Incidental Mutation 'R4895:Uggt2'
| ID |
377592 |
| 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 |
042499-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.097)
|
| Stock # |
R4895 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
14 |
| Chromosomal Location |
119222451-119336842 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 119256298 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Lysine to Asparagine
at position 1124
(K1124N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000121249
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000127153]
[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 damaging
Transcript: ENSMUST00000156203
AA Change: K1124N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000121249
Gene: ENSMUSG00000042104
AA Change: K1124N
| 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 benign
Transcript: ENSMUST00000173391
|
| SMART Domains |
Protein: ENSMUSP00000133772
Gene: ENSMUSG00000042104
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:UDP-g_GGTase
|
2 |
63 |
9.4e-18 |
PFAM |
|
SCOP:d1ga8a_
|
77 |
216 |
3e-21 |
SMART |
|
| Meta Mutation Damage Score |
0.4837 |
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 94.0%
|
| Validation Efficiency |
98% (84/86) |
| 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: 80 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930519P11Rik |
C |
A |
2: 154,454,990 (GRCm39) |
|
probably benign |
Het |
| Abat |
G |
A |
16: 8,433,826 (GRCm39) |
A392T |
probably benign |
Het |
| Abca14 |
G |
A |
7: 119,846,572 (GRCm39) |
|
probably null |
Het |
| Abcc6 |
A |
T |
7: 45,630,414 (GRCm39) |
L1282Q |
possibly damaging |
Het |
| Acss2 |
A |
G |
2: 155,392,401 (GRCm39) |
|
probably benign |
Het |
| Adgrf1 |
G |
T |
17: 43,621,511 (GRCm39) |
V583L |
probably benign |
Het |
| Aftph |
T |
C |
11: 20,646,801 (GRCm39) |
D825G |
probably damaging |
Het |
| Ahnak |
T |
C |
19: 8,994,805 (GRCm39) |
V5363A |
probably benign |
Het |
| Apba3 |
G |
A |
10: 81,107,117 (GRCm39) |
|
probably null |
Het |
| Asb13 |
T |
C |
13: 3,693,589 (GRCm39) |
Y116H |
probably damaging |
Het |
| Asb4 |
C |
A |
6: 5,398,266 (GRCm39) |
T77K |
probably damaging |
Het |
| Atp8b4 |
A |
T |
2: 126,256,289 (GRCm39) |
H223Q |
probably benign |
Het |
| Best1 |
A |
G |
19: 9,970,135 (GRCm39) |
L159P |
probably benign |
Het |
| Cacna1h |
A |
T |
17: 25,608,396 (GRCm39) |
M731K |
probably damaging |
Het |
| Catspere1 |
T |
A |
1: 177,687,427 (GRCm39) |
|
noncoding transcript |
Het |
| Cenpv |
A |
T |
11: 62,418,346 (GRCm39) |
Y202* |
probably null |
Het |
| Cep57 |
A |
T |
9: 13,727,449 (GRCm39) |
|
probably benign |
Het |
| Cfap100 |
T |
A |
6: 90,383,084 (GRCm39) |
D363V |
possibly damaging |
Het |
| Cluh |
A |
G |
11: 74,558,231 (GRCm39) |
Y1126C |
probably damaging |
Het |
| Cyp2j5 |
A |
G |
4: 96,551,347 (GRCm39) |
|
probably null |
Het |
| Dnajc11 |
T |
C |
4: 152,064,390 (GRCm39) |
F514L |
probably damaging |
Het |
| Efcab3 |
C |
T |
11: 104,611,112 (GRCm39) |
T318I |
probably benign |
Het |
| Efcab3 |
T |
A |
11: 105,008,227 (GRCm39) |
|
probably benign |
Het |
| Efcab3 |
A |
G |
11: 104,640,496 (GRCm39) |
D1026G |
probably damaging |
Het |
| Eif2b4 |
T |
G |
5: 31,350,298 (GRCm39) |
Q8P |
probably benign |
Het |
| Epha6 |
A |
T |
16: 59,486,918 (GRCm39) |
V1043E |
probably benign |
Het |
| Gm11562 |
G |
T |
11: 99,511,141 (GRCm39) |
Q20K |
unknown |
Het |
| Gm14415 |
A |
T |
2: 176,796,114 (GRCm39) |
|
noncoding transcript |
Het |
| Gm5431 |
A |
G |
11: 48,779,855 (GRCm39) |
S634P |
probably damaging |
Het |
| Gpld1 |
C |
A |
13: 25,163,711 (GRCm39) |
N501K |
probably damaging |
Het |
| Gsn |
C |
T |
2: 35,192,590 (GRCm39) |
R513C |
probably damaging |
Het |
| Gulp1 |
T |
C |
1: 44,827,757 (GRCm39) |
F300L |
probably benign |
Het |
| H2aj |
T |
C |
6: 136,785,660 (GRCm39) |
V108A |
possibly damaging |
Het |
| Haus3 |
T |
C |
5: 34,325,414 (GRCm39) |
R82G |
probably benign |
Het |
| Herc2 |
G |
A |
7: 55,872,734 (GRCm39) |
R4424H |
probably damaging |
Het |
| Hmcn1 |
T |
A |
1: 150,553,130 (GRCm39) |
Q2520L |
probably benign |
Het |
| Hs2st1 |
T |
C |
3: 144,171,014 (GRCm39) |
I53V |
probably benign |
Het |
| Inpp5e |
C |
T |
2: 26,287,924 (GRCm39) |
R624Q |
probably damaging |
Het |
| Ints8 |
G |
T |
4: 11,230,367 (GRCm39) |
C491* |
probably null |
Het |
| Itpkb |
C |
A |
1: 180,241,460 (GRCm39) |
A710D |
probably damaging |
Het |
| Kcnk4 |
A |
C |
19: 6,905,784 (GRCm39) |
|
probably null |
Het |
| Kmt2d |
T |
C |
15: 98,742,368 (GRCm39) |
|
probably benign |
Het |
| Lamb3 |
C |
T |
1: 193,014,622 (GRCm39) |
R594* |
probably null |
Het |
| Map3k20 |
A |
G |
2: 72,232,700 (GRCm39) |
|
probably benign |
Het |
| Maz |
A |
T |
7: 126,624,472 (GRCm39) |
|
probably null |
Het |
| Mtr |
T |
C |
13: 12,231,752 (GRCm39) |
T651A |
probably benign |
Het |
| Nbeal1 |
A |
G |
1: 60,332,062 (GRCm39) |
E2252G |
probably damaging |
Het |
| Ndufa10 |
A |
G |
1: 92,397,618 (GRCm39) |
Y61H |
probably damaging |
Het |
| Npat |
T |
A |
9: 53,481,789 (GRCm39) |
L1166M |
probably damaging |
Het |
| Or12e1 |
A |
C |
2: 87,022,192 (GRCm39) |
I54L |
probably benign |
Het |
| Or4c108 |
A |
T |
2: 88,804,055 (GRCm39) |
F60Y |
probably benign |
Het |
| Or5ak20 |
A |
T |
2: 85,183,341 (GRCm39) |
*310K |
probably null |
Het |
| Or5b97 |
C |
T |
19: 12,878,251 (GRCm39) |
V298M |
probably damaging |
Het |
| Or5h22 |
C |
T |
16: 58,895,020 (GRCm39) |
C141Y |
probably benign |
Het |
| Or5p66 |
A |
C |
7: 107,885,802 (GRCm39) |
I177S |
probably damaging |
Het |
| Pcdhb3 |
T |
C |
18: 37,434,759 (GRCm39) |
F242L |
probably damaging |
Het |
| Phip |
A |
G |
9: 82,841,648 (GRCm39) |
V57A |
probably benign |
Het |
| Plekha7 |
A |
T |
7: 115,788,626 (GRCm39) |
|
probably null |
Het |
| Pot1a |
A |
C |
6: 25,753,205 (GRCm39) |
F444V |
probably damaging |
Het |
| Ppm1a |
C |
T |
12: 72,831,126 (GRCm39) |
P217L |
probably damaging |
Het |
| Prepl |
A |
G |
17: 85,388,494 (GRCm39) |
F203S |
probably damaging |
Het |
| Prl8a1 |
T |
C |
13: 27,759,513 (GRCm39) |
I175V |
probably benign |
Het |
| Ranbp6 |
A |
T |
19: 29,787,175 (GRCm39) |
I1059N |
possibly damaging |
Het |
| Rhag |
A |
G |
17: 41,122,242 (GRCm39) |
Q59R |
probably benign |
Het |
| Sema4c |
A |
C |
1: 36,592,651 (GRCm39) |
|
probably null |
Het |
| Sf3b3 |
T |
C |
8: 111,542,656 (GRCm39) |
D902G |
probably benign |
Het |
| Tbc1d23 |
A |
G |
16: 57,019,220 (GRCm39) |
|
probably null |
Het |
| Tbrg1 |
A |
T |
9: 37,566,375 (GRCm39) |
I54N |
probably damaging |
Het |
| Tchh |
A |
T |
3: 93,352,993 (GRCm39) |
E811V |
unknown |
Het |
| Tenm3 |
T |
A |
8: 48,754,006 (GRCm39) |
D799V |
probably damaging |
Het |
| Tlr5 |
T |
C |
1: 182,801,764 (GRCm39) |
L342P |
probably damaging |
Het |
| Tppp |
C |
T |
13: 74,178,996 (GRCm39) |
R146* |
probably null |
Het |
| Trpm4 |
A |
T |
7: 44,967,482 (GRCm39) |
M574K |
probably damaging |
Het |
| Uggt1 |
A |
T |
1: 36,195,345 (GRCm39) |
F1288Y |
probably damaging |
Het |
| Usf3 |
A |
C |
16: 44,041,459 (GRCm39) |
S1980R |
possibly damaging |
Het |
| Vav2 |
T |
C |
2: 27,208,973 (GRCm39) |
D100G |
probably damaging |
Het |
| Vmn2r3 |
G |
T |
3: 64,167,182 (GRCm39) |
H650N |
probably benign |
Het |
| Vmn2r59 |
T |
A |
7: 41,695,218 (GRCm39) |
Y398F |
probably damaging |
Het |
| Zfp619 |
A |
G |
7: 39,187,396 (GRCm39) |
D1142G |
possibly damaging |
Het |
| Zfp933 |
G |
A |
4: 147,910,892 (GRCm39) |
R235* |
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 |
|
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'- TGGAATAGATAAGTCCTCAAAAGCC -3'
(R):5'- GATGAAGTCCTATCTCAAAACATGG -3'
Sequencing Primer
(F):5'- CTGTTATCCTGTTGAAAACCAGATC -3'
(R):5'- GTCCTATCTCAAAACATGGAAAAGC -3'
|
| Posted On |
2016-03-17 |
Incidental Mutation