Incidental Mutation 'R8880:Disp2'
| ID |
676815 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Disp2
|
| Ensembl Gene |
ENSMUSG00000040035 |
| Gene Name |
dispatched RND transporter family member 2 |
| Synonyms |
B230210L08Rik, DispB |
| MMRRC Submission |
068748-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.896)
|
| Stock # |
R8880 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
2 |
| Chromosomal Location |
118610183-118625656 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 118621239 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Phenylalanine to Serine
at position 657
(F657S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000037136
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000037547]
[ENSMUST00000063975]
[ENSMUST00000110843]
[ENSMUST00000110846]
|
| AlphaFold |
Q8CIP5 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000037547
AA Change: F657S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000037136
Gene: ENSMUSG00000040035
AA Change: F657S
| Domain | Start | End | E-Value | Type |
|---|
|
transmembrane domain
|
123 |
145 |
N/A |
INTRINSIC |
|
low complexity region
|
195 |
203 |
N/A |
INTRINSIC |
|
Pfam:MMPL
|
435 |
635 |
9.7e-8 |
PFAM |
|
Pfam:Sterol-sensing
|
458 |
611 |
9.1e-9 |
PFAM |
|
transmembrane domain
|
657 |
679 |
N/A |
INTRINSIC |
|
low complexity region
|
682 |
695 |
N/A |
INTRINSIC |
|
low complexity region
|
748 |
761 |
N/A |
INTRINSIC |
|
transmembrane domain
|
914 |
936 |
N/A |
INTRINSIC |
|
transmembrane domain
|
943 |
965 |
N/A |
INTRINSIC |
|
transmembrane domain
|
975 |
997 |
N/A |
INTRINSIC |
|
transmembrane domain
|
1018 |
1040 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000063975
|
| SMART Domains |
Protein: ENSMUSP00000070031
Gene: ENSMUSG00000040035
| Domain | Start | End | E-Value | Type |
|---|
|
transmembrane domain
|
123 |
145 |
N/A |
INTRINSIC |
|
low complexity region
|
195 |
203 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000110843
|
| SMART Domains |
Protein: ENSMUSP00000106467
Gene: ENSMUSG00000040035
| Domain | Start | End | E-Value | Type |
|---|
|
transmembrane domain
|
123 |
145 |
N/A |
INTRINSIC |
|
low complexity region
|
195 |
203 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000110846
|
| SMART Domains |
Protein: ENSMUSP00000106470
Gene: ENSMUSG00000040035
| Domain | Start | End | E-Value | Type |
|---|
|
transmembrane domain
|
123 |
145 |
N/A |
INTRINSIC |
|
low complexity region
|
195 |
203 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.8%
|
| Validation Efficiency |
100% (82/82) |
| MGI Phenotype |
FUNCTION: The pattern of cellular proliferation and differentiation that leads to normal development of embryonic structures often depends upon the localized production of secreted protein signals. Cells surrounding the source of a particular signal respond in a graded manner according to the effective concentration of the signal, and this response produces the pattern of cell types constituting the mature structure. A segment-polarity gene known as dispatched has been identified in Drosophila and its protein product is required for normal Hedgehog (Hh) signaling. [provided by RefSeq, Sep 2015]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 84 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 3425401B19Rik |
C |
T |
14: 32,382,837 (GRCm39) |
V1043I |
probably benign |
Het |
| 5031439G07Rik |
T |
A |
15: 84,839,867 (GRCm39) |
I176F |
possibly damaging |
Het |
| Adam6b |
T |
A |
12: 113,454,764 (GRCm39) |
M527K |
probably benign |
Het |
| Atp10b |
C |
T |
11: 43,106,811 (GRCm39) |
T615I |
probably benign |
Het |
| Atxn2 |
A |
G |
5: 121,948,973 (GRCm39) |
T1117A |
probably benign |
Het |
| AU021092 |
A |
T |
16: 5,032,585 (GRCm39) |
|
probably benign |
Het |
| Bcam |
C |
T |
7: 19,492,671 (GRCm39) |
V505M |
probably damaging |
Het |
| Bco2 |
A |
T |
9: 50,461,962 (GRCm39) |
L14Q |
probably damaging |
Het |
| Caps2 |
T |
G |
10: 112,030,824 (GRCm39) |
|
probably benign |
Het |
| Cblb |
T |
C |
16: 51,986,368 (GRCm39) |
V537A |
probably benign |
Het |
| Ccdc141 |
A |
T |
2: 76,845,556 (GRCm39) |
N1170K |
probably benign |
Het |
| Ccdc154 |
T |
G |
17: 25,389,129 (GRCm39) |
D442E |
probably benign |
Het |
| Col24a1 |
A |
G |
3: 145,019,798 (GRCm39) |
I60V |
probably null |
Het |
| Crb1 |
A |
T |
1: 139,164,886 (GRCm39) |
N1140K |
probably benign |
Het |
| Ddhd1 |
G |
A |
14: 45,846,430 (GRCm39) |
P621S |
probably benign |
Het |
| Ddx46 |
A |
T |
13: 55,814,033 (GRCm39) |
N663I |
probably benign |
Het |
| Dgki |
C |
T |
6: 37,011,652 (GRCm39) |
|
probably benign |
Het |
| Dnajc2 |
T |
C |
5: 21,973,670 (GRCm39) |
E262G |
probably damaging |
Het |
| Dvl2 |
T |
A |
11: 69,898,761 (GRCm39) |
L408Q |
possibly damaging |
Het |
| Egflam |
T |
C |
15: 7,267,249 (GRCm39) |
D712G |
probably damaging |
Het |
| Entpd7 |
A |
G |
19: 43,692,846 (GRCm39) |
|
probably benign |
Het |
| Epb41 |
A |
T |
4: 131,695,104 (GRCm39) |
W28R |
|
Het |
| Fabp9 |
C |
T |
3: 10,262,231 (GRCm39) |
|
probably benign |
Het |
| Fkbp15 |
T |
A |
4: 62,232,602 (GRCm39) |
M657L |
probably benign |
Het |
| Gfy |
A |
C |
7: 44,827,784 (GRCm39) |
L104R |
possibly damaging |
Het |
| Gm4884 |
A |
T |
7: 40,693,911 (GRCm39) |
I627F |
probably damaging |
Het |
| Gm9195 |
A |
T |
14: 72,691,320 (GRCm39) |
S1643T |
unknown |
Het |
| Gpsm2 |
C |
T |
3: 108,610,335 (GRCm39) |
A42T |
possibly damaging |
Het |
| Gvin2 |
T |
C |
7: 105,551,120 (GRCm39) |
K644R |
probably benign |
Het |
| Gys2 |
T |
C |
6: 142,402,113 (GRCm39) |
Y242C |
probably damaging |
Het |
| Hbs1l |
A |
G |
10: 21,185,868 (GRCm39) |
N430S |
probably damaging |
Het |
| Idh3b |
A |
T |
2: 130,126,004 (GRCm39) |
|
probably benign |
Het |
| Igdcc3 |
C |
T |
9: 65,088,550 (GRCm39) |
A384V |
probably benign |
Het |
| Ighv3-4 |
C |
T |
12: 114,217,535 (GRCm39) |
D19N |
possibly damaging |
Het |
| Igkv19-93 |
G |
T |
6: 68,713,494 (GRCm39) |
A45E |
probably damaging |
Het |
| Il10ra |
G |
A |
9: 45,175,631 (GRCm39) |
T230M |
probably damaging |
Het |
| Kalrn |
A |
G |
16: 34,038,305 (GRCm39) |
V1009A |
probably damaging |
Het |
| Kcnma1 |
G |
T |
14: 23,417,718 (GRCm39) |
A837D |
probably damaging |
Het |
| Kif7 |
T |
A |
7: 79,348,650 (GRCm39) |
R1231S |
probably benign |
Het |
| Klhdc1 |
A |
G |
12: 69,298,817 (GRCm39) |
D134G |
possibly damaging |
Het |
| Klk14 |
T |
C |
7: 43,343,459 (GRCm39) |
V97A |
probably damaging |
Het |
| Lamb3 |
G |
A |
1: 193,003,363 (GRCm39) |
V101M |
possibly damaging |
Het |
| Lrrc7 |
C |
T |
3: 157,867,381 (GRCm39) |
E787K |
probably damaging |
Het |
| Mep1a |
A |
G |
17: 43,808,808 (GRCm39) |
I94T |
possibly damaging |
Het |
| Mtrex |
T |
A |
13: 113,051,034 (GRCm39) |
K180N |
probably benign |
Het |
| Ncr1 |
C |
T |
7: 4,341,336 (GRCm39) |
S109L |
probably benign |
Het |
| Nell2 |
A |
T |
15: 95,129,329 (GRCm39) |
M678K |
probably damaging |
Het |
| Or12j5 |
C |
A |
7: 140,084,172 (GRCm39) |
A67S |
probably benign |
Het |
| Or14c42-ps1 |
G |
A |
7: 86,211,549 (GRCm39) |
C203Y |
unknown |
Het |
| Or2m13 |
A |
T |
16: 19,226,396 (GRCm39) |
Y123* |
probably null |
Het |
| Or8g19 |
T |
A |
9: 39,055,899 (GRCm39) |
F168I |
probably damaging |
Het |
| Pnpla1 |
A |
C |
17: 29,098,438 (GRCm39) |
Y248S |
probably damaging |
Het |
| Pramel27 |
T |
C |
4: 143,573,140 (GRCm39) |
|
probably null |
Het |
| Prdm10 |
T |
C |
9: 31,264,742 (GRCm39) |
F726L |
probably damaging |
Het |
| Prdm16 |
T |
C |
4: 154,613,370 (GRCm39) |
N19S |
probably damaging |
Het |
| Prss44 |
A |
G |
9: 110,643,263 (GRCm39) |
R53G |
probably benign |
Het |
| Rasgrp1 |
C |
T |
2: 117,115,425 (GRCm39) |
R721Q |
probably benign |
Het |
| Rassf1 |
A |
T |
9: 107,434,740 (GRCm39) |
N149I |
probably damaging |
Het |
| Rbp3 |
A |
C |
14: 33,678,796 (GRCm39) |
T915P |
probably benign |
Het |
| Reg3g |
A |
T |
6: 78,444,788 (GRCm39) |
D63E |
probably benign |
Het |
| Relch |
T |
C |
1: 105,592,220 (GRCm39) |
Y130H |
probably damaging |
Het |
| Rgs3 |
C |
A |
4: 62,543,373 (GRCm39) |
T236K |
probably damaging |
Het |
| Rin2 |
T |
C |
2: 145,690,772 (GRCm39) |
F147L |
probably damaging |
Het |
| Slc17a1 |
T |
C |
13: 24,062,732 (GRCm39) |
I266T |
probably benign |
Het |
| Slc34a3 |
A |
T |
2: 25,119,267 (GRCm39) |
N534K |
probably benign |
Het |
| Smc2 |
A |
T |
4: 52,462,856 (GRCm39) |
E615D |
probably benign |
Het |
| Snx16 |
A |
C |
3: 10,484,193 (GRCm39) |
D343E |
probably benign |
Het |
| St18 |
T |
A |
1: 6,865,619 (GRCm39) |
Y32* |
probably null |
Het |
| Svep1 |
C |
T |
4: 58,064,204 (GRCm39) |
V3260I |
possibly damaging |
Het |
| Synm |
C |
T |
7: 67,386,456 (GRCm39) |
R402H |
possibly damaging |
Het |
| Tacc2 |
A |
T |
7: 130,318,564 (GRCm39) |
E67V |
possibly damaging |
Het |
| Tarbp1 |
G |
T |
8: 127,198,044 (GRCm39) |
N302K |
probably damaging |
Het |
| Tenm2 |
A |
G |
11: 35,942,788 (GRCm39) |
S1294P |
probably damaging |
Het |
| Ttk |
T |
C |
9: 83,751,304 (GRCm39) |
S794P |
probably damaging |
Het |
| Ulk1 |
G |
A |
5: 110,934,288 (GRCm39) |
A999V |
probably damaging |
Het |
| Upf2 |
A |
G |
2: 6,030,983 (GRCm39) |
I808V |
unknown |
Het |
| Ush2a |
A |
G |
1: 188,460,733 (GRCm39) |
T2665A |
probably benign |
Het |
| Usp8 |
A |
G |
2: 126,590,229 (GRCm39) |
K672E |
probably damaging |
Het |
| Vmn2r105 |
T |
A |
17: 20,429,229 (GRCm39) |
I616F |
probably damaging |
Het |
| Vps33a |
T |
C |
5: 123,707,506 (GRCm39) |
M154V |
probably damaging |
Het |
| Wdfy4 |
A |
C |
14: 32,795,492 (GRCm39) |
Y2083* |
probably null |
Het |
| Zc3hav1 |
A |
G |
6: 38,288,212 (GRCm39) |
F875L |
probably benign |
Het |
| Zfp979 |
T |
C |
4: 147,697,836 (GRCm39) |
N291S |
probably benign |
Het |
| Zp2 |
T |
A |
7: 119,742,835 (GRCm39) |
Y99F |
possibly damaging |
Het |
|
| Other mutations in Disp2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00790:Disp2
|
APN |
2 |
118,616,759 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00970:Disp2
|
APN |
2 |
118,622,274 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01790:Disp2
|
APN |
2 |
118,621,361 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01809:Disp2
|
APN |
2 |
118,617,745 (GRCm39) |
splice site |
probably benign |
|
|
IGL02069:Disp2
|
APN |
2 |
118,621,161 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
IGL02140:Disp2
|
APN |
2 |
118,621,350 (GRCm39) |
missense |
probably benign |
|
|
IGL02143:Disp2
|
APN |
2 |
118,620,450 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02155:Disp2
|
APN |
2 |
118,622,285 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02884:Disp2
|
APN |
2 |
118,618,032 (GRCm39) |
splice site |
probably benign |
|
|
IGL03113:Disp2
|
APN |
2 |
118,621,259 (GRCm39) |
splice site |
probably null |
|
|
IGL03194:Disp2
|
APN |
2 |
118,618,110 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4453001:Disp2
|
UTSW |
2 |
118,618,125 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0109:Disp2
|
UTSW |
2 |
118,622,297 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0126:Disp2
|
UTSW |
2 |
118,620,819 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0603:Disp2
|
UTSW |
2 |
118,622,487 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0610:Disp2
|
UTSW |
2 |
118,622,717 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0639:Disp2
|
UTSW |
2 |
118,621,325 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R0673:Disp2
|
UTSW |
2 |
118,621,325 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R0755:Disp2
|
UTSW |
2 |
118,620,243 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0781:Disp2
|
UTSW |
2 |
118,620,920 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1110:Disp2
|
UTSW |
2 |
118,620,920 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1148:Disp2
|
UTSW |
2 |
118,636,899 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1148:Disp2
|
UTSW |
2 |
118,636,899 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1243:Disp2
|
UTSW |
2 |
118,622,303 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1587:Disp2
|
UTSW |
2 |
118,622,064 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1739:Disp2
|
UTSW |
2 |
118,622,031 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1771:Disp2
|
UTSW |
2 |
118,621,778 (GRCm39) |
nonsense |
probably null |
|
|
R1781:Disp2
|
UTSW |
2 |
118,623,042 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1918:Disp2
|
UTSW |
2 |
118,622,408 (GRCm39) |
missense |
probably benign |
|
|
R1956:Disp2
|
UTSW |
2 |
118,622,704 (GRCm39) |
missense |
probably benign |
0.02 |
|
R2167:Disp2
|
UTSW |
2 |
118,622,166 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2206:Disp2
|
UTSW |
2 |
118,622,725 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4031:Disp2
|
UTSW |
2 |
118,622,361 (GRCm39) |
missense |
probably benign |
0.27 |
|
R4617:Disp2
|
UTSW |
2 |
118,620,643 (GRCm39) |
missense |
probably benign |
|
|
R4656:Disp2
|
UTSW |
2 |
118,621,044 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4684:Disp2
|
UTSW |
2 |
118,623,237 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4696:Disp2
|
UTSW |
2 |
118,622,165 (GRCm39) |
nonsense |
probably null |
|
|
R4697:Disp2
|
UTSW |
2 |
118,622,165 (GRCm39) |
nonsense |
probably null |
|
|
R4738:Disp2
|
UTSW |
2 |
118,620,807 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R4834:Disp2
|
UTSW |
2 |
118,622,985 (GRCm39) |
missense |
probably benign |
0.09 |
|
R4914:Disp2
|
UTSW |
2 |
118,620,935 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4915:Disp2
|
UTSW |
2 |
118,620,935 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4918:Disp2
|
UTSW |
2 |
118,620,935 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5045:Disp2
|
UTSW |
2 |
118,622,543 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5208:Disp2
|
UTSW |
2 |
118,622,286 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5303:Disp2
|
UTSW |
2 |
118,641,329 (GRCm39) |
unclassified |
probably benign |
|
|
R5350:Disp2
|
UTSW |
2 |
118,618,056 (GRCm39) |
missense |
probably benign |
0.23 |
|
R5355:Disp2
|
UTSW |
2 |
118,617,392 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6011:Disp2
|
UTSW |
2 |
118,621,301 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R6031:Disp2
|
UTSW |
2 |
118,620,275 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6031:Disp2
|
UTSW |
2 |
118,620,275 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6139:Disp2
|
UTSW |
2 |
118,621,143 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6169:Disp2
|
UTSW |
2 |
118,622,031 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6187:Disp2
|
UTSW |
2 |
118,622,624 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6209:Disp2
|
UTSW |
2 |
118,617,402 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6250:Disp2
|
UTSW |
2 |
118,621,247 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6392:Disp2
|
UTSW |
2 |
118,621,230 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7138:Disp2
|
UTSW |
2 |
118,617,361 (GRCm39) |
missense |
probably benign |
|
|
R7156:Disp2
|
UTSW |
2 |
118,622,292 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7230:Disp2
|
UTSW |
2 |
118,622,286 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7400:Disp2
|
UTSW |
2 |
118,622,367 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7460:Disp2
|
UTSW |
2 |
118,620,261 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7505:Disp2
|
UTSW |
2 |
118,621,569 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7542:Disp2
|
UTSW |
2 |
118,621,599 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7728:Disp2
|
UTSW |
2 |
118,621,961 (GRCm39) |
missense |
probably benign |
0.31 |
|
R7757:Disp2
|
UTSW |
2 |
118,621,391 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7798:Disp2
|
UTSW |
2 |
118,622,360 (GRCm39) |
missense |
probably benign |
|
|
R7945:Disp2
|
UTSW |
2 |
118,623,270 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8013:Disp2
|
UTSW |
2 |
118,620,163 (GRCm39) |
nonsense |
probably null |
|
|
R8085:Disp2
|
UTSW |
2 |
118,617,452 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R8179:Disp2
|
UTSW |
2 |
118,623,030 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8288:Disp2
|
UTSW |
2 |
118,620,762 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8345:Disp2
|
UTSW |
2 |
118,641,284 (GRCm39) |
missense |
unknown |
|
|
R8385:Disp2
|
UTSW |
2 |
118,620,891 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8700:Disp2
|
UTSW |
2 |
118,620,340 (GRCm39) |
nonsense |
probably null |
|
|
R8808:Disp2
|
UTSW |
2 |
118,620,489 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8997:Disp2
|
UTSW |
2 |
118,617,467 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9022:Disp2
|
UTSW |
2 |
118,621,179 (GRCm39) |
missense |
probably benign |
0.22 |
|
R9181:Disp2
|
UTSW |
2 |
118,617,393 (GRCm39) |
missense |
probably benign |
0.08 |
|
R9660:Disp2
|
UTSW |
2 |
118,620,627 (GRCm39) |
missense |
probably benign |
|
|
Z1177:Disp2
|
UTSW |
2 |
118,621,308 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Disp2
|
UTSW |
2 |
118,620,183 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Predicted Primers |
PCR Primer
(F):5'- CTGCTGTACTAGTGCACATGG -3'
(R):5'- AACTGCTGGCGATACTCTG -3'
Sequencing Primer
(F):5'- TACTAGTGCACATGGGGCTCAC -3'
(R):5'- CTCTGCGTCAAAGCGTTCAAAGG -3'
|
| Posted On |
2021-07-15 |
Incidental Mutation