Incidental Mutation 'IGL01643:Slc37a2'
ID |
93610 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Slc37a2
|
Ensembl Gene |
ENSMUSG00000032122 |
Gene Name |
solute carrier family 37 (glycerol-3-phosphate transporter), member 2 |
Synonyms |
ci2, Slc37a1, G3PP, cI-2 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.086)
|
Stock # |
IGL01643
|
Quality Score |
|
Status
|
|
Chromosome |
9 |
Chromosomal Location |
37140445-37166709 bp(-) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
A to T
at 37146849 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000124569
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000115068]
[ENSMUST00000161114]
|
AlphaFold |
Q9WU81 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000115068
|
SMART Domains |
Protein: ENSMUSP00000110720 Gene: ENSMUSG00000032122
Domain | Start | End | E-Value | Type |
Pfam:MFS_1
|
23 |
424 |
1.2e-40 |
PFAM |
transmembrane domain
|
431 |
453 |
N/A |
INTRINSIC |
transmembrane domain
|
460 |
482 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000161114
|
SMART Domains |
Protein: ENSMUSP00000124569 Gene: ENSMUSG00000032122
Domain | Start | End | E-Value | Type |
Pfam:MFS_1
|
24 |
426 |
1.2e-40 |
PFAM |
transmembrane domain
|
431 |
453 |
N/A |
INTRINSIC |
transmembrane domain
|
460 |
482 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000162018
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933427D14Rik |
C |
T |
11: 72,082,414 (GRCm39) |
R304Q |
probably damaging |
Het |
Afap1l1 |
T |
A |
18: 61,884,897 (GRCm39) |
E196V |
probably damaging |
Het |
Bmp5 |
A |
T |
9: 75,746,895 (GRCm39) |
D251V |
probably damaging |
Het |
Ccser1 |
A |
G |
6: 61,288,839 (GRCm39) |
H334R |
probably benign |
Het |
Crnkl1 |
A |
G |
2: 145,773,268 (GRCm39) |
M126T |
probably damaging |
Het |
Ddrgk1 |
T |
C |
2: 130,500,214 (GRCm39) |
|
probably benign |
Het |
Dpy19l4 |
T |
C |
4: 11,290,184 (GRCm39) |
|
probably benign |
Het |
Eral1 |
A |
G |
11: 77,965,104 (GRCm39) |
|
probably null |
Het |
Ereg |
T |
A |
5: 91,234,637 (GRCm39) |
S17T |
probably benign |
Het |
Fgfr1 |
T |
A |
8: 26,056,751 (GRCm39) |
M280K |
probably benign |
Het |
Gpr65 |
A |
G |
12: 98,242,013 (GRCm39) |
E222G |
probably damaging |
Het |
Grid1 |
G |
T |
14: 35,045,392 (GRCm39) |
|
probably null |
Het |
Hspa12b |
A |
G |
2: 130,984,617 (GRCm39) |
T329A |
probably damaging |
Het |
Inpp4b |
A |
G |
8: 82,798,400 (GRCm39) |
I863V |
probably damaging |
Het |
Kash5 |
A |
T |
7: 44,849,710 (GRCm39) |
M71K |
probably damaging |
Het |
Krt8 |
G |
T |
15: 101,905,508 (GRCm39) |
S447Y |
possibly damaging |
Het |
Lama2 |
T |
A |
10: 26,946,368 (GRCm39) |
|
probably benign |
Het |
Lama4 |
A |
C |
10: 38,932,846 (GRCm39) |
N574T |
probably benign |
Het |
Lig3 |
T |
C |
11: 82,689,118 (GRCm39) |
S791P |
probably damaging |
Het |
Oas2 |
A |
T |
5: 120,874,252 (GRCm39) |
|
probably benign |
Het |
Or4c12b |
A |
T |
2: 89,647,017 (GRCm39) |
I116F |
probably damaging |
Het |
Pdk1 |
A |
G |
2: 71,728,049 (GRCm39) |
D370G |
probably damaging |
Het |
Popdc3 |
T |
A |
10: 45,190,976 (GRCm39) |
I29N |
probably damaging |
Het |
Rbp3 |
A |
T |
14: 33,678,793 (GRCm39) |
I914F |
probably benign |
Het |
Rnf207 |
C |
T |
4: 152,402,718 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
T |
A |
13: 11,707,563 (GRCm39) |
I2825F |
possibly damaging |
Het |
Vps8 |
T |
C |
16: 21,336,972 (GRCm39) |
V791A |
possibly damaging |
Het |
Wdr64 |
T |
C |
1: 175,599,877 (GRCm39) |
L127P |
probably damaging |
Het |
Whrn |
T |
C |
4: 63,334,672 (GRCm39) |
T368A |
possibly damaging |
Het |
|
Other mutations in Slc37a2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01719:Slc37a2
|
APN |
9 |
37,145,474 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02039:Slc37a2
|
APN |
9 |
37,144,980 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02286:Slc37a2
|
APN |
9 |
37,146,455 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02951:Slc37a2
|
APN |
9 |
37,166,611 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4581001:Slc37a2
|
UTSW |
9 |
37,148,701 (GRCm39) |
missense |
probably benign |
0.00 |
R0547:Slc37a2
|
UTSW |
9 |
37,144,418 (GRCm39) |
splice site |
probably null |
|
R0689:Slc37a2
|
UTSW |
9 |
37,146,846 (GRCm39) |
splice site |
probably benign |
|
R1301:Slc37a2
|
UTSW |
9 |
37,148,177 (GRCm39) |
missense |
probably benign |
0.05 |
R3927:Slc37a2
|
UTSW |
9 |
37,146,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R4834:Slc37a2
|
UTSW |
9 |
37,146,404 (GRCm39) |
missense |
probably damaging |
0.97 |
R5154:Slc37a2
|
UTSW |
9 |
37,142,939 (GRCm39) |
makesense |
probably null |
|
R5292:Slc37a2
|
UTSW |
9 |
37,150,453 (GRCm39) |
nonsense |
probably null |
|
R6150:Slc37a2
|
UTSW |
9 |
37,149,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R6959:Slc37a2
|
UTSW |
9 |
37,152,630 (GRCm39) |
missense |
probably benign |
|
R7014:Slc37a2
|
UTSW |
9 |
37,145,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R7605:Slc37a2
|
UTSW |
9 |
37,148,624 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7974:Slc37a2
|
UTSW |
9 |
37,150,421 (GRCm39) |
splice site |
probably null |
|
R8342:Slc37a2
|
UTSW |
9 |
37,149,510 (GRCm39) |
critical splice donor site |
probably null |
|
R8419:Slc37a2
|
UTSW |
9 |
37,148,726 (GRCm39) |
missense |
probably benign |
0.00 |
R9039:Slc37a2
|
UTSW |
9 |
37,148,658 (GRCm39) |
missense |
probably benign |
|
R9314:Slc37a2
|
UTSW |
9 |
37,150,482 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
Posted On |
2013-12-09 |