Incidental Mutation 'R8294:St3gal5'
| ID |
638847 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
St3gal5
|
| Ensembl Gene |
ENSMUSG00000056091 |
| Gene Name |
ST3 beta-galactoside alpha-2,3-sialyltransferase 5 |
| Synonyms |
GM3 synthase, GM3-specific sialytransferase, 3S-T, [a]2, ST3Gal V, mST3Gal V, Siat9 |
| MMRRC Submission |
067784-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.072)
|
| Stock # |
R8294 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
6 |
| Chromosomal Location |
72074576-72131555 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 72074816 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Glutamic Acid
at position 25
(D25E)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000069994]
[ENSMUST00000114112]
|
| AlphaFold |
O88829 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000069994
|
| SMART Domains |
Protein: ENSMUSP00000070414
Gene: ENSMUSG00000056091
| Domain | Start | End | E-Value | Type |
|---|
|
transmembrane domain
|
66 |
88 |
N/A |
INTRINSIC |
|
Pfam:Glyco_transf_29
|
141 |
411 |
3e-66 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000114112
|
| SMART Domains |
Protein: ENSMUSP00000109747
Gene: ENSMUSG00000056091
| Domain | Start | End | E-Value | Type |
|---|
|
transmembrane domain
|
39 |
61 |
N/A |
INTRINSIC |
|
Pfam:Glyco_transf_29
|
111 |
385 |
4.9e-71 |
PFAM |
|
| Predicted Effect |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.9%
|
| Validation Efficiency |
98% (42/43) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Ganglioside GM3 is known to participate in the induction of cell differentiation, modulation of cell proliferation, maintenance of fibroblast morphology, signal transduction, and integrin-mediated cell adhesion. The protein encoded by this gene is a type II membrane protein which catalyzes the formation of GM3 using lactosylceramide as the substrate. The encoded protein is a member of glycosyltransferase family 29 and may be localized to the Golgi apparatus. Mutation in this gene has been associated with Amish infantile epilepsy syndrome. Transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
PHENOTYPE: Targeted inactivation of this gene leads to inability to synthesize GM3 ganglioside. Homozygotes for a null allele exhibit enhanced sensitivity to insulin. Homozygotes for a different null allele show resistance to botulinum neurotoxin type C. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 44 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca4 |
T |
C |
3: 121,897,217 (GRCm39) |
V632A |
possibly damaging |
Het |
| Abcf2 |
CAT |
CATAAT |
5: 24,781,589 (GRCm39) |
|
probably benign |
Het |
| Acat2 |
T |
C |
17: 13,175,243 (GRCm39) |
I79V |
probably benign |
Het |
| Arid3a |
A |
T |
10: 79,786,535 (GRCm39) |
|
silent |
Het |
| Cecr2 |
C |
T |
6: 120,710,747 (GRCm39) |
A154V |
probably damaging |
Het |
| Cog3 |
A |
C |
14: 75,954,619 (GRCm39) |
L650R |
probably damaging |
Het |
| Col12a1 |
A |
T |
9: 79,606,594 (GRCm39) |
F610I |
possibly damaging |
Het |
| Col24a1 |
A |
G |
3: 145,186,844 (GRCm39) |
D1215G |
probably null |
Het |
| Ctsh |
C |
G |
9: 89,950,489 (GRCm39) |
A219G |
possibly damaging |
Het |
| Dnah10 |
C |
T |
5: 124,859,410 (GRCm39) |
L2126F |
probably damaging |
Het |
| Dock10 |
A |
G |
1: 80,488,079 (GRCm39) |
V2028A |
possibly damaging |
Het |
| Ece1 |
T |
C |
4: 137,675,931 (GRCm39) |
V435A |
possibly damaging |
Het |
| Epha8 |
G |
T |
4: 136,665,897 (GRCm39) |
L420M |
probably damaging |
Het |
| H4c1 |
A |
G |
13: 23,944,957 (GRCm39) |
F62L |
probably damaging |
Het |
| Hk1 |
T |
G |
10: 62,131,624 (GRCm39) |
I245L |
probably benign |
Het |
| Hyal6 |
A |
C |
6: 24,734,378 (GRCm39) |
K104Q |
possibly damaging |
Het |
| Kalrn |
T |
C |
16: 33,853,954 (GRCm39) |
I2017V |
probably benign |
Het |
| Khdc4 |
C |
T |
3: 88,603,915 (GRCm39) |
A244V |
probably damaging |
Het |
| Krt72 |
A |
T |
15: 101,694,472 (GRCm39) |
L141Q |
probably damaging |
Het |
| Map3k4 |
C |
A |
17: 12,537,500 (GRCm39) |
A6S |
unknown |
Het |
| Muc6 |
T |
C |
7: 141,217,263 (GRCm39) |
Y2470C |
possibly damaging |
Het |
| Nrip1 |
A |
G |
16: 76,089,418 (GRCm39) |
V713A |
probably damaging |
Het |
| Or10q1b |
A |
G |
19: 13,683,010 (GRCm39) |
D273G |
probably benign |
Het |
| Or11g26 |
A |
G |
14: 50,753,083 (GRCm39) |
T141A |
possibly damaging |
Het |
| Or2ah1 |
T |
A |
2: 85,653,531 (GRCm39) |
I72N |
probably damaging |
Het |
| Or6aa1 |
T |
C |
7: 86,044,487 (GRCm39) |
Y73C |
probably damaging |
Het |
| Paip1 |
C |
T |
13: 119,587,300 (GRCm39) |
T304I |
possibly damaging |
Het |
| Pde4dip |
A |
G |
3: 97,674,694 (GRCm39) |
L74P |
probably damaging |
Het |
| Prkch |
T |
A |
12: 73,806,484 (GRCm39) |
L577H |
probably damaging |
Het |
| Rp1 |
A |
G |
1: 4,416,220 (GRCm39) |
S1631P |
probably benign |
Het |
| Rph3a |
A |
G |
5: 121,099,429 (GRCm39) |
F154S |
probably damaging |
Het |
| S1pr5 |
A |
G |
9: 21,156,300 (GRCm39) |
V42A |
possibly damaging |
Het |
| Scaper |
G |
A |
9: 55,517,280 (GRCm39) |
L1052F |
possibly damaging |
Het |
| Slc44a2 |
G |
T |
9: 21,259,643 (GRCm39) |
V597F |
probably damaging |
Het |
| Srsf1 |
T |
A |
11: 87,939,467 (GRCm39) |
S116T |
probably benign |
Het |
| Ssh2 |
A |
G |
11: 77,345,027 (GRCm39) |
D1004G |
probably benign |
Het |
| Syt17 |
A |
T |
7: 118,009,228 (GRCm39) |
Y327N |
probably damaging |
Het |
| T |
T |
A |
17: 8,653,364 (GRCm39) |
M1K |
probably null |
Het |
| Tmem201 |
A |
T |
4: 149,815,554 (GRCm39) |
I132N |
possibly damaging |
Het |
| Tmprss15 |
A |
T |
16: 78,868,176 (GRCm39) |
C211S |
probably benign |
Het |
| Trim36 |
T |
C |
18: 46,331,588 (GRCm39) |
D7G |
probably benign |
Het |
| Trip11 |
T |
A |
12: 101,811,160 (GRCm39) |
K1863N |
possibly damaging |
Het |
| Vmn2r13 |
A |
T |
5: 109,322,978 (GRCm39) |
S104T |
probably benign |
Het |
| Zfp977 |
T |
C |
7: 42,229,689 (GRCm39) |
T279A |
probably benign |
Het |
|
| Other mutations in St3gal5 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02137:St3gal5
|
APN |
6 |
72,105,266 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02277:St3gal5
|
APN |
6 |
72,119,184 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
IGL02756:St3gal5
|
APN |
6 |
72,126,157 (GRCm39) |
missense |
probably null |
0.83 |
|
IGL02904:St3gal5
|
APN |
6 |
72,124,108 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R0107:St3gal5
|
UTSW |
6 |
72,119,133 (GRCm39) |
missense |
probably benign |
0.11 |
|
R1605:St3gal5
|
UTSW |
6 |
72,119,272 (GRCm39) |
missense |
probably benign |
0.42 |
|
R1854:St3gal5
|
UTSW |
6 |
72,109,077 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2875:St3gal5
|
UTSW |
6 |
72,124,114 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R3692:St3gal5
|
UTSW |
6 |
72,126,013 (GRCm39) |
missense |
probably benign |
0.05 |
|
R5071:St3gal5
|
UTSW |
6 |
72,109,037 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5265:St3gal5
|
UTSW |
6 |
72,126,115 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5609:St3gal5
|
UTSW |
6 |
72,130,446 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R8085:St3gal5
|
UTSW |
6 |
72,074,925 (GRCm39) |
missense |
unknown |
|
|
R8199:St3gal5
|
UTSW |
6 |
72,119,175 (GRCm39) |
missense |
probably benign |
|
|
R8251:St3gal5
|
UTSW |
6 |
72,126,144 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8332:St3gal5
|
UTSW |
6 |
72,119,165 (GRCm39) |
nonsense |
probably null |
|
|
R8410:St3gal5
|
UTSW |
6 |
72,119,281 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8730:St3gal5
|
UTSW |
6 |
72,130,461 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9363:St3gal5
|
UTSW |
6 |
72,119,301 (GRCm39) |
nonsense |
probably null |
|
|
R9599:St3gal5
|
UTSW |
6 |
72,130,580 (GRCm39) |
missense |
probably benign |
0.30 |
|
RF060:St3gal5
|
UTSW |
6 |
72,074,836 (GRCm39) |
frame shift |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- ACTTCTCGGCTGGAGTTGTC -3'
(R):5'- GCTCAGAAGGTTCCAGCAATG -3'
Sequencing Primer
(F):5'- TCGGCGCACTCTGATTG -3'
(R):5'- GGTTCCAGCAATGAATTAAAATCCC -3'
|
| Posted On |
2020-07-28 |
Incidental Mutation