Incidental Mutation 'R4601:Dennd3'
| ID |
345665 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Dennd3
|
| Ensembl Gene |
ENSMUSG00000036661 |
| Gene Name |
DENN domain containing 3 |
| Synonyms |
E030003N15Rik |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.189)
|
| Stock # |
R4601 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
15 |
| Chromosomal Location |
73384409-73444091 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 73439009 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tryptophan to Arginine
at position 1126
(W1126R)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000134002
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000043414]
[ENSMUST00000160267]
[ENSMUST00000173292]
|
| AlphaFold |
A2RT67 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000043414
AA Change: W1126R
PolyPhen 2
Score 0.316 (Sensitivity: 0.90; Specificity: 0.89)
|
| SMART Domains |
Protein: ENSMUSP00000046774
Gene: ENSMUSG00000036661
AA Change: W1126R
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:uDENN
|
12 |
161 |
3e-78 |
BLAST |
|
DENN
|
187 |
373 |
1.54e-62 |
SMART |
|
dDENN
|
436 |
499 |
6.81e-14 |
SMART |
|
WD40
|
1015 |
1054 |
3.68e1 |
SMART |
|
WD40
|
1057 |
1098 |
3.32e-5 |
SMART |
|
WD40
|
1232 |
1272 |
1.1e1 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000159322
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000160267
|
| SMART Domains |
Protein: ENSMUSP00000124538
Gene: ENSMUSG00000036661
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:WD40
|
51 |
90 |
2e-9 |
BLAST |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000160727
|
| Predicted Effect |
|
| SMART Domains |
Protein: ENSMUSP00000125657
Gene: ENSMUSG00000036661
AA Change: W1002R
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
5 |
19 |
N/A |
INTRINSIC |
|
Blast:DENN
|
33 |
104 |
5e-28 |
BLAST |
|
DENN
|
116 |
302 |
1.54e-62 |
SMART |
|
dDENN
|
312 |
376 |
5.63e-6 |
SMART |
|
WD40
|
892 |
931 |
3.68e1 |
SMART |
|
WD40
|
934 |
975 |
3.32e-5 |
SMART |
|
WD40
|
1109 |
1149 |
1.1e1 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000173292
AA Change: W1126R
PolyPhen 2
Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000134002
Gene: ENSMUSG00000036661
AA Change: W1126R
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:uDENN
|
12 |
161 |
2e-78 |
BLAST |
|
DENN
|
187 |
373 |
1.54e-62 |
SMART |
|
dDENN
|
436 |
499 |
6.81e-14 |
SMART |
|
WD40
|
1015 |
1054 |
3.68e1 |
SMART |
|
WD40
|
1057 |
1098 |
3.32e-5 |
SMART |
|
| Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.1%
- 20x: 94.5%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 91 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aars2 |
T |
A |
17: 45,827,847 (GRCm39) |
D555E |
probably damaging |
Het |
| Abca16 |
T |
G |
7: 120,035,920 (GRCm39) |
F334L |
probably damaging |
Het |
| Abcc4 |
T |
A |
14: 118,869,575 (GRCm39) |
M186L |
probably benign |
Het |
| Agap3 |
T |
C |
5: 24,681,406 (GRCm39) |
L120P |
probably damaging |
Het |
| Ak7 |
G |
A |
12: 105,679,834 (GRCm39) |
V123M |
probably benign |
Het |
| Aldh1a7 |
A |
T |
19: 20,693,343 (GRCm39) |
V192D |
probably damaging |
Het |
| Ankrd36 |
A |
G |
11: 5,520,102 (GRCm39) |
D59G |
probably benign |
Het |
| Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
| Cacna1e |
A |
G |
1: 154,347,359 (GRCm39) |
V936A |
probably benign |
Het |
| Camkv |
T |
C |
9: 107,823,295 (GRCm39) |
V107A |
probably damaging |
Het |
| Camp |
T |
C |
9: 109,677,730 (GRCm39) |
E80G |
probably damaging |
Het |
| Cblif |
A |
C |
19: 11,729,554 (GRCm39) |
D171A |
probably damaging |
Het |
| Ccdc66 |
T |
C |
14: 27,222,377 (GRCm39) |
N122S |
probably damaging |
Het |
| Cd101 |
G |
A |
3: 100,901,204 (GRCm39) |
T960M |
possibly damaging |
Het |
| Cdk18 |
A |
G |
1: 132,044,657 (GRCm39) |
V323A |
possibly damaging |
Het |
| Celf2 |
G |
T |
2: 6,590,831 (GRCm39) |
N279K |
possibly damaging |
Het |
| Cemip |
T |
C |
7: 83,600,826 (GRCm39) |
I932V |
probably damaging |
Het |
| Cep250 |
C |
A |
2: 155,803,973 (GRCm39) |
Q28K |
probably benign |
Het |
| Ces2f |
T |
C |
8: 105,676,596 (GRCm39) |
C97R |
probably damaging |
Het |
| Cfap126 |
G |
T |
1: 170,941,627 (GRCm39) |
G41C |
possibly damaging |
Het |
| Cfap96 |
A |
T |
8: 46,423,505 (GRCm39) |
I69N |
probably damaging |
Het |
| Chat |
T |
C |
14: 32,146,112 (GRCm39) |
M354V |
probably benign |
Het |
| Clca4b |
A |
T |
3: 144,632,945 (GRCm39) |
D168E |
possibly damaging |
Het |
| Cpxm1 |
T |
A |
2: 130,235,496 (GRCm39) |
M499L |
possibly damaging |
Het |
| Dgkb |
T |
C |
12: 38,652,819 (GRCm39) |
S735P |
probably damaging |
Het |
| Dlec1 |
T |
C |
9: 118,976,202 (GRCm39) |
|
probably null |
Het |
| Dnajc6 |
T |
C |
4: 101,468,461 (GRCm39) |
F166L |
probably damaging |
Het |
| Dph5 |
A |
G |
3: 115,693,426 (GRCm39) |
N115D |
possibly damaging |
Het |
| Ercc3 |
G |
A |
18: 32,378,624 (GRCm39) |
A202T |
probably benign |
Het |
| Erich3 |
A |
T |
3: 154,470,375 (GRCm39) |
D136V |
unknown |
Het |
| Exoc2 |
T |
C |
13: 31,066,251 (GRCm39) |
N475S |
probably benign |
Het |
| Fam217a |
T |
C |
13: 35,095,285 (GRCm39) |
D310G |
probably damaging |
Het |
| Fam53a |
C |
T |
5: 33,758,007 (GRCm39) |
S372N |
probably benign |
Het |
| Fbn2 |
C |
G |
18: 58,186,805 (GRCm39) |
G1699R |
probably damaging |
Het |
| Fbxo46 |
T |
C |
7: 18,869,489 (GRCm39) |
V36A |
probably benign |
Het |
| Fhip1a |
T |
C |
3: 85,648,487 (GRCm39) |
M26V |
probably damaging |
Het |
| G6pc1 |
A |
G |
11: 101,263,567 (GRCm39) |
Y127C |
probably damaging |
Het |
| Gba2 |
A |
G |
4: 43,573,810 (GRCm39) |
F161L |
probably damaging |
Het |
| Gja1 |
T |
C |
10: 56,264,325 (GRCm39) |
L228P |
probably damaging |
Het |
| Gm20834 |
A |
G |
Y: 10,323,178 (GRCm39) |
V86A |
probably benign |
Het |
| Hmcn1 |
A |
T |
1: 150,614,396 (GRCm39) |
C1337S |
probably damaging |
Het |
| Il1rl1 |
T |
A |
1: 40,480,460 (GRCm39) |
S30T |
possibly damaging |
Het |
| Itgb4 |
A |
G |
11: 115,896,548 (GRCm39) |
T1436A |
probably damaging |
Het |
| Itk |
T |
A |
11: 46,227,342 (GRCm39) |
Q427L |
probably benign |
Het |
| Klhdc4 |
T |
C |
8: 122,526,266 (GRCm39) |
E291G |
probably damaging |
Het |
| Map4 |
T |
A |
9: 109,881,887 (GRCm39) |
S250R |
possibly damaging |
Het |
| Mnt |
T |
A |
11: 74,727,285 (GRCm39) |
V57E |
possibly damaging |
Het |
| Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
| Mslnl |
G |
A |
17: 25,961,908 (GRCm39) |
V128M |
probably damaging |
Het |
| Mtcl2 |
T |
C |
2: 156,881,844 (GRCm39) |
K736R |
probably benign |
Het |
| Musk |
A |
T |
4: 58,301,625 (GRCm39) |
I128F |
probably damaging |
Het |
| Myh4 |
G |
A |
11: 67,141,136 (GRCm39) |
A733T |
possibly damaging |
Het |
| Myo5a |
T |
A |
9: 75,043,670 (GRCm39) |
F220I |
probably damaging |
Het |
| Npas3 |
A |
G |
12: 54,091,361 (GRCm39) |
H305R |
probably damaging |
Het |
| Nrcam |
A |
T |
12: 44,637,839 (GRCm39) |
Y1132F |
probably damaging |
Het |
| Nt5c3b |
A |
C |
11: 100,323,744 (GRCm39) |
D189E |
probably benign |
Het |
| Nuf2 |
A |
G |
1: 169,333,683 (GRCm39) |
L331P |
probably damaging |
Het |
| Nup214 |
C |
T |
2: 31,887,977 (GRCm39) |
T646I |
probably benign |
Het |
| Or14j9 |
T |
C |
17: 37,875,076 (GRCm39) |
N42S |
probably damaging |
Het |
| Pcdh18 |
T |
C |
3: 49,699,174 (GRCm39) |
E1096G |
probably damaging |
Het |
| Pgm2 |
T |
A |
5: 64,265,070 (GRCm39) |
F364I |
probably benign |
Het |
| Pikfyve |
A |
G |
1: 65,273,421 (GRCm39) |
N612S |
probably damaging |
Het |
| Pla2g4e |
T |
G |
2: 120,016,863 (GRCm39) |
H226P |
possibly damaging |
Het |
| Ppp3cb |
T |
C |
14: 20,570,714 (GRCm39) |
N339S |
possibly damaging |
Het |
| Prkd2 |
G |
T |
7: 16,577,573 (GRCm39) |
|
probably benign |
Het |
| Rnf133 |
T |
C |
6: 23,649,041 (GRCm39) |
E296G |
possibly damaging |
Het |
| Sav1 |
A |
T |
12: 70,031,095 (GRCm39) |
D142E |
probably benign |
Het |
| Scn3b |
C |
A |
9: 40,199,719 (GRCm39) |
P212T |
probably damaging |
Het |
| Sel1l |
A |
T |
12: 91,799,827 (GRCm39) |
|
probably null |
Het |
| Septin9 |
A |
G |
11: 117,251,310 (GRCm39) |
K543E |
probably damaging |
Het |
| Serpinb12 |
T |
A |
1: 106,876,883 (GRCm39) |
D66E |
probably benign |
Het |
| Slc35e2 |
T |
C |
4: 155,702,106 (GRCm39) |
F290S |
probably benign |
Het |
| Snrpa |
A |
G |
7: 26,894,958 (GRCm39) |
M1T |
probably null |
Het |
| Sptlc3 |
G |
A |
2: 139,478,600 (GRCm39) |
V520I |
probably benign |
Het |
| Srpk3 |
A |
G |
X: 72,818,547 (GRCm39) |
H79R |
possibly damaging |
Het |
| Stox2 |
A |
G |
8: 47,645,970 (GRCm39) |
S497P |
probably damaging |
Het |
| Stradb |
G |
A |
1: 59,032,731 (GRCm39) |
S361N |
probably damaging |
Het |
| Sult3a2 |
T |
C |
10: 33,658,083 (GRCm39) |
K10R |
probably benign |
Het |
| Susd4 |
A |
G |
1: 182,686,025 (GRCm39) |
N192D |
probably damaging |
Het |
| Tcp10a |
T |
A |
17: 7,593,374 (GRCm39) |
D32E |
probably benign |
Het |
| Tdpoz4 |
T |
A |
3: 93,704,339 (GRCm39) |
V212D |
probably damaging |
Het |
| Tdrd5 |
T |
A |
1: 156,111,944 (GRCm39) |
T479S |
probably benign |
Het |
| Tex10 |
T |
C |
4: 48,452,946 (GRCm39) |
D671G |
probably benign |
Het |
| Tex55 |
A |
G |
16: 38,648,380 (GRCm39) |
V243A |
probably benign |
Het |
| Traj37 |
T |
C |
14: 54,418,996 (GRCm39) |
|
probably benign |
Het |
| Ttc7b |
G |
A |
12: 100,466,376 (GRCm39) |
R79C |
probably damaging |
Het |
| Vmn2r115 |
T |
A |
17: 23,565,373 (GRCm39) |
L420Q |
probably benign |
Het |
| Wdr24 |
T |
A |
17: 26,047,181 (GRCm39) |
|
probably null |
Het |
| Wdr81 |
T |
A |
11: 75,336,484 (GRCm39) |
Q516L |
probably damaging |
Het |
| Zfp516 |
A |
G |
18: 82,974,164 (GRCm39) |
T121A |
probably benign |
Het |
| Zmat1 |
A |
T |
X: 133,873,694 (GRCm39) |
S566T |
probably damaging |
Homo |
|
| Other mutations in Dennd3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00089:Dennd3
|
APN |
15 |
73,438,982 (GRCm39) |
missense |
probably benign |
0.26 |
|
IGL00579:Dennd3
|
APN |
15 |
73,412,691 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
IGL02101:Dennd3
|
APN |
15 |
73,399,794 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
IGL02164:Dennd3
|
APN |
15 |
73,416,297 (GRCm39) |
missense |
probably benign |
0.26 |
|
IGL02389:Dennd3
|
APN |
15 |
73,438,905 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02604:Dennd3
|
APN |
15 |
73,428,252 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02697:Dennd3
|
APN |
15 |
73,396,085 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
IGL02885:Dennd3
|
APN |
15 |
73,440,545 (GRCm39) |
missense |
probably benign |
|
|
IGL03356:Dennd3
|
APN |
15 |
73,440,482 (GRCm39) |
missense |
probably benign |
0.19 |
|
IGL03388:Dennd3
|
APN |
15 |
73,416,208 (GRCm39) |
missense |
probably damaging |
0.98 |
|
BB006:Dennd3
|
UTSW |
15 |
73,436,423 (GRCm39) |
missense |
probably damaging |
1.00 |
|
BB016:Dennd3
|
UTSW |
15 |
73,436,423 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0118:Dennd3
|
UTSW |
15 |
73,436,925 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0925:Dennd3
|
UTSW |
15 |
73,405,284 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1076:Dennd3
|
UTSW |
15 |
73,412,582 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1355:Dennd3
|
UTSW |
15 |
73,412,703 (GRCm39) |
splice site |
probably benign |
|
|
R1370:Dennd3
|
UTSW |
15 |
73,412,703 (GRCm39) |
splice site |
probably benign |
|
|
R1480:Dennd3
|
UTSW |
15 |
73,404,695 (GRCm39) |
missense |
probably benign |
0.20 |
|
R1727:Dennd3
|
UTSW |
15 |
73,436,977 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1732:Dennd3
|
UTSW |
15 |
73,409,267 (GRCm39) |
splice site |
probably benign |
|
|
R1771:Dennd3
|
UTSW |
15 |
73,426,950 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R1776:Dennd3
|
UTSW |
15 |
73,426,950 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R1779:Dennd3
|
UTSW |
15 |
73,394,357 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1838:Dennd3
|
UTSW |
15 |
73,436,949 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2146:Dennd3
|
UTSW |
15 |
73,426,909 (GRCm39) |
missense |
probably benign |
0.35 |
|
R2146:Dennd3
|
UTSW |
15 |
73,395,345 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2147:Dennd3
|
UTSW |
15 |
73,395,336 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2148:Dennd3
|
UTSW |
15 |
73,426,909 (GRCm39) |
missense |
probably benign |
0.35 |
|
R2149:Dennd3
|
UTSW |
15 |
73,426,909 (GRCm39) |
missense |
probably benign |
0.35 |
|
R2150:Dennd3
|
UTSW |
15 |
73,426,909 (GRCm39) |
missense |
probably benign |
0.35 |
|
R2174:Dennd3
|
UTSW |
15 |
73,427,154 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2295:Dennd3
|
UTSW |
15 |
73,395,404 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2905:Dennd3
|
UTSW |
15 |
73,429,495 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3106:Dennd3
|
UTSW |
15 |
73,436,973 (GRCm39) |
nonsense |
probably null |
|
|
R3757:Dennd3
|
UTSW |
15 |
73,394,083 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3785:Dennd3
|
UTSW |
15 |
73,419,426 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R3786:Dennd3
|
UTSW |
15 |
73,419,426 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R3787:Dennd3
|
UTSW |
15 |
73,419,426 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R3847:Dennd3
|
UTSW |
15 |
73,414,581 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R4369:Dennd3
|
UTSW |
15 |
73,412,658 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4666:Dennd3
|
UTSW |
15 |
73,442,709 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4680:Dennd3
|
UTSW |
15 |
73,405,225 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R4708:Dennd3
|
UTSW |
15 |
73,395,344 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4789:Dennd3
|
UTSW |
15 |
73,394,131 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4920:Dennd3
|
UTSW |
15 |
73,412,574 (GRCm39) |
missense |
probably benign |
0.13 |
|
R5043:Dennd3
|
UTSW |
15 |
73,399,785 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5074:Dennd3
|
UTSW |
15 |
73,419,144 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5410:Dennd3
|
UTSW |
15 |
73,419,297 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5421:Dennd3
|
UTSW |
15 |
73,438,964 (GRCm39) |
missense |
probably benign |
|
|
R5560:Dennd3
|
UTSW |
15 |
73,404,744 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6008:Dennd3
|
UTSW |
15 |
73,438,929 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R6357:Dennd3
|
UTSW |
15 |
73,428,321 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R6563:Dennd3
|
UTSW |
15 |
73,416,229 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6687:Dennd3
|
UTSW |
15 |
73,428,215 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R6837:Dennd3
|
UTSW |
15 |
73,429,542 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6910:Dennd3
|
UTSW |
15 |
73,426,965 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7125:Dennd3
|
UTSW |
15 |
73,405,140 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R7297:Dennd3
|
UTSW |
15 |
73,429,459 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7524:Dennd3
|
UTSW |
15 |
73,396,095 (GRCm39) |
nonsense |
probably null |
|
|
R7580:Dennd3
|
UTSW |
15 |
73,428,296 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R7653:Dennd3
|
UTSW |
15 |
73,434,275 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7731:Dennd3
|
UTSW |
15 |
73,434,216 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7767:Dennd3
|
UTSW |
15 |
73,394,079 (GRCm39) |
missense |
probably benign |
|
|
R7806:Dennd3
|
UTSW |
15 |
73,442,624 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R7860:Dennd3
|
UTSW |
15 |
73,412,657 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7902:Dennd3
|
UTSW |
15 |
73,439,964 (GRCm39) |
critical splice donor site |
probably benign |
|
|
R7929:Dennd3
|
UTSW |
15 |
73,436,423 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8218:Dennd3
|
UTSW |
15 |
73,384,622 (GRCm39) |
missense |
probably benign |
0.31 |
|
R8436:Dennd3
|
UTSW |
15 |
73,434,198 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8444:Dennd3
|
UTSW |
15 |
73,442,672 (GRCm39) |
missense |
probably benign |
0.09 |
|
R8698:Dennd3
|
UTSW |
15 |
73,394,154 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R8967:Dennd3
|
UTSW |
15 |
73,419,426 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R9147:Dennd3
|
UTSW |
15 |
73,429,463 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9148:Dennd3
|
UTSW |
15 |
73,429,463 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9194:Dennd3
|
UTSW |
15 |
73,419,153 (GRCm39) |
missense |
probably benign |
0.04 |
|
R9449:Dennd3
|
UTSW |
15 |
73,429,477 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9501:Dennd3
|
UTSW |
15 |
73,419,041 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9616:Dennd3
|
UTSW |
15 |
73,440,563 (GRCm39) |
missense |
probably benign |
|
|
R9730:Dennd3
|
UTSW |
15 |
73,426,959 (GRCm39) |
missense |
probably damaging |
1.00 |
|
RF006:Dennd3
|
UTSW |
15 |
73,419,441 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- CCTACTGTGAATGGTGCCTTTC -3'
(R):5'- GCCATCTATACACCAGCCTG -3'
Sequencing Primer
(F):5'- CCCCCAAGGTTAGATGTGAG -3'
(R):5'- ATCTATACACCAGCCTGTCAAG -3'
|
| Posted On |
2015-09-25 |
Incidental Mutation