Incidental Mutation 'R7027:Zfp804b'
| ID |
546032 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Zfp804b
|
| Ensembl Gene |
ENSMUSG00000092094 |
| Gene Name |
zinc finger protein 804B |
| Synonyms |
LOC207618 |
| MMRRC Submission |
045128-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.113)
|
| Stock # |
R7027 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
5 |
| Chromosomal Location |
6819030-7394378 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 6820372 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Asparagine
at position 897
(S897N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000143568
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000164784]
[ENSMUST00000200317]
|
| AlphaFold |
A0A0G2JGH6 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000164784
AA Change: S861N
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000130571
Gene: ENSMUSG00000092094
AA Change: S861N
| Domain | Start | End | E-Value | Type |
|---|
|
ZnF_C2H2
|
20 |
44 |
4.81e0 |
SMART |
|
low complexity region
|
922 |
934 |
N/A |
INTRINSIC |
|
low complexity region
|
1119 |
1143 |
N/A |
INTRINSIC |
|
low complexity region
|
1160 |
1171 |
N/A |
INTRINSIC |
|
low complexity region
|
1179 |
1198 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000200317
AA Change: S897N
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000143568
Gene: ENSMUSG00000092094
AA Change: S897N
| Domain | Start | End | E-Value | Type |
|---|
|
ZnF_C2H2
|
56 |
80 |
2e-2 |
SMART |
|
low complexity region
|
958 |
970 |
N/A |
INTRINSIC |
|
low complexity region
|
1155 |
1179 |
N/A |
INTRINSIC |
|
low complexity region
|
1196 |
1207 |
N/A |
INTRINSIC |
|
low complexity region
|
1215 |
1234 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.2%
|
| Validation Efficiency |
98% (85/87) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 88 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acoxl |
A |
T |
2: 127,852,003 (GRCm39) |
M102L |
probably benign |
Het |
| Adcy10 |
A |
G |
1: 165,345,815 (GRCm39) |
E288G |
probably damaging |
Het |
| Agap1 |
A |
G |
1: 89,816,444 (GRCm39) |
H748R |
probably benign |
Het |
| Ahsg |
T |
C |
16: 22,711,007 (GRCm39) |
L48P |
probably damaging |
Het |
| Ankrd27 |
A |
G |
7: 35,311,951 (GRCm39) |
T394A |
probably benign |
Het |
| Apc |
T |
G |
18: 34,445,129 (GRCm39) |
V657G |
probably damaging |
Het |
| Arl2 |
T |
C |
19: 6,191,119 (GRCm39) |
T5A |
probably benign |
Het |
| B020011L13Rik |
A |
G |
1: 117,729,180 (GRCm39) |
Y229C |
probably benign |
Het |
| B3gnt5 |
T |
A |
16: 19,588,740 (GRCm39) |
S320T |
probably damaging |
Het |
| Bach1 |
G |
A |
16: 87,516,179 (GRCm39) |
R240Q |
probably benign |
Het |
| BC107364 |
T |
G |
3: 96,348,057 (GRCm39) |
R77S |
unknown |
Het |
| Brox |
G |
A |
1: 183,065,750 (GRCm39) |
P206L |
possibly damaging |
Het |
| Ccrl2 |
T |
C |
9: 110,884,953 (GRCm39) |
K182E |
probably benign |
Het |
| Cd19 |
A |
G |
7: 126,009,671 (GRCm39) |
V465A |
possibly damaging |
Het |
| Chrdl2 |
A |
T |
7: 99,671,240 (GRCm39) |
Q126H |
probably damaging |
Het |
| Cnbd1 |
G |
A |
4: 18,862,063 (GRCm39) |
P376S |
probably benign |
Het |
| Cobll1 |
A |
G |
2: 64,919,847 (GRCm39) |
S1194P |
probably benign |
Het |
| Col6a4 |
T |
C |
9: 105,944,213 (GRCm39) |
Y1087C |
probably damaging |
Het |
| Col9a2 |
G |
A |
4: 120,901,216 (GRCm39) |
|
probably null |
Het |
| Cyp4v3 |
A |
G |
8: 45,763,289 (GRCm39) |
S341P |
possibly damaging |
Het |
| Dnah7a |
T |
A |
1: 53,670,665 (GRCm39) |
Y529F |
probably benign |
Het |
| Eif3b |
C |
T |
5: 140,411,043 (GRCm39) |
R165W |
probably damaging |
Het |
| Erlec1 |
C |
A |
11: 30,900,790 (GRCm39) |
C126F |
probably damaging |
Het |
| Fads2b |
A |
G |
2: 85,315,871 (GRCm39) |
Y440H |
probably damaging |
Het |
| Fat2 |
T |
C |
11: 55,160,259 (GRCm39) |
T3285A |
probably benign |
Het |
| Fat2 |
G |
A |
11: 55,172,677 (GRCm39) |
R2679* |
probably null |
Het |
| Fbxo31 |
T |
C |
8: 122,305,224 (GRCm39) |
T91A |
probably damaging |
Het |
| Fkbp5 |
A |
G |
17: 28,631,037 (GRCm39) |
Y243H |
probably damaging |
Het |
| Flcn |
C |
T |
11: 59,686,632 (GRCm39) |
V374M |
probably damaging |
Het |
| Fndc5 |
A |
G |
4: 129,033,316 (GRCm39) |
M128V |
probably benign |
Het |
| Gal3st1 |
A |
G |
11: 3,949,002 (GRCm39) |
D403G |
probably damaging |
Het |
| Garem1 |
T |
C |
18: 21,263,051 (GRCm39) |
N588D |
probably benign |
Het |
| Gas1 |
T |
C |
13: 60,324,047 (GRCm39) |
T196A |
probably damaging |
Het |
| Gcn1 |
T |
C |
5: 115,754,605 (GRCm39) |
|
probably null |
Het |
| Gprc5d |
T |
G |
6: 135,093,646 (GRCm39) |
Q87P |
probably damaging |
Het |
| Grm1 |
A |
G |
10: 10,595,339 (GRCm39) |
L763P |
probably damaging |
Het |
| Hivep2 |
G |
T |
10: 14,025,321 (GRCm39) |
K2378N |
probably damaging |
Het |
| Hivep2 |
G |
T |
10: 14,025,322 (GRCm39) |
D2379Y |
probably damaging |
Het |
| Itgad |
A |
G |
7: 127,782,161 (GRCm39) |
Y199C |
probably damaging |
Het |
| Itm2c |
A |
G |
1: 85,834,206 (GRCm39) |
I174V |
probably benign |
Het |
| Khdrbs2 |
A |
G |
1: 32,453,997 (GRCm39) |
S128G |
probably benign |
Het |
| Map3k9 |
T |
C |
12: 81,777,398 (GRCm39) |
T528A |
probably benign |
Het |
| Mmp11 |
G |
A |
10: 75,768,230 (GRCm39) |
|
probably benign |
Het |
| Mycbpap |
T |
A |
11: 94,405,440 (GRCm39) |
I30F |
probably damaging |
Het |
| Nfya |
T |
C |
17: 48,696,340 (GRCm39) |
T335A |
probably benign |
Het |
| Npat |
T |
A |
9: 53,481,216 (GRCm39) |
S1008T |
possibly damaging |
Het |
| Or10al5 |
G |
A |
17: 38,063,300 (GRCm39) |
C185Y |
probably damaging |
Het |
| Or12e10 |
A |
G |
2: 87,641,060 (GRCm39) |
T299A |
possibly damaging |
Het |
| Or5p69 |
A |
T |
7: 107,967,557 (GRCm39) |
M287L |
probably damaging |
Het |
| Or6c219 |
C |
T |
10: 129,781,041 (GRCm39) |
A297T |
possibly damaging |
Het |
| Osbpl10 |
T |
C |
9: 115,052,766 (GRCm39) |
V613A |
probably damaging |
Het |
| Pcdhga8 |
T |
C |
18: 37,860,164 (GRCm39) |
W407R |
probably benign |
Het |
| Pcdhgb4 |
A |
G |
18: 37,854,415 (GRCm39) |
D270G |
probably damaging |
Het |
| Pde2a |
A |
C |
7: 101,160,804 (GRCm39) |
E918D |
probably damaging |
Het |
| Plekhg5 |
A |
G |
4: 152,198,431 (GRCm39) |
D873G |
probably benign |
Het |
| Pno1 |
A |
T |
11: 17,158,880 (GRCm39) |
S173T |
possibly damaging |
Het |
| Ppfia3 |
A |
G |
7: 45,004,160 (GRCm39) |
I494T |
possibly damaging |
Het |
| Prkrip1 |
C |
A |
5: 136,210,267 (GRCm39) |
|
probably benign |
Het |
| Psma5 |
A |
G |
3: 108,172,484 (GRCm39) |
I67V |
probably benign |
Het |
| Reep6 |
G |
A |
10: 80,169,799 (GRCm39) |
|
probably null |
Het |
| Rtl1 |
CTCTTCTTCTTCACCATCTTCCTCCTCCTCCCCTTCTTCTTCTTCACCATCTTCCTCCTCCTCCCCTTCTTCTTCTTCACCATCTTCCTCCTCCTC |
CTCTTCTTCTTCACCATCTTCCTCCTCCTCCCCTTCTTCTTCTTCACCATCTTCCTCCTCCTC |
12: 109,557,848 (GRCm39) |
|
probably benign |
Het |
| Scyl2 |
C |
G |
10: 89,481,323 (GRCm39) |
|
probably null |
Het |
| Sdk1 |
T |
A |
5: 142,082,481 (GRCm39) |
|
probably null |
Het |
| Senp5 |
C |
A |
16: 31,808,113 (GRCm39) |
K380N |
probably benign |
Het |
| Slc22a14 |
A |
T |
9: 119,060,281 (GRCm39) |
|
probably null |
Het |
| Slc26a5 |
T |
A |
5: 22,021,972 (GRCm39) |
T485S |
possibly damaging |
Het |
| Slc44a5 |
T |
C |
3: 153,959,356 (GRCm39) |
I349T |
probably benign |
Het |
| Smarca5 |
T |
C |
8: 81,463,355 (GRCm39) |
E71G |
probably benign |
Het |
| Smok2a |
A |
T |
17: 13,444,666 (GRCm39) |
H81L |
probably damaging |
Het |
| Snrnp200 |
A |
G |
2: 127,059,192 (GRCm39) |
D388G |
probably benign |
Het |
| Tank |
T |
C |
2: 61,483,766 (GRCm39) |
V404A |
probably benign |
Het |
| Tek |
A |
G |
4: 94,753,747 (GRCm39) |
D1063G |
probably damaging |
Het |
| Tfap2a |
C |
T |
13: 40,887,150 (GRCm39) |
C16Y |
probably benign |
Het |
| Tmc1 |
A |
G |
19: 20,918,267 (GRCm39) |
|
probably null |
Het |
| Tnc |
A |
G |
4: 63,902,826 (GRCm39) |
F1484L |
probably benign |
Het |
| Tnfsf13 |
T |
A |
11: 69,575,958 (GRCm39) |
|
probably null |
Het |
| Tnrc6c |
T |
A |
11: 117,624,444 (GRCm39) |
S919T |
probably damaging |
Het |
| Trim17 |
C |
A |
11: 58,859,442 (GRCm39) |
Q219K |
probably benign |
Het |
| Trim5 |
T |
A |
7: 103,914,875 (GRCm39) |
H389L |
probably benign |
Het |
| Trio |
T |
A |
15: 27,805,740 (GRCm39) |
M583L |
possibly damaging |
Het |
| Ttll10 |
A |
T |
4: 156,120,258 (GRCm39) |
H389Q |
possibly damaging |
Het |
| Usp24 |
T |
C |
4: 106,219,441 (GRCm39) |
S546P |
probably benign |
Het |
| Vmn1r19 |
T |
A |
6: 57,381,475 (GRCm39) |
Y9* |
probably null |
Het |
| Vmn2r50 |
T |
A |
7: 9,781,539 (GRCm39) |
D402V |
probably damaging |
Het |
| Vmn2r93 |
C |
A |
17: 18,533,548 (GRCm39) |
A484E |
probably benign |
Het |
| Vps13a |
T |
C |
19: 16,642,028 (GRCm39) |
T2200A |
probably benign |
Het |
| Wdr36 |
T |
A |
18: 32,974,958 (GRCm39) |
H103Q |
probably benign |
Het |
| Zfp534 |
G |
A |
4: 147,759,667 (GRCm39) |
T334I |
possibly damaging |
Het |
|
| Other mutations in Zfp804b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01085:Zfp804b
|
APN |
5 |
6,820,931 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01726:Zfp804b
|
APN |
5 |
7,230,707 (GRCm39) |
intron |
probably benign |
|
|
IGL02020:Zfp804b
|
APN |
5 |
6,819,118 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02567:Zfp804b
|
APN |
5 |
6,819,989 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL02679:Zfp804b
|
APN |
5 |
6,821,392 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
IGL03245:Zfp804b
|
APN |
5 |
6,822,253 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
IGL03352:Zfp804b
|
APN |
5 |
6,820,039 (GRCm39) |
missense |
probably benign |
0.45 |
|
Flush
|
UTSW |
5 |
6,820,217 (GRCm39) |
missense |
probably benign |
0.27 |
|
gozinta
|
UTSW |
5 |
6,820,153 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
healthy
|
UTSW |
5 |
6,820,013 (GRCm39) |
missense |
probably benign |
0.04 |
|
Paluka
|
UTSW |
5 |
6,820,534 (GRCm39) |
missense |
probably benign |
|
|
PIT4142001:Zfp804b
|
UTSW |
5 |
6,819,422 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0025:Zfp804b
|
UTSW |
5 |
6,821,665 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0044:Zfp804b
|
UTSW |
5 |
6,819,655 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0137:Zfp804b
|
UTSW |
5 |
6,820,534 (GRCm39) |
missense |
probably benign |
|
|
R0330:Zfp804b
|
UTSW |
5 |
6,821,994 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R0330:Zfp804b
|
UTSW |
5 |
6,821,029 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R0522:Zfp804b
|
UTSW |
5 |
6,822,014 (GRCm39) |
missense |
probably benign |
0.05 |
|
R1463:Zfp804b
|
UTSW |
5 |
7,229,372 (GRCm39) |
intron |
probably benign |
|
|
R1497:Zfp804b
|
UTSW |
5 |
6,821,105 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R1511:Zfp804b
|
UTSW |
5 |
6,819,771 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R1633:Zfp804b
|
UTSW |
5 |
7,229,513 (GRCm39) |
intron |
probably benign |
|
|
R1666:Zfp804b
|
UTSW |
5 |
6,821,323 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R1668:Zfp804b
|
UTSW |
5 |
6,821,323 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R1677:Zfp804b
|
UTSW |
5 |
7,229,533 (GRCm39) |
intron |
probably benign |
|
|
R1698:Zfp804b
|
UTSW |
5 |
6,819,509 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1716:Zfp804b
|
UTSW |
5 |
6,819,673 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1730:Zfp804b
|
UTSW |
5 |
6,821,938 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1747:Zfp804b
|
UTSW |
5 |
6,820,217 (GRCm39) |
missense |
probably benign |
0.27 |
|
R1776:Zfp804b
|
UTSW |
5 |
6,819,806 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1783:Zfp804b
|
UTSW |
5 |
6,821,938 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1804:Zfp804b
|
UTSW |
5 |
6,821,756 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R1885:Zfp804b
|
UTSW |
5 |
6,820,376 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R1887:Zfp804b
|
UTSW |
5 |
6,820,376 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R1900:Zfp804b
|
UTSW |
5 |
6,819,283 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1929:Zfp804b
|
UTSW |
5 |
6,819,748 (GRCm39) |
missense |
probably benign |
0.05 |
|
R2141:Zfp804b
|
UTSW |
5 |
6,822,583 (GRCm39) |
missense |
probably benign |
0.11 |
|
R2181:Zfp804b
|
UTSW |
5 |
6,821,674 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2401:Zfp804b
|
UTSW |
5 |
6,819,445 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2408:Zfp804b
|
UTSW |
5 |
7,229,410 (GRCm39) |
intron |
probably benign |
|
|
R3237:Zfp804b
|
UTSW |
5 |
6,819,239 (GRCm39) |
missense |
probably benign |
|
|
R3429:Zfp804b
|
UTSW |
5 |
7,230,625 (GRCm39) |
intron |
probably benign |
|
|
R3785:Zfp804b
|
UTSW |
5 |
6,820,153 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R4459:Zfp804b
|
UTSW |
5 |
6,821,481 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4460:Zfp804b
|
UTSW |
5 |
6,821,481 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4608:Zfp804b
|
UTSW |
5 |
6,822,584 (GRCm39) |
missense |
probably benign |
0.04 |
|
R4762:Zfp804b
|
UTSW |
5 |
6,822,250 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4871:Zfp804b
|
UTSW |
5 |
6,926,479 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4910:Zfp804b
|
UTSW |
5 |
6,820,540 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R4973:Zfp804b
|
UTSW |
5 |
6,821,198 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5199:Zfp804b
|
UTSW |
5 |
6,820,013 (GRCm39) |
missense |
probably benign |
0.04 |
|
R5219:Zfp804b
|
UTSW |
5 |
6,820,703 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5411:Zfp804b
|
UTSW |
5 |
6,820,071 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6001:Zfp804b
|
UTSW |
5 |
6,819,043 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6041:Zfp804b
|
UTSW |
5 |
6,821,231 (GRCm39) |
missense |
probably benign |
0.08 |
|
R6151:Zfp804b
|
UTSW |
5 |
6,819,910 (GRCm39) |
missense |
probably benign |
|
|
R6252:Zfp804b
|
UTSW |
5 |
6,819,478 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6283:Zfp804b
|
UTSW |
5 |
6,819,908 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6346:Zfp804b
|
UTSW |
5 |
6,820,534 (GRCm39) |
missense |
probably benign |
|
|
R6520:Zfp804b
|
UTSW |
5 |
6,819,283 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6714:Zfp804b
|
UTSW |
5 |
6,819,239 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6924:Zfp804b
|
UTSW |
5 |
6,819,902 (GRCm39) |
missense |
probably benign |
0.09 |
|
R6966:Zfp804b
|
UTSW |
5 |
6,821,615 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7042:Zfp804b
|
UTSW |
5 |
6,820,042 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7076:Zfp804b
|
UTSW |
5 |
6,819,751 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7099:Zfp804b
|
UTSW |
5 |
6,822,161 (GRCm39) |
missense |
probably benign |
0.37 |
|
R7574:Zfp804b
|
UTSW |
5 |
6,822,301 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R7609:Zfp804b
|
UTSW |
5 |
6,820,066 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R7654:Zfp804b
|
UTSW |
5 |
6,819,458 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7669:Zfp804b
|
UTSW |
5 |
6,819,362 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7717:Zfp804b
|
UTSW |
5 |
6,821,293 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R7721:Zfp804b
|
UTSW |
5 |
6,821,263 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R7830:Zfp804b
|
UTSW |
5 |
6,821,124 (GRCm39) |
missense |
probably benign |
|
|
R7937:Zfp804b
|
UTSW |
5 |
6,821,866 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R7941:Zfp804b
|
UTSW |
5 |
6,820,042 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8093:Zfp804b
|
UTSW |
5 |
6,820,082 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8275:Zfp804b
|
UTSW |
5 |
6,822,289 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8714:Zfp804b
|
UTSW |
5 |
6,822,378 (GRCm39) |
nonsense |
probably null |
|
|
R8788:Zfp804b
|
UTSW |
5 |
6,822,635 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9206:Zfp804b
|
UTSW |
5 |
6,822,154 (GRCm39) |
missense |
probably benign |
0.37 |
|
R9223:Zfp804b
|
UTSW |
5 |
6,821,496 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9276:Zfp804b
|
UTSW |
5 |
6,821,398 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R9285:Zfp804b
|
UTSW |
5 |
6,820,723 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9534:Zfp804b
|
UTSW |
5 |
6,819,115 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0027:Zfp804b
|
UTSW |
5 |
6,821,257 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- CAATACCGTTCTCCTACAGCATG -3'
(R):5'- TAATGGCCAGGAATCTCAGCAC -3'
Sequencing Primer
(F):5'- TCCTACAGCATGGTGGTCC -3'
(R):5'- AGGAATCTCAGCACAACAAATTG -3'
|
| Posted On |
2019-05-13 |
Incidental Mutation