ZMP
NP_001076338.1
Ensembl ID:
Description:
hypothetical protein LOC570314 [Source:RefSeq peptide;Acc:NP_001076338]
Human Orthologue:
FSCN1
Human Description:
fascin homolog 1, actin-bundling protein (Strongylocentrotus purpuratus) [Source:HGNC Symbol;Acc:111
Mouse Orthologue:
Fscn1
Mouse Description:
fascin homolog 1, actin bundling protein (Strongylocentrotus purpuratus) Gene [Source:MGI Symbol;Acc
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9138 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa39546 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9138
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000054989 | Essential Splice Site | 283 | 501 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 1 (position 7739455)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 7979260 |
| GRCz11 | 1 | 8663371 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAAGTGGTGCTCACCGCCAGCAATGACAGAAACATCTCCATGCGCCAGG[G/A]TGAGATGCCAATGCAGCATGCTCACTCATTAATATTAATAATGCTTATGG
Long Flanking Sequence:
CTACCTGGGCGGGACCGAGGACCGGATCGCGTGCTTTGCGCAAAGCATCTCTCCTGCGGAGAAGTGGAACGTGCACCTGGCCGTGCACCCGCAGGTCAACGTGTACAGCATCGCGCGCAAACGGTACGCGCACCTGTGCGCCGATAGGAATGAGCTCGCCGTAGACCGCGACGTGCCGTGGGGTGTGGACTCGCTGCTCACACTCGTGTATCTGGACCACCGCTATCACCTGCAGACCGCTGACAACCGCTTCCTCTCGTGCGGCGGAACCCTGACAGCCAAACCAGACCGGGACACCGGCTTCACGCTGGAATTCCGCGCGGGTAAGGTGGCTTTCCGAGACGCCACGGGAAAATACATCGCGCCTACGGGCCCCACCGGGACCATGAAGTCGGGCAGGAGCGCGCGTGTTGGCAAAGATGAGTTGTTTGTCCTCGAGCAAAGTCACGGGCAAGTGGTGCTCACCGCCAGCAATGACAGAAACATCTCCATGCGCCAGG[G/A]TGAGATGCCAATGCAGCATGCTCACTCATTAATATTAATAATGCTTATGGAGCGTTTTTTTAACTTATGCAAATGTTTGGATTTAGAAAGTAATCTAAAACAGCAGGCTGCTCTTTATTTCTTCTAAAACTTTCCATTTAGCTGCACTTCTACTTAGGTTTCAGCATAATTGTCTCATGTAGCAGATATCAAACGCAAAAGATTAAAAATACCTCTTAAAACGCAAATAATAATAATAAAAATAAACAAAACCAAATTGTTCATAACTTCTTGTACACTCTTAAACCTTTCACTGTTACGTTTTTCTTTTTAGTCGAGCCGATTATCACAGAACAATGTTAGTATTTGAGTATTTGAAAGTTCAAGTTCATGAAAGGACATTATTTTAAAGAAATATTTCCAGAATCCTTTAATCTAAAAATAACTAAATGTGGAAAAGAAACGTTCGATGGATCATCACTGAAAACAATAAAGAATGTACATTTTAACTGTGCTTTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39546
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000054989 | Essential Splice Site | 377 | 501 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 1 (position 7743634)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 7983439 |
| GRCz11 | 1 | 8667550 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATCATAGGTAACGATGTACTGTGTGTAGAGTAGCTGATGTTGTTTTACA[G/T]GCGAGCAGGAGGAGTTTGTGTTGAAGCTCATCAACAGGCCGCTGATTGTG
Long Flanking Sequence:
TCTATCTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTACTTGCCAAAATTCACTAGATCAGCATAACATATTTAATGTTTTCAGATCTAAAATATTAGAGAAAAGTGTACACCCTTTCACACTGAACTACATTATACTTTAGAAAGTAAAATAAAAACCTTGACTTATATAGAGACTTTTTCAGATACATTTATTCAAAGTAATAATCACTCAGTTGACCAGAAATGTACATTAGAGACTAAATCTAATTATTGCTCATATCCAGATCTCCCAGTTGTTTCTTCGACCTGGAGTGGAAGGGCTCAAAAGTGGCACTGAAGGCCAGCAATGGCAAATATCTGGCAGCCAAGAAGAACGGACAGCTGGCAGCCGCGGTGGACTCTGCAGGTCTGACCGGCTTCACACATATATTTCAGATATTGATCATAGGTAACGATGTACTGTGTGTAGAGTAGCTGATGTTGTTTTACA[G/T]GCGAGCAGGAGGAGTTTGTGTTGAAGCTCATCAACAGGCCGCTGATTGTGTTGCGCGGTGAACATGGCTTTATTGGCTGCCGCAAACAAGGAACCGGTACACTCGATTCCAACCGATCTTCCTATGATGTCTTCCAGTTAGAGTACAACAACAATGCATACAGCCTCAGAGGTGAGCGACAGAGCCAACAGTTACTCCTGATGCATTACTGACAGCTGGTAAGATGTAAAAACAGTTCCTTAAAGAAGCTGAATGGATATATATTACTGCATTCGCCATATTTGAGGAAATGCCAACTGGCCCAGCTTAGACTCGAACCAGCGACCTTCTTGCTGTGAGGCAACAGTGCTAACCACTGAGCCACGGTGCTGCCACCCCCCTTTGTTGTTGTTGCTTTATTAGAGTCCTACGAGTTTTCCTAAATTGTGTGTTTGTGTGATTTTCAGACTCCGTGGGGAAGTACTGGACGGTGGAGTCAGACGGCTCTGTGATCAGCAGTG
Associated Phenotype:
Not determined