Incidental Mutation 'R1709:Dennd4a'
ID |
190334 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dennd4a
|
Ensembl Gene |
ENSMUSG00000053641 |
Gene Name |
DENN domain containing 4A |
Synonyms |
F730015K02Rik |
MMRRC Submission |
039742-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.489)
|
Stock # |
R1709 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
9 |
Chromosomal Location |
64718622-64826949 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 64796887 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Alanine
at position 860
(T860A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000037915
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000038890]
|
AlphaFold |
E9Q8V6 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000038890
AA Change: T860A
PolyPhen 2
Score 0.918 (Sensitivity: 0.81; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000037915 Gene: ENSMUSG00000053641 AA Change: T860A
Domain | Start | End | E-Value | Type |
internal_repeat_1
|
45 |
93 |
3.26e-5 |
PROSPERO |
uDENN
|
169 |
276 |
1.71e-28 |
SMART |
DENN
|
309 |
493 |
2.4e-73 |
SMART |
dDENN
|
559 |
633 |
4.15e-27 |
SMART |
low complexity region
|
724 |
735 |
N/A |
INTRINSIC |
low complexity region
|
936 |
950 |
N/A |
INTRINSIC |
low complexity region
|
1176 |
1191 |
N/A |
INTRINSIC |
low complexity region
|
1249 |
1262 |
N/A |
INTRINSIC |
low complexity region
|
1402 |
1417 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000216098
|
Meta Mutation Damage Score |
0.0719 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.4%
- 20x: 92.9%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a DENN domain-containing protein that may function as a guanine nucleotide exchange factor that specifically activates ras-related protein Rab-10. This protein also contains a interferon stimulated response element-binding domain and may be involved in regulating the v-myc avian myelocytomatosis viral (MYC) oncogene. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 8. [provided by RefSeq, Mar 2016]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aacs |
A |
G |
5: 125,566,942 (GRCm39) |
K152E |
probably benign |
Het |
Adgrd1 |
T |
C |
5: 129,256,292 (GRCm39) |
V641A |
possibly damaging |
Het |
Adgrv1 |
A |
T |
13: 81,741,179 (GRCm39) |
V95E |
probably damaging |
Het |
Agbl5 |
G |
A |
5: 31,063,585 (GRCm39) |
C872Y |
probably damaging |
Het |
Aldh1a7 |
G |
T |
19: 20,693,316 (GRCm39) |
T201K |
probably damaging |
Het |
Aox1 |
C |
T |
1: 58,116,633 (GRCm39) |
A788V |
probably benign |
Het |
Apob |
T |
C |
12: 8,059,306 (GRCm39) |
V2563A |
probably damaging |
Het |
Atcay |
G |
A |
10: 81,049,065 (GRCm39) |
T179I |
probably damaging |
Het |
Atf5 |
A |
T |
7: 44,462,707 (GRCm39) |
L139Q |
probably benign |
Het |
Atp13a3 |
T |
C |
16: 30,134,659 (GRCm39) |
T1205A |
probably benign |
Het |
Atr |
C |
T |
9: 95,753,129 (GRCm39) |
T656I |
probably benign |
Het |
Bloc1s3 |
T |
C |
7: 19,241,453 (GRCm39) |
E25G |
possibly damaging |
Het |
Brap |
T |
C |
5: 121,803,353 (GRCm39) |
|
probably null |
Het |
C6 |
G |
T |
15: 4,820,452 (GRCm39) |
A488S |
probably benign |
Het |
Ccin |
T |
C |
4: 43,984,133 (GRCm39) |
F180S |
probably damaging |
Het |
Cd207 |
T |
C |
6: 83,649,818 (GRCm39) |
I256V |
possibly damaging |
Het |
Cdc42bpa |
G |
T |
1: 179,894,789 (GRCm39) |
C323F |
probably damaging |
Het |
Cfap57 |
T |
C |
4: 118,428,901 (GRCm39) |
T1022A |
probably benign |
Het |
Cmtr2 |
A |
T |
8: 110,948,581 (GRCm39) |
Q297L |
probably benign |
Het |
Coro7 |
A |
T |
16: 4,452,305 (GRCm39) |
|
probably null |
Het |
Cpsf2 |
T |
A |
12: 101,965,801 (GRCm39) |
Y589N |
probably damaging |
Het |
Cpxm2 |
T |
C |
7: 131,661,563 (GRCm39) |
Y408C |
probably damaging |
Het |
Crocc |
A |
G |
4: 140,753,410 (GRCm39) |
|
probably null |
Het |
Cryzl1 |
A |
C |
16: 91,509,124 (GRCm39) |
F59C |
probably damaging |
Het |
Csmd2 |
T |
C |
4: 128,389,988 (GRCm39) |
V2241A |
probably damaging |
Het |
Cxcl15 |
C |
A |
5: 90,949,275 (GRCm39) |
H147N |
unknown |
Het |
Dnah10 |
C |
T |
5: 124,837,155 (GRCm39) |
P966L |
probably damaging |
Het |
Dpp9 |
T |
A |
17: 56,501,431 (GRCm39) |
M594L |
probably benign |
Het |
Dspp |
C |
A |
5: 104,323,590 (GRCm39) |
N244K |
probably damaging |
Het |
Efcab8 |
T |
A |
2: 153,656,290 (GRCm39) |
|
probably null |
Het |
Elapor2 |
C |
T |
5: 9,490,726 (GRCm39) |
R579* |
probably null |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Fbxw17 |
A |
G |
13: 50,585,693 (GRCm39) |
M299V |
probably benign |
Het |
Fbxw7 |
T |
A |
3: 84,883,659 (GRCm39) |
I530N |
probably damaging |
Het |
Gp2 |
C |
A |
7: 119,050,808 (GRCm39) |
D308Y |
probably null |
Het |
Gpd2 |
G |
A |
2: 57,247,667 (GRCm39) |
V537M |
probably damaging |
Het |
Gpr18 |
T |
A |
14: 122,149,404 (GRCm39) |
Y207F |
probably damaging |
Het |
Grip1 |
A |
T |
10: 119,733,620 (GRCm39) |
D20V |
probably damaging |
Het |
Gzmf |
A |
C |
14: 56,444,397 (GRCm39) |
F59V |
probably damaging |
Het |
H3c1 |
T |
A |
13: 23,945,964 (GRCm39) |
I125F |
probably damaging |
Het |
Igfn1 |
T |
C |
1: 135,883,311 (GRCm39) |
I2732V |
probably benign |
Het |
Ipo8 |
A |
T |
6: 148,684,226 (GRCm39) |
D855E |
probably benign |
Het |
Klrk1 |
A |
T |
6: 129,591,682 (GRCm39) |
|
probably null |
Het |
Megf11 |
A |
G |
9: 64,602,694 (GRCm39) |
Y876C |
probably damaging |
Het |
Mettl8 |
G |
T |
2: 70,812,495 (GRCm39) |
Q12K |
probably benign |
Het |
Mrgprf |
T |
C |
7: 144,861,954 (GRCm39) |
F172S |
probably benign |
Het |
Mycbp2 |
G |
A |
14: 103,461,852 (GRCm39) |
T1432I |
probably damaging |
Het |
Nek11 |
A |
C |
9: 105,225,260 (GRCm39) |
L84R |
probably damaging |
Het |
Nlrp1b |
T |
C |
11: 71,092,099 (GRCm39) |
E9G |
probably benign |
Het |
Nrxn1 |
T |
C |
17: 90,344,615 (GRCm39) |
I433V |
probably damaging |
Het |
Nup153 |
A |
G |
13: 46,847,450 (GRCm39) |
C660R |
probably damaging |
Het |
Or1o11 |
T |
A |
17: 37,757,091 (GRCm39) |
Y226* |
probably null |
Het |
Or2a25 |
T |
C |
6: 42,889,078 (GRCm39) |
V207A |
possibly damaging |
Het |
Or4z4 |
G |
T |
19: 12,076,245 (GRCm39) |
P253T |
probably damaging |
Het |
Or5h26 |
T |
A |
16: 58,988,264 (GRCm39) |
M81L |
probably benign |
Het |
P2rx7 |
T |
A |
5: 122,808,528 (GRCm39) |
N303K |
possibly damaging |
Het |
Pank4 |
T |
C |
4: 155,054,504 (GRCm39) |
L159P |
probably damaging |
Het |
Pcdhb22 |
A |
T |
18: 37,651,553 (GRCm39) |
H7L |
probably benign |
Het |
Pdzd8 |
A |
T |
19: 59,289,771 (GRCm39) |
I543N |
probably benign |
Het |
Pramel25 |
T |
C |
4: 143,520,116 (GRCm39) |
V120A |
possibly damaging |
Het |
Prrc2b |
C |
A |
2: 32,084,473 (GRCm39) |
R313S |
probably damaging |
Het |
Rbm12b1 |
T |
C |
4: 12,145,827 (GRCm39) |
C600R |
probably benign |
Het |
Rem1 |
G |
A |
2: 152,476,455 (GRCm39) |
V238M |
probably damaging |
Het |
Rfx6 |
T |
A |
10: 51,554,498 (GRCm39) |
M113K |
possibly damaging |
Het |
Rlf |
A |
T |
4: 121,007,020 (GRCm39) |
D653E |
probably benign |
Het |
Rnf130 |
A |
G |
11: 49,978,213 (GRCm39) |
D258G |
possibly damaging |
Het |
Robo2 |
A |
G |
16: 73,753,411 (GRCm39) |
V822A |
possibly damaging |
Het |
Rps6kc1 |
G |
T |
1: 190,532,533 (GRCm39) |
Q490K |
possibly damaging |
Het |
Scn9a |
T |
C |
2: 66,313,850 (GRCm39) |
Y1945C |
probably damaging |
Het |
Setd2 |
T |
A |
9: 110,378,925 (GRCm39) |
D913E |
probably benign |
Het |
Sfr1 |
G |
T |
19: 47,723,442 (GRCm39) |
E315D |
possibly damaging |
Het |
Smarca5 |
G |
A |
8: 81,435,849 (GRCm39) |
R763* |
probably null |
Het |
Sugct |
A |
C |
13: 17,847,151 (GRCm39) |
I44S |
probably damaging |
Het |
Syce1l |
A |
G |
8: 114,380,662 (GRCm39) |
|
probably null |
Het |
Tbc1d8b |
A |
G |
X: 138,634,829 (GRCm39) |
I654V |
probably benign |
Het |
Tcf23 |
T |
A |
5: 31,130,852 (GRCm39) |
Y163* |
probably null |
Het |
Terf2ip |
TG |
T |
8: 112,738,238 (GRCm39) |
|
probably null |
Het |
Tmem158 |
T |
C |
9: 123,088,950 (GRCm39) |
S221G |
possibly damaging |
Het |
Tnrc6a |
A |
G |
7: 122,769,205 (GRCm39) |
T332A |
probably benign |
Het |
Trappc4 |
T |
C |
9: 44,318,508 (GRCm39) |
T31A |
probably benign |
Het |
Trim27 |
T |
C |
13: 21,372,235 (GRCm39) |
|
probably null |
Het |
Ttyh2 |
T |
A |
11: 114,599,301 (GRCm39) |
L330Q |
probably damaging |
Het |
Tubgcp3 |
A |
T |
8: 12,689,532 (GRCm39) |
L578* |
probably null |
Het |
Txndc11 |
C |
A |
16: 10,946,565 (GRCm39) |
E83* |
probably null |
Het |
Utp20 |
T |
C |
10: 88,585,159 (GRCm39) |
K2635R |
probably benign |
Het |
V1ra8 |
C |
T |
6: 90,180,304 (GRCm39) |
T169I |
probably damaging |
Het |
Vcl |
G |
A |
14: 21,069,441 (GRCm39) |
V706I |
probably benign |
Het |
Vmn2r106 |
A |
T |
17: 20,499,373 (GRCm39) |
D179E |
probably benign |
Het |
Vmn2r80 |
T |
C |
10: 79,030,223 (GRCm39) |
M683T |
probably benign |
Het |
Xirp2 |
A |
G |
2: 67,340,215 (GRCm39) |
I819V |
probably benign |
Het |
Zfp735 |
T |
C |
11: 73,602,589 (GRCm39) |
F511S |
probably benign |
Het |
Zfp831 |
T |
C |
2: 174,487,683 (GRCm39) |
V786A |
probably benign |
Het |
Zfp992 |
T |
A |
4: 146,550,949 (GRCm39) |
H223Q |
probably benign |
Het |
Zfyve19 |
A |
C |
2: 119,041,300 (GRCm39) |
Q72P |
probably damaging |
Het |
|
Other mutations in Dennd4a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00476:Dennd4a
|
APN |
9 |
64,819,044 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01610:Dennd4a
|
APN |
9 |
64,814,166 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01788:Dennd4a
|
APN |
9 |
64,749,903 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01827:Dennd4a
|
APN |
9 |
64,749,843 (GRCm39) |
nonsense |
probably null |
|
IGL01828:Dennd4a
|
APN |
9 |
64,749,843 (GRCm39) |
nonsense |
probably null |
|
IGL01829:Dennd4a
|
APN |
9 |
64,749,843 (GRCm39) |
nonsense |
probably null |
|
IGL01979:Dennd4a
|
APN |
9 |
64,801,691 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02100:Dennd4a
|
APN |
9 |
64,816,988 (GRCm39) |
splice site |
probably benign |
|
IGL02339:Dennd4a
|
APN |
9 |
64,749,843 (GRCm39) |
nonsense |
probably null |
|
IGL02341:Dennd4a
|
APN |
9 |
64,749,843 (GRCm39) |
nonsense |
probably null |
|
IGL02584:Dennd4a
|
APN |
9 |
64,758,580 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02607:Dennd4a
|
APN |
9 |
64,769,609 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02654:Dennd4a
|
APN |
9 |
64,817,473 (GRCm39) |
splice site |
probably benign |
|
IGL02701:Dennd4a
|
APN |
9 |
64,804,635 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL03051:Dennd4a
|
APN |
9 |
64,769,696 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03257:Dennd4a
|
APN |
9 |
64,779,156 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03346:Dennd4a
|
APN |
9 |
64,795,808 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL03349:Dennd4a
|
APN |
9 |
64,796,256 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03398:Dennd4a
|
APN |
9 |
64,779,164 (GRCm39) |
missense |
probably benign |
0.32 |
R0010:Dennd4a
|
UTSW |
9 |
64,803,997 (GRCm39) |
missense |
probably benign |
0.00 |
R0010:Dennd4a
|
UTSW |
9 |
64,803,997 (GRCm39) |
missense |
probably benign |
0.00 |
R0129:Dennd4a
|
UTSW |
9 |
64,800,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R0220:Dennd4a
|
UTSW |
9 |
64,759,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R0396:Dennd4a
|
UTSW |
9 |
64,769,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R0881:Dennd4a
|
UTSW |
9 |
64,758,665 (GRCm39) |
critical splice donor site |
probably null |
|
R1225:Dennd4a
|
UTSW |
9 |
64,818,957 (GRCm39) |
missense |
probably benign |
0.03 |
R1311:Dennd4a
|
UTSW |
9 |
64,817,286 (GRCm39) |
missense |
probably benign |
0.34 |
R1448:Dennd4a
|
UTSW |
9 |
64,813,327 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1450:Dennd4a
|
UTSW |
9 |
64,818,947 (GRCm39) |
missense |
probably benign |
0.03 |
R1630:Dennd4a
|
UTSW |
9 |
64,779,164 (GRCm39) |
missense |
probably benign |
0.32 |
R1824:Dennd4a
|
UTSW |
9 |
64,766,640 (GRCm39) |
critical splice donor site |
probably null |
|
R1851:Dennd4a
|
UTSW |
9 |
64,769,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R1870:Dennd4a
|
UTSW |
9 |
64,804,516 (GRCm39) |
missense |
probably benign |
0.00 |
R1900:Dennd4a
|
UTSW |
9 |
64,804,618 (GRCm39) |
missense |
probably damaging |
0.99 |
R1911:Dennd4a
|
UTSW |
9 |
64,796,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R1938:Dennd4a
|
UTSW |
9 |
64,749,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R1954:Dennd4a
|
UTSW |
9 |
64,759,749 (GRCm39) |
missense |
probably benign |
0.02 |
R1955:Dennd4a
|
UTSW |
9 |
64,759,749 (GRCm39) |
missense |
probably benign |
0.02 |
R2049:Dennd4a
|
UTSW |
9 |
64,796,887 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2129:Dennd4a
|
UTSW |
9 |
64,813,256 (GRCm39) |
splice site |
probably null |
|
R2138:Dennd4a
|
UTSW |
9 |
64,796,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R2929:Dennd4a
|
UTSW |
9 |
64,759,699 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3083:Dennd4a
|
UTSW |
9 |
64,813,363 (GRCm39) |
missense |
probably benign |
0.03 |
R3108:Dennd4a
|
UTSW |
9 |
64,819,669 (GRCm39) |
missense |
probably benign |
0.23 |
R3176:Dennd4a
|
UTSW |
9 |
64,796,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R3177:Dennd4a
|
UTSW |
9 |
64,796,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R3276:Dennd4a
|
UTSW |
9 |
64,796,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R3277:Dennd4a
|
UTSW |
9 |
64,796,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R3890:Dennd4a
|
UTSW |
9 |
64,779,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R3953:Dennd4a
|
UTSW |
9 |
64,759,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R3963:Dennd4a
|
UTSW |
9 |
64,769,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R4059:Dennd4a
|
UTSW |
9 |
64,819,174 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4499:Dennd4a
|
UTSW |
9 |
64,817,405 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4500:Dennd4a
|
UTSW |
9 |
64,817,405 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4501:Dennd4a
|
UTSW |
9 |
64,817,405 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4671:Dennd4a
|
UTSW |
9 |
64,801,689 (GRCm39) |
missense |
probably benign |
|
R4701:Dennd4a
|
UTSW |
9 |
64,804,639 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4821:Dennd4a
|
UTSW |
9 |
64,804,531 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4829:Dennd4a
|
UTSW |
9 |
64,796,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R4876:Dennd4a
|
UTSW |
9 |
64,803,872 (GRCm39) |
missense |
probably benign |
|
R4881:Dennd4a
|
UTSW |
9 |
64,746,126 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4962:Dennd4a
|
UTSW |
9 |
64,813,285 (GRCm39) |
missense |
probably benign |
0.00 |
R5225:Dennd4a
|
UTSW |
9 |
64,796,210 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5557:Dennd4a
|
UTSW |
9 |
64,811,509 (GRCm39) |
missense |
probably benign |
0.07 |
R5649:Dennd4a
|
UTSW |
9 |
64,758,491 (GRCm39) |
splice site |
probably null |
|
R5868:Dennd4a
|
UTSW |
9 |
64,804,011 (GRCm39) |
missense |
probably benign |
0.02 |
R5876:Dennd4a
|
UTSW |
9 |
64,819,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R6052:Dennd4a
|
UTSW |
9 |
64,794,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R6411:Dennd4a
|
UTSW |
9 |
64,779,181 (GRCm39) |
missense |
probably benign |
0.04 |
R6596:Dennd4a
|
UTSW |
9 |
64,759,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R6668:Dennd4a
|
UTSW |
9 |
64,794,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R6915:Dennd4a
|
UTSW |
9 |
64,759,771 (GRCm39) |
nonsense |
probably null |
|
R7056:Dennd4a
|
UTSW |
9 |
64,814,205 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7107:Dennd4a
|
UTSW |
9 |
64,801,681 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7203:Dennd4a
|
UTSW |
9 |
64,803,756 (GRCm39) |
missense |
probably benign |
0.05 |
R7238:Dennd4a
|
UTSW |
9 |
64,769,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R7373:Dennd4a
|
UTSW |
9 |
64,804,551 (GRCm39) |
missense |
probably benign |
0.01 |
R7454:Dennd4a
|
UTSW |
9 |
64,759,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R7546:Dennd4a
|
UTSW |
9 |
64,780,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R7590:Dennd4a
|
UTSW |
9 |
64,795,869 (GRCm39) |
missense |
probably benign |
0.01 |
R7662:Dennd4a
|
UTSW |
9 |
64,759,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R7782:Dennd4a
|
UTSW |
9 |
64,814,202 (GRCm39) |
missense |
probably damaging |
0.98 |
R7909:Dennd4a
|
UTSW |
9 |
64,780,275 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7976:Dennd4a
|
UTSW |
9 |
64,759,794 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8026:Dennd4a
|
UTSW |
9 |
64,780,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R8034:Dennd4a
|
UTSW |
9 |
64,795,850 (GRCm39) |
missense |
probably benign |
0.01 |
R8089:Dennd4a
|
UTSW |
9 |
64,756,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R8298:Dennd4a
|
UTSW |
9 |
64,814,157 (GRCm39) |
missense |
probably benign |
0.00 |
R8397:Dennd4a
|
UTSW |
9 |
64,796,391 (GRCm39) |
missense |
probably benign |
|
R8425:Dennd4a
|
UTSW |
9 |
64,746,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R8495:Dennd4a
|
UTSW |
9 |
64,794,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R8855:Dennd4a
|
UTSW |
9 |
64,819,672 (GRCm39) |
missense |
probably benign |
|
R9219:Dennd4a
|
UTSW |
9 |
64,796,376 (GRCm39) |
missense |
probably damaging |
0.96 |
R9275:Dennd4a
|
UTSW |
9 |
64,749,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R9376:Dennd4a
|
UTSW |
9 |
64,819,974 (GRCm39) |
missense |
probably benign |
0.00 |
R9485:Dennd4a
|
UTSW |
9 |
64,814,388 (GRCm39) |
nonsense |
probably null |
|
R9672:Dennd4a
|
UTSW |
9 |
64,800,640 (GRCm39) |
missense |
probably benign |
|
R9746:Dennd4a
|
UTSW |
9 |
64,801,793 (GRCm39) |
missense |
probably benign |
|
X0026:Dennd4a
|
UTSW |
9 |
64,804,602 (GRCm39) |
missense |
possibly damaging |
0.67 |
Z1088:Dennd4a
|
UTSW |
9 |
64,779,304 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- AGCTGGTATTGACCCCAATGCAATC -3'
(R):5'- AGGCTTCCAGAACCAGGTACTGTG -3'
Sequencing Primer
(F):5'- TTGACCCCAATGCAATCACTTATG -3'
(R):5'- gagccatctcatcagccc -3'
|
Posted On |
2014-05-14 |