Incidental Mutation 'R4706:Phf3'
| ID |
355181 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Phf3
|
| Ensembl Gene |
ENSMUSG00000048874 |
| Gene Name |
PHD finger protein 3 |
| Synonyms |
AU020177, 2310061N19Rik |
| MMRRC Submission |
041954-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R4706 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
1 |
| Chromosomal Location |
30841417-30912989 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 30844687 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 1424
(V1424A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000139610
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000088310]
[ENSMUST00000186733]
[ENSMUST00000191329]
|
| AlphaFold |
B2RQG2 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000088310
AA Change: V1424A
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000085650
Gene: ENSMUSG00000048874
AA Change: V1424A
| 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 |
probably damaging
Transcript: ENSMUST00000186733
AA Change: V1424A
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000139610
Gene: ENSMUSG00000048874
AA Change: V1424A
| 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: ENSMUST00000190190
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000191329
|
| SMART Domains |
Protein: ENSMUSP00000139662
Gene: ENSMUSG00000048874
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:SPOC
|
1 |
88 |
1.9e-17 |
PFAM |
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 97.1%
- 20x: 94.8%
|
| 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: 78 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca16 |
T |
A |
7: 120,064,988 (GRCm39) |
N548K |
probably damaging |
Het |
| Abcd2 |
T |
C |
15: 91,043,385 (GRCm39) |
D601G |
probably benign |
Het |
| Afap1l2 |
A |
T |
19: 56,925,672 (GRCm39) |
I152N |
possibly damaging |
Het |
| Ankrd52 |
T |
G |
10: 128,214,030 (GRCm39) |
M62R |
probably benign |
Het |
| Aox4 |
A |
T |
1: 58,305,946 (GRCm39) |
T1317S |
probably damaging |
Het |
| Apol7c |
T |
A |
15: 77,409,923 (GRCm39) |
Q341L |
probably benign |
Het |
| Arhgef4 |
C |
T |
1: 34,771,298 (GRCm39) |
R1202W |
probably benign |
Het |
| B4galnt2 |
C |
T |
11: 95,766,923 (GRCm39) |
|
probably null |
Het |
| Cecr2 |
A |
T |
6: 120,732,539 (GRCm39) |
E477V |
possibly damaging |
Het |
| Chmp7 |
A |
T |
14: 69,956,010 (GRCm39) |
D419E |
probably benign |
Het |
| Cmip |
A |
C |
8: 118,103,893 (GRCm39) |
K127T |
probably damaging |
Het |
| Csmd2 |
T |
C |
4: 128,438,544 (GRCm39) |
V3041A |
probably benign |
Het |
| Cyp1b1 |
T |
A |
17: 80,020,771 (GRCm39) |
I324F |
possibly damaging |
Het |
| Dapp1 |
T |
C |
3: 137,638,928 (GRCm39) |
D225G |
probably benign |
Het |
| Ddx10 |
T |
C |
9: 53,145,231 (GRCm39) |
T249A |
probably damaging |
Het |
| Dscaml1 |
T |
C |
9: 45,361,878 (GRCm39) |
Y213H |
probably damaging |
Het |
| Eef1a2 |
T |
C |
2: 180,797,150 (GRCm39) |
D17G |
probably damaging |
Het |
| Fbn1 |
T |
C |
2: 125,212,069 (GRCm39) |
I848V |
probably benign |
Het |
| Fbxw18 |
A |
G |
9: 109,519,585 (GRCm39) |
I307T |
probably benign |
Het |
| Fxr1 |
T |
A |
3: 34,118,278 (GRCm39) |
D500E |
probably damaging |
Het |
| Gars1 |
G |
A |
6: 55,046,363 (GRCm39) |
G492D |
probably damaging |
Het |
| Gria2 |
A |
T |
3: 80,648,297 (GRCm39) |
D146E |
probably benign |
Het |
| Gstz1 |
A |
G |
12: 87,205,894 (GRCm39) |
N37S |
probably benign |
Het |
| Hnrnph3 |
C |
A |
10: 62,853,059 (GRCm39) |
G194V |
probably damaging |
Het |
| Il2rb |
T |
C |
15: 78,370,600 (GRCm39) |
R172G |
possibly damaging |
Het |
| Itga11 |
T |
A |
9: 62,662,578 (GRCm39) |
V517D |
possibly damaging |
Het |
| Kcnq4 |
A |
G |
4: 120,561,683 (GRCm39) |
I462T |
probably benign |
Het |
| Klf6 |
T |
A |
13: 5,911,639 (GRCm39) |
M1K |
probably null |
Het |
| Lrp8 |
G |
A |
4: 107,718,470 (GRCm39) |
A817T |
probably benign |
Het |
| Map3k5 |
T |
A |
10: 19,934,684 (GRCm39) |
Y509N |
probably damaging |
Het |
| Mdc1 |
C |
T |
17: 36,163,671 (GRCm39) |
S1073F |
probably damaging |
Het |
| Mme |
A |
G |
3: 63,256,133 (GRCm39) |
D531G |
possibly damaging |
Het |
| Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
| Mroh7 |
A |
T |
4: 106,548,821 (GRCm39) |
V1014E |
possibly damaging |
Het |
| Msantd5l |
A |
T |
11: 51,144,668 (GRCm39) |
F204L |
possibly damaging |
Het |
| Myo1d |
C |
T |
11: 80,557,467 (GRCm39) |
C491Y |
probably damaging |
Het |
| Ncoa3 |
C |
A |
2: 165,889,799 (GRCm39) |
D61E |
probably damaging |
Het |
| Nmrk1 |
A |
G |
19: 18,622,491 (GRCm39) |
E190G |
probably benign |
Het |
| Nr4a2 |
G |
T |
2: 57,002,225 (GRCm39) |
P13H |
probably damaging |
Het |
| Nup205 |
T |
C |
6: 35,178,943 (GRCm39) |
L671P |
probably damaging |
Het |
| Omt2a |
T |
C |
9: 78,220,352 (GRCm39) |
I16V |
probably benign |
Het |
| Or4c116 |
A |
T |
2: 88,942,576 (GRCm39) |
F93L |
probably damaging |
Het |
| Or51f2 |
T |
A |
7: 102,526,640 (GRCm39) |
H104Q |
probably damaging |
Het |
| Or6n1 |
A |
G |
1: 173,917,268 (GRCm39) |
I221V |
probably damaging |
Het |
| Or8k24 |
G |
A |
2: 86,216,732 (GRCm39) |
T10I |
probably benign |
Het |
| Or8s5 |
G |
T |
15: 98,238,659 (GRCm39) |
H70Q |
possibly damaging |
Het |
| Osbpl9 |
A |
T |
4: 109,013,884 (GRCm39) |
I70N |
probably damaging |
Het |
| Pclo |
A |
T |
5: 14,764,221 (GRCm39) |
L4231F |
unknown |
Het |
| Per1 |
C |
T |
11: 68,991,444 (GRCm39) |
|
probably benign |
Het |
| Perm1 |
G |
T |
4: 156,301,531 (GRCm39) |
C25F |
probably damaging |
Het |
| Plxnb1 |
T |
G |
9: 108,941,096 (GRCm39) |
L1625R |
probably damaging |
Het |
| Ppid |
G |
A |
3: 79,506,359 (GRCm39) |
V216I |
probably benign |
Het |
| Ppp4r3a |
C |
T |
12: 101,008,175 (GRCm39) |
G754D |
probably damaging |
Het |
| Prex2 |
G |
T |
1: 11,270,212 (GRCm39) |
W1299L |
probably damaging |
Het |
| Ptprn2 |
C |
A |
12: 116,835,714 (GRCm39) |
Q350K |
probably benign |
Het |
| Ralyl |
G |
A |
3: 14,104,850 (GRCm39) |
|
probably null |
Het |
| Rbm8a |
G |
A |
3: 96,537,368 (GRCm39) |
|
probably benign |
Het |
| Relch |
T |
A |
1: 105,620,004 (GRCm39) |
M353K |
probably benign |
Het |
| Ros1 |
A |
G |
10: 51,977,990 (GRCm39) |
S1419P |
possibly damaging |
Het |
| Rps6ka5 |
C |
T |
12: 100,564,144 (GRCm39) |
|
probably null |
Het |
| Rps6ka5 |
T |
A |
12: 100,547,578 (GRCm39) |
I311F |
probably damaging |
Het |
| Rtel1 |
T |
C |
2: 180,965,539 (GRCm39) |
|
probably null |
Het |
| Sacs |
A |
G |
14: 61,441,722 (GRCm39) |
E1256G |
probably damaging |
Het |
| Sec23a |
A |
G |
12: 59,029,372 (GRCm39) |
V467A |
probably damaging |
Het |
| Sec24d |
T |
A |
3: 123,149,427 (GRCm39) |
N811K |
possibly damaging |
Het |
| Sf3b1 |
G |
A |
1: 55,029,666 (GRCm39) |
T1112M |
probably damaging |
Het |
| Shisa5 |
T |
A |
9: 108,885,128 (GRCm39) |
C133S |
probably null |
Het |
| Slc16a6 |
A |
G |
11: 109,354,193 (GRCm39) |
S59P |
probably benign |
Het |
| Slc25a31 |
G |
A |
3: 40,670,975 (GRCm39) |
A89T |
probably damaging |
Het |
| Slc6a1 |
G |
T |
6: 114,284,713 (GRCm39) |
R257L |
possibly damaging |
Het |
| Sntb1 |
C |
T |
15: 55,612,670 (GRCm39) |
V303M |
probably benign |
Het |
| Snx20 |
A |
G |
8: 89,354,439 (GRCm39) |
V97A |
probably damaging |
Het |
| Vmn1r29 |
T |
A |
6: 58,285,136 (GRCm39) |
N285K |
probably benign |
Het |
| Vmn2r98 |
T |
G |
17: 19,290,007 (GRCm39) |
S514R |
probably damaging |
Het |
| Zfp28 |
A |
T |
7: 6,392,793 (GRCm39) |
E156D |
probably damaging |
Het |
| Zfp39 |
A |
G |
11: 58,793,633 (GRCm39) |
V35A |
probably benign |
Het |
| Zfp536 |
A |
C |
7: 37,268,891 (GRCm39) |
I175S |
probably damaging |
Het |
| Zic5 |
A |
T |
14: 122,696,969 (GRCm39) |
S549T |
unknown |
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 |
|
R4757:Phf3
|
UTSW |
1 |
30,859,908 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4766:Phf3
|
UTSW |
1 |
30,853,020 (GRCm39) |
unclassified |
probably benign |
|
|
R4786:Phf3
|
UTSW |
1 |
30,855,638 (GRCm39) |
nonsense |
probably null |
|
|
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'- TTGGCGTCACCTTCAGTCAC -3'
(R):5'- AGAGCGCCCCAATAGTGTTG -3'
Sequencing Primer
(F):5'- CTCTACTTTTGGGTTAGCTTGATC -3'
(R):5'- TCATGCACAGAGGAAGCAGC -3'
|
| Posted On |
2015-10-21 |
Incidental Mutation