Incidental Mutation 'R1936:Zfp292'
ID |
215781 |
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 |
039954-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.843)
|
Stock # |
R1936 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
4 |
Chromosomal Location |
34803113-34882960 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 34807452 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Alanine
at position 1864
(V1864A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000095766
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000047950]
[ENSMUST00000098163]
|
AlphaFold |
Q9Z2U2 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000047950
AA Change: V1869A
PolyPhen 2
Score 0.143 (Sensitivity: 0.92; Specificity: 0.86)
|
SMART Domains |
Protein: ENSMUSP00000037233 Gene: ENSMUSG00000039967 AA Change: V1869A
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 benign
Transcript: ENSMUST00000098163
AA Change: V1864A
PolyPhen 2
Score 0.224 (Sensitivity: 0.91; Specificity: 0.88)
|
SMART Domains |
Protein: ENSMUSP00000095766 Gene: ENSMUSG00000039967 AA Change: V1864A
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 |
0.0898 |
Coding Region Coverage |
- 1x: 97.5%
- 3x: 97.0%
- 10x: 95.7%
- 20x: 93.5%
|
Validation Efficiency |
99% (98/99) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930590J08Rik |
A |
G |
6: 91,894,061 (GRCm39) |
Q226R |
possibly damaging |
Het |
Abca13 |
G |
A |
11: 9,243,595 (GRCm39) |
M1819I |
probably benign |
Het |
Abca4 |
G |
A |
3: 121,846,572 (GRCm39) |
V30M |
probably benign |
Het |
Ablim1 |
T |
A |
19: 57,204,397 (GRCm39) |
|
probably null |
Het |
Adgrf3 |
A |
T |
5: 30,407,304 (GRCm39) |
N207K |
probably benign |
Het |
Anapc4 |
T |
A |
5: 52,997,010 (GRCm39) |
D94E |
probably damaging |
Het |
Arfgef2 |
A |
G |
2: 166,705,523 (GRCm39) |
N918S |
probably benign |
Het |
Arhgap45 |
A |
G |
10: 79,866,788 (GRCm39) |
N1097S |
probably damaging |
Het |
Atp8a2 |
T |
C |
14: 60,097,719 (GRCm39) |
K770E |
probably benign |
Het |
AU016765 |
G |
A |
17: 64,826,873 (GRCm39) |
|
noncoding transcript |
Het |
Brd10 |
A |
G |
19: 29,731,077 (GRCm39) |
F712S |
possibly damaging |
Het |
Cacna2d2 |
T |
C |
9: 107,386,455 (GRCm39) |
F194S |
probably damaging |
Het |
Cacna2d4 |
A |
G |
6: 119,247,722 (GRCm39) |
D341G |
possibly damaging |
Het |
Cdc42bpg |
A |
G |
19: 6,360,339 (GRCm39) |
Y175C |
probably damaging |
Het |
Cep170b |
G |
T |
12: 112,702,172 (GRCm39) |
D322Y |
probably damaging |
Het |
Cflar |
T |
A |
1: 58,791,784 (GRCm39) |
Y362* |
probably null |
Het |
Chml |
A |
T |
1: 175,514,825 (GRCm39) |
C365* |
probably null |
Het |
Clrn3 |
A |
C |
7: 135,115,753 (GRCm39) |
I199S |
possibly damaging |
Het |
Crtam |
G |
C |
9: 40,915,846 (GRCm39) |
P13A |
probably benign |
Het |
Defb26 |
T |
A |
2: 152,350,195 (GRCm39) |
K28N |
possibly damaging |
Het |
Dennd1c |
G |
A |
17: 57,380,889 (GRCm39) |
|
probably benign |
Het |
Dgkz |
A |
T |
2: 91,768,323 (GRCm39) |
M761K |
possibly damaging |
Het |
Dnhd1 |
A |
T |
7: 105,323,183 (GRCm39) |
M564L |
probably benign |
Het |
Dusp15 |
A |
G |
2: 152,787,341 (GRCm39) |
|
probably benign |
Het |
Dync2h1 |
A |
G |
9: 7,139,159 (GRCm39) |
|
probably null |
Het |
Eapp |
A |
T |
12: 54,720,513 (GRCm39) |
M234K |
probably benign |
Het |
Epha8 |
T |
C |
4: 136,667,554 (GRCm39) |
D309G |
probably benign |
Het |
Gfi1b |
T |
C |
2: 28,500,125 (GRCm39) |
K302R |
possibly damaging |
Het |
Gimap3 |
A |
T |
6: 48,742,683 (GRCm39) |
F82L |
probably damaging |
Het |
Gm4862 |
T |
C |
3: 138,834,253 (GRCm39) |
|
noncoding transcript |
Het |
Gpatch1 |
A |
G |
7: 34,994,947 (GRCm39) |
S440P |
probably damaging |
Het |
Gpr152 |
A |
G |
19: 4,192,531 (GRCm39) |
D24G |
probably damaging |
Het |
Gpr6 |
T |
C |
10: 40,947,477 (GRCm39) |
E35G |
probably benign |
Het |
Hip1r |
T |
A |
5: 124,134,134 (GRCm39) |
M270K |
probably damaging |
Het |
Hk3 |
C |
T |
13: 55,159,204 (GRCm39) |
V451I |
probably damaging |
Het |
Itprid1 |
G |
T |
6: 55,874,666 (GRCm39) |
L205F |
probably damaging |
Het |
Jag1 |
C |
G |
2: 136,925,393 (GRCm39) |
V1070L |
possibly damaging |
Het |
Klf16 |
G |
A |
10: 80,412,739 (GRCm39) |
A99V |
probably benign |
Het |
Lama5 |
T |
C |
2: 179,832,714 (GRCm39) |
N1646S |
probably benign |
Het |
Lvrn |
A |
T |
18: 47,011,387 (GRCm39) |
Y448F |
probably benign |
Het |
Mark3 |
A |
G |
12: 111,584,799 (GRCm39) |
M132V |
probably damaging |
Het |
Mast3 |
A |
G |
8: 71,237,444 (GRCm39) |
Y577H |
probably damaging |
Het |
Med24 |
A |
T |
11: 98,609,642 (GRCm39) |
|
probably null |
Het |
Mif |
G |
T |
10: 75,695,681 (GRCm39) |
H41N |
possibly damaging |
Het |
Myo18b |
T |
C |
5: 112,908,222 (GRCm39) |
N2017S |
probably benign |
Het |
Neurl4 |
C |
T |
11: 69,797,959 (GRCm39) |
R740C |
probably damaging |
Het |
Nlgn1 |
G |
T |
3: 26,385,939 (GRCm39) |
|
probably benign |
Het |
Or10ad1c |
T |
A |
15: 98,085,462 (GRCm39) |
H72L |
probably benign |
Het |
Or2ak6 |
T |
A |
11: 58,593,172 (GRCm39) |
L215Q |
probably damaging |
Het |
Or5t15 |
A |
G |
2: 86,681,745 (GRCm39) |
M99T |
probably benign |
Het |
Or8b12i |
A |
G |
9: 20,082,477 (GRCm39) |
L130P |
probably damaging |
Het |
Paip1 |
T |
A |
13: 119,593,550 (GRCm39) |
M463K |
probably damaging |
Het |
Parp3 |
T |
A |
9: 106,351,931 (GRCm39) |
Y147F |
probably damaging |
Het |
Pgrmc2 |
C |
A |
3: 41,037,473 (GRCm39) |
|
probably benign |
Het |
Phldb3 |
G |
A |
7: 24,316,832 (GRCm39) |
A278T |
probably benign |
Het |
Plxnb1 |
T |
C |
9: 108,924,715 (GRCm39) |
|
probably null |
Het |
Pphln1 |
A |
G |
15: 93,386,868 (GRCm39) |
D234G |
possibly damaging |
Het |
Prdm2 |
T |
C |
4: 142,861,032 (GRCm39) |
S753G |
probably benign |
Het |
Prss32 |
A |
G |
17: 24,075,024 (GRCm39) |
R125G |
possibly damaging |
Het |
Psg22 |
A |
T |
7: 18,453,635 (GRCm39) |
N149I |
probably damaging |
Het |
Psmd11 |
T |
C |
11: 80,319,570 (GRCm39) |
L20P |
probably damaging |
Het |
Recql5 |
T |
C |
11: 115,788,017 (GRCm39) |
Y434C |
probably benign |
Het |
Rexo1 |
A |
G |
10: 80,386,303 (GRCm39) |
S252P |
probably benign |
Het |
Sdr9c7 |
A |
G |
10: 127,739,503 (GRCm39) |
K206R |
probably benign |
Het |
Slc17a8 |
T |
C |
10: 89,413,777 (GRCm39) |
M484V |
probably benign |
Het |
Slc1a2 |
A |
G |
2: 102,607,950 (GRCm39) |
N530D |
probably benign |
Het |
Slc25a14 |
G |
A |
X: 47,740,840 (GRCm39) |
V210I |
probably benign |
Het |
Slc25a24 |
A |
T |
3: 109,043,581 (GRCm39) |
E79D |
probably damaging |
Het |
Smchd1 |
T |
C |
17: 71,770,786 (GRCm39) |
Y132C |
probably damaging |
Het |
Sorcs1 |
T |
C |
19: 50,221,082 (GRCm39) |
D545G |
probably damaging |
Het |
Sorcs2 |
A |
G |
5: 36,228,731 (GRCm39) |
S104P |
possibly damaging |
Het |
Speg |
C |
T |
1: 75,408,052 (GRCm39) |
T3249I |
possibly damaging |
Het |
Spry4 |
A |
G |
18: 38,723,142 (GRCm39) |
I207T |
possibly damaging |
Het |
Srsf6 |
C |
T |
2: 162,776,403 (GRCm39) |
|
probably benign |
Het |
Tdrd6 |
A |
G |
17: 43,937,358 (GRCm39) |
L1230P |
probably damaging |
Het |
Tesk2 |
A |
G |
4: 116,599,021 (GRCm39) |
Y43C |
probably benign |
Het |
Tex101 |
A |
G |
7: 24,367,650 (GRCm39) |
V234A |
probably benign |
Het |
Tmem161b |
T |
A |
13: 84,441,585 (GRCm39) |
L210Q |
probably damaging |
Het |
Tmprss11f |
T |
A |
5: 86,692,723 (GRCm39) |
Q67L |
probably benign |
Het |
Tnfrsf23 |
A |
G |
7: 143,222,291 (GRCm39) |
F174L |
probably benign |
Het |
Tnrc6c |
A |
G |
11: 117,646,849 (GRCm39) |
D1450G |
possibly damaging |
Het |
Trdmt1 |
A |
G |
2: 13,516,420 (GRCm39) |
L386P |
probably damaging |
Het |
Trim25 |
A |
T |
11: 88,895,576 (GRCm39) |
T206S |
probably benign |
Het |
Trit1 |
T |
C |
4: 122,948,033 (GRCm39) |
I451T |
probably benign |
Het |
Trpc4 |
T |
A |
3: 54,187,311 (GRCm39) |
M421K |
probably damaging |
Het |
Ttc34 |
G |
A |
4: 154,950,139 (GRCm39) |
A1031T |
possibly damaging |
Het |
Ttn |
A |
C |
2: 76,715,834 (GRCm39) |
|
probably benign |
Het |
Ttn |
T |
A |
2: 76,577,522 (GRCm39) |
D24457V |
probably damaging |
Het |
Ubiad1 |
A |
G |
4: 148,528,468 (GRCm39) |
L147P |
probably damaging |
Het |
Vmn2r94 |
G |
A |
17: 18,464,554 (GRCm39) |
R579* |
probably null |
Het |
Vps72 |
T |
A |
3: 95,029,851 (GRCm39) |
V290D |
probably benign |
Het |
Wipf2 |
C |
T |
11: 98,783,236 (GRCm39) |
R221* |
probably null |
Het |
Zfp26 |
A |
G |
9: 20,348,849 (GRCm39) |
Y572H |
probably benign |
Het |
Zfp952 |
A |
T |
17: 33,222,643 (GRCm39) |
H374L |
possibly damaging |
Het |
Zfy2 |
C |
A |
Y: 2,121,496 (GRCm39) |
M132I |
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 |
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 |
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'- GTGTGCCCGGAGATTAGAATTTC -3'
(R):5'- TGTAATGCCAACAAAGTCTGAAGC -3'
Sequencing Primer
(F):5'- GAAGGTACTACACATTTAAATGGAGC -3'
(R):5'- TCTGAAGCATTACATAAGGAGGATC -3'
|
Posted On |
2014-07-14 |