Incidental Mutation 'R1942:Ugcg'
| ID |
216270 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ugcg
|
| Ensembl Gene |
ENSMUSG00000028381 |
| Gene Name |
UDP-glucose ceramide glucosyltransferase |
| Synonyms |
Epcs21, Ugcgl, GlcT-1 |
| MMRRC Submission |
039960-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R1942 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
4 |
| Chromosomal Location |
59189452-59222833 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 59207798 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Proline to Serine
at position 46
(P46S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000030074
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000030074]
|
| AlphaFold |
O88693 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000030074
AA Change: P46S
PolyPhen 2
Score 0.175 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000030074
Gene: ENSMUSG00000028381
AA Change: P46S
| Domain | Start | End | E-Value | Type |
|---|
|
transmembrane domain
|
10 |
32 |
N/A |
INTRINSIC |
|
Pfam:Glyco_tranf_2_3
|
51 |
278 |
1.3e-26 |
PFAM |
|
Pfam:Glyco_transf_21
|
106 |
278 |
8.4e-61 |
PFAM |
|
Pfam:Glyco_trans_2_3
|
139 |
368 |
9.6e-13 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000128227
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000133996
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000155153
|
| Meta Mutation Damage Score |
0.0799 |
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.7%
|
| Validation Efficiency |
100% (75/75) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes an enzyme that catalyzes the first glycosylation step in the biosynthesis of glycosphingolipids, which are membrane components containing lipid and sugar moieties. The product of this reaction is glucosylceramide, which is the core structure of many glycosphingolipids. [provided by RefSeq, Dec 2014]
PHENOTYPE: At embryonic day 7.5, embryos homozygous for a null mutation exhibit decreased size, markedly reduced extraembryonic tissues and a large increase in cells undergoing apoptosis. Mutants die by embryonic day 8.5. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 73 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930407I10Rik |
A |
T |
15: 81,949,625 (GRCm39) |
Y1174F |
probably damaging |
Het |
| Ahnak |
A |
G |
19: 8,992,447 (GRCm39) |
E4577G |
probably damaging |
Het |
| Anapc4 |
T |
C |
5: 53,004,056 (GRCm39) |
V291A |
probably benign |
Het |
| Apba2 |
A |
G |
7: 64,345,218 (GRCm39) |
E136G |
possibly damaging |
Het |
| Arhgap20 |
C |
A |
9: 51,742,998 (GRCm39) |
Q279K |
probably benign |
Het |
| B3galnt1 |
A |
T |
3: 69,483,258 (GRCm39) |
M1K |
probably null |
Het |
| C4bp |
C |
A |
1: 130,583,804 (GRCm39) |
|
probably benign |
Het |
| Catsperg1 |
G |
A |
7: 28,906,232 (GRCm39) |
T157I |
possibly damaging |
Het |
| Cfap90 |
A |
C |
13: 68,761,090 (GRCm39) |
I171L |
probably benign |
Het |
| Chrm1 |
T |
A |
19: 8,655,637 (GRCm39) |
M114K |
probably damaging |
Het |
| Clasp1 |
A |
G |
1: 118,429,078 (GRCm39) |
E329G |
possibly damaging |
Het |
| Clrn2 |
A |
C |
5: 45,611,337 (GRCm39) |
Y62S |
probably benign |
Het |
| Col12a1 |
T |
G |
9: 79,542,748 (GRCm39) |
D2339A |
probably damaging |
Het |
| Copa |
T |
A |
1: 171,939,455 (GRCm39) |
L564Q |
probably damaging |
Het |
| Cpeb2 |
C |
A |
5: 43,392,596 (GRCm39) |
|
probably benign |
Het |
| Dhx57 |
A |
T |
17: 80,572,573 (GRCm39) |
M647K |
probably damaging |
Het |
| Diaph3 |
C |
T |
14: 87,378,556 (GRCm39) |
|
probably benign |
Het |
| Eomes |
A |
G |
9: 118,313,716 (GRCm39) |
D587G |
probably benign |
Het |
| Gm5142 |
T |
A |
14: 59,416,156 (GRCm39) |
M1L |
probably benign |
Het |
| Gnl2 |
A |
G |
4: 124,923,957 (GRCm39) |
I12V |
probably benign |
Het |
| Gprin1 |
C |
T |
13: 54,887,752 (GRCm39) |
C174Y |
probably benign |
Het |
| Grin2b |
A |
T |
6: 135,709,730 (GRCm39) |
V1272E |
possibly damaging |
Het |
| Hdac9 |
A |
G |
12: 34,479,544 (GRCm39) |
L227S |
probably damaging |
Het |
| Helz |
T |
A |
11: 107,493,318 (GRCm39) |
L247Q |
probably benign |
Het |
| Hs6st1 |
T |
C |
1: 36,107,803 (GRCm39) |
V22A |
probably benign |
Het |
| Hspg2 |
C |
A |
4: 137,269,863 (GRCm39) |
A2304E |
possibly damaging |
Het |
| Htr3a |
T |
C |
9: 48,819,911 (GRCm39) |
Y73C |
probably damaging |
Het |
| Il1rap |
A |
C |
16: 26,541,205 (GRCm39) |
E482A |
probably damaging |
Het |
| Itsn2 |
T |
A |
12: 4,689,670 (GRCm39) |
L581* |
probably null |
Het |
| Msmb |
A |
G |
14: 31,870,034 (GRCm39) |
E2G |
probably benign |
Het |
| Muc19 |
T |
C |
15: 91,776,666 (GRCm39) |
|
noncoding transcript |
Het |
| Muc4 |
A |
C |
16: 32,569,460 (GRCm39) |
L173F |
probably damaging |
Het |
| Muc5b |
A |
T |
7: 141,411,421 (GRCm39) |
S1456C |
unknown |
Het |
| Mylip |
A |
T |
13: 45,560,172 (GRCm39) |
I203F |
probably damaging |
Het |
| Nckap5 |
A |
T |
1: 125,952,039 (GRCm39) |
D1504E |
probably damaging |
Het |
| Neil1 |
C |
G |
9: 57,053,891 (GRCm39) |
R143P |
probably benign |
Het |
| Nlrp2 |
T |
A |
7: 5,325,447 (GRCm39) |
T742S |
probably damaging |
Het |
| Nme8 |
A |
G |
13: 19,859,978 (GRCm39) |
V214A |
probably damaging |
Het |
| Nsun7 |
C |
T |
5: 66,441,588 (GRCm39) |
T419I |
probably benign |
Het |
| Nup210l |
G |
A |
3: 90,058,544 (GRCm39) |
E648K |
probably benign |
Het |
| Or10g6 |
T |
A |
9: 39,934,031 (GRCm39) |
L114H |
probably damaging |
Het |
| Or10g6 |
T |
C |
9: 39,934,048 (GRCm39) |
Y120H |
probably damaging |
Het |
| Or2y1c |
T |
C |
11: 49,360,981 (GRCm39) |
M1T |
probably null |
Het |
| Or8s2 |
A |
G |
15: 98,276,445 (GRCm39) |
L182P |
probably damaging |
Het |
| Parp11 |
A |
C |
6: 127,447,663 (GRCm39) |
|
probably null |
Het |
| Pomgnt1 |
G |
T |
4: 116,012,472 (GRCm39) |
|
probably null |
Het |
| Ppp1r14c |
T |
C |
10: 3,413,417 (GRCm39) |
I150T |
probably damaging |
Het |
| Psd4 |
A |
G |
2: 24,295,805 (GRCm39) |
E908G |
probably damaging |
Het |
| Psmd6 |
A |
T |
14: 14,116,442 (GRCm38) |
V91E |
probably damaging |
Het |
| Ptk2b |
A |
T |
14: 66,406,830 (GRCm39) |
V634D |
probably damaging |
Het |
| Rapgef6 |
A |
G |
11: 54,548,089 (GRCm39) |
I753V |
possibly damaging |
Het |
| Rbm45 |
G |
A |
2: 76,205,823 (GRCm39) |
|
probably null |
Het |
| Ric1 |
A |
G |
19: 29,578,416 (GRCm39) |
|
probably benign |
Het |
| Sh3rf2 |
A |
G |
18: 42,282,689 (GRCm39) |
K416E |
probably damaging |
Het |
| Six5 |
C |
T |
7: 18,830,858 (GRCm39) |
A495V |
possibly damaging |
Het |
| Slc27a6 |
T |
A |
18: 58,689,870 (GRCm39) |
M112K |
probably damaging |
Het |
| Slc5a4a |
T |
C |
10: 75,983,422 (GRCm39) |
S20P |
unknown |
Het |
| Smg1 |
A |
G |
7: 117,757,326 (GRCm39) |
|
probably benign |
Het |
| Sntb2 |
G |
A |
8: 107,737,984 (GRCm39) |
A511T |
probably damaging |
Het |
| Stk31 |
A |
T |
6: 49,416,061 (GRCm39) |
N622I |
probably damaging |
Het |
| Sulf1 |
T |
C |
1: 12,918,397 (GRCm39) |
F38S |
probably damaging |
Het |
| Szt2 |
G |
T |
4: 118,249,817 (GRCm39) |
T521K |
probably benign |
Het |
| Terf1 |
G |
T |
1: 15,876,038 (GRCm39) |
R46I |
probably benign |
Het |
| Tmem245 |
A |
G |
4: 56,923,511 (GRCm39) |
|
probably benign |
Het |
| Tmigd1 |
T |
C |
11: 76,804,905 (GRCm39) |
|
probably null |
Het |
| Umod |
A |
G |
7: 119,076,155 (GRCm39) |
Y204H |
probably damaging |
Het |
| Vcan |
T |
A |
13: 89,851,543 (GRCm39) |
Q1139L |
probably benign |
Het |
| Vmn1r85 |
T |
A |
7: 12,818,668 (GRCm39) |
T159S |
possibly damaging |
Het |
| Vmn2r103 |
T |
A |
17: 20,032,562 (GRCm39) |
S779T |
probably benign |
Het |
| Vmn2r27 |
C |
T |
6: 124,200,722 (GRCm39) |
A412T |
probably damaging |
Het |
| Zc3h12d |
A |
C |
10: 7,729,077 (GRCm39) |
D147A |
probably damaging |
Het |
| Zfp800 |
A |
T |
6: 28,243,272 (GRCm39) |
D564E |
probably benign |
Het |
| Zfp932 |
A |
G |
5: 110,154,853 (GRCm39) |
E17G |
probably damaging |
Het |
|
| Other mutations in Ugcg |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01447:Ugcg
|
APN |
4 |
59,213,865 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
IGL01768:Ugcg
|
APN |
4 |
59,217,216 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02636:Ugcg
|
APN |
4 |
59,207,763 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
IGL02672:Ugcg
|
APN |
4 |
59,218,587 (GRCm39) |
splice site |
probably benign |
|
|
IGL02798:Ugcg
|
APN |
4 |
59,220,346 (GRCm39) |
missense |
probably damaging |
1.00 |
|
congee
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
cream_o_wheat
|
UTSW |
4 |
59,220,387 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
gruel
|
UTSW |
4 |
59,189,690 (GRCm39) |
missense |
probably benign |
|
|
Porridge
|
UTSW |
4 |
59,219,530 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
slop
|
UTSW |
4 |
59,211,883 (GRCm39) |
missense |
probably benign |
0.16 |
|
wheatina
|
UTSW |
4 |
59,220,272 (GRCm39) |
missense |
probably damaging |
0.96 |
|
PIT4382001:Ugcg
|
UTSW |
4 |
59,213,246 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R0013:Ugcg
|
UTSW |
4 |
59,213,931 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R0013:Ugcg
|
UTSW |
4 |
59,213,931 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R0068:Ugcg
|
UTSW |
4 |
59,217,130 (GRCm39) |
missense |
probably benign |
0.16 |
|
R0068:Ugcg
|
UTSW |
4 |
59,217,130 (GRCm39) |
missense |
probably benign |
0.16 |
|
R0119:Ugcg
|
UTSW |
4 |
59,217,036 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R0230:Ugcg
|
UTSW |
4 |
59,189,739 (GRCm39) |
nonsense |
probably null |
|
|
R0299:Ugcg
|
UTSW |
4 |
59,217,036 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R0384:Ugcg
|
UTSW |
4 |
59,220,387 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R0499:Ugcg
|
UTSW |
4 |
59,217,036 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R0645:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R0688:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R0726:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R0802:Ugcg
|
UTSW |
4 |
59,189,685 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0803:Ugcg
|
UTSW |
4 |
59,189,685 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0811:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R0812:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R0828:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R0831:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R0944:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R0945:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R0947:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R1104:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R1209:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R1210:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R1252:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R1253:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R1255:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R1488:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R1490:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R1548:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R1698:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R1771:Ugcg
|
UTSW |
4 |
59,207,775 (GRCm39) |
missense |
probably benign |
0.05 |
|
R1776:Ugcg
|
UTSW |
4 |
59,207,775 (GRCm39) |
missense |
probably benign |
0.05 |
|
R1781:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R1794:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R1840:Ugcg
|
UTSW |
4 |
59,219,517 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2228:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R2229:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R2237:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R2239:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R2314:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R2337:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R2338:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R2340:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R2422:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R2426:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R2433:Ugcg
|
UTSW |
4 |
59,207,876 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R2680:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R3076:Ugcg
|
UTSW |
4 |
59,213,922 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3078:Ugcg
|
UTSW |
4 |
59,213,922 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3689:Ugcg
|
UTSW |
4 |
59,211,883 (GRCm39) |
missense |
probably benign |
0.16 |
|
R3732:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R3732:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R3733:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R3766:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R3767:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R3768:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R3769:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R3771:Ugcg
|
UTSW |
4 |
59,189,690 (GRCm39) |
missense |
probably benign |
|
|
R3847:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R3848:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R3916:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R3917:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R3958:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R3959:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R4023:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R4024:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R4025:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R4065:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R4066:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
R4427:Ugcg
|
UTSW |
4 |
59,219,555 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5842:Ugcg
|
UTSW |
4 |
59,219,545 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6012:Ugcg
|
UTSW |
4 |
59,220,272 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R6080:Ugcg
|
UTSW |
4 |
59,218,524 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R6762:Ugcg
|
UTSW |
4 |
59,219,530 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R7194:Ugcg
|
UTSW |
4 |
59,213,210 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7286:Ugcg
|
UTSW |
4 |
59,217,111 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7362:Ugcg
|
UTSW |
4 |
59,217,109 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7472:Ugcg
|
UTSW |
4 |
59,217,156 (GRCm39) |
missense |
probably benign |
|
|
R7638:Ugcg
|
UTSW |
4 |
59,220,299 (GRCm39) |
missense |
probably benign |
0.26 |
|
R7866:Ugcg
|
UTSW |
4 |
59,211,927 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R8170:Ugcg
|
UTSW |
4 |
59,211,974 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R8488:Ugcg
|
UTSW |
4 |
59,213,896 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8793:Ugcg
|
UTSW |
4 |
59,207,794 (GRCm39) |
missense |
probably benign |
0.22 |
|
R9441:Ugcg
|
UTSW |
4 |
59,207,843 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Y4336:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
Y4337:Ugcg
|
UTSW |
4 |
59,207,798 (GRCm39) |
missense |
probably benign |
0.17 |
|
| Predicted Primers |
PCR Primer
(F):5'- TCTTGCTCCTGGTTCTTGTGTTT -3'
(R):5'- AGGCTAGGCTGTTTTCACAATCA -3'
Sequencing Primer
(F):5'- TCTAACCCAACTCTGTTCAG -3'
(R):5'- CACGTATTCTTTCATTCCCC -3'
|
| Posted On |
2014-08-01 |
Incidental Mutation