ZMP
fbln2
Ensembl ID:
ZFIN ID:
Description:
Fbln2 protein [Source:UniProtKB/TrEMBL;Acc:Q5BLE3]
Human Orthologue:
FBLN2
Human Description:
fibulin 2 [Source:HGNC Symbol;Acc:3601]
Mouse Orthologue:
Fbln2
Mouse Description:
fibulin 2 Gene [Source:MGI Symbol;Acc:MGI:95488]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15910 | Nonsense | Available for shipment | Available now |
sa21928 | Nonsense | Available for shipment | Available now |
sa21929 | Nonsense | Available for shipment | Available now |
sa16218 | Essential Splice Site | Available for shipment | Available now |
sa812 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15910
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 |
---|---|---|---|---|---|
ENSDART00000024992 | None | None | 468 | None | 10 |
ENSDART00000103481 | Nonsense | 240 | 328 | 1 | 2 |
ENSDART00000113707 | None | None | 1231 | None | 33 |
ENSDART00000131752 | None | None | 650 | None | 13 |
ENSDART00000132865 | None | None | 207 | None | 5 |
ENSDART00000134504 | None | None | 304 | None | 8 |
The following transcripts of ENSDARG00000015156 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 28154111)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 27030097 |
GRCz11 | 11 | 27277271 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATATGAGAAAAATAGATGARAAAGAGGAGGATGAGGAAGACTATGATTA[T/A]CCACCCACTGAYTACTCAGCTCCTTCTCATGATGATTTTGCGGCTCCCAC
Long Flanking Sequence:
GCAGAAGGAGAGTCATACTTTGTGGACTTTGGGAGTACTGAATGCTCTTGTCCACAAGGGGGTGGACGGATCAGCTGCCATTTTATACCATGTCCTGAAGTTCCAGCTAACTGCATAGAATTGTCGGAGCCGGCAGATGGGTGCATTCAGTGCGAGCGAGTAGGATGCGTTCACAAGGATCAGAAGTACGAAGCTGGTCACACATTCCAAATTGACCCTTGTGAAGTATGCCACTGCCCAAATGGTGGTGGGGATCTAATGTGCTATCCGGTTCCAAGCTGCAATCCAAGTCGGGCTTCAAAACCCATGCTGATGACAACAACTGAAGAAACCACACAAGGGATGCCCTACCGAGACCCCATAATGCACATTTTTAACAATCAAGGCTCTAGAATTCCCTTTACCAAACATTTTCCCTTGCATGCCAATAACAATCGTCCTTTTAAGCTACATATGAGAAAAATAGATGAAAAAGAGGAGGATGAGGAAGACTATGATTA[T/A]CCACCCACTGATTACTCAGCTCCTTCTCATGATGATTTTGCGGCTCCCACAGAGTCATCCATCATGTCGGTATCTCGTTCAGATAATTTTACCCCCCACCAGGGTGTGCACAGGGGTGCTAAGCAAGAGCTGAGAGAGATGCTTGGTATTCATAGGTCCACAACAGAAAGGCCACAGTTTCCTTTCTATAAGGACAGTACAGACCGAATGAGAGTAGGCACTCGCAATGACAAACCAAAAAATGAGCTATTCAGCCCTCTGGAATATAAAACAGACCGGGAACGATTCATCCTTCCTGTGGAAACTACAAACAGACTGGGATTCTCCAGTCACAAAGACGCTTCTGAGATCCATAGCTTTAGTCTTTATAAAGACAGCTTCAATCAAGAGGCCCTAACAGATGATGAACAGCTTGAATTTCCTTCAGAAACTACTGATGGGGAAAGAGATACCTCACAGGAGGACACCACATACAGCAAGACAGTTACTGACTCTCCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21928
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024992 | None | None | 468 | None | 10 |
ENSDART00000103481 | None | None | 328 | None | 2 |
ENSDART00000113707 | Nonsense | 293 | 1231 | 4 | 33 |
ENSDART00000131752 | None | None | 650 | None | 13 |
ENSDART00000132865 | None | None | 207 | None | 5 |
ENSDART00000134504 | None | None | 304 | None | 8 |
The following transcripts of ENSDARG00000015156 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 28156027)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 27032013 |
GRCz11 | 11 | 27279187 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGCGTGACAAGATCACTGACTTGAGAATTTTTTATAGGTTTAGATGGT[G/T]AGCCAATAAGAGTCAACATTTTTTTTGCTGTTATATTGATACTATATTGA
Long Flanking Sequence:
CATGACAGGTTACCAATTAAAGTATTTCTGGTATCACACAGCGCTTAGGAAAACGGTTCGCTGTCATGTTTGATTTTGACACGTAAGTGGTAGCTAGTCTCTGGAATTGTGCATGAGCTGGAGCATAAATATTCAACTCAGGGGGGCCGTCTGGATCGCGAAGCCAAACATCGCTCCTGCTGGGAACATCCTCCCTGCTCAGTCATCATATTCACTCACACACCACCTAACACCCTTGTGTCGTTTAGCACACCCAAAGCTTCAATTAGCGGAAACATTGCTTGCTATAAACACACCATTGACTGGAAAATGGCTTGTGACTTTGAACCAAAAGGTGTTTATAGGTTTGTCTGTATAATTCATCTTGACTGGTGCTGGAACTGAAATATTTAATTGGACCTTTGAATGAGGCACCAAGGTAACTCAATGCTTTTCCAGTGCCTACTTAATATTGCGTGACAAGATCACTGACTTGAGAATTTTTTATAGGTTTAGATGGT[G/T]AGCCAATAAGAGTCAACATTTTTTTTGCTGTTATATTGATACTATATTGAAATATGTCCAGCAAAATTTAGTGTGCTATGCTAAAGGGATCATTCACTATATGTTAAGGGGTGGTCCATCTTGTATTTTTAAGGCTTTGTTGTGTTTATAAGATACAAAGCAATGTGTGCTCATGCTTCATTTGTAAAAAACCATGTTATTTTTTCATAAATCTTACTTTGATTATATACAACTACTCAGCTAACATGAAAAAGATTGCCATATTTCCTAGTTCCTTTGAAAGGCCCACTCTCAAGAGGCTCTGATTGGTCAGCTAACATAATGTGCTGGGATTTGCGAATCGGCTCCATGTCACCACATCACGCACCTACAAGCATGCGCTTTTGCACTGTGTAAACAGTAGCTGTTGTGCCTAAATGAGACAGAAAATGAAATAGACACATCTGAACCTCACACCTTCCCTCTAAAATAAAATCTAACAAGTGTCTTATATTTTCGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21929
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024992 | None | None | 468 | None | 10 |
ENSDART00000103481 | None | None | 328 | None | 2 |
ENSDART00000113707 | Nonsense | 679 | 1231 | 22 | 33 |
ENSDART00000131752 | Nonsense | 98 | 650 | 2 | 13 |
ENSDART00000132865 | None | None | 207 | None | 5 |
ENSDART00000134504 | None | None | 304 | None | 8 |
The following transcripts of ENSDARG00000015156 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 28220377)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 27096363 |
GRCz11 | 11 | 27343537 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCTACTACAGTTCCAGATAAACAACAAACTACCACTCAGATGCCGGTCT[T/G]ACATAACCCCTGTGCAGGTATGAACTGTTAAACATGCTGTAAATTTATTT
Long Flanking Sequence:
TGTCCCGTTTCCCTGGTAATTCGGCCAAACCCTAACAACACCACTGCATGATGTGATTGTCATCATGTGTCAATGTTGTTTTTGTGTCTCTGGTGACATAGAAGCGTTGATAGAGATAGACACTTGCCTCATGATCTCATGTCAGCAGTGAACTATTGACACAAACACGGAGAACTTCCTCAGTTGACTTCAGGAATGGCAGGAATTATGATGACAAGATATGTGTTGGCAAATCAAATCAAAACACACTCCATAATTTCTCATCTGGTCATGATTAAATGTTGGAGGAAAAACTCTCCATCGTATGTGCGGTTCTTTGACCAGAAGGTCCATCTGACAGAGCGTGTAATGAAAAAAGCGTGACTCATCGCTCGGAGATTTCACTCTTTTCTGTTTTGTGTAAACAGAGAACCAGGAGGAAGACAACAGAGTTAGCGAGGAAGACCGGATCCCTACTACAGTTCCAGATAAACAACAAACTACCACTCAGATGCCGGTCT[T/G]ACATAACCCCTGTGCAGGTATGAACTGTTAAACATGCTGTAAATTTATTTACCCCAAGGTCAAATACCATGTCATTGATGTTTGATTTTCAGTATAGTATCTTTATAAATAATGCCAGCTATATATTTTATTACCTTATATCCATAAGTTTTTTATTTTTTACTGCATCAATATATGTACTATACTGTTTATATTAAATTATGTCTTAAGGAGGGCCGGTGTCCCAGCAGGGTTTAGCTCCAGCTTGAACGTTTGAACACACCTGCCTAAACGTTTCAAGTATACCTAGCAAGACCTTGATTAGCTTGTTCAGGTGTGTTTGATTAGGGTTGGAGCTAAAATCTGCAGGACACCGGCCCTCCAGGAACAAGTTTGGTGACCACTGTCTTAAACAGTTGAAGGCACAATTATCAGCTCACCTGTGAATTTTTTATTATTTTAATATATTTCCTAAGTGATGTTTAACAGAGCAAGGACATTTTCACACCATTTCCTGTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16218
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024992 | Essential Splice Site | 3 | 468 | 2 | 10 |
ENSDART00000103481 | None | None | 328 | None | 2 |
ENSDART00000113707 | Essential Splice Site | 766 | 1231 | 25 | 33 |
ENSDART00000131752 | Essential Splice Site | 185 | 650 | 5 | 13 |
ENSDART00000132865 | None | None | 207 | None | 5 |
ENSDART00000134504 | Essential Splice Site | 24 | 304 | 2 | 8 |
The following transcripts of ENSDARG00000015156 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 28237778)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 27113764 |
GRCz11 | 11 | 27360938 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGATGTTTTATTTTAGAGTTTAGGAAGATAATGCTGTGCTTGTGTYTTGC[A/T]GATGTGAATGAKTGTGTGACGAACACACACACCTGTCGGGCAGRCGAGCG
Long Flanking Sequence:
TTCTCTTCTGTCCTAATGTGGCCATGCAGTAGAAAGCACAAACATTTCCACTCGGTCGCCTGAAATTATTTACCCTGGCAATAACATGACAGATTGAATCCTTTTCTTGGCCCGTAAATCAGCCATTGTCTAAGCTTCAAGTAATTATTTTCTCCTCTCTCTGGGCCATGCTCGCTTTCCAATCTTGTTTAGCCATTTTTTTTTTCAACATAGTCCAGAGTTATTGCCTTTAATATATCTGGCCAACCGAAGATCTTGACAGTTCACCACAGCACTGGCACTAAAGAATGAGAAGCAAAATGTGCCACAGCTTACAGAAACACACAACTCCTCTCTTTGTTTTTCACACTTCTGTCTCACCTGCTTGCTTTACGACCAGCTTCAGCTTCTCCATTGCCGGATCTTGTGGTTGCAACTGTCCATTATGTCTCAGGCTGTGTGCGAGGATGAGGATGTTTTATTTTAGAGTTTAGGAAGATAATGCTGTGCTTGTGTTTTGC[A/T]GATGTGAATGAGTGTGTGACGAACACACACACCTGTCGGGCAGACGAGCGCTGCGTGAACTCAGTTGGAGGATTTGTGTGCGAAAGGATGATCTTGTGTTCGAGTGGTTACCAGCTGAGAAATGGAGTATGTGAAGGTGAGTTGGGGATACAGTATTAATAAATGCACACATGTACACTTACCGGCCACTTTATTAGGTTCACCTTACTAGTACCAGGTTGGATCCTTTTTTGCCTTCAGAACTGCCTTAATCCTTCATGGCATAGATTCAACAAGGTACTGGAAATATTCCTCAGAGAAGTATTTTTTATTAAGCAAGTTTAGAACCCAAATGTACTGTAGGGCTTATTTTACAGTGCCATTTCATATTTAGCTCTTATGTATATTTGATTATATAAAAAAAACTTTTTAAAAAATTACACAATTAGGCTTTAATTTTACTAAAAGTGCACACAGAGCATTTTCTGTTAATTGAAAAATGCTAAATGTTATGTTTACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa812
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 |
---|---|---|---|---|---|
ENSDART00000024992 | Nonsense | 139 | 468 | 4 | 10 |
ENSDART00000103481 | None | None | 328 | None | 2 |
ENSDART00000113707 | Nonsense | 902 | 1231 | 27 | 33 |
ENSDART00000131752 | Nonsense | 321 | 650 | 7 | 13 |
ENSDART00000132865 | Nonsense | 120 | 207 | 3 | 5 |
ENSDART00000134504 | Nonsense | 160 | 304 | 4 | 8 |
The following transcripts of ENSDARG00000015156 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 28241896)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 27117882 |
GRCz11 | 11 | 27365056 |
KASP Assay ID:
554-0716.1 (used for ordering genotyping assays)
KASP Sequence:
GCAAGATCATCATGTGCAGTCGAGGTTACCATTCCAGTCCAGATGGAGCT[C/T]GATGTATTGGTGAGGACTATATAAATGTGCAAACATACAGCTCTGGACAA
Long Flanking Sequence:
ATATTTATTTCTAAAAGTACTGACTCTAAAATAGTGCACCTGTCGTGCTTTTTTGAAGTATTACCTTTCATGCTGTGTTTAATATAGCTGTTTGTGAATGTAAAATGCCTGAAAGGTTTTAAAGATCAAATGCATGGTGGATAGAGTTGTTGCCTGCCAAAAAATATATATAAACTGCCTGATCTGGGTTATAGTTTTAAACAAATTTGCATTGTCAGTGTATGTTCTTCTTTGGCTGCATGCAAACAGCATGGTCTTTGACGTCAATAGGTTTGACTTGTAGCCAGATCGATTTTGCTTAAGGCATTGTTGCCATTTTTTGCTTGATTTGCATTGATTTTGCCGATTTTTCTCACTTTCTCTTAGACATTGATGAATGCAGCAGTGTGAGAGAACCATGTACGACTGGCTTCAACTGCATAAATACTGTGGGCTCCTATACCTGTCAGCGCAAGATCATCATGTGCAGTCGAGGTTACCATTCCAGTCCAGATGGAGCT[C/T]GATGTATTGGTGAGGACTATATAAATGTGCAAACATACAGCTCTGGACAAAAAAAAAAATCAGAGCACTTCATAGTTATTATTGGTTGTGTGCCATAGGTAGAGCCAGACGGAATATGTTTGCCATATAATATATCTAGTAAAAGATATTGCTGTACAAACTGTACTGTACATAAATAATTTTCATATTAGTCAATAATATTACTGTAATTAATTTAAAAAATCTGCAGAAATCTGCGGAATTCTGCACGCGCAGATTCCGGGTAGGCCTATAGGTGTGCGTTTTGAGTACAGTGTTAATTTTGTGTTTTAATGAATAAATTACTAATAGATAAATTTTGATTTCAAAATTTCAAATAAGAATAGGGTCATTTAAAGCAACTATTTGCAGAAAATCATAGTAGGTCTTCATAAAATATTTTGGGGTTTAAACTCTTATTGAAGCTGATATATAAACTCATACCCAGTGTTGGACACTTTCCTTTAAAAGAGAAATTATAG
Associated Phenotype:
Not determined