Incidental Mutation 'IGL00155:Slc18a1'
| ID |
1398 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Slc18a1
|
| Ensembl Gene |
ENSMUSG00000036330 |
| Gene Name |
solute carrier family 18 (vesicular monoamine), member 1 |
| Synonyms |
4832416I10Rik |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL00155
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
8 |
| Chromosomal Location |
69490363-69541887 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 69503998 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Alanine to Threonine
at position 314
(A314T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000046924
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000037478]
|
| AlphaFold |
Q8R090 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000037478
AA Change: A314T
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000046924
Gene: ENSMUSG00000036330
AA Change: A314T
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:MFS_1
|
24 |
430 |
3.7e-34 |
PFAM |
|
Pfam:MFS_1
|
302 |
508 |
9e-17 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000162457
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The vesicular monoamine transporter acts to accumulate cytosolic monoamines into vesicles, using the proton gradient maintained across the vesicular membrane. Its proper function is essential to the correct activity of the monoaminergic systems that have been implicated in several human neuropsychiatric disorders. The transporter is a site of action of important drugs, including reserpine and tetrabenazine (Peter et al., 1993 [PubMed 7905859]). See also SLC18A2 (MIM 193001).[supplied by OMIM, Mar 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit increased neuron apoptosis, decreased neuron proliferation and impaired spatial object recognition. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 38 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aacs |
T |
C |
5: 125,590,235 (GRCm39) |
F498S |
probably damaging |
Het |
| Arhgap11a |
A |
G |
2: 113,664,601 (GRCm39) |
S561P |
probably benign |
Het |
| Best3 |
T |
C |
10: 116,824,632 (GRCm39) |
Y33H |
probably damaging |
Het |
| Cd209b |
T |
A |
8: 3,969,945 (GRCm39) |
|
probably benign |
Het |
| Cep152 |
A |
G |
2: 125,405,808 (GRCm39) |
S1575P |
probably benign |
Het |
| Crabp2 |
A |
G |
3: 87,859,506 (GRCm39) |
Y52C |
probably damaging |
Het |
| Crybg1 |
T |
C |
10: 43,868,505 (GRCm39) |
D1017G |
probably damaging |
Het |
| Ctnna2 |
A |
T |
6: 76,957,744 (GRCm39) |
W137R |
probably damaging |
Het |
| Cxcl9 |
T |
A |
5: 92,471,728 (GRCm39) |
H104L |
possibly damaging |
Het |
| Ddr2 |
A |
G |
1: 169,811,996 (GRCm39) |
I742T |
possibly damaging |
Het |
| Frem1 |
A |
G |
4: 82,877,626 (GRCm39) |
V223A |
possibly damaging |
Het |
| Fzd10 |
T |
A |
5: 128,678,592 (GRCm39) |
I104N |
probably damaging |
Het |
| Greb1 |
A |
G |
12: 16,761,962 (GRCm39) |
S473P |
probably damaging |
Het |
| Gtf2i |
T |
C |
5: 134,271,602 (GRCm39) |
Y873C |
probably damaging |
Het |
| Igsf6 |
T |
A |
7: 120,669,876 (GRCm39) |
K89* |
probably null |
Het |
| Ints3 |
A |
G |
3: 90,313,636 (GRCm39) |
F331L |
probably damaging |
Het |
| Kcnh3 |
A |
T |
15: 99,140,354 (GRCm39) |
H1080L |
possibly damaging |
Het |
| Mettl15 |
A |
T |
2: 108,923,521 (GRCm39) |
Y300* |
probably null |
Het |
| Mms19 |
A |
G |
19: 41,936,672 (GRCm39) |
F654L |
probably benign |
Het |
| Myc |
A |
G |
15: 61,861,669 (GRCm39) |
H425R |
probably benign |
Het |
| Ntn1 |
G |
T |
11: 68,117,445 (GRCm39) |
|
probably benign |
Het |
| Ormdl2 |
C |
A |
10: 128,655,944 (GRCm39) |
G69W |
probably damaging |
Het |
| Pdpr |
T |
C |
8: 111,828,704 (GRCm39) |
V69A |
possibly damaging |
Het |
| Rbbp6 |
T |
C |
7: 122,587,908 (GRCm39) |
I254T |
probably damaging |
Het |
| Sema6d |
A |
G |
2: 124,501,785 (GRCm39) |
R543G |
possibly damaging |
Het |
| Slc22a26 |
A |
G |
19: 7,760,201 (GRCm39) |
L514P |
probably damaging |
Het |
| Slc22a28 |
A |
C |
19: 8,107,567 (GRCm39) |
S167A |
possibly damaging |
Het |
| Speer1m |
A |
G |
5: 11,971,377 (GRCm39) |
S110G |
possibly damaging |
Het |
| Tchh |
A |
G |
3: 93,352,606 (GRCm39) |
E682G |
unknown |
Het |
| Thbs2 |
A |
T |
17: 14,889,097 (GRCm39) |
M1134K |
probably damaging |
Het |
| Tmem26 |
A |
G |
10: 68,611,184 (GRCm39) |
S218G |
probably damaging |
Het |
| Tmprss11c |
A |
T |
5: 86,387,254 (GRCm39) |
S208R |
probably benign |
Het |
| Tnfrsf8 |
T |
C |
4: 145,019,161 (GRCm39) |
|
probably null |
Het |
| Ush2a |
T |
C |
1: 188,596,875 (GRCm39) |
S3872P |
probably benign |
Het |
| Vmn1r69 |
T |
C |
7: 10,313,879 (GRCm39) |
N205S |
probably benign |
Het |
| Vmn2r54 |
T |
A |
7: 12,365,840 (GRCm39) |
|
probably benign |
Het |
| Wwtr1 |
A |
T |
3: 57,370,942 (GRCm39) |
M328K |
possibly damaging |
Het |
| Zfp64 |
G |
A |
2: 168,768,601 (GRCm39) |
S337L |
probably benign |
Het |
|
| Other mutations in Slc18a1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00661:Slc18a1
|
APN |
8 |
69,526,383 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01568:Slc18a1
|
APN |
8 |
69,518,278 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02199:Slc18a1
|
APN |
8 |
69,496,632 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL03011:Slc18a1
|
APN |
8 |
69,491,515 (GRCm39) |
missense |
probably benign |
|
|
IGL03260:Slc18a1
|
APN |
8 |
69,527,766 (GRCm39) |
missense |
probably benign |
0.24 |
|
R0349:Slc18a1
|
UTSW |
8 |
69,524,753 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1019:Slc18a1
|
UTSW |
8 |
69,527,685 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1759:Slc18a1
|
UTSW |
8 |
69,518,237 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1928:Slc18a1
|
UTSW |
8 |
69,526,464 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2058:Slc18a1
|
UTSW |
8 |
69,496,613 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4652:Slc18a1
|
UTSW |
8 |
69,496,583 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R4724:Slc18a1
|
UTSW |
8 |
69,526,301 (GRCm39) |
nonsense |
probably null |
|
|
R4818:Slc18a1
|
UTSW |
8 |
69,492,951 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6799:Slc18a1
|
UTSW |
8 |
69,493,633 (GRCm39) |
missense |
probably benign |
0.05 |
|
R6989:Slc18a1
|
UTSW |
8 |
69,491,514 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7557:Slc18a1
|
UTSW |
8 |
69,518,213 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7736:Slc18a1
|
UTSW |
8 |
69,518,206 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7956:Slc18a1
|
UTSW |
8 |
69,491,466 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8024:Slc18a1
|
UTSW |
8 |
69,527,799 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8146:Slc18a1
|
UTSW |
8 |
69,495,401 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R8339:Slc18a1
|
UTSW |
8 |
69,518,273 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R9055:Slc18a1
|
UTSW |
8 |
69,520,823 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9129:Slc18a1
|
UTSW |
8 |
69,491,533 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9190:Slc18a1
|
UTSW |
8 |
69,519,790 (GRCm39) |
critical splice donor site |
probably null |
|
|
| Posted On |
2011-07-12 |
Incidental Mutation