Incidental Mutation 'R0032:Dennd4c'
ID |
59382 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dennd4c
|
Ensembl Gene |
ENSMUSG00000038024 |
Gene Name |
DENN domain containing 4C |
Synonyms |
1700065A05Rik |
MMRRC Submission |
038326-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R0032 (G1)
of strain
731
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
4 |
Chromosomal Location |
86666792-86768840 bp(+) (GRCm39) |
Type of Mutation |
critical splice donor site (2 bp from exon) |
DNA Base Change (assembly) |
T to C
at 86746387 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000123367
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000045512]
[ENSMUST00000082026]
[ENSMUST00000142837]
|
AlphaFold |
A6H8H2 |
Predicted Effect |
probably null
Transcript: ENSMUST00000045512
|
SMART Domains |
Protein: ENSMUSP00000039860 Gene: ENSMUSG00000038024
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 null
Transcript: ENSMUST00000082026
|
SMART Domains |
Protein: ENSMUSP00000080685 Gene: ENSMUSG00000038024
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 |
probably null
Transcript: ENSMUST00000142837
|
SMART Domains |
Protein: ENSMUSP00000123367 Gene: ENSMUSG00000038024
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 |
0.9500 |
Coding Region Coverage |
- 1x: 99.4%
- 3x: 98.9%
- 10x: 97.4%
- 20x: 94.8%
|
Validation Efficiency |
100% (89/89) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acss3 |
T |
A |
10: 106,959,156 (GRCm39) |
T97S |
probably benign |
Het |
Adcy1 |
T |
C |
11: 7,094,729 (GRCm39) |
S552P |
possibly damaging |
Het |
Arrb1 |
T |
C |
7: 99,231,472 (GRCm39) |
F9L |
probably damaging |
Het |
Auts2 |
G |
C |
5: 131,468,931 (GRCm39) |
D571E |
probably damaging |
Het |
C2cd3 |
T |
A |
7: 100,093,652 (GRCm39) |
|
probably benign |
Het |
Ccbe1 |
T |
G |
18: 66,424,723 (GRCm39) |
T35P |
possibly damaging |
Het |
Cct6b |
G |
T |
11: 82,644,469 (GRCm39) |
T202K |
possibly damaging |
Het |
Cd86 |
A |
T |
16: 36,441,235 (GRCm39) |
S77R |
probably damaging |
Het |
Cdk5rap3 |
A |
T |
11: 96,799,579 (GRCm39) |
L412Q |
possibly damaging |
Het |
Cdsn |
G |
A |
17: 35,866,452 (GRCm39) |
G327D |
probably damaging |
Het |
Cfap54 |
C |
T |
10: 92,768,559 (GRCm39) |
R188H |
probably benign |
Het |
Clca3a2 |
T |
A |
3: 144,522,494 (GRCm39) |
I176F |
probably benign |
Het |
Cop1 |
T |
C |
1: 159,152,606 (GRCm39) |
|
probably null |
Het |
Cpne8 |
T |
A |
15: 90,453,771 (GRCm39) |
|
probably benign |
Het |
Ctsg |
T |
A |
14: 56,339,196 (GRCm39) |
I21F |
probably damaging |
Het |
Cyp2j9 |
T |
G |
4: 96,457,043 (GRCm39) |
N476T |
possibly damaging |
Het |
Dcaf4 |
G |
A |
12: 83,582,762 (GRCm39) |
|
probably benign |
Het |
Des |
A |
G |
1: 75,338,810 (GRCm39) |
E195G |
possibly damaging |
Het |
Dicer1 |
A |
T |
12: 104,671,057 (GRCm39) |
L995* |
probably null |
Het |
Dnah10 |
A |
G |
5: 124,877,955 (GRCm39) |
K2623R |
possibly damaging |
Het |
Dnajc21 |
G |
T |
15: 10,461,963 (GRCm39) |
T146K |
probably benign |
Het |
Dnmbp |
A |
C |
19: 43,891,158 (GRCm39) |
L203R |
probably damaging |
Het |
Eif4g1 |
C |
T |
16: 20,504,648 (GRCm39) |
S829F |
probably damaging |
Het |
Enkur |
T |
C |
2: 21,194,115 (GRCm39) |
I153V |
probably benign |
Het |
Epb41l3 |
G |
T |
17: 69,517,379 (GRCm39) |
|
probably null |
Het |
Erf |
T |
C |
7: 24,944,500 (GRCm39) |
Y277C |
possibly damaging |
Het |
Fcsk |
G |
A |
8: 111,618,735 (GRCm39) |
T341M |
possibly damaging |
Het |
Fstl5 |
T |
A |
3: 76,555,742 (GRCm39) |
|
probably benign |
Het |
Galnt16 |
T |
C |
12: 80,639,243 (GRCm39) |
V419A |
probably damaging |
Het |
Gm10226 |
A |
G |
17: 21,910,963 (GRCm39) |
D66G |
possibly damaging |
Het |
Gm15821 |
T |
A |
17: 34,431,199 (GRCm39) |
|
probably benign |
Het |
Grm3 |
A |
G |
5: 9,561,452 (GRCm39) |
|
probably null |
Het |
Il11ra1 |
A |
G |
4: 41,768,187 (GRCm39) |
E366G |
probably damaging |
Het |
Impdh2 |
A |
G |
9: 108,438,860 (GRCm39) |
D71G |
probably damaging |
Het |
Ipo11 |
A |
C |
13: 106,970,971 (GRCm39) |
|
probably benign |
Het |
Ipo8 |
A |
G |
6: 148,712,209 (GRCm39) |
C261R |
probably damaging |
Het |
Iqsec3 |
T |
C |
6: 121,450,089 (GRCm39) |
D145G |
possibly damaging |
Het |
Itga11 |
T |
C |
9: 62,681,377 (GRCm39) |
F998L |
probably benign |
Het |
Junb |
T |
C |
8: 85,704,415 (GRCm39) |
H215R |
probably benign |
Het |
Kcnh4 |
C |
T |
11: 100,637,758 (GRCm39) |
G633E |
probably benign |
Het |
Kcnn3 |
CGCAGCAGCAGCAGCAGCAGCAG |
CGCAGCAGCAGCAGCAGCAG |
3: 89,427,972 (GRCm39) |
|
probably benign |
Het |
Krt73 |
T |
C |
15: 101,702,487 (GRCm39) |
S459G |
probably benign |
Het |
Krt74 |
T |
A |
15: 101,669,887 (GRCm39) |
|
noncoding transcript |
Het |
Meis3 |
C |
A |
7: 15,916,210 (GRCm39) |
|
probably benign |
Het |
Mlh3 |
A |
G |
12: 85,292,523 (GRCm39) |
|
probably benign |
Het |
Mroh2a |
GT |
GTT |
1: 88,183,888 (GRCm39) |
|
probably null |
Het |
Naip6 |
C |
T |
13: 100,439,745 (GRCm39) |
E341K |
probably benign |
Het |
Nbeal2 |
G |
T |
9: 110,466,936 (GRCm39) |
|
probably benign |
Het |
Nfx1 |
T |
A |
4: 41,015,321 (GRCm39) |
V842E |
probably benign |
Het |
Oma1 |
T |
A |
4: 103,223,209 (GRCm39) |
S465T |
possibly damaging |
Het |
Opa1 |
A |
T |
16: 29,433,887 (GRCm39) |
H574L |
probably damaging |
Het |
Or10al2 |
T |
A |
17: 37,983,378 (GRCm39) |
W155R |
probably damaging |
Het |
Or6c210 |
T |
A |
10: 129,496,269 (GRCm39) |
V198D |
probably benign |
Het |
Or8c13 |
A |
G |
9: 38,091,904 (GRCm39) |
C72R |
probably damaging |
Het |
Otog |
T |
A |
7: 45,937,637 (GRCm39) |
L1782* |
probably null |
Het |
Otog |
G |
A |
7: 45,953,655 (GRCm39) |
V2638M |
probably damaging |
Het |
Pcsk5 |
T |
C |
19: 17,542,179 (GRCm39) |
N804S |
possibly damaging |
Het |
Pde4a |
C |
A |
9: 21,112,728 (GRCm39) |
|
probably benign |
Het |
Pilra |
T |
A |
5: 137,829,527 (GRCm39) |
D179V |
probably damaging |
Het |
Piwil1 |
G |
A |
5: 128,820,344 (GRCm39) |
S247N |
probably benign |
Het |
Ppp2r1a |
G |
A |
17: 21,165,846 (GRCm39) |
|
probably benign |
Het |
Prss58 |
T |
G |
6: 40,872,633 (GRCm39) |
T158P |
probably benign |
Het |
Setmar |
T |
A |
6: 108,053,377 (GRCm39) |
C290* |
probably null |
Het |
Slc35e3 |
T |
C |
10: 117,580,837 (GRCm39) |
M156V |
probably benign |
Het |
Slc4a5 |
T |
A |
6: 83,250,139 (GRCm39) |
I509N |
probably damaging |
Het |
Slit2 |
G |
A |
5: 48,414,198 (GRCm39) |
R938Q |
probably damaging |
Het |
Snrpn |
A |
G |
7: 59,634,830 (GRCm39) |
Y168H |
probably damaging |
Het |
Sycn |
C |
T |
7: 28,240,717 (GRCm39) |
A128V |
possibly damaging |
Het |
Synm |
C |
A |
7: 67,383,675 (GRCm39) |
R1329M |
possibly damaging |
Het |
Syt8 |
T |
C |
7: 141,992,926 (GRCm39) |
V152A |
probably benign |
Het |
Tcp10a |
T |
C |
17: 7,604,306 (GRCm39) |
M247T |
probably benign |
Het |
Tjp2 |
A |
G |
19: 24,086,059 (GRCm39) |
L821S |
probably damaging |
Het |
Tppp2 |
G |
T |
14: 52,156,866 (GRCm39) |
R81L |
possibly damaging |
Het |
Trim34b |
A |
G |
7: 103,985,784 (GRCm39) |
D473G |
possibly damaging |
Het |
Trpc3 |
A |
G |
3: 36,698,405 (GRCm39) |
I618T |
probably damaging |
Het |
Trpm5 |
A |
T |
7: 142,638,978 (GRCm39) |
D264E |
probably damaging |
Het |
Tuba8 |
A |
T |
6: 121,202,863 (GRCm39) |
D392V |
probably benign |
Het |
Vmn1r50 |
C |
A |
6: 90,084,782 (GRCm39) |
P176T |
probably damaging |
Het |
Vmn1r76 |
T |
C |
7: 11,665,194 (GRCm39) |
I7V |
probably benign |
Het |
Vmn2r26 |
T |
A |
6: 124,016,858 (GRCm39) |
W441R |
possibly damaging |
Het |
Vmn2r57 |
T |
C |
7: 41,049,157 (GRCm39) |
|
probably null |
Het |
Zc3h4 |
T |
A |
7: 16,168,565 (GRCm39) |
D891E |
unknown |
Het |
Zfp120 |
A |
T |
2: 149,959,512 (GRCm39) |
V270E |
possibly damaging |
Het |
Znhit1 |
G |
C |
5: 137,013,901 (GRCm39) |
R8G |
possibly damaging |
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 |
|
R0092:Dennd4c
|
UTSW |
4 |
86,699,844 (GRCm39) |
missense |
probably damaging |
1.00 |
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'- AGCACCCCATCGAGGTATGTCACATC -3'
(R):5'- GGCCCCATTCCACAAATTCAGTTTCAG -3'
Sequencing Primer
(F):5'- CGAGGTATGTCACATCTTGAATG -3'
(R):5'- AACTGGTCTGGTTGACAATACG -3'
|
Posted On |
2013-07-11 |