sult1st4

Ensembl ID:
ENSDARG00000003181
ZFIN ID:
ZDB-GENE-040426-2054
Description:
SULT1 sulfotransferase isoform 4 [Source:RefSeq peptide;Acc:NP_991183]
Human Orthologues:
SULT1A1, SULT1A2, SULT1A3, SULT1A4, SULT1B1, SULT1C3, SULT1E1
Human Descriptions:
sulfotransferase family 1E, estrogen-preferring, member 1 [Source:HGNC Symbol;Acc:11377]
sulfotransferase family, cytosolic, 1A, phenol-preferring, member 1 [Source:HGNC Symbol;Acc:11453]
sulfotransferase family, cytosolic, 1A, phenol-preferring, member 2 [Source:HGNC Symbol;Acc:11454]
sulfotransferase family, cytosolic, 1A, phenol-preferring, member 3 [Source:HGNC Symbol;Acc:11455]
sulfotransferase family, cytosolic, 1A, phenol-preferring, member 4 [Source:HGNC Symbol;Acc:30004]
sulfotransferase family, cytosolic, 1B, member 1 [Source:HGNC Symbol;Acc:17845]
sulfotransferase family, cytosolic, 1C, member 3 [Source:HGNC Symbol;Acc:33543]
Mouse Orthologues:
Sult1a1, Sult1b1, Sult1d1, Sult1e1
Mouse Descriptions:
sulfotransferase family 1A, phenol-preferring, member 1 Gene [Source:MGI Symbol;Acc:MGI:102896]
sulfotransferase family 1B, member 1 Gene [Source:MGI Symbol;Acc:MGI:2136282]
sulfotransferase family 1D, member 1 Gene [Source:MGI Symbol;Acc:MGI:1926341]
sulfotransferase family 1E, member 1 Gene [Source:MGI Symbol;Acc:MGI:98431]

Alleles

There are 2 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa41312 Nonsense Mutation detected in F1 DNA During 2018
sa2413 Nonsense F2 line generated During 2018

Mutation Details

Allele Name:
sa41312
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2018.
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000030557 Nonsense 131 304 4 8

The following transcripts of ENSDARG00000003181 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 55332337)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53295579
GRCz11 8 53174158
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TCATTAAAACCCATTTACCGGTCCAGCTCGTGCCCAAGTCCTTCTGGGAG[C/T]AGAACTCAAGGGTAAGAATACCATTTTCACAAAAAATATAGGCGATTATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2413
Current Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2018.
Mutation:
T > G
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000030557 Nonsense 289 304 8 8

The following transcripts of ENSDARG00000003181 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 55335165)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53292751
GRCz11 8 53171330
KASP Assay ID:
554-2437.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
TGGAAAAGTCACTTCACCGTGGCCCAGAACGAACGCTTCGATGAAGTCTA[T/G]AAACAGAAGATGAAGAACAGCGGCGTCACGTTTCGCACTGAGATTTAAAA
Associated Phenotype:
Not determined

GWAS

This gene's human homologue has been identified in the following GWAS studies:

(GWAS data comes from http://www.genome.gov/gwastudies/.)

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