Incidental Mutation 'R4917:Rufy4'
ID |
378251 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Rufy4
|
Ensembl Gene |
ENSMUSG00000061815 |
Gene Name |
RUN and FYVE domain containing 4 |
Synonyms |
F930048N03Rik |
MMRRC Submission |
042519-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.202)
|
Stock # |
R4917 (G1)
|
Quality Score |
204 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
74164700-74187382 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 74186822 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Cysteine to Arginine
at position 537
(C537R)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000115873
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000080167]
[ENSMUST00000127134]
|
AlphaFold |
Q3TYX8 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000080167
AA Change: C453R
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000079062 Gene: ENSMUSG00000061815 AA Change: C453R
Domain | Start | End | E-Value | Type |
Pfam:RUN
|
2 |
81 |
1.5e-8 |
PFAM |
coiled coil region
|
331 |
404 |
N/A |
INTRINSIC |
Blast:FYVE
|
415 |
472 |
2e-6 |
BLAST |
SCOP:d1vfya_
|
428 |
473 |
4e-7 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000127134
AA Change: C537R
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000115873 Gene: ENSMUSG00000061815 AA Change: C537R
Domain | Start | End | E-Value | Type |
Pfam:RUN
|
41 |
165 |
6.2e-10 |
PFAM |
coiled coil region
|
415 |
488 |
N/A |
INTRINSIC |
Blast:FYVE
|
499 |
556 |
2e-6 |
BLAST |
SCOP:d1vfya_
|
512 |
557 |
3e-7 |
SMART |
|
Meta Mutation Damage Score |
0.8605 |
Coding Region Coverage |
- 1x: 99.0%
- 3x: 98.3%
- 10x: 96.1%
- 20x: 91.7%
|
Validation Efficiency |
97% (111/114) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
C |
T |
13: 81,658,996 (GRCm39) |
V2783I |
probably benign |
Het |
Ago4 |
A |
C |
4: 126,400,635 (GRCm39) |
C693G |
probably damaging |
Het |
Apobec2 |
T |
C |
17: 48,730,153 (GRCm39) |
E171G |
probably benign |
Het |
Arfgef3 |
T |
A |
10: 18,492,638 (GRCm39) |
I1258F |
probably damaging |
Het |
Arhgef40 |
A |
G |
14: 52,227,556 (GRCm39) |
E434G |
probably damaging |
Het |
Bcas1 |
T |
C |
2: 170,220,806 (GRCm39) |
D324G |
probably damaging |
Het |
Bdp1 |
A |
T |
13: 100,191,713 (GRCm39) |
V1422E |
probably damaging |
Het |
Bfsp1 |
C |
T |
2: 143,669,391 (GRCm39) |
R396Q |
probably benign |
Het |
Bpifb9b |
T |
A |
2: 154,156,026 (GRCm39) |
|
probably null |
Het |
Cacna1s |
T |
A |
1: 136,029,302 (GRCm39) |
|
probably null |
Het |
Casp8 |
T |
C |
1: 58,866,377 (GRCm39) |
F126S |
probably damaging |
Het |
Cdh26 |
T |
C |
2: 178,091,614 (GRCm39) |
S58P |
probably benign |
Het |
Cds2 |
A |
G |
2: 132,140,398 (GRCm39) |
T182A |
probably damaging |
Het |
Cfap157 |
C |
T |
2: 32,669,965 (GRCm39) |
R206H |
probably benign |
Het |
Col7a1 |
G |
A |
9: 108,795,532 (GRCm39) |
G1529E |
unknown |
Het |
Crybg3 |
A |
G |
16: 59,350,782 (GRCm39) |
F2567L |
probably benign |
Het |
Cyp2e1 |
T |
C |
7: 140,354,527 (GRCm39) |
S393P |
possibly damaging |
Het |
D5Ertd579e |
A |
G |
5: 36,773,160 (GRCm39) |
Y412H |
probably damaging |
Het |
Dclk2 |
A |
T |
3: 86,732,049 (GRCm39) |
|
probably null |
Het |
Ddx50 |
A |
T |
10: 62,463,450 (GRCm39) |
C414* |
probably null |
Het |
Dip2c |
T |
A |
13: 9,671,905 (GRCm39) |
|
probably null |
Het |
Dmtn |
G |
T |
14: 70,843,159 (GRCm39) |
P283Q |
probably damaging |
Het |
Dspp |
C |
A |
5: 104,325,789 (GRCm39) |
D717E |
unknown |
Het |
Efcab11 |
T |
C |
12: 99,685,321 (GRCm39) |
D151G |
probably damaging |
Het |
Egfem1 |
T |
C |
3: 29,206,042 (GRCm39) |
V93A |
probably damaging |
Het |
Ehbp1 |
T |
C |
11: 22,096,592 (GRCm39) |
D299G |
probably benign |
Het |
Erlec1 |
A |
G |
11: 30,884,710 (GRCm39) |
Y448H |
possibly damaging |
Het |
Fer1l4 |
T |
C |
2: 155,873,220 (GRCm39) |
K1287E |
probably benign |
Het |
Fn1 |
A |
T |
1: 71,634,968 (GRCm39) |
|
probably null |
Het |
Fut8 |
G |
T |
12: 77,521,818 (GRCm39) |
A486S |
probably damaging |
Het |
Gfra1 |
A |
T |
19: 58,255,522 (GRCm39) |
S308R |
probably damaging |
Het |
Gm10764 |
A |
G |
10: 87,126,579 (GRCm39) |
|
noncoding transcript |
Het |
Gm5958 |
C |
A |
14: 100,073,189 (GRCm39) |
|
noncoding transcript |
Het |
Gm6788 |
C |
T |
19: 28,740,664 (GRCm39) |
|
noncoding transcript |
Het |
Gsdmd |
A |
G |
15: 75,736,241 (GRCm39) |
I123M |
probably benign |
Het |
H2bc13 |
A |
T |
13: 21,900,189 (GRCm39) |
V42E |
probably damaging |
Het |
Hsf4 |
A |
G |
8: 105,999,367 (GRCm39) |
E235G |
probably benign |
Het |
Ighv1-83 |
T |
C |
12: 115,927,580 (GRCm39) |
I57V |
probably benign |
Het |
Inhca |
A |
C |
9: 103,129,054 (GRCm39) |
Y235* |
probably null |
Het |
Inpp5f |
A |
T |
7: 128,286,840 (GRCm39) |
D573V |
probably damaging |
Het |
Kcnj1 |
T |
A |
9: 32,308,056 (GRCm39) |
L160Q |
probably damaging |
Het |
Kcnmb3 |
A |
T |
3: 32,526,653 (GRCm39) |
C179* |
probably null |
Het |
Lrig1 |
A |
G |
6: 94,586,700 (GRCm39) |
F659L |
probably damaging |
Het |
Lrrc3 |
T |
C |
10: 77,737,253 (GRCm39) |
D61G |
probably benign |
Het |
Marchf4 |
T |
G |
1: 72,467,938 (GRCm39) |
S365R |
probably benign |
Het |
Mccc1 |
A |
G |
3: 36,051,703 (GRCm39) |
L32S |
probably benign |
Het |
Mei4 |
A |
G |
9: 81,772,216 (GRCm39) |
T10A |
probably benign |
Het |
Meis1 |
T |
C |
11: 18,959,222 (GRCm39) |
|
probably benign |
Het |
Mllt1 |
T |
C |
17: 57,206,813 (GRCm39) |
T344A |
probably benign |
Het |
Mmp11 |
C |
T |
10: 75,761,419 (GRCm39) |
A31T |
probably damaging |
Het |
Mrps28 |
A |
G |
3: 8,947,614 (GRCm39) |
|
probably benign |
Het |
Mthfsl |
A |
C |
9: 88,597,550 (GRCm39) |
L67V |
probably damaging |
Het |
Ncaph2 |
A |
G |
15: 89,244,574 (GRCm39) |
I11V |
probably damaging |
Het |
Ncdn |
G |
A |
4: 126,643,731 (GRCm39) |
L364F |
possibly damaging |
Het |
Nfat5 |
T |
A |
8: 108,051,284 (GRCm39) |
D47E |
probably damaging |
Het |
Or51g2 |
A |
T |
7: 102,622,614 (GRCm39) |
I195N |
possibly damaging |
Het |
Or5b106 |
T |
A |
19: 13,123,355 (GRCm39) |
I223L |
possibly damaging |
Het |
Or5bw2 |
C |
T |
7: 6,573,643 (GRCm39) |
L218F |
possibly damaging |
Het |
Pcdhb3 |
A |
T |
18: 37,435,452 (GRCm39) |
I473F |
probably damaging |
Het |
Pcdhgb8 |
A |
T |
18: 37,897,191 (GRCm39) |
N754Y |
probably damaging |
Het |
Pgbd5 |
C |
A |
8: 125,097,305 (GRCm39) |
K408N |
probably benign |
Het |
Pnisr |
A |
G |
4: 21,859,330 (GRCm39) |
|
probably benign |
Het |
Poldip3 |
A |
T |
15: 83,016,776 (GRCm39) |
|
probably null |
Het |
Ppfia2 |
G |
C |
10: 106,597,978 (GRCm39) |
L180F |
probably damaging |
Het |
Psmc3 |
A |
G |
2: 90,896,317 (GRCm39) |
|
probably benign |
Het |
Rab3gap1 |
T |
A |
1: 127,816,914 (GRCm39) |
W58R |
possibly damaging |
Het |
Rere |
T |
A |
4: 150,703,601 (GRCm39) |
W1528R |
probably damaging |
Het |
Rhot1 |
A |
G |
11: 80,100,027 (GRCm39) |
|
probably benign |
Het |
Rsf1 |
T |
C |
7: 97,311,612 (GRCm39) |
S781P |
probably damaging |
Het |
Rtraf |
T |
C |
14: 19,873,784 (GRCm39) |
K5R |
probably damaging |
Het |
Ryr2 |
A |
G |
13: 11,609,872 (GRCm39) |
V753A |
probably damaging |
Het |
Ryr3 |
T |
C |
2: 112,661,530 (GRCm39) |
H1820R |
probably damaging |
Het |
Schip1 |
A |
T |
3: 68,315,818 (GRCm39) |
|
probably benign |
Het |
Scin |
T |
A |
12: 40,119,373 (GRCm39) |
I552F |
possibly damaging |
Het |
Selp |
A |
C |
1: 163,972,475 (GRCm39) |
T705P |
probably damaging |
Het |
Sh3rf3 |
A |
T |
10: 58,842,925 (GRCm39) |
D297V |
probably damaging |
Het |
Slc24a4 |
T |
A |
12: 102,231,203 (GRCm39) |
|
probably null |
Het |
Slc2a9 |
C |
A |
5: 38,574,603 (GRCm39) |
L224F |
probably benign |
Het |
Slc35e2 |
C |
A |
4: 155,700,693 (GRCm39) |
P272Q |
probably damaging |
Het |
Slf2 |
T |
G |
19: 44,960,100 (GRCm39) |
D1022E |
probably damaging |
Het |
Syne1 |
C |
T |
10: 5,007,909 (GRCm39) |
C7932Y |
probably damaging |
Het |
Tc2n |
A |
G |
12: 101,631,954 (GRCm39) |
L301P |
probably damaging |
Het |
Tchhl1 |
A |
G |
3: 93,377,623 (GRCm39) |
D109G |
possibly damaging |
Het |
Thoc7 |
T |
C |
14: 13,953,154 (GRCm38) |
I83V |
probably damaging |
Het |
Tm4sf1 |
C |
T |
3: 57,200,448 (GRCm39) |
G85S |
probably damaging |
Het |
Tmem63a |
T |
A |
1: 180,794,086 (GRCm39) |
I541N |
probably benign |
Het |
Tmpo |
A |
G |
10: 90,985,411 (GRCm39) |
V357A |
probably damaging |
Het |
Unc80 |
T |
C |
1: 66,685,709 (GRCm39) |
Y2278H |
possibly damaging |
Het |
Vmn1r26 |
A |
G |
6: 57,985,808 (GRCm39) |
F127S |
probably damaging |
Het |
Vmn2r8 |
A |
T |
5: 108,945,264 (GRCm39) |
M781K |
probably damaging |
Het |
Vps36 |
T |
G |
8: 22,708,280 (GRCm39) |
M348R |
possibly damaging |
Het |
Vps45 |
T |
C |
3: 95,926,943 (GRCm39) |
T535A |
probably damaging |
Het |
|
Other mutations in Rufy4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01617:Rufy4
|
APN |
1 |
74,168,513 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02075:Rufy4
|
APN |
1 |
74,168,518 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02604:Rufy4
|
APN |
1 |
74,173,348 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02606:Rufy4
|
APN |
1 |
74,172,509 (GRCm39) |
splice site |
probably benign |
|
IGL02928:Rufy4
|
APN |
1 |
74,168,241 (GRCm39) |
unclassified |
probably benign |
|
R0091:Rufy4
|
UTSW |
1 |
74,168,095 (GRCm39) |
unclassified |
probably benign |
|
R0507:Rufy4
|
UTSW |
1 |
74,185,875 (GRCm39) |
missense |
probably benign |
0.02 |
R0589:Rufy4
|
UTSW |
1 |
74,172,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R0595:Rufy4
|
UTSW |
1 |
74,180,089 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0742:Rufy4
|
UTSW |
1 |
74,185,875 (GRCm39) |
missense |
probably benign |
0.02 |
R1533:Rufy4
|
UTSW |
1 |
74,169,002 (GRCm39) |
critical splice donor site |
probably null |
|
R1666:Rufy4
|
UTSW |
1 |
74,186,837 (GRCm39) |
missense |
probably benign |
0.06 |
R1668:Rufy4
|
UTSW |
1 |
74,186,837 (GRCm39) |
missense |
probably benign |
0.06 |
R1827:Rufy4
|
UTSW |
1 |
74,173,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R2018:Rufy4
|
UTSW |
1 |
74,180,106 (GRCm39) |
missense |
possibly damaging |
0.49 |
R2095:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R2306:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R2307:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R2472:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R2475:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R3022:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R3054:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R3055:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R3056:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R3117:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R3118:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R3236:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R3237:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R3545:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R3546:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R3547:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R3548:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R3767:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R3768:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R3770:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R3816:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R3817:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R3818:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R3819:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R3895:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4050:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4091:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4117:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4124:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4125:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4127:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4231:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4233:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4234:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4236:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4254:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4255:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4319:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4320:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4321:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4321:Rufy4
|
UTSW |
1 |
74,171,943 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4322:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4323:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4324:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4360:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4361:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4406:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4408:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4516:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4517:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4520:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4522:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4524:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4531:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4533:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4617:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4661:Rufy4
|
UTSW |
1 |
74,172,266 (GRCm39) |
missense |
probably damaging |
0.99 |
R4778:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4779:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4840:Rufy4
|
UTSW |
1 |
74,168,198 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4897:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4898:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4899:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4915:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4918:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4997:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5092:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5097:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5189:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5191:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5195:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5196:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5197:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5226:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5227:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5228:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5230:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5372:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5373:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5374:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5375:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5376:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5377:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5378:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5699:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5748:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5750:Rufy4
|
UTSW |
1 |
74,172,068 (GRCm39) |
missense |
probably benign |
0.01 |
R5767:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R5865:Rufy4
|
UTSW |
1 |
74,185,914 (GRCm39) |
missense |
probably damaging |
0.99 |
R6083:Rufy4
|
UTSW |
1 |
74,168,556 (GRCm39) |
missense |
probably damaging |
0.99 |
R6149:Rufy4
|
UTSW |
1 |
74,186,892 (GRCm39) |
missense |
probably benign |
0.15 |
R6279:Rufy4
|
UTSW |
1 |
74,172,383 (GRCm39) |
missense |
probably benign |
0.00 |
R6300:Rufy4
|
UTSW |
1 |
74,172,383 (GRCm39) |
missense |
probably benign |
0.00 |
R6629:Rufy4
|
UTSW |
1 |
74,171,526 (GRCm39) |
splice site |
probably null |
|
R6809:Rufy4
|
UTSW |
1 |
74,172,206 (GRCm39) |
missense |
probably benign |
0.00 |
R7179:Rufy4
|
UTSW |
1 |
74,172,035 (GRCm39) |
missense |
probably benign |
0.12 |
R7218:Rufy4
|
UTSW |
1 |
74,172,174 (GRCm39) |
missense |
probably damaging |
0.99 |
R7453:Rufy4
|
UTSW |
1 |
74,168,493 (GRCm39) |
splice site |
probably null |
|
R9377:Rufy4
|
UTSW |
1 |
74,171,879 (GRCm39) |
missense |
probably benign |
0.08 |
X0023:Rufy4
|
UTSW |
1 |
74,180,208 (GRCm39) |
missense |
probably benign |
0.04 |
X0025:Rufy4
|
UTSW |
1 |
74,172,178 (GRCm39) |
missense |
probably benign |
|
|
Predicted Primers |
PCR Primer
(F):5'- CAAGCCATCAGGAGAAGCTG -3'
(R):5'- AGCTAGGCCTATCTGTGGACTG -3'
Sequencing Primer
(F):5'- GGAGAAGCTGCCACCTCAATTAG -3'
(R):5'- TGGACTGCCAGCTGTTCC -3'
|
Posted On |
2016-04-15 |