ZMP
Q567Y1_DANRE
Ensembl ID:
Description:
LOC553370 protein [Source:UniProtKB/TrEMBL;Acc:Q567Y1]
Human Orthologue:
FIBIN
Human Description:
fin bud initiation factor homolog (zebrafish) [Source:HGNC Symbol;Acc:33747]
Mouse Orthologue:
Fibin
Mouse Description:
fin bud initiation factor homolog (zebrafish) Gene [Source:MGI Symbol;Acc:MGI:1914856]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12540 | Nonsense | Available for shipment | Available now |
sa19373 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13086 | Nonsense | Available for shipment | Available now |
sa12551 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12540
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058443 | Nonsense | 149 | 225 | 1 | 1 |
ENSDART00000058443 | Nonsense | 149 | 225 | 1 | 1 |
ENSDART00000058443 | Nonsense | 149 | 225 | 1 | 1 |
ENSDART00000058443 | Nonsense | 149 | 225 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 25 (position 36590449)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 34998065 |
GRCz11 | 25 | 35503004 |
KASP Assay ID:
554-5565.1 (used for ordering genotyping assays)
KASP Sequence:
ACCTGAAGCGAGAGATCGAGCAGATCGGCGARGCTTTCACMAACGTGGAG[A/T]AATCYCTGCTGGAGCTGGAGAGCAAGTTCAAGCAGAGCCAGGAGACGGAG
Long Flanking Sequence:
CAGACTCGGATTACAGCCCTGTGGGTCTCCTCTAGTGCGCACACTTCTATGAAGCGCTCCAGATGTGGACGTCGCCTCTGTCAGGCCGGTCAGACCTCCGCCGTGGACAGAAGCGATCTATCATGTTACCCTTTGCCCTCGGCCTGTTTTTACTGCCTCTTTGTGGCGCGGTCTACGAGGGACCTTTGCTCCCCGAAATGTCCAATGGCACTTTTCACCACTTCTTCGTCCCGGACGGCGATTATGAAGAGACTGAAGACCCCGAGAAGTGCCAGATGCTCTTCAAATGGATCGACCGCAGACCGTGTCCACTGGAGGAAGACCGGGACACGGTTATTAGGGAGGATTTCGTTATAGTAAAGCAGCAGATTGAAGACGCGGCGCGCGTTCTGGAGACTCTCGGGAAGAGCATCTCGTTTGATCTGGACGGAGAGGACAGCTACGGGAAATACCTGAAGCGAGAGATCGAGCAGATCGGCGAGGCTTTCACCAACGTGGAG[A/T]AATCTCTGCTGGAGCTGGAGAGCAAGTTCAAGCAGAGCCAGGAGACGGAGCAGAGAGAGGAGAGCGAGTTCAGCAGTAACTTCATCAAGCCCGTGTATGATGTGAGAGAAACGCTGCAGGAGACGCTGGACATCTCATCCGGACTCAAGGATAAACACGAGCTCATTTCTCTGATCGTGAGGAATCACGGCTCCAGGCTAAGCAGGCTGAAAAACGACTATCTGAACGTTTAAGACTTCCTGGGCAGACTTCAGTCCACTTTGGATTGTTCATTTGCGAGTTGTTTTGAAAGACGGAGCTCTAAATGTTCTCCGCTTCTGAAAGTATTTGGTGGTTTTGAGGTTCATTCACTCGTAATAGTTGTAATGCGTTTCCTCGGAGATTAAACATCAGCTATTGATGCTTTAGTGTGCGTTCATAGAAGTTCTTTGATTCAATTCAATTTAATTCATCTTTATTTCTACACTGAAAAAAATTATTCAAAGATGACTCCTTGGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19373
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058443 | Nonsense | 149 | 225 | 1 | 1 |
ENSDART00000058443 | Nonsense | 149 | 225 | 1 | 1 |
ENSDART00000058443 | Nonsense | 149 | 225 | 1 | 1 |
ENSDART00000058443 | Nonsense | 149 | 225 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 25 (position 36590449)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 34998065 |
GRCz11 | 25 | 35503004 |
KASP Assay ID:
554-5565.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTGAAGCGAGAGATCGAGCAGATCGGCGAGGCTTTCACCAACGTGGAG[A/T]AATCTCTGCTGGAGCTGGAGAGCAAGTTCAAGCAGAGCCAGGAGACGGAG
Long Flanking Sequence:
CAGACTCGGATTACAGCCCTGTGGGTCTCCTCTAGTGCGCACACTTCTATGAAGCGCTCCAGATGTGGACGTCGCCTCTGTCAGGCCGGTCAGACCTCCGCCGTGGACAGAAGCGATCTATCATGTTACCCTTTGCCCTCGGCCTGTTTTTACTGCCTCTTTGTGGCGCGGTCTACGAGGGACCTTTGCTCCCCGAAATGTCCAATGGCACTTTTCACCACTTCTTCGTCCCGGACGGCGATTATGAAGAGACTGAAGACCCCGAGAAGTGCCAGATGCTCTTCAAATGGATCGACCGCAGACCGTGTCCACTGGAGGAAGACCGGGACACGGTTATTAGGGAGGATTTCGTTATAGTAAAGCAGCAGATTGAAGACGCGGCGCGCGTTCTGGAGACTCTCGGGAAGAGCATCTCGTTTGATCTGGACGGAGAGGACAGCTACGGGAAATACCTGAAGCGAGAGATCGAGCAGATCGGCGAGGCTTTCACCAACGTGGAG[A/T]AATCTCTGCTGGAGCTGGAGAGCAAGTTCAAGCAGAGCCAGGAGACGGAGCAGAGAGAGGAGAGCGAGTTCAGCAGTAACTTCATCAAGCCCGTGTATGATGTGAGAGAAACGCTGCAGGAGACGCTGGACATCTCATCCGGACTCAAGGATAAACACGAGCTCATTTCTCTGATCGTGAGGAATCACGGCTCCAGGCTAAGCAGGCTGAAAAACGACTATCTGAACGTTTAAGACTTCCTGGGCAGACTTCAGTCCACTTTGGATTGTTCATTTGCGAGTTGTTTTGAAAGACGGAGCTCTAAATGTTCTCCGCTTCTGAAAGTATTTGGTGGTTTTGAGGTTCATTCACTCGTAATAGTTGTAATGCGTTTCCTCGGAGATTAAACATCAGCTATTGATGCTTTAGTGTGCGTTCATAGAAGTTCTTTGATTCAATTCAATTTAATTCATCTTTATTTCTACACTGAAAAAAATTATTCAAAGATGACTCCTTGGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13086
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058443 | Nonsense | 149 | 225 | 1 | 1 |
ENSDART00000058443 | Nonsense | 149 | 225 | 1 | 1 |
ENSDART00000058443 | Nonsense | 149 | 225 | 1 | 1 |
ENSDART00000058443 | Nonsense | 149 | 225 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 25 (position 36590449)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 34998065 |
GRCz11 | 25 | 35503004 |
KASP Assay ID:
554-5565.1 (used for ordering genotyping assays)
KASP Sequence:
ACCTGAAGCGAGAGATCGAGCAGATCGGCGARGCTTTCACMAACGTGGAG[A/T]AATCYCTGCTGGAGCTGGAGAGCAAGTTCAAGCAGAGCCAGGAGACGGAG
Long Flanking Sequence:
CAGACTCGGATTACAGCCCTGTGGGTCTCCTCTAGTGCGCACACTTCTATGAAGCGCTCCAGATGTGGACGTCGCCTCTGTCAGGCCGGTCAGACCTCCGCCGTGGACAGAAGCGATCTATCATGTTACCCTTTGCCCTCGGCCTGTTTTTACTGCCTCTTTGTGGCGCGGTCTACGAGGGACCTTTGCTCCCCGAAATGTCCAATGGCACTTTTCACCACTTCTTCGTCCCGGACGGCGATTATGAAGAGACTGAAGACCCCGAGAAGTGCCAGATGCTCTTCAAATGGATCGACCGCAGACCGTGTCCACTGGAGGAAGACCGGGACACGGTTATTAGGGAGGATTTCGTTATAGTAAAGCAGCAGATTGAAGACGCGGCGCGCGTTCTGGAGACTCTCGGGAAGAGCATCTCGTTTGATCTGGACGGAGAGGACAGCTACGGGAAATACCTGAAGCGAGAGATCGAGCAGATCGGCGAGGCTTTCACCAACGTGGAG[A/T]AATCTCTGCTGGAGCTGGAGAGCAAGTTCAAGCAGAGCCAGGAGACGGAGCAGAGAGAGGAGAGCGAGTTCAGCAGTAACTTCATCAAGCCCGTGTATGATGTGAGAGAAACGCTGCAGGAGACGCTGGACATCTCATCCGGACTCAAGGATAAACACGAGCTCATTTCTCTGATCGTGAGGAATCACGGCTCCAGGCTAAGCAGGCTGAAAAACGACTATCTGAACGTTTAAGACTTCCTGGGCAGACTTCAGTCCACTTTGGATTGTTCATTTGCGAGTTGTTTTGAAAGACGGAGCTCTAAATGTTCTCCGCTTCTGAAAGTATTTGGTGGTTTTGAGGTTCATTCACTCGTAATAGTTGTAATGCGTTTCCTCGGAGATTAAACATCAGCTATTGATGCTTTAGTGTGCGTTCATAGAAGTTCTTTGATTCAATTCAATTTAATTCATCTTTATTTCTACACTGAAAAAAATTATTCAAAGATGACTCCTTGGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12551
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058443 | Nonsense | 149 | 225 | 1 | 1 |
ENSDART00000058443 | Nonsense | 149 | 225 | 1 | 1 |
ENSDART00000058443 | Nonsense | 149 | 225 | 1 | 1 |
ENSDART00000058443 | Nonsense | 149 | 225 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 25 (position 36590449)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 34998065 |
GRCz11 | 25 | 35503004 |
KASP Assay ID:
554-5565.1 (used for ordering genotyping assays)
KASP Sequence:
ACCTGAAGCGAGAGATCGAGCAGATCGGCGARGCTTTCACMAACGTGGAG[A/T]AATCYCTGCTGGAGCTGGAGAGCAAGTTCAAGCAGAGCCAGGAGACGGAG
Long Flanking Sequence:
CAGACTCGGATTACAGCCCTGTGGGTCTCCTCTAGTGCGCACACTTCTATGAAGCGCTCCAGATGTGGACGTCGCCTCTGTCAGGCCGGTCAGACCTCCGCCGTGGACAGAAGCGATCTATCATGTTACCCTTTGCCCTCGGCCTGTTTTTACTGCCTCTTTGTGGCGCGGTCTACGAGGGACCTTTGCTCCCCGAAATGTCCAATGGCACTTTTCACCACTTCTTCGTCCCGGACGGCGATTATGAAGAGACTGAAGACCCCGAGAAGTGCCAGATGCTCTTCAAATGGATCGACCGCAGACCGTGTCCACTGGAGGAAGACCGGGACACGGTTATTAGGGAGGATTTCGTTATAGTAAAGCAGCAGATTGAAGACGCGGCGCGCGTTCTGGAGACTCTCGGGAAGAGCATCTCGTTTGATCTGGACGGAGAGGACAGCTACGGGAAATACCTGAAGCGAGAGATCGAGCAGATCGGCGAGGCTTTCACCAACGTGGAG[A/T]AATCTCTGCTGGAGCTGGAGAGCAAGTTCAAGCAGAGCCAGGAGACGGAGCAGAGAGAGGAGAGCGAGTTCAGCAGTAACTTCATCAAGCCCGTGTATGATGTGAGAGAAACGCTGCAGGAGACGCTGGACATCTCATCCGGACTCAAGGATAAACACGAGCTCATTTCTCTGATCGTGAGGAATCACGGCTCCAGGCTAAGCAGGCTGAAAAACGACTATCTGAACGTTTAAGACTTCCTGGGCAGACTTCAGTCCACTTTGGATTGTTCATTTGCGAGTTGTTTTGAAAGACGGAGCTCTAAATGTTCTCCGCTTCTGAAAGTATTTGGTGGTTTTGAGGTTCATTCACTCGTAATAGTTGTAATGCGTTTCCTCGGAGATTAAACATCAGCTATTGATGCTTTAGTGTGCGTTCATAGAAGTTCTTTGATTCAATTCAATTTAATTCATCTTTATTTCTACACTGAAAAAAATTATTCAAAGATGACTCCTTGGATT
Associated Phenotype:
Not determined