Incidental Mutation 'IGL02861:Slc2a7'
| ID |
362172 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Slc2a7
|
| Ensembl Gene |
ENSMUSG00000062064 |
| Gene Name |
solute carrier family 2 (facilitated glucose transporter), member 7 |
| Synonyms |
OTTMUSG00000010396 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.055)
|
| Stock # |
IGL02861
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
4 |
| Chromosomal Location |
150233429-150252939 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 150252836 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Cysteine to Tyrosine
at position 492
(C492Y)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000059106
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000059893]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000059893
AA Change: C492Y
PolyPhen 2
Score 0.158 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000059106
Gene: ENSMUSG00000062064
AA Change: C492Y
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:MFS_1
|
22 |
319 |
2e-15 |
PFAM |
|
Pfam:Sugar_tr
|
26 |
494 |
7.6e-120 |
PFAM |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] SLC2A7 belongs to a family of transporters that catalyze the uptake of sugars through facilitated diffusion (Li et al., 2004). This family of transporters shows conservation of 12 transmembrane helices as well as functionally significant amino acid residues (Joost and Thorens, 2001 [PubMed 11780753]).[supplied by OMIM, Mar 2008]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 44 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930486L24Rik |
A |
T |
13: 61,001,146 (GRCm39) |
|
probably benign |
Het |
| 6430548M08Rik |
G |
A |
8: 120,876,863 (GRCm39) |
R157H |
probably damaging |
Het |
| Amer3 |
A |
G |
1: 34,627,206 (GRCm39) |
K482E |
probably damaging |
Het |
| Ankrd11 |
A |
T |
8: 123,622,566 (GRCm39) |
S429T |
probably damaging |
Het |
| Ano3 |
T |
A |
2: 110,569,157 (GRCm39) |
N125I |
probably damaging |
Het |
| BC106179 |
T |
A |
16: 23,042,746 (GRCm39) |
|
probably benign |
Het |
| Bclaf3 |
T |
C |
X: 158,338,524 (GRCm39) |
I457T |
possibly damaging |
Het |
| Cbr3 |
T |
G |
16: 93,482,007 (GRCm39) |
V121G |
probably damaging |
Het |
| Cd44 |
A |
G |
2: 102,662,826 (GRCm39) |
|
probably null |
Het |
| Cd72 |
G |
A |
4: 43,448,332 (GRCm39) |
A316V |
probably benign |
Het |
| Cdc27 |
A |
T |
11: 104,413,657 (GRCm39) |
|
probably benign |
Het |
| Cdon |
A |
T |
9: 35,398,253 (GRCm39) |
Q990L |
probably damaging |
Het |
| Clk2 |
T |
C |
3: 89,080,706 (GRCm39) |
W231R |
probably damaging |
Het |
| Cpsf2 |
G |
A |
12: 101,965,825 (GRCm39) |
V597I |
probably benign |
Het |
| D630003M21Rik |
A |
G |
2: 158,042,918 (GRCm39) |
V874A |
probably benign |
Het |
| Daam2 |
A |
G |
17: 49,776,455 (GRCm39) |
F811L |
probably damaging |
Het |
| Ddx54 |
T |
C |
5: 120,756,195 (GRCm39) |
|
probably benign |
Het |
| Dysf |
T |
A |
6: 84,016,519 (GRCm39) |
L59Q |
probably damaging |
Het |
| Eps8 |
A |
G |
6: 137,476,597 (GRCm39) |
Y601H |
probably damaging |
Het |
| Faf2 |
T |
C |
13: 54,796,235 (GRCm39) |
Y131H |
probably damaging |
Het |
| Hectd4 |
T |
A |
5: 121,445,067 (GRCm39) |
D101E |
possibly damaging |
Het |
| Hk2 |
T |
C |
6: 82,737,139 (GRCm39) |
T30A |
possibly damaging |
Het |
| Il27 |
A |
T |
7: 126,191,821 (GRCm39) |
L77Q |
probably damaging |
Het |
| Klhdc1 |
T |
A |
12: 69,298,225 (GRCm39) |
V83D |
possibly damaging |
Het |
| Manba |
T |
G |
3: 135,276,024 (GRCm39) |
S822A |
probably benign |
Het |
| Mterf2 |
A |
C |
10: 84,956,195 (GRCm39) |
V143G |
probably damaging |
Het |
| Ncapd3 |
A |
G |
9: 26,981,195 (GRCm39) |
D895G |
probably benign |
Het |
| Or4c115 |
T |
A |
2: 88,927,801 (GRCm39) |
I157L |
probably benign |
Het |
| Or6n1 |
T |
A |
1: 173,916,602 (GRCm39) |
|
probably benign |
Het |
| Panx1 |
T |
C |
9: 14,919,101 (GRCm39) |
K253E |
probably benign |
Het |
| Phc1 |
T |
A |
6: 122,300,748 (GRCm39) |
|
probably benign |
Het |
| Pkd1l2 |
G |
A |
8: 117,792,484 (GRCm39) |
T436I |
probably benign |
Het |
| Ptchd4 |
A |
G |
17: 42,688,208 (GRCm39) |
E250G |
probably damaging |
Het |
| Rp1 |
G |
T |
1: 4,416,375 (GRCm39) |
S1579* |
probably null |
Het |
| Rrp1 |
A |
G |
10: 78,245,056 (GRCm39) |
|
probably benign |
Het |
| Ryr3 |
A |
G |
2: 112,483,186 (GRCm39) |
L4187P |
possibly damaging |
Het |
| Serpinc1 |
A |
T |
1: 160,827,561 (GRCm39) |
I387F |
probably damaging |
Het |
| Slf1 |
A |
G |
13: 77,274,478 (GRCm39) |
|
probably benign |
Het |
| Spta1 |
T |
A |
1: 174,039,164 (GRCm39) |
L1169Q |
probably damaging |
Het |
| Stap1 |
T |
A |
5: 86,219,824 (GRCm39) |
|
probably benign |
Het |
| Taf6 |
A |
G |
5: 138,182,147 (GRCm39) |
L66P |
probably damaging |
Het |
| Ttn |
T |
C |
2: 76,632,841 (GRCm39) |
E14071G |
probably damaging |
Het |
| Unk |
A |
G |
11: 115,947,125 (GRCm39) |
H586R |
possibly damaging |
Het |
| Zfpm2 |
A |
C |
15: 40,966,662 (GRCm39) |
K917T |
probably damaging |
Het |
|
| Other mutations in Slc2a7 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01302:Slc2a7
|
APN |
4 |
150,242,021 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01990:Slc2a7
|
APN |
4 |
150,239,141 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
IGL02480:Slc2a7
|
APN |
4 |
150,244,569 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
IGL02607:Slc2a7
|
APN |
4 |
150,239,162 (GRCm39) |
missense |
probably benign |
|
|
IGL02716:Slc2a7
|
APN |
4 |
150,244,467 (GRCm39) |
splice site |
probably benign |
|
|
IGL03343:Slc2a7
|
APN |
4 |
150,252,797 (GRCm39) |
missense |
probably damaging |
1.00 |
|
anhedonic
|
UTSW |
4 |
150,243,015 (GRCm39) |
nonsense |
probably null |
|
|
Anorectic
|
UTSW |
4 |
150,242,667 (GRCm39) |
splice site |
probably null |
|
|
paunch
|
UTSW |
4 |
150,242,605 (GRCm39) |
missense |
probably damaging |
1.00 |
|
tablemuscle
|
UTSW |
4 |
150,252,797 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0116:Slc2a7
|
UTSW |
4 |
150,252,721 (GRCm39) |
missense |
probably benign |
0.31 |
|
R0302:Slc2a7
|
UTSW |
4 |
150,233,978 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0309:Slc2a7
|
UTSW |
4 |
150,242,528 (GRCm39) |
splice site |
probably benign |
|
|
R0367:Slc2a7
|
UTSW |
4 |
150,250,823 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1485:Slc2a7
|
UTSW |
4 |
150,250,853 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1542:Slc2a7
|
UTSW |
4 |
150,252,928 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1544:Slc2a7
|
UTSW |
4 |
150,239,143 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3973:Slc2a7
|
UTSW |
4 |
150,242,667 (GRCm39) |
splice site |
probably null |
|
|
R4399:Slc2a7
|
UTSW |
4 |
150,243,007 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4467:Slc2a7
|
UTSW |
4 |
150,247,731 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4712:Slc2a7
|
UTSW |
4 |
150,252,926 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5066:Slc2a7
|
UTSW |
4 |
150,244,573 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5510:Slc2a7
|
UTSW |
4 |
150,244,551 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5995:Slc2a7
|
UTSW |
4 |
150,252,797 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6017:Slc2a7
|
UTSW |
4 |
150,249,629 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6062:Slc2a7
|
UTSW |
4 |
150,252,884 (GRCm39) |
missense |
probably benign |
|
|
R6185:Slc2a7
|
UTSW |
4 |
150,233,450 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6730:Slc2a7
|
UTSW |
4 |
150,242,605 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7753:Slc2a7
|
UTSW |
4 |
150,239,141 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R8145:Slc2a7
|
UTSW |
4 |
150,252,818 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8203:Slc2a7
|
UTSW |
4 |
150,243,015 (GRCm39) |
nonsense |
probably null |
|
|
R8512:Slc2a7
|
UTSW |
4 |
150,247,752 (GRCm39) |
missense |
probably benign |
0.23 |
|
R9066:Slc2a7
|
UTSW |
4 |
150,250,872 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9074:Slc2a7
|
UTSW |
4 |
150,242,625 (GRCm39) |
missense |
probably benign |
0.44 |
|
R9129:Slc2a7
|
UTSW |
4 |
150,243,001 (GRCm39) |
missense |
probably benign |
0.31 |
|
R9773:Slc2a7
|
UTSW |
4 |
150,234,044 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
| Posted On |
2015-12-18 |
Incidental Mutation