ZMP
flncb
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate filamin C, gamma (Actin binding protein 280) (FLNC) [Source:UniP
Human Orthologue:
FLNC
Human Description:
filamin C, gamma [Source:HGNC Symbol;Acc:3756]
Mouse Orthologue:
Flnc
Mouse Description:
filamin C, gamma Gene [Source:MGI Symbol;Acc:MGI:95557]
Alleles
There are 19 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15601 | Nonsense | Available for shipment | Available now |
sa12735 | Nonsense | Available for shipment | Available now |
sa31379 | Nonsense | Available for shipment | Available now |
sa20216 | Essential Splice Site | Available for shipment | Available now |
sa11171 | Nonsense | Available for shipment | Available now |
sa11278 | Essential Splice Site | Available for shipment | Available now |
sa20217 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15601
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 |
---|---|---|---|---|---|
ENSDART00000026492 | Nonsense | 65 | 2743 | 1 | 48 |
ENSDART00000134286 | None | None | 2248 | None | 40 |
ENSDART00000026492 | Nonsense | 65 | 2743 | 1 | 48 |
ENSDART00000134286 | None | None | 2248 | None | 40 |
Genomic Location (Zv9):
Chromosome 4 (position 9129464)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10066222 |
GRCz11 | 4 | 10067032 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAACACCTTCACCAGGTGGTGCAACGAACACCTGAAATGCCTCAACAGA[A/T]AGATCCTRGAYCTGCAGAAGGACCTGACCGACGGGCTCAAGCTCATCGGG
Long Flanking Sequence:
TTTTTGTGACGACGACAGAAAAGTGGCGAATGGAAGACTTTAAATACGATTGTTTTTAAACTGTTCGTGGCTTGAAGGTAATTCCAAGTGGTCTCTGTATGACAGATACTTTATTACTACTGACTTTTTTCGCAAACGCTTCCAACTTTCTTTCGTTTCTTTCCTTCTTTTTTCATCAGAAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGCGCGCCTGCCCCACTCCCCCCTCACGCTGTAAGAGTCTCGTAGTTTGTAGAATAAAAGGGGGCACGAAAACATCGGAAAAACATGATGAGCAATAATACATACTACGACCAGCAGCTGCCGCCGCAGTATTACCAGGGCACCGACAACGGCGAGGACGGAGACGAGGAGATGCCGGCCACGGAGAAGGACCTGGCCGAGGATGCGCCCTGGAAGAAGATCCAGCAGAACACCTTCACCAGGTGGTGCAACGAACACCTGAAATGCCTCAACAGA[A/T]AGATCCTGGATCTGCAGAAGGACCTGACCGACGGGCTCAAGCTCATCGGGCTCCTGGAAGTTCTCAGCCAGAAGAAAATGTACAGAAAGTACCACGCCAGACCCAATTTCAGGCAGATGAAGCTGGAGAATGTGTCAGTGGCGCTGGAGTTTCTGGAAAGGGAACACATCAAACTGGTTTCAATAGGTAAGTGCGCTTTCCTGGCATACATATGCGCTCAATGCGGTGGCGAACGCACTTTGGTACAATGCCATGCCACTTAACTATTTATAACTATCATAAAAGTGTTTAAAAGGTTACAGAGTGCTTGTTACAAGTGATGTTTGAATGATCAATTAAGTGATGTGCTCGAGCTGCGTACTGTCGCTATGGTTACCTCATCAATTCGTCATGGTTTCTACTAAGTGCACTAGTAAGCTGACTTGTGTGGTTAGTGAAACGTTTCTAATCTTTCAACGTGTACTTATATAATGTAAACCTACTTTTAAAAGCCTCCTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12735
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 |
---|---|---|---|---|---|
ENSDART00000026492 | Nonsense | 65 | 2743 | 1 | 48 |
ENSDART00000134286 | None | None | 2248 | None | 40 |
ENSDART00000026492 | Nonsense | 65 | 2743 | 1 | 48 |
ENSDART00000134286 | None | None | 2248 | None | 40 |
Genomic Location (Zv9):
Chromosome 4 (position 9129464)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10066222 |
GRCz11 | 4 | 10067032 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAACACCTTCACCAGGTGGTGCAACGAACACCTGAAATGCCTCAACAGA[A/T]AGATCCTGGAYCTGCAGAAGGACCTGACCGACGGGCTCAAGCTCATCGGG
Long Flanking Sequence:
TTTTTGTGACGACGACAGAAAAGTGGCGAATGGAAGACTTTAAATACGATTGTTTTTAAACTGTTCGTGGCTTGAAGGTAATTCCAAGTGGTCTCTGTATGACAGATACTTTATTACTACTGACTTTTTTCGCAAACGCTTCCAACTTTCTTTCGTTTCTTTCCTTCTTTTTTCATCAGAAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGCGCGCCTGCCCCACTCCCCCCTCACGCTGTAAGAGTCTCGTAGTTTGTAGAATAAAAGGGGGCACGAAAACATCGGAAAAACATGATGAGCAATAATACATACTACGACCAGCAGCTGCCGCCGCAGTATTACCAGGGCACCGACAACGGCGAGGACGGAGACGAGGAGATGCCGGCCACGGAGAAGGACCTGGCCGAGGATGCGCCCTGGAAGAAGATCCAGCAGAACACCTTCACCAGGTGGTGCAACGAACACCTGAAATGCCTCAACAGA[A/T]AGATCCTGGATCTGCAGAAGGACCTGACCGACGGGCTCAAGCTCATCGGGCTCCTGGAAGTTCTCAGCCAGAAGAAAATGTACAGAAAGTACCACGCCAGACCCAATTTCAGGCAGATGAAGCTGGAGAATGTGTCAGTGGCGCTGGAGTTTCTGGAAAGGGAACACATCAAACTGGTTTCAATAGGTAAGTGCGCTTTCCTGGCATACATATGCGCTCAATGCGGTGGCGAACGCACTTTGGTACAATGCCATGCCACTTAACTATTTATAACTATCATAAAAGTGTTTAAAAGGTTACAGAGTGCTTGTTACAAGTGATGTTTGAATGATCAATTAAGTGATGTGCTCGAGCTGCGTACTGTCGCTATGGTTACCTCATCAATTCGTCATGGTTTCTACTAAGTGCACTAGTAAGCTGACTTGTGTGGTTAGTGAAACGTTTCTAATCTTTCAACGTGTACTTATATAATGTAAACCTACTTTTAAAAGCCTCCTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31379
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 |
---|---|---|---|---|---|
ENSDART00000026492 | Nonsense | 278 | 2743 | 4 | 48 |
ENSDART00000134286 | None | None | 2248 | None | 40 |
Genomic Location (Zv9):
Chromosome 4 (position 9161999)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10098757 |
GRCz11 | 4 | 10099622 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTACCTGTCGCAGTTCCCCAAAGCCAAACTCAAGCCTGGTGCACCACTG[C/T]GACCCAAAACTCTGCACCCCAAGAGAGCCAAGGCCTACGGACCAGGTCAG
Long Flanking Sequence:
ACGGGACTGAAGGGAGCGTAGAGACAGAAAATATTTTCCACAGCTCTCCTTAAGTGTACTTCATCAGTTTGTGCCGTAGACCATCACTATGTTTATATCTGACGATCGATTCTGGCAGTAGAAGTACTCAAAGGAAATGTCAAATAAAGACAGTGAGATGTGCTTCTTCATCTGTTTTAGCTCCTGAGGGCTGCGGCAATGGACATTTATGGTGTTTTGCCATCTGATAAAGCTATTATAGGTCAATGTTTCACTAATAGTAAATAAAATGACTTGTATTGAAGTGTTTGATGAGGAAAACATCCAAAATGTTGTACTAGTTTCCCCAAGAGCTTGACAGAGGAATTGGCACTATGACTGATCTCTAAGTTTGCACTCTGCTCTGTTTCATCCAGGTCATTGCTCCAGAGGAGATTGTGGATCCTAATGTGGACGAGCATTCGGTGATGACCTACCTGTCGCAGTTCCCCAAAGCCAAACTCAAGCCTGGTGCACCACTG[C/T]GACCCAAAACTCTGCACCCCAAGAGAGCCAAGGCCTACGGACCAGGTCAGACCAAAAAAAGATGATGTTAAAACTTTTGATTGGCAGACAGTGGTTATGAATCACGACTTTTACTGTAACACAAACTTCTGCATCTTTCATCTTCCTATAGGTATTGAGCCCAGAGGGAACGTTGTGTTGAAGCCAGCCGAGTTTGTGGTGGAGACCGTGGAGGCCGGGCTTGGAGAGGTGTTGGTCTACATTGAAGATCCAGAGGGACACACAGAAGAGGTCATCTACTAACTCAGCTCAACTTCTTTCATTGTCAAAGTCAAACGTCTTTCAGCCAGGGGTATTTACACATCGACTGGGTTTCTGGTTGCATTGGCTAAATTTAAGGCTATGTTTACACAGAAGTTTTACCATTGCATTTTAAAAGTTTCACTTTTAAGCAAGACCATTTTAAACAAAATCATTGGCATTTACATGTCCATGTAAATAGGTAAAAATGCTGAATTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20216
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026492 | Essential Splice Site | 479 | 2743 | 8 | 48 |
ENSDART00000134286 | None | None | 2248 | None | 40 |
Genomic Location (Zv9):
Chromosome 4 (position 9163938)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10100696 |
GRCz11 | 4 | 10101561 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCCGGCCAGCAAATACCCAGAAGTCCTTTCACTGTGCACATCTCAGAGG[G/T]TGAGACCCATGTCCTCACTTCTGGACTTAATTCCTTTAAGAAATGTATTG
Long Flanking Sequence:
TACAGTCTTCTTAAGTCTTCATATCAGTAGTTTTATTTCTGTTTTATTGTCTTGCAGGTGAAAGTTTTGTTTGCTGGACAGGACATTGACAGAAGCCCTTTCTTAGTAAATGTGTCTAAAGCACTGGGAGACCCAAACAAGGTGCAGGCCAGAGGGCCAGGTTTGGAACCGGTGGGCAACGTGGCCAATAAACCCACCTATTTTGACATCTACACTGCAGGTAATGTCAGGCAAATAATTCTGTTTGTTCTTAGACCCGAGAGCAGTTTAAGATCATCTGTGTATTTGTGACTCCTCAGGTGCAGGAGCAGGTGATGTTGGTGTGATCATTGTGGACTCTCAGGGCCGTAGAGACACAGTGGAGATCATTCTGGAAAACAAGGGTGACAGTGTTTTCCGTTGCACCTATGGCCCCATTCTGGAGGGCCCTCACACTATATATGTGACATTCGCCGGCCAGCAAATACCCAGAAGTCCTTTCACTGTGCACATCTCAGAGG[G/T]TGAGACCCATGTCCTCACTTCTGGACTTAATTCCTTTAAGAAATGTATTGATTTTCTGGAGTCATTTTGCAGTCACGTTGTTCTTTGGTACCTAAGCTGTTAATGCACCAAGAATACAACAAGTTCTTTGTTGACTTGATGTTTTTTGCTGCATTAAAAGCATGTCATGTGCTTTTTAAAATGTTTACTGCCCTCTCTGAAAAGGCCAGCTCAGACTAGTGTGGTAAAACTGCTTTACTTGCTGGTTTAGACGACTGGTGAAAACTCAAGGGCTAAATTCCGGATCTAATAAGTTTTATCAAGCTGGCTTTTTCAATGGGGGCATTATGCACAAATGGAGCTAGATTTTCCAAACTAAAGGTACGGTCACACTTATGATTAAATTTAATTAATCAAACAGGCAAAATTTACTCATTGGTAAAAGAGTGAAACGTTACACATGCAGACTTCTCTCATAATCATATTGTTTACAGAACTTCACCATGCTGACCAACAGAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11171
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 |
---|---|---|---|---|---|
ENSDART00000026492 | Nonsense | 728 | 2743 | 14 | 48 |
ENSDART00000134286 | Nonsense | 247 | 2248 | 6 | 40 |
Genomic Location (Zv9):
Chromosome 4 (position 9168177)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10104804 |
GRCz11 | 4 | 10105669 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTTGTCCTTCTTTTATYCAAGGACTCAGAAGGGTTTCCCATCAACATC[C/T]AGATCACAGATWAYGGCGACAGCACATATTTCTGCGTCTATATACCCATC
Long Flanking Sequence:
TTTCCATCGAAGGGCCCTCGCAGGCTAAGATAGAGTGTGATGACAAGGGTGATGGCTCTTGTGATGTTTTGTACTGGCCCACTGAGCCAGGGGACTATGCAGTCCATGTCATCTGCGATGATGAAGATATTAAAGACAGCCCCTTTATGGCCCACATCCTCCCTGCAGCCAGTGACGTTTTCCCTGAGAAGGTCTGTTTTGTGGTGCTTGGCAATAATGATTGTACATTCAATAGGGATAATAAATAACTGTGGTACTGAAAGTCATGTTTTTATGCAGGTTAAGTGTTACGGCCCCGGGCTGGAGCCAACCGGGTGCATCGTAAATAAACCTGCAGAGTTTACAATTGATGCCCGTGGAGCTGGAAGAGGACAGCTACAAATTTATGCTCAGGTACATTTTCATACAAGTCCCAGATGCCTCATGCTTCACTTCACTGGTGCAAAAACCTTTTTGTCCTTCTTTTATCCAAGGACTCAGAAGGGTTTCCCATCAACATC[C/T]AGATCACAGATAACGGCGACAGCACATATTTCTGCGTCTATATACCCATCAAGCCCATCAAACACACTATCATCATCACATGGGGAGAGGTCAACGTTCCCAACAGTCCTTTCAGGGTGAGAGCTCACTGTCAACAGGCAAATTTCACCCGGCTGATGACATTTTTATGATGCTGTTGGTCAAGAACGTTCATAAATTGGATCTGCAGCAAGCTTAGCCTTTCAATGAAAGTTCATGACCACATTTTTCCAGTGTTAGATTTCACACTTTGCCTTTGCGTGACCATGTTAGATCATAGGTTCCATATTGGATCATAAGCTTTACTAGAATCACTGTCCTCCATAAGATTTCAGTTACTACTTTTACAATATATTTATAAATATATAATTGACATATCTCAGGTGACCATTGGAGAAGGCAGTCACCCTGAGAATGTGAAGGTTCATGGACCAGGAGTAGAAAAGACTGGCTTAAAGGCCAACGAACCCACATACTTCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11278
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 |
---|---|---|---|---|---|
ENSDART00000026492 | Essential Splice Site | 861 | 2743 | 16 | 48 |
ENSDART00000134286 | Essential Splice Site | 375 | 2248 | 8 | 40 |
Genomic Location (Zv9):
Chromosome 4 (position 9168955)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10105582 |
GRCz11 | 4 | 10106447 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACCCCCTGGTGCTGGACGCTACACMATCATGGTGCTATTTGCAGATCAA[G/A]TAAGGCTCAKTCAATAATRTGATRTGACTCATAAGCAATCTAAAATCTGA
Long Flanking Sequence:
CGTGACCATGTTAGATCATAGGTTCCATATTGGATCATAAGCTTTACTAGAATCACTGTCCTCCATAAGATTTCAGTTACTACTTTTACAATATATTTATAAATATATAATTGACATATCTCAGGTGACCATTGGAGAAGGCAGTCACCCTGAGAATGTGAAGGTTCATGGACCAGGAGTAGAAAAGACTGGCTTAAAGGCCAACGAACCCACATACTTCACAGTGGACTGCAGTGAGGCTGGACAGGGTCAGAACCAACATCATTGATATCATTATTCTAATCTGCATTTTACATTTATTTAGTGATCATTACTTATTTGTCTTTTCCGATTCCATAGGAGATGTAAGCATTGGGATTAAGTGCGCTCCTGGTGTGGTGGGACCTGCGGAAGCAGATATTGATTTTGACATCATTAAAAATGACAATGACACATTCACAGTGAAGTATACACCCCCTGGTGCTGGACGCTACACAATCATGGTGCTATTTGCAGATCAA[G/A]TAAGGCTCAGTCAATAATGTGATATGACTCATAAGCAATCTAAAATCTGAAATCTAAAATCTACTTTTTCAATTTACCAACAGGAAATTCCCATCAGCCCCTTCCGTATCAAAGTTGATCCATCTCATGATGCTAATAAGGTCAAAGCAGAGGGTCCTGGCCTCAACAAGACAGGTCTGTTTTATAGACAATGACTGAAAGTTTGCAAAATAATAGGTGAGGATATCTAATCTCATCATAATTTATATGTCTATATCACAGGTGTGGAAGTGGGCAAGCCAACCCACTTTACAATCTACACTAAAGGAGCAGGCAAGGCCACACCTGAGGTTCACTTCACTGCATCTGGTAGAGGAGATGCTGTCAGTGACTTTGAGATCATCGATAACCATGACTATTCTTTCACTGTGCGCTACACTGCATTACAGCAGGTGAGACATTCTGGCACCAGGTTATAGTTCATATAAATGGACACTAAAGCCTGATTAATTCTTCTGCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20217
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026492 | Nonsense | 1936 | 2743 | 35 | 48 |
ENSDART00000134286 | Nonsense | 1449 | 2248 | 27 | 40 |
Genomic Location (Zv9):
Chromosome 4 (position 9180477)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10117104 |
GRCz11 | 4 | 10117974 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGATGGCACCTGCACTGTATCCTACCTGCCAACGGCCCCGGGAGACTA[C/A]AACATAATCGTCAAATTTGATGACAAGCACATCGCTGGAAGCCCCTTTAC
Long Flanking Sequence:
TACTTGCTCTCTTTAGATCCCAATATTGAATGTTAAATTGAATACATAAACTGTCTTTTCTTTGTGATTATTCAAAAATATTAAAATTTAAAACTTTTTATTTTAAACTTTCAGTTAAATGATTAAAAAATACACTTTTAATAACTATTCCACAAATTCTGGCTCTCTTTTATTATTTCCCTACAGGAAGCCCACTGCAGTTCTATGTGGATGCCATTAACAGCGGGCATGTGAATGCATACGGCCCTGGTCTGAGTCACGGGATGGTCAACAAATCCGCTACATTCACAATCGTCACTAAGGATGCTGGAGAAGGTAATGCCCACAGCAAACCTACAATCCCCCCATTCACATTGCATTAGTTTCACATTGCACTCTCATCTTCTCCCAGGTGGTCTGTCATTGGCAGTGGAAGGACCCTCCAAGGCAGAGATCAGCTGTAAGGATAATAAAGATGGCACCTGCACTGTATCCTACCTGCCAACGGCCCCGGGAGACTA[C/A]AACATAATCGTCAAATTTGATGACAAGCACATCGCTGGAAGCCCCTTTACAGCCAAGATCACAGGTTTGTGTGTGCCCATATTTGGGTATGAGTAAGAGAGCAGGAGGATGAACAAGAGAGGGCAAAGTTATGTCTCTCCATAATGTCTGTGAATCACTAAATTAGCTGGCATGTGTGTTTATGTGTGTGCGCGTGCATTCACACCGGGAGAATTTAACCACATCTGTAAAGTGCTTCTAAAAGTAGGAGGCCCTTTCAGAGAGTTTTAAGAAACAGGAAGCAGCTGTTTCCCCCCTCCTTTAGTCTCACTCTCACTTTGCCCCTCAAAAAACGGTTCTAGTCTGCGGAAATAGGGTTGCACCCACAGAGCAAATGCTTATTTTAATAATTATATCATATTTGTTAATTATAATAATTATAAAAGAACTATTTTTACGTTTTGGCTAGGTTTACATGTTTGAATAAACTCACAAAGATTGCATTTGTTTGATCAGGATTA
Associated Phenotype:
Not determined