ZMP
fga
Ensembl ID:
ZFIN ID:
Description:
fibrinogen alpha chain [Source:RefSeq peptide;Acc:NP_001181918]
Human Orthologue:
FGA
Human Description:
fibrinogen alpha chain [Source:HGNC Symbol;Acc:3661]
Mouse Orthologue:
Fga
Mouse Description:
fibrinogen alpha chain Gene [Source:MGI Symbol;Acc:MGI:1316726]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa651 | Essential Splice Site | F2 line generated | Not yet available |
| sa12469 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa651
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000033118 | Essential Splice Site | 19 | 684 | 2 | 6 |
| ENSDART00000080442 | None | None | 206 | None | 2 |
| ENSDART00000135522 | Essential Splice Site | 19 | 456 | 2 | 5 |
The following transcripts of ENSDARG00000020741 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 9146216)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 9386021 |
| GRCz11 | 1 | 10070132 |
KASP Assay ID:
554-0559.1 (used for ordering genotyping assays)
KASP Sequence:
AAAATGGCCTATGTTGGCAGACCTAANGTAGTTATAAAGTACTTACTTTTT[A/C]GGCCGAGGAGGACACAGTGGTGAACCCTAGAGGYGCTCGTCCTATTGAGC
Long Flanking Sequence:
GAAGGAAAATATTATCAGACATACTGTGAAAATTTCCTCGCTCTGTTAAACATCATTTAGGAAATATTTAAAAAGAAAATAAAATTCAAAGGGGGCTAATAATTCTGACTTCAACTGTATATTTTTTTTTACAGTGTATAGGATGCTCTACAATAATATATTTGTGCATATACATTAGATTAGTATTTATTTAAGCCAAAACTGGAACTAATCTGACAAAAAAATCGTGAGATCAAAGTCTAAAAATTAGTTAAAATATAGTAAAATTAATAAAAAAAAAAATTATAAAATTTTAATTAATATTAAAAATCAATAGAATAATAAAAAAGATCAAATTTTGTTGGAATGACATGTTTCAATTTAAATGTATTTTCTTGACTACATTCACTGAGAAATGGATAAAATAGTAGTTTTCAAAAGGGTGTACTTATTTGCTGAGCACTGTATGTTAAAATGGCCTATGTTGGCAGACCTAAGTAGTTATAAAGTACTTACTTTTT[A/C]GGCCGAGGAGGACACAGTGGTGAACCCTAGAGGCGCTCGTCCTATTGAGCACGGCTTCAAGGCACAAGACACCTGCCAGACAAAAGAATGGCCAGGGTGTACCGATGATGACTGGGTATGGGTTTCTCACTGTTTTTCTTCACTTCGTTCATTCCATCCATCCACCATCATGTGGATGAATGATAACAGCCTTCTAAGCCTATATGCGCAGAGGACCCCTACTGGCCCATATCTGTCAGCTGATAACCACTGATTACGCCCATACAATTGAGTGTAAAACATTCGAGTTGGCTGGATAAAAAATTTCAGACGGCATTTAGAAGTCTTCATATACTACCTATTACTATATATTATATAAGTCATAAATATTGACTCAATAATTAGACAAAACACAAAAATCTCTATCAACAAATTTGTTGCAGTAAATGTTTCTTTCAATCCTCAATATAGGGAAGCAAATGTCCATCTGGCTGCCGAGTTCAAGGCCTCATGGACAAAGC
Associated Phenotype:
Normal
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa12469
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 |
|---|---|---|---|---|---|
| ENSDART00000033118 | Nonsense | 400 | 684 | 5 | 6 |
| ENSDART00000080442 | None | None | 206 | None | 2 |
| ENSDART00000135522 | Nonsense | 400 | 456 | 5 | 5 |
The following transcripts of ENSDARG00000020741 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 9143431)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 9383236 |
| GRCz11 | 1 | 10067347 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAAGTATGCCTCATCTTCATCCTCAACATCCACAAAGAYAGTGTCAGAT[G/T]GAAGCAAARGTTACTCAAAGACCACCCTCACTAGCGACCCTATTTTTGGG
Long Flanking Sequence:
TTTATAAGAGCGGAACGGGCAAAGCTGAGCAGAAGCTGCTTTTTGGAGATGTAGGCCAGATGCAGCTCTCTCTGGAAGCTGAAGGCTCCACTGCCGAATCTGCCGCCACAGTTAGCAAGTTTCCCACATCAGGTACGGGCTCCACATCACAAACCTCCAGCAAGCAGTGCACCAAATCAGTTCGCAAAGTGATAACACACACCAAAGATGGCCCCGTGGAAAAGGTTGAAGTTTCGTCTAGCGGGCCCGGGTGTGATGATTTAGGAAAACTAGGAATTTCAGATTCAGAGTTTTTGACGGCAGCCAAAGATGGGAAAGATTTGAGTCGCGATGGCTTGAAAATAACAGTGACCGGCGGTGATGAAAAGTCCCTCACTTCTCTAAGCCACAGCACTTCTGATCTGGGTGGCTTCGGAGGAGACTTCTTTAAGAATCTTGGCACTGACAACCGAAAGTATGCCTCATCTTCATCCTCAACATCCACAAAGACAGTGTCAGAT[G/T]GAAGCAAAAGTTACTCAAAGACCACCCTCACTAGCGACCCTATTTTTGGGGATGACCTCGGGGCGTTCATGCGGGGCGACGTGGAAGAAGATATGCCCGACATCCATGCACGCAGTGTGAAATCGCAAGACGATCGCAAGGCTGGCTTTGTTGGCGGAGGTACACTCGAGTGAAACTCTTAACACAAGTGAACCATTGATAAACATAATGATAACACTATTAACAAGAGTTTGTTGGAAACATGTGGACTAACTGATATCTAAGTAAATACCAATCCATCACATTTATTAATACTCACCAAGAAGCAATTGTTTGGATCTCTGGAATGAATTTGCAATGCAGTTTTGCTCTAATCGGCAGGTGTGTAATCTTCTTTCAGATTGCGTTGAAATCCAGCAGAAGCATGTGAACGGCGGTCAGAGCGGGATGTTCAAAATAAAACCAGCGGGGTCTGAGGAGGTAGTAGAGGTTTACTGTGACCAGAGCACTGGGTTGGGGGG
Associated Phenotype:
Not determined