Incidental Mutation 'R0373:Uggt1'
ID |
30570 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Uggt1
|
Ensembl Gene |
ENSMUSG00000037470 |
Gene Name |
UDP-glucose glycoprotein glucosyltransferase 1 |
Synonyms |
C820010P03Rik, 0910001L17Rik, Ugcgl1, A930007H10Rik |
MMRRC Submission |
038579-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.470)
|
Stock # |
R0373 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
36179109-36283407 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 36218751 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Proline
at position 59
(S59P)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000134078
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000046875]
[ENSMUST00000173166]
[ENSMUST00000174266]
|
AlphaFold |
Q6P5E4 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000046875
AA Change: S676P
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
SMART Domains |
Protein: ENSMUSP00000037930 Gene: ENSMUSG00000037470 AA Change: S676P
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
42 |
N/A |
INTRINSIC |
Pfam:UDP-g_GGTase
|
44 |
1222 |
N/A |
PFAM |
SCOP:d1ga8a_
|
1256 |
1521 |
3e-45 |
SMART |
Blast:BROMO
|
1414 |
1453 |
3e-17 |
BLAST |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000173166
AA Change: S59P
PolyPhen 2
Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000174266
|
SMART Domains |
Protein: ENSMUSP00000134640 Gene: ENSMUSG00000037470
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
42 |
N/A |
INTRINSIC |
low complexity region
|
88 |
97 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000174716
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.1%
- 10x: 95.8%
- 20x: 91.5%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] UDP-glucose:glycoprotein glucosyltransferase (UGT) is a soluble protein of the endoplasmic reticulum (ER) that selectively reglucosylates unfolded glycoproteins, thus providing quality control for protein transport out of the ER.[supplied by OMIM, Oct 2009] PHENOTYPE: Heterozygous KO reduces susceptibility to and morbidity of RNA virus infection. Homozygous KO is embryonic lethal. The peptide is a folding sensor for glycoproteins in the ER. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930579F01Rik |
A |
T |
3: 137,879,343 (GRCm39) |
L235Q |
probably damaging |
Het |
Aadacl4fm4 |
A |
T |
4: 144,412,790 (GRCm39) |
M50K |
possibly damaging |
Het |
Adam6b |
T |
A |
12: 113,454,275 (GRCm39) |
V364D |
probably benign |
Het |
Akap13 |
T |
C |
7: 75,259,677 (GRCm39) |
L767P |
probably benign |
Het |
Akap13 |
T |
A |
7: 75,380,248 (GRCm39) |
S2193T |
probably damaging |
Het |
Anapc11 |
T |
C |
11: 120,496,203 (GRCm39) |
V69A |
probably benign |
Het |
Ankmy1 |
C |
T |
1: 92,823,912 (GRCm39) |
R118Q |
probably damaging |
Het |
Ankrd27 |
T |
C |
7: 35,337,478 (GRCm39) |
S931P |
probably benign |
Het |
Atp6v1c2 |
G |
A |
12: 17,338,169 (GRCm39) |
R280C |
probably damaging |
Het |
Bbs10 |
T |
A |
10: 111,135,913 (GRCm39) |
I342N |
probably damaging |
Het |
Calhm2 |
T |
C |
19: 47,121,389 (GRCm39) |
D260G |
possibly damaging |
Het |
Camk2a |
A |
G |
18: 61,091,310 (GRCm39) |
E264G |
probably damaging |
Het |
Ccdc146 |
T |
A |
5: 21,524,543 (GRCm39) |
M270L |
probably benign |
Het |
Cdc16 |
A |
G |
8: 13,829,264 (GRCm39) |
T517A |
probably benign |
Het |
Ces1g |
T |
C |
8: 94,057,821 (GRCm39) |
H160R |
probably benign |
Het |
Chst4 |
T |
C |
8: 110,757,026 (GRCm39) |
N196S |
probably damaging |
Het |
Ciz1 |
A |
T |
2: 32,257,479 (GRCm39) |
N175Y |
probably damaging |
Het |
Cyb5r4 |
G |
A |
9: 86,909,093 (GRCm39) |
V57I |
probably damaging |
Het |
Cyth3 |
A |
G |
5: 143,670,181 (GRCm39) |
|
probably benign |
Het |
Def6 |
A |
G |
17: 28,439,154 (GRCm39) |
E255G |
probably damaging |
Het |
Dhtkd1 |
T |
G |
2: 5,916,681 (GRCm39) |
Q665P |
probably damaging |
Het |
Dsg3 |
A |
C |
18: 20,672,804 (GRCm39) |
D825A |
probably damaging |
Het |
Eif3m |
T |
C |
2: 104,835,345 (GRCm39) |
T242A |
probably benign |
Het |
Emilin3 |
A |
G |
2: 160,751,737 (GRCm39) |
F101L |
probably benign |
Het |
Epha7 |
A |
G |
4: 28,935,700 (GRCm39) |
|
probably null |
Het |
Fbxo45 |
A |
T |
16: 32,057,223 (GRCm39) |
Y224N |
probably damaging |
Het |
Fhod3 |
A |
T |
18: 25,223,161 (GRCm39) |
M836L |
possibly damaging |
Het |
Fut4 |
C |
A |
9: 14,662,506 (GRCm39) |
V263F |
probably damaging |
Het |
Ggt1 |
C |
T |
10: 75,415,104 (GRCm39) |
T206M |
probably benign |
Het |
Gls |
T |
C |
1: 52,227,858 (GRCm39) |
R79G |
probably damaging |
Het |
Grhl1 |
T |
C |
12: 24,631,514 (GRCm39) |
S156P |
probably benign |
Het |
Ipo8 |
C |
T |
6: 148,676,540 (GRCm39) |
S983N |
probably benign |
Het |
Kcna7 |
C |
T |
7: 45,058,868 (GRCm39) |
A385V |
probably damaging |
Het |
Kpnb1 |
A |
T |
11: 97,075,916 (GRCm39) |
L40Q |
probably damaging |
Het |
Matn1 |
A |
T |
4: 130,677,417 (GRCm39) |
S209C |
probably damaging |
Het |
Mcc |
A |
G |
18: 44,608,289 (GRCm39) |
I501T |
probably benign |
Het |
Mdp1 |
A |
T |
14: 55,896,832 (GRCm39) |
F104L |
probably damaging |
Het |
Mib2 |
A |
T |
4: 155,740,745 (GRCm39) |
N626K |
probably damaging |
Het |
Mrgprh |
T |
C |
17: 13,095,843 (GRCm39) |
S28P |
possibly damaging |
Het |
Mup-ps23 |
T |
A |
4: 61,774,386 (GRCm39) |
|
noncoding transcript |
Het |
Myh15 |
A |
G |
16: 49,003,322 (GRCm39) |
T1794A |
possibly damaging |
Het |
Myo18a |
C |
G |
11: 77,711,868 (GRCm39) |
P680A |
probably benign |
Het |
Myom2 |
G |
T |
8: 15,148,419 (GRCm39) |
D532Y |
possibly damaging |
Het |
Ndufaf5 |
A |
G |
2: 140,012,801 (GRCm39) |
N57S |
probably benign |
Het |
Nectin3 |
C |
T |
16: 46,278,550 (GRCm39) |
V282M |
probably damaging |
Het |
Nup188 |
G |
T |
2: 30,221,000 (GRCm39) |
D997Y |
probably damaging |
Het |
Olfm3 |
T |
C |
3: 114,916,454 (GRCm39) |
V462A |
probably damaging |
Het |
Opcml |
A |
G |
9: 28,724,694 (GRCm39) |
H164R |
possibly damaging |
Het |
Or14a259 |
A |
T |
7: 86,013,013 (GRCm39) |
C177* |
probably null |
Het |
Or4c120 |
A |
T |
2: 89,000,757 (GRCm39) |
F266L |
probably benign |
Het |
Or8u9 |
A |
C |
2: 86,002,050 (GRCm39) |
F37C |
probably damaging |
Het |
Pacrg |
A |
G |
17: 10,622,347 (GRCm39) |
I209T |
probably damaging |
Het |
Pcf11 |
T |
C |
7: 92,310,423 (GRCm39) |
M522V |
probably benign |
Het |
Pck1 |
T |
A |
2: 172,995,183 (GRCm39) |
M1K |
probably null |
Het |
Pcm1 |
G |
T |
8: 41,729,148 (GRCm39) |
E707* |
probably null |
Het |
Pcsk5 |
G |
A |
19: 17,632,213 (GRCm39) |
R318W |
probably damaging |
Het |
Phf11d |
A |
T |
14: 59,590,793 (GRCm39) |
M188K |
possibly damaging |
Het |
Ppip5k2 |
A |
T |
1: 97,668,262 (GRCm39) |
C615* |
probably null |
Het |
Prkdc |
T |
A |
16: 15,609,791 (GRCm39) |
S3132T |
probably damaging |
Het |
Prl2c5 |
A |
T |
13: 13,357,609 (GRCm39) |
|
probably benign |
Het |
Prpsap2 |
A |
G |
11: 61,631,826 (GRCm39) |
I177T |
possibly damaging |
Het |
Rad50 |
A |
G |
11: 53,541,346 (GRCm39) |
S1297P |
probably damaging |
Het |
Rasip1 |
T |
A |
7: 45,284,668 (GRCm39) |
N678K |
possibly damaging |
Het |
Rubcn |
A |
G |
16: 32,656,350 (GRCm39) |
S544P |
probably damaging |
Het |
Rwdd2a |
A |
T |
9: 86,456,453 (GRCm39) |
T210S |
possibly damaging |
Het |
Scd2 |
A |
G |
19: 44,291,479 (GRCm39) |
D306G |
probably damaging |
Het |
Sema3b |
T |
C |
9: 107,480,117 (GRCm39) |
N207S |
probably benign |
Het |
Sf3b2 |
C |
T |
19: 5,324,852 (GRCm39) |
D845N |
probably damaging |
Het |
Sipa1l2 |
C |
A |
8: 126,191,149 (GRCm39) |
C947F |
probably damaging |
Het |
Slc12a1 |
A |
T |
2: 125,067,951 (GRCm39) |
T1013S |
probably damaging |
Het |
Slc18a2 |
A |
T |
19: 59,275,799 (GRCm39) |
I461L |
probably benign |
Het |
Slc1a6 |
C |
A |
10: 78,637,756 (GRCm39) |
Y427* |
probably null |
Het |
Slc30a4 |
A |
T |
2: 122,531,319 (GRCm39) |
I231K |
probably damaging |
Het |
Sos1 |
G |
T |
17: 80,761,192 (GRCm39) |
A168D |
probably damaging |
Het |
Spata31f1a |
T |
C |
4: 42,851,161 (GRCm39) |
I332V |
probably benign |
Het |
Sptb |
T |
C |
12: 76,668,145 (GRCm39) |
S651G |
probably benign |
Het |
Stk36 |
T |
C |
1: 74,672,779 (GRCm39) |
L1007P |
probably damaging |
Het |
Tek |
A |
T |
4: 94,692,578 (GRCm39) |
N229Y |
probably damaging |
Het |
Tep1 |
A |
G |
14: 51,074,225 (GRCm39) |
F1887L |
possibly damaging |
Het |
Tet1 |
A |
T |
10: 62,713,988 (GRCm39) |
C602* |
probably null |
Het |
Tnfrsf19 |
A |
G |
14: 61,209,485 (GRCm39) |
S262P |
possibly damaging |
Het |
Trim5 |
T |
C |
7: 103,914,891 (GRCm39) |
I393V |
probably benign |
Het |
Trpm6 |
A |
G |
19: 18,830,951 (GRCm39) |
E1272G |
probably benign |
Het |
Ttc21b |
A |
T |
2: 66,018,670 (GRCm39) |
Y1246N |
probably damaging |
Het |
Ttll3 |
T |
A |
6: 113,375,738 (GRCm39) |
L151H |
probably damaging |
Het |
U2surp |
C |
T |
9: 95,366,496 (GRCm39) |
V470I |
probably benign |
Het |
Ubr1 |
A |
T |
2: 120,777,138 (GRCm39) |
Y276N |
probably benign |
Het |
Unc45a |
T |
C |
7: 79,976,092 (GRCm39) |
T796A |
probably damaging |
Het |
Unc5b |
C |
A |
10: 60,614,719 (GRCm39) |
V193F |
possibly damaging |
Het |
Upp1 |
G |
T |
11: 9,079,590 (GRCm39) |
M50I |
probably benign |
Het |
Vps18 |
C |
T |
2: 119,124,386 (GRCm39) |
R438C |
probably damaging |
Het |
Zfp715 |
T |
C |
7: 42,948,760 (GRCm39) |
Y400C |
possibly damaging |
Het |
Zfp955b |
T |
C |
17: 33,521,496 (GRCm39) |
Y322H |
probably benign |
Het |
|
Other mutations in Uggt1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Uggt1
|
APN |
1 |
36,218,633 (GRCm39) |
splice site |
probably benign |
|
IGL00817:Uggt1
|
APN |
1 |
36,225,013 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01395:Uggt1
|
APN |
1 |
36,194,158 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01609:Uggt1
|
APN |
1 |
36,221,555 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01619:Uggt1
|
APN |
1 |
36,200,775 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02077:Uggt1
|
APN |
1 |
36,215,875 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02313:Uggt1
|
APN |
1 |
36,223,565 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02341:Uggt1
|
APN |
1 |
36,203,600 (GRCm39) |
makesense |
probably null |
|
IGL02346:Uggt1
|
APN |
1 |
36,218,751 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02447:Uggt1
|
APN |
1 |
36,189,223 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02883:Uggt1
|
APN |
1 |
36,216,696 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02930:Uggt1
|
APN |
1 |
36,196,537 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03153:Uggt1
|
APN |
1 |
36,241,899 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03162:Uggt1
|
APN |
1 |
36,247,037 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03170:Uggt1
|
APN |
1 |
36,202,342 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03266:Uggt1
|
APN |
1 |
36,189,129 (GRCm39) |
missense |
probably damaging |
1.00 |
K3955:Uggt1
|
UTSW |
1 |
36,201,434 (GRCm39) |
missense |
probably benign |
0.37 |
R0037:Uggt1
|
UTSW |
1 |
36,225,013 (GRCm39) |
missense |
probably benign |
0.03 |
R0037:Uggt1
|
UTSW |
1 |
36,225,013 (GRCm39) |
missense |
probably benign |
0.03 |
R0167:Uggt1
|
UTSW |
1 |
36,209,278 (GRCm39) |
critical splice donor site |
probably null |
|
R0502:Uggt1
|
UTSW |
1 |
36,199,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R0546:Uggt1
|
UTSW |
1 |
36,235,052 (GRCm39) |
missense |
probably benign |
0.00 |
R0610:Uggt1
|
UTSW |
1 |
36,204,587 (GRCm39) |
splice site |
probably benign |
|
R0671:Uggt1
|
UTSW |
1 |
36,194,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R0760:Uggt1
|
UTSW |
1 |
36,200,805 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0825:Uggt1
|
UTSW |
1 |
36,197,224 (GRCm39) |
missense |
probably benign |
0.01 |
R0827:Uggt1
|
UTSW |
1 |
36,195,394 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0884:Uggt1
|
UTSW |
1 |
36,214,159 (GRCm39) |
missense |
probably benign |
0.00 |
R1112:Uggt1
|
UTSW |
1 |
36,212,627 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1470:Uggt1
|
UTSW |
1 |
36,215,877 (GRCm39) |
missense |
probably benign |
0.13 |
R1470:Uggt1
|
UTSW |
1 |
36,215,877 (GRCm39) |
missense |
probably benign |
0.13 |
R1592:Uggt1
|
UTSW |
1 |
36,241,939 (GRCm39) |
missense |
probably benign |
0.04 |
R1730:Uggt1
|
UTSW |
1 |
36,260,342 (GRCm39) |
missense |
probably benign |
0.05 |
R1923:Uggt1
|
UTSW |
1 |
36,218,694 (GRCm39) |
missense |
probably damaging |
0.99 |
R1970:Uggt1
|
UTSW |
1 |
36,190,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R2086:Uggt1
|
UTSW |
1 |
36,231,495 (GRCm39) |
missense |
probably null |
1.00 |
R2829:Uggt1
|
UTSW |
1 |
36,201,375 (GRCm39) |
missense |
probably benign |
0.38 |
R3431:Uggt1
|
UTSW |
1 |
36,249,140 (GRCm39) |
nonsense |
probably null |
|
R3432:Uggt1
|
UTSW |
1 |
36,249,140 (GRCm39) |
nonsense |
probably null |
|
R3725:Uggt1
|
UTSW |
1 |
36,221,588 (GRCm39) |
nonsense |
probably null |
|
R3880:Uggt1
|
UTSW |
1 |
36,215,885 (GRCm39) |
intron |
probably benign |
|
R4052:Uggt1
|
UTSW |
1 |
36,203,570 (GRCm39) |
missense |
probably damaging |
0.98 |
R4133:Uggt1
|
UTSW |
1 |
36,197,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R4489:Uggt1
|
UTSW |
1 |
36,185,749 (GRCm39) |
nonsense |
probably null |
|
R4570:Uggt1
|
UTSW |
1 |
36,189,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R4866:Uggt1
|
UTSW |
1 |
36,241,936 (GRCm39) |
nonsense |
probably null |
|
R4895:Uggt1
|
UTSW |
1 |
36,195,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R4900:Uggt1
|
UTSW |
1 |
36,241,936 (GRCm39) |
nonsense |
probably null |
|
R5372:Uggt1
|
UTSW |
1 |
36,283,141 (GRCm39) |
splice site |
probably benign |
|
R5385:Uggt1
|
UTSW |
1 |
36,223,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R5652:Uggt1
|
UTSW |
1 |
36,255,234 (GRCm39) |
nonsense |
probably null |
|
R5694:Uggt1
|
UTSW |
1 |
36,218,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R5732:Uggt1
|
UTSW |
1 |
36,200,852 (GRCm39) |
splice site |
probably null |
|
R5893:Uggt1
|
UTSW |
1 |
36,266,709 (GRCm39) |
splice site |
probably null |
|
R6191:Uggt1
|
UTSW |
1 |
36,201,289 (GRCm39) |
missense |
probably damaging |
0.98 |
R6247:Uggt1
|
UTSW |
1 |
36,202,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R6259:Uggt1
|
UTSW |
1 |
36,273,997 (GRCm39) |
missense |
probably benign |
0.00 |
R6399:Uggt1
|
UTSW |
1 |
36,202,447 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6439:Uggt1
|
UTSW |
1 |
36,214,032 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6468:Uggt1
|
UTSW |
1 |
36,212,531 (GRCm39) |
missense |
probably benign |
0.00 |
R6788:Uggt1
|
UTSW |
1 |
36,269,769 (GRCm39) |
missense |
probably benign |
0.00 |
R7165:Uggt1
|
UTSW |
1 |
36,194,188 (GRCm39) |
missense |
probably benign |
0.41 |
R7255:Uggt1
|
UTSW |
1 |
36,185,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R7273:Uggt1
|
UTSW |
1 |
36,201,302 (GRCm39) |
missense |
probably damaging |
0.99 |
R7469:Uggt1
|
UTSW |
1 |
36,190,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R7490:Uggt1
|
UTSW |
1 |
36,203,589 (GRCm39) |
missense |
probably benign |
0.01 |
R7570:Uggt1
|
UTSW |
1 |
36,224,919 (GRCm39) |
missense |
probably benign |
0.09 |
R7612:Uggt1
|
UTSW |
1 |
36,202,316 (GRCm39) |
missense |
probably damaging |
0.99 |
R7759:Uggt1
|
UTSW |
1 |
36,185,806 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7792:Uggt1
|
UTSW |
1 |
36,247,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R7816:Uggt1
|
UTSW |
1 |
36,202,396 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7858:Uggt1
|
UTSW |
1 |
36,195,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R7887:Uggt1
|
UTSW |
1 |
36,247,115 (GRCm39) |
missense |
probably damaging |
0.99 |
R8040:Uggt1
|
UTSW |
1 |
36,250,554 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8093:Uggt1
|
UTSW |
1 |
36,266,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R8245:Uggt1
|
UTSW |
1 |
36,204,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R8338:Uggt1
|
UTSW |
1 |
36,266,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R8353:Uggt1
|
UTSW |
1 |
36,209,377 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8442:Uggt1
|
UTSW |
1 |
36,212,568 (GRCm39) |
missense |
probably damaging |
0.99 |
R8519:Uggt1
|
UTSW |
1 |
36,215,724 (GRCm39) |
splice site |
probably null |
|
R8529:Uggt1
|
UTSW |
1 |
36,223,513 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8730:Uggt1
|
UTSW |
1 |
36,236,624 (GRCm39) |
critical splice donor site |
probably null |
|
R8917:Uggt1
|
UTSW |
1 |
36,185,735 (GRCm39) |
missense |
|
|
R8947:Uggt1
|
UTSW |
1 |
36,197,229 (GRCm39) |
missense |
probably benign |
0.12 |
R9240:Uggt1
|
UTSW |
1 |
36,221,696 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9248:Uggt1
|
UTSW |
1 |
36,249,103 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9401:Uggt1
|
UTSW |
1 |
36,255,212 (GRCm39) |
critical splice donor site |
probably null |
|
R9414:Uggt1
|
UTSW |
1 |
36,223,507 (GRCm39) |
missense |
probably benign |
0.01 |
R9416:Uggt1
|
UTSW |
1 |
36,203,603 (GRCm39) |
missense |
|
|
R9441:Uggt1
|
UTSW |
1 |
36,260,306 (GRCm39) |
missense |
probably benign |
0.02 |
R9489:Uggt1
|
UTSW |
1 |
36,273,886 (GRCm39) |
critical splice donor site |
probably null |
|
R9563:Uggt1
|
UTSW |
1 |
36,204,627 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9605:Uggt1
|
UTSW |
1 |
36,273,886 (GRCm39) |
critical splice donor site |
probably null |
|
X0022:Uggt1
|
UTSW |
1 |
36,204,636 (GRCm39) |
missense |
possibly damaging |
0.67 |
Z1088:Uggt1
|
UTSW |
1 |
36,213,272 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Uggt1
|
UTSW |
1 |
36,200,776 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Uggt1
|
UTSW |
1 |
36,194,154 (GRCm39) |
missense |
probably null |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- ACCCCACCTTAAACTCCTGAGAGTG -3'
(R):5'- CTGGCACCCCAGTGTTTCAATAGAG -3'
Sequencing Primer
(F):5'- gccatctcttcagcccc -3'
(R):5'- CCCCAGTGTTTCAATAGAGTTAGAGG -3'
|
Posted On |
2013-04-24 |