Incidental Mutation 'R7117:Uggt2'
| ID |
551884 |
| 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 |
045208-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.097)
|
| Stock # |
R7117 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
14 |
| Chromosomal Location |
119222451-119336842 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 119251938 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Methionine
at position 1174
(I1174M)
|
| 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 benign
Transcript: ENSMUST00000156203
AA Change: I1174M
PolyPhen 2
Score 0.251 (Sensitivity: 0.91; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000121249
Gene: ENSMUSG00000042104
AA Change: I1174M
| 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 |
|
| SMART Domains |
Protein: ENSMUSP00000133772
Gene: ENSMUSG00000042104
AA Change: I47M
| 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 |
0.0898 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.2%
|
| Validation Efficiency |
97% (95/98) |
| 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: 98 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2900026A02Rik |
T |
C |
5: 113,339,250 (GRCm39) |
Y254C |
probably benign |
Het |
| 4930480E11Rik |
G |
T |
X: 77,414,311 (GRCm39) |
M345I |
probably benign |
Het |
| Adam12 |
T |
C |
7: 133,518,191 (GRCm39) |
I650V |
probably benign |
Het |
| Adam39 |
G |
T |
8: 41,279,279 (GRCm39) |
G557C |
probably damaging |
Het |
| Ak5 |
A |
G |
3: 152,321,493 (GRCm39) |
|
probably null |
Het |
| Arhgef10l |
C |
T |
4: 140,291,497 (GRCm39) |
|
probably null |
Het |
| Arhgef37 |
C |
T |
18: 61,637,481 (GRCm39) |
E394K |
probably benign |
Het |
| Baz2b |
A |
G |
2: 59,742,841 (GRCm39) |
V13A |
|
Het |
| Bnc1 |
G |
T |
7: 81,623,109 (GRCm39) |
A706E |
possibly damaging |
Het |
| Bscl2 |
G |
A |
19: 8,825,878 (GRCm39) |
A421T |
possibly damaging |
Het |
| Btn1a1 |
A |
C |
13: 23,643,415 (GRCm39) |
W345G |
possibly damaging |
Het |
| C3 |
A |
T |
17: 57,519,655 (GRCm39) |
M1199K |
probably benign |
Het |
| Ccdc18 |
T |
G |
5: 108,296,835 (GRCm39) |
L213V |
possibly damaging |
Het |
| Cers2 |
T |
C |
3: 95,228,072 (GRCm39) |
|
probably null |
Het |
| Chpt1 |
T |
A |
10: 88,316,711 (GRCm39) |
H249L |
probably damaging |
Het |
| Cited2 |
A |
G |
10: 17,600,364 (GRCm39) |
E224G |
possibly damaging |
Het |
| Cntn5 |
T |
A |
9: 10,904,704 (GRCm39) |
|
probably benign |
Het |
| Col28a1 |
A |
G |
6: 8,013,122 (GRCm39) |
S977P |
possibly damaging |
Het |
| Col6a1 |
T |
C |
10: 76,560,843 (GRCm39) |
K52E |
probably damaging |
Het |
| Cpne2 |
T |
A |
8: 95,282,172 (GRCm39) |
H239Q |
probably damaging |
Het |
| Cr2 |
A |
T |
1: 194,842,909 (GRCm39) |
N244K |
possibly damaging |
Het |
| Csf2rb2 |
T |
C |
15: 78,169,385 (GRCm39) |
D590G |
probably damaging |
Het |
| Defb25 |
A |
C |
2: 152,464,380 (GRCm39) |
C55G |
probably damaging |
Het |
| Dnah7b |
A |
T |
1: 46,391,973 (GRCm39) |
|
probably null |
Het |
| Dvl3 |
T |
A |
16: 20,346,072 (GRCm39) |
Y467* |
probably null |
Het |
| Elapor2 |
T |
A |
5: 9,495,384 (GRCm39) |
C729* |
probably null |
Het |
| Extl2 |
T |
C |
3: 115,821,088 (GRCm39) |
S312P |
probably damaging |
Het |
| Fam178b |
T |
C |
1: 36,639,548 (GRCm39) |
T313A |
probably benign |
Het |
| Fam186b |
A |
G |
15: 99,183,471 (GRCm39) |
Y58H |
probably damaging |
Het |
| Fat1 |
A |
T |
8: 45,484,505 (GRCm39) |
I3248L |
probably damaging |
Het |
| Fat2 |
A |
G |
11: 55,172,088 (GRCm39) |
F2875S |
probably damaging |
Het |
| Flnb |
T |
A |
14: 7,894,214 (GRCm38) |
N760K |
probably benign |
Het |
| Galnt14 |
T |
C |
17: 73,801,190 (GRCm39) |
H544R |
probably benign |
Het |
| Gpr137c |
A |
C |
14: 45,516,484 (GRCm39) |
R357S |
probably damaging |
Het |
| Grk2 |
A |
G |
19: 4,340,630 (GRCm39) |
|
probably null |
Het |
| Hectd2 |
A |
T |
19: 36,577,055 (GRCm39) |
T342S |
probably benign |
Het |
| Hjv |
G |
T |
3: 96,435,542 (GRCm39) |
V267L |
possibly damaging |
Het |
| Ildr2 |
G |
T |
1: 166,123,380 (GRCm39) |
G270C |
probably damaging |
Het |
| Insm2 |
C |
A |
12: 55,647,357 (GRCm39) |
A367D |
probably damaging |
Het |
| Kcnh5 |
T |
A |
12: 75,161,219 (GRCm39) |
I230F |
possibly damaging |
Het |
| Keg1 |
T |
A |
19: 12,687,042 (GRCm39) |
S24T |
probably damaging |
Het |
| Kera |
A |
T |
10: 97,448,714 (GRCm39) |
E311D |
probably benign |
Het |
| Kit |
T |
A |
5: 75,767,758 (GRCm39) |
I47K |
probably benign |
Het |
| Megf6 |
A |
G |
4: 154,343,379 (GRCm39) |
T663A |
possibly damaging |
Het |
| Mettl21c |
G |
A |
1: 44,049,808 (GRCm39) |
A79V |
probably damaging |
Het |
| Mfsd1 |
T |
A |
3: 67,507,391 (GRCm39) |
|
probably null |
Het |
| Mob3b |
A |
G |
4: 34,985,914 (GRCm39) |
|
probably null |
Het |
| Morc2b |
T |
A |
17: 33,356,926 (GRCm39) |
H282L |
probably benign |
Het |
| Mtpap |
T |
C |
18: 4,380,889 (GRCm39) |
|
probably null |
Het |
| Mtus1 |
A |
G |
8: 41,536,621 (GRCm39) |
V365A |
possibly damaging |
Het |
| Muc5ac |
T |
A |
7: 141,367,559 (GRCm39) |
Y2993* |
probably null |
Het |
| Mycbp2 |
A |
C |
14: 103,391,513 (GRCm39) |
F3422V |
probably benign |
Het |
| Ndufb7 |
T |
A |
8: 84,297,490 (GRCm39) |
D48E |
probably benign |
Het |
| Nxpe5 |
A |
G |
5: 138,237,704 (GRCm39) |
Y88C |
probably damaging |
Het |
| Or51a6 |
T |
A |
7: 102,604,185 (GRCm39) |
M208L |
probably benign |
Het |
| Or5d3 |
A |
G |
2: 88,174,905 (GRCm39) |
L64P |
probably damaging |
Het |
| Osbpl5 |
T |
A |
7: 143,263,520 (GRCm39) |
D121V |
probably benign |
Het |
| Oxnad1 |
A |
T |
14: 31,813,608 (GRCm39) |
H3L |
probably benign |
Het |
| Pam |
C |
A |
1: 97,904,841 (GRCm39) |
|
probably benign |
Het |
| Papolg |
T |
C |
11: 23,845,207 (GRCm39) |
|
probably benign |
Het |
| Pax1 |
G |
A |
2: 147,208,190 (GRCm39) |
G266D |
probably damaging |
Het |
| Pde11a |
A |
T |
2: 75,906,348 (GRCm39) |
M623K |
probably damaging |
Het |
| Peg3 |
GTGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTC |
GTGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTC |
7: 6,712,167 (GRCm39) |
|
probably benign |
Het |
| Phf21a |
A |
T |
2: 92,189,502 (GRCm39) |
Q587L |
probably benign |
Het |
| Plcb3 |
A |
G |
19: 6,941,746 (GRCm39) |
L336P |
probably damaging |
Het |
| Pnp2 |
T |
C |
14: 51,201,931 (GRCm39) |
*306Q |
probably null |
Het |
| Pou5f2 |
A |
G |
13: 78,173,392 (GRCm39) |
I111M |
probably benign |
Het |
| Pramel32 |
T |
A |
4: 88,547,195 (GRCm39) |
M246L |
probably damaging |
Het |
| Prmt3 |
G |
T |
7: 49,467,843 (GRCm39) |
A350S |
probably benign |
Het |
| Rac3 |
A |
T |
11: 120,614,343 (GRCm39) |
R163* |
probably null |
Het |
| Raly |
G |
T |
2: 154,699,432 (GRCm39) |
V79L |
probably benign |
Het |
| Rbm20 |
A |
T |
19: 53,839,989 (GRCm39) |
T993S |
possibly damaging |
Het |
| Rwdd3 |
A |
G |
3: 120,964,987 (GRCm39) |
L56P |
probably benign |
Het |
| Serpina3a |
C |
T |
12: 104,082,436 (GRCm39) |
H70Y |
possibly damaging |
Het |
| Sez6l2 |
A |
C |
7: 126,552,915 (GRCm39) |
E227A |
possibly damaging |
Het |
| Shank1 |
C |
T |
7: 43,976,585 (GRCm39) |
A561V |
unknown |
Het |
| Sidt2 |
C |
T |
9: 45,864,517 (GRCm39) |
V71I |
probably benign |
Het |
| Slc35f6 |
T |
C |
5: 30,815,051 (GRCm39) |
L326P |
probably damaging |
Het |
| Sox2 |
G |
A |
3: 34,705,075 (GRCm39) |
G171S |
possibly damaging |
Het |
| Spef2 |
G |
A |
15: 9,729,924 (GRCm39) |
R65C |
probably damaging |
Het |
| Spmap2 |
A |
T |
10: 79,420,741 (GRCm39) |
|
probably null |
Het |
| Stip1 |
C |
T |
19: 6,999,178 (GRCm39) |
G467S |
possibly damaging |
Het |
| Tada2a |
T |
A |
11: 83,976,514 (GRCm39) |
I327F |
probably damaging |
Het |
| Tex2 |
A |
G |
11: 106,435,071 (GRCm39) |
V785A |
unknown |
Het |
| Thada |
C |
A |
17: 84,538,214 (GRCm39) |
|
probably null |
Het |
| Tmed1 |
G |
A |
9: 21,420,550 (GRCm39) |
T94M |
possibly damaging |
Het |
| Tsr1 |
G |
T |
11: 74,790,360 (GRCm39) |
M149I |
probably benign |
Het |
| Ttc8 |
T |
C |
12: 98,942,761 (GRCm39) |
Y434H |
possibly damaging |
Het |
| Ttn |
A |
G |
2: 76,578,519 (GRCm39) |
Y24125H |
probably damaging |
Het |
| Ttn |
G |
T |
2: 76,552,253 (GRCm39) |
|
probably null |
Het |
| Ttn |
A |
G |
2: 76,773,235 (GRCm39) |
I2435T |
unknown |
Het |
| Unc13b |
T |
C |
4: 43,216,544 (GRCm39) |
I281T |
probably benign |
Het |
| Usp1 |
G |
T |
4: 98,817,127 (GRCm39) |
K106N |
possibly damaging |
Het |
| Vwa3b |
A |
G |
1: 37,174,634 (GRCm39) |
D15G |
|
Het |
| Zfp28 |
G |
A |
7: 6,397,461 (GRCm39) |
C632Y |
probably damaging |
Het |
| Zfp68 |
T |
C |
5: 138,604,580 (GRCm39) |
D581G |
probably benign |
Het |
| Zmynd10 |
A |
C |
9: 107,424,716 (GRCm39) |
S21R |
probably benign |
Het |
| Zswim4 |
C |
T |
8: 84,940,681 (GRCm39) |
R806H |
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 |
|
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 |
|
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 |
|
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'- GTTCTCTCTGGCTGTAGAGAC -3'
(R):5'- AAGCTGGCCTTTGACAGATAATC -3'
Sequencing Primer
(F):5'- CAAGCTCCCCTTTCATACA -3'
(R):5'- GGACATTTGTGTTCTTCTGC -3'
|
| Posted On |
2019-05-15 |
Incidental Mutation