ZMP
si:ch73-22c10.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
FERMT1
Human Description:
fermitin family member 1 [Source:HGNC Symbol;Acc:15889]
Mouse Orthologue:
Fermt1
Mouse Description:
fermitin family homolog 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2443583]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23801 | Essential Splice Site | Available for shipment | Available now |
sa11922 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23801
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 |
---|---|---|---|---|---|
ENSDART00000074546 | Essential Splice Site | 409 | 666 | 9 | 14 |
ENSDART00000147637 | None | None | 127 | None | 3 |
ENSDART00000147897 | Essential Splice Site | 404 | 661 | 10 | 15 |
The following transcripts of ENSDARG00000052652 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 45989820)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 45883509 |
GRCz11 | 20 | 45787229 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACAAAGATTCTGCCAATAAAGAGCCCATTGAGCAGCTTCATCTACGAG[G/A]TGAGCAGCCAATCAGAGAGCATGTCATTCACTTCAGTGCATTTGCAGAGC
Long Flanking Sequence:
GATAATTAACCCCGAAAAATCCAAAGCAAAGCAAACACTAGCAGATTACTATGGTATAAATACAGCACTGCAACATACAGAAGAGAGAAATCGACTTAGAATGTCACTTACCTGTTTTATAATGATTTGATCAGCTGTAGTTTGAAATTTACGCTGAGTTTTTCTCCCCTATGCGGTCTCTGTTGTCATCTTGTGGCAGAGCATCAACCGTGTTTGCTCTGCTCAATGACAGGCTAATGGCTGTCGTCGCGTTAAATCTCAGAAATTATAAATATTTAAAATAGGCACTCTCCTTATAAATAAACTGCATTTTTAAGGTTTAAATCCACAATTAAAGTTCATTATTTTCTTCTTTGTTCATTTTCCACTCTACAGGCCCAAGCGACTGACGTTAAAGCCGTATAAGGAGTACTGGTTTGTTTTTAGGGACACCACCATTTCTTATTTTAAAAACAAAGATTCTGCCAATAAAGAGCCCATTGAGCAGCTTCATCTACGAG[G/A]TGAGCAGCCAATCAGAGAGCATGTCATTCACTTCAGTGCATTTGCAGAGCGATCATTAACATTATCAATGTACAGGATGTGAGGTCATTCCTGATGTCAATGTGACCGAGAGGAAATTCGGCCTCAAGCTATTATTGCCCGCAGCTGATGGGATGAACGAGGTTTACATTCGCTGCGAAAATGTGAGTTTTGTATCTCTAATTTGCATGCAGATAGTTGTATATGTCTTGAAAAAAATTACATTCAAGAAACTTTTAGGTTTTAATAATATTTTAAGATAAACATTTACTGGAGCACTTTAAGAAGGGTAACGCTCAGTATAAATATAAGCAACGGCTCCAAATATTTTTCTTATTTTCACTACATCTTACTATAAGAGCCATAAAAGCCTATGAAGTCTTACCACTCAATAAAAACCATGCACAAGCATTTGTATTTAGATGTATTTAGCAGATTACCATGGTATAAATACAGCACCACAACAAAAAGAGAGAGCTCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11922
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 |
---|---|---|---|---|---|
ENSDART00000074546 | Nonsense | 512 | 666 | 11 | 14 |
ENSDART00000147637 | None | None | 127 | None | 3 |
ENSDART00000147897 | Nonsense | 507 | 661 | 12 | 15 |
The following transcripts of ENSDARG00000052652 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 45986241)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 45879930 |
GRCz11 | 20 | 45783650 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAWGTAGAGTCCATGGAGATGAACCCCGAGTGCTTTGTTTCTCCRCGATA[T/A]GCTAAGAAGTTYAAGACCAAACAGGTCAGATCACAATCTCAGGACCRGAT
Long Flanking Sequence:
CTTGCTGTGAGGCGCCAGCACTACCTACTGCACCACTGCTTCGCCGGCACCATGATTATTTAGCATATATTATTTGACATATATATAAGCCATTTAAAATTTAAATTGCTGCATGTTTGAGGTGATTATTATATAATATTACATAGAAACATAAACACACACACACATTCACACTTTGTGTAATATTTCATATGCTTTACCTTACAGGGTTACATTAAAATCCTCACAAGCAATGAAATATAGGATTTTGCATTCATTATTATAGTCCTCTACTAAGAAGAAGTGTCTTCTGAAATCCAGGAAACTCAGTACGCCAAGTGGAAAGCTGCCTGTATTTTGGCATCCAAAGGCAAGACGATGGCCTACAGCTCGTACCGCACCGAGGTGAAGAACATCCAGTCGTTCCTGCAGATGAAGAGTCTCGCTCCTCCTCCCGGTCAAGCGGCACCTGATGTAGAGTCCATGGAGATGAACCCCGAGTGCTTTGTTTCTCCGCGATA[T/A]GCTAAGAAGTTCAAGACCAAACAGGTCAGATCACAATCTCAGGACCGGATATAACTCGTCTTCATTACGACATCAGATTATTGTTTGATTTATTTTTGTGTTTAGTTATTTTTCCATTAGGGCTGCACGATATTGAAAAAAAAGGGGATTGTGATATTTTTTTTTCAGTAATAAATATTGTGATATAAATAAAATTACACCAGATGGCTTAAAAAGCTCCATCTGGAAAGAAAATTTCATATTTAGACTGATTGGGGGGATTTTGTATGGGTGTGAATCATGCATGCCTGTCAACATTGGCATGTGAAAATAAGAAAATAATTCCCCCCAAAATTGCTAAATATGTTCACCTGGAGCTGTTTGTAAATAAACAGTTGAAACGGACGGTAACATGTTTTATTATTATTATTATTATTATTATTCATTTATTCATTCATTTTCTTGTCGGCTAAGTCCCTTTATTAATCCGGGGTCGCCACAGCGGAATGAACCGCCAACTT
Associated Phenotype:
Not determined