ZMP
sult1st2
Ensembl ID:
ZFIN ID:
Description:
Cytosolic sulfotransferase 2 [Source:UniProtKB/Swiss-Prot;Acc:Q7ZUS4]
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]
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]
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 |
---|---|---|---|
sa41295 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15273 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41295
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000030482 | Nonsense | 82 | 301 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 8 (position 48673789)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 46512047 |
GRCz11 | 8 | 46519926 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATACTTTGGCAATGAAAGTCCAGAGCGTCAGACCTCCCAGCCTATCTA[T/A]ATGAGAGTGCCTTTCTTGGAGATGTGTTTTCAAGGATTACCATTAGGTCA
Long Flanking Sequence:
GCGAGAACAGCGCGGGCGCGAACTGCACGTTTGAAATGCGAAAAAGCGCACAACAGCGGCCTCTCGCGGATTCGCGAAAACTAAAACTGCAGCCGTACATACCTACCGGGACGTATTCCGCGGCCTCCAGAAACGTCCGTGGGACTACGTTTCTACAATGACCCTGGGTTAAATTCATTGCAAGTCTTTTTACATGAGGCCCCTGGTCTTTGATATCTGTCTGAATTAAATCTGCTGTAAAAGTGTGTAAGTTTTGCTAATAAAATGGGTTTTCTTATTCGCAGATACATACAATATTTTAAATGTCTGCACTTATCAGTGCTAACTTTTAAGCACATTATAAATTTACTTTATGTCTCTAAGAAAAGGTTTTGCAGCAAGCAATACTGTAAGTTCTACTCTGTATTTTTTCTTGTAGGTACCACCTGGGTTTCATACATACTTGACCTTCTATACTTTGGCAATGAAAGTCCAGAGCGTCAGACCTCCCAGCCTATCTA[T/A]ATGAGAGTGCCTTTCTTGGAGATGTGTTTTCAAGGATTACCATTAGGTCAGAAGCCAAAATATAATGAGTGTACAATAATTTATTAATGTTTTCGGATGGGTTTTCTTCATTTTCAGGTAGGAAGCTGGTAAAGGGTTGTTGTTTTTTTATGTCAGAATGTTTGGTCAAATTGTCTTATTTATGAAAACAGAGAAATTTTTGACTTTGGAATTGGTAGAGCCACTTTGCCAAACTCATAAAGTGTAGCTTCTACACTTAAGTGACAATAAATTTAACATTATTATCCTGTATTATTTAAATGTAATTTATATTATTGTGTATTTTACTGTAAGGACAACTCTAGAATCACATTTAATTTTGACTTTCAGGTACAGAGCTGGCTGATACTCTGCCCACCTCTCCTCGCCTCATTAAAACACATTTACCTGTGCAGCTTGTGCCCAAGTCCTTCTGGGAGCAGAACTCAAAGGTACAGCTATAGTATTAATGCTAATGAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15273
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000030482 | Nonsense | 288 | 301 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 8 (position 48668124)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 46506382 |
GRCz11 | 8 | 46514261 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAATCACTTCACTGTGGCACAAAATGAACAGTTTGATGAGGWCTACAAA[C/T]AAAAGATGAAGAAYACCACTGTYAAGTTCCGCACTGAGATTTAAAACYAG
Long Flanking Sequence:
GTATTTGGTCCTTGGTATGATCATGTTAATGGATATTGGAAGAAAAAACAGACATATTCTAACATACTGTACATGTTCTATGAGGATATGGTTGAAGTAAGTGAAGTTTATAAAGTTACTAACTTAGAAAAATTTGTAATAAAACAAAATCGGCAAGCATATTTAATGTACATGTCTTGCTCAGGACACTGGACGTGAAGTGGCTCGTTTGTGCTCCTTCTTGGGATTGTCCACTTCAGCCGCAGAGAGGGAGAGAATAACAAAAGGGGTTCAGTTTGATGCAATGAAACAGAACAAGATGACCAACTATTCCACTCTCCCTGTCATGGACTTCAAGATCTCGCCCTTCATGCGGAAAGGTCAATAAAGCATCTACTTTTAAATCTAAATTCTTTACTTCCACTCGCTTTGATTTTCGTTTTGTTTGTGTAGGTAAAGTTGGAGACTGGAGAAATCACTTCACTGTGGCACAAAATGAACAGTTTGATGAGGTCTACAAA[C/T]AAAAGATGAAGAACACCACTGTCAAGTTCCGCACTGAGATTTAAAACTAGAGTTCTTGATCTTTAACCAGAATAATCTATATATAAAAAAATATTATCATCCACTGGCCTACTTAGAAATCTGTTTACTTGCATATGTTATTTTATAAAGGATCATTTAAGATCTTCTAAGATATGAGTTTTGAACAGGATGATCTGTTTGACCAACCCTTCCTGCAGCTAGTAAGAATTGTTTTTTATGTGAATCAGAAACTCCAGATTGAAATTTTGTTGGTTGCCCAAAAAAATTGTGAAAGAACACTATTTAAAGCAGGGATGTCAAACTCAATTTCTGGAGGGCCACAGGCCTGCACAGTTTAGTTCCAACCCTGCTCCAACACACTTACCTGTAGGTTTCAAACAAGCCTGAAGGACTCAATTAGTTTGATCAGGTGTGTTTAATTAGGGTTGGAACTAAACTGTGCAGAGCTGCGGCCCTTTTGGAACTGAGTTTGACACCTG
Associated Phenotype:
Not determined