Incidental Mutation 'R5268:Dennd2b'
ID |
399933 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dennd2b
|
Ensembl Gene |
ENSMUSG00000031024 |
Gene Name |
DENN domain containing 2B |
Synonyms |
Denn2b, 2610305K15Rik, St5, 2010004M01Rik |
MMRRC Submission |
042860-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.390)
|
Stock # |
R5268 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
7 |
Chromosomal Location |
109123118-109302812 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 109156519 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Leucine to Proline
at position 77
(L77P)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000146747
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000077909]
[ENSMUST00000079282]
[ENSMUST00000084738]
[ENSMUST00000168005]
[ENSMUST00000207394]
[ENSMUST00000207745]
[ENSMUST00000208583]
|
AlphaFold |
Q924W7 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000077909
AA Change: L77P
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000077067 Gene: ENSMUSG00000031024 AA Change: L77P
Domain | Start | End | E-Value | Type |
low complexity region
|
28 |
46 |
N/A |
INTRINSIC |
low complexity region
|
197 |
213 |
N/A |
INTRINSIC |
low complexity region
|
314 |
326 |
N/A |
INTRINSIC |
low complexity region
|
327 |
348 |
N/A |
INTRINSIC |
low complexity region
|
365 |
379 |
N/A |
INTRINSIC |
low complexity region
|
407 |
426 |
N/A |
INTRINSIC |
low complexity region
|
577 |
609 |
N/A |
INTRINSIC |
low complexity region
|
624 |
638 |
N/A |
INTRINSIC |
low complexity region
|
645 |
656 |
N/A |
INTRINSIC |
uDENN
|
690 |
781 |
1.16e-30 |
SMART |
DENN
|
788 |
972 |
7.84e-78 |
SMART |
low complexity region
|
1007 |
1014 |
N/A |
INTRINSIC |
dDENN
|
1019 |
1086 |
3.12e-22 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000079282
AA Change: L77P
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000078264 Gene: ENSMUSG00000031024 AA Change: L77P
Domain | Start | End | E-Value | Type |
low complexity region
|
28 |
46 |
N/A |
INTRINSIC |
low complexity region
|
197 |
213 |
N/A |
INTRINSIC |
low complexity region
|
314 |
326 |
N/A |
INTRINSIC |
low complexity region
|
327 |
348 |
N/A |
INTRINSIC |
low complexity region
|
365 |
379 |
N/A |
INTRINSIC |
low complexity region
|
407 |
426 |
N/A |
INTRINSIC |
low complexity region
|
577 |
609 |
N/A |
INTRINSIC |
low complexity region
|
624 |
638 |
N/A |
INTRINSIC |
low complexity region
|
645 |
656 |
N/A |
INTRINSIC |
uDENN
|
690 |
781 |
1.16e-30 |
SMART |
DENN
|
788 |
972 |
7.84e-78 |
SMART |
low complexity region
|
1007 |
1014 |
N/A |
INTRINSIC |
dDENN
|
1019 |
1086 |
3.12e-22 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000084738
|
SMART Domains |
Protein: ENSMUSP00000081789 Gene: ENSMUSG00000031024
Domain | Start | End | E-Value | Type |
low complexity region
|
160 |
192 |
N/A |
INTRINSIC |
low complexity region
|
207 |
221 |
N/A |
INTRINSIC |
low complexity region
|
228 |
239 |
N/A |
INTRINSIC |
uDENN
|
273 |
364 |
1.16e-30 |
SMART |
DENN
|
371 |
555 |
7.84e-78 |
SMART |
low complexity region
|
590 |
597 |
N/A |
INTRINSIC |
dDENN
|
602 |
669 |
3.12e-22 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000168005
|
SMART Domains |
Protein: ENSMUSP00000130119 Gene: ENSMUSG00000031024
Domain | Start | End | E-Value | Type |
low complexity region
|
160 |
192 |
N/A |
INTRINSIC |
low complexity region
|
207 |
221 |
N/A |
INTRINSIC |
low complexity region
|
228 |
239 |
N/A |
INTRINSIC |
uDENN
|
273 |
364 |
1.16e-30 |
SMART |
DENN
|
371 |
555 |
7.84e-78 |
SMART |
low complexity region
|
590 |
597 |
N/A |
INTRINSIC |
dDENN
|
602 |
669 |
3.12e-22 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000207394
AA Change: L77P
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000207745
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000208583
AA Change: L77P
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000208981
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000208557
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 97.0%
- 20x: 94.9%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene was identified by its ability to suppress the tumorigenicity of Hela cells in nude mice. The protein encoded by this gene contains a C-terminal region that shares similarity with the Rab 3 family of small GTP binding proteins. This protein preferentially binds to the SH3 domain of c-Abl kinase, and acts as a regulator of MAPK1/ERK2 kinase, which may contribute to its ability to reduce the tumorigenic phenotype in cells. Three alternatively spliced transcript variants of this gene encoding distinct isoforms are identified. [provided by RefSeq, Jul 2008]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm2 |
A |
G |
3: 59,659,444 (GRCm39) |
E299G |
probably damaging |
Het |
Adamtsl4 |
C |
A |
3: 95,587,473 (GRCm39) |
R701L |
probably damaging |
Het |
Adgrf5 |
T |
C |
17: 43,761,890 (GRCm39) |
V1195A |
probably damaging |
Het |
Agpat5 |
A |
G |
8: 18,931,878 (GRCm39) |
T333A |
possibly damaging |
Het |
Aspm |
G |
T |
1: 139,392,033 (GRCm39) |
G795C |
probably damaging |
Het |
Car4 |
C |
A |
11: 84,856,626 (GRCm39) |
Q305K |
probably benign |
Het |
Catsperg1 |
T |
C |
7: 28,894,672 (GRCm39) |
N612S |
probably benign |
Het |
Cdc5l |
G |
A |
17: 45,726,511 (GRCm39) |
R354W |
probably damaging |
Het |
Cdh9 |
G |
A |
15: 16,851,099 (GRCm39) |
V623I |
probably benign |
Het |
Cfap65 |
A |
G |
1: 74,964,061 (GRCm39) |
V629A |
probably benign |
Het |
Chd1 |
G |
A |
17: 15,956,005 (GRCm39) |
V535I |
probably damaging |
Het |
Col12a1 |
A |
G |
9: 79,585,329 (GRCm39) |
V1316A |
probably damaging |
Het |
Col6a3 |
A |
T |
1: 90,712,965 (GRCm39) |
D1721E |
unknown |
Het |
Cop1 |
T |
A |
1: 159,154,734 (GRCm39) |
F647L |
probably damaging |
Het |
Corin |
A |
C |
5: 72,500,362 (GRCm39) |
S421A |
probably damaging |
Het |
Crb2 |
T |
C |
2: 37,680,833 (GRCm39) |
V587A |
probably damaging |
Het |
Ctc1 |
T |
A |
11: 68,920,636 (GRCm39) |
V646E |
possibly damaging |
Het |
Cyp2a12 |
A |
T |
7: 26,730,643 (GRCm39) |
M203L |
probably benign |
Het |
Dcdc2c |
T |
A |
12: 28,566,656 (GRCm39) |
K336M |
possibly damaging |
Het |
Ddx39a |
G |
A |
8: 84,448,950 (GRCm39) |
R275H |
probably benign |
Het |
Des |
A |
G |
1: 75,339,572 (GRCm39) |
N310S |
possibly damaging |
Het |
Dlk1 |
C |
A |
12: 109,425,764 (GRCm39) |
S212R |
probably benign |
Het |
Dnajc5b |
A |
G |
3: 19,633,224 (GRCm39) |
E149G |
probably benign |
Het |
Dpep1 |
A |
T |
8: 123,920,828 (GRCm39) |
I3F |
probably benign |
Het |
Eml6 |
T |
A |
11: 29,753,108 (GRCm39) |
R934S |
probably benign |
Het |
Ercc6l2 |
T |
C |
13: 64,016,925 (GRCm39) |
L676P |
possibly damaging |
Het |
Fkbpl |
G |
A |
17: 34,864,303 (GRCm39) |
A24T |
probably benign |
Het |
Frem2 |
T |
A |
3: 53,560,575 (GRCm39) |
I1311F |
probably damaging |
Het |
Gldc |
T |
A |
19: 30,123,125 (GRCm39) |
M257L |
probably damaging |
Het |
Gm8674 |
T |
G |
13: 50,055,390 (GRCm39) |
|
noncoding transcript |
Het |
Gnai3 |
C |
T |
3: 108,030,857 (GRCm39) |
|
probably null |
Het |
Gtf3a |
A |
G |
5: 146,891,965 (GRCm39) |
D300G |
probably damaging |
Het |
Haus3 |
A |
T |
5: 34,323,449 (GRCm39) |
V387D |
probably damaging |
Het |
Hpf1 |
T |
A |
8: 61,346,768 (GRCm39) |
F28I |
possibly damaging |
Het |
Iars1 |
A |
G |
13: 49,843,967 (GRCm39) |
D147G |
probably damaging |
Het |
Ibtk |
A |
T |
9: 85,625,743 (GRCm39) |
D2E |
probably benign |
Het |
Ift140 |
T |
A |
17: 25,239,601 (GRCm39) |
I86K |
possibly damaging |
Het |
Igf2bp2 |
T |
A |
16: 21,898,241 (GRCm39) |
I235F |
probably damaging |
Het |
Ighv3-8 |
G |
T |
12: 114,286,252 (GRCm39) |
A30E |
probably benign |
Het |
Kcnq5 |
T |
A |
1: 21,575,949 (GRCm39) |
T252S |
probably damaging |
Het |
Lrrc4b |
A |
T |
7: 44,110,787 (GRCm39) |
N220Y |
probably damaging |
Het |
Ltbr |
G |
A |
6: 125,289,757 (GRCm39) |
R146W |
probably damaging |
Het |
Mamdc4 |
T |
C |
2: 25,454,702 (GRCm39) |
T1037A |
possibly damaging |
Het |
Mbd5 |
A |
T |
2: 49,162,106 (GRCm39) |
I863F |
possibly damaging |
Het |
Muc4 |
T |
A |
16: 32,570,484 (GRCm39) |
S515T |
possibly damaging |
Het |
Mylk4 |
T |
A |
13: 32,892,864 (GRCm39) |
|
probably null |
Het |
Neu4 |
G |
A |
1: 93,952,669 (GRCm39) |
R346H |
probably benign |
Het |
Nxpe5 |
T |
A |
5: 138,238,200 (GRCm39) |
Y253* |
probably null |
Het |
Olfml2b |
A |
T |
1: 170,477,330 (GRCm39) |
E155V |
probably damaging |
Het |
Or14a258 |
A |
G |
7: 86,034,867 (GRCm39) |
*334Q |
probably null |
Het |
Or6a2 |
T |
A |
7: 106,600,111 (GRCm39) |
N319Y |
probably benign |
Het |
Or8a1b |
T |
A |
9: 37,623,300 (GRCm39) |
I92F |
probably damaging |
Het |
Pamr1 |
G |
A |
2: 102,417,029 (GRCm39) |
A114T |
probably damaging |
Het |
Pdzd2 |
T |
A |
15: 12,592,263 (GRCm39) |
N127I |
probably damaging |
Het |
Pglyrp4 |
C |
T |
3: 90,634,271 (GRCm39) |
L5F |
probably damaging |
Het |
Plce1 |
T |
A |
19: 38,747,279 (GRCm39) |
S1667T |
possibly damaging |
Het |
Qser1 |
A |
T |
2: 104,617,776 (GRCm39) |
V1012E |
possibly damaging |
Het |
R3hdm4 |
C |
T |
10: 79,748,292 (GRCm39) |
E162K |
possibly damaging |
Het |
Rcn3 |
A |
T |
7: 44,736,203 (GRCm39) |
D168E |
probably damaging |
Het |
Rdh1 |
T |
G |
10: 127,595,832 (GRCm39) |
V9G |
possibly damaging |
Het |
Rin2 |
A |
G |
2: 145,686,680 (GRCm39) |
T70A |
probably benign |
Het |
Rnf207 |
T |
C |
4: 152,398,346 (GRCm39) |
D276G |
probably damaging |
Het |
Rtel1 |
C |
T |
2: 180,982,354 (GRCm39) |
S368L |
probably benign |
Het |
Slc15a5 |
C |
A |
6: 138,056,751 (GRCm39) |
C55F |
probably damaging |
Het |
Slc36a4 |
T |
C |
9: 15,638,212 (GRCm39) |
F213L |
possibly damaging |
Het |
Snhg16 |
G |
T |
11: 116,562,582 (GRCm39) |
M18I |
probably benign |
Het |
Spata25 |
C |
T |
2: 164,669,954 (GRCm39) |
G19D |
probably damaging |
Het |
Tas2r102 |
A |
T |
6: 132,739,360 (GRCm39) |
L89F |
probably damaging |
Het |
Tbc1d1 |
A |
G |
5: 64,481,910 (GRCm39) |
K704E |
probably damaging |
Het |
Tert |
T |
G |
13: 73,775,473 (GRCm39) |
S75A |
probably damaging |
Het |
Tiparp |
T |
A |
3: 65,454,986 (GRCm39) |
L195Q |
possibly damaging |
Het |
Tmem205 |
A |
C |
9: 21,837,380 (GRCm39) |
Y57* |
probably null |
Het |
Tomm22 |
A |
G |
15: 79,555,428 (GRCm39) |
R5G |
probably benign |
Het |
Trav10 |
A |
T |
14: 53,743,515 (GRCm39) |
S39C |
probably benign |
Het |
Trav6-2 |
T |
A |
14: 52,905,205 (GRCm39) |
N75K |
probably benign |
Het |
Trio |
T |
C |
15: 27,748,372 (GRCm39) |
S2427G |
probably benign |
Het |
Ttc41 |
C |
A |
10: 86,580,342 (GRCm39) |
H763N |
possibly damaging |
Het |
Usp29 |
A |
T |
7: 6,964,583 (GRCm39) |
N142I |
probably damaging |
Het |
Vmn1r204 |
G |
T |
13: 22,740,912 (GRCm39) |
W181L |
probably damaging |
Het |
Vmn2r76 |
G |
A |
7: 85,875,267 (GRCm39) |
T570M |
probably damaging |
Het |
Wdr90 |
A |
G |
17: 26,069,819 (GRCm39) |
L1173P |
probably damaging |
Het |
Wnt9a |
T |
A |
11: 59,219,396 (GRCm39) |
C141S |
probably damaging |
Het |
Zfp462 |
A |
T |
4: 55,012,299 (GRCm39) |
I1422L |
probably benign |
Het |
|
Other mutations in Dennd2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00493:Dennd2b
|
APN |
7 |
109,126,915 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01132:Dennd2b
|
APN |
7 |
109,169,212 (GRCm39) |
splice site |
probably null |
|
IGL01288:Dennd2b
|
APN |
7 |
109,139,029 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01645:Dennd2b
|
APN |
7 |
109,126,841 (GRCm39) |
nonsense |
probably null |
|
IGL01714:Dennd2b
|
APN |
7 |
109,169,269 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02021:Dennd2b
|
APN |
7 |
109,156,579 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02302:Dennd2b
|
APN |
7 |
109,124,538 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02496:Dennd2b
|
APN |
7 |
109,155,442 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02795:Dennd2b
|
APN |
7 |
109,155,571 (GRCm39) |
missense |
probably damaging |
1.00 |
Bucolic
|
UTSW |
7 |
109,124,755 (GRCm39) |
nonsense |
probably null |
|
Halcyon
|
UTSW |
7 |
109,156,000 (GRCm39) |
nonsense |
probably null |
|
FR4340:Dennd2b
|
UTSW |
7 |
109,156,128 (GRCm39) |
unclassified |
probably benign |
|
FR4737:Dennd2b
|
UTSW |
7 |
109,156,128 (GRCm39) |
unclassified |
probably benign |
|
PIT4466001:Dennd2b
|
UTSW |
7 |
109,130,337 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4469001:Dennd2b
|
UTSW |
7 |
109,130,337 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4472001:Dennd2b
|
UTSW |
7 |
109,130,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R0024:Dennd2b
|
UTSW |
7 |
109,123,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R0124:Dennd2b
|
UTSW |
7 |
109,141,718 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0125:Dennd2b
|
UTSW |
7 |
109,155,545 (GRCm39) |
missense |
probably benign |
0.19 |
R0365:Dennd2b
|
UTSW |
7 |
109,138,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R0491:Dennd2b
|
UTSW |
7 |
109,156,411 (GRCm39) |
missense |
probably benign |
0.45 |
R0534:Dennd2b
|
UTSW |
7 |
109,140,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R0662:Dennd2b
|
UTSW |
7 |
109,156,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R0743:Dennd2b
|
UTSW |
7 |
109,156,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R0772:Dennd2b
|
UTSW |
7 |
109,141,527 (GRCm39) |
splice site |
probably null |
|
R0774:Dennd2b
|
UTSW |
7 |
109,141,527 (GRCm39) |
splice site |
probably null |
|
R0787:Dennd2b
|
UTSW |
7 |
109,124,827 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0884:Dennd2b
|
UTSW |
7 |
109,156,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R1518:Dennd2b
|
UTSW |
7 |
109,156,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R1908:Dennd2b
|
UTSW |
7 |
109,124,533 (GRCm39) |
nonsense |
probably null |
|
R1909:Dennd2b
|
UTSW |
7 |
109,124,533 (GRCm39) |
nonsense |
probably null |
|
R2232:Dennd2b
|
UTSW |
7 |
109,156,414 (GRCm39) |
missense |
probably benign |
|
R2358:Dennd2b
|
UTSW |
7 |
109,155,653 (GRCm39) |
missense |
probably benign |
0.01 |
R2847:Dennd2b
|
UTSW |
7 |
109,124,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R2869:Dennd2b
|
UTSW |
7 |
109,156,637 (GRCm39) |
missense |
probably benign |
0.01 |
R2869:Dennd2b
|
UTSW |
7 |
109,156,637 (GRCm39) |
missense |
probably benign |
0.01 |
R2870:Dennd2b
|
UTSW |
7 |
109,156,637 (GRCm39) |
missense |
probably benign |
0.01 |
R2870:Dennd2b
|
UTSW |
7 |
109,156,637 (GRCm39) |
missense |
probably benign |
0.01 |
R2871:Dennd2b
|
UTSW |
7 |
109,156,637 (GRCm39) |
missense |
probably benign |
0.01 |
R2871:Dennd2b
|
UTSW |
7 |
109,156,637 (GRCm39) |
missense |
probably benign |
0.01 |
R2873:Dennd2b
|
UTSW |
7 |
109,156,637 (GRCm39) |
missense |
probably benign |
0.01 |
R2874:Dennd2b
|
UTSW |
7 |
109,156,637 (GRCm39) |
missense |
probably benign |
0.01 |
R4534:Dennd2b
|
UTSW |
7 |
109,130,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R4536:Dennd2b
|
UTSW |
7 |
109,130,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R4559:Dennd2b
|
UTSW |
7 |
109,124,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R4798:Dennd2b
|
UTSW |
7 |
109,156,240 (GRCm39) |
missense |
probably damaging |
0.99 |
R4846:Dennd2b
|
UTSW |
7 |
109,156,043 (GRCm39) |
nonsense |
probably null |
|
R5110:Dennd2b
|
UTSW |
7 |
109,141,697 (GRCm39) |
missense |
probably benign |
0.02 |
R5181:Dennd2b
|
UTSW |
7 |
109,155,997 (GRCm39) |
missense |
probably benign |
|
R5403:Dennd2b
|
UTSW |
7 |
109,156,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R5836:Dennd2b
|
UTSW |
7 |
109,140,552 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5932:Dennd2b
|
UTSW |
7 |
109,169,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R5937:Dennd2b
|
UTSW |
7 |
109,156,478 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6180:Dennd2b
|
UTSW |
7 |
109,156,095 (GRCm39) |
missense |
probably benign |
0.11 |
R6741:Dennd2b
|
UTSW |
7 |
109,144,304 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6781:Dennd2b
|
UTSW |
7 |
109,124,511 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7086:Dennd2b
|
UTSW |
7 |
109,124,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R7466:Dennd2b
|
UTSW |
7 |
109,124,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R7644:Dennd2b
|
UTSW |
7 |
109,156,000 (GRCm39) |
nonsense |
probably null |
|
R8354:Dennd2b
|
UTSW |
7 |
109,124,755 (GRCm39) |
nonsense |
probably null |
|
R8745:Dennd2b
|
UTSW |
7 |
109,156,279 (GRCm39) |
missense |
probably benign |
0.02 |
R8859:Dennd2b
|
UTSW |
7 |
109,123,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R9016:Dennd2b
|
UTSW |
7 |
109,139,642 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9178:Dennd2b
|
UTSW |
7 |
109,156,291 (GRCm39) |
missense |
probably benign |
0.31 |
R9361:Dennd2b
|
UTSW |
7 |
109,126,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Dennd2b
|
UTSW |
7 |
109,125,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R9595:Dennd2b
|
UTSW |
7 |
109,155,973 (GRCm39) |
missense |
probably damaging |
0.96 |
RF062:Dennd2b
|
UTSW |
7 |
109,156,153 (GRCm39) |
unclassified |
probably benign |
|
X0067:Dennd2b
|
UTSW |
7 |
109,155,447 (GRCm39) |
missense |
probably benign |
0.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TCTCGGATACCCAGGCTATG -3'
(R):5'- TGAGACTTCTGCAGGAACATAAC -3'
Sequencing Primer
(F):5'- GGTACCAGTGCAACTCAGC -3'
(R):5'- GAAACACAGTCCCCCTGGTTTTTAG -3'
|
Posted On |
2016-07-06 |