Incidental Mutation 'R0092:Dennd4c'
| ID |
20267 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Dennd4c
|
| Ensembl Gene |
ENSMUSG00000038024 |
| Gene Name |
DENN domain containing 4C |
| Synonyms |
1700065A05Rik |
| MMRRC Submission |
038379-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R0092 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
(trace)
|
| Chromosome |
4 |
| Chromosomal Location |
86666792-86768840 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 86699844 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Phenylalanine to Isoleucine
at position 232
(F232I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000123367
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000045512]
[ENSMUST00000082026]
[ENSMUST00000142837]
|
| AlphaFold |
A6H8H2 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000045512
AA Change: F232I
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000039860
Gene: ENSMUSG00000038024
AA Change: F232I
| Domain | Start | End | E-Value | Type |
|---|
|
internal_repeat_1
|
43 |
91 |
2.15e-5 |
PROSPERO |
|
uDENN
|
168 |
275 |
3.96e-24 |
SMART |
|
DENN
|
307 |
491 |
7.16e-72 |
SMART |
|
dDENN
|
557 |
631 |
1.85e-24 |
SMART |
|
low complexity region
|
983 |
1001 |
N/A |
INTRINSIC |
|
low complexity region
|
1013 |
1025 |
N/A |
INTRINSIC |
|
low complexity region
|
1045 |
1052 |
N/A |
INTRINSIC |
|
low complexity region
|
1102 |
1113 |
N/A |
INTRINSIC |
|
low complexity region
|
1175 |
1186 |
N/A |
INTRINSIC |
|
low complexity region
|
1377 |
1392 |
N/A |
INTRINSIC |
|
low complexity region
|
1472 |
1486 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000082026
AA Change: F232I
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000080685
Gene: ENSMUSG00000038024
AA Change: F232I
| Domain | Start | End | E-Value | Type |
|---|
|
internal_repeat_1
|
43 |
91 |
3.19e-5 |
PROSPERO |
|
uDENN
|
168 |
275 |
3.96e-24 |
SMART |
|
DENN
|
307 |
491 |
7.16e-72 |
SMART |
|
dDENN
|
557 |
631 |
1.85e-24 |
SMART |
|
low complexity region
|
983 |
1001 |
N/A |
INTRINSIC |
|
low complexity region
|
1013 |
1025 |
N/A |
INTRINSIC |
|
low complexity region
|
1045 |
1052 |
N/A |
INTRINSIC |
|
low complexity region
|
1102 |
1113 |
N/A |
INTRINSIC |
|
low complexity region
|
1175 |
1186 |
N/A |
INTRINSIC |
|
low complexity region
|
1377 |
1392 |
N/A |
INTRINSIC |
|
low complexity region
|
1472 |
1486 |
N/A |
INTRINSIC |
|
low complexity region
|
1724 |
1739 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000128710
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000142837
AA Change: F232I
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000123367
Gene: ENSMUSG00000038024
AA Change: F232I
| Domain | Start | End | E-Value | Type |
|---|
|
internal_repeat_1
|
43 |
91 |
2.68e-5 |
PROSPERO |
|
uDENN
|
168 |
275 |
3.96e-24 |
SMART |
|
DENN
|
307 |
491 |
7.16e-72 |
SMART |
|
dDENN
|
557 |
631 |
1.85e-24 |
SMART |
|
low complexity region
|
934 |
952 |
N/A |
INTRINSIC |
|
low complexity region
|
964 |
976 |
N/A |
INTRINSIC |
|
low complexity region
|
996 |
1003 |
N/A |
INTRINSIC |
|
low complexity region
|
1053 |
1064 |
N/A |
INTRINSIC |
|
low complexity region
|
1126 |
1137 |
N/A |
INTRINSIC |
|
low complexity region
|
1328 |
1343 |
N/A |
INTRINSIC |
|
low complexity region
|
1423 |
1437 |
N/A |
INTRINSIC |
|
low complexity region
|
1675 |
1690 |
N/A |
INTRINSIC |
|
| Meta Mutation Damage Score |
0.2492 |
| Coding Region Coverage |
- 1x: 98.9%
- 3x: 97.9%
- 10x: 95.1%
- 20x: 88.6%
|
| Validation Efficiency |
99% (112/113) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 94 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcg2 |
T |
A |
6: 58,662,762 (GRCm39) |
S535T |
probably benign |
Het |
| Acad11 |
A |
T |
9: 103,967,540 (GRCm39) |
|
probably benign |
Het |
| Acadm |
A |
T |
3: 153,647,512 (GRCm39) |
|
probably benign |
Het |
| Acot12 |
T |
A |
13: 91,889,684 (GRCm39) |
M12K |
probably damaging |
Het |
| Actr2 |
A |
T |
11: 20,044,308 (GRCm39) |
N99K |
probably benign |
Het |
| Adam2 |
G |
A |
14: 66,291,336 (GRCm39) |
A314V |
probably damaging |
Het |
| Agl |
C |
T |
3: 116,587,453 (GRCm39) |
R34Q |
probably damaging |
Het |
| Agrn |
C |
T |
4: 156,263,410 (GRCm39) |
R338H |
probably damaging |
Het |
| AI661453 |
A |
G |
17: 47,778,440 (GRCm39) |
|
probably benign |
Het |
| Alpk3 |
A |
G |
7: 80,742,301 (GRCm39) |
D706G |
probably benign |
Het |
| Apbb1 |
T |
C |
7: 105,208,361 (GRCm39) |
E648G |
probably damaging |
Het |
| Astn2 |
C |
A |
4: 66,322,219 (GRCm39) |
A127S |
unknown |
Het |
| Asxl2 |
T |
C |
12: 3,546,313 (GRCm39) |
S366P |
probably benign |
Het |
| Bdh1 |
A |
T |
16: 31,266,380 (GRCm39) |
K92* |
probably null |
Het |
| Bltp1 |
A |
G |
3: 37,082,308 (GRCm39) |
D3790G |
probably benign |
Het |
| Cacna1g |
C |
T |
11: 94,348,090 (GRCm39) |
S666N |
probably damaging |
Het |
| Ces2b |
A |
G |
8: 105,563,144 (GRCm39) |
T361A |
possibly damaging |
Het |
| Col6a4 |
T |
A |
9: 105,890,513 (GRCm39) |
E1927V |
probably benign |
Het |
| Ctnnb1 |
T |
G |
9: 120,781,929 (GRCm39) |
I314S |
possibly damaging |
Het |
| Cyp2c66 |
T |
C |
19: 39,172,224 (GRCm39) |
|
probably benign |
Het |
| Dennd5a |
T |
C |
7: 109,499,013 (GRCm39) |
N950S |
possibly damaging |
Het |
| Dhx30 |
T |
C |
9: 109,914,078 (GRCm39) |
N14S |
possibly damaging |
Het |
| Dip2b |
T |
A |
15: 100,100,146 (GRCm39) |
V1004D |
probably damaging |
Het |
| Dnah1 |
A |
C |
14: 30,993,566 (GRCm39) |
S2872A |
probably benign |
Het |
| Dnajc10 |
T |
C |
2: 80,156,026 (GRCm39) |
V233A |
probably damaging |
Het |
| E230025N22Rik |
A |
G |
18: 36,822,277 (GRCm39) |
L162P |
probably damaging |
Het |
| Elmod3 |
T |
C |
6: 72,543,792 (GRCm39) |
D333G |
probably benign |
Het |
| Epb41l3 |
T |
A |
17: 69,593,745 (GRCm39) |
M846K |
probably damaging |
Het |
| Frem2 |
A |
G |
3: 53,497,217 (GRCm39) |
Y1766H |
probably benign |
Het |
| Fxr2 |
T |
C |
11: 69,532,972 (GRCm39) |
|
probably benign |
Het |
| Gmpr2 |
A |
G |
14: 55,915,402 (GRCm39) |
R258G |
probably benign |
Het |
| Helb |
T |
C |
10: 119,925,713 (GRCm39) |
Y888C |
probably damaging |
Het |
| Hephl1 |
TTCCAGATGTCC |
TTCC |
9: 15,001,899 (GRCm39) |
|
probably null |
Het |
| Hipk2 |
T |
C |
6: 38,720,164 (GRCm39) |
D482G |
probably damaging |
Het |
| Itgb4 |
G |
T |
11: 115,869,950 (GRCm39) |
R44L |
probably damaging |
Het |
| Itih1 |
T |
C |
14: 30,662,820 (GRCm39) |
|
probably benign |
Het |
| Kit |
T |
A |
5: 75,808,414 (GRCm39) |
S719R |
possibly damaging |
Het |
| Krt13 |
G |
A |
11: 100,012,258 (GRCm39) |
Q22* |
probably null |
Het |
| L3mbtl4 |
A |
C |
17: 68,732,698 (GRCm39) |
R59S |
probably benign |
Het |
| Lpp |
A |
G |
16: 24,580,352 (GRCm39) |
S23G |
probably benign |
Het |
| Magi3 |
G |
A |
3: 103,958,280 (GRCm39) |
Q602* |
probably null |
Het |
| Man2a1 |
A |
G |
17: 64,966,079 (GRCm39) |
|
probably benign |
Het |
| Muc5ac |
A |
G |
7: 141,372,367 (GRCm39) |
E2667G |
possibly damaging |
Het |
| Myef2l |
G |
A |
3: 10,153,633 (GRCm39) |
C134Y |
possibly damaging |
Het |
| Myo15b |
C |
G |
11: 115,753,812 (GRCm39) |
S842C |
possibly damaging |
Het |
| Naf1 |
T |
A |
8: 67,341,760 (GRCm39) |
S462T |
probably benign |
Het |
| Necab3 |
T |
C |
2: 154,400,659 (GRCm39) |
D34G |
possibly damaging |
Het |
| Nisch |
C |
A |
14: 30,913,410 (GRCm39) |
|
probably benign |
Het |
| Nlrc5 |
T |
C |
8: 95,216,222 (GRCm39) |
|
probably benign |
Het |
| Nmt1 |
T |
C |
11: 102,937,319 (GRCm39) |
F119L |
probably damaging |
Het |
| Nod1 |
T |
G |
6: 54,921,526 (GRCm39) |
D264A |
probably damaging |
Het |
| Nol8 |
C |
T |
13: 49,815,923 (GRCm39) |
A677V |
possibly damaging |
Het |
| Nt5e |
T |
A |
9: 88,252,338 (GRCm39) |
F567I |
probably benign |
Het |
| Obscn |
A |
T |
11: 58,942,073 (GRCm39) |
M4434K |
possibly damaging |
Het |
| Opa1 |
A |
T |
16: 29,444,412 (GRCm39) |
D866V |
probably damaging |
Het |
| Or10a3m |
T |
C |
7: 108,313,031 (GRCm39) |
V145A |
probably benign |
Het |
| Or10al3 |
T |
G |
17: 38,011,696 (GRCm39) |
L45R |
probably damaging |
Het |
| Or10p1 |
A |
G |
10: 129,444,090 (GRCm39) |
S87P |
probably damaging |
Het |
| Or1j21 |
A |
G |
2: 36,683,508 (GRCm39) |
T87A |
probably benign |
Het |
| Or51ai2 |
T |
C |
7: 103,586,934 (GRCm39) |
S116P |
probably damaging |
Het |
| Otop1 |
T |
A |
5: 38,457,174 (GRCm39) |
V311E |
probably damaging |
Het |
| Pcsk2 |
A |
G |
2: 143,642,944 (GRCm39) |
D407G |
probably damaging |
Het |
| Pdcd1 |
A |
G |
1: 93,980,149 (GRCm39) |
W23R |
possibly damaging |
Het |
| Pigp |
A |
G |
16: 94,166,321 (GRCm39) |
V129A |
probably damaging |
Het |
| Pik3r5 |
A |
G |
11: 68,383,629 (GRCm39) |
R483G |
probably benign |
Het |
| Pink1 |
A |
G |
4: 138,047,309 (GRCm39) |
V225A |
probably benign |
Het |
| Plcl1 |
C |
G |
1: 55,735,924 (GRCm39) |
Q422E |
probably damaging |
Het |
| Plec |
T |
C |
15: 76,067,943 (GRCm39) |
E1222G |
probably benign |
Het |
| Polr1a |
T |
C |
6: 71,944,439 (GRCm39) |
|
probably benign |
Het |
| Prokr2 |
C |
T |
2: 132,215,517 (GRCm39) |
V154M |
probably damaging |
Het |
| Rasgrp4 |
A |
G |
7: 28,844,557 (GRCm39) |
R280G |
possibly damaging |
Het |
| Rmnd5b |
T |
C |
11: 51,520,419 (GRCm39) |
E8G |
possibly damaging |
Het |
| Sbf2 |
T |
A |
7: 109,920,013 (GRCm39) |
|
probably benign |
Het |
| Sec23b |
A |
G |
2: 144,408,830 (GRCm39) |
M172V |
probably benign |
Het |
| Setx |
T |
C |
2: 29,036,305 (GRCm39) |
V930A |
probably benign |
Het |
| Sft2d2 |
G |
A |
1: 165,006,829 (GRCm39) |
A159V |
possibly damaging |
Het |
| Sh3gl1 |
G |
T |
17: 56,325,088 (GRCm39) |
R250S |
probably benign |
Het |
| Skor1 |
C |
A |
9: 63,053,277 (GRCm39) |
D231Y |
probably damaging |
Het |
| Slc24a1 |
T |
G |
9: 64,856,034 (GRCm39) |
E291A |
unknown |
Het |
| Slc28a2b |
G |
T |
2: 122,348,078 (GRCm39) |
|
probably benign |
Het |
| Smc1b |
A |
T |
15: 84,951,925 (GRCm39) |
|
probably benign |
Het |
| Tbccd1 |
A |
T |
16: 22,644,844 (GRCm39) |
N177K |
possibly damaging |
Het |
| Tdp1 |
T |
A |
12: 99,921,248 (GRCm39) |
Y595N |
probably damaging |
Het |
| Tle5 |
G |
A |
10: 81,397,054 (GRCm39) |
G10D |
possibly damaging |
Het |
| Tmem108 |
T |
C |
9: 103,366,504 (GRCm39) |
K496E |
possibly damaging |
Het |
| Tmprss7 |
T |
C |
16: 45,487,959 (GRCm39) |
D490G |
probably damaging |
Het |
| Tnrc6b |
A |
T |
15: 80,802,729 (GRCm39) |
N1511Y |
probably damaging |
Het |
| Top2b |
G |
A |
14: 16,409,263 (GRCm38) |
R802Q |
probably damaging |
Het |
| Trip10 |
A |
T |
17: 57,557,798 (GRCm39) |
K27N |
possibly damaging |
Het |
| Txlnb |
A |
G |
10: 17,718,503 (GRCm39) |
N445D |
possibly damaging |
Het |
| Txnrd1 |
T |
A |
10: 82,715,636 (GRCm39) |
I159N |
probably damaging |
Het |
| Ulk1 |
C |
A |
5: 110,944,193 (GRCm39) |
A164S |
probably null |
Het |
| Vmn2r83 |
T |
C |
10: 79,327,798 (GRCm39) |
V802A |
probably damaging |
Het |
| Zbtb4 |
A |
G |
11: 69,670,177 (GRCm39) |
I967V |
probably benign |
Het |
|
| Other mutations in Dennd4c |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01309:Dennd4c
|
APN |
4 |
86,723,724 (GRCm39) |
splice site |
probably benign |
|
|
IGL01810:Dennd4c
|
APN |
4 |
86,717,788 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
IGL02203:Dennd4c
|
APN |
4 |
86,721,173 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02217:Dennd4c
|
APN |
4 |
86,732,036 (GRCm39) |
missense |
probably benign |
|
|
IGL02236:Dennd4c
|
APN |
4 |
86,725,672 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
IGL02256:Dennd4c
|
APN |
4 |
86,717,778 (GRCm39) |
missense |
probably damaging |
0.96 |
|
IGL02396:Dennd4c
|
APN |
4 |
86,743,237 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02523:Dennd4c
|
APN |
4 |
86,692,490 (GRCm39) |
unclassified |
probably benign |
|
|
IGL02615:Dennd4c
|
APN |
4 |
86,739,704 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03069:Dennd4c
|
APN |
4 |
86,692,674 (GRCm39) |
nonsense |
probably null |
|
|
IGL03116:Dennd4c
|
APN |
4 |
86,707,057 (GRCm39) |
splice site |
probably benign |
|
|
IGL03117:Dennd4c
|
APN |
4 |
86,696,140 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL03273:Dennd4c
|
APN |
4 |
86,696,033 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03329:Dennd4c
|
APN |
4 |
86,696,113 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03365:Dennd4c
|
APN |
4 |
86,725,663 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
PIT4486001:Dennd4c
|
UTSW |
4 |
86,717,701 (GRCm39) |
nonsense |
probably null |
|
|
R0010:Dennd4c
|
UTSW |
4 |
86,699,814 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0032:Dennd4c
|
UTSW |
4 |
86,746,387 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0032:Dennd4c
|
UTSW |
4 |
86,746,387 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0103:Dennd4c
|
UTSW |
4 |
86,730,683 (GRCm39) |
missense |
probably benign |
0.07 |
|
R0103:Dennd4c
|
UTSW |
4 |
86,730,683 (GRCm39) |
missense |
probably benign |
0.07 |
|
R0511:Dennd4c
|
UTSW |
4 |
86,744,259 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0515:Dennd4c
|
UTSW |
4 |
86,731,703 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R0578:Dennd4c
|
UTSW |
4 |
86,730,659 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0759:Dennd4c
|
UTSW |
4 |
86,707,066 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0784:Dennd4c
|
UTSW |
4 |
86,763,145 (GRCm39) |
missense |
probably benign |
0.37 |
|
R1156:Dennd4c
|
UTSW |
4 |
86,725,703 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1370:Dennd4c
|
UTSW |
4 |
86,729,747 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1381:Dennd4c
|
UTSW |
4 |
86,692,769 (GRCm39) |
missense |
probably benign |
0.24 |
|
R1569:Dennd4c
|
UTSW |
4 |
86,704,331 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R1747:Dennd4c
|
UTSW |
4 |
86,725,675 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1764:Dennd4c
|
UTSW |
4 |
86,721,247 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1838:Dennd4c
|
UTSW |
4 |
86,743,415 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1997:Dennd4c
|
UTSW |
4 |
86,755,634 (GRCm39) |
missense |
probably benign |
|
|
R2244:Dennd4c
|
UTSW |
4 |
86,692,780 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2348:Dennd4c
|
UTSW |
4 |
86,729,764 (GRCm39) |
missense |
probably benign |
0.04 |
|
R2968:Dennd4c
|
UTSW |
4 |
86,699,881 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R3033:Dennd4c
|
UTSW |
4 |
86,743,557 (GRCm39) |
small deletion |
probably benign |
|
|
R3401:Dennd4c
|
UTSW |
4 |
86,692,780 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3402:Dennd4c
|
UTSW |
4 |
86,692,780 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3403:Dennd4c
|
UTSW |
4 |
86,692,780 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3855:Dennd4c
|
UTSW |
4 |
86,698,084 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3939:Dennd4c
|
UTSW |
4 |
86,692,517 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4164:Dennd4c
|
UTSW |
4 |
86,725,764 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4384:Dennd4c
|
UTSW |
4 |
86,729,687 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4435:Dennd4c
|
UTSW |
4 |
86,716,312 (GRCm39) |
missense |
probably benign |
0.44 |
|
R4788:Dennd4c
|
UTSW |
4 |
86,738,200 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4801:Dennd4c
|
UTSW |
4 |
86,738,121 (GRCm39) |
nonsense |
probably null |
|
|
R4802:Dennd4c
|
UTSW |
4 |
86,738,121 (GRCm39) |
nonsense |
probably null |
|
|
R4818:Dennd4c
|
UTSW |
4 |
86,743,511 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4923:Dennd4c
|
UTSW |
4 |
86,725,775 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4958:Dennd4c
|
UTSW |
4 |
86,699,916 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5025:Dennd4c
|
UTSW |
4 |
86,713,536 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5434:Dennd4c
|
UTSW |
4 |
86,729,693 (GRCm39) |
missense |
probably benign |
0.10 |
|
R5662:Dennd4c
|
UTSW |
4 |
86,713,525 (GRCm39) |
missense |
probably benign |
0.13 |
|
R5802:Dennd4c
|
UTSW |
4 |
86,729,690 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5849:Dennd4c
|
UTSW |
4 |
86,744,223 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
R5861:Dennd4c
|
UTSW |
4 |
86,709,589 (GRCm39) |
missense |
probably benign |
0.30 |
|
R5970:Dennd4c
|
UTSW |
4 |
86,743,749 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6163:Dennd4c
|
UTSW |
4 |
86,723,828 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R6356:Dennd4c
|
UTSW |
4 |
86,743,686 (GRCm39) |
missense |
probably benign |
|
|
R6661:Dennd4c
|
UTSW |
4 |
86,717,626 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R6855:Dennd4c
|
UTSW |
4 |
86,754,694 (GRCm39) |
missense |
probably benign |
|
|
R6983:Dennd4c
|
UTSW |
4 |
86,717,730 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7035:Dennd4c
|
UTSW |
4 |
86,730,574 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7126:Dennd4c
|
UTSW |
4 |
86,725,667 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7185:Dennd4c
|
UTSW |
4 |
86,729,687 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7212:Dennd4c
|
UTSW |
4 |
86,721,228 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7324:Dennd4c
|
UTSW |
4 |
86,747,975 (GRCm39) |
missense |
unknown |
|
|
R7329:Dennd4c
|
UTSW |
4 |
86,698,111 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R7329:Dennd4c
|
UTSW |
4 |
86,759,318 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7466:Dennd4c
|
UTSW |
4 |
86,692,568 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7479:Dennd4c
|
UTSW |
4 |
86,717,590 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7538:Dennd4c
|
UTSW |
4 |
86,692,753 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7599:Dennd4c
|
UTSW |
4 |
86,729,849 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7688:Dennd4c
|
UTSW |
4 |
86,713,377 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7725:Dennd4c
|
UTSW |
4 |
86,704,330 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7751:Dennd4c
|
UTSW |
4 |
86,747,179 (GRCm39) |
missense |
probably benign |
0.05 |
|
R7790:Dennd4c
|
UTSW |
4 |
86,717,754 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8056:Dennd4c
|
UTSW |
4 |
86,763,213 (GRCm39) |
missense |
probably null |
0.71 |
|
R8307:Dennd4c
|
UTSW |
4 |
86,744,109 (GRCm39) |
missense |
probably benign |
0.12 |
|
R8494:Dennd4c
|
UTSW |
4 |
86,759,312 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8531:Dennd4c
|
UTSW |
4 |
86,744,319 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9014:Dennd4c
|
UTSW |
4 |
86,754,666 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9014:Dennd4c
|
UTSW |
4 |
86,739,702 (GRCm39) |
missense |
probably benign |
0.07 |
|
R9017:Dennd4c
|
UTSW |
4 |
86,743,349 (GRCm39) |
missense |
probably benign |
0.33 |
|
R9142:Dennd4c
|
UTSW |
4 |
86,755,637 (GRCm39) |
missense |
probably benign |
0.32 |
|
R9224:Dennd4c
|
UTSW |
4 |
86,738,170 (GRCm39) |
nonsense |
probably null |
|
|
R9570:Dennd4c
|
UTSW |
4 |
86,747,208 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R9644:Dennd4c
|
UTSW |
4 |
86,713,363 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9649:Dennd4c
|
UTSW |
4 |
86,743,160 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9658:Dennd4c
|
UTSW |
4 |
86,754,625 (GRCm39) |
nonsense |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- CGTGTAGCTTTCAGCACTGTCTTACATT -3'
(R):5'- TCAACCTGACCCAAAGTCTGCTAATTC -3'
Sequencing Primer
(F):5'- ttctccatctaatggaaccctg -3'
(R):5'- GACCCAAAGTCTGCTAATTCTATCTG -3'
|
| Posted On |
2013-04-11 |
Incidental Mutation