Incidental Mutation 'R4786:Phf3'
| ID |
367049 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Phf3
|
| Ensembl Gene |
ENSMUSG00000048874 |
| Gene Name |
PHD finger protein 3 |
| Synonyms |
AU020177, 2310061N19Rik |
| MMRRC Submission |
041995-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R4786 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
1 |
| Chromosomal Location |
30841417-30912989 bp(-) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
C to A
at 30855638 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamic Acid to Stop codon
at position 983
(E983*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000139610
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000088310]
[ENSMUST00000186733]
[ENSMUST00000191064]
|
| AlphaFold |
B2RQG2 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000088310
AA Change: E983*
|
| SMART Domains |
Protein: ENSMUSP00000085650
Gene: ENSMUSG00000048874
AA Change: E983*
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
212 |
223 |
N/A |
INTRINSIC |
|
low complexity region
|
337 |
344 |
N/A |
INTRINSIC |
|
low complexity region
|
600 |
611 |
N/A |
INTRINSIC |
|
low complexity region
|
651 |
660 |
N/A |
INTRINSIC |
|
PHD
|
697 |
748 |
3.82e-10 |
SMART |
|
low complexity region
|
847 |
859 |
N/A |
INTRINSIC |
|
low complexity region
|
876 |
887 |
N/A |
INTRINSIC |
|
TFS2M
|
908 |
1008 |
1.28e-47 |
SMART |
|
Pfam:SPOC
|
1188 |
1294 |
4.2e-26 |
PFAM |
|
low complexity region
|
1367 |
1373 |
N/A |
INTRINSIC |
|
low complexity region
|
1516 |
1529 |
N/A |
INTRINSIC |
|
low complexity region
|
1597 |
1620 |
N/A |
INTRINSIC |
|
low complexity region
|
1796 |
1811 |
N/A |
INTRINSIC |
|
low complexity region
|
1813 |
1846 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000186105
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000186733
AA Change: E983*
|
| SMART Domains |
Protein: ENSMUSP00000139610
Gene: ENSMUSG00000048874
AA Change: E983*
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
212 |
223 |
N/A |
INTRINSIC |
|
low complexity region
|
337 |
344 |
N/A |
INTRINSIC |
|
low complexity region
|
600 |
611 |
N/A |
INTRINSIC |
|
low complexity region
|
651 |
660 |
N/A |
INTRINSIC |
|
PHD
|
697 |
748 |
3.82e-10 |
SMART |
|
low complexity region
|
847 |
859 |
N/A |
INTRINSIC |
|
low complexity region
|
876 |
887 |
N/A |
INTRINSIC |
|
TFS2M
|
908 |
1008 |
1.28e-47 |
SMART |
|
Pfam:SPOC
|
1188 |
1294 |
4.2e-26 |
PFAM |
|
low complexity region
|
1367 |
1373 |
N/A |
INTRINSIC |
|
low complexity region
|
1516 |
1529 |
N/A |
INTRINSIC |
|
low complexity region
|
1597 |
1620 |
N/A |
INTRINSIC |
|
low complexity region
|
1796 |
1811 |
N/A |
INTRINSIC |
|
low complexity region
|
1813 |
1846 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000187316
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000188847
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000191064
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000191245
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.0%
- 20x: 94.7%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of a PHD finger-containing gene family. This gene may function as a transcription factor and may be involved in glioblastomas development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 86 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2700097O09Rik |
A |
T |
12: 55,106,321 (GRCm39) |
I134N |
possibly damaging |
Het |
| Acvr1c |
T |
C |
2: 58,170,366 (GRCm39) |
Y414C |
probably damaging |
Het |
| Adam32 |
A |
C |
8: 25,353,509 (GRCm39) |
S693R |
probably damaging |
Het |
| Aldh2 |
A |
T |
5: 121,710,887 (GRCm39) |
F314Y |
probably benign |
Het |
| Anks1 |
A |
G |
17: 28,271,704 (GRCm39) |
D874G |
possibly damaging |
Het |
| Ap4b1 |
T |
A |
3: 103,726,120 (GRCm39) |
V372E |
probably benign |
Het |
| Aqp12 |
G |
A |
1: 92,934,177 (GRCm39) |
C18Y |
probably damaging |
Het |
| Arap1 |
T |
A |
7: 101,034,212 (GRCm39) |
I218N |
possibly damaging |
Het |
| Arhgap42 |
C |
A |
9: 9,238,703 (GRCm39) |
E28* |
probably null |
Het |
| Asb5 |
G |
A |
8: 55,038,874 (GRCm39) |
E247K |
probably benign |
Het |
| Atg9b |
T |
C |
5: 24,591,087 (GRCm39) |
D781G |
possibly damaging |
Het |
| Atxn10 |
A |
G |
15: 85,271,344 (GRCm39) |
H294R |
probably benign |
Het |
| Bod1l |
G |
T |
5: 41,976,781 (GRCm39) |
T1511K |
probably benign |
Het |
| Btnl2 |
A |
T |
17: 34,582,322 (GRCm39) |
N296I |
probably damaging |
Het |
| Camta1 |
A |
T |
4: 151,374,496 (GRCm39) |
L168H |
probably damaging |
Het |
| Cant1 |
A |
T |
11: 118,299,665 (GRCm39) |
V265E |
possibly damaging |
Het |
| Ccdc157 |
T |
C |
11: 4,101,861 (GRCm39) |
D20G |
probably damaging |
Het |
| Cd209c |
T |
G |
8: 3,995,698 (GRCm39) |
T35P |
possibly damaging |
Het |
| Cdc20b |
G |
A |
13: 113,215,268 (GRCm39) |
V279M |
probably damaging |
Het |
| Cdh18 |
T |
A |
15: 23,410,873 (GRCm39) |
W453R |
probably null |
Het |
| Cdh24 |
A |
G |
14: 54,875,007 (GRCm39) |
S333P |
possibly damaging |
Het |
| Ceacam11 |
T |
C |
7: 17,706,239 (GRCm39) |
|
probably null |
Het |
| Ciz1 |
C |
T |
2: 32,267,539 (GRCm39) |
P150L |
probably damaging |
Het |
| Crip3 |
C |
A |
17: 46,741,968 (GRCm39) |
Q152K |
possibly damaging |
Het |
| Dars2 |
G |
A |
1: 160,888,330 (GRCm39) |
R197W |
probably damaging |
Het |
| Dctn4 |
A |
G |
18: 60,688,267 (GRCm39) |
D394G |
probably damaging |
Het |
| Dido1 |
T |
C |
2: 180,312,664 (GRCm39) |
Y1077C |
possibly damaging |
Het |
| Dnhd1 |
A |
G |
7: 105,323,651 (GRCm39) |
T641A |
probably benign |
Het |
| Egln3 |
A |
T |
12: 54,232,367 (GRCm39) |
I146N |
probably damaging |
Het |
| Eif2ak3 |
C |
T |
6: 70,869,602 (GRCm39) |
T763M |
possibly damaging |
Het |
| Etfbkmt |
A |
T |
6: 149,048,744 (GRCm39) |
M1L |
probably benign |
Het |
| Fam171a1 |
A |
T |
2: 3,226,615 (GRCm39) |
I583F |
probably damaging |
Het |
| Fbxo38 |
A |
C |
18: 62,662,745 (GRCm39) |
L249W |
probably damaging |
Het |
| Fxyd5 |
T |
C |
7: 30,740,907 (GRCm39) |
|
probably benign |
Het |
| Gabrr3 |
C |
A |
16: 59,250,463 (GRCm39) |
T154K |
probably benign |
Het |
| Gm7233 |
C |
A |
14: 43,038,347 (GRCm39) |
D90E |
probably benign |
Het |
| Gm8186 |
A |
G |
17: 26,318,014 (GRCm39) |
V61A |
probably benign |
Het |
| Gnao1 |
A |
G |
8: 94,670,931 (GRCm39) |
I137V |
probably benign |
Het |
| Gnptab |
A |
G |
10: 88,272,044 (GRCm39) |
M945V |
probably damaging |
Het |
| Gpsm1 |
G |
A |
2: 26,212,493 (GRCm39) |
A78T |
probably benign |
Het |
| Gtf2b |
T |
C |
3: 142,487,230 (GRCm39) |
L222P |
probably damaging |
Het |
| Hnrnpf |
A |
G |
6: 117,900,857 (GRCm39) |
Y47C |
probably damaging |
Het |
| Itga6 |
A |
G |
2: 71,669,034 (GRCm39) |
N608S |
possibly damaging |
Het |
| Kdm2b |
T |
C |
5: 123,018,917 (GRCm39) |
|
probably null |
Het |
| Krit1 |
T |
A |
5: 3,862,467 (GRCm39) |
H207Q |
possibly damaging |
Het |
| Ky |
A |
G |
9: 102,419,186 (GRCm39) |
N398D |
probably benign |
Het |
| Lama1 |
T |
A |
17: 68,080,854 (GRCm39) |
V1294E |
possibly damaging |
Het |
| Lef1 |
C |
T |
3: 130,905,173 (GRCm39) |
T18I |
probably damaging |
Het |
| Lrp2 |
T |
C |
2: 69,368,300 (GRCm39) |
N178S |
probably damaging |
Het |
| Lrrc36 |
A |
G |
8: 106,181,910 (GRCm39) |
T525A |
probably benign |
Het |
| Map3k8 |
A |
T |
18: 4,340,647 (GRCm39) |
C222* |
probably null |
Het |
| Mapre2 |
G |
C |
18: 24,011,016 (GRCm39) |
S199T |
probably benign |
Het |
| Mcm3ap |
A |
G |
10: 76,324,300 (GRCm39) |
N911S |
probably benign |
Het |
| Mroh4 |
G |
T |
15: 74,482,083 (GRCm39) |
H722Q |
probably benign |
Het |
| Muc21 |
A |
T |
17: 35,930,221 (GRCm39) |
|
probably benign |
Het |
| Myo5b |
A |
C |
18: 74,828,451 (GRCm39) |
Y701S |
probably benign |
Het |
| Myt1l |
G |
T |
12: 29,861,457 (GRCm39) |
V80L |
unknown |
Het |
| Ncoa7 |
C |
A |
10: 30,531,638 (GRCm39) |
V24L |
probably benign |
Het |
| Nlrp10 |
A |
T |
7: 108,524,445 (GRCm39) |
V345D |
probably damaging |
Het |
| Nmral1 |
C |
A |
16: 4,534,288 (GRCm39) |
G51V |
probably damaging |
Het |
| Npc1 |
A |
G |
18: 12,332,554 (GRCm39) |
I797T |
probably benign |
Het |
| Or4x6 |
A |
T |
2: 89,949,351 (GRCm39) |
I197N |
possibly damaging |
Het |
| Or8g22 |
T |
A |
9: 38,958,783 (GRCm39) |
R22* |
probably null |
Het |
| Or8g34 |
A |
T |
9: 39,373,137 (GRCm39) |
I134L |
probably benign |
Het |
| Pclo |
A |
T |
5: 14,773,281 (GRCm39) |
I4419F |
unknown |
Het |
| Pitpnm2 |
A |
T |
5: 124,259,806 (GRCm39) |
Y1149* |
probably null |
Het |
| Sdc3 |
A |
T |
4: 130,550,079 (GRCm39) |
T430S |
probably damaging |
Het |
| Sema3f |
A |
G |
9: 107,559,881 (GRCm39) |
V671A |
probably benign |
Het |
| Sigirr |
T |
G |
7: 140,671,346 (GRCm39) |
S379R |
probably benign |
Het |
| Slc25a23 |
T |
A |
17: 57,354,326 (GRCm39) |
N360I |
possibly damaging |
Het |
| Slco6c1 |
A |
T |
1: 97,015,720 (GRCm39) |
M357K |
probably benign |
Het |
| Sox14 |
C |
A |
9: 99,757,018 (GRCm39) |
M240I |
probably benign |
Het |
| Stradb |
A |
T |
1: 59,030,367 (GRCm39) |
|
probably benign |
Het |
| Szt2 |
A |
T |
4: 118,256,259 (GRCm39) |
M200K |
probably benign |
Het |
| Tef |
T |
C |
15: 81,699,453 (GRCm39) |
S85P |
probably benign |
Het |
| Thada |
T |
A |
17: 84,766,283 (GRCm39) |
H41L |
possibly damaging |
Het |
| Tinagl1 |
A |
G |
4: 130,067,724 (GRCm39) |
F90S |
probably benign |
Het |
| Tnfaip1 |
G |
A |
11: 78,421,045 (GRCm39) |
T5I |
possibly damaging |
Het |
| Tnfrsf23 |
A |
T |
7: 143,233,801 (GRCm39) |
V59D |
probably damaging |
Het |
| Tnpo3 |
A |
G |
6: 29,578,541 (GRCm39) |
V311A |
probably benign |
Het |
| Trak1 |
T |
A |
9: 121,301,560 (GRCm39) |
M772K |
probably benign |
Het |
| Ubash3a |
A |
G |
17: 31,436,938 (GRCm39) |
D185G |
probably benign |
Het |
| Vmn2r120 |
T |
C |
17: 57,829,048 (GRCm39) |
T516A |
probably benign |
Het |
| Wdr4 |
A |
C |
17: 31,728,785 (GRCm39) |
L130R |
probably damaging |
Het |
| Zfp12 |
T |
C |
5: 143,231,257 (GRCm39) |
I528T |
probably damaging |
Het |
| Zfp607a |
T |
C |
7: 27,578,838 (GRCm39) |
L636P |
probably damaging |
Het |
|
| Other mutations in Phf3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00234:Phf3
|
APN |
1 |
30,850,928 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL00704:Phf3
|
APN |
1 |
30,843,919 (GRCm39) |
missense |
probably benign |
|
|
IGL01147:Phf3
|
APN |
1 |
30,843,250 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01360:Phf3
|
APN |
1 |
30,847,809 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01376:Phf3
|
APN |
1 |
30,869,566 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
IGL01396:Phf3
|
APN |
1 |
30,843,386 (GRCm39) |
nonsense |
probably null |
|
|
IGL01830:Phf3
|
APN |
1 |
30,853,148 (GRCm39) |
nonsense |
probably null |
|
|
IGL02108:Phf3
|
APN |
1 |
30,869,032 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02156:Phf3
|
APN |
1 |
30,847,859 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02576:Phf3
|
APN |
1 |
30,869,117 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL03031:Phf3
|
APN |
1 |
30,843,734 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03334:Phf3
|
APN |
1 |
30,844,810 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL03411:Phf3
|
APN |
1 |
30,843,482 (GRCm39) |
missense |
probably damaging |
1.00 |
|
FR4976:Phf3
|
UTSW |
1 |
30,844,104 (GRCm39) |
utr 3 prime |
probably benign |
|
|
PIT4458001:Phf3
|
UTSW |
1 |
30,855,622 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0037:Phf3
|
UTSW |
1 |
30,843,999 (GRCm39) |
missense |
probably benign |
0.03 |
|
R0052:Phf3
|
UTSW |
1 |
30,847,848 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0114:Phf3
|
UTSW |
1 |
30,844,524 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R0123:Phf3
|
UTSW |
1 |
30,844,146 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0225:Phf3
|
UTSW |
1 |
30,844,146 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0715:Phf3
|
UTSW |
1 |
30,850,919 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0835:Phf3
|
UTSW |
1 |
30,869,632 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0848:Phf3
|
UTSW |
1 |
30,902,253 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1473:Phf3
|
UTSW |
1 |
30,845,021 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1522:Phf3
|
UTSW |
1 |
30,844,729 (GRCm39) |
missense |
probably benign |
0.05 |
|
R1549:Phf3
|
UTSW |
1 |
30,843,923 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1555:Phf3
|
UTSW |
1 |
30,844,958 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R1780:Phf3
|
UTSW |
1 |
30,851,023 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1789:Phf3
|
UTSW |
1 |
30,845,287 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1875:Phf3
|
UTSW |
1 |
30,869,704 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R1912:Phf3
|
UTSW |
1 |
30,843,426 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1957:Phf3
|
UTSW |
1 |
30,870,601 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2019:Phf3
|
UTSW |
1 |
30,850,928 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2259:Phf3
|
UTSW |
1 |
30,843,424 (GRCm39) |
missense |
probably benign |
0.20 |
|
R2305:Phf3
|
UTSW |
1 |
30,844,556 (GRCm39) |
nonsense |
probably null |
|
|
R2345:Phf3
|
UTSW |
1 |
30,844,432 (GRCm39) |
nonsense |
probably null |
|
|
R2424:Phf3
|
UTSW |
1 |
30,845,430 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2497:Phf3
|
UTSW |
1 |
30,869,095 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2504:Phf3
|
UTSW |
1 |
30,849,870 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3522:Phf3
|
UTSW |
1 |
30,844,684 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3816:Phf3
|
UTSW |
1 |
30,844,834 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4152:Phf3
|
UTSW |
1 |
30,870,539 (GRCm39) |
missense |
probably benign |
0.13 |
|
R4403:Phf3
|
UTSW |
1 |
30,843,490 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4658:Phf3
|
UTSW |
1 |
30,902,169 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4663:Phf3
|
UTSW |
1 |
30,860,296 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4669:Phf3
|
UTSW |
1 |
30,869,027 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4706:Phf3
|
UTSW |
1 |
30,844,687 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4757:Phf3
|
UTSW |
1 |
30,859,908 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4766:Phf3
|
UTSW |
1 |
30,853,020 (GRCm39) |
unclassified |
probably benign |
|
|
R5107:Phf3
|
UTSW |
1 |
30,870,566 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5155:Phf3
|
UTSW |
1 |
30,863,457 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R5310:Phf3
|
UTSW |
1 |
30,842,887 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5823:Phf3
|
UTSW |
1 |
30,843,764 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5944:Phf3
|
UTSW |
1 |
30,859,785 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5979:Phf3
|
UTSW |
1 |
30,844,827 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6007:Phf3
|
UTSW |
1 |
30,843,426 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6024:Phf3
|
UTSW |
1 |
30,902,307 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6072:Phf3
|
UTSW |
1 |
30,869,769 (GRCm39) |
missense |
probably benign |
0.08 |
|
R6533:Phf3
|
UTSW |
1 |
30,845,399 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6649:Phf3
|
UTSW |
1 |
30,844,104 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R6653:Phf3
|
UTSW |
1 |
30,844,104 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R6852:Phf3
|
UTSW |
1 |
30,843,711 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6855:Phf3
|
UTSW |
1 |
30,859,204 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6862:Phf3
|
UTSW |
1 |
30,853,063 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6930:Phf3
|
UTSW |
1 |
30,850,958 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7135:Phf3
|
UTSW |
1 |
30,870,190 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R7323:Phf3
|
UTSW |
1 |
30,852,211 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7352:Phf3
|
UTSW |
1 |
30,843,407 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R7455:Phf3
|
UTSW |
1 |
30,876,239 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R7549:Phf3
|
UTSW |
1 |
30,870,556 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7609:Phf3
|
UTSW |
1 |
30,844,582 (GRCm39) |
missense |
probably benign |
0.05 |
|
R7720:Phf3
|
UTSW |
1 |
30,868,938 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7745:Phf3
|
UTSW |
1 |
30,843,305 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8134:Phf3
|
UTSW |
1 |
30,863,552 (GRCm39) |
missense |
unknown |
|
|
R8264:Phf3
|
UTSW |
1 |
30,870,138 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R8545:Phf3
|
UTSW |
1 |
30,863,391 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R8821:Phf3
|
UTSW |
1 |
30,860,347 (GRCm39) |
nonsense |
probably null |
|
|
R8831:Phf3
|
UTSW |
1 |
30,860,347 (GRCm39) |
nonsense |
probably null |
|
|
R8873:Phf3
|
UTSW |
1 |
30,843,773 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R9101:Phf3
|
UTSW |
1 |
30,843,026 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R9402:Phf3
|
UTSW |
1 |
30,850,928 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9426:Phf3
|
UTSW |
1 |
30,870,625 (GRCm39) |
nonsense |
probably null |
|
|
R9594:Phf3
|
UTSW |
1 |
30,869,003 (GRCm39) |
missense |
probably benign |
0.07 |
|
R9707:Phf3
|
UTSW |
1 |
30,868,923 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9803:Phf3
|
UTSW |
1 |
30,869,872 (GRCm39) |
missense |
probably benign |
0.16 |
|
Z1177:Phf3
|
UTSW |
1 |
30,851,049 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
Z1177:Phf3
|
UTSW |
1 |
30,844,132 (GRCm39) |
missense |
unknown |
|
|
Z1177:Phf3
|
UTSW |
1 |
30,843,376 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- AAGAGAATCACCTGGCCCAG -3'
(R):5'- AAGCTGCTAGGCTGTATGTACTAGG -3'
Sequencing Primer
(F):5'- CCAGATCGGGTGGGGTGAG -3'
(R):5'- CCAGGCTTTAAAGTGGCTT -3'
|
| Posted On |
2015-12-29 |
Incidental Mutation