ZMP
fnbp1l
Ensembl ID:
ZFIN ID:
Description:
formin-binding protein 1-like [Source:RefSeq peptide;Acc:NP_001003634]
Human Orthologue:
FNBP1L
Human Description:
formin binding protein 1-like [Source:HGNC Symbol;Acc:20851]
Mouse Orthologue:
Fnbp1l
Mouse Description:
formin binding protein 1-like Gene [Source:MGI Symbol;Acc:MGI:1925642]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34354 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa41155 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa34355 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34354
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 |
|---|---|---|---|---|---|
| ENSDART00000045038 | Nonsense | 124 | 548 | 5 | 14 |
The following transcripts of ENSDARG00000020131 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 15573727)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 15019071 |
| GRCz11 | 8 | 15056776 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTGTGTGATCAACAGCATCTTCAGGAGGGACGGAAGGCCCAGCAGTA[T/A]CTAGACCAGTGCTGGAAACACATGGACAATGTGAGTCATTTTAGCGTTAC
Long Flanking Sequence:
CAATGATTTTTTTAAAACACCTGTTGTTTTTTTTCTAATTCACACACCTGCTTTTTGCCTGCAGCCTTGTGTTTATAACCGAATAACAGCCATGCTAATATATAGTTACATATTGTAATCCTACAAATTCATAGCATGATTTGTATTTGGTGTAGGGAAGTAGTAATTAAGTACTTCAATTTCTGCCTTATAAAACAATGGTGAAATGTTCTTCATTTGTTGTATATTGTCTTCTTGCAGGTTCACGTCTTGTCTGTCATTCTACGCCATCCTGAATGAGCTGAATGACTATGCTGGTCAGCGAGAGGTTGTTGCAGAGGAGATGGGCCACAAAGTGTATGGAGAGCTCATGAGATACTCACAAGACCTGAAGGGAGAGAGGAAACATGTGAGTGCCCGAAATACACCCCTGGGGCATGCTGGTGCAGGACAAGACTATAATAATGTGCTTGTGTGTGTGATCAACAGCATCTTCAGGAGGGACGGAAGGCCCAGCAGTA[T/A]CTAGACCAGTGCTGGAAACACATGGACAATGTGAGTCATTTTAGCGTTACTAATATTTTGGATACTGATACTTTGGTTCTGGAAATGAGTTGTACTGGGTAGAGTCTCGGTTATGGTCCTGTGCATGTTTTTATTCCGCTGCACATGCTTGTGAAACTCTACTTGGTTGATTTATACAAACATTTGTGTATAATCATCTGTCATTTGTCAATCTATATTCATTTGTTATTAATATTAATCGTAACAACAACAAATAGTTATTTATATTCATTTGACTACATGATATTAAAATAAAAACAAAATCATTTTAATTTTCTCCAGATATTCTCTTCATAGTAATATTTATATGTCAATGTTTTATTATTTGTATTAATAGTATTAGTATTGTTGTTATTATTATTTTTATTATTATTATTAGTAGTAGTAGTAGTAGTAGCACCAACATATAATTATTAAATTAATTAATGCTATTTAATTATTATTGGTTTTTATTCTTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41155
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 |
|---|---|---|---|---|---|
| ENSDART00000045038 | Essential Splice Site | 169 | 548 | 6 | 14 |
The following transcripts of ENSDARG00000020131 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 15578833)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 15024177 |
| GRCz11 | 8 | 15061882 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGAGAGGTTAGACAATGACATCAACGCCACAAAGTCAGAAGTCGAAAAG[G/A]TATTCCTGTTCTTCACTTGAATTCTTACAGTTATTGACTGAATCTTGTTC
Long Flanking Sequence:
AAGTCTGAAATTTCATTCGTAATGATCTCAAAAAGGTCTTTAAAAGTCTTTAATTTGACCAGGAGAAACCTGTTGAAACCCTGATTTGCACTACTAATCAAAAGTCTGCCAAAGAAGAAACCTTTTTCTCATTGCCAATATTACATTTAGTTAATACAAATAATTAAATTGATCATGAATATGCAGGCTATTTGACCAGTATACACTTCTTTTTAAAAACCAATTGTACTCCCTCAAACTTTTGACTGGATGTGTATGCCACTGCTGCATCATCTCCTGACAGATTTTGGGACTGTATTTACGCAGAAAGATCATTAATGATCTGGTAGGGTTGCAGGAAATGTGTCATGCTTGTTTGGACTACATGTGTCTGCATTTCTGTATGGATTTAACAGAGTAAAAAGAAGTTTGAACGGGAATGCAAAGAGGCGGAGAAATCGCAGATGATGTACGAGAGGTTAGACAATGACATCAACGCCACAAAGTCAGAAGTCGAAAAG[G/A]TATTCCTGTTCTTCACTTGAATTCTTACAGTTATTGACTGAATCTTGTTCTGATAACATTGTAAAACATCACTTGCTGTTGGGGCTAATACTGGAAGCCTCGGCTGTATTCCTGAGGTATTAGTAATACAGATGACCAATCATTCTGTCCTAGGCAAAGTCCCAGCTGTATCTGAGACAACACATGGCGGAGGAGAGCAAGAACGAGTACGCGGCCCAGTTGCAGAACTTTAATGGTGAACAGTGGAAACATTTCAACCAGGCCATCCCTCAGATATTCACTGTAATGACATCTCTCATCTTTTAGTTTCTAAAAATTCAATTGTGATGTTTGAGTTAGTTCATCAAAGCTAAGCTTAAAGTTAAAACCATTTGTTAGCATGTTTTAGCATGTTTGCAGCATAATGTAGCACACTGCTTGTGTGTTTTAGCGCTTACTTAGCATCTTTCCACTATGATTTACTTTCCTGCTTGTGTTCTGGCACATTTCTGCCATCTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34355
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000045038 | Nonsense | 343 | 548 | 10 | 14 |
The following transcripts of ENSDARG00000020131 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 15587171)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 15032515 |
| GRCz11 | 8 | 15070220 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTGTACAGGCGCCAACACTAGAGGATCTCAGCCACCTTCCCCCTGAA[C/T]AGAGACGCAAAAAACTACAACAGCGGATCGATGAGCTGAATAAAGAACTG
Long Flanking Sequence:
GTAGGCCTGCCATTCTGTGGCTAAAATCATCAGCCAAAAGACATTCACTTGACTGGTGTTGATGAGCGATTTGTTGTCTTTGTTCTTGCTGAATTGGCGTGACCTAACCTTAACCTCTCAGTGGTCTTTAAAGCTGGTAAGTGTAGTGTGTTTTGGACTGCTGTACTCTAGATATAAGGTTTGAGAATAGACTTTGTGTTTAGTTGTAGTATTCAGCCATAAAACCCCTTTACTCCTCTTGTCGTTCAGCTTCAAGATGTCTTTCTTACAGTGCGGCTTAAAGTTTATAAACTATCGTCTGAATTCCAGAATTGGAATGTATGCAAACATAAGGGCTCAGCGTTAAACTGTAGGAAAGACATCTCTCTTAAGAGTGACTGTTTATATAATGTGTGCTCAGACTGTGCCGGGATGTTTGTCAGTGCATCTTTGCCTCCAACCAATAACCTGTGTTTGTACAGGCGCCAACACTAGAGGATCTCAGCCACCTTCCCCCTGAA[C/T]AGAGACGCAAAAAACTACAACAGCGGATCGATGAGCTGAATAAAGAACTGCAGAAGGAACAGGACCAAAGGTAGACAATGAAGACATTTTATTATGTAGCATAGTGTTTTTGTTCAGATTTGCTATCTTTGTAATTGTATTCTGTATGCTACTAACCATCAATACAGGAAAACGCATTCATTTTTTAATTTATTTAATTTGGTATTATCTAATACAAGATGTCTTTTAAAAATATTTTATATTAACTAATTTATGCATTATTTGCTTGTTCAATTGTACAACAATACATTTTTATTATACTTTTATAATTTTTTATAATACTATAAATTATTTTGATGATAAAATTACATTGTTTATTGTAATTGTAATATTTTTAAAATAAAAATAAATTAAACATTTTCAGTAATTATTTTATAAATTTACTTGCTTAATTTTAGATATTAACAAATTAAAATAGTATTTATTTATAGTTTGTTGTTTTTTCGGCATTGTCGTTGTTG
Associated Phenotype:
Not determined