ZMP
f2
Ensembl ID:
ZFIN ID:
Description:
prothrombin [Source:RefSeq peptide;Acc:NP_998555]
Human Orthologue:
F2
Human Description:
coagulation factor II (thrombin) [Source:HGNC Symbol;Acc:3535]
Mouse Orthologue:
F2
Mouse Description:
coagulation factor II Gene [Source:MGI Symbol;Acc:MGI:88380]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa10601 | Nonsense | Available for shipment | Available now |
| sa21024 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10601
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 |
|---|---|---|---|---|---|
| ENSDART00000052325 | Nonsense | 197 | 635 | 6 | 14 |
| ENSDART00000114238 | Nonsense | 197 | 539 | 6 | 14 |
The following transcripts of ENSDARG00000036041 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 40144853)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 38481493 |
| GRCz11 | 7 | 38752751 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCACAAAGATGGCCCTTGGTGTTTTACCAGAGACCCGACTGTCAGGAGG[G/T]AGACCTGCAATGTGCCAAAATGYGGTAGAGAAAACTTACTAAAACATAAC
Long Flanking Sequence:
AACAAAACGAGACATTCTGTTAAGGTGAGTCCTTTCTACATTGTAAAATAACCCAAATTGTTTAATGTGTGATTGATAGGGGACTGTTTCATAAATATTGGAGCAAAGTATGCTGGTAAAGTATCTGTCACCAAGTCTGGAAAGGCATGCCAGTACTGGAAAAGCAACTTTCCCCACAAGATTGAGTATGCACCACTACTCTCGTATTTTTATTGTACTGAACCACCTTTAACAGTGTCTAACTGTGTCATCTCCCAGTGTTGGCCAGTGGGGAAAAACATTTCATATTGATTGAATAGAAAACACAAAAGCCTTCAGTAAAGAAAAGGTTGTTTTGTTTTACATGCCTTTAGTGATGTTCCTCTGTCTTATGATCCATTTGTTTCCCCCGCAGCGAATTTAATGTGACACAGCTGAAGCTACCGGAGAACTTCTGCAGGAACCCAGATAAGCACAAAGATGGCCCTTGGTGTTTTACCAGAGACCCGACTGTCAGGAGG[G/T]AGACCTGCAATGTGCCAAAATGTGGTAGAGAAAACTTACTAAAACATAACAGCAAAATGTACTAAAGTGCAGTAACTGGCAGTCAGAAATTTGAAATCAATCAAAACTGTATTATTTATAGCATTTGTTACCATCACCTGTTTGGGCATTGTGTTTATTGCACAGTCCAGGCTTGAGTTAAAGGGATTATTTACCCCAAACATCATTGACTCACCCTATACTCGTTTTAAACATTTCTTTATTCTGTTAAACACAAAAGAAGATATTTTGAAGAAAGCTGGAAATATGTAACCATTGACCTCTATTCATTCATTGACTTTCAGCTTTTTTTTTTTTTTGAGGCTCAGTAAATCATGAATAAGTTATCATTTTTGGTGAACTATCCCTTTAAGATTGTCTGCAGAGTGCCTTTAATTATCTTTTTACAGGTTTTACATTTACTCTACTTTTAACAAAAAATTAGTCTGTCATACTTAAAGAGTTTTTATTTTGTTGTAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21024
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 |
|---|---|---|---|---|---|
| ENSDART00000052325 | Nonsense | 258 | 635 | 7 | 14 |
| ENSDART00000114238 | None | None | 539 | None | 14 |
The following transcripts of ENSDARG00000036041 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 40145642)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 38482282 |
| GRCz11 | 7 | 38753540 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTGACTCTGGGGCTACACACCTGCCTGCAGTGGAGCTCCGCAGAAGTA[C/T]AAGCCTTGATTAAGAAGAAAGAACTTCTGCCTCAAGTTCAGCTGGTGAAG
Long Flanking Sequence:
TAACCATTGACCTCTATTCATTCATTGACTTTCAGCTTTTTTTTTTTTTTGAGGCTCAGTAAATCATGAATAAGTTATCATTTTTGGTGAACTATCCCTTTAAGATTGTCTGCAGAGTGCCTTTAATTATCTTTTTACAGGTTTTACATTTACTCTACTTTTAACAAAAAATTAGTCTGTCATACTTAAAGAGTTTTTATTTTGTTGTAAAGTATGTAAATTACTGAACAAAAAGGTACACCCAACAGAAAAGTGGACAAAAGAGCTGCATTTGAATACCATCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCCTCCTCCTCAGGTGAGGCTGTTGTTCCTCCTCCAAAAGCTCCTACTGCAAAACCTGAGCAGCGTCATGTGATAAGCAAATGTCTGCCTGGAAACGGGGAGACCTACACCGGGGAGTTGTTTGTGACTCTGGGGCTACACACCTGCCTGCAGTGGAGCTCCGCAGAAGTA[C/T]AAGCCTTGATTAAGAAGAAAGAACTTCTGCCTCAAGTTCAGCTGGTGAAGAACCATTGCAGAAACCCAGATGGAGATATGGAGGGTCCCTGGTGTTACATAAAGGCAGCAAGCGGAAACATTACCATTGATTACTGTGATTTAGAGTTGTGCGGTGAGTGAACAGTACTTTCTTTAAAACTTCATTAACCACTAAAAATATTCATATCCTTGCATTGAACCTAGGATCTCCCTTGAAAGGGAGTTCTGCAGCAGACTTAATTAATTAGGATTAAATGTCAGGATTTTAATGAGGCAAAAACACTTCTTAAATGTCAACTGTTAAAGAGTTAGTTCACCCCAGAATGAAGATTCCCTTAAAATACCATTATCATTTCTCAATTCCTTTCTTTAGAACACTAAAGGAAGGAATTTAATTTTTTTTTTTAGAAGTTGAATATTTTTTAATCATATCTGATAGGGCAAGCAGACTTTACATTTAATCTTTACAACATACTAGTA
Associated Phenotype:
Not determined