Incidental Mutation 'R1929:Focad'
ID |
215154 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Focad
|
Ensembl Gene |
ENSMUSG00000038368 |
Gene Name |
focadhesin |
Synonyms |
BC057079 |
MMRRC Submission |
039947-MU
|
Accession Numbers |
|
Essential gene? |
Possibly essential
(E-score: 0.515)
|
Stock # |
R1929 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
4 |
Chromosomal Location |
88012866-88329248 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 88315416 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Glycine
at position 1525
(S1525G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000095602
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000097992]
[ENSMUST00000107147]
[ENSMUST00000132493]
[ENSMUST00000159342]
|
AlphaFold |
A2AKG8 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000097992
AA Change: S1525G
PolyPhen 2
Score 0.317 (Sensitivity: 0.90; Specificity: 0.89)
|
SMART Domains |
Protein: ENSMUSP00000095602 Gene: ENSMUSG00000038368 AA Change: S1525G
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 |
probably benign
Transcript: ENSMUST00000107147
|
SMART Domains |
Protein: ENSMUSP00000102765 Gene: ENSMUSG00000038368
Domain | Start | End | E-Value | Type |
Pfam:DUF3028
|
1 |
204 |
8.6e-136 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000107148
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000132493
|
SMART Domains |
Protein: ENSMUSP00000119411 Gene: ENSMUSG00000028497
Domain | Start | End | E-Value | Type |
transmembrane domain
|
33 |
55 |
N/A |
INTRINSIC |
Pfam:PTPLA
|
80 |
234 |
1.5e-32 |
PFAM |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000159342
AA Change: S1439G
|
SMART Domains |
Protein: ENSMUSP00000124298 Gene: ENSMUSG00000038368 AA Change: S1439G
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 |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000162039
|
Meta Mutation Damage Score |
0.0720 |
Coding Region Coverage |
- 1x: 97.5%
- 3x: 96.9%
- 10x: 95.3%
- 20x: 92.4%
|
Validation Efficiency |
98% (107/109) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy10 |
A |
T |
1: 165,337,866 (GRCm39) |
E160V |
probably damaging |
Het |
Amdhd2 |
T |
C |
17: 24,376,860 (GRCm39) |
|
probably null |
Het |
Angel1 |
A |
C |
12: 86,749,093 (GRCm39) |
L656V |
probably damaging |
Het |
Ankrd12 |
G |
A |
17: 66,293,681 (GRCm39) |
S584L |
possibly damaging |
Het |
Apbb2 |
T |
A |
5: 66,464,958 (GRCm39) |
N679Y |
probably benign |
Het |
Arid3c |
T |
A |
4: 41,724,744 (GRCm39) |
I364F |
probably damaging |
Het |
Bcan |
T |
A |
3: 87,900,401 (GRCm39) |
S611C |
probably damaging |
Het |
Bnip3 |
T |
G |
7: 138,496,359 (GRCm39) |
|
silent |
Het |
Btc |
T |
C |
5: 91,510,260 (GRCm39) |
Y111C |
probably damaging |
Het |
Carnmt1 |
T |
C |
19: 18,680,734 (GRCm39) |
L336P |
probably damaging |
Het |
Ccdc83 |
C |
T |
7: 89,873,285 (GRCm39) |
V357I |
probably damaging |
Het |
Cd2bp2 |
T |
C |
7: 126,793,050 (GRCm39) |
D324G |
probably benign |
Het |
Cdc20b |
A |
G |
13: 113,208,451 (GRCm39) |
T216A |
probably benign |
Het |
Cdk17 |
T |
C |
10: 93,064,540 (GRCm39) |
Y270H |
probably damaging |
Het |
Cenpv |
T |
C |
11: 62,416,059 (GRCm39) |
E230G |
probably benign |
Het |
Chst11 |
T |
C |
10: 83,027,004 (GRCm39) |
Y144H |
probably damaging |
Het |
Cracr2a |
T |
A |
6: 127,584,261 (GRCm39) |
F107I |
probably damaging |
Het |
Cyfip1 |
G |
T |
7: 55,549,705 (GRCm39) |
R624L |
probably null |
Het |
Cyp27b1 |
T |
A |
10: 126,884,181 (GRCm39) |
V11D |
probably damaging |
Het |
Ddc |
T |
C |
11: 11,785,764 (GRCm39) |
N308D |
probably damaging |
Het |
Des |
T |
G |
1: 75,340,137 (GRCm39) |
M348R |
probably damaging |
Het |
Dis3l |
T |
A |
9: 64,238,165 (GRCm39) |
D109V |
probably damaging |
Het |
Dnah3 |
T |
A |
7: 119,574,352 (GRCm39) |
I2136F |
probably benign |
Het |
Dnah9 |
T |
C |
11: 65,867,224 (GRCm39) |
S2785G |
probably benign |
Het |
Dop1a |
T |
G |
9: 86,376,471 (GRCm39) |
V235G |
probably damaging |
Het |
Dtx3l |
A |
T |
16: 35,754,059 (GRCm39) |
D182E |
possibly damaging |
Het |
Efcab6 |
A |
G |
15: 83,777,163 (GRCm39) |
|
probably benign |
Het |
Elac2 |
T |
A |
11: 64,870,015 (GRCm39) |
S27T |
probably benign |
Het |
Emsy |
T |
G |
7: 98,275,830 (GRCm39) |
K352N |
probably damaging |
Het |
Erbb4 |
T |
C |
1: 68,238,047 (GRCm39) |
N814S |
probably damaging |
Het |
Fgd6 |
T |
C |
10: 93,880,868 (GRCm39) |
V574A |
probably benign |
Het |
Filip1 |
T |
C |
9: 79,727,212 (GRCm39) |
E469G |
probably damaging |
Het |
Fmo1 |
A |
T |
1: 162,661,424 (GRCm39) |
D286E |
probably damaging |
Het |
Fmo4 |
A |
T |
1: 162,626,616 (GRCm39) |
I310N |
possibly damaging |
Het |
Fras1 |
T |
C |
5: 96,815,296 (GRCm39) |
W1338R |
probably benign |
Het |
Fry |
A |
G |
5: 150,324,389 (GRCm39) |
I1151V |
probably null |
Het |
Garin5b |
T |
A |
7: 4,761,186 (GRCm39) |
T509S |
probably benign |
Het |
Gm10076 |
T |
G |
14: 105,919,304 (GRCm39) |
|
noncoding transcript |
Het |
Gm5698 |
T |
G |
1: 31,017,042 (GRCm39) |
D3A |
probably damaging |
Het |
Gngt2 |
C |
T |
11: 95,735,972 (GRCm39) |
|
probably benign |
Het |
Gsdma |
T |
C |
11: 98,562,193 (GRCm39) |
|
probably null |
Het |
Gtf2h3 |
A |
T |
5: 124,740,262 (GRCm39) |
|
probably benign |
Het |
Hkdc1 |
T |
C |
10: 62,253,677 (GRCm39) |
T35A |
probably benign |
Het |
Irs1 |
T |
C |
1: 82,266,180 (GRCm39) |
S679G |
probably benign |
Het |
Itpr1 |
T |
A |
6: 108,470,716 (GRCm39) |
C2214S |
probably damaging |
Het |
Kcnh8 |
GAGACCAACGAGCAGCTGATGCTTCAGA |
GAGA |
17: 53,032,934 (GRCm39) |
74 |
probably benign |
Het |
Kcnk16 |
A |
G |
14: 20,315,347 (GRCm39) |
V72A |
probably damaging |
Het |
Lipa |
T |
A |
19: 34,488,290 (GRCm39) |
R119* |
probably null |
Het |
Matr3 |
T |
A |
18: 35,721,378 (GRCm39) |
|
probably benign |
Het |
Med13l |
T |
G |
5: 118,866,898 (GRCm39) |
F651V |
probably benign |
Het |
Mfsd11 |
T |
C |
11: 116,764,740 (GRCm39) |
V388A |
probably benign |
Het |
Mki67 |
C |
T |
7: 135,299,794 (GRCm39) |
V1747I |
possibly damaging |
Het |
Mms22l |
T |
C |
4: 24,535,936 (GRCm39) |
|
probably benign |
Het |
Msh5 |
A |
G |
17: 35,263,366 (GRCm39) |
I154T |
probably benign |
Het |
Myo5b |
G |
T |
18: 74,866,996 (GRCm39) |
L1382F |
probably damaging |
Het |
Ncbp2 |
T |
C |
16: 31,775,769 (GRCm39) |
Y138H |
probably damaging |
Het |
Ndufv1 |
C |
A |
19: 4,058,347 (GRCm39) |
R359L |
probably benign |
Het |
Ntrk3 |
A |
C |
7: 78,166,471 (GRCm39) |
|
probably null |
Het |
Or1e1c |
T |
A |
11: 73,266,427 (GRCm39) |
V287E |
probably damaging |
Het |
Or4a15 |
A |
G |
2: 89,193,353 (GRCm39) |
V140A |
probably benign |
Het |
Or8b12i |
T |
A |
9: 20,082,705 (GRCm39) |
H54L |
possibly damaging |
Het |
P4ha1 |
A |
G |
10: 59,206,859 (GRCm39) |
E523G |
probably damaging |
Het |
Per3 |
T |
A |
4: 151,103,342 (GRCm39) |
Y530F |
probably damaging |
Het |
Pes1 |
C |
A |
11: 3,919,524 (GRCm39) |
L66I |
probably damaging |
Het |
Pigr |
G |
A |
1: 130,774,399 (GRCm39) |
|
probably benign |
Het |
Pkd1l1 |
A |
T |
11: 8,786,197 (GRCm39) |
|
probably benign |
Het |
Plch1 |
T |
A |
3: 63,651,956 (GRCm39) |
K378N |
probably damaging |
Het |
Plxnb1 |
T |
C |
9: 108,931,776 (GRCm39) |
|
probably null |
Het |
Pramel22 |
G |
A |
4: 143,380,712 (GRCm39) |
T437I |
probably damaging |
Het |
Prkdc |
A |
G |
16: 15,472,681 (GRCm39) |
|
probably null |
Het |
Prrc1 |
G |
T |
18: 57,514,718 (GRCm39) |
D312Y |
probably damaging |
Het |
Psma5-ps |
A |
G |
10: 85,149,595 (GRCm39) |
|
noncoding transcript |
Het |
Rab3gap2 |
T |
A |
1: 185,015,739 (GRCm39) |
|
probably null |
Het |
Rgs3 |
A |
G |
4: 62,620,384 (GRCm39) |
I537V |
probably damaging |
Het |
Rhobtb2 |
T |
G |
14: 70,033,893 (GRCm39) |
D444A |
probably damaging |
Het |
Rnf40 |
T |
C |
7: 127,190,956 (GRCm39) |
S314P |
probably damaging |
Het |
Rngtt |
T |
A |
4: 33,500,302 (GRCm39) |
C565* |
probably null |
Het |
Samd3 |
A |
G |
10: 26,139,884 (GRCm39) |
|
probably benign |
Het |
Sec61a2 |
A |
G |
2: 5,878,547 (GRCm39) |
|
probably benign |
Het |
Serpina3m |
G |
A |
12: 104,355,581 (GRCm39) |
A83T |
probably damaging |
Het |
Serpinb13 |
A |
T |
1: 106,926,756 (GRCm39) |
I251L |
possibly damaging |
Het |
Sez6 |
C |
T |
11: 77,863,758 (GRCm39) |
T439I |
probably damaging |
Het |
Shc1 |
G |
A |
3: 89,330,849 (GRCm39) |
G91S |
probably damaging |
Het |
Slc26a2 |
A |
G |
18: 61,331,650 (GRCm39) |
C594R |
possibly damaging |
Het |
Specc1l |
C |
T |
10: 75,081,438 (GRCm39) |
S278F |
probably damaging |
Het |
Spg11 |
C |
T |
2: 121,890,688 (GRCm39) |
V2044M |
probably damaging |
Het |
Stx18 |
T |
A |
5: 38,285,383 (GRCm39) |
|
probably null |
Het |
Suclg2 |
T |
C |
6: 95,566,075 (GRCm39) |
|
probably benign |
Het |
Tlr4 |
A |
T |
4: 66,757,681 (GRCm39) |
H158L |
probably damaging |
Het |
Tmem131 |
A |
G |
1: 36,851,352 (GRCm39) |
V966A |
possibly damaging |
Het |
Tram1l1 |
T |
A |
3: 124,115,635 (GRCm39) |
I265N |
probably damaging |
Het |
Trim58 |
T |
A |
11: 58,531,493 (GRCm39) |
F67Y |
possibly damaging |
Het |
Ttc19 |
A |
G |
11: 62,172,650 (GRCm39) |
Q74R |
probably benign |
Het |
Usp7 |
T |
C |
16: 8,516,333 (GRCm39) |
S649G |
probably benign |
Het |
Vmn2r16 |
A |
G |
5: 109,487,124 (GRCm39) |
Y115C |
possibly damaging |
Het |
Zfp444 |
T |
C |
7: 6,192,554 (GRCm39) |
C191R |
probably damaging |
Het |
Zfp451 |
A |
G |
1: 33,821,274 (GRCm39) |
F151L |
probably damaging |
Het |
Zfp451 |
G |
A |
1: 33,822,937 (GRCm39) |
P99S |
probably benign |
Het |
Zfp729b |
A |
T |
13: 67,740,352 (GRCm39) |
C648S |
probably damaging |
Het |
Zfp799 |
A |
G |
17: 33,040,777 (GRCm39) |
Y58H |
probably damaging |
Het |
Zfp804b |
A |
G |
5: 6,819,748 (GRCm39) |
V1069A |
probably benign |
Het |
Zfp938 |
C |
T |
10: 82,061,381 (GRCm39) |
G413D |
probably 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 |
|
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 |
R7380:Focad
|
UTSW |
4 |
88,192,435 (GRCm39) |
missense |
unknown |
|
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'- TGGTATCCATGCCTCTGTGG -3'
(R):5'- GCTTTGGTTCTAAACACTGAACC -3'
Sequencing Primer
(F):5'- TGGGCAAAGCACGTGTCTG -3'
(R):5'- ACCTACTCCTAGTTAAGAATGTGTC -3'
|
Posted On |
2014-07-14 |