Incidental Mutation 'R7473:Znfx1'
| ID |
579248 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Znfx1
|
| Ensembl Gene |
ENSMUSG00000039501 |
| Gene Name |
zinc finger, NFX1-type containing 1 |
| Synonyms |
|
| MMRRC Submission |
045547-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R7473 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
2 |
| Chromosomal Location |
166877713-166904935 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 166880744 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Cysteine to Serine
at position 1211
(C1211S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000049404
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000018143]
[ENSMUST00000048988]
[ENSMUST00000067584]
|
| AlphaFold |
Q8R151 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000018143
|
| SMART Domains |
Protein: ENSMUSP00000018143
Gene: ENSMUSG00000017999
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
20 |
33 |
N/A |
INTRINSIC |
|
coiled coil region
|
78 |
106 |
N/A |
INTRINSIC |
|
low complexity region
|
133 |
148 |
N/A |
INTRINSIC |
|
low complexity region
|
157 |
166 |
N/A |
INTRINSIC |
|
DEXDc
|
203 |
404 |
2.24e-56 |
SMART |
|
HELICc
|
443 |
524 |
1.71e-29 |
SMART |
|
coiled coil region
|
577 |
613 |
N/A |
INTRINSIC |
|
low complexity region
|
622 |
629 |
N/A |
INTRINSIC |
|
low complexity region
|
644 |
657 |
N/A |
INTRINSIC |
|
low complexity region
|
679 |
692 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000048988
AA Change: C1211S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000049404
Gene: ENSMUSG00000039501
AA Change: C1211S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:AAA_11
|
590 |
855 |
2.2e-17 |
PFAM |
|
Pfam:AAA_19
|
597 |
684 |
1.7e-10 |
PFAM |
|
Pfam:AAA_11
|
829 |
1033 |
1.4e-18 |
PFAM |
|
Pfam:AAA_12
|
1044 |
1228 |
3.7e-42 |
PFAM |
|
internal_repeat_2
|
1281 |
1374 |
1.33e-7 |
PROSPERO |
|
internal_repeat_1
|
1292 |
1410 |
1.32e-16 |
PROSPERO |
|
low complexity region
|
1422 |
1433 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
1434 |
1547 |
1.32e-16 |
PROSPERO |
|
internal_repeat_2
|
1453 |
1555 |
1.33e-7 |
PROSPERO |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000067584
AA Change: C347S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000072867
Gene: ENSMUSG00000039501
AA Change: C347S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:AAA_11
|
8 |
170 |
1.2e-17 |
PFAM |
|
Pfam:AAA_12
|
180 |
364 |
7.4e-42 |
PFAM |
|
internal_repeat_2
|
417 |
510 |
1.08e-6 |
PROSPERO |
|
internal_repeat_1
|
428 |
546 |
1.81e-14 |
PROSPERO |
|
low complexity region
|
558 |
569 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
570 |
683 |
1.81e-14 |
PROSPERO |
|
internal_repeat_2
|
589 |
691 |
1.08e-6 |
PROSPERO |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
| Validation Efficiency |
96% (80/83) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 82 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4933434E20Rik |
T |
C |
3: 89,965,960 (GRCm39) |
|
probably null |
Het |
| A630095N17Rik |
G |
A |
1: 75,208,675 (GRCm39) |
T15I |
unknown |
Het |
| Actr1b |
A |
G |
1: 36,748,900 (GRCm39) |
V12A |
probably benign |
Het |
| Add1 |
A |
G |
5: 34,776,697 (GRCm39) |
T473A |
possibly damaging |
Het |
| Akap11 |
A |
T |
14: 78,751,328 (GRCm39) |
V353E |
|
Het |
| Alcam |
G |
A |
16: 52,272,882 (GRCm39) |
|
probably benign |
Het |
| Alpi |
A |
G |
1: 87,027,369 (GRCm39) |
|
probably null |
Het |
| Ap3s2 |
A |
G |
7: 79,565,779 (GRCm39) |
F49S |
probably damaging |
Het |
| Arpc1a |
A |
G |
5: 145,037,886 (GRCm39) |
K174E |
probably benign |
Het |
| Bbox1 |
A |
T |
2: 110,095,843 (GRCm39) |
S374T |
probably damaging |
Het |
| Bean1 |
CT |
C |
8: 104,908,664 (GRCm39) |
|
probably null |
Het |
| Bltp2 |
T |
C |
11: 78,157,941 (GRCm39) |
S368P |
possibly damaging |
Het |
| Bmp2k |
A |
G |
5: 97,204,871 (GRCm39) |
N402S |
probably benign |
Het |
| Bmper |
C |
A |
9: 23,286,926 (GRCm39) |
A284D |
probably benign |
Het |
| Bnip5 |
G |
A |
17: 29,124,298 (GRCm39) |
R335W |
probably damaging |
Het |
| Bpifb2 |
A |
T |
2: 153,723,116 (GRCm39) |
H124L |
possibly damaging |
Het |
| Bsn |
C |
T |
9: 107,989,449 (GRCm39) |
R2101Q |
probably damaging |
Het |
| Cacng1 |
T |
A |
11: 107,607,018 (GRCm39) |
D67V |
probably damaging |
Het |
| Catsperg1 |
A |
G |
7: 28,894,903 (GRCm39) |
S565P |
probably damaging |
Het |
| Cep126 |
C |
T |
9: 8,101,779 (GRCm39) |
E252K |
probably damaging |
Het |
| Cep55 |
G |
A |
19: 38,058,384 (GRCm39) |
E326K |
probably damaging |
Het |
| Cfap58 |
T |
A |
19: 47,963,064 (GRCm39) |
Y491* |
probably null |
Het |
| Cpeb2 |
T |
C |
5: 43,434,848 (GRCm39) |
S747P |
|
Het |
| Cryz |
T |
A |
3: 154,312,157 (GRCm39) |
S85T |
probably benign |
Het |
| D2hgdh |
T |
C |
1: 93,765,800 (GRCm39) |
V367A |
probably damaging |
Het |
| Dgkh |
T |
C |
14: 78,836,483 (GRCm39) |
N703S |
probably benign |
Het |
| Dnah11 |
T |
C |
12: 117,866,911 (GRCm39) |
S4077G |
probably benign |
Het |
| Dnah14 |
A |
G |
1: 181,579,704 (GRCm39) |
H3079R |
probably damaging |
Het |
| Dnah2 |
T |
A |
11: 69,382,484 (GRCm39) |
T1209S |
probably damaging |
Het |
| Dnmt3b |
A |
G |
2: 153,526,370 (GRCm39) |
D804G |
probably damaging |
Het |
| Ell2 |
A |
G |
13: 75,898,154 (GRCm39) |
E143G |
probably damaging |
Het |
| Exoc2 |
A |
G |
13: 31,006,613 (GRCm39) |
|
probably null |
Het |
| Fahd2a |
A |
T |
2: 127,282,376 (GRCm39) |
I131N |
probably damaging |
Het |
| Fer1l5 |
A |
G |
1: 36,460,689 (GRCm39) |
N1976D |
possibly damaging |
Het |
| Flt1 |
A |
G |
5: 147,531,405 (GRCm39) |
S853P |
probably damaging |
Het |
| Frg2f1 |
C |
T |
4: 119,387,990 (GRCm39) |
V170I |
probably benign |
Het |
| Gcn1 |
G |
A |
5: 115,719,863 (GRCm39) |
V373M |
probably benign |
Het |
| Gm19965 |
A |
G |
1: 116,749,602 (GRCm39) |
T428A |
unknown |
Het |
| Gm4792 |
A |
G |
10: 94,129,730 (GRCm39) |
I124T |
unknown |
Het |
| Grik2 |
A |
T |
10: 48,989,618 (GRCm39) |
C804S |
probably benign |
Het |
| Heatr6 |
T |
A |
11: 83,672,217 (GRCm39) |
I1075N |
probably damaging |
Het |
| Hunk |
G |
A |
16: 90,250,588 (GRCm39) |
A211T |
probably damaging |
Het |
| Ighe |
T |
C |
12: 113,234,976 (GRCm39) |
I395V |
probably damaging |
Het |
| Ino80e |
A |
T |
7: 126,456,484 (GRCm39) |
S104T |
probably damaging |
Het |
| Inpp4a |
A |
G |
1: 37,408,534 (GRCm39) |
Y305C |
probably benign |
Het |
| Insrr |
T |
A |
3: 87,711,838 (GRCm39) |
|
probably null |
Het |
| Itgae |
T |
G |
11: 73,031,504 (GRCm39) |
D1073E |
possibly damaging |
Het |
| Klf11 |
G |
T |
12: 24,705,141 (GRCm39) |
|
probably null |
Het |
| Lrguk |
A |
T |
6: 34,006,630 (GRCm39) |
K80M |
probably benign |
Het |
| Map2 |
A |
T |
1: 66,454,617 (GRCm39) |
D1169V |
probably damaging |
Het |
| Mpst |
G |
T |
15: 78,297,726 (GRCm39) |
C248F |
probably damaging |
Het |
| Myo9a |
C |
A |
9: 59,802,527 (GRCm39) |
Q2005K |
probably benign |
Het |
| Nfatc4 |
C |
T |
14: 56,069,421 (GRCm39) |
T649I |
probably benign |
Het |
| Nmt1 |
A |
G |
11: 102,937,226 (GRCm39) |
R88G |
probably benign |
Het |
| Nqo1 |
G |
A |
8: 108,129,729 (GRCm39) |
|
probably benign |
Het |
| Nudt2 |
T |
G |
4: 41,477,576 (GRCm39) |
M19R |
probably benign |
Het |
| Or10a49 |
T |
A |
7: 108,467,476 (GRCm39) |
K295M |
probably damaging |
Het |
| Or12d2 |
T |
A |
17: 37,624,522 (GRCm39) |
Y251F |
probably benign |
Het |
| Or9q2 |
C |
T |
19: 13,772,526 (GRCm39) |
V150M |
probably benign |
Het |
| P2ry1 |
T |
A |
3: 60,911,509 (GRCm39) |
I216N |
probably damaging |
Het |
| Pcx |
T |
A |
19: 4,669,589 (GRCm39) |
L823* |
probably null |
Het |
| Pkhd1 |
A |
G |
1: 20,619,980 (GRCm39) |
V880A |
probably damaging |
Het |
| Plcb1 |
A |
T |
2: 135,186,196 (GRCm39) |
N721I |
probably damaging |
Het |
| Prdm15 |
T |
C |
16: 97,623,046 (GRCm39) |
K269E |
possibly damaging |
Het |
| Prl7b1 |
A |
G |
13: 27,785,996 (GRCm39) |
V224A |
possibly damaging |
Het |
| Reln |
A |
G |
5: 22,134,125 (GRCm39) |
V2601A |
probably benign |
Het |
| Rspo4 |
G |
A |
2: 151,714,993 (GRCm39) |
R210Q |
unknown |
Het |
| Slc7a5 |
A |
T |
8: 122,615,162 (GRCm39) |
D228E |
probably benign |
Het |
| Spopfm2 |
T |
A |
3: 94,083,509 (GRCm39) |
K101* |
probably null |
Het |
| Tas2r115 |
A |
G |
6: 132,714,214 (GRCm39) |
S246P |
probably damaging |
Het |
| Tenm4 |
A |
G |
7: 96,423,353 (GRCm39) |
Y716C |
probably damaging |
Het |
| Tgfb3 |
T |
C |
12: 86,108,923 (GRCm39) |
K269E |
possibly damaging |
Het |
| Thoc6 |
A |
G |
17: 23,889,841 (GRCm39) |
I27T |
probably benign |
Het |
| Tigd5 |
G |
A |
15: 75,781,748 (GRCm39) |
G37S |
probably benign |
Het |
| Tmem259 |
C |
T |
10: 79,815,506 (GRCm39) |
D102N |
possibly damaging |
Het |
| Tpo |
T |
G |
12: 30,142,589 (GRCm39) |
I712L |
probably benign |
Het |
| Ttn |
G |
A |
2: 76,700,892 (GRCm39) |
T21M |
possibly damaging |
Het |
| Utp20 |
A |
T |
10: 88,656,572 (GRCm39) |
|
probably null |
Het |
| Xrcc5 |
A |
G |
1: 72,351,748 (GRCm39) |
D106G |
probably damaging |
Het |
| Xrn1 |
T |
A |
9: 95,861,194 (GRCm39) |
F451L |
probably benign |
Het |
| Zar1l |
T |
A |
5: 150,441,203 (GRCm39) |
D141V |
probably damaging |
Het |
| Zfp27 |
A |
T |
7: 29,595,324 (GRCm39) |
C214S |
possibly damaging |
Het |
|
| Other mutations in Znfx1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00324:Znfx1
|
APN |
2 |
166,878,649 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
IGL00492:Znfx1
|
APN |
2 |
166,878,843 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01285:Znfx1
|
APN |
2 |
166,880,615 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
IGL01343:Znfx1
|
APN |
2 |
166,879,283 (GRCm39) |
missense |
probably benign |
0.16 |
|
IGL01767:Znfx1
|
APN |
2 |
166,897,643 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01983:Znfx1
|
APN |
2 |
166,898,270 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02006:Znfx1
|
APN |
2 |
166,897,683 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02254:Znfx1
|
APN |
2 |
166,897,643 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02421:Znfx1
|
APN |
2 |
166,902,000 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL02496:Znfx1
|
APN |
2 |
166,889,550 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
IGL02525:Znfx1
|
APN |
2 |
166,879,457 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02528:Znfx1
|
APN |
2 |
166,892,324 (GRCm39) |
missense |
probably benign |
0.11 |
|
IGL02537:Znfx1
|
APN |
2 |
166,898,087 (GRCm39) |
missense |
probably benign |
0.37 |
|
IGL03065:Znfx1
|
APN |
2 |
166,897,685 (GRCm39) |
missense |
probably benign |
0.00 |
|
raywing
|
UTSW |
2 |
166,879,738 (GRCm39) |
missense |
probably damaging |
1.00 |
|
sharkfin
|
UTSW |
2 |
166,898,237 (GRCm39) |
missense |
probably benign |
0.03 |
|
skate
|
UTSW |
2 |
166,880,137 (GRCm39) |
missense |
probably benign |
0.06 |
|
R0127:Znfx1
|
UTSW |
2 |
166,886,130 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R0331:Znfx1
|
UTSW |
2 |
166,888,898 (GRCm39) |
missense |
probably benign |
0.11 |
|
R0488:Znfx1
|
UTSW |
2 |
166,884,483 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R0497:Znfx1
|
UTSW |
2 |
166,897,331 (GRCm39) |
missense |
probably benign |
0.03 |
|
R0537:Znfx1
|
UTSW |
2 |
166,883,621 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0542:Znfx1
|
UTSW |
2 |
166,897,575 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0650:Znfx1
|
UTSW |
2 |
166,889,574 (GRCm39) |
nonsense |
probably null |
|
|
R0655:Znfx1
|
UTSW |
2 |
166,898,827 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1104:Znfx1
|
UTSW |
2 |
166,897,560 (GRCm39) |
nonsense |
probably null |
|
|
R1470:Znfx1
|
UTSW |
2 |
166,884,507 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R1470:Znfx1
|
UTSW |
2 |
166,884,507 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R1512:Znfx1
|
UTSW |
2 |
166,898,237 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1533:Znfx1
|
UTSW |
2 |
166,898,708 (GRCm39) |
missense |
probably benign |
0.10 |
|
R1541:Znfx1
|
UTSW |
2 |
166,898,110 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1642:Znfx1
|
UTSW |
2 |
166,880,930 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1720:Znfx1
|
UTSW |
2 |
166,885,986 (GRCm39) |
nonsense |
probably null |
|
|
R1760:Znfx1
|
UTSW |
2 |
166,881,786 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1865:Znfx1
|
UTSW |
2 |
166,880,729 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1959:Znfx1
|
UTSW |
2 |
166,892,270 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2088:Znfx1
|
UTSW |
2 |
166,897,730 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4581:Znfx1
|
UTSW |
2 |
166,892,236 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4622:Znfx1
|
UTSW |
2 |
166,883,673 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R4649:Znfx1
|
UTSW |
2 |
166,898,276 (GRCm39) |
missense |
probably benign |
0.08 |
|
R4685:Znfx1
|
UTSW |
2 |
166,880,950 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4798:Znfx1
|
UTSW |
2 |
166,880,489 (GRCm39) |
splice site |
probably null |
|
|
R4827:Znfx1
|
UTSW |
2 |
166,886,151 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R4870:Znfx1
|
UTSW |
2 |
166,897,189 (GRCm39) |
missense |
probably benign |
|
|
R4910:Znfx1
|
UTSW |
2 |
166,879,402 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4910:Znfx1
|
UTSW |
2 |
166,878,724 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5022:Znfx1
|
UTSW |
2 |
166,881,746 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5023:Znfx1
|
UTSW |
2 |
166,881,746 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5057:Znfx1
|
UTSW |
2 |
166,881,746 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5061:Znfx1
|
UTSW |
2 |
166,907,318 (GRCm39) |
unclassified |
probably benign |
|
|
R5119:Znfx1
|
UTSW |
2 |
166,907,307 (GRCm39) |
unclassified |
probably benign |
|
|
R5125:Znfx1
|
UTSW |
2 |
166,888,859 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R5896:Znfx1
|
UTSW |
2 |
166,880,920 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6107:Znfx1
|
UTSW |
2 |
166,879,001 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R6112:Znfx1
|
UTSW |
2 |
166,880,126 (GRCm39) |
missense |
probably benign |
|
|
R6158:Znfx1
|
UTSW |
2 |
166,898,646 (GRCm39) |
missense |
probably benign |
0.19 |
|
R6281:Znfx1
|
UTSW |
2 |
166,897,805 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6464:Znfx1
|
UTSW |
2 |
166,888,842 (GRCm39) |
missense |
probably benign |
0.34 |
|
R6749:Znfx1
|
UTSW |
2 |
166,898,519 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6888:Znfx1
|
UTSW |
2 |
166,880,860 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R6973:Znfx1
|
UTSW |
2 |
166,898,681 (GRCm39) |
missense |
probably benign |
0.18 |
|
R7017:Znfx1
|
UTSW |
2 |
166,890,454 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7138:Znfx1
|
UTSW |
2 |
166,898,697 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7192:Znfx1
|
UTSW |
2 |
166,884,110 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7426:Znfx1
|
UTSW |
2 |
166,890,475 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7431:Znfx1
|
UTSW |
2 |
166,897,712 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7593:Znfx1
|
UTSW |
2 |
166,898,145 (GRCm39) |
missense |
probably benign |
0.28 |
|
R7732:Znfx1
|
UTSW |
2 |
166,884,589 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R7835:Znfx1
|
UTSW |
2 |
166,881,747 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7993:Znfx1
|
UTSW |
2 |
166,897,857 (GRCm39) |
nonsense |
probably null |
|
|
R8154:Znfx1
|
UTSW |
2 |
166,897,157 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8351:Znfx1
|
UTSW |
2 |
166,897,575 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8790:Znfx1
|
UTSW |
2 |
166,892,500 (GRCm39) |
intron |
probably benign |
|
|
R8953:Znfx1
|
UTSW |
2 |
166,897,421 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9005:Znfx1
|
UTSW |
2 |
166,880,656 (GRCm39) |
missense |
|
|
|
R9131:Znfx1
|
UTSW |
2 |
166,892,298 (GRCm39) |
missense |
probably benign |
|
|
R9163:Znfx1
|
UTSW |
2 |
166,898,261 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9169:Znfx1
|
UTSW |
2 |
166,897,185 (GRCm39) |
missense |
probably benign |
|
|
R9181:Znfx1
|
UTSW |
2 |
166,880,137 (GRCm39) |
missense |
probably benign |
0.06 |
|
R9181:Znfx1
|
UTSW |
2 |
166,879,738 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9300:Znfx1
|
UTSW |
2 |
166,897,860 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9448:Znfx1
|
UTSW |
2 |
166,888,844 (GRCm39) |
missense |
probably benign |
0.04 |
|
R9569:Znfx1
|
UTSW |
2 |
166,897,875 (GRCm39) |
missense |
|
|
|
X0064:Znfx1
|
UTSW |
2 |
166,897,176 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- ATACAAGGGTGTGGGTCTCAG -3'
(R):5'- GTCACCAGAACCAGCATGAG -3'
Sequencing Primer
(F):5'- CTCAGGGTGGTTCTGGCAAC -3'
(R):5'- TGGAGCTGTGCCAGTACCTC -3'
|
| Posted On |
2019-10-07 |
Incidental Mutation