Incidental Mutation 'IGL02137:St3gal5'
| ID |
281361 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| 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 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.065)
|
| Stock # |
IGL02137
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
6 |
| Chromosomal Location |
72074576-72131555 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to A
at 72105266 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Asparagine
at position 6
(T6N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000145599
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000069994]
[ENSMUST00000114112]
[ENSMUST00000188366]
|
| AlphaFold |
O88829 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000069994
AA Change: T33N
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000070414
Gene: ENSMUSG00000056091
AA Change: T33N
| 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
AA Change: T6N
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000109747
Gene: ENSMUSG00000056091
AA Change: T6N
| 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 |
probably benign
Transcript: ENSMUST00000187007
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000188366
AA Change: T6N
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| 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: 39 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930595M18Rik |
T |
C |
X: 80,501,262 (GRCm39) |
D116G |
probably benign |
Het |
| Acp2 |
G |
T |
2: 91,034,028 (GRCm39) |
G66V |
probably damaging |
Het |
| Adam32 |
C |
T |
8: 25,362,610 (GRCm39) |
G605D |
probably damaging |
Het |
| Adam4 |
T |
C |
12: 81,467,877 (GRCm39) |
D248G |
possibly damaging |
Het |
| Adamts15 |
C |
A |
9: 30,821,956 (GRCm39) |
G494W |
probably damaging |
Het |
| Arfgef1 |
A |
T |
1: 10,283,338 (GRCm39) |
N190K |
probably damaging |
Het |
| Bach2 |
C |
T |
4: 32,501,621 (GRCm39) |
|
probably benign |
Het |
| Bloc1s1 |
T |
C |
10: 128,758,517 (GRCm39) |
|
probably benign |
Het |
| Casz1 |
G |
T |
4: 149,017,925 (GRCm39) |
A405S |
possibly damaging |
Het |
| Cplx4 |
T |
C |
18: 66,090,125 (GRCm39) |
D98G |
probably benign |
Het |
| Dync2h1 |
T |
C |
9: 7,134,349 (GRCm39) |
N1553D |
probably benign |
Het |
| Erich5 |
G |
A |
15: 34,470,900 (GRCm39) |
C43Y |
probably damaging |
Het |
| Exosc10 |
A |
C |
4: 148,645,590 (GRCm39) |
R123S |
probably damaging |
Het |
| Hoatz |
T |
C |
9: 50,997,408 (GRCm39) |
|
probably benign |
Het |
| Inpp5f |
T |
C |
7: 128,296,853 (GRCm39) |
V377A |
probably damaging |
Het |
| Lrp1b |
T |
C |
2: 40,620,700 (GRCm39) |
|
probably benign |
Het |
| Mrps17 |
G |
A |
5: 129,793,847 (GRCm39) |
V14M |
probably benign |
Het |
| Mtrr |
G |
A |
13: 68,716,920 (GRCm39) |
S431F |
possibly damaging |
Het |
| Myo5a |
T |
C |
9: 75,068,817 (GRCm39) |
|
probably null |
Het |
| Nsfl1c |
T |
A |
2: 151,351,509 (GRCm39) |
I291N |
probably damaging |
Het |
| Ntsr1 |
T |
A |
2: 180,180,628 (GRCm39) |
|
probably null |
Het |
| Or4n4 |
T |
C |
14: 50,519,135 (GRCm39) |
T192A |
probably benign |
Het |
| Park7 |
T |
C |
4: 150,988,288 (GRCm39) |
I102M |
probably benign |
Het |
| Pik3c2a |
T |
A |
7: 115,950,039 (GRCm39) |
Q1326L |
probably benign |
Het |
| Rapgef3 |
T |
C |
15: 97,648,025 (GRCm39) |
D693G |
probably benign |
Het |
| Rep15 |
G |
A |
6: 146,934,845 (GRCm39) |
R228H |
probably benign |
Het |
| Slc25a1 |
A |
G |
16: 17,745,234 (GRCm39) |
V100A |
probably benign |
Het |
| Slc9a4 |
T |
C |
1: 40,640,059 (GRCm39) |
F284L |
possibly damaging |
Het |
| Sox10 |
G |
T |
15: 79,043,393 (GRCm39) |
D52E |
probably benign |
Het |
| Tbc1d22a |
A |
G |
15: 86,183,870 (GRCm39) |
D243G |
probably benign |
Het |
| Tll1 |
T |
C |
8: 64,469,132 (GRCm39) |
Y997C |
possibly damaging |
Het |
| Tmem8b |
A |
T |
4: 43,689,434 (GRCm39) |
H276L |
probably benign |
Het |
| Tnpo3 |
T |
C |
6: 29,609,450 (GRCm39) |
Y12C |
probably damaging |
Het |
| Tns3 |
A |
T |
11: 8,442,578 (GRCm39) |
M595K |
possibly damaging |
Het |
| Trav18 |
T |
A |
14: 54,069,192 (GRCm39) |
M78K |
probably benign |
Het |
| Uba7 |
A |
G |
9: 107,856,952 (GRCm39) |
|
probably benign |
Het |
| Vmn1r167 |
A |
T |
7: 23,204,864 (GRCm39) |
S51T |
probably damaging |
Het |
| Vmn1r83 |
A |
T |
7: 12,055,761 (GRCm39) |
Y99N |
probably damaging |
Het |
| Wdr38 |
A |
T |
2: 38,888,424 (GRCm39) |
N7I |
probably damaging |
Het |
|
| Other mutations in St3gal5 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
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 |
|
R8294:St3gal5
|
UTSW |
6 |
72,074,816 (GRCm39) |
missense |
|
|
|
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 |
|
|
| Posted On |
2015-04-16 |
Incidental Mutation