ZMP
sez6l
Ensembl ID:
ZFIN ID:
Human Orthologue:
SEZ6L
Human Description:
seizure related 6 homolog (mouse)-like [Source:HGNC Symbol;Acc:10763]
Mouse Orthologue:
Sez6l
Mouse Description:
seizure related 6 homolog like Gene [Source:MGI Symbol;Acc:MGI:1935121]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21892 | Essential Splice Site | Available for shipment | Available now |
| sa12945 | Essential Splice Site | Available for shipment | Available now |
| sa12754 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21892
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114839 | Essential Splice Site | 414 | 937 | 6 | 17 |
| ENSDART00000141454 | Essential Splice Site | 232 | 755 | 4 | 15 |
Genomic Location (Zv9):
Chromosome 11 (position 21621953)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 44803733 |
| GRCz11 | 10 | 44650345 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCGGCTGCACCTACACCTGGAGAGAATGGTGTTGGGCACCACAGACAGG[T/G]AAACCCAGGTACCATCAACATCAATGCATGCTTCTCCTACGACAGCTCTG
Long Flanking Sequence:
AGCATCATAACAACGTAGTAACAACTTCTTATAAACTTAGCAACACCCTGGCAACAACCCAGAACACCATAGCAACATAGTAACAACTTCTTATAAACTTAGCAACACCCTGGCAACCACCAAGAACACCATAACAATACTGCAACAGCTTCTTATAAAATTTAGCAACAACCTGGAAACCACCCAACCTTTCAGTACCTTAGCAACACTTGACAGACCCTGAACACAATAACACAGAAACAAACTCTCAGAGTTTTCACAACCACCCAGTATAAGACAGTATTATAGTTAGCTTATTAATGCAATGTTCCATATGTTCTCGTCCAGCTCTGTGTGGCGGTGTTGTTAAGAACGCAACAGTGGGACGAGTGTTGTCCCCCTCACCCCATTCAGGCCCCAACAGCACTCTGGACCGCAGCTGCTCATGGTCTCTGGAGGCTCCAAGCGGCCAGCGGCTGCACCTACACCTGGAGAGAATGGTGTTGGGCACCACAGACAGG[T/G]AAACCCAGGTACCATCAACATCAATGCATGCTTCTCCTACGACAGCTCTGCTAGAATTGTTATGTTGGGGCTGTTTTTGCCCTATTGACTTCCATTATAATCACATTTTTGGATTACAAATCTCTGTGTCGTTCAGACTGACTCCCCTTTGGTTATGTTGGTTTGTTTTTGTCCCACTGACTTCCATTATAATCACATTTATTGATTGCAAAGCCATGGCACTCTTGATTGGTGCTGGTTTTCACTGTTGGACCCATCTAAAGGGATAATGATGACAACTGATGATCAACAGTAAAATGACAAATGTTACCTCTTAATCCTAACAGGGTAAATCAGCAGCAATCAGTAATGCATGATTATCTGCTGTCATGGCTTTGCAATCAATTAATGTGATTATAATGGAAGTCAATGGGGCACAAACAGCCCCCAACATAACCAAAGGTGAGTAAATCTTCCTCCATGATTTAGGCTTGTGTTATGGAGTGGTCTCGACGCTGGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12945
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 |
|---|---|---|---|---|---|
| ENSDART00000114839 | Essential Splice Site | 470 | 937 | 7 | 17 |
| ENSDART00000141454 | Essential Splice Site | 288 | 755 | 5 | 15 |
Genomic Location (Zv9):
Chromosome 11 (position 21621314)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 44804372 |
| GRCz11 | 10 | 44650984 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACAGACCAGCCGAACAGCCACAACACCGGCTTCAATATACGATTTGAAG[G/A]YAGGCTGACAATGCACCGAGTAGATTCAATTCAATGTGCAATGGACTAAA
Long Flanking Sequence:
TGACTCCCCTTTGGTTATGTTGGTTTGTTTTTGTCCCACTGACTTCCATTATAATCACATTTATTGATTGCAAAGCCATGGCACTCTTGATTGGTGCTGGTTTTCACTGTTGGACCCATCTAAAGGGATAATGATGACAACTGATGATCAACAGTAAAATGACAAATGTTACCTCTTAATCCTAACAGGGTAAATCAGCAGCAATCAGTAATGCATGATTATCTGCTGTCATGGCTTTGCAATCAATTAATGTGATTATAATGGAAGTCAATGGGGCACAAACAGCCCCCAACATAACCAAAGGTGAGTAAATCTTCCTCCATGATTTAGGCTTGTGTTATGGAGTGGTCTCGACGCTGGTTCGGTGGTCCTGTTTGATTCTGGACGTGGAGGTCCGATCCCATTTGAGGGAGTGATCAGCGAAGGTCCGGCAGTTCGGGTTCAGTTTATAACAGACCAGCCGAACAGCCACAACACCGGCTTCAATATACGATTTGAAG[G/A]TAGGCTGACAATGCACCGAGTAGATTCAATTCAATGTGCAATGGACTAAAAATATTTACAGTATTTATCCCACTTGGACGTTAAATATGGAAGGTAAATCCTGCCAATTTTAAATAAATCAAATAAACATTGGAAATGAAAATTAAATGAAATTATTTAGTTTTAATTTTCACTTTGACAACACATCGTCCCTGTCAAACTGATAATTAAAATGAAGTTGCCGATTTAACATTTCATTTTCCCTGCATTTCCGCATCAAGACTGCCAATATTAAAATGAAAAGCCAAACTGAAAAATAAAATGCAAACACAATTTTTACACAGCGTGTTATTAATGTTCACGCTATAATAGTGACACAATTCAAATGAAAATGTAAATTTAAGCTTTCCTTTTATTGACACTTTTTCATTTCAGTTTTCATTTTCGATTTCATTTTCAACTTAAAGCTGTATGCAAAGCCTATGCTAATCAGTGGGAGGGGCGTATTCGAGTGACGTCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12754
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114839 | Essential Splice Site | 471 | 937 | 7 | 17 |
| ENSDART00000141454 | Essential Splice Site | 289 | 755 | 5 | 15 |
| ENSDART00000114839 | Essential Splice Site | 471 | 937 | 7 | 17 |
| ENSDART00000141454 | Essential Splice Site | 289 | 755 | 5 | 15 |
Genomic Location (Zv9):
Chromosome 11 (position 21621313)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 44804373 |
| GRCz11 | 10 | 44650985 |
KASP Assay ID:
2260-4199.1 (used for ordering genotyping assays)
KASP Sequence:
ACAGACCAGCCGAACAGCCACAACACCGGCTTCAATATACGATTTGAAGR[T/C]AGGCTGACAATGCACCGAGTAGATTCAATTCAATGTGCAATGGACTAAAA
Long Flanking Sequence:
GACTCCCCTTTGGTTATGTTGGTTTGTTTTTGTCCCACTGACTTCCATTATAATCACATTTATTGATTGCAAAGCCATGGCACTCTTGATTGGTGCTGGTTTTCACTGTTGGACCCATCTAAAGGGATAATGATGACAACTGATGATCAACAGTAAAATGACAAATGTTACCTCTTAATCCTAACAGGGTAAATCAGCAGCAATCAGTAATGCATGATTATCTGCTGTCATGGCTTTGCAATCAATTAATGTGATTATAATGGAAGTCAATGGGGCACAAACAGCCCCCAACATAACCAAAGGTGAGTAAATCTTCCTCCATGATTTAGGCTTGTGTTATGGAGTGGTCTCGACGCTGGTTCGGTGGTCCTGTTTGATTCTGGACGTGGAGGTCCGATCCCATTTGAGGGAGTGATCAGCGAAGGTCCGGCAGTTCGGGTTCAGTTTATAACAGACCAGCCGAACAGCCACAACACCGGCTTCAATATACGATTTGAAGG[T/C]AGGCTGACAATGCACCGAGTAGATTCAATTCAATGTGCAATGGACTAAAAATATTTACAGTATTTATCCCACTTGGACGTTAAATATGGAAGGTAAATCCTGCCAATTTTAAATAAATCAAATAAACATTGGAAATGAAAATTAAATGAAATTATTTAGTTTTAATTTTCACTTTGACAACACATCGTCCCTGTCAAACTGATAATTAAAATGAAGTTGCCGATTTAACATTTCATTTTCCCTGCATTTCCGCATCAAGACTGCCAATATTAAAATGAAAAGCCAAACTGAAAAATAAAATGCAAACACAATTTTTACACAGCGTGTTATTAATGTTCACGCTATAATAGTGACACAATTCAAATGAAAATGTAAATTTAAGCTTTCCTTTTATTGACACTTTTTCATTTCAGTTTTCATTTTCGATTTCATTTTCAACTTAAAGCTGTATGCAAAGCCTATGCTAATCAGTGGGAGGGGCGTATTCGAGTGACGTCGAG
Associated Phenotype:
Not determined