ZMP
f5
Ensembl ID:
ZFIN ID:
Description:
coagulation factor V [Source:RefSeq peptide;Acc:NP_001007209]
Human Orthologue:
F5
Human Description:
coagulation factor V (proaccelerin, labile factor) [Source:HGNC Symbol;Acc:3542]
Mouse Orthologue:
F5
Mouse Description:
coagulation factor V Gene [Source:MGI Symbol;Acc:MGI:88382]
Alleles
There are 13 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa13037 | Nonsense | Available for shipment | Available now |
| sa21530 | Essential Splice Site | Available for shipment | Available now |
| sa21531 | Essential Splice Site | Available for shipment | Available now |
| sa13751 | Nonsense | Available for shipment | Available now |
| sa13402 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13037
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 |
|---|---|---|---|---|---|
| ENSDART00000078065 | Nonsense | 66 | 2101 | 2 | 25 |
| ENSDART00000128539 | None | None | 406 | 2 | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 35101085)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 34320596 |
| GRCz11 | 9 | 34129781 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACAATCATATAAAAAAGTAGTATACAGGGAATATAATGAGGGATTCAAA[C/T]AGCCAAAAGCTCATCCCTTGTCCTCAGGTAYACCGRTCACTTAACTTTAA
Long Flanking Sequence:
AATTTCAAATATCTATGTAACAAAATAGTTTTGTATACATATTTTTTCTATGTATGTGTATCACATATACATAATAATTACATATATATATATATATATATATGTATATGTATATGTATATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAATACACACACATAAATTTGTAAAAACAAACTTTATATTTAGACCCAATTTCATTGCAATTAATTGCAATTAAAGAGAGAGAGAACGAAAGTGAGAGAGAGTGAGAGAGAATAATTCATTCACTCACTCACTCACTCACTCACTTACTCACTCACTCACTCACTCACTCACTCACTCGCTCACTCACTCGCTCACTCACTCACTCACTGCTCATACTTATTTACTGTTGTTGTATTTCAGAACCGGACAATCATATAAAAAAGTAGTATACAGGGAATATAATGAGGGATTCAAA[C/T]AGCCAAAAGCTCATCCCTTGTCCTCAGGTATACCGGTCACTTAACTTTAAAACCCATTCAGTATAAAGCAAAGCATGAATCTAACAATTGCTCAAAACAAATGTTCTAGGGTTACTTGGGCCTACATTGCGTGGACAAGAGGGTGACACAATCATCGTCACGTTCAGGAACATGGCAGATCATCCTTGCAGCCTCCACCCCCATGGCATTGCTTACGGGAAGCAGTCAGAGGGTGTGTATTCAGATGTGATTGCGGTAACAGTATGACCCATGTAGCAATGTTGTAACATACACCATAATTTTAACAAGCAGACACTGTGCTTTGAAATGACAGAGATGATGCATTTCAAGTGGAATTTTGTTTAGAGGACATTATGGATTATTTTAGTGCTCATCGTTTAGCTGAGTAAACAGTTTGAGCAACACAAACATTTGTGTTTGATGTCTTTGGAAATATTAACCCAAGATACAAATTAACCAAAGGCTGTACCTAAGTCCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21530
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000078065 | Essential Splice Site | 75 | 2101 | None | 25 |
| ENSDART00000128539 | Essential Splice Site | None | 406 | None | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 35101193)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 34320704 |
| GRCz11 | 9 | 34129889 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGTATAAAGCAAAGCATGAATCTAACAATTGCTCAAAACAAATGTTCT[A/G]GGGTTACTTGGGCCTACATTGCGTGGACAAGAGGGTGACACAATCATCGT
Long Flanking Sequence:
TGTATATGTATATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAATACACACACATAAATTTGTAAAAACAAACTTTATATTTAGACCCAATTTCATTGCAATTAATTGCAATTAAAGAGAGAGAGAACGAAAGTGAGAGAGAGTGAGAGAGAATAATTCATTCACTCACTCACTCACTCACTCACTTACTCACTCACTCACTCACTCACTCACTCACTCGCTCACTCACTCGCTCACTCACTCACTCACTGCTCATACTTATTTACTGTTGTTGTATTTCAGAACCGGACAATCATATAAAAAAGTAGTATACAGGGAATATAATGAGGGATTCAAACAGCCAAAAGCTCATCCCTTGTCCTCAGGTATACCGGTCACTTAACTTTAAAACCCATTCAGTATAAAGCAAAGCATGAATCTAACAATTGCTCAAAACAAATGTTCT[A/G]GGGTTACTTGGGCCTACATTGCGTGGACAAGAGGGTGACACAATCATCGTCACGTTCAGGAACATGGCAGATCATCCTTGCAGCCTCCACCCCCATGGCATTGCTTACGGGAAGCAGTCAGAGGGTGTGTATTCAGATGTGATTGCGGTAACAGTATGACCCATGTAGCAATGTTGTAACATACACCATAATTTTAACAAGCAGACACTGTGCTTTGAAATGACAGAGATGATGCATTTCAAGTGGAATTTTGTTTAGAGGACATTATGGATTATTTTAGTGCTCATCGTTTAGCTGAGTAAACAGTTTGAGCAACACAAACATTTGTGTTTGATGTCTTTGGAAATATTAACCCAAGATACAAATTAACCAAAGGCTGTACCTAAGTCCAAAGCTGTCAGTCCCTGATAAATATTTACTTTTTGTTCCGAAAAATCTTAAGCAAAATTACTTTTTCCCCTAAAAATGCATGTCTGTTAGTTTCATTAAATCCTTTATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21531
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 |
|---|---|---|---|---|---|
| ENSDART00000078065 | Essential Splice Site | 115 | 2101 | 3 | 25 |
| ENSDART00000128539 | Essential Splice Site | None | 406 | 3 | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 35101318)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 34320829 |
| GRCz11 | 9 | 34130014 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTTGCAGCCTCCACCCCCATGGCATTGCTTACGGGAAGCAGTCAGAGG[G/T]TGTGTATTCAGATGTGATTGCGGTAACAGTATGACCCATGTAGCAATGTT
Long Flanking Sequence:
AACTTTATATTTAGACCCAATTTCATTGCAATTAATTGCAATTAAAGAGAGAGAGAACGAAAGTGAGAGAGAGTGAGAGAGAATAATTCATTCACTCACTCACTCACTCACTCACTTACTCACTCACTCACTCACTCACTCACTCACTCGCTCACTCACTCGCTCACTCACTCACTCACTGCTCATACTTATTTACTGTTGTTGTATTTCAGAACCGGACAATCATATAAAAAAGTAGTATACAGGGAATATAATGAGGGATTCAAACAGCCAAAAGCTCATCCCTTGTCCTCAGGTATACCGGTCACTTAACTTTAAAACCCATTCAGTATAAAGCAAAGCATGAATCTAACAATTGCTCAAAACAAATGTTCTAGGGTTACTTGGGCCTACATTGCGTGGACAAGAGGGTGACACAATCATCGTCACGTTCAGGAACATGGCAGATCATCCTTGCAGCCTCCACCCCCATGGCATTGCTTACGGGAAGCAGTCAGAGG[G/T]TGTGTATTCAGATGTGATTGCGGTAACAGTATGACCCATGTAGCAATGTTGTAACATACACCATAATTTTAACAAGCAGACACTGTGCTTTGAAATGACAGAGATGATGCATTTCAAGTGGAATTTTGTTTAGAGGACATTATGGATTATTTTAGTGCTCATCGTTTAGCTGAGTAAACAGTTTGAGCAACACAAACATTTGTGTTTGATGTCTTTGGAAATATTAACCCAAGATACAAATTAACCAAAGGCTGTACCTAAGTCCAAAGCTGTCAGTCCCTGATAAATATTTACTTTTTGTTCCGAAAAATCTTAAGCAAAATTACTTTTTCCCCTAAAAATGCATGTCTGTTAGTTTCATTAAATCCTTTATCCTTCAATGTTTCCATTAGGGTCTTTATACTTTGACAACACGTCACTCCTTGAGAAAAATGATGATGTAATTCAACCTGGTGAAGAGCACACTTACCAGTGGGACGTGACGTCTGATGTGACCCCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13751
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 |
|---|---|---|---|---|---|
| ENSDART00000078065 | Nonsense | 799 | 2101 | 13 | 25 |
| ENSDART00000128539 | None | None | 406 | 13 | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 35111089)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 34330600 |
| GRCz11 | 9 | 34139785 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGGTTTATTAATGGAGGAAGGWGATTTAGACAAGGGAGAATCTTCTAAT[A/T]AAGWCTTGAATGACAGCACWGACAAGKCATTGCTAGAGACAACAACTACT
Long Flanking Sequence:
CTATACAAACATACACATTGTACAACAAAAACTGAATGCAACCTCAATATCTCCACTTTACAGGTATTTGGCTTTTGGCATCATTGAACTCGCATGATTCCACTAAAGGGATGAGGGTGAAATTCAAAGACCTCGAATGCTTCAGAGATTATGTAATAGAATATGATTATGAGGACGGGAAATTCACTGCATGGAAACCACCGACTATTAATGAAATCAAAAAAGAGGAACCGGTCCGTGCAAGACCTGACGTGGTCGACGAGTACTCTGATTTATTTGCTGAAACCCTCAACTTAAGGACGTTCAACAATGTTAAAGATGAAGTTGAGATAATCGACTTGACATTTCTAGATCAAGATGATGGTTTGTTGCCCATTGTTGAAGAAAAAAGCCTGGGATCAAGCAACGAGAACTTACACAATGCTACTTTACAATCTTTCATTGAGACTCATGGTTTATTAATGGAGGAAGGTGATTTAGACAAGGGAGAATCTTCTAAT[A/T]AAGTCTTGAATGACAGCACAGACAAGGCATTGCTAGAGACAACAACTACTTTTGATTCCAATAGAGTTGTCGCATTAAACAACGAAACGGACAGTATAATTTTAGATTTTCCAATTGTAGAAAGAAAGGTTCGTAGTGCACCATCAAAGCCAATGAACGAACCTGAAAGTGTCACTATGAACTTTAAAACAACAGAACATATCAATTCATCATTAGAGAGAATCAATGCTATATATTCCCCAATAACTGAAACAAACATCAACACAATGACTGAGACACACACTGATTTCAGTATCACTCCATTTGATGGTTCAACTGGAGAAATGAACTTCACACTAGAGGATGACACCGCACTTCTAAATTCATCTGAATCAGAGCCCCTGCAATCAAACCAAAACTCCGAAAACAGAATAGCTTTTCAAGAAGAGCTAAATGCAAAAGATGGCACAGATGTTGACAGTAATAATTCTGTGAAAAATCAGATCTTCAAATACAACGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13402
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 |
|---|---|---|---|---|---|
| ENSDART00000078065 | Essential Splice Site | 1467 | 2101 | None | 25 |
| ENSDART00000128539 | Essential Splice Site | None | 406 | None | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 35114295)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 34333806 |
| GRCz11 | 9 | 34142991 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACRTTTTMAATAAATRAATCTAAARCTAATTTGCTAATTCCTGTTTGCAA[A/C]GGCGACTTGATAAAACAGCTCAAAATGAGAGGCCCACGGTTTTCAGAAAA
Long Flanking Sequence:
AAATTTACTGTAAAATAACAGTCCTTAAATTACAGAAATTTACCATAAAACAACGGCTGTTAAATTACAAAATTTCCTTAAATTTTTAATTTCCGGTAAATTTCTGTTTTTTAATATCTGTTATTTTACAGTAAATTTCTGTAATTTAACGGACGTTATTTTATGTCTTTTTCCAGTACCCTAGTACTAAACCGAAGGAGATGAATGAATAAATAGTGTTTTTTTTTTAAGTGAGACATTTAATTCCTAACTGAATTTGATGAGCCAAGACAAGTTTAGCATTTTTAACATATTAGGAATACAAATAAGACTGAATGTGTGCATGTTTTAAAATAATATTTGGAAATAATTAAAAATTATAACTTCCCACCTAGAATTCGACTACATCATTCTGTTTCTTCAAATGTTATTTAAAAATAAGTCCCTCAAAATCATCAGAATTTCTGGAGAACGTTTTAAATAAATGAATCTAAAACTAATTTGCTAATTCCTGTTTGCAA[A/C]GGCGACTTGATAAAACAGCTCAAAATGAGAGGCCCACGGTTTTCAGAAAAGTGGTGTTCCGAAGGTACCTGGACAGCACCTTTAGCATCCGAGACATCCGAGGAGAAATGGACGAACACCTGGGAATTCTTGGTCCGCTCATTAAAGCGGAAGTTGATCAGACCGTTATGGTAAACCACACACTTGTGAAGAAATCAGAATTGGAAAGCATCACGTCTATAAAATGAATATTAACAATTGCATTCTGGTTTTCCATGCTAGGTATTTTTCAGGAACCGTGCAAGTCGTCCATACTCTTTGCATGCAAATGGAGTAAAATACTTAAAACAAATGGAAGGCCTGAGTTATGATGATGAATCTCCATACTGGTACAAACAGGACGATGCTGTTCCACCCAATGGCACCTTTACCTACATGTGGACCATAAATCCCAAATCTGGACCTCAAAATAATGAATCTGACTGCCGAACTTGGACCTACTACTCTGCAGTGAATCCTGT
Associated Phenotype:
Not determined