Incidental Mutation 'IGL03231:Slc19a2'
| ID |
413922 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Slc19a2
|
| Ensembl Gene |
ENSMUSG00000040918 |
| Gene Name |
solute carrier family 19 (thiamine transporter), member 2 |
| Synonyms |
TRMA, DDA1, THTR1 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.159)
|
| Stock # |
IGL03231
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
1 |
| Chromosomal Location |
164076615-164092954 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to T
at 164088449 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tryptophan to Leucine
at position 98
(W98L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000131327
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000044021]
[ENSMUST00000159230]
[ENSMUST00000169394]
|
| AlphaFold |
Q9EQN9 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000044021
AA Change: W299L
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000037561
Gene: ENSMUSG00000040918
AA Change: W299L
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
5 |
24 |
N/A |
INTRINSIC |
|
Pfam:Folate_carrier
|
28 |
459 |
2.7e-180 |
PFAM |
|
Pfam:MFS_1
|
34 |
441 |
2.6e-11 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000159230
AA Change: W261L
PolyPhen 2
Score 0.955 (Sensitivity: 0.79; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000123870
Gene: ENSMUSG00000040918
AA Change: W261L
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
5 |
24 |
N/A |
INTRINSIC |
|
Pfam:Folate_carrier
|
28 |
421 |
1.6e-176 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000160773
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000169394
AA Change: W98L
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000131327
Gene: ENSMUSG00000040918
AA Change: W98L
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
5 |
24 |
N/A |
INTRINSIC |
|
Pfam:Folate_carrier
|
28 |
70 |
3.7e-17 |
PFAM |
|
Pfam:Folate_carrier
|
65 |
258 |
6.7e-85 |
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 the thiamin transporter protein. Mutations in this gene cause thiamin-responsive megaloblastic anemia syndrome (TRMA), which is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural deafness. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]
PHENOTYPE: Homozygotes for targeted null alleles exhibit a grossly normal phenotype except for reduced testis size and male infertility. On a low-thiamine diet, mutants show premature death and sensorineural deafness, while homozygotes for one targeted allele also display diabetes mellitus and megaloblastosis. [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 |
|---|
| Abca9 |
A |
C |
11: 110,046,094 (GRCm39) |
F277V |
probably damaging |
Het |
| Arel1 |
T |
A |
12: 84,981,084 (GRCm39) |
T308S |
probably benign |
Het |
| Asic1 |
T |
A |
15: 99,596,983 (GRCm39) |
H548Q |
probably benign |
Het |
| B3galt1 |
T |
C |
2: 67,948,947 (GRCm39) |
Y221H |
probably damaging |
Het |
| Bltp2 |
A |
G |
11: 78,159,528 (GRCm39) |
T526A |
probably benign |
Het |
| Brs3 |
G |
T |
X: 56,090,804 (GRCm39) |
C221F |
probably benign |
Het |
| Capn7 |
G |
A |
14: 31,077,247 (GRCm39) |
G322R |
probably damaging |
Het |
| Ccdc138 |
T |
C |
10: 58,409,528 (GRCm39) |
L619P |
probably damaging |
Het |
| Cdh22 |
C |
T |
2: 164,958,126 (GRCm39) |
V614I |
probably benign |
Het |
| Dnah5 |
C |
T |
15: 28,311,294 (GRCm39) |
R1758W |
probably damaging |
Het |
| Dr1 |
T |
C |
5: 108,423,474 (GRCm39) |
V87A |
probably benign |
Het |
| F830045P16Rik |
A |
G |
2: 129,302,393 (GRCm39) |
S400P |
probably damaging |
Het |
| Fcgbpl1 |
A |
G |
7: 27,853,147 (GRCm39) |
E1478G |
possibly damaging |
Het |
| Fyb2 |
T |
A |
4: 104,843,460 (GRCm39) |
Y353* |
probably null |
Het |
| Gm28043 |
A |
G |
17: 29,854,916 (GRCm39) |
D457G |
probably damaging |
Het |
| Gsap |
T |
C |
5: 21,434,164 (GRCm39) |
V260A |
probably damaging |
Het |
| Kcnt2 |
A |
T |
1: 140,461,740 (GRCm39) |
|
probably benign |
Het |
| Magee2 |
A |
T |
X: 103,899,944 (GRCm39) |
L236M |
probably damaging |
Het |
| Map4k3 |
A |
T |
17: 80,905,104 (GRCm39) |
V729E |
probably damaging |
Het |
| Myh13 |
A |
G |
11: 67,242,817 (GRCm39) |
E910G |
possibly damaging |
Het |
| Nbeal1 |
G |
T |
1: 60,275,618 (GRCm39) |
A651S |
probably benign |
Het |
| Nhsl3 |
C |
T |
4: 129,117,474 (GRCm39) |
V385I |
possibly damaging |
Het |
| Nuak2 |
A |
T |
1: 132,255,915 (GRCm39) |
D188V |
probably damaging |
Het |
| Nup210l |
A |
G |
3: 90,096,852 (GRCm39) |
T1354A |
probably damaging |
Het |
| Or10q1 |
A |
T |
19: 13,726,749 (GRCm39) |
Q93L |
probably benign |
Het |
| Pof1b |
C |
T |
X: 111,554,987 (GRCm39) |
S506N |
possibly damaging |
Het |
| Prrt3 |
A |
G |
6: 113,474,485 (GRCm39) |
S246P |
possibly damaging |
Het |
| Rps6ka6 |
T |
A |
X: 110,360,018 (GRCm39) |
T43S |
probably benign |
Het |
| Snap29 |
C |
T |
16: 17,244,964 (GRCm39) |
S195L |
probably benign |
Het |
| Stt3b |
C |
T |
9: 115,073,062 (GRCm39) |
G815S |
unknown |
Het |
| Tm9sf2 |
T |
G |
14: 122,378,664 (GRCm39) |
I256R |
possibly damaging |
Het |
| Tpbpb |
A |
T |
13: 61,049,996 (GRCm39) |
N44K |
probably damaging |
Het |
| Trim13 |
A |
G |
14: 61,842,994 (GRCm39) |
E337G |
probably benign |
Het |
| Trmt6 |
A |
T |
2: 132,657,756 (GRCm39) |
D33E |
probably benign |
Het |
| Trpm6 |
T |
A |
19: 18,796,545 (GRCm39) |
S800R |
probably benign |
Het |
| V1rd19 |
A |
G |
7: 23,703,328 (GRCm39) |
I265V |
probably benign |
Het |
| Xkrx |
A |
G |
X: 133,051,391 (GRCm39) |
L420P |
probably damaging |
Het |
| Zfp618 |
T |
C |
4: 63,012,716 (GRCm39) |
Y167H |
probably damaging |
Het |
|
| Other mutations in Slc19a2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01464:Slc19a2
|
APN |
1 |
164,088,430 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0324:Slc19a2
|
UTSW |
1 |
164,084,344 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0709:Slc19a2
|
UTSW |
1 |
164,084,367 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1117:Slc19a2
|
UTSW |
1 |
164,091,025 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R1165:Slc19a2
|
UTSW |
1 |
164,091,014 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1463:Slc19a2
|
UTSW |
1 |
164,084,766 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1833:Slc19a2
|
UTSW |
1 |
164,089,753 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2148:Slc19a2
|
UTSW |
1 |
164,089,657 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2680:Slc19a2
|
UTSW |
1 |
164,076,982 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4010:Slc19a2
|
UTSW |
1 |
164,088,451 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5850:Slc19a2
|
UTSW |
1 |
164,091,025 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6279:Slc19a2
|
UTSW |
1 |
164,084,344 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6300:Slc19a2
|
UTSW |
1 |
164,084,344 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6907:Slc19a2
|
UTSW |
1 |
164,090,323 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R6917:Slc19a2
|
UTSW |
1 |
164,088,578 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6982:Slc19a2
|
UTSW |
1 |
164,084,428 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R6993:Slc19a2
|
UTSW |
1 |
164,088,391 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7424:Slc19a2
|
UTSW |
1 |
164,088,445 (GRCm39) |
missense |
probably benign |
0.31 |
|
R7575:Slc19a2
|
UTSW |
1 |
164,084,691 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8193:Slc19a2
|
UTSW |
1 |
164,084,794 (GRCm39) |
missense |
probably benign |
0.13 |
|
R8831:Slc19a2
|
UTSW |
1 |
164,084,443 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9424:Slc19a2
|
UTSW |
1 |
164,076,895 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2016-08-02 |
Incidental Mutation