Incidental Mutation 'R6247:Uggt1'
| ID |
505654 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Uggt1
|
| Ensembl Gene |
ENSMUSG00000037470 |
| Gene Name |
UDP-glucose glycoprotein glucosyltransferase 1 |
| Synonyms |
C820010P03Rik, 0910001L17Rik, Ugcgl1, A930007H10Rik |
| MMRRC Submission |
044366-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.470)
|
| Stock # |
R6247 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
1 |
| Chromosomal Location |
36179109-36283407 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 36202309 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Leucine to Glutamine
at position 1096
(L1096Q)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000037930
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000046875]
[ENSMUST00000173166]
[ENSMUST00000174266]
|
| AlphaFold |
Q6P5E4 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000046875
AA Change: L1096Q
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000037930
Gene: ENSMUSG00000037470
AA Change: L1096Q
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
42 |
N/A |
INTRINSIC |
|
Pfam:UDP-g_GGTase
|
44 |
1222 |
N/A |
PFAM |
|
SCOP:d1ga8a_
|
1256 |
1521 |
3e-45 |
SMART |
|
Blast:BROMO
|
1414 |
1453 |
3e-17 |
BLAST |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000173082
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000173166
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000173999
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000174224
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000174266
|
| SMART Domains |
Protein: ENSMUSP00000134640
Gene: ENSMUSG00000037470
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
42 |
N/A |
INTRINSIC |
|
low complexity region
|
88 |
97 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.7%
- 10x: 98.4%
- 20x: 95.4%
|
| 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]
PHENOTYPE: Heterozygous KO reduces susceptibility to and morbidity of RNA virus infection. Homozygous KO is embryonic lethal. The peptide is a folding sensor for glycoproteins in the ER. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 86 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4933427D14Rik |
T |
C |
11: 72,049,768 (GRCm39) |
D871G |
probably benign |
Het |
| A4galt |
G |
T |
15: 83,112,020 (GRCm39) |
H254Q |
probably damaging |
Het |
| AA986860 |
C |
A |
1: 130,670,780 (GRCm39) |
T334K |
possibly damaging |
Het |
| Abca13 |
T |
C |
11: 9,353,874 (GRCm39) |
I3732T |
probably benign |
Het |
| Abcf1 |
C |
T |
17: 36,271,956 (GRCm39) |
D353N |
probably damaging |
Het |
| Adss1 |
A |
G |
12: 112,594,790 (GRCm39) |
H83R |
probably damaging |
Het |
| Amer2 |
C |
A |
14: 60,616,321 (GRCm39) |
A172E |
probably damaging |
Het |
| Ankhd1 |
A |
G |
18: 36,787,199 (GRCm39) |
T2300A |
probably benign |
Het |
| Ano5 |
G |
A |
7: 51,215,879 (GRCm39) |
|
probably null |
Het |
| Apob |
G |
A |
12: 8,051,801 (GRCm39) |
G1109D |
probably damaging |
Het |
| Arhgef26 |
A |
T |
3: 62,288,381 (GRCm39) |
N484Y |
probably damaging |
Het |
| C6 |
A |
G |
15: 4,793,023 (GRCm39) |
D376G |
probably damaging |
Het |
| Caml |
T |
C |
13: 55,772,986 (GRCm39) |
|
probably null |
Het |
| Capn12 |
T |
C |
7: 28,588,077 (GRCm39) |
L473S |
probably benign |
Het |
| Cdk6 |
G |
A |
5: 3,394,553 (GRCm39) |
|
probably null |
Het |
| Cers5 |
A |
T |
15: 99,643,805 (GRCm39) |
C153S |
probably benign |
Het |
| Cfap206 |
T |
C |
4: 34,692,530 (GRCm39) |
M499V |
probably benign |
Het |
| Chd6 |
A |
G |
2: 160,791,968 (GRCm39) |
M2463T |
probably damaging |
Het |
| Chn1 |
T |
C |
2: 73,537,350 (GRCm39) |
E58G |
possibly damaging |
Het |
| Clec4a1 |
T |
C |
6: 122,905,001 (GRCm39) |
V100A |
probably benign |
Het |
| Col7a1 |
G |
C |
9: 108,810,130 (GRCm39) |
|
probably benign |
Het |
| Csmd1 |
A |
G |
8: 16,246,249 (GRCm39) |
V1050A |
possibly damaging |
Het |
| Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
| Dennd5a |
A |
T |
7: 109,497,889 (GRCm39) |
C1044S |
probably damaging |
Het |
| Dnah7b |
A |
G |
1: 46,265,048 (GRCm39) |
T2181A |
probably benign |
Het |
| Dnai1 |
T |
C |
4: 41,605,775 (GRCm39) |
V255A |
probably benign |
Het |
| Dync2h1 |
A |
G |
9: 7,135,078 (GRCm39) |
C1518R |
probably damaging |
Het |
| Dysf |
T |
C |
6: 84,043,981 (GRCm39) |
V273A |
probably damaging |
Het |
| Eif1 |
C |
T |
11: 100,211,223 (GRCm39) |
|
probably benign |
Het |
| Eml3 |
T |
C |
19: 8,908,313 (GRCm39) |
I58T |
probably benign |
Het |
| Fam171b |
T |
A |
2: 83,709,552 (GRCm39) |
I408N |
probably damaging |
Het |
| Fchsd2 |
A |
G |
7: 100,902,747 (GRCm39) |
E351G |
probably benign |
Het |
| Focad |
G |
A |
4: 88,325,377 (GRCm39) |
A81T |
possibly damaging |
Het |
| Fpr-rs4 |
G |
A |
17: 18,242,748 (GRCm39) |
V252I |
probably benign |
Het |
| Fryl |
A |
G |
5: 73,222,824 (GRCm39) |
L1919P |
probably damaging |
Het |
| Gm12185 |
C |
T |
11: 48,806,735 (GRCm39) |
R152H |
probably damaging |
Het |
| Gm14410 |
C |
T |
2: 176,885,517 (GRCm39) |
G249E |
probably damaging |
Het |
| Gm6685 |
A |
T |
11: 28,289,706 (GRCm39) |
S37T |
possibly damaging |
Het |
| Greb1 |
G |
A |
12: 16,766,676 (GRCm39) |
P374L |
probably damaging |
Het |
| Hdac4 |
A |
T |
1: 91,940,560 (GRCm39) |
|
probably null |
Het |
| Hecw1 |
A |
T |
13: 14,409,010 (GRCm39) |
L1099* |
probably null |
Het |
| Hivep1 |
T |
C |
13: 42,310,966 (GRCm39) |
S1069P |
probably benign |
Het |
| Itgad |
T |
C |
7: 127,784,959 (GRCm39) |
I288T |
possibly damaging |
Het |
| Kif9 |
A |
G |
9: 110,317,612 (GRCm39) |
M96V |
possibly damaging |
Het |
| Kncn |
T |
A |
4: 115,741,987 (GRCm39) |
V18E |
probably damaging |
Het |
| Lrrc74a |
G |
A |
12: 86,805,330 (GRCm39) |
G384D |
probably damaging |
Het |
| Ltb4r2 |
T |
C |
14: 56,000,108 (GRCm39) |
V243A |
probably damaging |
Het |
| Mtnr1b |
T |
A |
9: 15,774,082 (GRCm39) |
I326L |
probably benign |
Het |
| Mylip |
C |
T |
13: 45,561,957 (GRCm39) |
T253I |
probably damaging |
Het |
| Necap1 |
T |
A |
6: 122,857,611 (GRCm39) |
|
probably null |
Het |
| Nedd4 |
C |
T |
9: 72,633,720 (GRCm39) |
P409S |
probably damaging |
Het |
| Npat |
A |
T |
9: 53,456,538 (GRCm39) |
E36D |
probably damaging |
Het |
| Ovch2 |
C |
T |
7: 107,384,648 (GRCm39) |
V490M |
probably damaging |
Het |
| Pax9 |
T |
C |
12: 56,756,480 (GRCm39) |
S273P |
probably benign |
Het |
| Plce1 |
A |
G |
19: 38,734,289 (GRCm39) |
E1563G |
probably damaging |
Het |
| Podxl2 |
C |
A |
6: 88,826,299 (GRCm39) |
G336* |
probably null |
Het |
| Prdm1 |
A |
G |
10: 44,322,782 (GRCm39) |
|
probably null |
Het |
| Psme4 |
T |
C |
11: 30,803,245 (GRCm39) |
I29T |
possibly damaging |
Het |
| Ptprd |
A |
T |
4: 75,984,528 (GRCm39) |
D780E |
probably benign |
Het |
| Retsat |
T |
C |
6: 72,581,918 (GRCm39) |
M294T |
probably benign |
Het |
| Robo2 |
A |
T |
16: 73,764,672 (GRCm39) |
V652D |
probably damaging |
Het |
| Rptn |
C |
G |
3: 93,305,437 (GRCm39) |
H923Q |
possibly damaging |
Het |
| Serpinb3d |
G |
T |
1: 107,010,490 (GRCm39) |
T66K |
probably benign |
Het |
| Setd1b |
A |
T |
5: 123,296,461 (GRCm39) |
|
probably benign |
Het |
| Slc7a10 |
G |
T |
7: 34,886,012 (GRCm39) |
A36S |
possibly damaging |
Het |
| Sstr3 |
T |
A |
15: 78,423,788 (GRCm39) |
I320F |
probably damaging |
Het |
| Syne1 |
G |
T |
10: 5,299,071 (GRCm39) |
A1005E |
probably damaging |
Het |
| Syngap1 |
C |
A |
17: 27,181,931 (GRCm39) |
S975* |
probably null |
Het |
| Tinagl1 |
C |
T |
4: 130,066,725 (GRCm39) |
C124Y |
probably null |
Het |
| Tm9sf1 |
C |
T |
14: 55,873,827 (GRCm39) |
R557H |
probably damaging |
Het |
| Tmed2 |
T |
A |
5: 124,685,055 (GRCm39) |
I68K |
possibly damaging |
Het |
| Tmem104 |
A |
G |
11: 115,134,819 (GRCm39) |
T451A |
probably benign |
Het |
| Tmem141 |
T |
C |
2: 25,511,693 (GRCm39) |
|
probably null |
Het |
| Tmem184a |
C |
A |
5: 139,798,827 (GRCm39) |
V41L |
probably benign |
Het |
| Tmem39b |
C |
T |
4: 129,580,584 (GRCm39) |
V303I |
possibly damaging |
Het |
| Tsn |
T |
C |
1: 118,232,939 (GRCm39) |
I122V |
probably benign |
Het |
| Ttc41 |
G |
T |
10: 86,612,527 (GRCm39) |
V1267L |
probably benign |
Het |
| Usp50 |
A |
T |
2: 126,617,713 (GRCm39) |
I244N |
probably benign |
Het |
| Vil1 |
A |
G |
1: 74,471,498 (GRCm39) |
S760G |
probably benign |
Het |
| Wasf1 |
T |
A |
10: 40,813,741 (GRCm39) |
V541E |
unknown |
Het |
| Zc3h13 |
G |
T |
14: 75,581,176 (GRCm39) |
S1721I |
probably benign |
Het |
| Zfp180 |
G |
T |
7: 23,804,530 (GRCm39) |
K316N |
probably damaging |
Het |
| Zfp582 |
T |
C |
7: 6,356,945 (GRCm39) |
C253R |
probably damaging |
Het |
| Zfp709 |
TCGACG |
TCG |
8: 72,644,552 (GRCm39) |
|
probably benign |
Het |
| Zfp759 |
A |
G |
13: 67,288,524 (GRCm39) |
T692A |
probably benign |
Het |
| Zfyve26 |
A |
G |
12: 79,329,758 (GRCm39) |
V476A |
probably benign |
Het |
|
| Other mutations in Uggt1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00091:Uggt1
|
APN |
1 |
36,218,633 (GRCm39) |
splice site |
probably benign |
|
|
IGL00817:Uggt1
|
APN |
1 |
36,225,013 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL01395:Uggt1
|
APN |
1 |
36,194,158 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01609:Uggt1
|
APN |
1 |
36,221,555 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01619:Uggt1
|
APN |
1 |
36,200,775 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02077:Uggt1
|
APN |
1 |
36,215,875 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02313:Uggt1
|
APN |
1 |
36,223,565 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02341:Uggt1
|
APN |
1 |
36,203,600 (GRCm39) |
makesense |
probably null |
|
|
IGL02346:Uggt1
|
APN |
1 |
36,218,751 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02447:Uggt1
|
APN |
1 |
36,189,223 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02883:Uggt1
|
APN |
1 |
36,216,696 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL02930:Uggt1
|
APN |
1 |
36,196,537 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL03153:Uggt1
|
APN |
1 |
36,241,899 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
IGL03162:Uggt1
|
APN |
1 |
36,247,037 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03170:Uggt1
|
APN |
1 |
36,202,342 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03266:Uggt1
|
APN |
1 |
36,189,129 (GRCm39) |
missense |
probably damaging |
1.00 |
|
K3955:Uggt1
|
UTSW |
1 |
36,201,434 (GRCm39) |
missense |
probably benign |
0.37 |
|
R0037:Uggt1
|
UTSW |
1 |
36,225,013 (GRCm39) |
missense |
probably benign |
0.03 |
|
R0037:Uggt1
|
UTSW |
1 |
36,225,013 (GRCm39) |
missense |
probably benign |
0.03 |
|
R0167:Uggt1
|
UTSW |
1 |
36,209,278 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0373:Uggt1
|
UTSW |
1 |
36,218,751 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0502:Uggt1
|
UTSW |
1 |
36,199,027 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0546:Uggt1
|
UTSW |
1 |
36,235,052 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0610:Uggt1
|
UTSW |
1 |
36,204,587 (GRCm39) |
splice site |
probably benign |
|
|
R0671:Uggt1
|
UTSW |
1 |
36,194,209 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0760:Uggt1
|
UTSW |
1 |
36,200,805 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R0825:Uggt1
|
UTSW |
1 |
36,197,224 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0827:Uggt1
|
UTSW |
1 |
36,195,394 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R0884:Uggt1
|
UTSW |
1 |
36,214,159 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1112:Uggt1
|
UTSW |
1 |
36,212,627 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R1470:Uggt1
|
UTSW |
1 |
36,215,877 (GRCm39) |
missense |
probably benign |
0.13 |
|
R1470:Uggt1
|
UTSW |
1 |
36,215,877 (GRCm39) |
missense |
probably benign |
0.13 |
|
R1592:Uggt1
|
UTSW |
1 |
36,241,939 (GRCm39) |
missense |
probably benign |
0.04 |
|
R1730:Uggt1
|
UTSW |
1 |
36,260,342 (GRCm39) |
missense |
probably benign |
0.05 |
|
R1923:Uggt1
|
UTSW |
1 |
36,218,694 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1970:Uggt1
|
UTSW |
1 |
36,190,862 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2086:Uggt1
|
UTSW |
1 |
36,231,495 (GRCm39) |
missense |
probably null |
1.00 |
|
R2829:Uggt1
|
UTSW |
1 |
36,201,375 (GRCm39) |
missense |
probably benign |
0.38 |
|
R3431:Uggt1
|
UTSW |
1 |
36,249,140 (GRCm39) |
nonsense |
probably null |
|
|
R3432:Uggt1
|
UTSW |
1 |
36,249,140 (GRCm39) |
nonsense |
probably null |
|
|
R3725:Uggt1
|
UTSW |
1 |
36,221,588 (GRCm39) |
nonsense |
probably null |
|
|
R3880:Uggt1
|
UTSW |
1 |
36,215,885 (GRCm39) |
intron |
probably benign |
|
|
R4052:Uggt1
|
UTSW |
1 |
36,203,570 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4133:Uggt1
|
UTSW |
1 |
36,197,240 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4489:Uggt1
|
UTSW |
1 |
36,185,749 (GRCm39) |
nonsense |
probably null |
|
|
R4570:Uggt1
|
UTSW |
1 |
36,189,154 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4866:Uggt1
|
UTSW |
1 |
36,241,936 (GRCm39) |
nonsense |
probably null |
|
|
R4895:Uggt1
|
UTSW |
1 |
36,195,345 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4900:Uggt1
|
UTSW |
1 |
36,241,936 (GRCm39) |
nonsense |
probably null |
|
|
R5372:Uggt1
|
UTSW |
1 |
36,283,141 (GRCm39) |
splice site |
probably benign |
|
|
R5385:Uggt1
|
UTSW |
1 |
36,223,493 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5652:Uggt1
|
UTSW |
1 |
36,255,234 (GRCm39) |
nonsense |
probably null |
|
|
R5694:Uggt1
|
UTSW |
1 |
36,218,737 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5732:Uggt1
|
UTSW |
1 |
36,200,852 (GRCm39) |
splice site |
probably null |
|
|
R5893:Uggt1
|
UTSW |
1 |
36,266,709 (GRCm39) |
splice site |
probably null |
|
|
R6191:Uggt1
|
UTSW |
1 |
36,201,289 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6259:Uggt1
|
UTSW |
1 |
36,273,997 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6399:Uggt1
|
UTSW |
1 |
36,202,447 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R6439:Uggt1
|
UTSW |
1 |
36,214,032 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R6468:Uggt1
|
UTSW |
1 |
36,212,531 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6788:Uggt1
|
UTSW |
1 |
36,269,769 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7165:Uggt1
|
UTSW |
1 |
36,194,188 (GRCm39) |
missense |
probably benign |
0.41 |
|
R7255:Uggt1
|
UTSW |
1 |
36,185,187 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7273:Uggt1
|
UTSW |
1 |
36,201,302 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7469:Uggt1
|
UTSW |
1 |
36,190,814 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7490:Uggt1
|
UTSW |
1 |
36,203,589 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7570:Uggt1
|
UTSW |
1 |
36,224,919 (GRCm39) |
missense |
probably benign |
0.09 |
|
R7612:Uggt1
|
UTSW |
1 |
36,202,316 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7759:Uggt1
|
UTSW |
1 |
36,185,806 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R7792:Uggt1
|
UTSW |
1 |
36,247,065 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7816:Uggt1
|
UTSW |
1 |
36,202,396 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7858:Uggt1
|
UTSW |
1 |
36,195,339 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7887:Uggt1
|
UTSW |
1 |
36,247,115 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8040:Uggt1
|
UTSW |
1 |
36,250,554 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R8093:Uggt1
|
UTSW |
1 |
36,266,566 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8245:Uggt1
|
UTSW |
1 |
36,204,645 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8338:Uggt1
|
UTSW |
1 |
36,266,602 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8353:Uggt1
|
UTSW |
1 |
36,209,377 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R8442:Uggt1
|
UTSW |
1 |
36,212,568 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8519:Uggt1
|
UTSW |
1 |
36,215,724 (GRCm39) |
splice site |
probably null |
|
|
R8529:Uggt1
|
UTSW |
1 |
36,223,513 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R8730:Uggt1
|
UTSW |
1 |
36,236,624 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8917:Uggt1
|
UTSW |
1 |
36,185,735 (GRCm39) |
missense |
|
|
|
R8947:Uggt1
|
UTSW |
1 |
36,197,229 (GRCm39) |
missense |
probably benign |
0.12 |
|
R9240:Uggt1
|
UTSW |
1 |
36,221,696 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R9248:Uggt1
|
UTSW |
1 |
36,249,103 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R9401:Uggt1
|
UTSW |
1 |
36,255,212 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9414:Uggt1
|
UTSW |
1 |
36,223,507 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9416:Uggt1
|
UTSW |
1 |
36,203,603 (GRCm39) |
missense |
|
|
|
R9441:Uggt1
|
UTSW |
1 |
36,260,306 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9489:Uggt1
|
UTSW |
1 |
36,273,886 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9563:Uggt1
|
UTSW |
1 |
36,204,627 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R9605:Uggt1
|
UTSW |
1 |
36,273,886 (GRCm39) |
critical splice donor site |
probably null |
|
|
X0022:Uggt1
|
UTSW |
1 |
36,204,636 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
Z1088:Uggt1
|
UTSW |
1 |
36,213,272 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Uggt1
|
UTSW |
1 |
36,200,776 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Uggt1
|
UTSW |
1 |
36,194,154 (GRCm39) |
missense |
probably null |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- TCTGAATAAAGCAGCTGCCG -3'
(R):5'- GCTGAGACTGCATCAAGAAATACC -3'
Sequencing Primer
(F):5'- CGTAAGGGAGCATCAACGTAAGG -3'
(R):5'- AGCTTTTACCGTTACGTCTTAGAG -3'
|
| Posted On |
2018-02-28 |
Incidental Mutation