Incidental Mutation 'R1853:Dhx57'
| ID |
208385 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Dhx57
|
| Ensembl Gene |
ENSMUSG00000035051 |
| Gene Name |
DExH-box helicase 57 |
| Synonyms |
|
| MMRRC Submission |
039877-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.171)
|
| Stock # |
R1853 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
17 |
| Chromosomal Location |
80545733-80597620 bp(-) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
A to T
at 80582308 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Stop codon
at position 432
(Y432*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000083742
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000038166]
[ENSMUST00000086555]
|
| AlphaFold |
Q6P5D3 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000038166
AA Change: Y379*
|
| SMART Domains |
Protein: ENSMUSP00000041069
Gene: ENSMUSG00000035051
AA Change: Y379*
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
6 |
50 |
N/A |
INTRINSIC |
|
low complexity region
|
116 |
125 |
N/A |
INTRINSIC |
|
UBA
|
129 |
166 |
1.04e-3 |
SMART |
|
ZnF_C3H1
|
246 |
272 |
4.07e-6 |
SMART |
|
low complexity region
|
357 |
368 |
N/A |
INTRINSIC |
|
low complexity region
|
381 |
390 |
N/A |
INTRINSIC |
|
low complexity region
|
423 |
432 |
N/A |
INTRINSIC |
|
DEXDc
|
490 |
678 |
1.27e-28 |
SMART |
|
Blast:DEXDc
|
688 |
752 |
2e-28 |
BLAST |
|
HELICc
|
810 |
918 |
3.22e-16 |
SMART |
|
HA2
|
984 |
1074 |
1.64e-24 |
SMART |
|
Pfam:OB_NTP_bind
|
1113 |
1262 |
1.5e-20 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000086555
AA Change: Y432*
|
| SMART Domains |
Protein: ENSMUSP00000083742
Gene: ENSMUSG00000035051
AA Change: Y432*
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
6 |
50 |
N/A |
INTRINSIC |
|
low complexity region
|
169 |
178 |
N/A |
INTRINSIC |
|
UBA
|
182 |
219 |
1.04e-3 |
SMART |
|
ZnF_C3H1
|
299 |
325 |
4.07e-6 |
SMART |
|
low complexity region
|
410 |
421 |
N/A |
INTRINSIC |
|
low complexity region
|
434 |
443 |
N/A |
INTRINSIC |
|
low complexity region
|
476 |
485 |
N/A |
INTRINSIC |
|
DEXDc
|
543 |
731 |
1.27e-28 |
SMART |
|
Blast:DEXDc
|
741 |
805 |
1e-28 |
BLAST |
|
HELICc
|
863 |
971 |
3.22e-16 |
SMART |
|
HA2
|
1037 |
1127 |
1.64e-24 |
SMART |
|
Pfam:OB_NTP_bind
|
1166 |
1315 |
8.5e-25 |
PFAM |
|
| Coding Region Coverage |
- 1x: 97.4%
- 3x: 96.8%
- 10x: 95.1%
- 20x: 92.2%
|
| Validation Efficiency |
|
| Allele List at MGI |
All alleles(25) : Gene trapped(25)
|
| Other mutations in this stock |
Total: 97 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acadvl |
T |
C |
11: 69,901,696 (GRCm39) |
K554E |
probably damaging |
Het |
| Acap2 |
C |
T |
16: 30,936,122 (GRCm39) |
E322K |
probably damaging |
Het |
| Adam32 |
T |
C |
8: 25,388,642 (GRCm39) |
Y354C |
probably benign |
Het |
| Agl |
A |
T |
3: 116,572,971 (GRCm39) |
Y789* |
probably null |
Het |
| Aida |
A |
G |
1: 183,087,380 (GRCm39) |
T68A |
probably benign |
Het |
| Aldh3b3 |
T |
A |
19: 4,015,822 (GRCm39) |
L264Q |
probably damaging |
Het |
| Anks6 |
T |
C |
4: 47,049,387 (GRCm39) |
T173A |
probably benign |
Het |
| Ankzf1 |
A |
G |
1: 75,174,772 (GRCm39) |
|
probably null |
Het |
| Apob |
A |
T |
12: 8,060,928 (GRCm39) |
K3137* |
probably null |
Het |
| Arhgef16 |
C |
T |
4: 154,375,563 (GRCm39) |
V144I |
probably benign |
Het |
| Arhgef2 |
A |
T |
3: 88,540,222 (GRCm39) |
T107S |
possibly damaging |
Het |
| Ark2c |
T |
A |
18: 77,550,671 (GRCm39) |
S279C |
possibly damaging |
Het |
| Atad2 |
G |
A |
15: 57,960,685 (GRCm39) |
P971L |
possibly damaging |
Het |
| Atp6ap1l |
T |
C |
13: 91,031,707 (GRCm39) |
E325G |
probably damaging |
Het |
| BC035947 |
T |
C |
1: 78,475,653 (GRCm39) |
N293S |
possibly damaging |
Het |
| Bhmt |
C |
T |
13: 93,761,843 (GRCm39) |
V147M |
probably damaging |
Het |
| Ccdc112 |
A |
T |
18: 46,418,767 (GRCm39) |
H447Q |
probably benign |
Het |
| Cd274 |
T |
A |
19: 29,357,882 (GRCm39) |
N191K |
probably damaging |
Het |
| Ckmt1 |
C |
T |
2: 121,191,131 (GRCm39) |
T181I |
probably damaging |
Het |
| Cnih3 |
C |
A |
1: 181,282,186 (GRCm39) |
S140* |
probably null |
Het |
| Col28a1 |
T |
G |
6: 8,014,574 (GRCm39) |
I944L |
probably benign |
Het |
| Cttnbp2 |
T |
C |
6: 18,408,601 (GRCm39) |
T1007A |
probably benign |
Het |
| Cux2 |
G |
T |
5: 122,007,184 (GRCm39) |
P826T |
possibly damaging |
Het |
| Cyren |
A |
G |
6: 34,852,494 (GRCm39) |
V67A |
probably damaging |
Het |
| Dap3 |
A |
T |
3: 88,838,233 (GRCm39) |
V86E |
probably damaging |
Het |
| Ddah1 |
A |
G |
3: 145,597,304 (GRCm39) |
I180M |
probably benign |
Het |
| Ddt |
T |
C |
10: 75,609,138 (GRCm39) |
E7G |
possibly damaging |
Het |
| Dpp9 |
T |
C |
17: 56,509,885 (GRCm39) |
I314V |
probably benign |
Het |
| Enpp2 |
C |
T |
15: 54,709,219 (GRCm39) |
E803K |
probably damaging |
Het |
| Ercc6 |
T |
A |
14: 32,298,773 (GRCm39) |
I1387N |
possibly damaging |
Het |
| Fancg |
T |
C |
4: 43,009,727 (GRCm39) |
E57G |
probably benign |
Het |
| Fcgbpl1 |
C |
T |
7: 27,854,971 (GRCm39) |
Q1866* |
probably null |
Het |
| Fkbp5 |
A |
T |
17: 28,648,281 (GRCm39) |
C103S |
possibly damaging |
Het |
| Gm14403 |
C |
A |
2: 177,200,932 (GRCm39) |
H293N |
probably damaging |
Het |
| Gm4353 |
G |
A |
7: 115,682,804 (GRCm39) |
P259L |
probably benign |
Het |
| Gm4787 |
T |
A |
12: 81,425,108 (GRCm39) |
H350L |
probably damaging |
Het |
| Hibch |
T |
C |
1: 52,940,494 (GRCm39) |
|
probably null |
Het |
| Impg2 |
T |
C |
16: 56,080,640 (GRCm39) |
S815P |
probably damaging |
Het |
| Ipo11 |
A |
T |
13: 106,997,395 (GRCm39) |
I688K |
probably benign |
Het |
| Kcnd3 |
A |
T |
3: 105,367,068 (GRCm39) |
T313S |
probably damaging |
Het |
| Kctd14 |
A |
T |
7: 97,102,631 (GRCm39) |
S38C |
possibly damaging |
Het |
| Kdm3b |
G |
T |
18: 34,966,446 (GRCm39) |
R1660L |
probably damaging |
Het |
| Kdr |
C |
T |
5: 76,113,565 (GRCm39) |
G768S |
possibly damaging |
Het |
| Klhl2 |
G |
A |
8: 65,275,658 (GRCm39) |
H82Y |
probably benign |
Het |
| Lama3 |
A |
T |
18: 12,646,762 (GRCm39) |
T1759S |
possibly damaging |
Het |
| Lamb1 |
T |
G |
12: 31,368,271 (GRCm39) |
C1134G |
probably damaging |
Het |
| Macf1 |
T |
C |
4: 123,406,513 (GRCm39) |
|
probably null |
Het |
| Mlph |
C |
T |
1: 90,873,389 (GRCm39) |
Q567* |
probably null |
Het |
| Mocos |
A |
C |
18: 24,829,026 (GRCm39) |
E777A |
probably damaging |
Het |
| Neil1 |
T |
A |
9: 57,051,999 (GRCm39) |
Q214L |
probably damaging |
Het |
| Nes |
A |
G |
3: 87,883,114 (GRCm39) |
T458A |
possibly damaging |
Het |
| Nlgn1 |
A |
T |
3: 26,187,671 (GRCm39) |
N71K |
possibly damaging |
Het |
| Nr4a1 |
T |
C |
15: 101,169,645 (GRCm39) |
I305T |
probably benign |
Het |
| Nup58 |
T |
C |
14: 60,481,996 (GRCm39) |
T123A |
possibly damaging |
Het |
| Oas1c |
A |
T |
5: 120,946,060 (GRCm39) |
V146E |
probably damaging |
Het |
| Oit3 |
C |
T |
10: 59,277,444 (GRCm39) |
|
probably null |
Het |
| Or12k8 |
A |
T |
2: 36,975,232 (GRCm39) |
F176Y |
probably damaging |
Het |
| Or4k15c |
A |
G |
14: 50,321,577 (GRCm39) |
L187P |
probably damaging |
Het |
| Osbp |
T |
C |
19: 11,951,255 (GRCm39) |
S267P |
possibly damaging |
Het |
| Pclo |
T |
A |
5: 14,726,698 (GRCm39) |
|
probably benign |
Het |
| Pde9a |
C |
T |
17: 31,674,094 (GRCm39) |
P60S |
probably damaging |
Het |
| Pdia3 |
T |
C |
2: 121,262,144 (GRCm39) |
I205T |
probably benign |
Het |
| Pdia4 |
A |
T |
6: 47,790,161 (GRCm39) |
D26E |
unknown |
Het |
| Pds5a |
A |
G |
5: 65,781,372 (GRCm39) |
V1036A |
possibly damaging |
Het |
| Pitx3 |
C |
T |
19: 46,125,912 (GRCm39) |
G4R |
probably benign |
Het |
| Pnn |
T |
A |
12: 59,118,399 (GRCm39) |
N327K |
probably damaging |
Het |
| Pole |
T |
G |
5: 110,454,719 (GRCm39) |
I984R |
possibly damaging |
Het |
| Psme2 |
T |
A |
14: 55,825,936 (GRCm39) |
I124F |
probably damaging |
Het |
| Pstpip2 |
T |
A |
18: 77,959,499 (GRCm39) |
L198Q |
probably damaging |
Het |
| Siglece |
A |
G |
7: 43,309,360 (GRCm39) |
F66S |
probably benign |
Het |
| Slc1a6 |
T |
A |
10: 78,648,758 (GRCm39) |
V493E |
probably damaging |
Het |
| Snd1 |
T |
A |
6: 28,545,563 (GRCm39) |
I373N |
probably damaging |
Het |
| Srrm2 |
A |
G |
17: 24,039,499 (GRCm39) |
T2144A |
probably damaging |
Het |
| Sst |
A |
G |
16: 23,709,403 (GRCm39) |
L31P |
probably damaging |
Het |
| Stab1 |
C |
T |
14: 30,862,420 (GRCm39) |
V2305M |
probably damaging |
Het |
| Stard9 |
T |
C |
2: 120,519,232 (GRCm39) |
I545T |
probably damaging |
Het |
| Tcaim |
T |
C |
9: 122,655,271 (GRCm39) |
W248R |
probably damaging |
Het |
| Tepsin |
A |
C |
11: 119,989,462 (GRCm39) |
F13C |
probably damaging |
Het |
| Terf1 |
T |
A |
1: 15,889,162 (GRCm39) |
L197* |
probably null |
Het |
| Tiam2 |
C |
T |
17: 3,465,410 (GRCm39) |
R380C |
probably damaging |
Het |
| Tmem63b |
G |
A |
17: 45,972,223 (GRCm39) |
H745Y |
possibly damaging |
Het |
| Trim40 |
A |
G |
17: 37,199,970 (GRCm39) |
L36P |
probably damaging |
Het |
| Trim72 |
A |
G |
7: 127,608,254 (GRCm39) |
I251V |
probably benign |
Het |
| Trio |
T |
C |
15: 27,756,622 (GRCm39) |
Y914C |
probably damaging |
Het |
| Vmn2r113 |
G |
A |
17: 23,164,501 (GRCm39) |
V135I |
probably benign |
Het |
| Vmn2r117 |
T |
A |
17: 23,696,429 (GRCm39) |
H326L |
probably damaging |
Het |
| Vmn2r28 |
A |
T |
7: 5,484,246 (GRCm39) |
C651* |
probably null |
Het |
| Xpnpep1 |
T |
C |
19: 52,994,641 (GRCm39) |
E329G |
probably benign |
Het |
| Xpo4 |
G |
A |
14: 57,823,364 (GRCm39) |
T1042M |
possibly damaging |
Het |
| Ypel1 |
A |
C |
16: 16,925,087 (GRCm39) |
D28E |
probably benign |
Het |
| Zdbf2 |
GAAAAA |
GAAAAAA |
1: 63,344,701 (GRCm39) |
|
probably null |
Het |
| Zfp51 |
A |
T |
17: 21,684,585 (GRCm39) |
H400L |
probably damaging |
Het |
| Zfp518b |
A |
T |
5: 38,830,750 (GRCm39) |
F418L |
probably benign |
Het |
| Zfp54 |
T |
A |
17: 21,654,404 (GRCm39) |
Y299* |
probably null |
Het |
| Zfp672 |
T |
C |
11: 58,207,790 (GRCm39) |
H177R |
probably benign |
Het |
| Zfp692 |
C |
A |
11: 58,200,805 (GRCm39) |
P229T |
possibly damaging |
Het |
| Zswim4 |
A |
T |
8: 84,950,829 (GRCm39) |
C533S |
probably damaging |
Het |
|
| Other mutations in Dhx57 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00642:Dhx57
|
APN |
17 |
80,582,405 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL00811:Dhx57
|
APN |
17 |
80,560,672 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01389:Dhx57
|
APN |
17 |
80,588,652 (GRCm39) |
missense |
probably benign |
0.28 |
|
IGL01468:Dhx57
|
APN |
17 |
80,563,039 (GRCm39) |
nonsense |
probably null |
|
|
IGL01908:Dhx57
|
APN |
17 |
80,558,872 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01965:Dhx57
|
APN |
17 |
80,576,279 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02147:Dhx57
|
APN |
17 |
80,567,752 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL02275:Dhx57
|
APN |
17 |
80,582,268 (GRCm39) |
missense |
probably benign |
0.13 |
|
IGL02349:Dhx57
|
APN |
17 |
80,563,000 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02405:Dhx57
|
APN |
17 |
80,562,979 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02588:Dhx57
|
APN |
17 |
80,576,300 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02673:Dhx57
|
APN |
17 |
80,574,974 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02836:Dhx57
|
APN |
17 |
80,574,978 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02889:Dhx57
|
APN |
17 |
80,554,581 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
IGL03085:Dhx57
|
APN |
17 |
80,565,526 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
P0014:Dhx57
|
UTSW |
17 |
80,582,620 (GRCm39) |
missense |
probably benign |
0.00 |
|
PIT4377001:Dhx57
|
UTSW |
17 |
80,571,404 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R0100:Dhx57
|
UTSW |
17 |
80,582,585 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R0100:Dhx57
|
UTSW |
17 |
80,582,585 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R0129:Dhx57
|
UTSW |
17 |
80,546,343 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0200:Dhx57
|
UTSW |
17 |
80,558,902 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0309:Dhx57
|
UTSW |
17 |
80,582,310 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0375:Dhx57
|
UTSW |
17 |
80,565,550 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0396:Dhx57
|
UTSW |
17 |
80,582,226 (GRCm39) |
missense |
probably benign |
0.34 |
|
R0520:Dhx57
|
UTSW |
17 |
80,565,604 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R0554:Dhx57
|
UTSW |
17 |
80,567,665 (GRCm39) |
nonsense |
probably null |
|
|
R0661:Dhx57
|
UTSW |
17 |
80,576,293 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0883:Dhx57
|
UTSW |
17 |
80,577,800 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0900:Dhx57
|
UTSW |
17 |
80,583,011 (GRCm39) |
missense |
probably benign |
|
|
R0963:Dhx57
|
UTSW |
17 |
80,582,956 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1469:Dhx57
|
UTSW |
17 |
80,561,847 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1469:Dhx57
|
UTSW |
17 |
80,561,847 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1660:Dhx57
|
UTSW |
17 |
80,553,157 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R1707:Dhx57
|
UTSW |
17 |
80,582,655 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1822:Dhx57
|
UTSW |
17 |
80,560,514 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1942:Dhx57
|
UTSW |
17 |
80,572,573 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2043:Dhx57
|
UTSW |
17 |
80,560,509 (GRCm39) |
splice site |
probably benign |
|
|
R2106:Dhx57
|
UTSW |
17 |
80,582,792 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2127:Dhx57
|
UTSW |
17 |
80,580,477 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2183:Dhx57
|
UTSW |
17 |
80,582,760 (GRCm39) |
missense |
probably benign |
0.07 |
|
R2249:Dhx57
|
UTSW |
17 |
80,588,663 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2400:Dhx57
|
UTSW |
17 |
80,567,845 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2404:Dhx57
|
UTSW |
17 |
80,561,733 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2513:Dhx57
|
UTSW |
17 |
80,549,378 (GRCm39) |
splice site |
probably null |
|
|
R2869:Dhx57
|
UTSW |
17 |
80,558,805 (GRCm39) |
missense |
probably benign |
0.22 |
|
R2869:Dhx57
|
UTSW |
17 |
80,558,805 (GRCm39) |
missense |
probably benign |
0.22 |
|
R2870:Dhx57
|
UTSW |
17 |
80,558,805 (GRCm39) |
missense |
probably benign |
0.22 |
|
R2870:Dhx57
|
UTSW |
17 |
80,558,805 (GRCm39) |
missense |
probably benign |
0.22 |
|
R2871:Dhx57
|
UTSW |
17 |
80,558,805 (GRCm39) |
missense |
probably benign |
0.22 |
|
R2871:Dhx57
|
UTSW |
17 |
80,558,805 (GRCm39) |
missense |
probably benign |
0.22 |
|
R2874:Dhx57
|
UTSW |
17 |
80,558,805 (GRCm39) |
missense |
probably benign |
0.22 |
|
R3819:Dhx57
|
UTSW |
17 |
80,572,503 (GRCm39) |
critical splice donor site |
probably null |
|
|
R3964:Dhx57
|
UTSW |
17 |
80,572,541 (GRCm39) |
nonsense |
probably null |
|
|
R4535:Dhx57
|
UTSW |
17 |
80,582,511 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4666:Dhx57
|
UTSW |
17 |
80,582,390 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4788:Dhx57
|
UTSW |
17 |
80,582,760 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4822:Dhx57
|
UTSW |
17 |
80,549,596 (GRCm39) |
splice site |
probably null |
|
|
R4863:Dhx57
|
UTSW |
17 |
80,560,540 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4988:Dhx57
|
UTSW |
17 |
80,558,827 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5391:Dhx57
|
UTSW |
17 |
80,582,510 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5559:Dhx57
|
UTSW |
17 |
80,561,808 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R5644:Dhx57
|
UTSW |
17 |
80,546,302 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R5997:Dhx57
|
UTSW |
17 |
80,553,235 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R6090:Dhx57
|
UTSW |
17 |
80,571,375 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6177:Dhx57
|
UTSW |
17 |
80,580,395 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R6283:Dhx57
|
UTSW |
17 |
80,582,234 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6802:Dhx57
|
UTSW |
17 |
80,582,750 (GRCm39) |
missense |
probably benign |
0.43 |
|
R6924:Dhx57
|
UTSW |
17 |
80,546,244 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R7151:Dhx57
|
UTSW |
17 |
80,580,476 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7386:Dhx57
|
UTSW |
17 |
80,575,006 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R7393:Dhx57
|
UTSW |
17 |
80,563,000 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7451:Dhx57
|
UTSW |
17 |
80,554,542 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7602:Dhx57
|
UTSW |
17 |
80,582,290 (GRCm39) |
missense |
probably benign |
0.06 |
|
R7733:Dhx57
|
UTSW |
17 |
80,572,503 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7748:Dhx57
|
UTSW |
17 |
80,572,546 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7749:Dhx57
|
UTSW |
17 |
80,546,287 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7772:Dhx57
|
UTSW |
17 |
80,580,507 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R8213:Dhx57
|
UTSW |
17 |
80,582,585 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R8370:Dhx57
|
UTSW |
17 |
80,553,192 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8371:Dhx57
|
UTSW |
17 |
80,582,919 (GRCm39) |
missense |
probably benign |
0.18 |
|
R8403:Dhx57
|
UTSW |
17 |
80,585,718 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8467:Dhx57
|
UTSW |
17 |
80,561,853 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8690:Dhx57
|
UTSW |
17 |
80,577,794 (GRCm39) |
critical splice donor site |
probably benign |
|
|
R9210:Dhx57
|
UTSW |
17 |
80,576,338 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9212:Dhx57
|
UTSW |
17 |
80,576,338 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9447:Dhx57
|
UTSW |
17 |
80,549,523 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9562:Dhx57
|
UTSW |
17 |
80,561,817 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9669:Dhx57
|
UTSW |
17 |
80,553,130 (GRCm39) |
missense |
probably benign |
0.09 |
|
R9717:Dhx57
|
UTSW |
17 |
80,582,447 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1088:Dhx57
|
UTSW |
17 |
80,558,777 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Dhx57
|
UTSW |
17 |
80,553,234 (GRCm39) |
missense |
probably damaging |
0.96 |
|
| Predicted Primers |
PCR Primer
(F):5'- TGTTCAGGACCACGGGAAAG -3'
(R):5'- TTTATTCCACCAATGAGAACCTACC -3'
Sequencing Primer
(F):5'- GAGTCCTCATCTAGCCTCAAAGTG -3'
(R):5'- AATGAGAACCTACCTCTGGCTTG -3'
|
| Posted On |
2014-06-23 |
Incidental Mutation