ZMP
sult2st3
Ensembl ID:
ZFIN ID:
Description:
sulfotransferase family 2, cytosolic sulfotransferase 3 [Source:RefSeq peptide;Acc:NP_001071636]
Human Orthologues:
SULT2A1, SULT2B1
Human Descriptions:
sulfotransferase family, cytosolic, 2A, dehydroepiandrosterone (DHEA)-preferring, member 1 [Source:H
sulfotransferase family, cytosolic, 2B, member 1 [Source:HGNC Symbol;Acc:11459]
sulfotransferase family, cytosolic, 2B, member 1 [Source:HGNC Symbol;Acc:11459]
Mouse Orthologues:
2810007J24Rik, Sult2a1, Sult2a2, Sult2a3, Sult2a4, Sult2a5, Sult2a6, Sult2b1
Mouse Descriptions:
RIKEN cDNA 2810007J24 gene Gene [Source:MGI Symbol;Acc:MGI:1924221]
sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 1 Gene [Source:MGI Symb
sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 2 Gene [Source:MGI Symb
sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 3 Gene [Source:MGI Symb
sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 4 Gene [Source:MGI Symb
sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 5 Gene [Source:MGI Symb
sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 6 Gene [Source:MGI Symb
sulfotransferase family, cytosolic, 2B, member 1 Gene [Source:MGI Symbol;Acc:MGI:1926342]
sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 1 Gene [Source:MGI Symb
sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 2 Gene [Source:MGI Symb
sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 3 Gene [Source:MGI Symb
sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 4 Gene [Source:MGI Symb
sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 5 Gene [Source:MGI Symb
sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 6 Gene [Source:MGI Symb
sulfotransferase family, cytosolic, 2B, member 1 Gene [Source:MGI Symbol;Acc:MGI:1926342]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22938 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22938
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037797 | Nonsense | 185 | 288 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 16 (position 47824749)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 45022945 |
GRCz11 | 16 | 44989661 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAGCTGGCGAAACCCAGAGCTCAAAGACAGAATTCTGTACGTCACCTA[T/A]GAAGAAATGCTTCAGGTAAAGTGAAATTGTGCCACTCACTCAGAGATCAG
Long Flanking Sequence:
ACCCCTTTGAGGTATGCGTTATATATGAAAAACGAAAATAATATGTGCGTCTCTTGATAATACACTTCTAAAGTATTATGAAGCAAAACAACCAAATGCACATTTCAGAGGCTGTATATTAAAGGTAAAATATTGAAATGATGATTTTCTTGCAGAGATTTTTTGTAATGATTGTAAAGACCTCAAGGAATTATTAGGAGCCATGAATATTAGTTGTGTTTTCCCTACATGTCTATTTTTGACTCCCAAAGTGCTGGTATCTTCTGATTTTCTGAACCACCAACGGCCACTGTCTGTCATTTTCAGCAGAAATCTTCTTCAATGTTTAGTTGAAGCAAAATGTCACCAGTTCCACAGAAACAGTAAGAATAGGTTGTGAATCAGAACTTTTAAACTGATCAGTTTGCACTTGCTTTCACAGTTGTTTTTGGTAAATGGTCTGACCACATCAAAAGCTGGCGAAACCCAGAGCTCAAAGACAGAATTCTGTACGTCACCTA[T/A]GAAGAAATGCTTCAGGTAAAGTGAAATTGTGCCACTCACTCAGAGATCAGACGAATCATTTTTGGTTATTTACATCAAACAAAAAATATCATATCTAATGTTTTTAATGTAAATGTTTTAATTTTATTGATTTATTTTTTGGGGTGTCATATTTGTTGAATTATGAAGTTATAACTTATATGCTGTTAGTGTCACACTTTACAATAAGGTTTTATTAGTTAATGCATTTACTAACGTGAACCAATTATGAACCACACTTGTTCAGTGTTTATTAGTTCACCATTTAGTAACGCTTATAAACATCCAAATTCATGATTCACAGTATTGTTCATTGTTTGTTCATGTTATGCATTAACTAACATGTTAAGTTAACCTTATTGTAAAGTGTTACCATTTTATCTATATTAAACTTGCTGTGAAATAGCCATAAGTTGCTCGTGAGGAAATAAACAAACAAGCAAAGATCAAAGATTATTAGTAACAAGTCCAGTGTTGTTGTT
Associated Phenotype:
Not determined