ZMP
fgb
Ensembl ID:
ZFIN ID:
Description:
fibrinogen beta chain [Source:RefSeq peptide;Acc:NP_997939]
Human Orthologue:
FGB
Human Description:
fibrinogen beta chain [Source:HGNC Symbol;Acc:3662]
Mouse Orthologue:
Fgb
Mouse Description:
fibrinogen beta chain Gene [Source:MGI Symbol;Acc:MGI:99501]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9621 | Essential Splice Site | Available for shipment | Available now |
| sa298 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa9621
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000011701 | Essential Splice Site | 159 | 485 | None | 8 |
| ENSDART00000041987 | Essential Splice Site | None | 216 | None | 11 |
The following transcripts of ENSDARG00000008969 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 9130967)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 9370772 |
| GRCz11 | 1 | 10054883 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATTCTMRACTATTAAAAATACCCACAAGTAATKGTTTATGTYCTTTCAC[A/C]GGCAATGGACTTGTGGTTGATCAGTACACAGACAGCTTAGAAACCCAGCA
Long Flanking Sequence:
AAAGCCAACTGTAGAGCAGCTGAAAAGAGCTGTGGACGACTTGACTCAATCCACCAACTCCATCCACGGCTACGTCCTCGATATGACCGCAGAAGTAGCTCAAAGACAAAAAGTCAGCGAGGGTAACTACACTTCAGAAAGTTTTGTTTATATGATATTTGTTTTAAAGTAATAGTTGTCTAATGACTTGCCTAATTATGACTGATTACTATAGTATCTTTTCAAATATCTAGTAAAAAATTCTGTACTGACTGTCATCATGGCCGAGAAAAAAGAAATGAGTTATAGGAAATGAGTTATTAAAGCTATTATGTTTAAAAAGGACTTTTAAAAAGAATGAAAAGTTCACAGGAGGTCTAATAATTTCATTGCATGTCGAGTAAATTAATAAAAGTATAAGCATCCGCCTGACTAATACTGGTAGGCAACCTATTTTTTATATTTAATAGACATTCTCGACTATTAAAAATACCCACAAGTAATGGTTTATGTTCTTTCAC[A/C]GGCAATGGACTTGTGGTTGATCAGTACACAGACAGCTTAGAAACCCAGCATGCTTATATTAAGGACACGGTGGACGTCACCTTCCCCCAGAACATTAAAGTCCTTCAGGGAGTGCTGGATAAGATCCGTGAGAAGATCCAGCGCTTGGAGAAAGCCATCACTACTCAGAGAGCCAAGTGCCAAGCGCCCTGTAAAGTCACCTGCCCCATTCCTGTTGTGTCCGGCAAGGAGTGCGAAGACATCATCCGCAAAGGAGGAGAGGACTCGCAGATGTACATCATACGGCCTGATCCGCTTGGAACGCCTTACAAGGTCTTCTGCGATCAGACCAGTAAAAATGGAGGTATGGCAACTTTGGCCTTGTCTACTCTATTACATTTTACAGTTACCCTAGACACAGCTTTTTCTGTAAACACACACAAAAAAAAAATCCATGTGGATATATTTGAAACTCACATAGAAATCTGATATATGCAAATTATTATGCAAAAACTGTTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa298
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000011701 | Nonsense | 177 | 485 | 5 | 8 |
| ENSDART00000041987 | None | None | 216 | 5 | 11 |
The following transcripts of ENSDARG00000008969 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 9131024)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 9370829 |
| GRCz11 | 1 | 10054940 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGACTTGTGGTTGATCAGTACACAGACAGCTTAGAAACCCAGCATGCTTA[T/A]ATTAAGGACACGGTGGACGTCACCTTCCCCCAGAACATTAAAGTCCTTCA
Long Flanking Sequence:
CTCCATCCACGGCTACGTCCTCGATATGACCGCAGAAGTAGCTCAAAGACAAAAAGTCAGCGAGGGTAACTACACTTCAGAAAGTTTTGTTTATATGATATTTGTTTTAAAGTAATAGTTGTCTAATGACTTGCCTAATTATGACTGATTACTATAGTATCTTTTCAAATATCTAGTAAAAAATTCTGTACTGACTGTCATCATGGCCGAGAAAAAAGAAATGAGTTATAGGAAATGAGTTATTAAAGCTATTATGTTTAAAAAGGACTTTTAAAAAGAATGAAAAGTTCACAGGAGGTCTAATAATTTCATTGCATGTCGAGTAAATTAATAAAAGTATAAGCATCCGCCTGACTAATACTGGTAGGCAACCTATTTTTTATATTTAATAGACATTCTCGACTATTAAAAATACCCACAAGTAATGGTTTATGTTCTTTCACAGGCAATGGACTTGTGGTTGATCAGTACACAGACAGCTTAGAAACCCAGCATGCTTA[T/A]ATTAAGGACACGGTGGACGTCACCTTCCCCCAGAACATTAAAGTCCTTCAGGGAGTGCTGGATAAGATCCGTGAGAAGATCCAGCGCTTGGAGAAAGCCATCACTACTCAGAGAGCCAAGTGCCAAGCGCCCTGTAAAGTCACCTGCCCCATTCCTGTTGTGTCCGGCAAGGAGTGCGAAGACATCATCCGCAAAGGAGGAGAGGACTCGCAGATGTACATCATACGGCCTGATCCGCTTGGAACGCCTTACAAGGTCTTCTGCGATCAGACCAGTAAAAATGGAGGTATGGCAACTTTGGCCTTGTCTACTCTATTACATTTTACAGTTACCCTAGACACAGCTTTTTCTGTAAACACACACAAAAAAAAAATCCATGTGGATATATTTGAAACTCACATAGAAATCTGATATATGCAAATTATTATGCAAAAACTGTTTACTAATTACAAATATGTGCATATATGTTAAATTATATTAGCTATAATTTTATATATCGG
Associated Phenotype:
Not determined