ZMP
zgc:163025
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100038778 [Source:RefSeq peptide;Acc:NP_001083027]
Human Orthologue:
F7
Human Description:
coagulation factor VII (serum prothrombin conversion accelerator) [Source:HGNC Symbol;Acc:3544]
Mouse Orthologue:
F7
Mouse Description:
coagulation factor VII Gene [Source:MGI Symbol;Acc:MGI:109325]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa32569 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa15303 | Essential Splice Site | Available for shipment | Available now |
| sa5652 | Nonsense | F2 line generated | Not yet available |
| sa45061 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32569
Status:
Mutation detected in F1 DNA
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109479 | Nonsense | 123 | 431 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 5625)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 111623 |
| GRCz11 | 1 | 111623 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTGTGTGGACCAGATCAACACATACATCTGCATCTGTCCAGTCAACCTC[G/T]AAGGGCGACACTGCGACAAAGGTAACACACAACACAACACAACTACACAA
Long Flanking Sequence:
AATAAATGTGAGACAGCAGAGGAAGATAACTCAGATCTCCTGCTGTGTTTCAGGAGGACTTCTGGAAGAGGTACACAGGTATGTGCAGAGCCGGCTGCATGCCAAAACACGCTTGTCTCACTTATTGTGTGTCTTGTTTCTAGTCCAAATATCTCACAACTCTTAAATCAGGAAGCATTTTGTAGACAGGCAAACAATACAGTGCTGCTTCCAGAAATAATGAAATAATAATGAGTCAAAGTGAAGCGAGTTTCTCCTTACAGCAAGCAGAATATTCAGCCAGTAGAGAATCACTGGACAAACTCTCCCTCACAACTCAATAGCGACACCCTCAAACCAGTCAGTACGGTACTGCCCAGCCGTGTGCCGTCCTGCTGCTGATGGGTTTCTGTGATTGCTGTTGTTCAGAGGTGGATCACTGTCAGTCCGAGCCGTGTCAGAACGGCGCCACGTGTGTGGACCAGATCAACACATACATCTGCATCTGTCCAGTCAACCTC[G/T]AAGGGCGACACTGCGACAAAGGTAACACACAACACAACACAACTACACAACACACCACAACACACAACACAACTACACAACACACCACAACACAACACAACACAACACACCACACAACACCACACAACAAAACACAACTACACAACACAACACAACACATCACACCACAACACAACTACACAACACAATACAACACAACACCACACAACACAACACCACACAACACAACTATACAACACAACACAACACAACACCACACAACACAACTATACAACACAACACAACACAACACAACACACCACACAACACCACACAACACAACACAACTACACAACACAACACAACACATCACACCACACCACACAACACAACTACACAACACAACACCACACAACACCACACCACACAACACACAACACAACTATACAACACAACTATACAACACCACACAACACCACACCACACCACACAACTATACAACACAACACAACACACAACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15303
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 |
|---|---|---|---|---|---|
| ENSDART00000109479 | Essential Splice Site | 250 | 431 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 13071)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 117069 |
| GRCz11 | 1 | 117069 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACTACTGCTGTCCACACATATAACCTGTGTCTGTTTGCKGTGGTCCTGC[A/T]GGTGAGCACATCCGCGATAGAGACGAAGGYACGGAGCAGATGAGGAAGGT
Long Flanking Sequence:
AACTGATAGCTCCACCCAAAAGCACTGATAACCCCACCCTAAATAACTGATAGCTCCACCCAAAAGCACTGATAACCCCACCCTAAATAACTGATAGCTCCACCCAAAAGCACTCATATCCATGCTCAAAATCAGGGATAACCCCACCCTAAATAACTGATAGCTCCACCCAAAAGCACTCATATCCATGATCAAAATCAGGGATAACCCCACCCTAAATAACTGATAGCTCCACCCAAAAGCACTCATATCCATGCTCAAAATCACGGATAGCCCCACCTTAAATGATTGATAGCCCCGCCCTAAAAGACTGATAGTCCCTGCCTTTAATTACTCATAGCCCCGCCCTAAATGAAGATGGCGAGGGGAAGGTTGTTGTATTTGGAGTTTAATGGGGTGAATGAATGTTATCACAGTAATGAGGTGCACAGATGCATCATGCATAAGCAGCACTACTGCTGTCCACACATATAACCTGTGTCTGTTTGCGGTGGTCCTGC[A/T]GGTGAGCACATCCGCGATAGAGACGAAGGCACGGAGCAGATGAGGAAGGTGTCAGAAGTCTTCCTCCACCCTCAGTATAATCACTCCAGCACAGACAGCGATGTGGCTCTGCTGCGTCTGCACCGGCCCGTGACTCTCGGACCCTACGCCCTGCCCGTCTGCCTGCCTCCGCCCAACGGCACCTTCAGCCGCACACTGGCCTCCATCCGCATGTCTACGGTGAGCGGCTGGGGCCGGCTGGCGCAGTCTGGACCTCCGTCTACTGTGCTGCAGCGGCTGCAGGTGCCGCGGGTCTCCTCTGAGGACTGCAGGGCTCGATCCGGCCTGACCGTCAGCAGGAACATGCTGTGCGCCGGCTTTGCCGAGGGAGGGCGCGACTCCTGCCAGGGCGACAGTGGTGGTCCGCTGGTCACGCGCTACAGAAACACCTGGTTTCTGACCGGCATCGTCAGCTGGGGGAAAGGCTGCGCTCGCGCAGACGTCTACGGCATTTACACACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5652
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109479 | Nonsense | 371 | 431 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 13435)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 117433 |
| GRCz11 | 1 | 117433 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCGATCCGGCCTGACCGTCAGCAGGAACATGCTGTGCGCCGGCTTTGCC[G/T]AGGGAGGGCGCGACTCCTGCCAGGGCGACAGTGGTGGTCCKCTGGTCACG
Long Flanking Sequence:
GGGGAAGGTTGTTGTATTTGGAGTTTAATGGGGTGAATGAATGTTATCACAGTAATGAGGTGCACAGATGCATCATGCATAAGCAGCACTACTGCTGTCCACACATATAACCTGTGTCTGTTTGCGGTGGTCCTGCAGGTGAGCACATCCGCGATAGAGACGAAGGCACGGAGCAGATGAGGAAGGTGTCAGAAGTCTTCCTCCACCCTCAGTATAATCACTCCAGCACAGACAGCGATGTGGCTCTGCTGCGTCTGCACCGGCCCGTGACTCTCGGACCCTACGCCCTGCCCGTCTGCCTGCCTCCGCCCAACGGCACCTTCAGCCGCACACTGGCCTCCATCCGCATGTCTACGGTGAGCGGCTGGGGCCGGCTGGCGCAGTCTGGACCTCCGTCTACTGTGCTGCAGCGGCTGCAGGTGCCGCGGGTCTCCTCTGAGGACTGCAGGGCTCGATCCGGCCTGACCGTCAGCAGGAACATGCTGTGCGCCGGCTTTGCC[G/T]AGGGAGGGCGCGACTCCTGCCAGGGCGACAGTGGTGGTCCGCTGGTCACGCGCTACAGAAACACCTGGTTTCTGACCGGCATCGTCAGCTGGGGGAAAGGCTGCGCTCGCGCAGACGTCTACGGCATTTACACACGTGTGTCTGTGTTCGTGGAGTGGATCTTGAAGACTGTGGCCAGCGCATGAACATAACCACGATCACGCTTACTGCTCAGAGTGATCTGTACAGCGCTCTCACTATAATTACTGCTCCACAGATGAAGATGCTCATTATCATGCTACAGTACGATCGCCACCATATCACAATACTCTTCCTATTTCTATATGTATAAAATATGCATCATATGCAGTAATTCCTGTTATAAATGATGTATCTGTACACTTACATTAATTTGCCCTCATAAACTCTGATCAAAGTTTTGAACACATTAAATTCCTTAAGGGCTATCAGTCATTTAGGGCGGGTCTATTAATTGTTTAGGGAGGGGCTATCAGTCCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45061
Status:
Mutation detected in F1 DNA
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109479 | Nonsense | 393 | 431 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 13503)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 117501 |
| GRCz11 | 1 | 117501 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCAGGGCGACAGTGGTGGTCCGCTGGTCACGCGCTACAGAAACACCTG[G/A]TTTCTGACCGGCATCGTCAGCTGGGGGAAAGGCTGCGCTCGCGCAGACGT
Long Flanking Sequence:
TGCATCATGCATAAGCAGCACTACTGCTGTCCACACATATAACCTGTGTCTGTTTGCGGTGGTCCTGCAGGTGAGCACATCCGCGATAGAGACGAAGGCACGGAGCAGATGAGGAAGGTGTCAGAAGTCTTCCTCCACCCTCAGTATAATCACTCCAGCACAGACAGCGATGTGGCTCTGCTGCGTCTGCACCGGCCCGTGACTCTCGGACCCTACGCCCTGCCCGTCTGCCTGCCTCCGCCCAACGGCACCTTCAGCCGCACACTGGCCTCCATCCGCATGTCTACGGTGAGCGGCTGGGGCCGGCTGGCGCAGTCTGGACCTCCGTCTACTGTGCTGCAGCGGCTGCAGGTGCCGCGGGTCTCCTCTGAGGACTGCAGGGCTCGATCCGGCCTGACCGTCAGCAGGAACATGCTGTGCGCCGGCTTTGCCGAGGGAGGGCGCGACTCCTGCCAGGGCGACAGTGGTGGTCCGCTGGTCACGCGCTACAGAAACACCTG[G/A]TTTCTGACCGGCATCGTCAGCTGGGGGAAAGGCTGCGCTCGCGCAGACGTCTACGGCATTTACACACGTGTGTCTGTGTTCGTGGAGTGGATCTTGAAGACTGTGGCCAGCGCATGAACATAACCACGATCACGCTTACTGCTCAGAGTGATCTGTACAGCGCTCTCACTATAATTACTGCTCCACAGATGAAGATGCTCATTATCATGCTACAGTACGATCGCCACCATATCACAATACTCTTCCTATTTCTATATGTATAAAATATGCATCATATGCAGTAATTCCTGTTATAAATGATGTATCTGTACACTTACATTAATTTGCCCTCATAAACTCTGATCAAAGTTTTGAACACATTAAATTCCTTAAGGGCTATCAGTCATTTAGGGCGGGTCTATTAATTGTTTAGGGAGGGGCTATCAGTCCTTTAGGGCGGGGCTTTTAGTTCTTTGGAGAGAGGCTTTTAGTGATAAAAAGTGGGATACCAGTCCTTTTGG
Associated Phenotype:
Not determined