Incidental Mutation 'R6056:Uggt2'
| ID |
484431 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Uggt2
|
| Ensembl Gene |
ENSMUSG00000042104 |
| Gene Name |
UDP-glucose glycoprotein glucosyltransferase 2 |
| Synonyms |
3110001A05Rik, A230065J02Rik, 3110027P15Rik, 1810064L21Rik, Ugcgl2 |
| MMRRC Submission |
044223-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.104)
|
| Stock # |
R6056 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
14 |
| Chromosomal Location |
119222451-119336842 bp(-) (GRCm39) |
| Type of Mutation |
critical splice donor site (1 bp from exon) |
| DNA Base Change (assembly) |
C to T
at 119273381 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000121249
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000127153]
[ENSMUST00000156203]
[ENSMUST00000156203]
|
| AlphaFold |
E9Q4X2 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000127153
|
| SMART Domains |
Protein: ENSMUSP00000117738
Gene: ENSMUSG00000042104
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
327 |
334 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000153693
|
| SMART Domains |
Protein: ENSMUSP00000123327
Gene: ENSMUSG00000042104
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:UDP-g_GGTase
|
1 |
106 |
3.3e-40 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000156203
|
| SMART Domains |
Protein: ENSMUSP00000121249
Gene: ENSMUSG00000042104
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
|
Pfam:UDP-g_GGTase
|
23 |
1189 |
N/A |
PFAM |
|
SCOP:d1ga8a_
|
1219 |
1485 |
9e-44 |
SMART |
|
Blast:BROMO
|
1377 |
1427 |
4e-16 |
BLAST |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000156203
|
| SMART Domains |
Protein: ENSMUSP00000121249
Gene: ENSMUSG00000042104
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
|
Pfam:UDP-g_GGTase
|
23 |
1189 |
N/A |
PFAM |
|
SCOP:d1ga8a_
|
1219 |
1485 |
9e-44 |
SMART |
|
Blast:BROMO
|
1377 |
1427 |
4e-16 |
BLAST |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000173470
|
| Meta Mutation Damage Score |
0.9483 |
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.7%
- 10x: 98.4%
- 20x: 95.4%
|
| Validation Efficiency |
96% (99/103) |
| 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]
|
| Allele List at MGI |
All alleles(5) : Targeted(2) Gene trapped(3)
|
| Other mutations in this stock |
Total: 101 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2310002L09Rik |
A |
T |
4: 73,861,115 (GRCm39) |
W162R |
probably benign |
Het |
| 4930438A08Rik |
C |
A |
11: 58,184,464 (GRCm39) |
P394H |
probably damaging |
Het |
| Aggf1 |
C |
T |
13: 95,508,123 (GRCm39) |
C81Y |
probably benign |
Het |
| Agxt2 |
A |
T |
15: 10,378,963 (GRCm39) |
D188V |
probably damaging |
Het |
| Angpt2 |
T |
C |
8: 18,748,132 (GRCm39) |
K376R |
probably benign |
Het |
| Anxa5 |
A |
G |
3: 36,504,840 (GRCm39) |
S241P |
probably damaging |
Het |
| Aox3 |
A |
T |
1: 58,209,018 (GRCm39) |
K850N |
probably damaging |
Het |
| Arid5a |
T |
C |
1: 36,358,473 (GRCm39) |
M415T |
probably benign |
Het |
| Aspa |
T |
A |
11: 73,199,578 (GRCm39) |
N233I |
probably damaging |
Het |
| Atp4b |
C |
T |
8: 13,438,782 (GRCm39) |
R198Q |
probably damaging |
Het |
| Atp8b2 |
A |
T |
3: 89,853,528 (GRCm39) |
V719E |
possibly damaging |
Het |
| Bltp2 |
C |
A |
11: 78,162,210 (GRCm39) |
L691I |
possibly damaging |
Het |
| Cacna1s |
T |
G |
1: 136,033,574 (GRCm39) |
V1017G |
probably damaging |
Het |
| Chrna4 |
G |
T |
2: 180,671,235 (GRCm39) |
Q174K |
probably damaging |
Het |
| Chrnb1 |
A |
T |
11: 69,677,765 (GRCm39) |
V329D |
probably damaging |
Het |
| Chst14 |
T |
C |
2: 118,758,214 (GRCm39) |
L336P |
probably damaging |
Het |
| Clec2e |
T |
C |
6: 129,077,772 (GRCm39) |
D22G |
probably benign |
Het |
| Csrnp2 |
A |
C |
15: 100,380,263 (GRCm39) |
S343A |
probably benign |
Het |
| Dapl1 |
C |
A |
2: 59,315,057 (GRCm39) |
A2E |
probably damaging |
Het |
| Dlec1 |
G |
T |
9: 118,950,991 (GRCm39) |
R519L |
probably damaging |
Het |
| Dmgdh |
T |
A |
13: 93,845,251 (GRCm39) |
F415I |
possibly damaging |
Het |
| Dmgdh |
T |
C |
13: 93,888,834 (GRCm39) |
V824A |
probably damaging |
Het |
| Dnah11 |
T |
G |
12: 117,892,191 (GRCm39) |
T3661P |
probably benign |
Het |
| Dnah3 |
A |
G |
7: 119,629,254 (GRCm39) |
F1434L |
probably damaging |
Het |
| Dnajc11 |
C |
A |
4: 152,062,583 (GRCm39) |
|
probably benign |
Het |
| Dot1l |
A |
G |
10: 80,621,929 (GRCm39) |
E527G |
probably damaging |
Het |
| Drc7 |
T |
C |
8: 95,801,679 (GRCm39) |
L680P |
probably damaging |
Het |
| Dysf |
T |
C |
6: 84,083,844 (GRCm39) |
Y742H |
probably benign |
Het |
| Ece1 |
A |
G |
4: 137,688,958 (GRCm39) |
Y665C |
probably damaging |
Het |
| Emc1 |
A |
G |
4: 139,081,533 (GRCm39) |
K54E |
possibly damaging |
Het |
| Enoph1 |
C |
T |
5: 100,215,760 (GRCm39) |
T247M |
probably damaging |
Het |
| Exoc2 |
T |
C |
13: 31,084,812 (GRCm39) |
K383R |
probably benign |
Het |
| Fam227b |
A |
T |
2: 125,962,972 (GRCm39) |
H181Q |
probably damaging |
Het |
| Fsip2 |
A |
T |
2: 82,816,017 (GRCm39) |
M3917L |
probably benign |
Het |
| Gtf3a |
T |
A |
5: 146,892,338 (GRCm39) |
|
probably benign |
Het |
| Hgfac |
T |
A |
5: 35,198,973 (GRCm39) |
C11* |
probably null |
Het |
| Hmcn1 |
C |
A |
1: 150,539,660 (GRCm39) |
A2944S |
probably damaging |
Het |
| Hps5 |
T |
A |
7: 46,416,521 (GRCm39) |
Y947F |
probably benign |
Het |
| Ighv2-5 |
A |
T |
12: 113,649,120 (GRCm39) |
I111K |
probably benign |
Het |
| Inpp5e |
A |
T |
2: 26,297,860 (GRCm39) |
L247* |
probably null |
Het |
| Kbtbd11 |
T |
C |
8: 15,077,577 (GRCm39) |
S59P |
probably benign |
Het |
| Kctd19 |
G |
A |
8: 106,123,082 (GRCm39) |
H111Y |
probably damaging |
Het |
| Kif1a |
T |
C |
1: 92,952,370 (GRCm39) |
D1303G |
probably damaging |
Het |
| Kif7 |
A |
G |
7: 79,363,842 (GRCm39) |
V22A |
possibly damaging |
Het |
| Lrit3 |
A |
T |
3: 129,583,004 (GRCm39) |
C328S |
probably damaging |
Het |
| Lrrc37a |
G |
T |
11: 103,388,484 (GRCm39) |
Q2314K |
unknown |
Het |
| LTO1 |
G |
T |
7: 144,469,023 (GRCm39) |
V17L |
possibly damaging |
Het |
| Lurap1 |
G |
T |
4: 115,994,599 (GRCm39) |
P211T |
possibly damaging |
Het |
| Mbd2 |
T |
A |
18: 70,713,874 (GRCm39) |
N5K |
possibly damaging |
Het |
| Mbtps1 |
A |
C |
8: 120,242,341 (GRCm39) |
L894V |
probably benign |
Het |
| Mefv |
G |
A |
16: 3,525,906 (GRCm39) |
S787F |
possibly damaging |
Het |
| Miip |
T |
A |
4: 147,946,792 (GRCm39) |
I289F |
probably damaging |
Het |
| Mogat2 |
T |
A |
7: 98,872,720 (GRCm39) |
I155F |
possibly damaging |
Het |
| Mpp3 |
C |
A |
11: 101,902,515 (GRCm39) |
|
probably null |
Het |
| Mrrf |
A |
G |
2: 36,067,233 (GRCm39) |
K220E |
probably damaging |
Het |
| Mtmr6 |
C |
T |
14: 60,535,619 (GRCm39) |
P485L |
probably damaging |
Het |
| Mtor |
G |
A |
4: 148,621,892 (GRCm39) |
R1896K |
probably benign |
Het |
| Myh3 |
C |
T |
11: 66,978,371 (GRCm39) |
P453S |
probably benign |
Het |
| Nebl |
A |
G |
2: 17,455,045 (GRCm39) |
V112A |
probably benign |
Het |
| Nmnat2 |
G |
A |
1: 152,950,480 (GRCm39) |
W55* |
probably null |
Het |
| Nprl3 |
A |
G |
11: 32,217,432 (GRCm39) |
S37P |
probably damaging |
Het |
| Or4a73 |
T |
C |
2: 89,421,445 (GRCm39) |
N5D |
possibly damaging |
Het |
| Pcdhga4 |
T |
G |
18: 37,819,383 (GRCm39) |
S311A |
probably benign |
Het |
| Pcdhgb6 |
T |
C |
18: 37,876,165 (GRCm39) |
V291A |
probably benign |
Het |
| Peg10 |
GAT |
GATCAT |
6: 4,756,449 (GRCm39) |
|
probably benign |
Het |
| Peg3 |
T |
C |
7: 6,712,570 (GRCm39) |
E884G |
probably damaging |
Het |
| Pgpep1 |
G |
A |
8: 71,105,101 (GRCm39) |
T53M |
probably damaging |
Het |
| Phf12 |
A |
G |
11: 77,900,341 (GRCm39) |
T146A |
probably benign |
Het |
| Polr3k |
C |
G |
2: 181,506,281 (GRCm39) |
N10K |
probably damaging |
Het |
| Prickle4 |
C |
A |
17: 48,001,135 (GRCm39) |
G144C |
probably damaging |
Het |
| Ptpn6 |
T |
C |
6: 124,709,398 (GRCm39) |
Y25C |
probably damaging |
Het |
| Rad1 |
A |
G |
15: 10,488,160 (GRCm39) |
I95V |
probably damaging |
Het |
| Rad23b |
A |
G |
4: 55,382,540 (GRCm39) |
T248A |
probably benign |
Het |
| Rapgef3 |
T |
C |
15: 97,656,742 (GRCm39) |
D299G |
probably damaging |
Het |
| Rcc2 |
T |
G |
4: 140,444,335 (GRCm39) |
V342G |
possibly damaging |
Het |
| Rgs3 |
G |
T |
4: 62,544,143 (GRCm39) |
R136L |
probably damaging |
Het |
| Scube2 |
A |
T |
7: 109,432,220 (GRCm39) |
C399* |
probably null |
Het |
| Serpinb3d |
T |
C |
1: 107,007,452 (GRCm39) |
Y178C |
probably damaging |
Het |
| Slc1a7 |
A |
G |
4: 107,869,458 (GRCm39) |
T508A |
probably benign |
Het |
| Slc29a4 |
C |
T |
5: 142,705,832 (GRCm39) |
R439C |
probably damaging |
Het |
| Sntg2 |
A |
G |
12: 30,362,560 (GRCm39) |
I62T |
probably benign |
Het |
| Sowaha |
G |
A |
11: 53,369,914 (GRCm39) |
P274L |
probably damaging |
Het |
| Sptan1 |
A |
G |
2: 29,886,794 (GRCm39) |
N869S |
probably benign |
Het |
| Stx18 |
C |
A |
5: 38,263,908 (GRCm39) |
A64D |
probably damaging |
Het |
| Stxbp5 |
A |
G |
10: 9,646,430 (GRCm39) |
V94A |
probably benign |
Het |
| Sult1a1 |
T |
A |
7: 126,275,624 (GRCm39) |
|
probably null |
Het |
| Susd1 |
G |
T |
4: 59,379,687 (GRCm39) |
H313Q |
possibly damaging |
Het |
| Tdrd9 |
A |
T |
12: 111,951,475 (GRCm39) |
K88N |
probably damaging |
Het |
| Tlr5 |
A |
C |
1: 182,801,603 (GRCm39) |
R302S |
possibly damaging |
Het |
| Tnr |
C |
T |
1: 159,714,479 (GRCm39) |
T786I |
probably damaging |
Het |
| Tprg1l |
A |
G |
4: 154,244,552 (GRCm39) |
S148P |
probably damaging |
Het |
| Trpc4ap |
T |
A |
2: 155,512,994 (GRCm39) |
N127I |
probably damaging |
Het |
| Tulp2 |
T |
A |
7: 45,139,797 (GRCm39) |
|
probably null |
Het |
| Ulk4 |
T |
A |
9: 121,102,021 (GRCm39) |
Y19F |
probably damaging |
Het |
| Upf1 |
T |
C |
8: 70,785,687 (GRCm39) |
Y1053C |
probably damaging |
Het |
| Vars2 |
A |
T |
17: 35,976,680 (GRCm39) |
H223Q |
probably benign |
Het |
| Vmn2r106 |
T |
A |
17: 20,487,806 (GRCm39) |
|
probably null |
Het |
| Ythdc2 |
T |
A |
18: 44,973,277 (GRCm39) |
F305I |
probably damaging |
Het |
| Zfp281 |
T |
C |
1: 136,553,178 (GRCm39) |
F52S |
possibly damaging |
Het |
| Zfp292 |
A |
T |
4: 34,809,784 (GRCm39) |
C1087S |
probably damaging |
Het |
| Zfp335 |
A |
T |
2: 164,737,018 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in Uggt2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00158:Uggt2
|
APN |
14 |
119,286,688 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
IGL00430:Uggt2
|
APN |
14 |
119,263,841 (GRCm39) |
nonsense |
probably null |
|
|
IGL00433:Uggt2
|
APN |
14 |
119,250,899 (GRCm39) |
missense |
probably benign |
|
|
IGL00572:Uggt2
|
APN |
14 |
119,280,203 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL00577:Uggt2
|
APN |
14 |
119,272,312 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
IGL00671:Uggt2
|
APN |
14 |
119,280,211 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
IGL01482:Uggt2
|
APN |
14 |
119,295,057 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01630:Uggt2
|
APN |
14 |
119,280,184 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01787:Uggt2
|
APN |
14 |
119,319,146 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02063:Uggt2
|
APN |
14 |
119,326,605 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
IGL02809:Uggt2
|
APN |
14 |
119,328,150 (GRCm39) |
missense |
probably benign |
0.17 |
|
IGL02894:Uggt2
|
APN |
14 |
119,319,211 (GRCm39) |
missense |
probably damaging |
0.96 |
|
IGL03062:Uggt2
|
APN |
14 |
119,312,758 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03139:Uggt2
|
APN |
14 |
119,332,722 (GRCm39) |
missense |
probably benign |
0.25 |
|
IGL03142:Uggt2
|
APN |
14 |
119,235,603 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03168:Uggt2
|
APN |
14 |
119,315,080 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL03348:Uggt2
|
APN |
14 |
119,308,300 (GRCm39) |
missense |
probably benign |
0.38 |
|
P0014:Uggt2
|
UTSW |
14 |
119,281,950 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0006:Uggt2
|
UTSW |
14 |
119,287,075 (GRCm39) |
missense |
probably benign |
0.07 |
|
R0063:Uggt2
|
UTSW |
14 |
119,244,542 (GRCm39) |
splice site |
probably benign |
|
|
R0063:Uggt2
|
UTSW |
14 |
119,244,542 (GRCm39) |
splice site |
probably benign |
|
|
R0383:Uggt2
|
UTSW |
14 |
119,286,863 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0433:Uggt2
|
UTSW |
14 |
119,312,741 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0472:Uggt2
|
UTSW |
14 |
119,332,748 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0609:Uggt2
|
UTSW |
14 |
119,332,748 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0645:Uggt2
|
UTSW |
14 |
119,295,010 (GRCm39) |
missense |
probably benign |
0.27 |
|
R0788:Uggt2
|
UTSW |
14 |
119,332,812 (GRCm39) |
splice site |
probably benign |
|
|
R0940:Uggt2
|
UTSW |
14 |
119,328,604 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1567:Uggt2
|
UTSW |
14 |
119,246,505 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
R1627:Uggt2
|
UTSW |
14 |
119,295,075 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1682:Uggt2
|
UTSW |
14 |
119,292,055 (GRCm39) |
missense |
probably benign |
0.19 |
|
R1746:Uggt2
|
UTSW |
14 |
119,250,915 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1785:Uggt2
|
UTSW |
14 |
119,298,788 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1786:Uggt2
|
UTSW |
14 |
119,298,788 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1799:Uggt2
|
UTSW |
14 |
119,269,688 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1894:Uggt2
|
UTSW |
14 |
119,287,130 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1918:Uggt2
|
UTSW |
14 |
119,245,467 (GRCm39) |
splice site |
probably benign |
|
|
R2149:Uggt2
|
UTSW |
14 |
119,312,757 (GRCm39) |
missense |
probably benign |
0.02 |
|
R2168:Uggt2
|
UTSW |
14 |
119,256,917 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2219:Uggt2
|
UTSW |
14 |
119,312,749 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2220:Uggt2
|
UTSW |
14 |
119,312,749 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2240:Uggt2
|
UTSW |
14 |
119,232,461 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2331:Uggt2
|
UTSW |
14 |
119,264,011 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R2904:Uggt2
|
UTSW |
14 |
119,296,521 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R2906:Uggt2
|
UTSW |
14 |
119,256,919 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2907:Uggt2
|
UTSW |
14 |
119,256,919 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2908:Uggt2
|
UTSW |
14 |
119,256,919 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2998:Uggt2
|
UTSW |
14 |
119,286,797 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3407:Uggt2
|
UTSW |
14 |
119,328,682 (GRCm39) |
missense |
probably benign |
0.39 |
|
R3722:Uggt2
|
UTSW |
14 |
119,278,930 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3749:Uggt2
|
UTSW |
14 |
119,295,084 (GRCm39) |
missense |
probably benign |
0.13 |
|
R4015:Uggt2
|
UTSW |
14 |
119,263,845 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R4016:Uggt2
|
UTSW |
14 |
119,263,845 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R4017:Uggt2
|
UTSW |
14 |
119,263,845 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R4206:Uggt2
|
UTSW |
14 |
119,286,674 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4536:Uggt2
|
UTSW |
14 |
119,256,970 (GRCm39) |
missense |
probably benign |
|
|
R4642:Uggt2
|
UTSW |
14 |
119,272,347 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4654:Uggt2
|
UTSW |
14 |
119,269,670 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R4770:Uggt2
|
UTSW |
14 |
119,266,466 (GRCm39) |
splice site |
probably null |
|
|
R4810:Uggt2
|
UTSW |
14 |
119,250,933 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4832:Uggt2
|
UTSW |
14 |
119,239,259 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4856:Uggt2
|
UTSW |
14 |
119,273,376 (GRCm39) |
splice site |
probably null |
|
|
R4886:Uggt2
|
UTSW |
14 |
119,273,376 (GRCm39) |
splice site |
probably null |
|
|
R4888:Uggt2
|
UTSW |
14 |
119,315,062 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4888:Uggt2
|
UTSW |
14 |
119,286,665 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4895:Uggt2
|
UTSW |
14 |
119,256,298 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5353:Uggt2
|
UTSW |
14 |
119,319,182 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5423:Uggt2
|
UTSW |
14 |
119,256,898 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5476:Uggt2
|
UTSW |
14 |
119,328,121 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5561:Uggt2
|
UTSW |
14 |
119,278,939 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5607:Uggt2
|
UTSW |
14 |
119,326,611 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R5608:Uggt2
|
UTSW |
14 |
119,326,611 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R5625:Uggt2
|
UTSW |
14 |
119,315,136 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5698:Uggt2
|
UTSW |
14 |
119,280,138 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5986:Uggt2
|
UTSW |
14 |
119,286,838 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6031:Uggt2
|
UTSW |
14 |
119,308,238 (GRCm39) |
missense |
probably benign |
0.06 |
|
R6031:Uggt2
|
UTSW |
14 |
119,308,238 (GRCm39) |
missense |
probably benign |
0.06 |
|
R6289:Uggt2
|
UTSW |
14 |
119,279,014 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6480:Uggt2
|
UTSW |
14 |
119,294,976 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6515:Uggt2
|
UTSW |
14 |
119,315,131 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R6706:Uggt2
|
UTSW |
14 |
119,308,293 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6745:Uggt2
|
UTSW |
14 |
119,280,022 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
R6819:Uggt2
|
UTSW |
14 |
119,263,847 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6879:Uggt2
|
UTSW |
14 |
119,239,271 (GRCm39) |
missense |
probably benign |
0.10 |
|
R7117:Uggt2
|
UTSW |
14 |
119,251,938 (GRCm39) |
missense |
probably benign |
0.25 |
|
R7183:Uggt2
|
UTSW |
14 |
119,257,049 (GRCm39) |
splice site |
probably null |
|
|
R7337:Uggt2
|
UTSW |
14 |
119,323,587 (GRCm39) |
missense |
probably benign |
0.28 |
|
R7342:Uggt2
|
UTSW |
14 |
119,232,384 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R7615:Uggt2
|
UTSW |
14 |
119,326,681 (GRCm39) |
missense |
probably benign |
0.12 |
|
R7625:Uggt2
|
UTSW |
14 |
119,263,905 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7685:Uggt2
|
UTSW |
14 |
119,312,759 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7842:Uggt2
|
UTSW |
14 |
119,235,516 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7891:Uggt2
|
UTSW |
14 |
119,280,059 (GRCm39) |
missense |
probably benign |
0.09 |
|
R7938:Uggt2
|
UTSW |
14 |
119,296,519 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R8050:Uggt2
|
UTSW |
14 |
119,263,834 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9007:Uggt2
|
UTSW |
14 |
119,326,724 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9080:Uggt2
|
UTSW |
14 |
119,295,017 (GRCm39) |
missense |
probably benign |
0.42 |
|
R9203:Uggt2
|
UTSW |
14 |
119,294,975 (GRCm39) |
missense |
probably benign |
0.08 |
|
R9215:Uggt2
|
UTSW |
14 |
119,279,006 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9324:Uggt2
|
UTSW |
14 |
119,312,741 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9459:Uggt2
|
UTSW |
14 |
119,286,595 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9647:Uggt2
|
UTSW |
14 |
119,256,312 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9781:Uggt2
|
UTSW |
14 |
119,232,384 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
Z1177:Uggt2
|
UTSW |
14 |
119,244,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- GAAGCACTGTCCCTAGCCAG -3'
(R):5'- CGTCTCCTGGAAGATATCTGAC -3'
|
| Posted On |
2017-07-14 |
Incidental Mutation