Incidental Mutation 'R7380:Focad'
| ID |
572617 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Focad
|
| Ensembl Gene |
ENSMUSG00000038368 |
| Gene Name |
focadhesin |
| Synonyms |
BC057079 |
| MMRRC Submission |
045462-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.515)
|
| Stock # |
R7380 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
4 |
| Chromosomal Location |
88012866-88329248 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 88192435 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Aspartic acid
at position 588
(V588D)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000124298
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000097992]
[ENSMUST00000159342]
|
| AlphaFold |
A2AKG8 |
| Predicted Effect |
unknown
Transcript: ENSMUST00000097992
AA Change: V674D
|
| SMART Domains |
Protein: ENSMUSP00000095602
Gene: ENSMUSG00000038368
AA Change: V674D
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
150 |
161 |
N/A |
INTRINSIC |
|
low complexity region
|
194 |
203 |
N/A |
INTRINSIC |
|
low complexity region
|
264 |
273 |
N/A |
INTRINSIC |
|
low complexity region
|
328 |
338 |
N/A |
INTRINSIC |
|
low complexity region
|
348 |
361 |
N/A |
INTRINSIC |
|
Pfam:DUF3730
|
490 |
714 |
1.5e-71 |
PFAM |
|
low complexity region
|
957 |
969 |
N/A |
INTRINSIC |
|
low complexity region
|
1032 |
1047 |
N/A |
INTRINSIC |
|
low complexity region
|
1200 |
1209 |
N/A |
INTRINSIC |
|
Pfam:DUF3028
|
1210 |
1798 |
1.5e-291 |
PFAM |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000159342
AA Change: V588D
|
| SMART Domains |
Protein: ENSMUSP00000124298
Gene: ENSMUSG00000038368
AA Change: V588D
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF3730
|
20 |
250 |
5.8e-27 |
PFAM |
|
low complexity region
|
264 |
273 |
N/A |
INTRINSIC |
|
low complexity region
|
328 |
338 |
N/A |
INTRINSIC |
|
low complexity region
|
348 |
361 |
N/A |
INTRINSIC |
|
Pfam:DUF3730
|
403 |
633 |
2.8e-61 |
PFAM |
|
low complexity region
|
871 |
883 |
N/A |
INTRINSIC |
|
low complexity region
|
946 |
961 |
N/A |
INTRINSIC |
|
low complexity region
|
1114 |
1123 |
N/A |
INTRINSIC |
|
Pfam:DUF3028
|
1124 |
1712 |
N/A |
PFAM |
|
| Meta Mutation Damage Score |
0.6114 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.8%
|
| Validation Efficiency |
98% (79/81) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 81 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700030J22Rik |
T |
C |
8: 117,700,376 (GRCm39) |
T9A |
probably benign |
Het |
| Abcc5 |
A |
T |
16: 20,215,784 (GRCm39) |
S414R |
possibly damaging |
Het |
| Acads |
C |
A |
5: 115,249,057 (GRCm39) |
Q365H |
probably damaging |
Het |
| Ankib1 |
G |
T |
5: 3,772,576 (GRCm39) |
Q487K |
probably benign |
Het |
| BC034090 |
T |
G |
1: 155,108,229 (GRCm39) |
S11R |
probably damaging |
Het |
| Car12 |
A |
G |
9: 66,654,945 (GRCm39) |
N125S |
probably benign |
Het |
| Casq1 |
A |
G |
1: 172,044,416 (GRCm39) |
V137A |
probably benign |
Het |
| Cfap54 |
C |
A |
10: 92,883,840 (GRCm39) |
V305F |
probably damaging |
Het |
| Clstn3 |
T |
C |
6: 124,433,948 (GRCm39) |
E404G |
probably benign |
Het |
| Copg1 |
T |
G |
6: 87,870,824 (GRCm39) |
L209R |
probably damaging |
Het |
| Cpb2 |
A |
T |
14: 75,493,449 (GRCm39) |
Q42L |
possibly damaging |
Het |
| Cpd |
G |
A |
11: 76,693,151 (GRCm39) |
Q712* |
probably null |
Het |
| Csmd3 |
T |
A |
15: 47,450,361 (GRCm39) |
Y2690F |
|
Het |
| Dchs1 |
G |
T |
7: 105,407,835 (GRCm39) |
T1999K |
probably benign |
Het |
| Ddx10 |
T |
A |
9: 53,151,786 (GRCm39) |
T80S |
probably damaging |
Het |
| Dmtn |
G |
A |
14: 70,854,768 (GRCm39) |
T69I |
probably damaging |
Het |
| Dnah5 |
T |
A |
15: 28,370,524 (GRCm39) |
H2821Q |
probably damaging |
Het |
| Fam162b |
T |
A |
10: 51,466,572 (GRCm39) |
|
probably benign |
Het |
| Fam193b |
A |
C |
13: 55,690,612 (GRCm39) |
S717A |
probably benign |
Het |
| Far2 |
T |
C |
6: 148,082,493 (GRCm39) |
F500L |
unknown |
Het |
| Gm12728 |
T |
C |
4: 105,651,593 (GRCm39) |
F68L |
probably damaging |
Het |
| Gm1527 |
T |
A |
3: 28,974,621 (GRCm39) |
M478K |
probably benign |
Het |
| Gm57858 |
T |
A |
3: 36,080,070 (GRCm39) |
D229V |
possibly damaging |
Het |
| Gpd2 |
A |
T |
2: 57,230,171 (GRCm39) |
I308F |
probably damaging |
Het |
| Igf2bp3 |
T |
C |
6: 49,085,933 (GRCm39) |
T249A |
probably benign |
Het |
| Igfn1 |
C |
A |
1: 135,889,746 (GRCm39) |
V2434F |
probably damaging |
Het |
| Inhca |
G |
A |
9: 103,156,680 (GRCm39) |
Q127* |
probably null |
Het |
| Kdm5a |
C |
A |
6: 120,382,879 (GRCm39) |
Q737K |
probably benign |
Het |
| Khdrbs2 |
T |
C |
1: 32,372,685 (GRCm39) |
S120P |
unknown |
Het |
| Lmx1a |
T |
C |
1: 167,519,609 (GRCm39) |
F46L |
probably damaging |
Het |
| Lrba |
C |
G |
3: 86,232,381 (GRCm39) |
T776R |
probably damaging |
Het |
| Lrrc8c |
A |
G |
5: 105,755,701 (GRCm39) |
N492S |
possibly damaging |
Het |
| Mapk3 |
A |
T |
7: 126,363,967 (GRCm39) |
I365F |
|
Het |
| Mcee |
A |
G |
7: 64,061,657 (GRCm39) |
I153M |
possibly damaging |
Het |
| Mllt3 |
T |
C |
4: 87,710,180 (GRCm39) |
D415G |
possibly damaging |
Het |
| Muc4 |
A |
T |
16: 32,575,740 (GRCm39) |
T1747S |
unknown |
Het |
| Myh14 |
A |
T |
7: 44,310,466 (GRCm39) |
V139E |
probably damaging |
Het |
| Myo10 |
A |
T |
15: 25,779,706 (GRCm39) |
I772L |
probably benign |
Het |
| Naa15 |
T |
G |
3: 51,367,268 (GRCm39) |
|
probably null |
Het |
| Nbeal1 |
T |
A |
1: 60,283,969 (GRCm39) |
I841N |
probably damaging |
Het |
| Nf1 |
C |
T |
11: 79,437,102 (GRCm39) |
T2006I |
probably damaging |
Het |
| Npr2 |
T |
A |
4: 43,641,254 (GRCm39) |
W427R |
probably damaging |
Het |
| Nr1h3 |
A |
T |
2: 91,020,540 (GRCm39) |
F324L |
possibly damaging |
Het |
| Obscn |
T |
C |
11: 58,947,740 (GRCm39) |
K4430E |
|
Het |
| Or1e1d-ps1 |
T |
A |
11: 73,819,013 (GRCm39) |
Y61N |
possibly damaging |
Het |
| Or5ac21 |
A |
G |
16: 59,124,391 (GRCm39) |
R292G |
probably damaging |
Het |
| Or6c2 |
A |
T |
10: 129,362,530 (GRCm39) |
T145S |
probably benign |
Het |
| Or6d13 |
T |
C |
6: 116,517,894 (GRCm39) |
L160P |
probably benign |
Het |
| Osgin1 |
T |
A |
8: 120,172,170 (GRCm39) |
H321Q |
probably benign |
Het |
| P4ha1 |
A |
G |
10: 59,186,273 (GRCm39) |
I251V |
probably benign |
Het |
| Padi2 |
G |
A |
4: 140,644,997 (GRCm39) |
W77* |
probably null |
Het |
| Pkd1 |
T |
A |
17: 24,800,616 (GRCm39) |
I3086N |
probably damaging |
Het |
| Plk3 |
T |
C |
4: 116,988,350 (GRCm39) |
N360S |
probably benign |
Het |
| Prr14 |
A |
T |
7: 127,075,614 (GRCm39) |
S541C |
probably null |
Het |
| Ptch2 |
C |
A |
4: 116,971,843 (GRCm39) |
Q1122K |
possibly damaging |
Het |
| Rab3gap1 |
T |
C |
1: 127,865,727 (GRCm39) |
V764A |
possibly damaging |
Het |
| Rad50 |
T |
C |
11: 53,586,223 (GRCm39) |
I258V |
probably benign |
Het |
| Rapgef3 |
G |
T |
15: 97,664,672 (GRCm39) |
R64S |
probably benign |
Het |
| Rbm44 |
A |
G |
1: 91,079,938 (GRCm39) |
N42S |
possibly damaging |
Het |
| Ring1 |
T |
C |
17: 34,240,694 (GRCm39) |
Y361C |
probably damaging |
Het |
| Robo3 |
T |
C |
9: 37,329,852 (GRCm39) |
T1155A |
probably damaging |
Het |
| Rsf1 |
GGCGG |
GGCGGTGGCCGCGG |
7: 97,229,122 (GRCm39) |
|
probably benign |
Het |
| Ryr3 |
T |
C |
2: 112,470,502 (GRCm39) |
T4682A |
probably damaging |
Het |
| Scart1 |
A |
T |
7: 139,804,790 (GRCm39) |
N598Y |
possibly damaging |
Het |
| Sema7a |
T |
C |
9: 57,868,847 (GRCm39) |
V653A |
unknown |
Het |
| Slc16a13 |
T |
C |
11: 70,110,105 (GRCm39) |
Y132C |
probably damaging |
Het |
| Slc24a1 |
A |
G |
9: 64,855,815 (GRCm39) |
V364A |
unknown |
Het |
| Slc8a2 |
C |
T |
7: 15,868,278 (GRCm39) |
A170V |
probably damaging |
Het |
| Slfn8 |
C |
T |
11: 82,894,566 (GRCm39) |
R691Q |
not run |
Het |
| Snx2 |
T |
C |
18: 53,327,640 (GRCm39) |
V122A |
probably benign |
Het |
| Sstr1 |
A |
T |
12: 58,260,066 (GRCm39) |
M230L |
probably benign |
Het |
| Themis2 |
C |
T |
4: 132,513,528 (GRCm39) |
V233I |
possibly damaging |
Het |
| Tmem106b |
T |
C |
6: 13,078,167 (GRCm39) |
S121P |
probably damaging |
Het |
| Tmem63c |
A |
G |
12: 87,124,722 (GRCm39) |
I529V |
probably benign |
Het |
| Tmem94 |
T |
C |
11: 115,686,971 (GRCm39) |
|
probably null |
Het |
| Trmt10c |
A |
T |
16: 55,854,619 (GRCm39) |
W339R |
probably damaging |
Het |
| Ugt2b1 |
A |
T |
5: 87,065,578 (GRCm39) |
F487Y |
not run |
Het |
| Vmn2r91 |
T |
A |
17: 18,356,838 (GRCm39) |
L835* |
probably null |
Het |
| Vps52 |
C |
A |
17: 34,177,283 (GRCm39) |
N108K |
possibly damaging |
Het |
| Wdpcp |
T |
A |
11: 21,661,585 (GRCm39) |
C286S |
possibly damaging |
Het |
| Zfp959 |
T |
A |
17: 56,205,551 (GRCm39) |
H529Q |
possibly damaging |
Het |
|
| Other mutations in Focad |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00326:Focad
|
APN |
4 |
88,275,711 (GRCm39) |
missense |
unknown |
|
|
IGL00562:Focad
|
APN |
4 |
88,267,046 (GRCm39) |
missense |
unknown |
|
|
IGL00563:Focad
|
APN |
4 |
88,267,046 (GRCm39) |
missense |
unknown |
|
|
IGL00900:Focad
|
APN |
4 |
88,047,260 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL00984:Focad
|
APN |
4 |
88,263,022 (GRCm39) |
missense |
unknown |
|
|
IGL01016:Focad
|
APN |
4 |
88,310,252 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
IGL01069:Focad
|
APN |
4 |
88,244,383 (GRCm39) |
missense |
unknown |
|
|
IGL01305:Focad
|
APN |
4 |
88,311,784 (GRCm39) |
missense |
probably benign |
0.32 |
|
IGL01409:Focad
|
APN |
4 |
88,260,542 (GRCm39) |
missense |
unknown |
|
|
IGL01447:Focad
|
APN |
4 |
88,244,465 (GRCm39) |
missense |
unknown |
|
|
IGL01521:Focad
|
APN |
4 |
88,328,927 (GRCm39) |
makesense |
probably null |
|
|
IGL01672:Focad
|
APN |
4 |
88,278,827 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL01739:Focad
|
APN |
4 |
88,289,043 (GRCm39) |
missense |
unknown |
|
|
IGL02082:Focad
|
APN |
4 |
88,148,815 (GRCm39) |
nonsense |
probably null |
|
|
IGL02139:Focad
|
APN |
4 |
88,047,291 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02381:Focad
|
APN |
4 |
88,192,327 (GRCm39) |
splice site |
probably benign |
|
|
IGL02898:Focad
|
APN |
4 |
88,310,234 (GRCm39) |
missense |
probably benign |
0.02 |
|
certitude
|
UTSW |
4 |
88,096,370 (GRCm39) |
missense |
probably damaging |
1.00 |
|
impression
|
UTSW |
4 |
88,196,479 (GRCm39) |
missense |
unknown |
|
|
Microscope
|
UTSW |
4 |
88,260,441 (GRCm39) |
missense |
unknown |
|
|
Nuance
|
UTSW |
4 |
88,115,083 (GRCm39) |
intron |
probably benign |
|
|
Objective
|
UTSW |
4 |
88,319,305 (GRCm39) |
nonsense |
probably null |
|
|
ANU22:Focad
|
UTSW |
4 |
88,311,784 (GRCm39) |
missense |
probably benign |
0.32 |
|
R0025:Focad
|
UTSW |
4 |
88,327,196 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0554:Focad
|
UTSW |
4 |
88,267,126 (GRCm39) |
missense |
unknown |
|
|
R0617:Focad
|
UTSW |
4 |
88,039,525 (GRCm39) |
unclassified |
probably benign |
|
|
R0688:Focad
|
UTSW |
4 |
88,192,450 (GRCm39) |
missense |
unknown |
|
|
R0746:Focad
|
UTSW |
4 |
88,315,451 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R0907:Focad
|
UTSW |
4 |
88,196,498 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1109:Focad
|
UTSW |
4 |
88,114,984 (GRCm39) |
intron |
probably benign |
|
|
R1136:Focad
|
UTSW |
4 |
88,244,417 (GRCm39) |
missense |
unknown |
|
|
R1185:Focad
|
UTSW |
4 |
88,096,424 (GRCm39) |
missense |
probably benign |
0.40 |
|
R1185:Focad
|
UTSW |
4 |
88,096,424 (GRCm39) |
missense |
probably benign |
0.40 |
|
R1185:Focad
|
UTSW |
4 |
88,096,424 (GRCm39) |
missense |
probably benign |
0.40 |
|
R1412:Focad
|
UTSW |
4 |
88,196,498 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1453:Focad
|
UTSW |
4 |
88,275,679 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R1697:Focad
|
UTSW |
4 |
88,327,225 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1739:Focad
|
UTSW |
4 |
88,316,128 (GRCm39) |
missense |
probably benign |
0.05 |
|
R1767:Focad
|
UTSW |
4 |
88,275,705 (GRCm39) |
missense |
unknown |
|
|
R1827:Focad
|
UTSW |
4 |
88,147,620 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1866:Focad
|
UTSW |
4 |
88,325,402 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R1867:Focad
|
UTSW |
4 |
88,096,326 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1929:Focad
|
UTSW |
4 |
88,260,449 (GRCm39) |
missense |
unknown |
|
|
R1929:Focad
|
UTSW |
4 |
88,315,416 (GRCm39) |
missense |
probably benign |
0.32 |
|
R1937:Focad
|
UTSW |
4 |
88,319,318 (GRCm39) |
start codon destroyed |
probably null |
|
|
R1989:Focad
|
UTSW |
4 |
88,151,021 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2176:Focad
|
UTSW |
4 |
88,197,481 (GRCm39) |
missense |
unknown |
|
|
R2393:Focad
|
UTSW |
4 |
88,039,567 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R2431:Focad
|
UTSW |
4 |
88,249,264 (GRCm39) |
missense |
unknown |
|
|
R3195:Focad
|
UTSW |
4 |
88,325,588 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R3196:Focad
|
UTSW |
4 |
88,325,588 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R3730:Focad
|
UTSW |
4 |
88,327,162 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R3772:Focad
|
UTSW |
4 |
88,254,398 (GRCm39) |
splice site |
probably benign |
|
|
R4391:Focad
|
UTSW |
4 |
88,104,195 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4491:Focad
|
UTSW |
4 |
88,278,142 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4492:Focad
|
UTSW |
4 |
88,278,142 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4703:Focad
|
UTSW |
4 |
88,260,558 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4788:Focad
|
UTSW |
4 |
88,275,706 (GRCm39) |
missense |
unknown |
|
|
R4923:Focad
|
UTSW |
4 |
88,115,083 (GRCm39) |
intron |
probably benign |
|
|
R5026:Focad
|
UTSW |
4 |
88,262,819 (GRCm39) |
missense |
unknown |
|
|
R5122:Focad
|
UTSW |
4 |
88,325,602 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5153:Focad
|
UTSW |
4 |
88,278,121 (GRCm39) |
missense |
unknown |
|
|
R5369:Focad
|
UTSW |
4 |
88,039,610 (GRCm39) |
splice site |
probably benign |
|
|
R5414:Focad
|
UTSW |
4 |
88,328,939 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R5839:Focad
|
UTSW |
4 |
88,115,083 (GRCm39) |
intron |
probably benign |
|
|
R5916:Focad
|
UTSW |
4 |
88,275,778 (GRCm39) |
missense |
unknown |
|
|
R5953:Focad
|
UTSW |
4 |
88,147,572 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5991:Focad
|
UTSW |
4 |
88,319,256 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R6230:Focad
|
UTSW |
4 |
88,260,441 (GRCm39) |
missense |
unknown |
|
|
R6247:Focad
|
UTSW |
4 |
88,325,377 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R6324:Focad
|
UTSW |
4 |
88,319,305 (GRCm39) |
nonsense |
probably null |
|
|
R6543:Focad
|
UTSW |
4 |
88,197,493 (GRCm39) |
missense |
unknown |
|
|
R6639:Focad
|
UTSW |
4 |
88,196,479 (GRCm39) |
missense |
unknown |
|
|
R6802:Focad
|
UTSW |
4 |
88,262,921 (GRCm39) |
missense |
unknown |
|
|
R6802:Focad
|
UTSW |
4 |
88,192,440 (GRCm39) |
missense |
unknown |
|
|
R6866:Focad
|
UTSW |
4 |
88,321,623 (GRCm39) |
missense |
probably benign |
0.34 |
|
R6902:Focad
|
UTSW |
4 |
88,148,713 (GRCm39) |
missense |
unknown |
|
|
R6928:Focad
|
UTSW |
4 |
88,267,112 (GRCm39) |
missense |
unknown |
|
|
R7036:Focad
|
UTSW |
4 |
88,042,874 (GRCm39) |
missense |
probably benign |
0.05 |
|
R7057:Focad
|
UTSW |
4 |
88,192,342 (GRCm39) |
missense |
unknown |
|
|
R7077:Focad
|
UTSW |
4 |
88,328,914 (GRCm39) |
missense |
unknown |
|
|
R7242:Focad
|
UTSW |
4 |
88,228,143 (GRCm39) |
missense |
unknown |
|
|
R7357:Focad
|
UTSW |
4 |
88,147,572 (GRCm39) |
missense |
probably benign |
0.19 |
|
R7427:Focad
|
UTSW |
4 |
88,286,988 (GRCm39) |
missense |
unknown |
|
|
R7582:Focad
|
UTSW |
4 |
88,147,615 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7661:Focad
|
UTSW |
4 |
88,221,772 (GRCm39) |
missense |
unknown |
|
|
R7688:Focad
|
UTSW |
4 |
88,096,370 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7789:Focad
|
UTSW |
4 |
88,147,643 (GRCm39) |
missense |
unknown |
|
|
R7880:Focad
|
UTSW |
4 |
88,319,407 (GRCm39) |
missense |
unknown |
|
|
R7887:Focad
|
UTSW |
4 |
88,100,853 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8024:Focad
|
UTSW |
4 |
88,315,237 (GRCm39) |
missense |
unknown |
|
|
R8129:Focad
|
UTSW |
4 |
88,151,000 (GRCm39) |
missense |
unknown |
|
|
R8369:Focad
|
UTSW |
4 |
88,150,905 (GRCm39) |
missense |
unknown |
|
|
R8837:Focad
|
UTSW |
4 |
88,072,905 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R9014:Focad
|
UTSW |
4 |
88,275,763 (GRCm39) |
missense |
unknown |
|
|
R9282:Focad
|
UTSW |
4 |
88,115,059 (GRCm39) |
missense |
unknown |
|
|
R9431:Focad
|
UTSW |
4 |
88,321,583 (GRCm39) |
missense |
unknown |
|
|
R9435:Focad
|
UTSW |
4 |
88,267,076 (GRCm39) |
missense |
unknown |
|
|
R9676:Focad
|
UTSW |
4 |
88,273,682 (GRCm39) |
missense |
unknown |
|
|
X0035:Focad
|
UTSW |
4 |
88,316,159 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
| Predicted Primers |
PCR Primer
(F):5'- GCATGGGGTACTTTCTGCC -3'
(R):5'- GCTTTTAAAGTCTTGACAATTCTCG -3'
Sequencing Primer
(F):5'- AGACAGGGTATTGCTACATTGCCC -3'
(R):5'- CGAAAAGCGGTCATCATA -3'
|
| Posted On |
2019-09-13 |
Incidental Mutation