ZMP
sly1
Ensembl ID:
ZFIN ID:
Description:
sec1 family domain-containing protein 1 [Source:RefSeq peptide;Acc:NP_878281]
Human Orthologue:
SCFD1
Human Description:
sec1 family domain containing 1 [Source:HGNC Symbol;Acc:20726]
Mouse Orthologue:
Scfd1
Mouse Description:
Sec1 family domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:1924233]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23101 | Essential Splice Site | Available for shipment | Available now |
sa42953 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23100 | Nonsense | Available for shipment | Available now |
sa42952 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23101
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104166 | Essential Splice Site | 94 | 632 | 4 | 25 |
ENSDART00000134735 | Essential Splice Site | 94 | 623 | 4 | 25 |
Genomic Location (Zv9):
Chromosome 17 (position 28852678)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 28776605 |
GRCz11 | 17 | 28793568 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATTTACTTTATAATGCCCACAGAGGAGAACATCGACAGGATATGTCAA[G/A]TAAATATGCTTGTTTTGGTCAGTCCCATTCAAAGATAATTTGTTTGAATA
Long Flanking Sequence:
TTTATAAAGATTGACACTGTCAAATCTTGCATGTTAACTGTTGTTTAGAATTGCTAATATATGTCGTTGCTGTTTCTCTCCTCAGCTGCTCTCAAACGAATGCTCAACTTTAATGCCCCACCCCTTAAAAACACAACAGCTGAGCCAGTATGGAAGGTAAGAGACAAACCTAGAAGTTTCCCCTTTTTAAATGTGCTTCAGTGATGCTTTTTTGGCTCACACGTTGCTATTCTTGTTAGGTTCTTATTTACGATCGCTTTGGCCAAGACATTATATCTCCGCTTCTGTCTGTGAAAGAGCTACGAGACATGGGCATCACTCTGCACCTGTGAGCACCTCTAAAACATCCAGTCAGCAGTTTCATAATACTAATCGAAATGATCGTTCACAATTGTTTGTTTCTCTCTAGCTTGTTGCACTCAGATCGCGACCCCATTCCAGACGTTCCTGCCATTTACTTTATAATGCCCACAGAGGAGAACATCGACAGGATATGTCAA[G/A]TAAATATGCTTGTTTTGGTCAGTCCCATTCAAAGATAATTTGTTTGAATAATTTCAGAACATTTATATGCTCCATCACAGGACCTCCGAAACCAACTATATGAGTCCTACTATTTGAACTTCATCTCCGCAATTTCCAGAAGCAAATTGGAGGATATAGCAAGTGCTGCGCTTGCGGCTAATGCAGTAAACCAGGTGACCAAAGTAAGTCCGACATGTTTGTTCACAGTGAGTGTCTGTTGTGCTTTTGCTAGAGCTCGAGCTCAGTGAAGTCCTGCAGAAAGCCAAATAACATGCTGCTCATATTTATTTCAGCTTAAATGTTAGACTGTTCTGTTTCTCCTCAGGTATTTGATCAGTATTTGAACTTCATCACACTTGAGGATGATATGTTCATTCTCTGTAATCAAAACAAAGAGCACATCTCCTACCATGGTAAGCTGTTAAACCCACTTGAAATATTAATTATTTTTAAATATAATCCAGAGTTATTAATAGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42953
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 |
---|---|---|---|---|---|
ENSDART00000104166 | Nonsense | 106 | 632 | 5 | 25 |
ENSDART00000134735 | Nonsense | 106 | 623 | 5 | 25 |
Genomic Location (Zv9):
Chromosome 17 (position 28852563)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 28776490 |
GRCz11 | 17 | 28793453 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATGCTCCATCACAGGACCTCCGAAACCAACTATATGAGTCCTACTATT[T/A]GAACTTCATCTCCGCAATTTCCAGAAGCAAATTGGAGGATATAGCAAGTG
Long Flanking Sequence:
CCCCACCCCTTAAAAACACAACAGCTGAGCCAGTATGGAAGGTAAGAGACAAACCTAGAAGTTTCCCCTTTTTAAATGTGCTTCAGTGATGCTTTTTTGGCTCACACGTTGCTATTCTTGTTAGGTTCTTATTTACGATCGCTTTGGCCAAGACATTATATCTCCGCTTCTGTCTGTGAAAGAGCTACGAGACATGGGCATCACTCTGCACCTGTGAGCACCTCTAAAACATCCAGTCAGCAGTTTCATAATACTAATCGAAATGATCGTTCACAATTGTTTGTTTCTCTCTAGCTTGTTGCACTCAGATCGCGACCCCATTCCAGACGTTCCTGCCATTTACTTTATAATGCCCACAGAGGAGAACATCGACAGGATATGTCAAGTAAATATGCTTGTTTTGGTCAGTCCCATTCAAAGATAATTTGTTTGAATAATTTCAGAACATTTATATGCTCCATCACAGGACCTCCGAAACCAACTATATGAGTCCTACTATT[T/A]GAACTTCATCTCCGCAATTTCCAGAAGCAAATTGGAGGATATAGCAAGTGCTGCGCTTGCGGCTAATGCAGTAAACCAGGTGACCAAAGTAAGTCCGACATGTTTGTTCACAGTGAGTGTCTGTTGTGCTTTTGCTAGAGCTCGAGCTCAGTGAAGTCCTGCAGAAAGCCAAATAACATGCTGCTCATATTTATTTCAGCTTAAATGTTAGACTGTTCTGTTTCTCCTCAGGTATTTGATCAGTATTTGAACTTCATCACACTTGAGGATGATATGTTCATTCTCTGTAATCAAAACAAAGAGCACATCTCCTACCATGGTAAGCTGTTAAACCCACTTGAAATATTAATTATTTTTAAATATAATCCAGAGTTATTAATAGTTGTCTTGTTCTGTTTCCTCAGCAATCAATAAGCCAGATATCATGGACACAGACATGGAGGGTATAATGGACACAATAGTGGATAGTCTCTTCTGCTTCTTTGTTACTCTTGGTAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23100
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 |
---|---|---|---|---|---|
ENSDART00000104166 | Nonsense | 281 | 632 | 11 | 25 |
ENSDART00000134735 | Nonsense | 281 | 623 | 11 | 25 |
Genomic Location (Zv9):
Chromosome 17 (position 28845973)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 28769900 |
GRCz11 | 17 | 28786863 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCATTTCTATTAACCAACCAATCCCCCATATTAGGACTTCCACCTGAAC[C/T]GAGTGAGTGTGGACGAGTCTCATGGGTCAGAGGCCAGTCCAGCCGGAGCA
Long Flanking Sequence:
ATATAACTTGTAATATTAGTTTTTTAGGGCAACAGTATCTCCACATCAAAAGCTATTGGTCAGGCCACGATTCAGCAAAAATTTGATAAACAAATCGCCTAGTGCAGTGGTTTTACTTTATATCCAAAGAAAAGAAAGATATCCAAAGATGAAAAAAAATTTTTGTTTTTTAATCTAATGAAGACAGCGGAAGTCAGTGATTTATTTGAATTATTTAGCCTGACATGTTTGCTGTTCCAAAAATATTTCACATTTTTATTCAATTAAAATAAACTGTGTTTAATAGGGGGAAAAGTTGTTGTTTTTTACCCTGACATTTAAAAATAGATCATATTTTACAGCAGTAATCACAATGCCGTTATAGAGTGAAACTGTGATATTTTCATCCAAGGTTATCATACCATCAGAATGTGACACCGGCCCATGCCTAGTTCCTGCATTGTGCTTTGGTTCATTTCTATTAACCAACCAATCCCCCATATTAGGACTTCCACCTGAAC[C/T]GAGTGAGTGTGGACGAGTCTCATGGGTCAGAGGCCAGTCCAGCCGGAGCACGACCCAAAAAGAAAAACAAGAAGAGCTATGATCTCACTGCTGCTGACAAGTTTTGGCAAAAACACAAAGGAAGGTAAACATCTAATGCTGATAAATCTAATGTATACAAATTAAAGGGTTAGTTCACCCAAAATTGAAAGTTCTGTCAATAATTACTCAACAGTCATCCCAAACTCTTGAGAAGCTTGTTTGTCTTTGGAATAAGGAGATATTTTAGATTAAATCTGAGAGCTCCCTCATACTGTCCCGACTCATTCAAAGTCCAGAGTGGTGCCAAAAAAAAGGCCATATGACTTCAGTGGTCTGAGTATTATGAAGTTATGAGGATACATTTGTGTGCACATAGGGTAACTGTTAGACATTTTATGTTATATTAATTTTATATAACATAAAATCTTTAACAGTTACCCTATGCACACTATACTGACACAGAGAAGAAACTGTTAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42952
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 |
---|---|---|---|---|---|
ENSDART00000104166 | Nonsense | 530 | 632 | 19 | 25 |
ENSDART00000134735 | Nonsense | 530 | 623 | 19 | 25 |
Genomic Location (Zv9):
Chromosome 17 (position 28836887)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 28760814 |
GRCz11 | 17 | 28777777 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGAACACCGGCTCCCAGTTTGTGATGGAGGGAGTGAAAAATCTGGTCT[T/A]GAAACAGCATGTGAGTATTTAATAGCACTTAAGGAAATAAAAATCATAAA
Long Flanking Sequence:
TAAAAACAGCTCCTCTTGAACTATTTAGTTTTTTATCTTCGAGTGTTGAAATAATAAAGACATTTTGTTCTTTTTAGGCTGATCTAGAACAGTACAAGAAAGCCATGGTTGATGCAGGCTGCGACCTATCCCCACTTAACTACATTAAACAGTGGAAGTAAGTTCTCGCCATAGTCAACAAACACACCATAACATGCTGTCACATTTGCCTAGTTACTACATTAAATTCAACAGAAAGATCAGAACAGTAGTGTTGCAACTAATATAACCTATTTTCCAGAGCTTTCACCAAGATGGCTGCGACGCCAGCCAATTACGGGAGCAGTGGAGTGAAACCTATGGGGTATGAGGCTACACCACATTTAATTCTCAAAATGTGAATCCTTTTGTTAGTGGCATAAGTGATTTGAATGCAATGGACTGTCACTTTTCCAGACTGTTCTCAAGGGTGATGAACACCGGCTCCCAGTTTGTGATGGAGGGAGTGAAAAATCTGGTCT[T/A]GAAACAGCATGTGAGTATTTAATAGCACTTAAGGAAATAAAAATCATAAAGAAGTGTACAAACCTATTCAATTCAATCCAATCTGCTACCATTTGACCAAATAATGCATCTTATTATGGATATGTGAGTAAATGTATTTTGATGGTCCGTTTGAGTAGACTGTCTGCTTAATATCTGTTGATACTGCTCCTTCAACAGGCATTTATCTGACTCTAAAAAACTTGTCAACTTACACTAACCCTAATCCCAACCCCATCCTAACAGTCTACTTATAGTCTAATGAGAATTAGTTGACATGTAGATGCTATGTAACAAATGGACCATCAAAATAAAGTGTGACCGATATGTGCATTATAGCTTATTCTAATTAAAGAACAAACATAAAGTGTATCTAGGGACCAGAAGATTGTACTAAAATATGTTTGTTGCTCCAATAACAAGTGTAGACCGGGTCAACTTCGGACCACTTCACAATAACGCATTTGCCCAGATTGTTTTTT
Associated Phenotype:
Not determined