |
V1307A |
probably benign |
Het |
| Kmt2a |
T |
A |
9: 44,758,868 (GRCm39) |
S1027C |
probably damaging |
Het |
| Kprp |
G |
C |
3: 92,731,664 (GRCm39) |
P462R |
unknown |
Het |
| Lrit3 |
A |
T |
3: 129,584,945 (GRCm39) |
V271D |
probably damaging |
Het |
| Map4 |
T |
A |
9: 109,808,171 (GRCm39) |
|
probably benign |
Het |
| Mark4 |
A |
C |
7: 19,182,598 (GRCm39) |
|
probably benign |
Het |
| Mfsd14b |
A |
G |
13: 65,226,259 (GRCm39) |
V142A |
probably benign |
Het |
| Mis18bp1 |
A |
T |
12: 65,208,227 (GRCm39) |
I162N |
possibly damaging |
Het |
| Mrpl43 |
A |
T |
19: 44,994,391 (GRCm39) |
|
probably benign |
Het |
| Mrpl47 |
A |
G |
3: 32,790,842 (GRCm39) |
F16S |
probably benign |
Het |
| Myh2 |
G |
T |
11: 67,069,793 (GRCm39) |
G380C |
probably damaging |
Het |
| Myo15a |
T |
C |
11: 60,412,464 (GRCm39) |
Y3284H |
probably damaging |
Het |
| Nectin2 |
A |
G |
7: 19,467,148 (GRCm39) |
|
probably benign |
Het |
| Neu3 |
A |
G |
7: 99,463,390 (GRCm39) |
V111A |
probably damaging |
Het |
| Nol4l |
T |
C |
2: 153,259,604 (GRCm39) |
|
probably null |
Het |
| Nphp3 |
C |
A |
9: 103,900,633 (GRCm39) |
H510Q |
probably damaging |
Het |
| Nprl3 |
T |
A |
11: 32,183,118 (GRCm39) |
|
probably null |
Het |
| Or14c39 |
A |
G |
7: 86,344,516 (GRCm39) |
N284S |
probably damaging |
Het |
| Or4c58 |
T |
C |
2: 89,674,787 (GRCm39) |
T177A |
probably benign |
Het |
| Or52ab7 |
T |
C |
7: 102,978,170 (GRCm39) |
V159A |
probably benign |
Het |
| Or6c2 |
T |
C |
10: 129,362,765 (GRCm39) |
I223T |
possibly damaging |
Het |
| Pex1 |
A |
G |
5: 3,656,130 (GRCm39) |
E319G |
possibly damaging |
Het |
| Pgap6 |
T |
C |
17: 26,336,088 (GRCm39) |
L130S |
probably benign |
Het |
| Phtf1 |
C |
A |
3: 103,911,785 (GRCm39) |
T709K |
probably damaging |
Het |
| Plek2 |
A |
T |
12: 78,938,946 (GRCm39) |
L271Q |
probably damaging |
Het |
| Plekhg5 |
T |
A |
4: 152,191,926 (GRCm39) |
C421* |
probably null |
Het |
| Polk |
A |
C |
13: 96,620,687 (GRCm39) |
C525W |
probably damaging |
Het |
| Ppfibp2 |
T |
C |
7: 107,328,381 (GRCm39) |
S471P |
probably damaging |
Het |
| Prickle2 |
A |
T |
6: 92,435,546 (GRCm39) |
F74L |
probably benign |
Het |
| Prl7d1 |
A |
T |
13: 27,896,038 (GRCm39) |
V113D |
probably benign |
Het |
| Prr14 |
C |
T |
7: 127,071,267 (GRCm39) |
|
probably benign |
Het |
| Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
| Ret |
A |
G |
6: 118,155,571 (GRCm39) |
V375A |
probably damaging |
Het |
| Rora |
T |
C |
9: 69,269,028 (GRCm39) |
F41S |
probably damaging |
Het |
| Sall1 |
T |
C |
8: 89,758,386 (GRCm39) |
T573A |
probably benign |
Het |
| Shb |
A |
G |
4: 45,458,321 (GRCm39) |
V281A |
possibly damaging |
Het |
| Slc25a26 |
A |
T |
6: 94,569,391 (GRCm39) |
|
probably null |
Het |
| Sltm |
T |
C |
9: 70,493,363 (GRCm39) |
F769L |
probably damaging |
Het |
| Snx9 |
T |
A |
17: 5,968,688 (GRCm39) |
M328K |
probably damaging |
Het |
| Stk25 |
G |
T |
1: 93,552,313 (GRCm39) |
Q356K |
probably benign |
Het |
| Svep1 |
T |
A |
4: 58,128,858 (GRCm39) |
Y613F |
possibly damaging |
Het |
| Syne4 |
G |
A |
7: 30,016,169 (GRCm39) |
A195T |
probably damaging |
Het |
| Tmem217b |
A |
T |
17: 29,738,545 (GRCm39) |
F74I |
probably benign |
Het |
| Trcg1 |
C |
T |
9: 57,149,616 (GRCm39) |
T396M |
probably damaging |
Het |
| Trim30b |
A |
G |
7: 104,006,505 (GRCm39) |
V117A |
possibly damaging |
Het |
| Trpc4 |
T |
C |
3: 54,209,511 (GRCm39) |
|
probably benign |
Het |
| Ttll4 |
A |
G |
1: 74,727,439 (GRCm39) |
H827R |
probably damaging |
Het |
| Tut7 |
A |
G |
13: 59,948,131 (GRCm39) |
V328A |
probably benign |
Het |
| Urgcp |
T |
C |
11: 5,667,477 (GRCm39) |
E287G |
probably damaging |
Het |
| Usp2 |
G |
T |
9: 44,004,081 (GRCm39) |
L319F |
probably damaging |
Het |
| Vmn1r167 |
A |
T |
7: 23,204,512 (GRCm39) |
V168D |
probably damaging |
Het |
| Vmn2r100 |
C |
A |
17: 19,742,382 (GRCm39) |
P252Q |
possibly damaging |
Het |
| Vmn2r61 |
A |
T |
7: 41,915,442 (GRCm39) |
I130F |
probably benign |
Het |
| Vmn2r63 |
A |
T |
7: 42,577,952 (GRCm39) |
Y195* |
probably null |
Het |
| Vmn2r81 |
T |
C |
10: 79,129,283 (GRCm39) |
S725P |
probably damaging |
Het |
| Wnt10b |
A |
G |
15: 98,670,818 (GRCm39) |
|
probably benign |
Het |
| Zfyve16 |
A |
G |
13: 92,653,028 (GRCm39) |
|
probably benign |
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 |
|
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 |
|
R8947:Zfp292
|
UTSW |
4 |
34,811,835 (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'- GCATTAGCAAGTGCAGCATCACC -3'
(R):5'- CCCTTTGTGTGTCAAAACCAAGGC -3'
Sequencing Primer
(F):5'- ATCACCTGTTGCTGCTGG -3'
(R):5'- GGCTGTAACTACAGTGCTATGAC -3'
|
| Posted On |
2013-06-11 |
Incidental Mutation