Incidental Mutation 'R1720:Znfx1'
| ID |
191355 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Znfx1
|
| Ensembl Gene |
ENSMUSG00000039501 |
| Gene Name |
zinc finger, NFX1-type containing 1 |
| Synonyms |
|
| MMRRC Submission |
039752-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R1720 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
2 |
| Chromosomal Location |
166877713-166904935 bp(-) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
A to T
at 166885986 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Leucine to Stop codon
at position 858
(L858*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000121750
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000048988]
[ENSMUST00000067584]
[ENSMUST00000128676]
[ENSMUST00000155281]
|
| AlphaFold |
Q8R151 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000048988
AA Change: L858*
|
| SMART Domains |
Protein: ENSMUSP00000049404
Gene: ENSMUSG00000039501
AA Change: L858*
| 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 benign
Transcript: ENSMUST00000067584
|
| SMART Domains |
Protein: ENSMUSP00000072867
Gene: ENSMUSG00000039501
| 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 |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000128676
|
| SMART Domains |
Protein: ENSMUSP00000121598
Gene: ENSMUSG00000039501
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:AAA_11
|
590 |
837 |
1.8e-17 |
PFAM |
|
Pfam:AAA_19
|
597 |
684 |
3.4e-11 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000155281
AA Change: L858*
|
| SMART Domains |
Protein: ENSMUSP00000121750
Gene: ENSMUSG00000039501
AA Change: L858*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:AAA_11
|
590 |
854 |
1.7e-17 |
PFAM |
|
Pfam:AAA_19
|
597 |
684 |
3.6e-11 |
PFAM |
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 96.7%
- 20x: 93.8%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 82 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acot5 |
A |
G |
12: 84,122,655 (GRCm39) |
D413G |
probably benign |
Het |
| Actr5 |
G |
T |
2: 158,478,057 (GRCm39) |
V476F |
possibly damaging |
Het |
| Adhfe1 |
G |
A |
1: 9,637,125 (GRCm39) |
D426N |
probably benign |
Het |
| Adra1a |
T |
C |
14: 66,875,727 (GRCm39) |
L234P |
probably damaging |
Het |
| Akap9 |
G |
T |
5: 4,022,791 (GRCm39) |
V1207L |
possibly damaging |
Het |
| Anapc2 |
A |
G |
2: 25,164,724 (GRCm39) |
D36G |
probably benign |
Het |
| Apol8 |
A |
G |
15: 77,633,566 (GRCm39) |
S337P |
possibly damaging |
Het |
| Asxl3 |
A |
T |
18: 22,585,492 (GRCm39) |
D139V |
probably damaging |
Het |
| Atp13a4 |
A |
T |
16: 29,227,746 (GRCm39) |
V1037E |
probably damaging |
Het |
| Baat |
A |
T |
4: 49,490,231 (GRCm39) |
F284L |
probably benign |
Het |
| Bltp3b |
T |
C |
10: 89,618,448 (GRCm39) |
V141A |
probably damaging |
Het |
| C1qtnf6 |
A |
T |
15: 78,411,640 (GRCm39) |
F40Y |
probably damaging |
Het |
| Caskin2 |
G |
A |
11: 115,693,608 (GRCm39) |
H508Y |
probably damaging |
Het |
| Cass4 |
A |
T |
2: 172,269,654 (GRCm39) |
I579F |
probably damaging |
Het |
| Cdk15 |
A |
G |
1: 59,328,917 (GRCm39) |
Y277C |
probably damaging |
Het |
| Cit |
G |
A |
5: 116,105,956 (GRCm39) |
D947N |
probably damaging |
Het |
| Clint1 |
T |
A |
11: 45,778,237 (GRCm39) |
I126K |
probably damaging |
Het |
| Col6a4 |
C |
T |
9: 105,903,671 (GRCm39) |
G1640E |
probably damaging |
Het |
| Ddx10 |
T |
C |
9: 53,149,371 (GRCm39) |
K119E |
probably damaging |
Het |
| Dennd1a |
G |
A |
2: 37,690,209 (GRCm39) |
Q964* |
probably null |
Het |
| Dnhd1 |
T |
C |
7: 105,343,035 (GRCm39) |
F1460L |
probably benign |
Het |
| Edc3 |
T |
C |
9: 57,655,462 (GRCm39) |
|
probably null |
Het |
| Edn1 |
A |
G |
13: 42,458,826 (GRCm39) |
E163G |
probably benign |
Het |
| Efl1 |
A |
T |
7: 82,332,929 (GRCm39) |
D317V |
possibly damaging |
Het |
| Elapor2 |
T |
G |
5: 9,478,407 (GRCm39) |
C424G |
probably damaging |
Het |
| F2 |
A |
T |
2: 91,459,175 (GRCm39) |
Y430* |
probably null |
Het |
| Faap100 |
C |
T |
11: 120,265,407 (GRCm39) |
V490M |
probably damaging |
Het |
| Fuz |
G |
T |
7: 44,546,415 (GRCm39) |
G104W |
probably damaging |
Het |
| Greb1l |
C |
A |
18: 10,553,848 (GRCm39) |
H1616Q |
probably benign |
Het |
| Grm1 |
G |
T |
10: 10,622,538 (GRCm39) |
|
probably null |
Het |
| Gucy2d |
G |
T |
7: 98,126,437 (GRCm39) |
A1098S |
probably benign |
Het |
| H1f0 |
T |
A |
15: 78,913,195 (GRCm39) |
S92T |
possibly damaging |
Het |
| Hbb-bt |
T |
A |
7: 103,463,083 (GRCm39) |
|
probably benign |
Het |
| Heg1 |
G |
A |
16: 33,527,549 (GRCm39) |
A170T |
probably benign |
Het |
| Hspa4l |
A |
T |
3: 40,736,049 (GRCm39) |
K578* |
probably null |
Het |
| Ikbke |
A |
G |
1: 131,186,947 (GRCm39) |
S582P |
possibly damaging |
Het |
| Itga6 |
T |
A |
2: 71,650,510 (GRCm39) |
F185L |
probably damaging |
Het |
| Itgal |
T |
A |
7: 126,906,099 (GRCm39) |
D396E |
probably benign |
Het |
| Kif5b |
T |
C |
18: 6,213,427 (GRCm39) |
H687R |
probably benign |
Het |
| Kmt2c |
T |
C |
5: 25,504,182 (GRCm39) |
N3709D |
probably benign |
Het |
| Lipf |
A |
T |
19: 33,943,066 (GRCm39) |
K125* |
probably null |
Het |
| Lrif1 |
A |
T |
3: 106,640,452 (GRCm39) |
E512D |
probably damaging |
Het |
| Matn2 |
T |
A |
15: 34,345,420 (GRCm39) |
Y142* |
probably null |
Het |
| Med13l |
A |
G |
5: 118,880,060 (GRCm39) |
T1051A |
probably damaging |
Het |
| Mpp3 |
T |
A |
11: 101,916,582 (GRCm39) |
M1L |
possibly damaging |
Het |
| Mro |
C |
T |
18: 74,009,806 (GRCm39) |
S159L |
probably benign |
Het |
| Myh15 |
T |
A |
16: 48,913,145 (GRCm39) |
D367E |
probably damaging |
Het |
| Myo1g |
T |
C |
11: 6,462,490 (GRCm39) |
Q547R |
probably benign |
Het |
| Neb |
T |
C |
2: 52,097,733 (GRCm39) |
I902M |
probably benign |
Het |
| Nsd1 |
G |
A |
13: 55,394,711 (GRCm39) |
D771N |
probably damaging |
Het |
| Or10x4 |
A |
G |
1: 174,219,486 (GRCm39) |
I284V |
probably benign |
Het |
| Or14a256 |
T |
C |
7: 86,265,664 (GRCm39) |
N63S |
probably damaging |
Het |
| Or2a20 |
T |
C |
6: 43,194,494 (GRCm39) |
S216P |
probably damaging |
Het |
| Or4e5 |
A |
C |
14: 52,728,051 (GRCm39) |
Y40* |
probably null |
Het |
| Or8b48 |
C |
T |
9: 38,492,585 (GRCm39) |
T4I |
probably benign |
Het |
| Penk |
A |
G |
4: 4,134,240 (GRCm39) |
Y136H |
probably damaging |
Het |
| Prdm6 |
C |
T |
18: 53,673,272 (GRCm39) |
S144L |
probably benign |
Het |
| Ptprq |
T |
A |
10: 107,522,155 (GRCm39) |
I599F |
probably damaging |
Het |
| Racgap1 |
A |
T |
15: 99,526,650 (GRCm39) |
C304* |
probably null |
Het |
| Rbp3 |
T |
C |
14: 33,678,866 (GRCm39) |
V938A |
probably benign |
Het |
| Rpp30 |
A |
G |
19: 36,071,827 (GRCm39) |
K132E |
probably damaging |
Het |
| Rxfp2 |
A |
T |
5: 149,966,564 (GRCm39) |
R101* |
probably null |
Het |
| Ryr1 |
A |
T |
7: 28,801,295 (GRCm39) |
V823E |
probably damaging |
Het |
| S100pbp |
A |
T |
4: 129,075,886 (GRCm39) |
D146E |
probably damaging |
Het |
| Sdr9c7 |
T |
A |
10: 127,738,127 (GRCm39) |
V135E |
probably damaging |
Het |
| Serpinb12 |
A |
G |
1: 106,874,344 (GRCm39) |
D23G |
probably damaging |
Het |
| Serpinf1 |
T |
A |
11: 75,304,807 (GRCm39) |
T185S |
probably null |
Het |
| Slc23a1 |
A |
C |
18: 35,758,904 (GRCm39) |
C96G |
possibly damaging |
Het |
| Slc5a4a |
C |
T |
10: 76,025,103 (GRCm39) |
|
probably null |
Het |
| Spmap1 |
A |
G |
11: 97,662,435 (GRCm39) |
F146L |
probably damaging |
Het |
| Suco |
A |
T |
1: 161,661,623 (GRCm39) |
L936Q |
probably damaging |
Het |
| Tmem144 |
T |
C |
3: 79,732,606 (GRCm39) |
Y224C |
probably damaging |
Het |
| Tpm4 |
T |
A |
8: 72,898,598 (GRCm39) |
|
probably null |
Het |
| Ttn |
T |
C |
2: 76,560,414 (GRCm39) |
E29329G |
probably damaging |
Het |
| Txn1 |
T |
C |
4: 57,943,922 (GRCm39) |
I101V |
probably benign |
Het |
| Ube2o |
A |
T |
11: 116,435,433 (GRCm39) |
C452S |
probably benign |
Het |
| Uxs1 |
A |
T |
1: 43,804,081 (GRCm39) |
I278N |
probably damaging |
Het |
| Vps54 |
T |
C |
11: 21,256,519 (GRCm39) |
F663L |
probably damaging |
Het |
| Wdfy3 |
CG |
C |
5: 102,074,391 (GRCm39) |
|
probably null |
Het |
| Zc3h11a |
A |
G |
1: 133,549,439 (GRCm39) |
S741P |
probably damaging |
Het |
| Zdbf2 |
G |
A |
1: 63,342,436 (GRCm39) |
V272I |
possibly damaging |
Het |
| Zdhhc24 |
A |
G |
19: 4,928,979 (GRCm39) |
N68S |
probably 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 |
|
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 |
|
R7473:Znfx1
|
UTSW |
2 |
166,880,744 (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'- TCTACCCTCAGGTTATGTCAGCCAG -3'
(R):5'- TGCAGTGACACTCTTTCTCTGCAAC -3'
Sequencing Primer
(F):5'- CTGTGGATGAAGTGATGATGTAAC -3'
(R):5'- acactctttctcTGCAACCTCTC -3'
|
| Posted On |
2014-05-14 |
Incidental Mutation