Incidental Mutation 'IGL03062:Sult2a5'
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ID409520
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Sult2a5
Ensembl Gene ENSMUSG00000078799
Gene Namesulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 5
SynonymsGm15438, EG434264
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.113) question?
Stock #IGL03062
Quality Score
Status
Chromosome7
Chromosomal Location13623967-13670807 bp(+) (GRCm38)
Type of Mutationcritical splice donor site (2 bp from exon)
DNA Base Change (assembly) T to A at 13624182 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000104165 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000108525] [ENSMUST00000108525]
Predicted Effect probably null
Transcript: ENSMUST00000108525
SMART Domains Protein: ENSMUSP00000104165
Gene: ENSMUSG00000078799

DomainStartEndE-ValueType
Pfam:Sulfotransfer_1 34 278 2e-82 PFAM
Pfam:Sulfotransfer_3 35 205 3.3e-12 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000108525
SMART Domains Protein: ENSMUSP00000104165
Gene: ENSMUSG00000078799

DomainStartEndE-ValueType
Pfam:Sulfotransfer_1 34 278 2e-82 PFAM
Pfam:Sulfotransfer_3 35 205 3.3e-12 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: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4932438A13Rik T C 3: 37,038,517 probably benign Het
Abcb10 C T 8: 123,954,315 R714Q possibly damaging Het
Abcb5 T A 12: 118,936,087 I282L probably benign Het
Aox1 A T 1: 58,078,465 E835D probably benign Het
Arhgap17 C T 7: 123,321,874 probably null Het
Calcr C T 6: 3,693,718 V359I probably benign Het
Chd9 T A 8: 91,015,267 probably benign Het
Col28a1 T C 6: 8,017,029 probably benign Het
Dnajc11 A G 4: 151,970,861 E171G possibly damaging Het
Efhd1 T C 1: 87,264,684 F79L possibly damaging Het
Fam83a A T 15: 57,993,077 probably null Het
Fam98a A G 17: 75,540,105 probably benign Het
Ficd A G 5: 113,738,253 Y163C probably damaging Het
Filip1l T C 16: 57,506,804 S66P probably damaging Het
Fmo5 A G 3: 97,635,593 Y73C probably damaging Het
Galnt12 C A 4: 47,122,566 R574S possibly damaging Het
Klc3 C A 7: 19,395,062 G461W probably damaging Het
Lmo7 A T 14: 101,912,079 T973S possibly damaging Het
Loxl1 C A 9: 58,311,910 G326V possibly damaging Het
Lrrc24 A G 15: 76,718,304 V127A probably benign Het
Lyrm1 T C 7: 119,916,131 probably benign Het
Med28 G A 5: 45,522,469 V65I probably damaging Het
Mgat4c T C 10: 102,388,461 Y179H probably damaging Het
Micall1 A C 15: 79,114,681 N58T probably damaging Het
Ncoa4 T A 14: 32,173,420 M72K possibly damaging Het
Nutm1 T C 2: 112,248,933 Q879R probably benign Het
Olfr1428 C T 19: 12,109,148 V133I probably benign Het
Olfr870 T A 9: 20,171,167 I135F probably damaging Het
Olfr965 T A 9: 39,720,035 D269E probably benign Het
Phf11b T C 14: 59,324,924 I177M probably damaging Het
Pin1rt1 T G 2: 104,714,707 I27L probably benign Het
Plxna2 T C 1: 194,762,550 V750A possibly damaging Het
Pou5f1 A T 17: 35,510,039 N126I possibly damaging Het
Ptprn A T 1: 75,247,873 H946Q possibly damaging Het
Rnf43 G T 11: 87,732,304 G744* probably null Het
Rsbn1 C A 3: 103,953,629 probably benign Het
Sars2 T A 7: 28,746,781 I145N possibly damaging Het
Sh3tc2 A T 18: 62,011,880 E1135V probably damaging Het
Shroom1 A G 11: 53,463,379 D42G probably benign Het
Sidt2 A G 9: 45,942,683 probably null Het
Slc39a8 T C 3: 135,886,797 probably benign Het
Slc9c1 T C 16: 45,599,758 S1059P probably benign Het
Socs6 A T 18: 88,869,846 M315K probably benign Het
Soga3 T A 10: 29,198,949 F911Y probably damaging Het
Speer2 T C 16: 69,857,977 E200G probably damaging Het
Tmbim1 A T 1: 74,291,699 I168N possibly damaging Het
Trim38 T C 13: 23,782,963 V131A probably damaging Het
Ube2o A G 11: 116,541,642 S833P probably damaging Het
Uggt2 T C 14: 119,075,346 I350M probably damaging Het
Unc80 A G 1: 66,509,489 D640G probably damaging Het
Vmn2r13 A G 5: 109,156,282 F761S probably damaging Het
Vmn2r54 C T 7: 12,632,428 C193Y probably damaging Het
Other mutations in Sult2a5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01757:Sult2a5 APN 7 13665154 missense probably damaging 1.00
IGL02352:Sult2a5 APN 7 13628802 missense probably benign 0.10
IGL02359:Sult2a5 APN 7 13628802 missense probably benign 0.10
IGL02453:Sult2a5 APN 7 13662507 missense possibly damaging 0.66
R0285:Sult2a5 UTSW 7 13628760 missense probably damaging 1.00
R0918:Sult2a5 UTSW 7 13625409 missense probably benign 0.12
R1869:Sult2a5 UTSW 7 13624120 missense probably benign 0.01
R1917:Sult2a5 UTSW 7 13670684 missense probably damaging 1.00
R2117:Sult2a5 UTSW 7 13625434 missense probably damaging 1.00
R4867:Sult2a5 UTSW 7 13624051 missense probably benign 0.02
R4890:Sult2a5 UTSW 7 13625386 missense probably benign 0.06
R4901:Sult2a5 UTSW 7 13625263 missense probably benign 0.10
R5236:Sult2a5 UTSW 7 13665049 missense probably benign
R6355:Sult2a5 UTSW 7 13662537 missense probably benign 0.00
R6692:Sult2a5 UTSW 7 13624132 missense probably damaging 0.99
R6735:Sult2a5 UTSW 7 13665058 nonsense probably null
R6873:Sult2a5 UTSW 7 13625386 missense probably benign 0.00
R7616:Sult2a5 UTSW 7 13670682 missense probably benign
R7828:Sult2a5 UTSW 7 13628843 critical splice donor site probably null
X0024:Sult2a5 UTSW 7 13665216 critical splice donor site probably null
Posted On2016-08-02