Incidental Mutation 'IGL00589:Slc17a5'
| ID |
6149 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Slc17a5
|
| Ensembl Gene |
ENSMUSG00000049624 |
| Gene Name |
solute carrier family 17 (anion/sugar transporter), member 5 |
| Synonyms |
4631416G20Rik |
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.705)
|
| Stock # |
IGL00589
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
9 |
| Chromosomal Location |
78443770-78495323 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 78485816 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Valine
at position 90
(I90V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000113003
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000052441]
[ENSMUST00000117645]
|
| AlphaFold |
Q8BN82 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000052441
AA Change: I90V
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000056182
Gene: ENSMUSG00000049624
AA Change: I90V
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:MFS_1
|
46 |
441 |
1.8e-61 |
PFAM |
|
transmembrane domain
|
456 |
478 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000117645
AA Change: I90V
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000113003
Gene: ENSMUSG00000049624
AA Change: I90V
| Domain | Start | End | E-Value | Type |
|---|
|
transmembrane domain
|
43 |
65 |
N/A |
INTRINSIC |
|
Pfam:MFS_1
|
97 |
415 |
2.5e-50 |
PFAM |
|
transmembrane domain
|
430 |
452 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000119213
|
| SMART Domains |
Protein: ENSMUSP00000113340
Gene: ENSMUSG00000049624
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Sugar_tr
|
43 |
175 |
4.9e-8 |
PFAM |
|
Pfam:MFS_1
|
45 |
189 |
5.5e-16 |
PFAM |
|
| 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 a membrane transporter that exports free sialic acids that have been cleaved off of cell surface lipids and proteins from lysosomes. Mutations in this gene cause sialic acid storage diseases, including infantile sialic acid storage disorder and and Salla disease, an adult form. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous mutant mice exhibit numerous neurological abnormalities, including impaired exploratory and locomotor activity, hearing deficits, and an increased depressive-like response. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 21 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acot9 |
A |
T |
X: 154,078,236 (GRCm39) |
I261L |
possibly damaging |
Het |
| Adcy8 |
A |
T |
15: 64,659,216 (GRCm39) |
F525I |
probably damaging |
Het |
| Ahr |
A |
T |
12: 35,554,096 (GRCm39) |
Y674* |
probably null |
Het |
| Baz1b |
A |
G |
5: 135,225,346 (GRCm39) |
E43G |
possibly damaging |
Het |
| Ccz1 |
T |
C |
5: 143,949,713 (GRCm39) |
T72A |
probably damaging |
Het |
| Chd9 |
G |
A |
8: 91,742,474 (GRCm39) |
R1629H |
probably damaging |
Het |
| Ell3 |
A |
T |
2: 121,270,761 (GRCm39) |
D257E |
probably benign |
Het |
| Fbxw26 |
T |
C |
9: 109,547,016 (GRCm39) |
|
probably benign |
Het |
| Isg20 |
G |
A |
7: 78,566,332 (GRCm39) |
D94N |
probably damaging |
Het |
| Mettl13 |
A |
T |
1: 162,369,960 (GRCm39) |
S392R |
probably damaging |
Het |
| Ms4a1 |
T |
A |
19: 11,231,923 (GRCm39) |
T151S |
probably benign |
Het |
| Nphp1 |
A |
G |
2: 127,605,769 (GRCm39) |
I352T |
probably damaging |
Het |
| Or1e1 |
T |
A |
11: 73,244,869 (GRCm39) |
C97S |
probably damaging |
Het |
| Pds5a |
T |
C |
5: 65,813,687 (GRCm39) |
D266G |
probably damaging |
Het |
| Rnf103 |
T |
C |
6: 71,486,067 (GRCm39) |
Y233H |
probably benign |
Het |
| Rwdd4a |
A |
T |
8: 47,997,219 (GRCm39) |
E146V |
probably damaging |
Het |
| Serpinb1c |
T |
C |
13: 33,067,958 (GRCm39) |
K213E |
probably damaging |
Het |
| Slc38a3 |
G |
A |
9: 107,535,876 (GRCm39) |
L86F |
probably damaging |
Het |
| Tbc1d2b |
T |
C |
9: 90,108,262 (GRCm39) |
T430A |
probably benign |
Het |
| Utrn |
C |
T |
10: 12,554,362 (GRCm39) |
V1576M |
possibly damaging |
Het |
| Vwa8 |
T |
A |
14: 79,275,635 (GRCm39) |
L806Q |
probably damaging |
Het |
|
| Other mutations in Slc17a5 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00828:Slc17a5
|
APN |
9 |
78,485,833 (GRCm39) |
missense |
probably benign |
0.37 |
|
IGL01603:Slc17a5
|
APN |
9 |
78,481,989 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01945:Slc17a5
|
APN |
9 |
78,495,214 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL03250:Slc17a5
|
APN |
9 |
78,485,846 (GRCm39) |
missense |
probably damaging |
0.99 |
|
PIT4618001:Slc17a5
|
UTSW |
9 |
78,445,530 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R0136:Slc17a5
|
UTSW |
9 |
78,485,956 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0245:Slc17a5
|
UTSW |
9 |
78,448,206 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0305:Slc17a5
|
UTSW |
9 |
78,464,819 (GRCm39) |
missense |
probably benign |
0.25 |
|
R0481:Slc17a5
|
UTSW |
9 |
78,445,584 (GRCm39) |
splice site |
probably null |
|
|
R0657:Slc17a5
|
UTSW |
9 |
78,485,956 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0763:Slc17a5
|
UTSW |
9 |
78,460,372 (GRCm39) |
splice site |
probably benign |
|
|
R1543:Slc17a5
|
UTSW |
9 |
78,468,082 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1564:Slc17a5
|
UTSW |
9 |
78,485,981 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2155:Slc17a5
|
UTSW |
9 |
78,484,455 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2483:Slc17a5
|
UTSW |
9 |
78,445,556 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3623:Slc17a5
|
UTSW |
9 |
78,445,556 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4193:Slc17a5
|
UTSW |
9 |
78,466,388 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
R4794:Slc17a5
|
UTSW |
9 |
78,481,997 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5115:Slc17a5
|
UTSW |
9 |
78,484,394 (GRCm39) |
missense |
probably benign |
0.12 |
|
R5141:Slc17a5
|
UTSW |
9 |
78,448,270 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5205:Slc17a5
|
UTSW |
9 |
78,485,899 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5953:Slc17a5
|
UTSW |
9 |
78,464,780 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6481:Slc17a5
|
UTSW |
9 |
78,445,553 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R7375:Slc17a5
|
UTSW |
9 |
78,495,174 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8309:Slc17a5
|
UTSW |
9 |
78,478,311 (GRCm39) |
nonsense |
probably null |
|
|
R8720:Slc17a5
|
UTSW |
9 |
78,485,945 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9286:Slc17a5
|
UTSW |
9 |
78,445,566 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9425:Slc17a5
|
UTSW |
9 |
78,484,457 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9567:Slc17a5
|
UTSW |
9 |
78,445,562 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
| Posted On |
2012-04-20 |
Incidental Mutation