ZMP
vasp
Ensembl ID:
ZFIN ID:
Description:
vasodilator-stimulated phosphoprotein [Source:RefSeq peptide;Acc:NP_001017790]
Human Orthologue:
VASP
Human Description:
vasodilator-stimulated phosphoprotein [Source:HGNC Symbol;Acc:12652]
Mouse Orthologue:
Vasp
Mouse Description:
vasodilator-stimulated phosphoprotein Gene [Source:MGI Symbol;Acc:MGI:109268]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23365 | Nonsense | Available for shipment | Available now |
sa15540 | Essential Splice Site, Missense | Available for shipment | Available now |
sa16008 | Splice Site, Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23365
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042473 | Nonsense | 82 | 185 | 3 | 6 |
ENSDART00000098862 | Nonsense | 83 | 411 | 2 | 19 |
ENSDART00000098865 | Nonsense | 82 | 445 | 3 | 14 |
ENSDART00000133797 | None | None | 96 | None | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 39089509)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 40802226 |
GRCz11 | 18 | 40792418 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTGTAAAGGGATTAAAATATAATCAGGCCACGCCAAACTTCCACCAGT[G/A]GCGGGACGCCCGGCAGGTGTGGGGACTCAATTTTGGCAGCAAGGAAGATG
Long Flanking Sequence:
GAACAACAGATATATCTCATTAATTAATTCATTCATTCATTAATTCATTCATTCATTCATTTTCTTTTCAGCTTAGTCACATTGTTAATCAGGGATTGCCACAGTGGAATGAACCGCCAACTTGTCCAATATATGTTTTACGCAGCAGATGAATGATATATCTATATTGCGTAAATCACAATAAACTGCTTAGTTGTTTTATTATCGTTTTAAATATGTTGAAGACACATAAATAGTCAATTAATTCAGAAACTGAAAATATGTTTGCACAAAAAAAAAAATGTATTTAAAGAAATTCTGTACGAATTACATTTTAAAACTAAATGAAATTAATGAACAAAATATACACCAAATTGAACTCAAAAGAGAGAGAATACCACAGCGTAAGATAAAACCACCATATTTTACATTCATACATTTGTGTCTCCTCCAGGTTGTGATAAACTGTCCAATTGTAAAGGGATTAAAATATAATCAGGCCACGCCAAACTTCCACCAGT[G/A]GCGGGACGCCCGGCAGGTGTGGGGACTCAATTTTGGCAGCAAGGAAGATGCGGCGTTGTTTGCCAATGGCATGATGCACGCTCTCGATGTGCTCAGCTCGATCCCTGATGGAGGTAACACACACATATACACAGCACCATGACACAGCATATCTGTTAATGTATAATGAAAACAGTCAACACAACCTCTCTAATATCTTTAGGTTACTCCGCACGGCCTGTGTCTAATGGACCATCACCAGAAGAGCTGGAACAGCAGAGAAGGTACAGGCCTGGGGTCGAAATTAGACTGGGGTTTATTTTATTTCCAGAATTGAAGTCATTTAAGCTTTCTTCACTTTCTGTGTCCTTGTGTGAATTGCTGTAAGACAGCGTTTCCTGGTCAGACTTTGACCTCATTTCTGAAGCACACACACTCCTTTACACACAAGCACACACTCTCAAGGGATTTACTGGTATTAACGCTGGAGTCTTTAGCTTTCCGTGAGCCCCTGAAGTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15540
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:
T > C
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042473 | Essential Splice Site | 140 | 185 | None | 6 |
ENSDART00000098862 | Missense | 142 | 411 | 3 | 19 |
ENSDART00000098865 | Essential Splice Site | 140 | 445 | None | 14 |
ENSDART00000133797 | None | None | 96 | None | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 39089244)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 40801961 |
GRCz11 | 18 | 40792153 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GRCCTGYGTCTAATGGACCATCACCAGAAGAGCTGGAACAGCAGAGRAGG[T/C]ACAGGCCTGGGGTCGAAATTAGACTGGGGTTTATTTTATTTYCAGAATTG
Long Flanking Sequence:
TGCACAAAAAAAAAAATGTATTTAAAGAAATTCTGTACGAATTACATTTTAAAACTAAATGAAATTAATGAACAAAATATACACCAAATTGAACTCAAAAGAGAGAGAATACCACAGCGTAAGATAAAACCACCATATTTTACATTCATACATTTGTGTCTCCTCCAGGTTGTGATAAACTGTCCAATTGTAAAGGGATTAAAATATAATCAGGCCACGCCAAACTTCCACCAGTGGCGGGACGCCCGGCAGGTGTGGGGACTCAATTTTGGCAGCAAGGAAGATGCGGCGTTGTTTGCCAATGGCATGATGCACGCTCTCGATGTGCTCAGCTCGATCCCTGATGGAGGTAACACACACATATACACAGCACCATGACACAGCATATCTGTTAATGTATAATGAAAACAGTCAACACAACCTCTCTAATATCTTTAGGTTACTCCGCACGGCCTGTGTCTAATGGACCATCACCAGAAGAGCTGGAACAGCAGAGAAGG[T/C]ACAGGCCTGGGGTCGAAATTAGACTGGGGTTTATTTTATTTCCAGAATTGAAGTCATTTAAGCTTTCTTCACTTTCTGTGTCCTTGTGTGAATTGCTGTAAGACAGCGTTTCCTGGTCAGACTTTGACCTCATTTCTGAAGCACACACACTCCTTTACACACAAGCACACACTCTCAAGGGATTTACTGGTATTAACGCTGGAGTCTTTAGCTTTCCGTGAGCCCCTGAAGTGACGGGGCAGAAGTCCGGGTCAGGCTTTCTGACTCACAAATCCTCTTCCACATTCTCCTCTTGCTTTCAATTTCGAGACTACAGTTTAGAAATATTGCTGCATTTACAAATCTTGACTTTTTTTTTTGGTTTTGATTCGTAATTAAGTTGATTAAAAAACGATGAAGAGAAGTGCATAGAGGGAGACACTGCTTGCTGCAGAGCCACTTGGGCTCCCATGAGGGGGCGCTTGAGCTTCAACTCCTCCTATAAGCTGTTTTAGGCCCCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16008
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042473 | Splice Site | None | 185 | None | 6 |
ENSDART00000098862 | None | None | 411 | None | 19 |
ENSDART00000098865 | Nonsense | 178 | 445 | 5 | 14 |
ENSDART00000133797 | None | None | 96 | None | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 39082703)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 40795420 |
GRCz11 | 18 | 40785612 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
KAGAACGGCAGGAAAGGGAAAGACAAGAGAGAGAAAGACWAGAGAGAGAA[C/T]RACAAGAGAGAGAACGGCCAGTAGCTTCAGGTCAGCAGAAACTCTTTTAC
Long Flanking Sequence:
TAAGCCCCTTTGAGCTATGTATTTTAAATTGTCCACAGAACAAACCACCGTTATACAATAGCTTGCCTAATTACTTTAACCTGCCTAGTTAATCTAGTTAAGCCTTAAATTGCACTTTAAGCTGAAGACTAGTATCTTGAACAATATCTGGTAAAATATTATTTACTGTCATCATGGCAAAGATAAAATAAATCAGTTATTAAAAATGAGTCATTAAAACTATTATGTTTAGAATTGTGTTGAAAAAATCTTCTCTCCGTTAAGCAGAAATATAGGGAAAATTATACAGGGGTAATAATAATTCAGGACGTCTAATAATTCAGACTTCAACTGTATATGCTGGTATTTTTTTGTGTATTTTGACTTTAAATGTTGTTTTTTCTTGCAGATTGGAACAACAGAGGCTGGAGCAGCAAGAGAGAGAGAGACTAGAAAGAGAGAGACAAGAGAGAGAACGGCAGGAAAGGGAAAGACAAGAGAGAGAAAGACAAGAGAGAGAA[C/T]GACAAGAGAGAGAACGGCCAGTAGCTTCAGGTCAGCAGAAACTCTTTTACCTCAGTGGACATGAGTTTGCACTTATTTCTGAGTAAAAACCAGCAAAGGTGTTTTTTTTAATGGTATGGGGGGGGGGGGTGTATATAAGGGGTATATAAATATAAATGGGGAAAAGACAAGATATCCCTTTTTGGTTTCTGCATCATATTAAATTTTCAAAAGTGAGTTTATATGAAAAGAAAAGTTTAAAGTGTCTTCTTCAATGTTTAAAAATTTTCTCTGAAAGTAAAAATAAAATAGGTAACTGTAATATCTACACAGTATGAATCATTTGTTAAGCTTTAGCTAATAGTGAATTTATTATCTGTTAAGCATTAACTCTACATTAATAAACCTTAATAAGCAATTTATAAATACAAATGCTGTATTCTTGAATTATAAGCACATGTATAATAAGCTTAATGATTGTGTTTTCATACTTTGTTATCTTATTAATTGTTCATTTCTAT
Associated Phenotype:
Not determined