Incidental Mutation 'R1853:Dhx57'
| ID |
208385 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Dhx57
|
| Ensembl Gene |
ENSMUSG00000035051 |
| Gene Name |
DEAH (Asp-Glu-Ala-Asp/His) box polypeptide 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 |
80238304-80290476 bp(-) (GRCm38) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
A to T
at 80274879 bp (GRCm38)
|
| 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: 70,010,870 (GRCm38) |
K554E |
probably damaging |
Het |
| Acap2 |
C |
T |
16: 31,117,304 (GRCm38) |
E322K |
probably damaging |
Het |
| Adam32 |
T |
C |
8: 24,898,626 (GRCm38) |
Y354C |
probably benign |
Het |
| Agl |
A |
T |
3: 116,779,322 (GRCm38) |
Y789* |
probably null |
Het |
| Aida |
A |
G |
1: 183,306,445 (GRCm38) |
T68A |
probably benign |
Het |
| Aldh3b3 |
T |
A |
19: 3,965,822 (GRCm38) |
L264Q |
probably damaging |
Het |
| Anks6 |
T |
C |
4: 47,049,387 (GRCm38) |
T173A |
probably benign |
Het |
| Ankzf1 |
A |
G |
1: 75,198,128 (GRCm38) |
|
probably null |
Het |
| Apob |
A |
T |
12: 8,010,928 (GRCm38) |
K3137* |
probably null |
Het |
| Arhgef16 |
C |
T |
4: 154,291,106 (GRCm38) |
V144I |
probably benign |
Het |
| Arhgef2 |
A |
T |
3: 88,632,915 (GRCm38) |
T107S |
possibly damaging |
Het |
| Ark2c |
T |
A |
18: 77,462,975 (GRCm38) |
S279C |
possibly damaging |
Het |
| Atad2 |
G |
A |
15: 58,097,289 (GRCm38) |
P971L |
possibly damaging |
Het |
| Atp6ap1l |
T |
C |
13: 90,883,588 (GRCm38) |
E325G |
probably damaging |
Het |
| BC035947 |
T |
C |
1: 78,499,016 (GRCm38) |
N293S |
possibly damaging |
Het |
| Bhmt |
C |
T |
13: 93,625,335 (GRCm38) |
V147M |
probably damaging |
Het |
| Ccdc112 |
A |
T |
18: 46,285,700 (GRCm38) |
H447Q |
probably benign |
Het |
| Cd274 |
T |
A |
19: 29,380,482 (GRCm38) |
N191K |
probably damaging |
Het |
| Ckmt1 |
C |
T |
2: 121,360,650 (GRCm38) |
T181I |
probably damaging |
Het |
| Cnih3 |
C |
A |
1: 181,454,621 (GRCm38) |
S140* |
probably null |
Het |
| Col28a1 |
T |
G |
6: 8,014,574 (GRCm38) |
I944L |
probably benign |
Het |
| Cttnbp2 |
T |
C |
6: 18,408,602 (GRCm38) |
T1007A |
probably benign |
Het |
| Cux2 |
G |
T |
5: 121,869,121 (GRCm38) |
P826T |
possibly damaging |
Het |
| Cyren |
A |
G |
6: 34,875,559 (GRCm38) |
V67A |
probably damaging |
Het |
| Dap3 |
A |
T |
3: 88,930,926 (GRCm38) |
V86E |
probably damaging |
Het |
| Ddah1 |
A |
G |
3: 145,891,549 (GRCm38) |
I180M |
probably benign |
Het |
| Ddt |
T |
C |
10: 75,773,304 (GRCm38) |
E7G |
possibly damaging |
Het |
| Dpp9 |
T |
C |
17: 56,202,885 (GRCm38) |
I314V |
probably benign |
Het |
| Enpp2 |
C |
T |
15: 54,845,823 (GRCm38) |
E803K |
probably damaging |
Het |
| Ercc6 |
T |
A |
14: 32,576,816 (GRCm38) |
I1387N |
possibly damaging |
Het |
| Fancg |
T |
C |
4: 43,009,727 (GRCm38) |
E57G |
probably benign |
Het |
| Fcgbpl1 |
C |
T |
7: 28,155,546 (GRCm38) |
Q1866* |
probably null |
Het |
| Fkbp5 |
A |
T |
17: 28,429,307 (GRCm38) |
C103S |
possibly damaging |
Het |
| Gm14403 |
C |
A |
2: 177,509,139 (GRCm38) |
H293N |
probably damaging |
Het |
| Gm4353 |
G |
A |
7: 116,083,569 (GRCm38) |
P259L |
probably benign |
Het |
| Gm4787 |
T |
A |
12: 81,378,334 (GRCm38) |
H350L |
probably damaging |
Het |
| Hibch |
T |
C |
1: 52,901,335 (GRCm38) |
|
probably null |
Het |
| Impg2 |
T |
C |
16: 56,260,277 (GRCm38) |
S815P |
probably damaging |
Het |
| Ipo11 |
A |
T |
13: 106,860,887 (GRCm38) |
I688K |
probably benign |
Het |
| Kcnd3 |
A |
T |
3: 105,459,752 (GRCm38) |
T313S |
probably damaging |
Het |
| Kctd14 |
A |
T |
7: 97,453,424 (GRCm38) |
S38C |
possibly damaging |
Het |
| Kdm3b |
G |
T |
18: 34,833,393 (GRCm38) |
R1660L |
probably damaging |
Het |
| Kdr |
C |
T |
5: 75,952,905 (GRCm38) |
G768S |
possibly damaging |
Het |
| Klhl2 |
G |
A |
8: 64,823,006 (GRCm38) |
H82Y |
probably benign |
Het |
| Lama3 |
A |
T |
18: 12,513,705 (GRCm38) |
T1759S |
possibly damaging |
Het |
| Lamb1 |
T |
G |
12: 31,318,272 (GRCm38) |
C1134G |
probably damaging |
Het |
| Macf1 |
T |
C |
4: 123,512,720 (GRCm38) |
|
probably null |
Het |
| Mlph |
C |
T |
1: 90,945,667 (GRCm38) |
Q567* |
probably null |
Het |
| Mocos |
A |
C |
18: 24,695,969 (GRCm38) |
E777A |
probably damaging |
Het |
| Neil1 |
T |
A |
9: 57,144,715 (GRCm38) |
Q214L |
probably damaging |
Het |
| Nes |
A |
G |
3: 87,975,807 (GRCm38) |
T458A |
possibly damaging |
Het |
| Nlgn1 |
A |
T |
3: 26,133,522 (GRCm38) |
N71K |
possibly damaging |
Het |
| Nr4a1 |
T |
C |
15: 101,271,764 (GRCm38) |
I305T |
probably benign |
Het |
| Nup58 |
T |
C |
14: 60,244,547 (GRCm38) |
T123A |
possibly damaging |
Het |
| Oas1c |
A |
T |
5: 120,807,995 (GRCm38) |
V146E |
probably damaging |
Het |
| Oit3 |
C |
T |
10: 59,441,622 (GRCm38) |
|
probably null |
Het |
| Or12k8 |
A |
T |
2: 37,085,220 (GRCm38) |
F176Y |
probably damaging |
Het |
| Or4k15c |
A |
G |
14: 50,084,120 (GRCm38) |
L187P |
probably damaging |
Het |
| Osbp |
T |
C |
19: 11,973,891 (GRCm38) |
S267P |
possibly damaging |
Het |
| Pclo |
T |
A |
5: 14,676,684 (GRCm38) |
|
probably benign |
Het |
| Pde9a |
C |
T |
17: 31,455,120 (GRCm38) |
P60S |
probably damaging |
Het |
| Pdia3 |
T |
C |
2: 121,431,663 (GRCm38) |
I205T |
probably benign |
Het |
| Pdia4 |
A |
T |
6: 47,813,227 (GRCm38) |
D26E |
unknown |
Het |
| Pds5a |
A |
G |
5: 65,624,029 (GRCm38) |
V1036A |
possibly damaging |
Het |
| Pitx3 |
C |
T |
19: 46,137,473 (GRCm38) |
G4R |
probably benign |
Het |
| Pnn |
T |
A |
12: 59,071,613 (GRCm38) |
N327K |
probably damaging |
Het |
| Pole |
T |
G |
5: 110,306,853 (GRCm38) |
I984R |
possibly damaging |
Het |
| Psme2 |
T |
A |
14: 55,588,479 (GRCm38) |
I124F |
probably damaging |
Het |
| Pstpip2 |
T |
A |
18: 77,871,799 (GRCm38) |
L198Q |
probably damaging |
Het |
| Siglece |
A |
G |
7: 43,659,936 (GRCm38) |
F66S |
probably benign |
Het |
| Slc1a6 |
T |
A |
10: 78,812,924 (GRCm38) |
V493E |
probably damaging |
Het |
| Snd1 |
T |
A |
6: 28,545,564 (GRCm38) |
I373N |
probably damaging |
Het |
| Srrm2 |
A |
G |
17: 23,820,525 (GRCm38) |
T2144A |
probably damaging |
Het |
| Sst |
A |
G |
16: 23,890,653 (GRCm38) |
L31P |
probably damaging |
Het |
| Stab1 |
C |
T |
14: 31,140,463 (GRCm38) |
V2305M |
probably damaging |
Het |
| Stard9 |
T |
C |
2: 120,688,751 (GRCm38) |
I545T |
probably damaging |
Het |
| Tcaim |
T |
C |
9: 122,826,206 (GRCm38) |
W248R |
probably damaging |
Het |
| Tepsin |
A |
C |
11: 120,098,636 (GRCm38) |
F13C |
probably damaging |
Het |
| Terf1 |
T |
A |
1: 15,818,938 (GRCm38) |
L197* |
probably null |
Het |
| Tiam2 |
C |
T |
17: 3,415,135 (GRCm38) |
R380C |
probably damaging |
Het |
| Tmem63b |
G |
A |
17: 45,661,297 (GRCm38) |
H745Y |
possibly damaging |
Het |
| Trim40 |
A |
G |
17: 36,889,078 (GRCm38) |
L36P |
probably damaging |
Het |
| Trim72 |
A |
G |
7: 128,009,082 (GRCm38) |
I251V |
probably benign |
Het |
| Trio |
T |
C |
15: 27,756,536 (GRCm38) |
Y914C |
probably damaging |
Het |
| Vmn2r113 |
G |
A |
17: 22,945,527 (GRCm38) |
V135I |
probably benign |
Het |
| Vmn2r117 |
T |
A |
17: 23,477,455 (GRCm38) |
H326L |
probably damaging |
Het |
| Vmn2r28 |
A |
T |
7: 5,481,247 (GRCm38) |
C651* |
probably null |
Het |
| Xpnpep1 |
T |
C |
19: 53,006,210 (GRCm38) |
E329G |
probably benign |
Het |
| Xpo4 |
G |
A |
14: 57,585,907 (GRCm38) |
T1042M |
possibly damaging |
Het |
| Ypel1 |
A |
C |
16: 17,107,223 (GRCm38) |
D28E |
probably benign |
Het |
| Zdbf2 |
GAAAAA |
GAAAAAA |
1: 63,305,542 (GRCm38) |
|
probably null |
Het |
| Zfp51 |
A |
T |
17: 21,464,323 (GRCm38) |
H400L |
probably damaging |
Het |
| Zfp518b |
A |
T |
5: 38,673,407 (GRCm38) |
F418L |
probably benign |
Het |
| Zfp54 |
T |
A |
17: 21,434,142 (GRCm38) |
Y299* |
probably null |
Het |
| Zfp672 |
T |
C |
11: 58,316,964 (GRCm38) |
H177R |
probably benign |
Het |
| Zfp692 |
C |
A |
11: 58,309,979 (GRCm38) |
P229T |
possibly damaging |
Het |
| Zswim4 |
A |
T |
8: 84,224,200 (GRCm38) |
C533S |
probably damaging |
Het |
|
| Other mutations in Dhx57 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00642:Dhx57
|
APN |
17 |
80,274,976 (GRCm38) |
missense |
probably benign |
0.00 |
|
IGL00811:Dhx57
|
APN |
17 |
80,253,243 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL01389:Dhx57
|
APN |
17 |
80,281,223 (GRCm38) |
missense |
probably benign |
0.28 |
|
IGL01468:Dhx57
|
APN |
17 |
80,255,610 (GRCm38) |
nonsense |
probably null |
|
|
IGL01908:Dhx57
|
APN |
17 |
80,251,443 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL01965:Dhx57
|
APN |
17 |
80,268,850 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02147:Dhx57
|
APN |
17 |
80,260,323 (GRCm38) |
missense |
possibly damaging |
0.95 |
|
IGL02275:Dhx57
|
APN |
17 |
80,274,839 (GRCm38) |
missense |
probably benign |
0.13 |
|
IGL02349:Dhx57
|
APN |
17 |
80,255,571 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02405:Dhx57
|
APN |
17 |
80,255,550 (GRCm38) |
critical splice donor site |
probably null |
|
|
IGL02588:Dhx57
|
APN |
17 |
80,268,871 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02673:Dhx57
|
APN |
17 |
80,267,545 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02836:Dhx57
|
APN |
17 |
80,267,549 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02889:Dhx57
|
APN |
17 |
80,247,152 (GRCm38) |
missense |
possibly damaging |
0.90 |
|
IGL03085:Dhx57
|
APN |
17 |
80,258,097 (GRCm38) |
missense |
possibly damaging |
0.48 |
|
P0014:Dhx57
|
UTSW |
17 |
80,275,191 (GRCm38) |
missense |
probably benign |
0.00 |
|
PIT4377001:Dhx57
|
UTSW |
17 |
80,263,975 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R0100:Dhx57
|
UTSW |
17 |
80,275,156 (GRCm38) |
missense |
possibly damaging |
0.82 |
|
R0100:Dhx57
|
UTSW |
17 |
80,275,156 (GRCm38) |
missense |
possibly damaging |
0.82 |
|
R0129:Dhx57
|
UTSW |
17 |
80,238,914 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0200:Dhx57
|
UTSW |
17 |
80,251,473 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0309:Dhx57
|
UTSW |
17 |
80,274,881 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0375:Dhx57
|
UTSW |
17 |
80,258,121 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0396:Dhx57
|
UTSW |
17 |
80,274,797 (GRCm38) |
missense |
probably benign |
0.34 |
|
R0520:Dhx57
|
UTSW |
17 |
80,258,175 (GRCm38) |
missense |
possibly damaging |
0.95 |
|
R0554:Dhx57
|
UTSW |
17 |
80,260,236 (GRCm38) |
nonsense |
probably null |
|
|
R0661:Dhx57
|
UTSW |
17 |
80,268,864 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0883:Dhx57
|
UTSW |
17 |
80,270,371 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0900:Dhx57
|
UTSW |
17 |
80,275,582 (GRCm38) |
missense |
probably benign |
|
|
R0963:Dhx57
|
UTSW |
17 |
80,275,527 (GRCm38) |
missense |
probably benign |
0.01 |
|
R1469:Dhx57
|
UTSW |
17 |
80,254,418 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1469:Dhx57
|
UTSW |
17 |
80,254,418 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1660:Dhx57
|
UTSW |
17 |
80,245,728 (GRCm38) |
missense |
possibly damaging |
0.83 |
|
R1707:Dhx57
|
UTSW |
17 |
80,275,226 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R1822:Dhx57
|
UTSW |
17 |
80,253,085 (GRCm38) |
critical splice donor site |
probably null |
|
|
R1942:Dhx57
|
UTSW |
17 |
80,265,144 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2043:Dhx57
|
UTSW |
17 |
80,253,080 (GRCm38) |
splice site |
probably benign |
|
|
R2106:Dhx57
|
UTSW |
17 |
80,275,363 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2127:Dhx57
|
UTSW |
17 |
80,273,048 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2183:Dhx57
|
UTSW |
17 |
80,275,331 (GRCm38) |
missense |
probably benign |
0.07 |
|
R2249:Dhx57
|
UTSW |
17 |
80,281,234 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R2400:Dhx57
|
UTSW |
17 |
80,260,416 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R2404:Dhx57
|
UTSW |
17 |
80,254,304 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R2513:Dhx57
|
UTSW |
17 |
80,241,949 (GRCm38) |
splice site |
probably null |
|
|
R2869:Dhx57
|
UTSW |
17 |
80,251,376 (GRCm38) |
missense |
probably benign |
0.22 |
|
R2869:Dhx57
|
UTSW |
17 |
80,251,376 (GRCm38) |
missense |
probably benign |
0.22 |
|
R2870:Dhx57
|
UTSW |
17 |
80,251,376 (GRCm38) |
missense |
probably benign |
0.22 |
|
R2870:Dhx57
|
UTSW |
17 |
80,251,376 (GRCm38) |
missense |
probably benign |
0.22 |
|
R2871:Dhx57
|
UTSW |
17 |
80,251,376 (GRCm38) |
missense |
probably benign |
0.22 |
|
R2871:Dhx57
|
UTSW |
17 |
80,251,376 (GRCm38) |
missense |
probably benign |
0.22 |
|
R2874:Dhx57
|
UTSW |
17 |
80,251,376 (GRCm38) |
missense |
probably benign |
0.22 |
|
R3819:Dhx57
|
UTSW |
17 |
80,265,074 (GRCm38) |
critical splice donor site |
probably null |
|
|
R3964:Dhx57
|
UTSW |
17 |
80,265,112 (GRCm38) |
nonsense |
probably null |
|
|
R4535:Dhx57
|
UTSW |
17 |
80,275,082 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4666:Dhx57
|
UTSW |
17 |
80,274,961 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4788:Dhx57
|
UTSW |
17 |
80,275,331 (GRCm38) |
missense |
probably benign |
0.01 |
|
R4822:Dhx57
|
UTSW |
17 |
80,242,167 (GRCm38) |
splice site |
probably null |
|
|
R4863:Dhx57
|
UTSW |
17 |
80,253,111 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4988:Dhx57
|
UTSW |
17 |
80,251,398 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5391:Dhx57
|
UTSW |
17 |
80,275,081 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5559:Dhx57
|
UTSW |
17 |
80,254,379 (GRCm38) |
missense |
possibly damaging |
0.53 |
|
R5644:Dhx57
|
UTSW |
17 |
80,238,873 (GRCm38) |
missense |
possibly damaging |
0.73 |
|
R5997:Dhx57
|
UTSW |
17 |
80,245,806 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R6090:Dhx57
|
UTSW |
17 |
80,263,946 (GRCm38) |
critical splice donor site |
probably null |
|
|
R6177:Dhx57
|
UTSW |
17 |
80,272,966 (GRCm38) |
missense |
possibly damaging |
0.91 |
|
R6283:Dhx57
|
UTSW |
17 |
80,274,805 (GRCm38) |
missense |
probably benign |
0.00 |
|
R6802:Dhx57
|
UTSW |
17 |
80,275,321 (GRCm38) |
missense |
probably benign |
0.43 |
|
R6924:Dhx57
|
UTSW |
17 |
80,238,815 (GRCm38) |
missense |
possibly damaging |
0.71 |
|
R7151:Dhx57
|
UTSW |
17 |
80,273,047 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7386:Dhx57
|
UTSW |
17 |
80,267,577 (GRCm38) |
missense |
possibly damaging |
0.89 |
|
R7393:Dhx57
|
UTSW |
17 |
80,255,571 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7451:Dhx57
|
UTSW |
17 |
80,247,113 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7602:Dhx57
|
UTSW |
17 |
80,274,861 (GRCm38) |
missense |
probably benign |
0.06 |
|
R7733:Dhx57
|
UTSW |
17 |
80,265,074 (GRCm38) |
critical splice donor site |
probably null |
|
|
R7748:Dhx57
|
UTSW |
17 |
80,265,117 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7749:Dhx57
|
UTSW |
17 |
80,238,858 (GRCm38) |
missense |
probably benign |
0.04 |
|
R7772:Dhx57
|
UTSW |
17 |
80,273,078 (GRCm38) |
missense |
possibly damaging |
0.71 |
|
R8213:Dhx57
|
UTSW |
17 |
80,275,156 (GRCm38) |
missense |
possibly damaging |
0.82 |
|
R8370:Dhx57
|
UTSW |
17 |
80,245,763 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8371:Dhx57
|
UTSW |
17 |
80,275,490 (GRCm38) |
missense |
probably benign |
0.18 |
|
R8403:Dhx57
|
UTSW |
17 |
80,278,289 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8467:Dhx57
|
UTSW |
17 |
80,254,424 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8690:Dhx57
|
UTSW |
17 |
80,270,365 (GRCm38) |
critical splice donor site |
probably benign |
|
|
R9210:Dhx57
|
UTSW |
17 |
80,268,909 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9212:Dhx57
|
UTSW |
17 |
80,268,909 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9447:Dhx57
|
UTSW |
17 |
80,242,094 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9562:Dhx57
|
UTSW |
17 |
80,254,388 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9669:Dhx57
|
UTSW |
17 |
80,245,701 (GRCm38) |
missense |
probably benign |
0.09 |
|
R9717:Dhx57
|
UTSW |
17 |
80,275,018 (GRCm38) |
missense |
probably damaging |
1.00 |
|
Z1088:Dhx57
|
UTSW |
17 |
80,251,348 (GRCm38) |
missense |
probably damaging |
1.00 |
|
Z1176:Dhx57
|
UTSW |
17 |
80,245,805 (GRCm38) |
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