ZMP
sulf1
Ensembl ID:
ZFIN ID:
Description:
extracellular sulfatase Sulf-1 [Source:RefSeq peptide;Acc:NP_001003846]
Human Orthologue:
SULF1
Human Description:
sulfatase 1 [Source:HGNC Symbol;Acc:20391]
Mouse Orthologue:
Sulf1
Mouse Description:
sulfatase 1 Gene [Source:MGI Symbol;Acc:MGI:2138563]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa199 | Nonsense | Available for shipment | Available now |
sa11702 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa199
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 |
---|---|---|---|---|---|
ENSDART00000027022 | Nonsense | 569 | 874 | 12 | 20 |
ENSDART00000056080 | Nonsense | 569 | 892 | 12 | 21 |
ENSDART00000056081 | Nonsense | 569 | 1099 | 12 | 19 |
ENSDART00000137175 | None | None | 118 | None | 4 |
ENSDART00000140379 | Nonsense | 569 | 874 | 11 | 19 |
ENSDART00000142830 | Nonsense | 569 | 892 | 11 | 20 |
The following transcripts of ENSDARG00000038428 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 20123653)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 19429807 |
GRCz11 | 24 | 19574226 |
KASP Assay ID:
554-0110.1 (used for ordering genotyping assays)
KASP Sequence:
AAATCTATGACGTTGATCTGCAGGCTGATGATAAAACGCCACTCGAGCCT[C/T]GACCAATCAGCAAGCGCCACTATGAGCCAGAGCCAGGTTTTGATTCGGAC
Long Flanking Sequence:
TTCTGTTGTATGTCGCTGCAAAAAAAGCTAGCGATTTGTCTATGTTTTGAATTTCTGTCCAGAAGAGGTCATGTTTTGATCCTAGATTGGTCTAACGCAGTCAAGTGATGCGATTTTACCAAGCTTGAACTTCACCATGTTTCAAGATAAATTCACCAAGCTTGAACTTTGCACTGCATCAACCTGCGAAACTTGCCACATGACCTTGCGTTTTCGGTCTGATGCGTTCGTGTGCGTATGAATGGAAGTCTATGGGGTTGTGACTGCAGCTTAAGTGTGCTGAAGCAGGGTTGAAACTAAACTGTGCAGGGCTGCGGCACCCCTGCTTTTTAGCTATGGATCATAAACATTGAAATATGTGCAGCTTACACTGATGTCCTCCCTCAGGATACAGACCTCGTTTTGTGCACACACGGCCAGCCAGATCCCTGTCAGTCGAGTTTGAGGGGGAAATCTATGACGTTGATCTGCAGGCTGATGATAAAACGCCACTCGAGCCT[C/T]GACCAATCAGCAAGCGCCACTATGAGCCAGAGCCAGGTTTTGATTCGGACTTTGGGTTGGAGTCTGATGACGGATCCGAGGAGATGCAGTCAGATGACACAAATGCTGTGGGGTACCCGAATTCTCTCAAAGTCACCCACAAGTAAGCCTCGAAGCATAATCTTTATTTTATTGTTATTAAAAAAAATGTGTTAGAACCAATATCCAAAATCCACTTGCAGCCAATCAGCAGTAGGGGTGTGTCTTGTAATTAGAGTTGAGAAATCAAAAAGGGGCGTGATTTTAAGTTATGGGCGTGTTTATTTTTGTGCCTTCCGATATCAGAAACTGTATAAAGACATAAAGAATACAATAAATGAATAAAATCGTTTTACATGATTTTCATATAGGATAAACAGGAAAAAAGAGAACTAATTTTAATATAATTAAACAAAAATAATTTAAATGAGGCTGCATGAAAAATCTCATCATATTTCTTCAAAAAAGAAACACATTTCTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11702
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 |
---|---|---|---|---|---|
ENSDART00000027022 | None | None | 874 | 20 | 20 |
ENSDART00000056080 | None | None | 892 | 21 | 21 |
ENSDART00000056081 | Nonsense | 1002 | 1099 | 19 | 19 |
ENSDART00000137175 | None | None | 118 | None | 4 |
ENSDART00000140379 | None | None | 874 | None | 19 |
ENSDART00000142830 | None | None | 892 | None | 20 |
The following transcripts of ENSDARG00000038428 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 20135720)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 19441874 |
GRCz11 | 24 | 19586293 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGCCCCCTTCCACGCGGAGACACCTGGKTTCATCAGCTGGAAAATGAGT[T/A]GGGCGATGATGGATTGACGTTTAGTGGCAATGGCGTCACTGAACTAGAGA
Long Flanking Sequence:
GCGCAGCAGTCATCAGCCCTTACTGACTTTTCCCCGCTTCTCCCGTTTCTCAGAACACAGCCAACCTGGGACGTCCACAAAGGTTAAGCTGCCCAATTTCACAGAGGACGTCGACTGGCAAGGACTGGCAGATTTGTACAGCATGAACGAGAGTCTGTACGAACACAGACACAACTACAGTCCCGTTCTGGATGACTGGATGAACTTTTGGAAGGATGTAGATAGTATGTTTGCACTGCTGAGAAATTTAAAGACACTCAACCAAACCGATAAGCTTGATCCCCTGGTAGAGCTGGGTTCCGGGGTCCTGGAGGAAGCCAGTGGAGCTGGATCCCTCATCCTAGAGAACCTCGCAACCGCAGGTCCCTCAGTAGACCTGACCCCAAGAACATTTCAAGAAAGTCACCTCAAGTCTCTTAATGAACTCCCGGAAGGCCGCCCGACAAAAGTGAGCCCCCTTCCACGCGGAGACACCTGGGTTCATCAGCTGGAAAATGAGT[T/A]GGGCGATGATGGATTGACGTTTAGTGGCAATGGCGTCACTGAACTAGAGACCCGCCATGACTTTGTGTTGCGCAGCTCTAAAATGCTGGATCTCCACCAGCAGGAAGAAGAGGAGGACATTTTTCAGGCCCAGGGTTACCTTCCCGTATCGCCCCAACCAGAGCCTGCTGAGGAAACTCCTCCAGCCCAGAGCGACCGACCACAGGAGAGGTGGAACTTTAGCATCAAATCCTTTACCCATAAGCCCAGGGACATTCAAGACTCAGAGGGTAGTGCCTCAGGCCTGTCCCATTGAGAAAGGACTGCTGCCATGCACTGTGAAGCCAGCCAACTCAGAGACACTAACCCCACAGAGCATGGACTGCTCTCCTGTATAATCCGATGAATTATTTTATTTTTTACAGGTGCTTCCATTTATTAGAAATCAGTGTTATGTATTTTGTAAAAAAAAAAAGAAAATCTATATATAAATATAAAAATGTAGAGGTAAAGTATCGGAT
Associated Phenotype:
Not determined