ZMP
si:ch211-225g23.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
FNBP1
Human Description:
formin binding protein 1 [Source:HGNC Symbol;Acc:17069]
Mouse Orthologue:
Fnbp1
Mouse Description:
formin binding protein 1 Gene [Source:MGI Symbol;Acc:MGI:109606]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37226 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17043 | Nonsense | Available for shipment | Available now |
sa18638 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37226
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065862 | None | None | 639 | None | 18 |
ENSDART00000132002 | Nonsense | 65 | 562 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 6227717)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 6201921 |
GRCz11 | 21 | 6307429 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATGTTGTATTAATGATGAATGTGTTTGTTTGTGTGTGTGTGTCAGATA[T/A]ACGTGGTGCCGTGCATTTCATTCAACGTTGAACGAGCTGAACGATTACGC
Long Flanking Sequence:
ATTTTTGTGACACACAACTTTAAAAGGTGTGTGTTAAAGCTGTTATAGTCTGTCAGATCTGTGTTTCAAACACGAGAGAAAATGTTATAGTGAGCCCCGTTTCTTTTCGTTCTGCTTAATCACGTGCCCTAAAAAAAGATATTAAAAATAAACAAAACAAAATGAAGTCTTTTGACTGCTTTCTTTAATAACTACATTACACAATACTTGTACTTTTACTTTCAGTACTTGAGTAGTACATTTTAAAAATTAACAACTTGCAATACTTAAGTACAAAAAATGTTGTATACTTTAGCACTTCCACTTAAGTATGGTGCTTAAAGAGCACTTCAACTTCAACTCAAGTCACTTTTTTAATAGAGCACTTGTACTTTTACTAAAGTCTGGGTCTTTAGTACTTTGTACATCTCTGCCGACATTTTTGTTTGGGAAATTTTAGATTAGTCTCATGCATGTTGTATTAATGATGAATGTGTTTGTTTGTGTGTGTGTGTCAGATA[T/A]ACGTGGTGCCGTGCATTTCATTCAACGTTGAACGAGCTGAACGATTACGCCGGTCAGCATGAGGTCATCGCGGAGAATATGATGTCACAGATCATCGCTGAGCTCACCAGATACTCTCAGGAGATCAAAACAGAGAGGAAAACGGTGAGTCCAAATATTCAGCTCATCTTTATTTCTATAGCGCTTTTACAATGTAGACTGCCAGAGCAGCTTGACATAAAAACCTTCTAATAAATTATAACTGCTTCAGTCCAGTTTTCAGAGTTGAAGTTCAGTTTAGATTAATATAAATGTCACTGCTAAAGCCCAAACACTGAAGAGCGAAAGAAAAAACGTCATAATACTGTGATTGAACTATTGAGCTGCCTTTTATCTAGAGTTTATAAACACATATAATATTTTTTTCACAATTTTTGTATCCATCCTAATTGTAAGTTGGTGGCTTAGTGGTTAGCACAGTCGCCTCACAGCAAGAAGGTCACTCATTTGAGTCCTGGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17043
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 |
---|---|---|---|---|---|
ENSDART00000065862 | Nonsense | 246 | 639 | 8 | 18 |
ENSDART00000132002 | Nonsense | 246 | 562 | 8 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 6294380)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 6232716 |
GRCz11 | 21 | 6338224 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGACGTTTGCGGAGGTGGACCGACAGATTCTGCCCATCATTGGGAAATG[T/A]CTGGATGGAATGACACAAGCRGCCGAGTCCATTGAATCCAAGACTGTTAG
Long Flanking Sequence:
CTAAATCAGGTGTGTTTGGTTGAGGAGAGATGTAAAATGTGCAGAGCTGGTGGTCCGCGGTTGAGAAACACTGCCCTAAACTGTCTGTATTATACATTATAAAACAAAATGATTATGTGTGATTGAAACATAAGGGTCCCCTCAATATAAAAATACAACATAGACACACACACACACACATGCACTGAGAATGAATTATAGCTACTGATGTTATCATTTATTTGCATGCACTGCCTGCATTGTTGTAGAGTTCTTTAAAAGAATTATGCAAATGAGCTTACTGTGAAAACACGCCCCAAAATCGTGAATGATTTGCATATGCAGTAGTGTGATTCCCGATCATGCAGCTGTCTGCTCTTAAATACACACTGTAACTTTTCATGTGTGTCTGTGGAGCAGAAAATCCAGGCGATGGAAGAGAAGAGAATAGAGCGGATGGGTGAGTCTCTGAAGACGTTTGCGGAGGTGGACCGACAGATTCTGCCCATCATTGGGAAATG[T/A]CTGGATGGAATGACACAAGCAGCCGAGTCCATTGAATCCAAGACTGTTAGTAACTCACACACACACGCACTTACACTCTCACATAACATACCATGTGCATAACACACATGCATCACAGATTTACACACACTCGACACACACATACACACACACACATACAGATTTATTCACGCTAAACTCTAGCGCTCTCTTCTGTCAGAATTATCTCTCATGTTTCCATTGCACAACACATTTTCTTCTTGAACACGACTCCTAATAAATTTAAACCTGCACTAATGCTGATCTAGGATCAGTCTGCCCTGAATGGATTAGATTATTGTAAGCCGCTGATACCTGATCCTACATCTGCAGGAAGTGTCGTTTTAGCAGGAGGAAATGTGTTGTAAAATTAAATTAAACTCTACCATTCAAAAGTTGAGGGTCATAATAGATTTAATAACTAATTTCTTATAACTCATTTCTTTTGTCTTTGCCATGATGACAGTATTATCTGCTATAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18638
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 |
---|---|---|---|---|---|
ENSDART00000065862 | Nonsense | 331 | 639 | 10 | 18 |
ENSDART00000132002 | None | None | 562 | None | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 6305713)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 6244049 |
GRCz11 | 21 | 6349557 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TYGCTGCTCTCTCTGTGGCTCGTGTCTTTACCGGTAGCTTATGTCCCTGT[T/A]AACGTCCCCCGTACCTCGCCAGCCCCCCCCTGACCCCCCCTCACCTTCTG
Long Flanking Sequence:
AAACAGCATAAATATCCTCCCTTGTGTTCCTCAGGAAAGTCAAAGTCACTGGCAGTGTTTGTTTTTGGTTGAACTGTCTCTTTAAGTGGTTCTGCAGTGATCTGAGCTCTGCATGCGACCCCTGATATGTATCTATATATATATAATATCCAGTTTAACGCACTAACTCTCTCGCTCAGTGATAACACCACCACAGCCACAGCGCAGTCTTTTGTTTTTTTGTTAATACTGTTTATTTACGTTTCATTTTTTGTCTTTCGGTTGCCCTTATTATTATTTTTTTTGGTTTCGTTTTTTTGTTCATTCCATTAATTGATTAATTGATTAATTCGTTGCCTTTAGTTCTGTAACATTTTTTGGGTCCTTATTTCTCTTGTTTTGTGTTCCCCTCCCTTCCTTCCTTTTGATTTTTTCCGGACCGATTTCTTTCCCCCCTCTGTCTGTCACTGGTCGCTGCTCTCTCTGTGGCTCGTGTCTTTACCGGTAGCTTATGTCCCTGT[T/A]AACGTCCCCCGTACCTCGCCAGCCCCCCCCTGACCCCCCCTCACCTTCTGCTGTGACCCCTGACCCCTGCCCCGCTCCCCAGACCCCCAAACAGTGCAAGGAGCCCCTGTCGCACCGCTTCAACGACCTCATGACCTCCAAGCCCAGAATGCAGTGCCTCAGGAGCCTGCGGCGAGGGGTGAGTATCTGCATGCTCTGCTCTGCCGGTCTGTCTGTCATCATCTGCTGCTGGACGTGTGCTGGAGGGAAAAAGGAGATGCATGAGGATTTCCTGCTGGTTTTTTGCATCGTAATGTAAATGTAAAACAACTGATAATGGCTGGCTGCTGATGTTATAGCAGAATGATTGTATTTAAACCTTAGGTCTCAAACTCAATTCCTGGAAGGCCGCAGCTCTGCACAGTTTTGTTCGAACCTTTCTTAATCCAACTAATCAAGATGATCCAAATGCTCAAGATGTTCAAGACTACTAGACACTAGTTGTCTTGAACACCTTTATT
Associated Phenotype:
Not determined