Incidental Mutation 'R4832:Uggt2'
| ID |
372937 |
| 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 |
042448-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.104)
|
| Stock # |
R4832 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
14 |
| Chromosomal Location |
119222451-119336842 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 119239259 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Asparagine
at position 1391
(I1391N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000121249
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000156203]
|
| AlphaFold |
E9Q4X2 |
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000123350
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000126023
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000131424
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000138720
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000148022
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000148648
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000154130
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000156203
AA Change: I1391N
PolyPhen 2
Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000121249
Gene: ENSMUSG00000042104
AA Change: I1391N
| 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 |
0.2749 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 93.9%
|
| Validation Efficiency |
98% (106/108) |
| 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 |
|---|
| 1110032F04Rik |
T |
C |
3: 68,777,597 (GRCm39) |
V186A |
possibly damaging |
Het |
| 1700088E04Rik |
A |
T |
15: 79,019,409 (GRCm39) |
M198K |
probably damaging |
Het |
| 4933402J07Rik |
A |
G |
8: 88,294,601 (GRCm39) |
K84R |
probably null |
Het |
| Aamdc |
T |
C |
7: 97,199,773 (GRCm39) |
|
probably null |
Het |
| Abcc9 |
A |
G |
6: 142,617,282 (GRCm39) |
V594A |
probably damaging |
Het |
| Adamts13 |
G |
A |
2: 26,879,414 (GRCm39) |
D656N |
probably benign |
Het |
| Adcy10 |
G |
T |
1: 165,334,213 (GRCm39) |
C122F |
probably damaging |
Het |
| Adi1 |
A |
G |
12: 28,725,252 (GRCm39) |
M1V |
probably null |
Het |
| Ahnak |
G |
A |
19: 8,989,824 (GRCm39) |
|
probably benign |
Het |
| Akt1 |
G |
T |
12: 112,623,521 (GRCm39) |
P313Q |
probably damaging |
Het |
| Ano3 |
A |
T |
2: 110,498,067 (GRCm39) |
M758K |
probably damaging |
Het |
| Baz2a |
T |
A |
10: 127,958,999 (GRCm39) |
N1168K |
probably benign |
Het |
| Bbs10 |
A |
G |
10: 111,136,995 (GRCm39) |
K703E |
probably benign |
Het |
| Bcap29 |
A |
G |
12: 31,674,202 (GRCm39) |
I131T |
probably benign |
Het |
| Brd10 |
G |
T |
19: 29,694,616 (GRCm39) |
L1626I |
possibly damaging |
Het |
| Btnl6 |
T |
C |
17: 34,732,966 (GRCm39) |
D299G |
possibly damaging |
Het |
| Ccdc66 |
A |
G |
14: 27,222,524 (GRCm39) |
I73T |
probably benign |
Het |
| Cdh2 |
A |
G |
18: 16,760,754 (GRCm39) |
S538P |
probably benign |
Het |
| Cfap54 |
T |
A |
10: 92,803,390 (GRCm39) |
M1551L |
probably benign |
Het |
| Chd2 |
G |
A |
7: 73,151,873 (GRCm39) |
A243V |
probably damaging |
Het |
| Cntnap1 |
T |
A |
11: 101,073,845 (GRCm39) |
N665K |
probably damaging |
Het |
| Colgalt2 |
C |
T |
1: 152,360,749 (GRCm39) |
T262I |
possibly damaging |
Het |
| Cyp24a1 |
T |
C |
2: 170,338,098 (GRCm39) |
I149V |
probably benign |
Het |
| Cyp2a5 |
T |
A |
7: 26,534,970 (GRCm39) |
|
probably null |
Het |
| Dab2 |
A |
G |
15: 6,366,080 (GRCm39) |
|
probably null |
Het |
| Dnah17 |
T |
A |
11: 117,917,606 (GRCm39) |
I4158F |
probably damaging |
Het |
| Dnm2 |
G |
A |
9: 21,385,975 (GRCm39) |
|
probably null |
Het |
| Dpp7 |
A |
T |
2: 25,242,398 (GRCm39) |
|
probably benign |
Het |
| Epha6 |
T |
A |
16: 59,780,776 (GRCm39) |
I642F |
probably damaging |
Het |
| Erbb4 |
T |
C |
1: 68,369,397 (GRCm39) |
S415G |
probably benign |
Het |
| Fancd2 |
A |
G |
6: 113,530,683 (GRCm39) |
T439A |
probably benign |
Het |
| Fat1 |
G |
A |
8: 45,466,102 (GRCm39) |
V1431M |
possibly damaging |
Het |
| Fhod3 |
G |
A |
18: 25,223,305 (GRCm39) |
A884T |
probably benign |
Het |
| Fsip2 |
A |
G |
2: 82,820,515 (GRCm39) |
D5416G |
possibly damaging |
Het |
| Gabarap |
C |
T |
11: 69,882,678 (GRCm39) |
|
probably benign |
Het |
| Garre1 |
T |
C |
7: 33,938,333 (GRCm39) |
|
probably benign |
Het |
| Gm11544 |
C |
T |
11: 94,736,532 (GRCm39) |
|
noncoding transcript |
Het |
| Gnat2 |
A |
C |
3: 108,007,964 (GRCm39) |
K304Q |
probably benign |
Het |
| Gpr141b |
T |
A |
13: 19,913,840 (GRCm39) |
|
noncoding transcript |
Het |
| Gramd4 |
C |
T |
15: 86,019,057 (GRCm39) |
A575V |
probably benign |
Het |
| Gtpbp10 |
G |
A |
5: 5,589,295 (GRCm39) |
A274V |
possibly damaging |
Het |
| Gzmb |
A |
G |
14: 56,497,679 (GRCm39) |
I187T |
probably damaging |
Het |
| H2-M10.2 |
G |
A |
17: 36,595,219 (GRCm39) |
T315I |
probably damaging |
Het |
| Haus5 |
A |
T |
7: 30,356,452 (GRCm39) |
F524I |
probably damaging |
Het |
| Herc1 |
A |
G |
9: 66,403,253 (GRCm39) |
S4391G |
probably benign |
Het |
| Herc2 |
T |
A |
7: 55,748,165 (GRCm39) |
L511* |
probably null |
Het |
| Htt |
T |
A |
5: 34,982,184 (GRCm39) |
C923S |
probably benign |
Het |
| Idua |
T |
C |
5: 108,817,247 (GRCm39) |
S7P |
probably benign |
Het |
| Ighv16-1 |
A |
T |
12: 114,032,466 (GRCm39) |
L112Q |
probably damaging |
Het |
| Igkv1-110 |
A |
G |
6: 68,248,185 (GRCm39) |
K98R |
probably benign |
Het |
| Kif15 |
G |
A |
9: 122,831,191 (GRCm39) |
|
probably null |
Het |
| Leng9 |
C |
A |
7: 4,152,029 (GRCm39) |
G216W |
probably damaging |
Het |
| Lrpprc |
A |
G |
17: 85,014,584 (GRCm39) |
L1306S |
probably benign |
Het |
| Lztfl1 |
C |
A |
9: 123,544,454 (GRCm39) |
E20D |
possibly damaging |
Het |
| Maob |
T |
C |
X: 16,582,662 (GRCm39) |
T400A |
probably benign |
Het |
| Map3k4 |
C |
T |
17: 12,490,667 (GRCm39) |
E255K |
probably damaging |
Het |
| Megf9 |
G |
A |
4: 70,452,665 (GRCm39) |
T132M |
probably damaging |
Het |
| Mob4 |
T |
C |
1: 55,184,411 (GRCm39) |
|
probably benign |
Het |
| Mttp |
G |
A |
3: 137,821,811 (GRCm39) |
A252V |
probably benign |
Het |
| Mxi1 |
A |
G |
19: 53,358,745 (GRCm39) |
D226G |
probably damaging |
Het |
| Myh14 |
A |
G |
7: 44,274,566 (GRCm39) |
S1249P |
probably benign |
Het |
| Mylk |
G |
A |
16: 34,742,737 (GRCm39) |
G1083D |
probably benign |
Het |
| Mylk4 |
T |
G |
13: 32,905,960 (GRCm39) |
I408L |
probably benign |
Het |
| Nbas |
A |
G |
12: 13,533,740 (GRCm39) |
S1792G |
probably benign |
Het |
| Nelfb |
A |
G |
2: 25,099,981 (GRCm39) |
V212A |
probably damaging |
Het |
| Nisch |
T |
C |
14: 30,899,587 (GRCm39) |
|
probably benign |
Het |
| Nqo1 |
C |
G |
8: 108,115,477 (GRCm39) |
D267H |
probably benign |
Het |
| Or8u10 |
C |
A |
2: 85,915,190 (GRCm39) |
L310F |
probably benign |
Het |
| Pcid2 |
T |
A |
8: 13,135,425 (GRCm39) |
I195F |
probably damaging |
Het |
| Pcnx2 |
A |
T |
8: 126,478,927 (GRCm39) |
M2107K |
probably damaging |
Het |
| Pgd |
A |
T |
4: 149,241,048 (GRCm39) |
|
probably benign |
Het |
| Prim2 |
T |
C |
1: 33,503,145 (GRCm39) |
M430V |
probably benign |
Het |
| Prkaa1 |
A |
G |
15: 5,190,101 (GRCm39) |
T40A |
probably damaging |
Het |
| Ptges |
T |
C |
2: 30,793,232 (GRCm39) |
|
probably benign |
Het |
| Ptprn |
T |
C |
1: 75,234,909 (GRCm39) |
E226G |
probably benign |
Het |
| Rab14 |
A |
G |
2: 35,079,978 (GRCm39) |
F55S |
probably damaging |
Het |
| Ralgps2 |
A |
T |
1: 156,684,637 (GRCm39) |
|
probably benign |
Het |
| Rgs11 |
C |
T |
17: 26,426,542 (GRCm39) |
H258Y |
probably benign |
Het |
| Rhpn2 |
T |
C |
7: 35,075,774 (GRCm39) |
|
probably null |
Het |
| Rprd2 |
A |
T |
3: 95,681,483 (GRCm39) |
V452E |
probably damaging |
Het |
| Scube3 |
C |
A |
17: 28,384,989 (GRCm39) |
H646Q |
probably damaging |
Het |
| Selp |
A |
T |
1: 163,953,909 (GRCm39) |
I70F |
probably damaging |
Het |
| Septin2 |
A |
G |
1: 93,426,849 (GRCm39) |
I153V |
probably damaging |
Het |
| Sh3rf3 |
G |
A |
10: 58,649,905 (GRCm39) |
S170N |
probably benign |
Het |
| Skint4 |
A |
T |
4: 112,000,963 (GRCm39) |
I353F |
possibly damaging |
Het |
| Slc16a12 |
A |
G |
19: 34,657,780 (GRCm39) |
I41T |
possibly damaging |
Het |
| Snai2 |
T |
C |
16: 14,524,881 (GRCm39) |
F129S |
probably damaging |
Het |
| Top3b |
C |
T |
16: 16,708,526 (GRCm39) |
R629* |
probably null |
Het |
| Trim17 |
T |
A |
11: 58,862,270 (GRCm39) |
V434E |
probably damaging |
Het |
| Ttn |
G |
A |
2: 76,615,327 (GRCm39) |
P15051L |
probably damaging |
Het |
| Usp8 |
A |
T |
2: 126,596,958 (GRCm39) |
M923L |
probably damaging |
Het |
| Vmn1r176 |
T |
C |
7: 23,534,463 (GRCm39) |
H230R |
possibly damaging |
Het |
| Vmn1r217 |
C |
A |
13: 23,298,159 (GRCm39) |
D248Y |
probably damaging |
Het |
| Vmn2r14 |
A |
T |
5: 109,363,976 (GRCm39) |
C647S |
probably damaging |
Het |
| Vwa5b1 |
A |
G |
4: 138,332,851 (GRCm39) |
I237T |
probably damaging |
Het |
| Zan |
T |
A |
5: 137,391,423 (GRCm39) |
D4687V |
unknown |
Het |
| Zfp273 |
T |
C |
13: 67,973,484 (GRCm39) |
V204A |
probably benign |
Het |
| Zfp956 |
T |
G |
6: 47,928,987 (GRCm39) |
|
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 |
|
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'- CTGAGCTTCAAATAGGAAGTTATGG -3'
(R):5'- CAGAACACTGGACTCAAATTTCTG -3'
Sequencing Primer
(F):5'- GCTTCAAATAGGAAGTTATGGGTAAG -3'
(R):5'- TTGCTGCTTACAGTCCACCATAAAG -3'
|
| Posted On |
2016-03-01 |
Incidental Mutation