Incidental Mutation 'IGL01529:Syde1'
| ID |
89667 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Syde1
|
| Ensembl Gene |
ENSMUSG00000032714 |
| Gene Name |
synapse defective 1, Rho GTPase, homolog 1 (C. elegans) |
| Synonyms |
1200008N06Rik, mSYD1A |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL01529
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
10 |
| Chromosomal Location |
78420337-78427798 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 78426015 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Proline
at position 51
(S51P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000043085
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000040580]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000040580
AA Change: S51P
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000043085
Gene: ENSMUSG00000032714
AA Change: S51P
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
37 |
45 |
N/A |
INTRINSIC |
|
low complexity region
|
56 |
69 |
N/A |
INTRINSIC |
|
low complexity region
|
114 |
127 |
N/A |
INTRINSIC |
|
low complexity region
|
147 |
160 |
N/A |
INTRINSIC |
|
low complexity region
|
176 |
191 |
N/A |
INTRINSIC |
|
low complexity region
|
321 |
335 |
N/A |
INTRINSIC |
|
RhoGAP
|
411 |
601 |
1.49e-56 |
SMART |
|
low complexity region
|
638 |
652 |
N/A |
INTRINSIC |
|
low complexity region
|
681 |
694 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000218641
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a Rho GTPase-activating protein highly expressed in placenta. The encoded protein is involved in cytoskeletal remodeling and trophoblast cell migration. Decreased expression of this gene has been associated with intrauterine growth restriction (IUGR). [provided by RefSeq, Feb 2017]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit reduced miniature excitatory postsynaptic current freuqency and docked vesciles in CA1 synpases. Mice homozygous for another allele exhibit reduced embryos and placental weight with abnormal placenta morphology and placental vasculature. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 36 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abhd17c |
A |
T |
7: 83,800,622 (GRCm39) |
I144N |
possibly damaging |
Het |
| Adamts19 |
T |
A |
18: 59,096,535 (GRCm39) |
H588Q |
probably damaging |
Het |
| Ankrd2 |
A |
G |
19: 42,028,349 (GRCm39) |
K46E |
probably damaging |
Het |
| Arhgap10 |
A |
C |
8: 78,072,920 (GRCm39) |
L513V |
possibly damaging |
Het |
| Arhgef12 |
C |
A |
9: 42,901,351 (GRCm39) |
R817L |
probably damaging |
Het |
| Asxl3 |
T |
A |
18: 22,650,712 (GRCm39) |
N900K |
probably damaging |
Het |
| Atp9b |
A |
T |
18: 80,887,826 (GRCm39) |
|
probably benign |
Het |
| Cdc27 |
T |
C |
11: 104,398,042 (GRCm39) |
N773D |
probably damaging |
Het |
| Cep97 |
A |
G |
16: 55,750,981 (GRCm39) |
|
probably benign |
Het |
| Dgkd |
T |
C |
1: 87,808,133 (GRCm39) |
F67S |
probably damaging |
Het |
| Dolk |
T |
C |
2: 30,175,749 (GRCm39) |
T99A |
probably benign |
Het |
| Egfr |
A |
T |
11: 16,813,014 (GRCm39) |
R165W |
probably benign |
Het |
| Fat2 |
T |
A |
11: 55,172,982 (GRCm39) |
D2577V |
probably damaging |
Het |
| Hsph1 |
T |
C |
5: 149,559,499 (GRCm39) |
I15V |
probably benign |
Het |
| Idh2 |
T |
C |
7: 79,747,693 (GRCm39) |
T276A |
probably benign |
Het |
| Jag1 |
T |
C |
2: 136,926,897 (GRCm39) |
Y954C |
probably damaging |
Het |
| Kat2a |
A |
T |
11: 100,602,735 (GRCm39) |
W118R |
probably damaging |
Het |
| Kcnh6 |
G |
T |
11: 105,911,522 (GRCm39) |
R636L |
probably benign |
Het |
| Klk1b16 |
G |
T |
7: 43,790,163 (GRCm39) |
K144N |
probably benign |
Het |
| Lrrk2 |
T |
A |
15: 91,696,516 (GRCm39) |
L2435I |
possibly damaging |
Het |
| Ltbp3 |
A |
G |
19: 5,797,867 (GRCm39) |
D502G |
probably benign |
Het |
| Ltn1 |
A |
T |
16: 87,178,359 (GRCm39) |
N1623K |
probably benign |
Het |
| Mcm10 |
C |
A |
2: 5,013,439 (GRCm39) |
E64D |
probably benign |
Het |
| Med13l |
A |
G |
5: 118,880,400 (GRCm39) |
N1164S |
probably damaging |
Het |
| Myo1a |
A |
G |
10: 127,556,529 (GRCm39) |
N1025D |
probably benign |
Het |
| Or2m12 |
A |
T |
16: 19,105,450 (GRCm39) |
D14E |
probably benign |
Het |
| Or8g27 |
C |
T |
9: 39,129,427 (GRCm39) |
T258I |
probably benign |
Het |
| Pdcd11 |
A |
G |
19: 47,098,068 (GRCm39) |
N785D |
probably benign |
Het |
| Psmd8 |
A |
T |
7: 28,878,576 (GRCm39) |
I81N |
probably damaging |
Het |
| Rigi |
G |
A |
4: 40,225,685 (GRCm39) |
H194Y |
probably benign |
Het |
| Ryr1 |
C |
T |
7: 28,774,652 (GRCm39) |
G2330R |
probably damaging |
Het |
| Scrib |
T |
C |
15: 75,921,084 (GRCm39) |
T80A |
possibly damaging |
Het |
| Sergef |
A |
T |
7: 46,092,942 (GRCm39) |
W356R |
probably damaging |
Het |
| Slc22a19 |
T |
C |
19: 7,660,300 (GRCm39) |
N370S |
probably damaging |
Het |
| Umodl1 |
A |
T |
17: 31,215,233 (GRCm39) |
D1019V |
possibly damaging |
Het |
| Vmn2r45 |
A |
G |
7: 8,486,493 (GRCm39) |
M265T |
probably benign |
Het |
|
| Other mutations in Syde1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00229:Syde1
|
APN |
10 |
78,421,643 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01285:Syde1
|
APN |
10 |
78,424,721 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01869:Syde1
|
APN |
10 |
78,424,753 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
IGL02098:Syde1
|
APN |
10 |
78,425,205 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03187:Syde1
|
APN |
10 |
78,424,943 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R0014:Syde1
|
UTSW |
10 |
78,425,868 (GRCm39) |
missense |
probably benign |
|
|
R0561:Syde1
|
UTSW |
10 |
78,425,210 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0605:Syde1
|
UTSW |
10 |
78,424,929 (GRCm39) |
unclassified |
probably benign |
|
|
R1713:Syde1
|
UTSW |
10 |
78,421,530 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1756:Syde1
|
UTSW |
10 |
78,422,814 (GRCm39) |
missense |
probably benign |
|
|
R4491:Syde1
|
UTSW |
10 |
78,426,062 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4846:Syde1
|
UTSW |
10 |
78,424,731 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5092:Syde1
|
UTSW |
10 |
78,425,252 (GRCm39) |
missense |
probably benign |
|
|
R5287:Syde1
|
UTSW |
10 |
78,425,871 (GRCm39) |
missense |
probably benign |
|
|
R5611:Syde1
|
UTSW |
10 |
78,421,725 (GRCm39) |
missense |
probably benign |
|
|
R5951:Syde1
|
UTSW |
10 |
78,425,150 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R5957:Syde1
|
UTSW |
10 |
78,425,951 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6169:Syde1
|
UTSW |
10 |
78,421,938 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7083:Syde1
|
UTSW |
10 |
78,422,903 (GRCm39) |
missense |
probably benign |
0.44 |
|
R7150:Syde1
|
UTSW |
10 |
78,422,032 (GRCm39) |
nonsense |
probably null |
|
|
R7239:Syde1
|
UTSW |
10 |
78,424,615 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7799:Syde1
|
UTSW |
10 |
78,425,741 (GRCm39) |
missense |
probably benign |
|
|
R7947:Syde1
|
UTSW |
10 |
78,425,916 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8876:Syde1
|
UTSW |
10 |
78,425,325 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8946:Syde1
|
UTSW |
10 |
78,424,683 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9104:Syde1
|
UTSW |
10 |
78,421,670 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9132:Syde1
|
UTSW |
10 |
78,425,340 (GRCm39) |
missense |
probably benign |
|
|
R9703:Syde1
|
UTSW |
10 |
78,421,557 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9728:Syde1
|
UTSW |
10 |
78,424,638 (GRCm39) |
frame shift |
probably null |
|
|
Z1176:Syde1
|
UTSW |
10 |
78,421,965 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
| Posted On |
2013-12-03 |
Incidental Mutation