Incidental Mutation 'IGL02353:Sult2a3'
ID |
289560 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Sult2a3
|
Ensembl Gene |
ENSMUSG00000074375 |
Gene Name |
sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 3 |
Synonyms |
Gm6955 |
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
IGL02353
|
Quality Score |
|
Status
|
|
Chromosome |
7 |
Chromosomal Location |
13801480-13856973 bp(-) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
G to A
at 13855575 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Stop codon
at position 94
(R94*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000096407
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000098809]
|
AlphaFold |
D3Z1W5 |
Predicted Effect |
probably null
Transcript: ENSMUST00000098809
AA Change: R94*
|
SMART Domains |
Protein: ENSMUSP00000096407 Gene: ENSMUSG00000074375 AA Change: R94*
Domain | Start | End | E-Value | Type |
Pfam:Sulfotransfer_1
|
34 |
278 |
1.5e-83 |
PFAM |
Pfam:Sulfotransfer_3
|
35 |
205 |
3.4e-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 |
Aldh18a1 |
A |
T |
19: 40,566,364 (GRCm39) |
V102D |
probably damaging |
Het |
Car4 |
C |
T |
11: 84,856,593 (GRCm39) |
P294S |
probably damaging |
Het |
Casp6 |
C |
T |
3: 129,704,175 (GRCm39) |
S87L |
probably damaging |
Het |
Ccdc121rt1 |
T |
C |
1: 181,338,190 (GRCm39) |
E254G |
possibly damaging |
Het |
Ccnl1 |
A |
C |
3: 65,856,141 (GRCm39) |
C255G |
probably damaging |
Het |
Celf4 |
T |
C |
18: 25,619,955 (GRCm39) |
I485M |
probably damaging |
Het |
Cntln |
A |
G |
4: 84,968,087 (GRCm39) |
R769G |
probably damaging |
Het |
Cstdc1 |
A |
G |
2: 148,625,387 (GRCm39) |
|
probably benign |
Het |
Cyp2d12 |
T |
C |
15: 82,443,171 (GRCm39) |
V360A |
probably benign |
Het |
Dgki |
T |
C |
6: 36,824,324 (GRCm39) |
E1068G |
probably damaging |
Het |
Fbxl4 |
A |
G |
4: 22,433,684 (GRCm39) |
N607S |
probably benign |
Het |
Fgd4 |
T |
C |
16: 16,279,909 (GRCm39) |
I383V |
probably damaging |
Het |
Fgd6 |
C |
T |
10: 93,974,258 (GRCm39) |
T1333I |
possibly damaging |
Het |
Got1 |
A |
G |
19: 43,512,882 (GRCm39) |
S5P |
probably damaging |
Het |
Herc2 |
T |
A |
7: 55,764,560 (GRCm39) |
N995K |
probably damaging |
Het |
Kcnma1 |
A |
G |
14: 23,641,681 (GRCm39) |
F159S |
probably damaging |
Het |
Krt87 |
T |
C |
15: 101,383,339 (GRCm39) |
S456G |
probably benign |
Het |
Lhb |
T |
C |
7: 45,070,718 (GRCm39) |
V32A |
possibly damaging |
Het |
Mau2 |
A |
T |
8: 70,472,288 (GRCm39) |
V602E |
probably damaging |
Het |
Mpst |
C |
T |
15: 78,294,285 (GRCm39) |
L6F |
probably damaging |
Het |
Nlrp2 |
G |
A |
7: 5,340,598 (GRCm39) |
T72I |
probably damaging |
Het |
Or8g20 |
A |
G |
9: 39,396,444 (GRCm39) |
I32T |
probably benign |
Het |
Phldb2 |
T |
C |
16: 45,569,142 (GRCm39) |
Y1239C |
probably damaging |
Het |
Slc22a8 |
T |
C |
19: 8,585,619 (GRCm39) |
F328S |
possibly damaging |
Het |
Spns1 |
C |
T |
7: 125,974,312 (GRCm39) |
R94Q |
probably damaging |
Het |
Syt16 |
A |
G |
12: 74,176,245 (GRCm39) |
N38S |
probably damaging |
Het |
Tbc1d1 |
G |
A |
5: 64,414,179 (GRCm39) |
R180Q |
probably damaging |
Het |
Ush2a |
T |
C |
1: 188,460,635 (GRCm39) |
I2632T |
probably benign |
Het |
Vcam1 |
T |
A |
3: 115,909,543 (GRCm39) |
I595F |
possibly damaging |
Het |
|
Other mutations in Sult2a3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00583:Sult2a3
|
APN |
7 |
13,856,905 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02360:Sult2a3
|
APN |
7 |
13,855,575 (GRCm39) |
nonsense |
probably null |
|
IGL02806:Sult2a3
|
APN |
7 |
13,856,857 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03252:Sult2a3
|
APN |
7 |
13,801,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R0029:Sult2a3
|
UTSW |
7 |
13,806,999 (GRCm39) |
missense |
probably benign |
0.11 |
R1480:Sult2a3
|
UTSW |
7 |
13,856,836 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1491:Sult2a3
|
UTSW |
7 |
13,856,867 (GRCm39) |
missense |
probably benign |
0.01 |
R4078:Sult2a3
|
UTSW |
7 |
13,855,662 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4668:Sult2a3
|
UTSW |
7 |
13,856,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R4928:Sult2a3
|
UTSW |
7 |
13,845,482 (GRCm39) |
missense |
probably benign |
0.06 |
R6311:Sult2a3
|
UTSW |
7 |
13,845,482 (GRCm39) |
missense |
probably benign |
0.00 |
R6749:Sult2a3
|
UTSW |
7 |
13,816,629 (GRCm39) |
missense |
probably benign |
0.00 |
R7030:Sult2a3
|
UTSW |
7 |
13,801,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R7232:Sult2a3
|
UTSW |
7 |
13,816,685 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7394:Sult2a3
|
UTSW |
7 |
13,845,449 (GRCm39) |
missense |
probably benign |
0.05 |
R7617:Sult2a3
|
UTSW |
7 |
13,806,981 (GRCm39) |
missense |
probably benign |
0.00 |
R8029:Sult2a3
|
UTSW |
7 |
13,855,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R8097:Sult2a3
|
UTSW |
7 |
13,816,635 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9154:Sult2a3
|
UTSW |
7 |
13,806,981 (GRCm39) |
missense |
probably benign |
0.00 |
|
Posted On |
2015-04-16 |