Incidental Mutation 'R1682:Uggt2'
| ID |
189281 |
| 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 |
039718-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.097)
|
| Stock # |
R1682 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
14 |
| Chromosomal Location |
119222451-119336842 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 119292055 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Glutamic Acid
at position 581
(D581E)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000121249
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000127153]
[ENSMUST00000156203]
|
| AlphaFold |
E9Q4X2 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000127153
AA Change: D105E
PolyPhen 2
Score 0.014 (Sensitivity: 0.96; Specificity: 0.79)
|
| SMART Domains |
Protein: ENSMUSP00000117738
Gene: ENSMUSG00000042104
AA Change: D105E
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
327 |
334 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000136924
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000138923
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000156203
AA Change: D581E
PolyPhen 2
Score 0.187 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000121249
Gene: ENSMUSG00000042104
AA Change: D581E
| 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 |
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.5%
|
| 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]
|
| Allele List at MGI |
All alleles(5) : Targeted(2) Gene trapped(3)
|
| Other mutations in this stock |
Total: 88 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acaca |
A |
G |
11: 84,283,043 (GRCm39) |
D2203G |
probably benign |
Het |
| Acin1 |
A |
G |
14: 54,901,175 (GRCm39) |
S629P |
probably damaging |
Het |
| Agbl2 |
T |
A |
2: 90,614,434 (GRCm39) |
I22N |
probably benign |
Het |
| Ank1 |
A |
G |
8: 23,599,343 (GRCm39) |
E796G |
probably damaging |
Het |
| Ankrd13d |
A |
G |
19: 4,332,961 (GRCm39) |
L13P |
probably damaging |
Het |
| Ankrd36 |
T |
C |
11: 5,557,143 (GRCm39) |
S364P |
possibly damaging |
Het |
| Ap2a1 |
T |
C |
7: 44,565,362 (GRCm39) |
T126A |
probably benign |
Het |
| Apob |
A |
G |
12: 8,062,365 (GRCm39) |
I3616V |
probably benign |
Het |
| Arl5a |
A |
T |
2: 52,306,214 (GRCm39) |
N39K |
probably benign |
Het |
| Baiap2 |
G |
A |
11: 119,888,366 (GRCm39) |
R334H |
probably damaging |
Het |
| Bbox1 |
T |
A |
2: 110,122,893 (GRCm39) |
N132I |
possibly damaging |
Het |
| Bcl11b |
A |
G |
12: 107,882,908 (GRCm39) |
L469P |
probably damaging |
Het |
| Brca1 |
A |
G |
11: 101,416,391 (GRCm39) |
I581T |
probably damaging |
Het |
| Cacng2 |
T |
C |
15: 78,002,997 (GRCm39) |
Y32C |
probably damaging |
Het |
| Capn9 |
G |
T |
8: 125,338,304 (GRCm39) |
|
probably null |
Het |
| Cdh18 |
A |
G |
15: 23,400,671 (GRCm39) |
T290A |
probably benign |
Het |
| Cdk5rap2 |
C |
T |
4: 70,220,387 (GRCm39) |
V593I |
possibly damaging |
Het |
| Cep128 |
G |
C |
12: 91,197,596 (GRCm39) |
D91E |
probably damaging |
Het |
| Cep295 |
T |
C |
9: 15,245,217 (GRCm39) |
M1080V |
probably benign |
Het |
| Coq8b |
T |
A |
7: 26,939,549 (GRCm39) |
M193K |
probably benign |
Het |
| Csn1s2b |
A |
G |
5: 87,970,162 (GRCm39) |
Y131C |
probably damaging |
Het |
| D130043K22Rik |
T |
C |
13: 25,066,539 (GRCm39) |
S779P |
probably damaging |
Het |
| Dgat1 |
C |
T |
15: 76,387,219 (GRCm39) |
C356Y |
probably benign |
Het |
| Dipk1c |
A |
T |
18: 84,754,988 (GRCm39) |
I155F |
possibly damaging |
Het |
| Dnah12 |
A |
T |
14: 26,500,840 (GRCm39) |
T1543S |
possibly damaging |
Het |
| Dock3 |
T |
C |
9: 106,851,040 (GRCm39) |
S821G |
probably damaging |
Het |
| Dock4 |
G |
A |
12: 40,775,779 (GRCm39) |
C574Y |
probably damaging |
Het |
| Dr1 |
T |
C |
5: 108,417,604 (GRCm39) |
I50T |
probably damaging |
Het |
| Dzip3 |
A |
T |
16: 48,778,780 (GRCm39) |
|
probably null |
Het |
| Eln |
C |
A |
5: 134,732,636 (GRCm39) |
*861L |
probably null |
Het |
| Eml6 |
T |
A |
11: 29,709,065 (GRCm39) |
H24L |
probably benign |
Het |
| Eps8l3 |
A |
C |
3: 107,798,622 (GRCm39) |
T503P |
possibly damaging |
Het |
| Fgf1 |
C |
A |
18: 38,974,985 (GRCm39) |
D155Y |
possibly damaging |
Het |
| Fkbp15 |
A |
T |
4: 62,242,431 (GRCm39) |
M507K |
probably damaging |
Het |
| Flnb |
A |
T |
14: 7,913,121 (GRCm38) |
R1463S |
probably benign |
Het |
| Fras1 |
C |
T |
5: 96,793,732 (GRCm39) |
T1018I |
probably benign |
Het |
| Gm10803 |
T |
A |
2: 93,394,533 (GRCm39) |
C102S |
probably damaging |
Het |
| Gpatch1 |
C |
A |
7: 35,002,812 (GRCm39) |
V233L |
possibly damaging |
Het |
| Gramd1a |
T |
C |
7: 30,842,325 (GRCm39) |
|
probably null |
Het |
| Gsk3a |
T |
C |
7: 24,935,133 (GRCm39) |
T106A |
possibly damaging |
Het |
| Hap1 |
A |
G |
11: 100,240,302 (GRCm39) |
V136A |
possibly damaging |
Het |
| Helq |
A |
T |
5: 100,940,679 (GRCm39) |
S307T |
probably benign |
Het |
| Herc2 |
T |
A |
7: 55,738,148 (GRCm39) |
S264T |
possibly damaging |
Het |
| Htr4 |
A |
G |
18: 62,561,137 (GRCm39) |
M133V |
possibly damaging |
Het |
| Iqca1 |
C |
A |
1: 90,070,453 (GRCm39) |
G133V |
probably null |
Het |
| Jakmip2 |
A |
G |
18: 43,714,896 (GRCm39) |
|
probably null |
Het |
| Ldhd |
T |
A |
8: 112,354,745 (GRCm39) |
S358C |
possibly damaging |
Het |
| Lrp1 |
A |
T |
10: 127,410,201 (GRCm39) |
V1515E |
probably damaging |
Het |
| Ltbp3 |
A |
G |
19: 5,801,782 (GRCm39) |
D700G |
probably benign |
Het |
| Magel2 |
T |
G |
7: 62,029,983 (GRCm39) |
S962R |
unknown |
Het |
| Map2 |
A |
C |
1: 66,454,781 (GRCm39) |
|
probably null |
Het |
| Map3k1 |
T |
A |
13: 111,893,684 (GRCm39) |
E704V |
probably damaging |
Het |
| Mrpl39 |
A |
T |
16: 84,527,347 (GRCm39) |
V180D |
probably damaging |
Het |
| Myef2 |
T |
C |
2: 124,939,978 (GRCm39) |
M383V |
probably damaging |
Het |
| Myh3 |
A |
G |
11: 66,979,891 (GRCm39) |
Y610C |
probably damaging |
Het |
| Or10ak7 |
A |
G |
4: 118,791,778 (GRCm39) |
L89P |
probably damaging |
Het |
| Or51h1 |
T |
C |
7: 102,308,904 (GRCm39) |
V292A |
probably damaging |
Het |
| Or8g54 |
T |
A |
9: 39,706,954 (GRCm39) |
Y94* |
probably null |
Het |
| Oxtr |
C |
T |
6: 112,454,138 (GRCm39) |
R42Q |
probably benign |
Het |
| Pabpc1 |
T |
A |
15: 36,605,785 (GRCm39) |
N135I |
possibly damaging |
Het |
| Pcsk6 |
T |
A |
7: 65,559,976 (GRCm39) |
H100Q |
probably damaging |
Het |
| Pdss1 |
A |
G |
2: 22,805,531 (GRCm39) |
K270E |
probably damaging |
Het |
| Pigx |
A |
T |
16: 31,906,268 (GRCm39) |
S18T |
possibly damaging |
Het |
| Plbd2 |
T |
A |
5: 120,623,849 (GRCm39) |
T558S |
probably damaging |
Het |
| Plppr1 |
A |
T |
4: 49,325,617 (GRCm39) |
|
probably null |
Het |
| Plppr2 |
T |
A |
9: 21,855,717 (GRCm39) |
V230E |
possibly damaging |
Het |
| Pola2 |
A |
G |
19: 6,003,091 (GRCm39) |
|
probably null |
Het |
| Ppp2r3d |
A |
G |
9: 101,089,505 (GRCm39) |
S273P |
probably benign |
Het |
| Prkdc |
A |
G |
16: 15,494,853 (GRCm39) |
E741G |
probably benign |
Het |
| Prom2 |
C |
A |
2: 127,382,082 (GRCm39) |
V111L |
possibly damaging |
Het |
| Rapgef4 |
A |
G |
2: 72,056,912 (GRCm39) |
D557G |
possibly damaging |
Het |
| Rgs10 |
T |
C |
7: 127,975,694 (GRCm39) |
T158A |
probably benign |
Het |
| Rnf123 |
A |
C |
9: 107,954,597 (GRCm39) |
Y40D |
probably benign |
Het |
| Rnf14 |
A |
G |
18: 38,441,242 (GRCm39) |
T211A |
probably benign |
Het |
| Rp1l1 |
T |
A |
14: 64,266,417 (GRCm39) |
S668T |
probably damaging |
Het |
| Sema6d |
T |
A |
2: 124,507,069 (GRCm39) |
L946Q |
probably benign |
Het |
| Sgcd |
T |
G |
11: 47,085,869 (GRCm39) |
K94Q |
probably benign |
Het |
| Skor2 |
A |
T |
18: 76,947,211 (GRCm39) |
D311V |
unknown |
Het |
| Slc34a1 |
A |
T |
13: 23,996,623 (GRCm39) |
I43F |
probably damaging |
Het |
| Spdye4c |
C |
A |
2: 128,434,542 (GRCm39) |
P40T |
probably damaging |
Het |
| Srp72 |
C |
A |
5: 77,135,717 (GRCm39) |
Q216K |
possibly damaging |
Het |
| Tmem62 |
C |
T |
2: 120,837,538 (GRCm39) |
T485I |
probably benign |
Het |
| Tmem94 |
G |
T |
11: 115,681,056 (GRCm39) |
V432L |
probably damaging |
Het |
| Trio |
T |
C |
15: 27,744,232 (GRCm39) |
|
probably null |
Het |
| Unc5d |
T |
A |
8: 29,249,109 (GRCm39) |
S319C |
probably damaging |
Het |
| Vmn1r211 |
T |
C |
13: 23,035,813 (GRCm39) |
I285V |
probably damaging |
Het |
| Vmn2r68 |
A |
G |
7: 84,882,574 (GRCm39) |
Y393H |
possibly damaging |
Het |
| Vmn2r99 |
A |
C |
17: 19,598,207 (GRCm39) |
N77T |
probably damaging |
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 |
|
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 |
|
R6056:Uggt2
|
UTSW |
14 |
119,273,381 (GRCm39) |
critical splice donor site |
probably null |
|
|
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'- CTTCACACATCTGTAAGTTCACAGGCAT -3'
(R):5'- TGGAATACTTGCCAGACAAACATGAACC -3'
Sequencing Primer
(F):5'- tcttaaacttctggtctaactgaatg -3'
(R):5'- tgggacaatgaaaacgaaagg -3'
|
| Posted On |
2014-05-14 |
Incidental Mutation