Incidental Mutation 'R7570:Uggt1'
ID |
585673 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Uggt1
|
Ensembl Gene |
ENSMUSG00000037470 |
Gene Name |
UDP-glucose glycoprotein glucosyltransferase 1 |
Synonyms |
C820010P03Rik, 0910001L17Rik, Ugcgl1, A930007H10Rik |
MMRRC Submission |
045631-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.470)
|
Stock # |
R7570 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
36179109-36283407 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 36224919 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Serine
at position 572
(T572S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000037930
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000046875]
[ENSMUST00000173166]
[ENSMUST00000174266]
|
AlphaFold |
Q6P5E4 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000046875
AA Change: T572S
PolyPhen 2
Score 0.090 (Sensitivity: 0.93; Specificity: 0.85)
|
SMART Domains |
Protein: ENSMUSP00000037930 Gene: ENSMUSG00000037470 AA Change: T572S
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
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000174142
|
SMART Domains |
Protein: ENSMUSP00000133929 Gene: ENSMUSG00000037470
Domain | Start | End | E-Value | Type |
Pfam:UDP-g_GGTase
|
1 |
52 |
7.8e-11 |
PFAM |
|
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 |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.1%
|
Validation Efficiency |
98% (104/106) |
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: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930590J08Rik |
C |
T |
6: 91,911,591 (GRCm39) |
T613I |
probably benign |
Het |
Ajuba |
T |
C |
14: 54,813,859 (GRCm39) |
E288G |
probably damaging |
Het |
Ankrd12 |
C |
T |
17: 66,292,355 (GRCm39) |
R1026K |
probably benign |
Het |
Apol7b |
T |
C |
15: 77,307,674 (GRCm39) |
T274A |
probably benign |
Het |
Arid4a |
A |
T |
12: 71,109,916 (GRCm39) |
R86* |
probably null |
Het |
Asnsd1 |
C |
T |
1: 53,387,417 (GRCm39) |
G70D |
probably damaging |
Het |
Atg4c |
T |
A |
4: 99,116,797 (GRCm39) |
V313D |
possibly damaging |
Het |
Atp13a5 |
A |
C |
16: 29,085,715 (GRCm39) |
C885G |
probably damaging |
Het |
Bpifb9a |
A |
T |
2: 154,104,183 (GRCm39) |
I209F |
possibly damaging |
Het |
Bsn |
T |
C |
9: 107,990,742 (GRCm39) |
D1670G |
probably damaging |
Het |
Cct8 |
T |
A |
16: 87,288,210 (GRCm39) |
I121F |
probably benign |
Het |
Cd209a |
T |
G |
8: 3,794,151 (GRCm39) |
D217A |
probably damaging |
Het |
Cdk19 |
C |
T |
10: 40,353,954 (GRCm39) |
S456L |
possibly damaging |
Het |
Chd9 |
C |
T |
8: 91,721,208 (GRCm39) |
H999Y |
unknown |
Het |
Col5a1 |
G |
A |
2: 27,841,395 (GRCm39) |
V339M |
unknown |
Het |
Cr2 |
G |
A |
1: 194,851,648 (GRCm39) |
R115* |
probably null |
Het |
Cyb561 |
A |
T |
11: 105,828,470 (GRCm39) |
F62I |
probably damaging |
Het |
Cyp2c38 |
A |
T |
19: 39,393,187 (GRCm39) |
N293K |
possibly damaging |
Het |
Cyp2c69 |
A |
T |
19: 39,848,342 (GRCm39) |
D293E |
probably damaging |
Het |
Dcbld2 |
T |
A |
16: 58,244,932 (GRCm39) |
C69S |
possibly damaging |
Het |
Dcdc2a |
T |
C |
13: 25,303,356 (GRCm39) |
S296P |
probably benign |
Het |
Dmxl1 |
T |
A |
18: 50,027,024 (GRCm39) |
I2044K |
possibly damaging |
Het |
Dnah5 |
A |
G |
15: 28,347,098 (GRCm39) |
D2527G |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,126,413 (GRCm39) |
T1305A |
probably benign |
Het |
Dnajc9 |
A |
G |
14: 20,438,712 (GRCm39) |
V47A |
probably benign |
Het |
Dnmt3b |
A |
G |
2: 153,518,619 (GRCm39) |
Y594C |
probably damaging |
Het |
Dph7 |
A |
G |
2: 24,855,642 (GRCm39) |
D147G |
probably damaging |
Het |
Drap1 |
T |
C |
19: 5,473,380 (GRCm39) |
H164R |
possibly damaging |
Het |
Dsg3 |
T |
A |
18: 20,660,837 (GRCm39) |
V392E |
possibly damaging |
Het |
Dxo |
A |
G |
17: 35,056,616 (GRCm39) |
D81G |
probably benign |
Het |
E230025N22Rik |
G |
T |
18: 36,828,645 (GRCm39) |
T11K |
probably benign |
Het |
Esyt1 |
A |
G |
10: 128,354,801 (GRCm39) |
V533A |
possibly damaging |
Het |
Etv3 |
T |
A |
3: 87,443,338 (GRCm39) |
C307* |
probably null |
Het |
Fam114a1 |
T |
A |
5: 65,187,402 (GRCm39) |
|
probably null |
Het |
Fam3c |
T |
A |
6: 22,326,404 (GRCm39) |
|
probably benign |
Het |
Fbn1 |
G |
T |
2: 125,239,772 (GRCm39) |
T305K |
probably benign |
Het |
Ggt1 |
A |
T |
10: 75,421,428 (GRCm39) |
I484F |
probably damaging |
Het |
Gpatch1 |
T |
C |
7: 34,993,237 (GRCm39) |
D536G |
probably damaging |
Het |
Gpx4 |
T |
C |
10: 79,890,875 (GRCm39) |
I189T |
probably damaging |
Het |
Gsr |
T |
A |
8: 34,159,193 (GRCm39) |
C85S |
probably damaging |
Het |
Gsta5 |
A |
T |
9: 78,211,751 (GRCm39) |
D171V |
possibly damaging |
Het |
Havcr1 |
T |
A |
11: 46,661,369 (GRCm39) |
|
probably null |
Het |
Heatr4 |
T |
C |
12: 84,026,418 (GRCm39) |
T280A |
probably benign |
Het |
Hmcn2 |
A |
T |
2: 31,313,923 (GRCm39) |
E3532D |
probably benign |
Het |
Hnrnpc |
T |
C |
14: 52,312,556 (GRCm39) |
N308S |
possibly damaging |
Het |
Ighv8-9 |
A |
G |
12: 115,432,358 (GRCm39) |
V13A |
probably benign |
Het |
Itgb2l |
A |
T |
16: 96,227,439 (GRCm39) |
F535I |
probably benign |
Het |
Kdm5a |
T |
G |
6: 120,404,803 (GRCm39) |
D1348E |
probably damaging |
Het |
Kndc1 |
CT |
C |
7: 139,503,691 (GRCm39) |
|
probably null |
Het |
Ky |
A |
G |
9: 102,419,528 (GRCm39) |
I512V |
probably benign |
Het |
Lamc1 |
A |
T |
1: 153,119,021 (GRCm39) |
F866Y |
possibly damaging |
Het |
Lbx1 |
C |
A |
19: 45,223,687 (GRCm39) |
|
probably benign |
Het |
Magel2 |
A |
G |
7: 62,028,658 (GRCm39) |
T521A |
possibly damaging |
Het |
Mgam |
A |
T |
6: 40,723,367 (GRCm39) |
I491L |
probably benign |
Het |
Mitd1 |
T |
C |
1: 37,929,273 (GRCm39) |
E40G |
probably damaging |
Het |
Mpzl3 |
A |
G |
9: 44,981,985 (GRCm39) |
T218A |
probably benign |
Het |
Mrpl42 |
A |
G |
10: 95,316,827 (GRCm39) |
S77P |
probably benign |
Het |
Mup5 |
C |
T |
4: 61,752,911 (GRCm39) |
W37* |
probably null |
Het |
Myh14 |
T |
C |
7: 44,281,850 (GRCm39) |
I803V |
probably benign |
Het |
Ncor2 |
T |
A |
5: 125,107,153 (GRCm39) |
T744S |
|
Het |
Ndufv3 |
A |
G |
17: 31,746,596 (GRCm39) |
D162G |
probably damaging |
Het |
Nostrin |
A |
G |
2: 69,006,150 (GRCm39) |
E278G |
probably damaging |
Het |
Nrxn1 |
T |
G |
17: 90,469,807 (GRCm39) |
E1288A |
probably benign |
Het |
Or4c11c |
A |
G |
2: 88,661,472 (GRCm39) |
N4D |
possibly damaging |
Het |
Or51b6b |
C |
A |
7: 103,310,088 (GRCm39) |
R123L |
probably damaging |
Het |
Or52h1 |
T |
A |
7: 103,828,955 (GRCm39) |
Y220F |
probably damaging |
Het |
Or8g55 |
A |
T |
9: 39,784,751 (GRCm39) |
Y60F |
possibly damaging |
Het |
Patj |
T |
A |
4: 98,312,737 (GRCm39) |
|
probably null |
Het |
Pcm1 |
T |
G |
8: 41,720,381 (GRCm39) |
I314R |
possibly damaging |
Het |
Pcsk6 |
A |
G |
7: 65,683,646 (GRCm39) |
T754A |
probably benign |
Het |
Pde2a |
A |
T |
7: 101,152,041 (GRCm39) |
N326I |
probably benign |
Het |
Plekhg4 |
T |
C |
8: 106,105,316 (GRCm39) |
S594P |
possibly damaging |
Het |
Plekhm3 |
T |
C |
1: 64,977,065 (GRCm39) |
D135G |
probably damaging |
Het |
Plin4 |
A |
T |
17: 56,413,776 (GRCm39) |
M283K |
probably benign |
Het |
Ppfia3 |
T |
C |
7: 44,990,172 (GRCm39) |
|
probably null |
Het |
Prdm9 |
T |
C |
17: 15,775,914 (GRCm39) |
N179S |
probably benign |
Het |
Prrt3 |
T |
C |
6: 113,471,449 (GRCm39) |
S908G |
probably damaging |
Het |
Psg22 |
C |
A |
7: 18,456,660 (GRCm39) |
S181Y |
possibly damaging |
Het |
Rcor3 |
C |
A |
1: 191,822,173 (GRCm39) |
G8V |
probably damaging |
Het |
Rp1l1 |
T |
A |
14: 64,269,023 (GRCm39) |
C1536* |
probably null |
Het |
Rpp25l |
T |
C |
4: 41,712,529 (GRCm39) |
H82R |
probably damaging |
Het |
Rps3a1 |
T |
A |
3: 86,046,396 (GRCm39) |
M172L |
probably benign |
Het |
Rtbdn |
T |
C |
8: 85,679,556 (GRCm39) |
L110P |
probably damaging |
Het |
Ryr1 |
T |
A |
7: 28,778,010 (GRCm39) |
Q2169L |
probably damaging |
Het |
Scn4a |
A |
T |
11: 106,211,299 (GRCm39) |
C1573S |
possibly damaging |
Het |
Sec16b |
A |
T |
1: 157,358,965 (GRCm39) |
|
probably null |
Het |
Serpina1a |
A |
T |
12: 103,820,096 (GRCm39) |
D383E |
possibly damaging |
Het |
Sh3gl3 |
T |
C |
7: 81,934,285 (GRCm39) |
M262T |
probably benign |
Het |
Sos2 |
G |
A |
12: 69,637,654 (GRCm39) |
T1052M |
probably damaging |
Het |
Spag16 |
G |
A |
1: 70,036,000 (GRCm39) |
V343I |
probably benign |
Het |
Spocd1 |
T |
G |
4: 129,823,957 (GRCm39) |
D251E |
|
Het |
Stc2 |
G |
T |
11: 31,317,798 (GRCm39) |
N74K |
probably damaging |
Het |
Tasor2 |
A |
G |
13: 3,623,621 (GRCm39) |
Y2110H |
probably damaging |
Het |
Thbs3 |
C |
T |
3: 89,126,359 (GRCm39) |
Q227* |
probably null |
Het |
Tmem92 |
A |
C |
11: 94,669,816 (GRCm39) |
I105R |
probably benign |
Het |
Tmod1 |
T |
A |
4: 46,083,632 (GRCm39) |
N20K |
probably benign |
Het |
Tns1 |
T |
C |
1: 73,992,638 (GRCm39) |
D53G |
probably damaging |
Het |
Tspan33 |
T |
A |
6: 29,717,337 (GRCm39) |
L246Q |
probably damaging |
Het |
Ttc16 |
A |
G |
2: 32,658,980 (GRCm39) |
L392P |
probably damaging |
Het |
Usp17la |
A |
T |
7: 104,509,604 (GRCm39) |
T70S |
probably damaging |
Het |
Usp31 |
C |
T |
7: 121,274,186 (GRCm39) |
R370H |
probably damaging |
Het |
Wdr83 |
C |
T |
8: 85,806,463 (GRCm39) |
V112M |
probably damaging |
Het |
Zbtb25 |
T |
A |
12: 76,416,366 (GRCm39) |
|
probably benign |
Het |
Zfp110 |
T |
A |
7: 12,583,267 (GRCm39) |
N638K |
possibly damaging |
Het |
Zfp747l1 |
T |
A |
7: 126,984,455 (GRCm39) |
S216C |
probably benign |
Het |
Zfp820 |
T |
C |
17: 22,037,994 (GRCm39) |
T445A |
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 |
|
R0373:Uggt1
|
UTSW |
1 |
36,218,751 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
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'- GTTGTACTCAACCTCCCACCAG -3'
(R):5'- CGGGTTGCCTTATAAGATGCC -3'
Sequencing Primer
(F):5'- TCCCACCAGTACTGCAGC -3'
(R):5'- GCCTTATAAGATGCCCCTTTTTCTG -3'
|
Posted On |
2019-10-17 |