Incidental Mutation 'R5000:Nsd3'
ID |
389829 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Nsd3
|
Ensembl Gene |
ENSMUSG00000054823 |
Gene Name |
nuclear receptor binding SET domain protein 3 |
Synonyms |
Whsc1l1, WHISTLE |
MMRRC Submission |
042594-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.361)
|
Stock # |
R5000 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
8 |
Chromosomal Location |
26091617-26209694 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 26172593 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Cysteine
at position 784
(Y784C)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000117778
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000084026]
[ENSMUST00000139966]
[ENSMUST00000142395]
[ENSMUST00000146919]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000084026
AA Change: Y784C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000081040 Gene: ENSMUSG00000054823 AA Change: Y784C
Domain | Start | End | E-Value | Type |
low complexity region
|
128 |
151 |
N/A |
INTRINSIC |
low complexity region
|
193 |
225 |
N/A |
INTRINSIC |
PWWP
|
278 |
341 |
1.6e-12 |
SMART |
low complexity region
|
680 |
701 |
N/A |
INTRINSIC |
PHD
|
713 |
756 |
4.49e-7 |
SMART |
PHD
|
761 |
808 |
5.82e-1 |
SMART |
PHD
|
809 |
861 |
3.06e0 |
SMART |
PHD
|
874 |
963 |
1e-4 |
SMART |
PWWP
|
968 |
1030 |
8.62e-18 |
SMART |
AWS
|
1103 |
1154 |
2.61e-17 |
SMART |
SET
|
1155 |
1278 |
2.17e-41 |
SMART |
PostSET
|
1279 |
1295 |
2.63e-3 |
SMART |
low complexity region
|
1309 |
1326 |
N/A |
INTRINSIC |
PHD
|
1332 |
1375 |
4.32e-9 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000139966
AA Change: Y784C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000122096 Gene: ENSMUSG00000054823 AA Change: Y784C
Domain | Start | End | E-Value | Type |
low complexity region
|
128 |
151 |
N/A |
INTRINSIC |
low complexity region
|
193 |
225 |
N/A |
INTRINSIC |
PWWP
|
278 |
341 |
1.6e-12 |
SMART |
low complexity region
|
680 |
701 |
N/A |
INTRINSIC |
PHD
|
713 |
756 |
4.49e-7 |
SMART |
PHD
|
761 |
808 |
5.82e-1 |
SMART |
PHD
|
809 |
861 |
3.06e0 |
SMART |
PHD
|
874 |
914 |
5.24e-8 |
SMART |
PWWP
|
919 |
981 |
8.62e-18 |
SMART |
AWS
|
1054 |
1105 |
2.61e-17 |
SMART |
SET
|
1106 |
1229 |
2.17e-41 |
SMART |
PostSET
|
1230 |
1246 |
2.63e-3 |
SMART |
low complexity region
|
1260 |
1277 |
N/A |
INTRINSIC |
PHD
|
1283 |
1326 |
4.32e-9 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000141781
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000142395
AA Change: Y784C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000117778 Gene: ENSMUSG00000054823 AA Change: Y784C
Domain | Start | End | E-Value | Type |
low complexity region
|
128 |
151 |
N/A |
INTRINSIC |
low complexity region
|
193 |
225 |
N/A |
INTRINSIC |
PWWP
|
278 |
341 |
1.6e-12 |
SMART |
low complexity region
|
680 |
701 |
N/A |
INTRINSIC |
PHD
|
713 |
756 |
4.49e-7 |
SMART |
PHD
|
761 |
808 |
5.82e-1 |
SMART |
PHD
|
809 |
861 |
3.06e0 |
SMART |
PHD
|
874 |
963 |
1e-4 |
SMART |
PWWP
|
968 |
1030 |
8.62e-18 |
SMART |
AWS
|
1103 |
1154 |
2.61e-17 |
SMART |
SET
|
1155 |
1278 |
2.17e-41 |
SMART |
PostSET
|
1279 |
1295 |
2.63e-3 |
SMART |
low complexity region
|
1309 |
1326 |
N/A |
INTRINSIC |
PHD
|
1332 |
1375 |
4.32e-9 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000146919
|
SMART Domains |
Protein: ENSMUSP00000115470 Gene: ENSMUSG00000054823
Domain | Start | End | E-Value | Type |
low complexity region
|
128 |
151 |
N/A |
INTRINSIC |
low complexity region
|
193 |
225 |
N/A |
INTRINSIC |
Pfam:PWWP
|
278 |
388 |
1.6e-25 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000157551
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000210452
|
Meta Mutation Damage Score |
0.9618 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.4%
|
Validation Efficiency |
98% (97/99) |
MGI Phenotype |
FUNCTION: This gene encodes a member of the SET domain family of histone lysine N-methyltransferase proteins. This protein methylates histone H3 at lysine residues 4 and 27, which represses gene transcription. It acts in opposition to the histone demethylase Jmjd1c. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2015]
|
Allele List at MGI |
All alleles(5) : Gene trapped(5)
|
Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310022A10Rik |
T |
A |
7: 27,255,946 (GRCm39) |
F11Y |
probably benign |
Het |
Abca5 |
A |
G |
11: 110,201,050 (GRCm39) |
L450P |
probably damaging |
Het |
Abi1 |
T |
A |
2: 22,840,211 (GRCm39) |
R357W |
probably damaging |
Het |
Acot7 |
G |
A |
4: 152,270,820 (GRCm39) |
G55R |
probably benign |
Het |
Aicda |
G |
A |
6: 122,538,826 (GRCm39) |
V14I |
probably damaging |
Het |
Anxa4 |
G |
T |
6: 86,742,766 (GRCm39) |
|
probably benign |
Het |
Apobr |
T |
A |
7: 126,185,729 (GRCm39) |
D413E |
possibly damaging |
Het |
Ash1l |
T |
C |
3: 88,965,941 (GRCm39) |
Y2448H |
probably damaging |
Het |
Atf7ip |
A |
G |
6: 136,559,426 (GRCm39) |
E749G |
probably damaging |
Het |
Atp8b3 |
A |
T |
10: 80,357,676 (GRCm39) |
N1114K |
possibly damaging |
Het |
Bdnf |
C |
A |
2: 109,553,993 (GRCm39) |
N122K |
probably benign |
Het |
Boc |
A |
T |
16: 44,310,517 (GRCm39) |
I801N |
probably damaging |
Het |
Brap |
A |
T |
5: 121,800,089 (GRCm39) |
K37* |
probably null |
Het |
Ccar1 |
C |
T |
10: 62,586,784 (GRCm39) |
E885K |
unknown |
Het |
Ccdc103 |
A |
G |
11: 102,774,932 (GRCm39) |
N177S |
probably benign |
Het |
Ccdc116 |
G |
A |
16: 16,959,657 (GRCm39) |
P344L |
possibly damaging |
Het |
Cdca5 |
T |
C |
19: 6,135,463 (GRCm39) |
S28P |
possibly damaging |
Het |
Ceacam20 |
T |
C |
7: 19,699,453 (GRCm39) |
I14T |
probably damaging |
Het |
Chrnb1 |
A |
T |
11: 69,677,858 (GRCm39) |
V298E |
probably damaging |
Het |
Cnksr3 |
G |
A |
10: 7,076,746 (GRCm39) |
Q149* |
probably null |
Het |
Csnk1a1 |
T |
C |
18: 61,711,840 (GRCm39) |
F97L |
probably damaging |
Het |
Dag1 |
A |
T |
9: 108,085,216 (GRCm39) |
S642T |
probably benign |
Het |
Dedd2 |
A |
G |
7: 24,903,068 (GRCm39) |
V297A |
possibly damaging |
Het |
Dhcr7 |
C |
T |
7: 143,395,060 (GRCm39) |
T189M |
possibly damaging |
Het |
Dlgap1 |
T |
C |
17: 71,073,053 (GRCm39) |
S691P |
probably damaging |
Het |
Dmgdh |
A |
C |
13: 93,825,046 (GRCm39) |
H123P |
probably damaging |
Het |
Dnah6 |
C |
T |
6: 73,121,798 (GRCm39) |
V1395I |
probably benign |
Het |
Dnah7a |
T |
C |
1: 53,606,201 (GRCm39) |
Y1273C |
probably damaging |
Het |
Dnah7b |
T |
A |
1: 46,138,663 (GRCm39) |
L235* |
probably null |
Het |
Elac2 |
T |
C |
11: 64,876,379 (GRCm39) |
F3L |
probably benign |
Het |
Elovl7 |
A |
T |
13: 108,410,915 (GRCm39) |
K163N |
probably benign |
Het |
Epg5 |
T |
C |
18: 77,997,376 (GRCm39) |
V413A |
probably benign |
Het |
Espl1 |
T |
A |
15: 102,206,986 (GRCm39) |
L150Q |
probably damaging |
Het |
F2rl3 |
T |
A |
8: 73,489,307 (GRCm39) |
L178Q |
probably damaging |
Het |
Fam120a |
T |
C |
13: 49,051,143 (GRCm39) |
E754G |
probably damaging |
Het |
Fam53b |
T |
C |
7: 132,317,730 (GRCm39) |
N304S |
probably benign |
Het |
Fbxo41 |
T |
C |
6: 85,460,901 (GRCm39) |
E269G |
probably damaging |
Het |
Fcrla |
T |
C |
1: 170,749,959 (GRCm39) |
T4A |
probably benign |
Het |
Frmpd1 |
A |
T |
4: 45,261,931 (GRCm39) |
|
probably null |
Het |
Gm9376 |
A |
G |
14: 118,504,702 (GRCm39) |
M45V |
probably benign |
Het |
Gpr68 |
G |
A |
12: 100,844,596 (GRCm39) |
A316V |
probably benign |
Het |
Hmgcl |
G |
A |
4: 135,689,511 (GRCm39) |
C323Y |
probably benign |
Het |
Hnrnpu |
T |
C |
1: 178,156,941 (GRCm39) |
|
probably benign |
Het |
Ier2 |
T |
A |
8: 85,389,353 (GRCm39) |
I10F |
probably damaging |
Het |
Ip6k1 |
C |
T |
9: 107,922,798 (GRCm39) |
Q234* |
probably null |
Het |
Llgl2 |
T |
C |
11: 115,735,728 (GRCm39) |
V108A |
probably benign |
Het |
Lrfn3 |
T |
C |
7: 30,059,805 (GRCm39) |
N140S |
possibly damaging |
Het |
Lrig1 |
T |
A |
6: 94,588,430 (GRCm39) |
H573L |
probably damaging |
Het |
Lrrk2 |
T |
A |
15: 91,634,081 (GRCm39) |
W1393R |
probably damaging |
Het |
Mrc1 |
T |
A |
2: 14,249,000 (GRCm39) |
Y179N |
probably damaging |
Het |
Mtfr1 |
C |
T |
3: 19,265,743 (GRCm39) |
L93F |
probably damaging |
Het |
Muc19 |
T |
C |
15: 91,757,429 (GRCm39) |
|
noncoding transcript |
Het |
Ndst2 |
C |
T |
14: 20,774,975 (GRCm39) |
|
probably null |
Het |
Nmd3 |
A |
T |
3: 69,624,735 (GRCm39) |
|
probably benign |
Het |
Or4a27 |
A |
T |
2: 88,559,910 (GRCm39) |
I11N |
probably damaging |
Het |
Or7a36 |
G |
A |
10: 78,820,514 (GRCm39) |
V297I |
probably benign |
Het |
Papln |
A |
G |
12: 83,821,663 (GRCm39) |
Y297C |
probably damaging |
Het |
Pdhx |
T |
C |
2: 102,871,385 (GRCm39) |
|
probably null |
Het |
Pdpk1 |
T |
C |
17: 24,330,019 (GRCm39) |
T6A |
possibly damaging |
Het |
Prcp |
T |
C |
7: 92,568,368 (GRCm39) |
W267R |
probably damaging |
Het |
Prg2 |
T |
C |
2: 84,812,367 (GRCm39) |
S26P |
probably benign |
Het |
Psg26 |
A |
T |
7: 18,214,057 (GRCm39) |
Y202N |
possibly damaging |
Het |
Psrc1 |
T |
C |
3: 108,287,839 (GRCm39) |
|
probably benign |
Het |
Rap1gds1 |
A |
T |
3: 138,662,011 (GRCm39) |
M366K |
probably damaging |
Het |
Robo4 |
G |
T |
9: 37,319,664 (GRCm39) |
R527L |
probably benign |
Het |
Sel1l3 |
G |
A |
5: 53,357,776 (GRCm39) |
T72M |
probably damaging |
Het |
Selenoo |
G |
A |
15: 88,978,387 (GRCm39) |
R270H |
probably damaging |
Het |
Sema3d |
A |
G |
5: 12,498,005 (GRCm39) |
T4A |
probably benign |
Het |
Shroom1 |
A |
T |
11: 53,357,944 (GRCm39) |
|
probably benign |
Het |
Slc25a19 |
T |
C |
11: 115,507,497 (GRCm39) |
|
probably null |
Het |
Snx29 |
A |
C |
16: 11,221,371 (GRCm39) |
I266L |
probably damaging |
Het |
Spo11 |
T |
C |
2: 172,831,193 (GRCm39) |
S255P |
probably damaging |
Het |
Spock3 |
T |
C |
8: 63,698,158 (GRCm39) |
V167A |
possibly damaging |
Het |
Tmc7 |
A |
G |
7: 118,158,077 (GRCm39) |
|
probably null |
Het |
Tmtc4 |
A |
G |
14: 123,170,743 (GRCm39) |
V509A |
possibly damaging |
Het |
Trim24 |
A |
G |
6: 37,935,547 (GRCm39) |
D880G |
probably benign |
Het |
Ube2j2 |
G |
A |
4: 156,030,841 (GRCm39) |
M1I |
probably null |
Het |
Ubr4 |
T |
A |
4: 139,163,480 (GRCm39) |
C2627S |
probably damaging |
Het |
Unc5d |
A |
T |
8: 29,205,775 (GRCm39) |
M512K |
possibly damaging |
Het |
Usp18 |
A |
G |
6: 121,229,479 (GRCm39) |
R33G |
possibly damaging |
Het |
Utp23 |
T |
A |
15: 51,745,569 (GRCm39) |
V23D |
probably damaging |
Het |
Wdr17 |
T |
A |
8: 55,118,161 (GRCm39) |
M512L |
possibly damaging |
Het |
Wdr64 |
T |
A |
1: 175,553,941 (GRCm39) |
|
probably null |
Het |
Zbtb6 |
T |
C |
2: 37,319,251 (GRCm39) |
T226A |
probably benign |
Het |
Zc3hc1 |
T |
A |
6: 30,375,987 (GRCm39) |
H191L |
possibly damaging |
Het |
Zdhhc4 |
C |
A |
5: 143,310,688 (GRCm39) |
C48F |
probably damaging |
Het |
Zfp335 |
T |
A |
2: 164,736,588 (GRCm39) |
T1016S |
probably benign |
Het |
Zfp583 |
A |
G |
7: 6,328,473 (GRCm39) |
Y39H |
probably damaging |
Het |
|
Other mutations in Nsd3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00435:Nsd3
|
APN |
8 |
26,166,728 (GRCm39) |
missense |
probably benign |
0.40 |
IGL00718:Nsd3
|
APN |
8 |
26,196,562 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00727:Nsd3
|
APN |
8 |
26,131,174 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01324:Nsd3
|
APN |
8 |
26,152,836 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01614:Nsd3
|
APN |
8 |
26,156,095 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL01834:Nsd3
|
APN |
8 |
26,130,668 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02066:Nsd3
|
APN |
8 |
26,203,515 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02229:Nsd3
|
APN |
8 |
26,200,775 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02481:Nsd3
|
APN |
8 |
26,181,143 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02686:Nsd3
|
APN |
8 |
26,156,086 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03394:Nsd3
|
APN |
8 |
26,165,765 (GRCm39) |
splice site |
probably benign |
|
Pine
|
UTSW |
8 |
26,169,952 (GRCm39) |
missense |
possibly damaging |
0.87 |
D3080:Nsd3
|
UTSW |
8 |
26,203,572 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02802:Nsd3
|
UTSW |
8 |
26,130,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R0136:Nsd3
|
UTSW |
8 |
26,149,870 (GRCm39) |
nonsense |
probably null |
|
R0195:Nsd3
|
UTSW |
8 |
26,170,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R0207:Nsd3
|
UTSW |
8 |
26,173,273 (GRCm39) |
missense |
probably benign |
0.02 |
R0471:Nsd3
|
UTSW |
8 |
26,138,450 (GRCm39) |
splice site |
probably benign |
|
R0511:Nsd3
|
UTSW |
8 |
26,168,732 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0524:Nsd3
|
UTSW |
8 |
26,190,605 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0581:Nsd3
|
UTSW |
8 |
26,200,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R0589:Nsd3
|
UTSW |
8 |
26,131,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R0645:Nsd3
|
UTSW |
8 |
26,199,096 (GRCm39) |
missense |
probably benign |
0.08 |
R0664:Nsd3
|
UTSW |
8 |
26,204,267 (GRCm39) |
missense |
probably damaging |
0.97 |
R0738:Nsd3
|
UTSW |
8 |
26,168,725 (GRCm39) |
splice site |
probably null |
|
R1148:Nsd3
|
UTSW |
8 |
26,203,407 (GRCm39) |
missense |
probably benign |
0.09 |
R1148:Nsd3
|
UTSW |
8 |
26,203,407 (GRCm39) |
missense |
probably benign |
0.09 |
R1265:Nsd3
|
UTSW |
8 |
26,172,578 (GRCm39) |
missense |
probably benign |
|
R1298:Nsd3
|
UTSW |
8 |
26,169,952 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1424:Nsd3
|
UTSW |
8 |
26,190,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R1493:Nsd3
|
UTSW |
8 |
26,203,407 (GRCm39) |
missense |
probably benign |
0.09 |
R1528:Nsd3
|
UTSW |
8 |
26,188,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R2051:Nsd3
|
UTSW |
8 |
26,181,116 (GRCm39) |
missense |
probably damaging |
0.99 |
R2199:Nsd3
|
UTSW |
8 |
26,156,073 (GRCm39) |
missense |
probably damaging |
0.99 |
R3414:Nsd3
|
UTSW |
8 |
26,190,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R3522:Nsd3
|
UTSW |
8 |
26,196,642 (GRCm39) |
missense |
probably benign |
|
R3623:Nsd3
|
UTSW |
8 |
26,152,835 (GRCm39) |
missense |
probably damaging |
0.98 |
R3624:Nsd3
|
UTSW |
8 |
26,152,835 (GRCm39) |
missense |
probably damaging |
0.98 |
R3798:Nsd3
|
UTSW |
8 |
26,188,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R4345:Nsd3
|
UTSW |
8 |
26,131,333 (GRCm39) |
missense |
probably benign |
0.04 |
R4370:Nsd3
|
UTSW |
8 |
26,138,524 (GRCm39) |
missense |
probably benign |
0.13 |
R4421:Nsd3
|
UTSW |
8 |
26,131,288 (GRCm39) |
missense |
probably damaging |
0.99 |
R4583:Nsd3
|
UTSW |
8 |
26,200,703 (GRCm39) |
missense |
probably benign |
0.20 |
R4664:Nsd3
|
UTSW |
8 |
26,188,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R4741:Nsd3
|
UTSW |
8 |
26,163,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R4876:Nsd3
|
UTSW |
8 |
26,181,161 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4888:Nsd3
|
UTSW |
8 |
26,188,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R5132:Nsd3
|
UTSW |
8 |
26,168,855 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5632:Nsd3
|
UTSW |
8 |
26,169,985 (GRCm39) |
missense |
probably benign |
0.00 |
R5760:Nsd3
|
UTSW |
8 |
26,149,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R5778:Nsd3
|
UTSW |
8 |
26,149,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R5779:Nsd3
|
UTSW |
8 |
26,172,685 (GRCm39) |
nonsense |
probably null |
|
R5860:Nsd3
|
UTSW |
8 |
26,156,107 (GRCm39) |
missense |
probably damaging |
0.98 |
R5911:Nsd3
|
UTSW |
8 |
26,156,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R6168:Nsd3
|
UTSW |
8 |
26,181,188 (GRCm39) |
missense |
probably null |
1.00 |
R6467:Nsd3
|
UTSW |
8 |
26,130,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R6490:Nsd3
|
UTSW |
8 |
26,204,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R6519:Nsd3
|
UTSW |
8 |
26,152,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R6554:Nsd3
|
UTSW |
8 |
26,152,891 (GRCm39) |
missense |
probably damaging |
0.99 |
R7038:Nsd3
|
UTSW |
8 |
26,131,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R7088:Nsd3
|
UTSW |
8 |
26,156,050 (GRCm39) |
missense |
probably benign |
0.40 |
R7244:Nsd3
|
UTSW |
8 |
26,156,055 (GRCm39) |
missense |
probably damaging |
0.96 |
R7308:Nsd3
|
UTSW |
8 |
26,130,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R7678:Nsd3
|
UTSW |
8 |
26,149,833 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7717:Nsd3
|
UTSW |
8 |
26,172,578 (GRCm39) |
missense |
probably benign |
|
R8064:Nsd3
|
UTSW |
8 |
26,190,698 (GRCm39) |
nonsense |
probably null |
|
R8242:Nsd3
|
UTSW |
8 |
26,196,567 (GRCm39) |
nonsense |
probably null |
|
R8312:Nsd3
|
UTSW |
8 |
26,153,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R8547:Nsd3
|
UTSW |
8 |
26,184,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R8954:Nsd3
|
UTSW |
8 |
26,163,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R8995:Nsd3
|
UTSW |
8 |
26,131,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R9026:Nsd3
|
UTSW |
8 |
26,172,576 (GRCm39) |
missense |
probably benign |
0.10 |
R9281:Nsd3
|
UTSW |
8 |
26,152,961 (GRCm39) |
missense |
probably benign |
0.00 |
R9320:Nsd3
|
UTSW |
8 |
26,199,088 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9563:Nsd3
|
UTSW |
8 |
26,204,230 (GRCm39) |
missense |
|
|
R9703:Nsd3
|
UTSW |
8 |
26,131,228 (GRCm39) |
missense |
probably benign |
0.00 |
X0026:Nsd3
|
UTSW |
8 |
26,190,621 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Nsd3
|
UTSW |
8 |
26,131,018 (GRCm39) |
small deletion |
probably benign |
|
|
Predicted Primers |
PCR Primer
(F):5'- TAAGCCCAACACTTTGAATGGTTC -3'
(R):5'- ACTGTGTGTCTCAGCTTTTGAAC -3'
Sequencing Primer
(F):5'- AGGACAGCACCCATGTTT -3'
(R):5'- CTTGGAAATAAACAGAAGGCCTGCC -3'
|
Posted On |
2016-06-06 |