Incidental Mutation 'IGL00896:Sult2a1'
ID |
27751 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Sult2a1
|
Ensembl Gene |
ENSMUSG00000078798 |
Gene Name |
sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 1 |
Synonyms |
Std, Sth1, mSTa1 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.078)
|
Stock # |
IGL00896
|
Quality Score |
|
Status
|
|
Chromosome |
7 |
Chromosomal Location |
13530171-13571334 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 13566565 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Serine
at position 137
(T137S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000104162
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000108522]
|
AlphaFold |
P52843 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000108522
AA Change: T137S
PolyPhen 2
Score 0.021 (Sensitivity: 0.95; Specificity: 0.80)
|
SMART Domains |
Protein: ENSMUSP00000104162 Gene: ENSMUSG00000078798 AA Change: T137S
Domain | Start | End | E-Value | Type |
Pfam:Sulfotransfer_1
|
34 |
278 |
4.6e-83 |
PFAM |
Pfam:Sulfotransfer_3
|
35 |
205 |
5.8e-11 |
PFAM |
|
Coding Region Coverage |
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: This is one of seven sulfotransferase family 2A genes in a chromosome 7 A1 cluster. [provided by RefSeq, May 2010]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam6a |
A |
G |
12: 113,509,030 (GRCm39) |
T468A |
possibly damaging |
Het |
Ankrd35 |
A |
G |
3: 96,591,592 (GRCm39) |
E626G |
probably damaging |
Het |
Arhgef4 |
A |
G |
1: 34,850,777 (GRCm39) |
Y1812C |
possibly damaging |
Het |
Aurkc |
T |
C |
7: 7,005,513 (GRCm39) |
Y260H |
possibly damaging |
Het |
Bltp1 |
A |
G |
3: 37,093,611 (GRCm39) |
T4352A |
probably benign |
Het |
Cpb1 |
A |
G |
3: 20,306,193 (GRCm39) |
V329A |
probably benign |
Het |
Cyp2d11 |
G |
T |
15: 82,275,275 (GRCm39) |
|
probably benign |
Het |
Dnase1 |
G |
A |
16: 3,857,076 (GRCm39) |
S28N |
probably benign |
Het |
Drgx |
C |
T |
14: 32,327,171 (GRCm39) |
|
probably benign |
Het |
Evpl |
C |
A |
11: 116,113,410 (GRCm39) |
E1427* |
probably null |
Het |
Gimap6 |
T |
C |
6: 48,679,394 (GRCm39) |
N214S |
probably benign |
Het |
Htr1f |
A |
T |
16: 64,746,469 (GRCm39) |
H274Q |
probably benign |
Het |
Ipo9 |
A |
T |
1: 135,327,797 (GRCm39) |
V538E |
probably damaging |
Het |
Lmf2 |
T |
C |
15: 89,237,539 (GRCm39) |
K308E |
probably benign |
Het |
Mog |
T |
A |
17: 37,328,377 (GRCm39) |
|
probably null |
Het |
Myo19 |
T |
C |
11: 84,800,324 (GRCm39) |
V903A |
probably benign |
Het |
Myt1l |
A |
G |
12: 29,876,885 (GRCm39) |
T179A |
unknown |
Het |
Nckap1 |
C |
T |
2: 80,411,297 (GRCm39) |
V5M |
possibly damaging |
Het |
Or1e23 |
T |
C |
11: 73,407,167 (GRCm39) |
N286S |
probably damaging |
Het |
Or51l4 |
T |
C |
7: 103,404,213 (GRCm39) |
D193G |
probably damaging |
Het |
Or9a2 |
A |
T |
6: 41,749,047 (GRCm39) |
L62Q |
probably damaging |
Het |
Pcdhb5 |
T |
G |
18: 37,455,838 (GRCm39) |
|
probably null |
Het |
Pcm1 |
C |
A |
8: 41,729,160 (GRCm39) |
Q711K |
possibly damaging |
Het |
Pde6a |
A |
G |
18: 61,353,864 (GRCm39) |
D63G |
possibly damaging |
Het |
Piezo1 |
T |
C |
8: 123,224,609 (GRCm39) |
M711V |
possibly damaging |
Het |
Rev1 |
G |
A |
1: 38,138,021 (GRCm39) |
T88I |
probably damaging |
Het |
Sntg1 |
A |
T |
1: 8,665,634 (GRCm39) |
|
probably null |
Het |
Txndc15 |
G |
A |
13: 55,873,488 (GRCm39) |
A283T |
probably damaging |
Het |
Zswim8 |
A |
G |
14: 20,766,069 (GRCm39) |
E785G |
probably damaging |
Het |
|
Other mutations in Sult2a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00990:Sult2a1
|
APN |
7 |
13,537,961 (GRCm39) |
missense |
probably benign |
|
IGL01322:Sult2a1
|
APN |
7 |
13,566,604 (GRCm39) |
nonsense |
probably null |
|
IGL02558:Sult2a1
|
APN |
7 |
13,566,520 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03033:Sult2a1
|
APN |
7 |
13,566,635 (GRCm39) |
splice site |
probably benign |
|
IGL03199:Sult2a1
|
APN |
7 |
13,566,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R1633:Sult2a1
|
UTSW |
7 |
13,535,351 (GRCm39) |
missense |
probably benign |
0.01 |
R1903:Sult2a1
|
UTSW |
7 |
13,569,900 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2295:Sult2a1
|
UTSW |
7 |
13,569,884 (GRCm39) |
critical splice donor site |
probably null |
|
R4207:Sult2a1
|
UTSW |
7 |
13,535,472 (GRCm39) |
missense |
probably benign |
0.00 |
R5444:Sult2a1
|
UTSW |
7 |
13,569,944 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6233:Sult2a1
|
UTSW |
7 |
13,566,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R6317:Sult2a1
|
UTSW |
7 |
13,569,945 (GRCm39) |
missense |
probably benign |
0.00 |
R6853:Sult2a1
|
UTSW |
7 |
13,535,412 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7098:Sult2a1
|
UTSW |
7 |
13,549,978 (GRCm39) |
splice site |
probably null |
|
R8948:Sult2a1
|
UTSW |
7 |
13,530,342 (GRCm39) |
missense |
probably damaging |
0.99 |
R8950:Sult2a1
|
UTSW |
7 |
13,530,342 (GRCm39) |
missense |
probably damaging |
0.99 |
R9207:Sult2a1
|
UTSW |
7 |
13,566,627 (GRCm39) |
missense |
probably benign |
0.40 |
Z1088:Sult2a1
|
UTSW |
7 |
13,537,961 (GRCm39) |
missense |
probably benign |
|
Z1088:Sult2a1
|
UTSW |
7 |
13,535,360 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Sult2a1
|
UTSW |
7 |
13,535,339 (GRCm39) |
missense |
probably benign |
|
Z1176:Sult2a1
|
UTSW |
7 |
13,537,961 (GRCm39) |
missense |
probably benign |
|
Z1176:Sult2a1
|
UTSW |
7 |
13,535,360 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Sult2a1
|
UTSW |
7 |
13,535,339 (GRCm39) |
missense |
probably benign |
|
Z1176:Sult2a1
|
UTSW |
7 |
13,569,892 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sult2a1
|
UTSW |
7 |
13,535,360 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Sult2a1
|
UTSW |
7 |
13,535,339 (GRCm39) |
missense |
probably benign |
|
Z1177:Sult2a1
|
UTSW |
7 |
13,530,288 (GRCm39) |
frame shift |
probably null |
|
Z1177:Sult2a1
|
UTSW |
7 |
13,537,961 (GRCm39) |
missense |
probably benign |
|
|
Posted On |
2013-04-17 |