ZMP
si:dkey-219c10.5
Ensembl ID:
ZFIN ID:
Description:
CLIP-associating protein 1 [Source:RefSeq peptide;Acc:NP_001108611]
Human Orthologue:
CLASP1
Human Description:
cytoplasmic linker associated protein 1 [Source:HGNC Symbol;Acc:17088]
Mouse Orthologue:
Clasp1
Mouse Description:
CLIP associating protein 1 Gene [Source:MGI Symbol;Acc:MGI:1923957]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15630 | Nonsense | Available for shipment | Available now |
sa41484 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34705 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15630
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 |
---|---|---|---|---|---|
ENSDART00000102445 | Nonsense | 14 | 1534 | 1 | 40 |
ENSDART00000131334 | None | None | 126 | None | 5 |
ENSDART00000137955 | Nonsense | 14 | 1492 | 2 | 38 |
ENSDART00000142853 | None | None | 63 | None | 3 |
Genomic Location (Zv9):
Chromosome 9 (position 39220360)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 38358256 |
GRCz11 | 9 | 38168051 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATCRTAGRCCATGGAGCCCAATATGGAGTACTGTCTGACCCAGGTGCTA[C/T]AGAAGGATGTTGCRCGAAGGTTGCAGATGGGTCCGGAGCTCATCGACTAC
Long Flanking Sequence:
TCTCATAAGTGGCTGTTGATCTGAGCTGACAAAAATGCAGCTCTTGCCGCACTGGCATTTGATATCCAGAGGTGGTACTCCACTAACAGCTCCCTTTTCTCATCCTTAGCAGGGAGGACTTCTGAATTATGAAGCAACGCTCCGCCGGACCCTCTCTCTCCTGCTCTAGTTACCACGACTCCTGCCGCAACCGTGATCACTTCTGCCTCTGCTACTAGTGCTTGTGGCTGGGACAAAAAGGAGAATTCGCAGTTCTCGTCAGCTGTTGTCTGGTCACATATGGTGCATCGTTTGCATTCCTGAGTCGACATCCCTACCACTCAGTTTCTTGCCAGCCTGTGGATTTATCAACACAGGATATTAATAAGCGTGTCTTCTTGTTTTGCCTGGATCACACACGCTAAAGGCCTATTTTTTTCACTTTCCACTGCCACACGGGTGGTGGCAGGACATCATAGGCCATGGAGCCCAATATGGAGTACTGTCTGACCCAGGTGCTA[C/T]AGAAGGATGTTGCGCGAAGGTTGCAGATGGGTCCGGAGCTCATCGACTACATCACAGATGCTGAAAAGTGTCAGGACTTGGAGAGTGACCAGACTGCGCTGGATAAAATGGTGGACGGTATTGCCACCTCATGGGTTAACTCCAGCAACTTTAAGGTAAGGGGCGTTTTATAGCATTAAGATGATTAACAGTAAATTTCCTGCAGGTTTGATGGATTTCTTGAGATAATAAAGGGTCTTGAAGCGCCTTGGTTCAATGGGATAAGGTTAGAAATCAAGGGCTTTTCTTTTGGAATCTCTTTCAGGCTGTTGTCTGGCATAGAATTGAGGGCTTGAATCGGTCCCTTGAGCGAAAGGGAGCAGGCTTTTGAGGTCACTGGAACATTTACAGGCCTTCATGTTGACATATTCAGAGATCGGACACAATGAGAGACTTCACTTTGTGTCTACGTTCTTGGATCATAATTAAAGCATTCGTTCACCCAGAAATGAAAATTCGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41484
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102445 | Nonsense | 696 | 1534 | 21 | 40 |
ENSDART00000131334 | None | None | 126 | None | 5 |
ENSDART00000137955 | Nonsense | 685 | 1492 | 21 | 38 |
ENSDART00000142853 | None | None | 63 | None | 3 |
Genomic Location (Zv9):
Chromosome 9 (position 39308132)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 38446028 |
GRCz11 | 9 | 38255823 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGCCGGCAGCCGATCCAGTTCACCAGGGAAGCTTTTGGGACATGCGTA[T/A]GGCAGAATTCCTAGAGCCACTGCGCCAACAACTCCCTCAGACAAGTACTC
Long Flanking Sequence:
ATTTGTGCTGTATGTCCCCACTAATGTCAAGAGCAAATATACACGCTTGGATGACAAAGATTTCATTTTTGGGTGAACTATCACTTTAAATTTTGTATAAAAGTTATACCATTAAGATTATAAATAGACTTTTCACTTTCTTTCTTTTTTTCAAGTCATTACTTTTGTAACATTATTAATGTAATTTTTATCTGTTATAAAGTTTAGCTATCTAGGCAATGGTAAATTCATCAAATAATGGAAAAGAACATTGTAACTATCATGTTCACATATGTGCAGTTAAGTATTTAAGAGGTTGATTCCAGTGCCTAAAACAACCCTTTTTTTATGATCTTTTCATTTTGTTATGCTTTATTTCACATTTAAAACAGCGAGCAGAGCAGCCAGTGGCAATTGGAAGATAATCCCCCACCATATTACTCACAGCAGCCTTGCTTTTCATTCCCTCTTGCAGCCGGCAGCCGATCCAGTTCACCAGGGAAGCTTTTGGGACATGCGTA[T/A]GGCAGAATTCCTAGAGCCACTGCGCCAACAACTCCCTCAGACAAGTACTCCAGAATCCCACGAAGCCAGGGATGCAGCCGTGAGACCAGCCCCAATAGACTGGGCATAGGTAGGGGCAACACATATTCACATCTAACACTTTAACACAAAGGATGCCTATAAATAGCAGACACATCAAACAACTTGATCACAAAACGCAAACGGACCTAAAACAGTCCCTTAAGAAATCTCTATGGAATATGCAGTAAAACCTGCAGATTGTTTGCTGCTTTATGCCTTGATTGTGGTAAGCATGGTGTTTTTTTAAGCTTTCTTTGAACAAAAAGAAGACATTAACTAGCTGGATCGTTGTATAGTGCAAATCCCATTAGATTTGACTAGTTTAGAAAGACAGGGGGCTTTTTTGCTGGGTTACTGAGGAGCGACGTTTGTTTAAAAGGTGAATGCGGGTGTTTTGATTGCCAAAACTGAATTAGTGGCTATTCATTGCCACATTTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34705
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102445 | Nonsense | 1272 | 1534 | 34 | 40 |
ENSDART00000131334 | None | None | 126 | None | 5 |
ENSDART00000137955 | Nonsense | 1217 | 1492 | 32 | 38 |
ENSDART00000142853 | None | None | 63 | None | 3 |
Genomic Location (Zv9):
Chromosome 9 (position 39330607)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 38468503 |
GRCz11 | 9 | 38278298 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGTCCAGAGAGTTTGCACCCTACGGCTATGGAGACACAATCACAGCCTA[T/A]GATAAAAGTGCCCTGAAAGAGGCCGTCTTTGATGACGATGTGGAGCAGTT
Long Flanking Sequence:
GGGATCATTAAAAAAAATAACAAAATAATAATGACAAAAGTAAAAGAAAAAATATAATATTAATTAAATATTGTTTATTTTATATGTTGTTGTTGTTTGTGGTGGTGATGGTATTATTATTTTTATTATTGCAGCAAAAAATGTGATCATAAAATACTACTAGTAATACAATAAAATATTACTAATAAAATACTACTAATAATAATAATAGTAGTGTTACATTAATCAAAAAAATGATAATAAAGATAGTTTAGTAACATAAAATATGTTACTATAAATTATTATTTTAAAAAACATATTTCACTTTTCCTGTCGCAGACTGGAAAAGAAGCAGCATCTCCGGGCTCTGATGCGAGACTGGGATTGGATGTAGTGGAAGGTGGTCGAACCGCTCTGGATAACAAGACCTCTCTTCTCAACACCCCGTCCCCGCGGTCTTTCGCTGGGCCCCGGTCCAGAGAGTTTGCACCCTACGGCTATGGAGACACAATCACAGCCTA[T/A]GATAAAAGTGCCCTGAAAGAGGCCGTCTTTGATGACGATGTGGAGCAGTTCAGAGACTGTGAGTCAATACACTGATTAGAGCATGTAAATCCACTCTCACTTCATCTGCACTCCATACTGCGCACCCATTGTCTGAGAGTGTGTAAAGAAACATGAGAAGATGAGGATAAAATTTTAAAATACATACATTTTTATCACACTCTTACATGAACCATACAACCTCCGCTTTTTATAGCTTGTTACAAAAAACTTAGCGGATTGAAATTAATATTTGTCGAATTTAAAATTTGAAAAAAGATTTTTTCTGGATTTATTATGTATGCATTTGAGTAAAATTTTTATAGTGTTTGTGTTTTATTTATTTAGTTTTATTTATTTATTTATTTTAGAATATCAAATAAAACTAAATAAATAAAACACAAATATTAACATTTTACTCAGGCATTTTACATTTTACTCAAAATGTACAAAATGTATATATATTATATATTTTGTTTTAT
Associated Phenotype:
Not determined