ZMP
si:dkey-273o13.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A2BIB0]
Human Orthologue:
CLIP1
Human Description:
CAP-GLY domain containing linker protein 1 [Source:HGNC Symbol;Acc:10461]
Mouse Orthologue:
Clip1
Mouse Description:
CAP-GLY domain containing linker protein 1 Gene [Source:MGI Symbol;Acc:MGI:1928401]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38528 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33768 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9135 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7278 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38528
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 |
---|---|---|---|---|---|
ENSDART00000114783 | Nonsense | 232 | 1411 | 4 | 29 |
ENSDART00000145122 | None | None | 436 | None | 13 |
Genomic Location (Zv9):
Chromosome 5 (position 70232747)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 66558857 |
GRCz11 | 5 | 67237226 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCGTTTCTTAGGGGAAACTGATTTTGCCAAGGGTGAGTGGTGTGGAGTT[G/T]AGCTGGATGAGCCCTTGGGGAAGAACGATGGAGCTGTGGCTGGAACCAGG
Long Flanking Sequence:
TCACTATGACAGAACTGACGTGTTTGTTTCGATTTAAAAATGAAAATTATTTTCTGTTTCAAGAGAAAGGGACTAGTAGAAAGTAAAAAGATCCCTGCAAAAATGCAAACCCTATAGCCTTCTGAAAACATGAACTGCCATTCGGTAATATTCAGTCAAAGTCTGAATATTTGCTTTACGTTTGGTGTGGTGGTCCTGTCAGTTTGACCAGCCACAATATTCTAAACCACGCCCCTCTTACCGTTAATTTGCTGTTAGGGAATGATGCACCAAAAGAAAGCCCCGCCTCCTACTCAATATTCCATTTCAGTTGAAAGCACATTAACATACTGATACTCGAAGGTTAATGATTGGCCATTTAATTTCAGAAGACTATCACCTATTGCTCAATTACGTTATTTTTTTCTACACATCTATAATTATAGGTTGCTGGCTCAAAAGCTGGCGTGGTGCGTTTCTTAGGGGAAACTGATTTTGCCAAGGGTGAGTGGTGTGGAGTT[G/T]AGCTGGATGAGCCCTTGGGGAAGAACGATGGAGCTGTGGCTGGAACCAGGTATTGTGTCCTGTTCTTACATCACAATCTAAAGGTGAATTGTCTATGAACAATGGGGGTATACATGCACAGAGACGTTTTATTTCAGTCAGCCAGCTCAAGCACTACTGGTGAGCTTTTTTTTTGTTGGCTGACAAACACTAGCTGTGCTTAAAGTATTTTACATGAATGCATTTGTTTATCTTCAGGTATTTCCAGTGTCAGCCCAAGTATGGTCTCTTTGCACCAGTGCACAAGGTGACCCGTATAGGTTTTCCCTCCACTACCCCAGCAAAGGCAAAAACCACTGTGCGGAAGACGACCGCCACCACCGCCGCCACTCCGTCAGCACTGAAGCGCAGCCCGAGTGCCTCCTCCATCAGCTCCATGAGCTCTGTAGCCTCTTCTGCTAGTTGCAAGCCAAGCCGTACAGGACTGGTGAGTCCTCACATGCATGCATATTTTTTGGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33768
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 |
---|---|---|---|---|---|
ENSDART00000114783 | Nonsense | 1112 | 1411 | 21 | 29 |
ENSDART00000145122 | Nonsense | 82 | 436 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 5 (position 70196661)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 66522819 |
GRCz11 | 5 | 67201188 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGCAGCTGGATGCTCTAAAACAGCAGAACTCTCAGTATCAGGAGAGTT[T/A]GAGTTCTGACAGTGAGAGAATTAACAGCCTCAGTAAAGAGATGTGAGTGA
Long Flanking Sequence:
CAGTTGGAAATTTGTTAATGATTTTAATTAATATTACAAAGATTTTGGTATAAAGGAAAAATCAATAATTGACACACACACACACACAGTGTATTTTTGGTTATTGCTAAACATAATACCCTGTGCCAGGTTTTGTTGTCCAGGATCACATTAATAGTTTGTGTGAAACACTTAATGAATATGATAAGTTTGATTACTGATTTTAAATGTGCTGTTATATTTATTATAAATAAGTATTTTAACTTTTTTTTTTTAAATAAAATATTTTAAAAAAATATTAGCAATAGACTGTTCACATGGGTAAAAAATGTAACTACATTAAAATATACCTGGAAGATTCAGAGTAGTTCTGCTTTCCCGCAACAAGATGAGATGCCAAAATGTTAAGCGAGCCCTTGTGGATAGATGATTAGAAGATAGAGCATGTTTCTGAATGCTTTCTCTGTACTCTTTGCAGCTGGATGCTCTAAAACAGCAGAACTCTCAGTATCAGGAGAGTT[T/A]GAGTTCTGACAGTGAGAGAATTAACAGCCTCAGTAAAGAGATGTGAGTGATCTCCATTGTGAAACCTGAATCTTTTCACCTTGATATTTATTTGTCTAGAGGTGTTTTTCTTCATGTTTAATTTAGTATCAACATCTTACTTGACTTTTTTACTATTTTGTTTTTTTGTTTTTTGCATTTGCACAATATTTTATAGTAAGGAATTACACAGATTATGCAATTTCATAACTATAATAATGATATTATACAGTAATATAATACGCATTTCTTGATATATATATATATATATATATATATATATATATATATATATATGTATATGTATGTATATATATATATATATATATATATATGTATGTATGTATATATATATATATATGTATATGTATGTGTATATATATATGTATGTGTGTATATATATGTATATGTATGTGTATATATGTTTGTATGTATATATATATATGTATGCATATATATATATATATATATATATATATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9135
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 |
---|---|---|---|---|---|
ENSDART00000114783 | Nonsense | 1129 | 1411 | 22 | 29 |
ENSDART00000145122 | Nonsense | 99 | 436 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 5 (position 70195769)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 66521927 |
GRCz11 | 5 | 67200296 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATTGAANNNNNNTCTGTGTTCAAACAAATGWYGGTTATGCGTTTCAGTGAGGAGT[T/A]GAAACAAGCCGCTGTCGAGAAATCCCAGGCAGTGGACGATCTGAAAAATG
Long Flanking Sequence:
GTATATATATATGTATGTGTGTATATATATGTATATGTATGTGTATATATGTTTGTATGTATATATATATATGTATGCATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATTGTTTGTTAATATATATAAGTTTGTAAAACTTCTTCTCAGTCCTTGGAGACTCCTCTGAGAAATGAGGTAATTTTAAATGTACATTTTGAGAAAATGAAAGTAATTTTGAACTTAAATGCATTTCAACCTATTGTGGGACTCCTCCAAAACAAAATCTGCAATATTTTCAATTGCATAATGGATTTTTAGTATTCCCCTCCTCTGAAAGAGATGCATCTTATTTCATGCATATGCAATACAGTATTGGCATTGGTTTATTGGTATTGTTTATTAGTAACATTTCACTGTGGTTCATGTTTTAACGCTAAAAGAGCATTGAATCTGTGTTCAAACAAATGTCGGTTATGCGTTTCAGTGAGGAGT[T/A]GAAACAAGCCGCTGTCGAGAAATCCCAGGCAGTGGACGATCTGAAAAATGAGAAGGAAAAGCTAACCATGGATCTCGCCAACAGCCTCAAAGACAGCAACATACTGCTAAATGTATGTTCAATCAGATTTATATACTATAGATTAGGAAGTTTGTCTAATAGAACTAATTAGTGTCAAGACCATTCAACATAATTGTTAGACCTGCTGTTTAGTACATGATTTACGATAAATATTATTATTATTGTTATTATTTTTGTATTTATATTATAAATTGATGTGTAGTATATGTATTCAAATATAATGTATATGTATTCAAATATAACACTATTTATTGTTGTTATTATTATTATTATTATTATTAATATTTTATTAATATATATTATAAAATAATGTATAATATATATTCATTTCCTAGAGATGGGTTGCAGCTGGAAGGGCATCCGCTGCGTAAAACATATGCTGGATAAGTTGGTAGTTCATTCTGCTATGGCGACCCCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7278
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114783 | Essential Splice Site | 1226 | 1411 | 24 | 29 |
ENSDART00000145122 | None | None | 436 | None | 13 |
Genomic Location (Zv9):
Chromosome 5 (position 70189947)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 66516105 |
GRCz11 | 5 | 67194474 |
KASP Assay ID:
554-4521.1 (used for ordering genotyping assays)
KASP Sequence:
TCTCAGAAAAGGACAAAGAGCTAGACTCYATGAGAAACGAGGTAACAGTC[G/A]CTTTGGGTTTTTTGAGTGTGYGAGTGCACGTTACTGTTTTTTGCTCAGTT
Long Flanking Sequence:
GGTTTCATCTTCATCCTCCTGCTAATGTAGATGTTGGACTGAAGCAGCTGATATTCATTTACACTGAAGAAGGGCAGAGGGTTGCTGAACTACTGAGAGATTTCAGCTGCTGTCTGGGCTTTTACTGGCTTTCTACACATACCTTTCTTTGTGTTCAATCATTTTTCCGTGTCATTTAATTATTTTACACATAAAGTAATTAGTTTGTTTGCATAAATGGATTTCTTTGGTTCTTACCAACATCTGGTGAAAATTTCAAGTCAACAGCACCTTTAGAAATATGTTTTCTGAGTAAAATGGTGAAGTGTTCAATACTTACTTCCCCCACTGTAACTAAACTTGAACATGAACCTGCGGTCTGTCTTCTGCACAGGGAAAGCACTTTAACGAAAGAAACGGAAAAGGAGAAAGCAGCACTTCAGCAATCTCTTCAAACCCAGAGTGCCTTGATCTCAGAAAAGGACAAAGAGCTAGACTCTATGAGAAACGAGGTAACAGTC[G/A]CTTTGGGTTTTTTGAGTGTGCGAGTGCACGTTACTGTTTTTTGCTCAGTTCTTCTGGTGTGGGTCGCGTGCAGATGGGTGGTCTGCGGGATCAGACACAGACGCTGCAGTCCAGTCTCAAATCTCAAAAGAGTGAGAATATTCAGCTTCAGGAGCGACTGAAGGGTCTGGAGAGGAGTTTAGCCGACGCTCAGATCCCCAGCAAAGGAGATAACGCCTCAGGTACAGCACCACACATGATTTTATAGCTTATATTAAATGGTTAGTTCACCCAACAATGAACATTTACTCATTTATTTACCGACACGTGGTTCTAAACCAGTTTGAGTTTCTTTATTCTGTTGAACACAAAAAAAAAAGAAATTTTGAAGAATGATAAACCCAACAACTGACTTCCATAGTAGGAAAACAAATACTATGGATGCCACAGGTTTTCAGCTTTCTTCAAGTGACCTATTTTTGCATTCAACAGAAGAAAGAAACTCAGGGTGCTTTCACAAC
Associated Phenotype:
Not determined