ZMP
si:dkey-32e23.4
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens DNM1L, dynamin 1-like (DNM1L) [Source:UniProtKB/TrEMBL;Acc:B8JIY8
Human Orthologue:
DNM1L
Human Description:
dynamin 1-like [Source:HGNC Symbol;Acc:2973]
Mouse Orthologue:
Dnm1l
Mouse Description:
dynamin 1-like Gene [Source:MGI Symbol;Acc:MGI:1921256]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21391 | Nonsense | Available for shipment | Available now |
sa13350 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21391
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 |
---|---|---|---|---|---|
ENSDART00000092024 | Nonsense | 409 | 675 | 10 | 17 |
ENSDART00000137808 | None | None | 108 | None | 3 |
ENSDART00000142061 | Nonsense | 394 | 479 | 9 | 11 |
The following transcripts of ENSDARG00000063159 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 53282830)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 51025355 |
GRCz11 | 8 | 51014377 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATTGACCCACTTGGAGGACTCACTGAGCTCGATATTCTCACAGCTATT[C/T]GAAATGCTACGGTATAATGTTTACATGGTTTTGCATGCGTGTGTGTGTGA
Long Flanking Sequence:
ATTACCAAGGCCACATTCCTACTAAACCTCTTTTTTTCTCTCTCTTCTCTCTCTGCGACTCCGGCAGCGTCTCAGTCTGTCATTTTCGCACCGAAGCTCATGACAGATATCAAGCACACCATGTTTACTTTGTCTGCTTGGCTGCATTTTGACGGGCAGATAATCCGCAAGTCTGCCCGGCTCTTATTTACACCGTGTTCACTGTGGGATGAAATGGCGTTCATCTCTCATATCTGGCTAAGTCCACACCGGCTATCGATTAATTAAGTGGCTCGTATTGACGCTTTCTGGCTGGACAGTTGGGCTGGAATCCAGGCCTGTGTGAATGTGCCAACAGAAGATTGTTAATTTGTGCAGGATGGACTGACTGTGAGCGCTTGTCTCTCGTTAGGTGCGGAGGAGCTCGCATGTGTTACATTTTCCACGAGACGTTTGGAAGAACCCTGCAGTCCATTGACCCACTTGGAGGACTCACTGAGCTCGATATTCTCACAGCTATT[C/T]GAAATGCTACGGTATAATGTTTACATGGTTTTGCATGCGTGTGTGTGTGAACAGATAAGTACTTTCTGAATACGTTTGCTCACTTTCTTAAATGTAAAGCACAGTTGACGTCATAATTATTCGCCCCCCTCCTCATGTGAAATGTTGATTGCAAGACACTGCAAGTCCTAATACAGCTCTTATATTAGTAATAAACAGATAATAAGATAGTAGTAATGTAAAACGCTGGATATACAGATTAAAAATGTATTCAGCACCACCCTAAAGAGAAAAAATCATTGCTTTATATACTTTAAATGGTCACAATTTACATACAACTATAGTTTCATTAACATACATGGCCACACTTTATTTTAACGTGTAATTCATGCTATTAACGACCCTTTAAATAAGACATTTAGCTCAATAAACTACTAATTAGTTGCTTTTAAATAGTAAGGTAGTAGTTGGATTTAGGTATTAATAAGAATTAGGGATGTAGAATAAAATCATACTTTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13350
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 |
---|---|---|---|---|---|
ENSDART00000092024 | Essential Splice Site | 657 | 675 | 16 | 17 |
ENSDART00000137808 | Essential Splice Site | 90 | 108 | 2 | 3 |
ENSDART00000142061 | None | None | 479 | None | 11 |
The following transcripts of ENSDARG00000063159 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 53291589)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 51034114 |
GRCz11 | 8 | 51023136 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
RTCTCAGGAAACAGCACAGCAGCGCACTGAGGTCGCACACATGCTGGAGG[T/C]ACGTCAAAATGGRCAGTATTATCAGGGGAAATCGAATTGGCACAAAAMAA
Long Flanking Sequence:
CAACAGCCCCTTTAGAAATGTGATTTCTAAGAAAAATGGTTGTTCAATATTTATTTACCCCACTGTATTTCAAAGAGGGTATGATCATTTTCTATAGGCACTTTAATATCGCCTATTTACATGTTTACCAGAAGACAAAATAAATCAATTGCAATATTTTTTATGATGTATTACCCTTCAAAAACAACAAAAAATAAAAAATAAAACTGTTTAGTCGTACACTTCTCTAAATAATTGATAATGAACCTTTTAGTGGAGCTTTGAAGCAAGATTTCATTTTTTTATTAGTGATTTTTTTATTCTTTTTTTATATGTTTTTTTTTATTCTGCTTCCTGTAGTGTGCCAAAGACAGTGATGCATTTCCTGGTGAATTTCGTGAAGGAGCATCTGCAGAGTGAGCTGGTGGGTCAGCTTTACAAACAGCCTCTGCTGCAGGAGTTGCTCATCGAGTCTCAGGAAACAGCACAGCAGCGCACTGAGGTCGCACACATGCTGGAGG[T/C]ACGTCAAAATGGGCAGTATTATCAGGGGAAATCGAATTGGCACAAAACAAAACCTTTTTTTTTTTTTTTTTTGATTTAGAAATTGAAAGTTTTCTGTCACTTGACCTGTGCAGAGGCTGCCAGGCAAAAAAAAAAATGAGCCGTAATGGCAGCTACACTGAAATCTTCATAGAAACGCAGCACAAACTGCTCAAATTTCCACATTGTTCCATTTCCATATTTTGGTTATTACAACTTTAAAATGAGAAGTGTAAATTCACATAATTATATTTAGTTTTTTTTTTAATTCAGTTACTTTTAATTAGTTTTTAGAGGCAGATTTACTAGTTTTTATATTTCCAAATTGCTTAGTTTTAGTTTAGTTTTTATTAGTTTCAGTTTTTTGTTTGTTTGTAATTTATAAATTGGAATATTTATTAGGTGCAAGATTCAAAATCATCTGAATAAATTTTGTTAAATAAATACTCAACCAAAGATACGTTTTGAAACGTATTCAGAGG
Associated Phenotype:
Not determined