Incidental Mutation 'R7816:Uggt1'
ID |
601499 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Uggt1
|
Ensembl Gene |
ENSMUSG00000037470 |
Gene Name |
UDP-glucose glycoprotein glucosyltransferase 1 |
Synonyms |
C820010P03Rik, 0910001L17Rik, Ugcgl1, A930007H10Rik |
MMRRC Submission |
045870-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.470)
|
Stock # |
R7816 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
36179109-36283407 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 36202396 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Phenylalanine
at position 1067
(S1067F)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000037930
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000046875]
[ENSMUST00000173166]
[ENSMUST00000174266]
|
AlphaFold |
Q6P5E4 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000046875
AA Change: S1067F
PolyPhen 2
Score 0.954 (Sensitivity: 0.79; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000037930 Gene: ENSMUSG00000037470 AA Change: S1067F
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 |
probably benign
Transcript: ENSMUST00000173166
|
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: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.9%
|
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: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
A |
G |
1: 71,331,588 (GRCm39) |
S1321P |
probably benign |
Het |
Abcb1a |
T |
C |
5: 8,736,132 (GRCm39) |
V175A |
possibly damaging |
Het |
Adamts20 |
T |
A |
15: 94,220,725 (GRCm39) |
M1403L |
probably benign |
Het |
Akap13 |
G |
A |
7: 75,380,213 (GRCm39) |
R462H |
probably damaging |
Het |
Amotl2 |
T |
A |
9: 102,608,853 (GRCm39) |
I789K |
probably benign |
Het |
BC005537 |
C |
T |
13: 24,987,382 (GRCm39) |
R7W |
possibly damaging |
Het |
Bcar3 |
C |
T |
3: 122,220,343 (GRCm39) |
T80I |
probably benign |
Het |
Bcas1 |
G |
T |
2: 170,248,347 (GRCm39) |
F181L |
probably benign |
Het |
Cacnb1 |
T |
C |
11: 97,896,115 (GRCm39) |
E389G |
probably damaging |
Het |
Cd52 |
A |
T |
4: 133,821,199 (GRCm39) |
|
probably benign |
Het |
Cmtm1 |
CGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGT |
CGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGT |
8: 105,036,102 (GRCm39) |
|
probably benign |
Het |
Coro2a |
T |
C |
4: 46,546,809 (GRCm39) |
D182G |
probably benign |
Het |
Crp |
T |
C |
1: 172,526,277 (GRCm39) |
S121P |
possibly damaging |
Het |
Csnka2ip |
T |
C |
16: 64,299,852 (GRCm39) |
|
probably benign |
Het |
Cttnbp2 |
T |
C |
6: 18,448,413 (GRCm39) |
D82G |
probably damaging |
Het |
Cyp2b9 |
A |
G |
7: 25,900,517 (GRCm39) |
N385S |
probably benign |
Het |
Dppa1 |
A |
G |
11: 46,507,003 (GRCm39) |
S26P |
possibly damaging |
Het |
Eif4e3 |
T |
C |
6: 99,617,599 (GRCm39) |
R91G |
probably damaging |
Het |
F13a1 |
A |
T |
13: 37,209,745 (GRCm39) |
N73K |
probably benign |
Het |
Fbxl13 |
T |
C |
5: 21,748,785 (GRCm39) |
Y378C |
probably benign |
Het |
Glis2 |
G |
A |
16: 4,431,328 (GRCm39) |
R285H |
probably damaging |
Het |
Gm17174 |
T |
A |
14: 51,829,569 (GRCm39) |
|
probably benign |
Het |
Golga1 |
G |
A |
2: 38,942,110 (GRCm39) |
S102F |
probably damaging |
Het |
Hdac1 |
A |
T |
4: 129,411,888 (GRCm39) |
Y336N |
probably damaging |
Het |
Hfe |
G |
T |
13: 23,888,382 (GRCm39) |
T168K |
possibly damaging |
Het |
Idh2 |
TCCCAGG |
T |
7: 79,748,079 (GRCm39) |
|
probably benign |
Het |
Ighv1-56 |
T |
C |
12: 115,206,846 (GRCm39) |
S4G |
probably benign |
Het |
Ino80d |
A |
G |
1: 63,125,556 (GRCm39) |
Y74H |
probably damaging |
Het |
Ints1 |
A |
T |
5: 139,757,134 (GRCm39) |
H427Q |
possibly damaging |
Het |
Itpkb |
T |
A |
1: 180,241,454 (GRCm39) |
V708E |
probably damaging |
Het |
Jmjd4 |
G |
T |
11: 59,341,162 (GRCm39) |
G31V |
probably benign |
Het |
Kcnh5 |
C |
T |
12: 75,023,457 (GRCm39) |
C537Y |
probably damaging |
Het |
Kcnj11 |
A |
T |
7: 45,749,281 (GRCm39) |
L14Q |
probably damaging |
Het |
Lipo4 |
A |
T |
19: 33,491,642 (GRCm39) |
W114R |
probably damaging |
Het |
Lrrc9 |
T |
A |
12: 72,542,466 (GRCm39) |
I1096N |
probably damaging |
Het |
Lyzl6 |
C |
T |
11: 103,527,680 (GRCm39) |
V15I |
probably benign |
Het |
Map4k4 |
A |
G |
1: 40,053,368 (GRCm39) |
T856A |
possibly damaging |
Het |
Mks1 |
T |
A |
11: 87,751,542 (GRCm39) |
W346R |
probably damaging |
Het |
Mtmr14 |
T |
C |
6: 113,243,263 (GRCm39) |
Y32H |
probably damaging |
Het |
Muc13 |
A |
G |
16: 33,619,386 (GRCm39) |
S45G |
unknown |
Het |
Mx2 |
G |
A |
16: 97,346,812 (GRCm39) |
G93D |
probably damaging |
Het |
Noc4l |
A |
T |
5: 110,797,539 (GRCm39) |
V365E |
probably benign |
Het |
Odf2l |
T |
C |
3: 144,856,776 (GRCm39) |
I577T |
probably damaging |
Het |
Or4l1 |
T |
C |
14: 50,166,622 (GRCm39) |
I126M |
probably damaging |
Het |
Peg10 |
C |
CTCT |
6: 4,756,453 (GRCm39) |
|
probably benign |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Pnoc |
A |
T |
14: 65,639,307 (GRCm39) |
I186N |
possibly damaging |
Het |
Pou4f3 |
A |
G |
18: 42,528,251 (GRCm39) |
I65V |
probably benign |
Het |
Pramel23 |
G |
T |
4: 143,424,764 (GRCm39) |
N226K |
probably benign |
Het |
Prss1l |
T |
C |
6: 41,371,707 (GRCm39) |
L51P |
probably damaging |
Het |
Ptpn21 |
G |
A |
12: 98,648,791 (GRCm39) |
A955V |
probably damaging |
Het |
Rabgap1 |
G |
T |
2: 37,453,476 (GRCm39) |
R968L |
probably benign |
Het |
Rarres1 |
T |
C |
3: 67,386,677 (GRCm39) |
N282S |
probably damaging |
Het |
Rgs17 |
T |
C |
10: 5,791,501 (GRCm39) |
N72S |
probably benign |
Het |
Rp1 |
T |
A |
1: 4,417,926 (GRCm39) |
N1062I |
probably damaging |
Het |
Rpn1 |
T |
A |
6: 88,080,378 (GRCm39) |
V559D |
possibly damaging |
Het |
Rrbp1 |
A |
T |
2: 143,830,855 (GRCm39) |
N437K |
probably damaging |
Het |
Rtn4r |
C |
A |
16: 17,969,399 (GRCm39) |
Q276K |
probably benign |
Het |
Rwdd4a |
T |
C |
8: 47,990,335 (GRCm39) |
S16P |
probably damaging |
Het |
S1pr1 |
A |
G |
3: 115,505,947 (GRCm39) |
S216P |
possibly damaging |
Het |
Scn8a |
C |
A |
15: 100,908,917 (GRCm39) |
T795K |
possibly damaging |
Het |
Spryd3 |
A |
C |
15: 102,026,141 (GRCm39) |
F401C |
probably damaging |
Het |
Stk36 |
G |
T |
1: 74,650,328 (GRCm39) |
E287* |
probably null |
Het |
Tbc1d1 |
G |
T |
5: 64,507,095 (GRCm39) |
S1104I |
probably damaging |
Het |
Tex15 |
A |
G |
8: 34,071,683 (GRCm39) |
D2410G |
probably benign |
Het |
Tmem92 |
T |
A |
11: 94,669,784 (GRCm39) |
I116F |
possibly damaging |
Het |
Trp53bp2 |
A |
G |
1: 182,276,260 (GRCm39) |
E747G |
probably damaging |
Het |
Trp63 |
A |
T |
16: 25,707,990 (GRCm39) |
D562V |
probably damaging |
Het |
Ttc21b |
A |
G |
2: 66,077,705 (GRCm39) |
Y167H |
possibly damaging |
Het |
Ubr5 |
G |
A |
15: 37,980,076 (GRCm39) |
A2434V |
probably null |
Het |
Vmn2r103 |
T |
A |
17: 20,014,476 (GRCm39) |
Y423N |
probably benign |
Het |
Vmn2r111 |
A |
G |
17: 22,792,083 (GRCm39) |
Y58H |
probably damaging |
Het |
Ypel3 |
T |
A |
7: 126,377,013 (GRCm39) |
V2E |
probably damaging |
Het |
Ythdf3 |
T |
C |
3: 16,243,681 (GRCm39) |
V34A |
probably damaging |
Het |
Zfp180 |
A |
T |
7: 23,804,570 (GRCm39) |
S330C |
probably damaging |
Het |
Zfp292 |
G |
A |
4: 34,809,865 (GRCm39) |
P1060S |
probably benign |
Het |
Zfp354c |
TCACACTCGGCACA |
TCACA |
11: 50,706,067 (GRCm39) |
|
probably benign |
Het |
Zfp981 |
C |
T |
4: 146,622,100 (GRCm39) |
R342C |
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 |
R6247:Uggt1
|
UTSW |
1 |
36,202,309 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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'- ACCACTCAGTTCAGGAATCGC -3'
(R):5'- AGAAGGCTTGGCTTATTGTCC -3'
Sequencing Primer
(F):5'- TCGCCACTGACTGAATGATG -3'
(R):5'- ATTTGGAAGGCTACTGTCCAAGC -3'
|
Posted On |
2019-12-03 |