ZMP
si:dkey-269p14.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate MCF.2 cell line derived transforming sequence-like (MCF2L) [Sour
Human Orthologue:
MCF2L
Human Description:
MCF.2 cell line derived transforming sequence-like [Source:HGNC Symbol;Acc:14576]
Mouse Orthologue:
Mcf2l
Mouse Description:
mcf.2 transforming sequence-like Gene [Source:MGI Symbol;Acc:MGI:103263]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9961 | Nonsense | Available for shipment | Available now |
| sa31232 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9961
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 |
|---|---|---|---|---|---|
| ENSDART00000114083 | Nonsense | 704 | 1166 | 19 | 31 |
| ENSDART00000144821 | None | None | 213 | None | 7 |
| ENSDART00000114083 | Nonsense | 704 | 1166 | 19 | 31 |
| ENSDART00000144821 | None | None | 213 | None | 7 |
The following transcripts of ENSDARG00000075859 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 47073771)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 45885432 |
| GRCz11 | 1 | 46576664 |
KASP Assay ID:
2259-0994.1 (used for ordering genotyping assays)
KASP Sequence:
TTTATGAGAAGTACTGWCAGAACAAACCTCGCTCAGAGTCTTTATGGAGA[C/T]AGTGCTCTGACTGCGCTTTCTTCCAGGTCTTCTTACTTTTTATATGCGTT
Long Flanking Sequence:
GAGCCTATTTTTCAGAAATAGTTCCTTTAAAGATCTGTTTTTTTCATTTGACTTCTCAAATGATTTCGTATTTAGGGTTATGCAGCAGAAATGGACAATCCTGCCATGTCTCACCTCATCCCCAACACACTGCTTCACAAGAAGGACATCCTCTTCGGAAACATGTCTGAGATCTACCAGTTCCACAAGAAGTGAGTGAACAATCTCTGTGTTTCTGTTATGTAGCGTTATAAAGCTAAAGCACATCTCTTATATTAACTCTTAATATATTTTAGGACTTTTCTTCGTGAACTGGAGGCTTACACAGATTATCCTGAGCTTGTGGGACAGTGTTTCTTGGAAAGAGTGAGTATTGAGGTCACGGTGCTAGTTGTTTTTGGTTTTCTAGGTGATTTGGTTGATTATTCAGATGTGTTTGCTCCTCTTTTCCTCAGATGACAGATCTGCAGATTTATGAGAAGTACTGTCAGAACAAACCTCGCTCAGAGTCTTTATGGAGA[C/T]AGTGCTCTGACTGCGCTTTCTTCCAGGTCTTCTTACTTTTTATATGCGTTACATATTTGTGCATATTTATTTTTGTAAACTAAAGGAGTCATATTGTAAGGAAATGAATTTGCTAAATAGTTTTTCTGAAAACGGAGTGAGGAAATCACATTTAAAAAAATCTGTAAAACATGGGTATTGAGGGGATGATGTAACATTTGTAGAGTAGATGTAAAAGCTTGCTTGTTTGATTCTGTCATAAGCTTCCAGTATTCTCAGAAAATAACAATAATAATTAAAAAGTAGTAAAATAAAGCATTTTACTTTACATTATTTTTCTTTTATAAGTAGTTTTCTGTTTAATTTGAGCTCATTGTTTCTTAAATTGCTAATAACATGCTATTAGAATAACAGTTGCAATTAATTTGATTTTAAATGACCAATTAAGCAATTATAATAGTATTTATTAATAAAGTTAGTTAATATAGCACTTTCATACAAACACTTAATTCAAAGTGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31232
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 |
|---|---|---|---|---|---|
| ENSDART00000114083 | Essential Splice Site | 743 | 1166 | 20 | 31 |
| ENSDART00000144821 | None | None | 213 | None | 7 |
The following transcripts of ENSDARG00000075859 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 47075579)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 45887240 |
| GRCz11 | 1 | 46578472 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTGCTGAAACCTGTGCAGAGAATAACCAAATACCAGCTTTTACTAAAG[G/A]TAAACTACACGGTCGCCTCTCACTGATGTAGGTACAGATATATTGCAGTA
Long Flanking Sequence:
ATTACAAACTGATAAAAAAAATATTTAAAGATATTTAAAAAGTTAAATAAAGACACAAACAGTGGGATCTGTTAATTAAAGTAACAGTTGCTGGAGTAAAAGCTGACTTCATTCTGAAAACTCTTTTAATAACAATTAAATTAACTTGAAATTAATAAAATAAGGCAATTCAGTTGCAATTATTTTATTATACTTATATATGTGCAGTTACATAACGGTAATATCACTGAATATTTTATGTGACAATAAAAATTTAAATTAAAACATTTTTAAATATAATATAATACATTCCAATTATTTCTTCATTAATGATAATACATTTCTATTCATTGAGAGCTTGTAGTATATAAAATAAGATCAGAAAATGCATTATTATTATTAAAACATGCTTTTTGTTGTGCTTTCAGGAGTGTCAAAAGAAACTGGAACATAAGCTTGGTCTGGACTCATACCTGCTGAAACCTGTGCAGAGAATAACCAAATACCAGCTTTTACTAAAG[G/A]TAAACTACACGGTCGCCTCTCACTGATGTAGGTACAGATATATTGCAGTATATTTACACCTCTCACTGTCAATGTGTCAGGAGCTGCTGAAGTACAGTAAAGGCTGTGAGGGTGAGGAGGACCTACAGGAGGCGCTCTCATCCATTCTTGGCATCCTAAAAGCTGTGAACGACTCTATGCACCTCATCGCCATCACTGGATACGAAGTAAGCGTTTGATTTAGTGTAAAATTTAGAAGTGCTTTCAATTTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGAGCAATATCACACGAGTAGCAGTGCAATATGGCTGTATATCGGCACTGGTGGAAGGCGTGTATTGTCCCATTAATGGCAATATACAGCCATATTGCACTGCTATGAGTGTGATATTGCGTTTATACTACAGTTTGACGGCATTATCGTGTACATAAAAAGAAAATCAAACCCAGAGAGTCTCA
Associated Phenotype:
Not determined