Incidental Mutation 'IGL02421:Sgce'
| ID |
292699 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Sgce
|
| Ensembl Gene |
ENSMUSG00000004631 |
| Gene Name |
sarcoglycan, epsilon |
| Synonyms |
e-SG |
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.550)
|
| Stock # |
IGL02421
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
6 |
| Chromosomal Location |
4674350-4747180 bp(-) (GRCm39) |
| Type of Mutation |
splice site |
| DNA Base Change (assembly) |
G to A
at 4694187 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000121964
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000004750]
[ENSMUST00000090686]
[ENSMUST00000101677]
[ENSMUST00000115577]
[ENSMUST00000115579]
[ENSMUST00000126151]
[ENSMUST00000133306]
|
| AlphaFold |
O70258 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000004750
|
| SMART Domains |
Protein: ENSMUSP00000004750
Gene: ENSMUSG00000004631
| Domain | Start | End | E-Value | Type |
|---|
|
CADG
|
49 |
157 |
1.86e-10 |
SMART |
|
low complexity region
|
412 |
423 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000090686
|
| SMART Domains |
Protein: ENSMUSP00000088185
Gene: ENSMUSG00000004631
| Domain | Start | End | E-Value | Type |
|---|
|
CADG
|
49 |
157 |
1.86e-10 |
SMART |
|
low complexity region
|
412 |
423 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000101677
|
| SMART Domains |
Protein: ENSMUSP00000099200
Gene: ENSMUSG00000004631
| Domain | Start | End | E-Value | Type |
|---|
|
CADG
|
49 |
157 |
1.86e-10 |
SMART |
|
low complexity region
|
421 |
432 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000115577
|
| SMART Domains |
Protein: ENSMUSP00000111240
Gene: ENSMUSG00000004631
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
28 |
40 |
N/A |
INTRINSIC |
|
CADG
|
85 |
193 |
1.86e-10 |
SMART |
|
low complexity region
|
457 |
468 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000115579
|
| SMART Domains |
Protein: ENSMUSP00000111242
Gene: ENSMUSG00000004631
| Domain | Start | End | E-Value | Type |
|---|
|
CADG
|
49 |
157 |
1.86e-10 |
SMART |
|
low complexity region
|
421 |
432 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000123907
|
| SMART Domains |
Protein: ENSMUSP00000120910
Gene: ENSMUSG00000004631
| Domain | Start | End | E-Value | Type |
|---|
|
CADG
|
32 |
140 |
1.86e-10 |
SMART |
|
low complexity region
|
395 |
406 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000126151
|
| SMART Domains |
Protein: ENSMUSP00000120718
Gene: ENSMUSG00000004631
| Domain | Start | End | E-Value | Type |
|---|
|
CADG
|
26 |
134 |
1.86e-10 |
SMART |
|
low complexity region
|
389 |
400 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000153284
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000139029
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000128109
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000133306
|
| SMART Domains |
Protein: ENSMUSP00000121964
Gene: ENSMUSG00000004631
| Domain | Start | End | E-Value | Type |
|---|
|
CADG
|
26 |
134 |
1.86e-10 |
SMART |
|
low complexity region
|
398 |
409 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes the epsilon member of the sarcoglycan family. Sarcoglycans are transmembrane proteins that are components of the dystrophin-glycoprotein complex, which link the actin cytoskeleton to the extracellular matrix. Unlike other family members which are predominantly expressed in striated muscle, the epsilon sarcoglycan is more broadly expressed. Mutations in this gene are associated with myoclonus-dystonia syndrome. This gene is imprinted, with preferential expression from the paternal allele. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. A pseudogene associated with this gene is located on chromosome 2. [provided by RefSeq, Oct 2016]
PHENOTYPE: Mice homozygous or heterozygous for a knock-out allele display significantly increased myoclonus and deficits in motor coordination and balance. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 45 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| a |
T |
C |
2: 154,892,672 (GRCm39) |
F117S |
probably damaging |
Het |
| A930011G23Rik |
A |
G |
5: 99,377,236 (GRCm39) |
S404P |
probably damaging |
Het |
| A930011G23Rik |
G |
A |
5: 99,377,241 (GRCm39) |
P402L |
probably damaging |
Het |
| Acacb |
A |
G |
5: 114,361,939 (GRCm39) |
T1394A |
probably benign |
Het |
| Adam19 |
A |
G |
11: 46,028,380 (GRCm39) |
N671S |
probably damaging |
Het |
| Akap13 |
A |
T |
7: 75,367,554 (GRCm39) |
N1815I |
possibly damaging |
Het |
| Aloxe3 |
A |
G |
11: 69,020,872 (GRCm39) |
D199G |
possibly damaging |
Het |
| Ap1g2 |
G |
A |
14: 55,339,859 (GRCm39) |
A440V |
probably damaging |
Het |
| Bmt2 |
G |
T |
6: 13,628,841 (GRCm39) |
Q281K |
probably damaging |
Het |
| Celsr3 |
T |
C |
9: 108,717,662 (GRCm39) |
F2243L |
probably damaging |
Het |
| Cenpb |
G |
A |
2: 131,021,601 (GRCm39) |
R66C |
probably damaging |
Het |
| Chl1 |
A |
T |
6: 103,694,541 (GRCm39) |
H1121L |
probably damaging |
Het |
| Cpb1 |
T |
C |
3: 20,306,148 (GRCm39) |
Y344C |
probably damaging |
Het |
| Cspg5 |
T |
A |
9: 110,076,460 (GRCm39) |
|
probably benign |
Het |
| Dnah11 |
T |
C |
12: 118,150,637 (GRCm39) |
N374D |
probably damaging |
Het |
| Dnah3 |
A |
G |
7: 119,550,215 (GRCm39) |
V3368A |
possibly damaging |
Het |
| Eml4 |
T |
C |
17: 83,785,321 (GRCm39) |
S829P |
probably benign |
Het |
| Got2-ps1 |
T |
C |
5: 138,362,811 (GRCm39) |
|
noncoding transcript |
Het |
| Hal |
T |
C |
10: 93,339,335 (GRCm39) |
C475R |
probably damaging |
Het |
| Mapkbp1 |
C |
T |
2: 119,850,136 (GRCm39) |
P806S |
possibly damaging |
Het |
| Mmrn1 |
A |
T |
6: 60,921,806 (GRCm39) |
T88S |
probably benign |
Het |
| Napsa |
A |
G |
7: 44,234,479 (GRCm39) |
H237R |
probably damaging |
Het |
| Opn5 |
C |
T |
17: 42,907,446 (GRCm39) |
|
probably benign |
Het |
| Or1d2 |
T |
C |
11: 74,256,017 (GRCm39) |
I174T |
probably damaging |
Het |
| Or4c110 |
T |
C |
2: 88,831,688 (GRCm39) |
|
probably null |
Het |
| Or51f2 |
T |
C |
7: 102,526,966 (GRCm39) |
I213T |
probably damaging |
Het |
| Or56b2 |
A |
G |
7: 104,337,740 (GRCm39) |
N173D |
probably benign |
Het |
| Pira12 |
T |
C |
7: 3,899,994 (GRCm39) |
N203D |
possibly damaging |
Het |
| Polb |
C |
T |
8: 23,130,389 (GRCm39) |
G179D |
probably damaging |
Het |
| Primpol |
G |
T |
8: 47,060,830 (GRCm39) |
|
probably benign |
Het |
| Prom2 |
T |
A |
2: 127,373,802 (GRCm39) |
|
probably null |
Het |
| Psmb10 |
A |
G |
8: 106,664,124 (GRCm39) |
|
probably null |
Het |
| Ranbp2 |
T |
G |
10: 58,316,376 (GRCm39) |
S2365R |
probably damaging |
Het |
| Slc25a34 |
A |
G |
4: 141,348,753 (GRCm39) |
V237A |
probably benign |
Het |
| Slc39a2 |
A |
T |
14: 52,131,329 (GRCm39) |
T25S |
probably benign |
Het |
| Smarca4 |
T |
C |
9: 21,550,535 (GRCm39) |
C423R |
probably damaging |
Het |
| Stt3b |
G |
A |
9: 115,080,920 (GRCm39) |
|
probably benign |
Het |
| Tbl1xr1 |
A |
T |
3: 22,257,327 (GRCm39) |
I397F |
probably damaging |
Het |
| Tie1 |
A |
G |
4: 118,343,591 (GRCm39) |
V117A |
probably damaging |
Het |
| Tmc3 |
T |
C |
7: 83,271,952 (GRCm39) |
F1035L |
probably benign |
Het |
| Trhde |
T |
A |
10: 114,248,366 (GRCm39) |
K944N |
probably damaging |
Het |
| Vmn1r54 |
G |
A |
6: 90,246,133 (GRCm39) |
A16T |
probably benign |
Het |
| Washc4 |
T |
A |
10: 83,415,414 (GRCm39) |
N801K |
probably damaging |
Het |
| Xylt2 |
A |
G |
11: 94,558,588 (GRCm39) |
Y523H |
possibly damaging |
Het |
| Znfx1 |
T |
C |
2: 166,902,000 (GRCm39) |
R5G |
probably damaging |
Het |
|
| Other mutations in Sgce |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00156:Sgce
|
APN |
6 |
4,689,750 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01399:Sgce
|
APN |
6 |
4,746,997 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01796:Sgce
|
APN |
6 |
4,711,326 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02403:Sgce
|
APN |
6 |
4,694,059 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02547:Sgce
|
APN |
6 |
4,711,301 (GRCm39) |
splice site |
probably benign |
|
|
IGL02585:Sgce
|
APN |
6 |
4,711,388 (GRCm39) |
splice site |
probably benign |
|
|
IGL03355:Sgce
|
APN |
6 |
4,689,738 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03374:Sgce
|
APN |
6 |
4,689,718 (GRCm39) |
nonsense |
probably null |
|
|
PIT4445001:Sgce
|
UTSW |
6 |
4,689,654 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R0345:Sgce
|
UTSW |
6 |
4,718,019 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0611:Sgce
|
UTSW |
6 |
4,689,621 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0719:Sgce
|
UTSW |
6 |
4,689,753 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1162:Sgce
|
UTSW |
6 |
4,691,419 (GRCm39) |
splice site |
probably benign |
|
|
R1630:Sgce
|
UTSW |
6 |
4,719,476 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1694:Sgce
|
UTSW |
6 |
4,689,709 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1759:Sgce
|
UTSW |
6 |
4,689,765 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1897:Sgce
|
UTSW |
6 |
4,691,511 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2231:Sgce
|
UTSW |
6 |
4,730,066 (GRCm39) |
missense |
probably benign |
0.44 |
|
R3429:Sgce
|
UTSW |
6 |
4,730,008 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4011:Sgce
|
UTSW |
6 |
4,691,563 (GRCm39) |
nonsense |
probably null |
|
|
R4426:Sgce
|
UTSW |
6 |
4,691,459 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R4427:Sgce
|
UTSW |
6 |
4,691,459 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R4651:Sgce
|
UTSW |
6 |
4,689,560 (GRCm39) |
intron |
probably benign |
|
|
R4652:Sgce
|
UTSW |
6 |
4,689,560 (GRCm39) |
intron |
probably benign |
|
|
R4921:Sgce
|
UTSW |
6 |
4,694,153 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4974:Sgce
|
UTSW |
6 |
4,689,630 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6271:Sgce
|
UTSW |
6 |
4,730,015 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R6898:Sgce
|
UTSW |
6 |
4,689,666 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7317:Sgce
|
UTSW |
6 |
4,691,615 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7347:Sgce
|
UTSW |
6 |
4,694,106 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7512:Sgce
|
UTSW |
6 |
4,707,192 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R7671:Sgce
|
UTSW |
6 |
4,691,564 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8009:Sgce
|
UTSW |
6 |
4,691,636 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8378:Sgce
|
UTSW |
6 |
4,691,525 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8378:Sgce
|
UTSW |
6 |
4,689,760 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8942:Sgce
|
UTSW |
6 |
4,730,027 (GRCm39) |
missense |
probably benign |
|
|
R9187:Sgce
|
UTSW |
6 |
4,711,362 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9276:Sgce
|
UTSW |
6 |
4,674,585 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9334:Sgce
|
UTSW |
6 |
4,707,205 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9517:Sgce
|
UTSW |
6 |
4,694,153 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0026:Sgce
|
UTSW |
6 |
4,689,638 (GRCm39) |
missense |
probably benign |
0.41 |
|
| Posted On |
2015-04-16 |
Incidental Mutation