Incidental Mutation 'R7337:Uggt2'
| ID |
569612 |
| 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 |
045427-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.104)
|
| Stock # |
R7337 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
14 |
| Chromosomal Location |
119222451-119336842 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 119323587 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Glutamic Acid
at position 231
(D231E)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000121249
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000156203]
|
| AlphaFold |
E9Q4X2 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000156203
AA Change: D231E
PolyPhen 2
Score 0.282 (Sensitivity: 0.91; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000121249
Gene: ENSMUSG00000042104
AA Change: D231E
| 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: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
| Validation Efficiency |
100% (88/88) |
| 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 |
|---|
| Abcb11 |
A |
T |
2: 69,076,113 (GRCm39) |
H1198Q |
probably damaging |
Het |
| Adamts14 |
A |
G |
10: 61,043,239 (GRCm39) |
V743A |
probably damaging |
Het |
| Adgrg6 |
A |
G |
10: 14,343,095 (GRCm39) |
V284A |
possibly damaging |
Het |
| Alb |
A |
G |
5: 90,622,452 (GRCm39) |
K560R |
probably damaging |
Het |
| Aqp9 |
A |
T |
9: 71,069,764 (GRCm39) |
F8L |
probably benign |
Het |
| Arhgef7 |
T |
C |
8: 11,835,789 (GRCm39) |
L182P |
probably damaging |
Het |
| Atr |
A |
G |
9: 95,753,501 (GRCm39) |
D701G |
probably damaging |
Het |
| Calr3 |
C |
T |
8: 73,185,339 (GRCm39) |
D187N |
probably damaging |
Het |
| Ccdc198 |
A |
G |
14: 49,471,948 (GRCm39) |
M163T |
possibly damaging |
Het |
| Ccdc65 |
A |
G |
15: 98,618,977 (GRCm39) |
T319A |
probably benign |
Het |
| Ccdc66 |
A |
T |
14: 27,222,290 (GRCm39) |
L151H |
probably damaging |
Het |
| Ces2e |
T |
A |
8: 105,657,688 (GRCm39) |
|
probably null |
Het |
| Cfap46 |
A |
G |
7: 139,210,492 (GRCm39) |
|
probably null |
Het |
| Cfap74 |
A |
G |
4: 155,544,472 (GRCm39) |
T1034A |
unknown |
Het |
| Cldnd1 |
T |
G |
16: 58,549,322 (GRCm39) |
|
probably null |
Het |
| Clec4f |
C |
A |
6: 83,630,190 (GRCm39) |
V123L |
probably benign |
Het |
| Cntn6 |
C |
T |
6: 104,627,491 (GRCm39) |
T108I |
probably damaging |
Het |
| Crygn |
T |
G |
5: 24,961,147 (GRCm39) |
D53A |
possibly damaging |
Het |
| Cyp27a1 |
T |
A |
1: 74,774,594 (GRCm39) |
V204E |
probably damaging |
Het |
| Cyp2c67 |
A |
T |
19: 39,597,708 (GRCm39) |
|
probably null |
Het |
| Ddb1 |
T |
C |
19: 10,605,195 (GRCm39) |
V1061A |
possibly damaging |
Het |
| Dnah12 |
G |
T |
14: 26,488,534 (GRCm39) |
|
probably null |
Het |
| Draxin |
T |
C |
4: 148,197,216 (GRCm39) |
T194A |
probably benign |
Het |
| Drosha |
T |
A |
15: 12,846,285 (GRCm39) |
D473E |
possibly damaging |
Het |
| Ecpas |
T |
C |
4: 58,827,047 (GRCm39) |
T1029A |
possibly damaging |
Het |
| G6pd2 |
T |
A |
5: 61,967,562 (GRCm39) |
C446S |
probably benign |
Het |
| Gm29106 |
C |
T |
1: 118,104,642 (GRCm39) |
S3L |
unknown |
Het |
| Grin3a |
T |
C |
4: 49,702,762 (GRCm39) |
Y908C |
probably damaging |
Het |
| Ints2 |
G |
A |
11: 86,108,668 (GRCm39) |
A893V |
probably benign |
Het |
| Ippk |
C |
T |
13: 49,602,767 (GRCm39) |
T371I |
probably benign |
Het |
| Irf2 |
T |
A |
8: 47,260,316 (GRCm39) |
C83S |
probably damaging |
Het |
| Jph3 |
C |
T |
8: 122,480,441 (GRCm39) |
A373V |
probably benign |
Het |
| Kcnj6 |
C |
T |
16: 94,634,073 (GRCm39) |
V13I |
probably benign |
Het |
| Lama3 |
T |
C |
18: 12,640,097 (GRCm39) |
|
probably null |
Het |
| Lmo7 |
A |
T |
14: 102,121,640 (GRCm39) |
Q235L |
probably damaging |
Het |
| Marchf7 |
A |
G |
2: 60,071,189 (GRCm39) |
|
probably null |
Het |
| Mfsd6l |
A |
T |
11: 68,448,109 (GRCm39) |
Y320F |
possibly damaging |
Het |
| Mroh1 |
T |
A |
15: 76,335,676 (GRCm39) |
W1440R |
probably benign |
Het |
| Mrps17 |
G |
A |
5: 129,793,863 (GRCm39) |
G19D |
probably damaging |
Het |
| Myt1 |
A |
G |
2: 181,444,756 (GRCm39) |
H566R |
possibly damaging |
Het |
| Nav2 |
T |
C |
7: 49,201,521 (GRCm39) |
L176P |
possibly damaging |
Het |
| Nop58 |
T |
A |
1: 59,737,599 (GRCm39) |
C139S |
probably benign |
Het |
| Nsd1 |
A |
G |
13: 55,394,022 (GRCm39) |
D644G |
probably damaging |
Het |
| Nsd2 |
T |
A |
5: 34,042,816 (GRCm39) |
C1027S |
probably damaging |
Het |
| Nsmce2 |
A |
G |
15: 59,473,265 (GRCm39) |
I235V |
probably damaging |
Het |
| Nyap2 |
T |
C |
1: 81,314,230 (GRCm39) |
V642A |
possibly damaging |
Het |
| Or14n1-ps1 |
A |
T |
7: 86,092,328 (GRCm39) |
L46F |
unknown |
Het |
| Or8g51 |
A |
G |
9: 38,609,161 (GRCm39) |
V167A |
probably benign |
Het |
| Paqr7 |
A |
G |
4: 134,234,431 (GRCm39) |
D96G |
probably benign |
Het |
| Parp4 |
A |
G |
14: 56,839,852 (GRCm39) |
Y520C |
probably damaging |
Het |
| Pde5a |
A |
G |
3: 122,542,107 (GRCm39) |
N199S |
probably damaging |
Het |
| Piezo1 |
A |
T |
8: 123,212,463 (GRCm39) |
Y1955N |
|
Het |
| Pnma8a |
A |
G |
7: 16,695,315 (GRCm39) |
K390R |
probably benign |
Het |
| Prdm10 |
G |
T |
9: 31,227,537 (GRCm39) |
Q47H |
probably damaging |
Het |
| Psg22 |
T |
A |
7: 18,453,499 (GRCm39) |
F104I |
probably benign |
Het |
| Ptprf |
T |
C |
4: 118,068,322 (GRCm39) |
E1738G |
probably damaging |
Het |
| Rad21l |
A |
T |
2: 151,500,365 (GRCm39) |
L218Q |
probably damaging |
Het |
| Rad54l2 |
A |
G |
9: 106,583,024 (GRCm39) |
I798T |
probably damaging |
Het |
| Rgs5 |
G |
T |
1: 169,483,149 (GRCm39) |
M1I |
probably null |
Het |
| Rhbdl2 |
T |
C |
4: 123,711,659 (GRCm39) |
V132A |
possibly damaging |
Het |
| Rmi1 |
T |
A |
13: 58,557,393 (GRCm39) |
Y547* |
probably null |
Het |
| Rptn |
A |
T |
3: 93,304,212 (GRCm39) |
D515V |
probably benign |
Het |
| Rsph10b |
A |
G |
5: 143,898,033 (GRCm39) |
N505D |
probably benign |
Het |
| Samhd1 |
T |
C |
2: 156,948,164 (GRCm39) |
D539G |
probably damaging |
Het |
| Scube3 |
A |
T |
17: 28,387,156 (GRCm39) |
I885F |
probably damaging |
Het |
| Sfmbt1 |
A |
G |
14: 30,506,696 (GRCm39) |
I247V |
possibly damaging |
Het |
| Slc25a21 |
T |
C |
12: 56,904,828 (GRCm39) |
I62V |
probably benign |
Het |
| Slc4a11 |
T |
A |
2: 130,527,452 (GRCm39) |
N648Y |
probably damaging |
Het |
| Slc7a11 |
A |
G |
3: 50,397,448 (GRCm39) |
V88A |
possibly damaging |
Het |
| Slc7a8 |
A |
C |
14: 54,964,263 (GRCm39) |
F397V |
possibly damaging |
Het |
| Sox12 |
A |
C |
2: 152,239,377 (GRCm39) |
L81R |
probably damaging |
Het |
| Spg11 |
T |
C |
2: 121,915,474 (GRCm39) |
I1057V |
probably benign |
Het |
| St8sia3 |
G |
A |
18: 64,402,987 (GRCm39) |
V265I |
probably benign |
Het |
| Stxbp5 |
A |
G |
10: 9,684,874 (GRCm39) |
S509P |
possibly damaging |
Het |
| Svep1 |
T |
C |
4: 58,108,323 (GRCm39) |
Y1129C |
probably damaging |
Het |
| Tenm4 |
G |
T |
7: 96,523,333 (GRCm39) |
R1625L |
probably benign |
Het |
| Tlr4 |
T |
C |
4: 66,758,191 (GRCm39) |
F328S |
possibly damaging |
Het |
| Tmprss15 |
T |
C |
16: 78,868,164 (GRCm39) |
T215A |
probably benign |
Het |
| Tmprss9 |
A |
T |
10: 80,718,504 (GRCm39) |
I62L |
probably benign |
Het |
| Trpm5 |
C |
T |
7: 142,642,756 (GRCm39) |
A64T |
probably benign |
Het |
| Txk |
A |
C |
5: 72,889,109 (GRCm39) |
Y148* |
probably null |
Het |
| Uba5 |
C |
T |
9: 103,932,454 (GRCm39) |
G170R |
possibly damaging |
Het |
| Ulk4 |
A |
T |
9: 121,077,993 (GRCm39) |
D525E |
probably benign |
Het |
| Vmn1r158 |
T |
A |
7: 22,489,649 (GRCm39) |
T187S |
probably benign |
Het |
| Vmn1r52 |
T |
A |
6: 90,156,605 (GRCm39) |
M303K |
probably benign |
Het |
| Vmn2r54 |
A |
G |
7: 12,356,044 (GRCm39) |
F454S |
probably benign |
Het |
| Zbp1 |
A |
T |
2: 173,060,546 (GRCm39) |
L8* |
probably null |
Het |
| Zmym2 |
A |
T |
14: 57,181,557 (GRCm39) |
D924V |
probably benign |
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 |
|
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 |
|
|
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'- GTCGTCGAGTTACTAGGAACG -3'
(R):5'- CATTTCACAGTGGCTACAAGC -3'
Sequencing Primer
(F):5'- CGAGTTACTAGGAACGTGTGC -3'
(R):5'- TGTTAGAGAACTTGCCGAGCACTC -3'
|
| Posted On |
2019-09-13 |
Incidental Mutation