ZMP
cluap1
Ensembl ID:
ZFIN ID:
Description:
Clusterin-associated protein 1 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q7ZVC2]
Human Orthologue:
CLUAP1
Human Description:
clusterin associated protein 1 [Source:HGNC Symbol;Acc:19009]
Mouse Orthologue:
Cluap1
Mouse Description:
clusterin associated protein 1 Gene [Source:MGI Symbol;Acc:MGI:1924029]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa5703 | Essential Splice Site | F2 line generated | Not yet available |
sa44181 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa5703
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111623 | Essential Splice Site | None | 427 | 2 | 12 |
ENSDART00000134152 | None | None | 184 | None | 6 |
ENSDART00000111623 | Essential Splice Site | None | 427 | 2 | 12 |
ENSDART00000134152 | None | None | 184 | None | 6 |
The following transcripts of ENSDARG00000079110 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 38997095)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 37595991 |
GRCz11 | 24 | 37483711 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTGTTTTACGTTTTGWTAATGAAATGTGTATTCATTCTTCTTGTCTWAT[A/T]GGTGACAGTTGTGTGTTTACTGGATTAAAGGACAGCAATCATGTCTTTTA
Long Flanking Sequence:
TGGTTCTAAAGTAATTTCGCGATAATGTTTTAGATCATCATCTGTAAACGCGTTTTTCTAGTTTGTGGTTATTGGGCTTCCGTAGGGTTGCATGGGTGCCATAGTGACGAACACAGCAACAGACGCCTTTTCGAGGCAAAAACATCCGCTTTATATGCTAATCATTACTGTTATTTTTACATGATTTACAACTAAAACGGTAAAGGTTTTGTTATATTCCTCCATTATCAGAATTTAGTAGTTAATTTTAGGCGGAAGACAAAAGATGATGCTCAAGCTACTTAACGTCATCATGCTAGCTTTAACAGTTGAGGCTAACCACATTTTCCAGTGAAGATTAACTTTAACATTAGACAAATGCAAAATGCCGTCTTTTATTGAAGGAAATGTGTGACTACTCGCTTTCAGTTTGAGTATTCAATATCTGTGCATGAATAATTTAATTGTATAATTGTTTTACGTTTTGTTAATGAAATGTGTATTCATTCTTCTTGTCTTAT[A/T]GGTGACAGTTGTGTGTTTACTGGATTAAAGGACAGCAATCATGTCTTTTAGAGATCTGAGAAGTAAGTGACCCCAAATCCATCAATTACTGTAAAATATATTCTAGTGTTACTCTGTGCTAAGTTAAGCTGTGGTTTGTGTTTATGTGATTATATATGTCAGCTGAAATATAATATTACCCTACCGCATGCTTGGAAAGGTTTCATTTCTGGTGTTTTTACAATAATATATTTGTGCATGCACATTAGATTAGGCAGTAATGAAGACAAATCTAACAAAATAACTTGCAATAACTGTCCTAAAACTAGTACACCCAAATTTGTTATAGAAAAATATAAACAAAAATTTCAAAAATAGTAAAAATCAAGCGAAGCAAAAAATTGAAATTATCTTGTTGAGATTTTGTAGGTTGTATTTTTTTTTTTGCTATATTTAACTTGAATTTAATTATATTATCCTTCAATTTCTAAATATCTTTGGTGACTAAAATATTATTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44181
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 |
---|---|---|---|---|---|
ENSDART00000111623 | Essential Splice Site | 8 | 427 | 3 | 12 |
ENSDART00000134152 | None | None | 184 | None | 6 |
The following transcripts of ENSDARG00000079110 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 38996121)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 37595017 |
GRCz11 | 24 | 37482737 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTAATGTTTTGATGGTTTTAAATATCTTTTCAATTTTTATCCATATGTA[G/A]ATTTTACAGAGATGATGCGAGCGCTTGGCTACCCTCGACTCATTTCCATG
Long Flanking Sequence:
TCTTTGGTGACTAAAATATTATTTTAATAAATTTATCTGTTAAATAAATCTGTTTTGTTTAAATGCACCAAAATACATCGCCTATATTCACTGAGAAATGGAGAAAAATGAAAAATATTCATTTTCAAAATGGGGTGTACTCAATTTTGCTGAGGTCTGTATATACATAAGAGCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATACACACACATATATATAAATATATTTAAATATATTGATATTTTTGTGGGTGTTCTAAAGGGTTAATTTACCCAAAAATGAACATTTCTTCACACGAAAGTGGTTCTAAACTTTAATGAATTTCTTTCCTCCATTGAACACAAATATGAACACTATCAGGACACCTTCTAATGTACAGAAATAAAAATAAGCTGAACTACAGTTAATGTTTTGATGGTTTTAAATATCTTTTCAATTTTTATCCATATGTA[G/A]ATTTTACAGAGATGATGCGAGCGCTTGGCTACCCTCGACTCATTTCCATGGAAAACTTCAGATCTCCAAACTTCCCTTTAGTAGCTGAGATTCTCATCTGGCTTGTCAAGAGGTAATAGAAATGGATGTGTTTTAAAAAAAAGAGAGTCGGGAGGAGAGATGTGTGTGTTGAAAGGACTTTTAACAAAAATGAAAATTCTGTCATTATTTATTCATCCTCCACTTGTTTGAGTTTCTGTCTTATTTTATATTCTGAAGATATATATATATATATATATATATATATATATATATATATATATATATTAAGGGTGGAGCCGAACCCGAATACGGTATTCGGAAAGGCACGAATAGCGTGTGTTTACGAATACTTATTTCGAACAAATACTTGAAAAATTATTTGTATTCGGGAGCAAGAAAAGCATTATATCAAAAAGCTGTGTTTCCTCCTGAGACCACAGTGCGTGAGAGAGAGCGAGAGAGAGAGAGAGAGAGAGAGA
Associated Phenotype:
Not determined