ZMP
si:dkey-94n12.1
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100151400 [Source:RefSeq peptide;Acc:NP_001121890]
Human Orthologue:
CPAMD8
Human Description:
C3 and PZP-like, alpha-2-macroglobulin domain containing 8 [Source:HGNC Symbol;Acc:23228]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37504 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa43829 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa43830 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37504
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079046 | Essential Splice Site | 195 | 1749 | None | 39 |
ENSDART00000134893 | None | None | 734 | None | 18 |
The following transcripts of ENSDARG00000056530 do not overlap with this mutation:
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 21582140)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 21235388 |
GRCz11 | 22 | 21260366 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGATGCAAGGCCACACGTACAACAAATCGTTTGAAGTGCAGAAGTACGG[T/G]AAGCATTTATGTATTAATATATACTGTAAAATGTAAATAGAAGTAGAAAT
Long Flanking Sequence:
ATGTGTTTGCTTAAGCTTGATTCTTTGCTGCCTTTTAACGAGTGTAAAGTGGCCTTCAGATTTAAGCAAAACAAATAAGCAAGAATGTGACTATTTGTACCACAAACTGTTTAAGATTACCACGTTGTTTACCCAGGACCCCAGAGGATCCCACATAGTCCATTGGAAAGATCTGAAGTCAATTTGTTGTGGTAAGGACTGTTACTATTATGTTCCTATGGATGTAGTCAGGATTTCAATTTTGTAATCTTTTTTCAATCATTGCATCATACTGTAAAACTTTTATGACAGTATTTATGATTTATAATATATTTTAACATTATGATGTGTGTACAGTGTGTATACATATAGTGTTAATATAAAAAATTATTATTGTCTCTATTAGGAATTGTCAATATGAGCTTTCCACTATCAGACCAACCAGTTTTTGGTGAATGGTTAGTCTTTGTCGAGATGCAAGGCCACACGTACAACAAATCGTTTGAAGTGCAGAAGTACGG[T/G]AAGCATTTATGTATTAATATATACTGTAAAATGTAAATAGAAGTAGAAATGCTTAGTTTTTCAGAAGTTCAGGTTTTTCCGAACAAGAAAGTTACAAGAGTTTTGTATGTGTTGTACGTTGTTTTCACAGTACATACAAAGTTTGTTTTTGAATAGACTGTTTTCATATTATCAAGTCAAATTTTAATGTTGATTTAAGAGCCCATATTATGCATTAAAATGGTTATATTTTGGTATAAGCCAACAACAGGCTTATATGCGTGCAAGGTCAAAACGTCAACAAAACGAACAACAAACGGCAGTGGATTGTGAGCTTACAAACGCATTTAAATTTATAAACAATGCGGCATGTGTCGCGTTTTCAACATGGCTTTAGATGCGAAATGAGAATATAAAGAGTTACCCAGAATCCAGATACAGTACAAGCAGTTACAAGTAACAAAACACTATTAAATACATAATTTGCAAGCTAGAGAAAACAACGAGGCAACCATTTTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43829
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079046 | Essential Splice Site | 661 | 1749 | None | 39 |
ENSDART00000134893 | None | None | 734 | None | 18 |
The following transcripts of ENSDARG00000056530 do not overlap with this mutation:
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 21586645)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 21239893 |
GRCz11 | 22 | 21264871 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTCCATGGCACTGGGACATCACTAAAGATGCCCGTTTTGCTTTTACGG[T/A]GAGGACATGACTTTCTCCACTTCCCCGTATTGTTTTAAGCTCAGGCAGCA
Long Flanking Sequence:
GTCCCGCTTCGAAAATGAGGTTGATTAATTTCAGTTCACCAATTGTCAATTCAGAAAATTCACCATAAAAAGAAAGTTCTGTCTTCTATTTGTTTAACAAACCTTCTTGTCTTCAGATCTCTGTGTCTTTGTCCACAAATGAGTCGATGCCAGGAAGCCCGATCAGTCTGAAGGTTAAAGCAGAAAGTGGCTCATGTGTATGTGTAGCTTCTGTGGACAAAAGCATGTACCTTCTCAAACCAGGCTTCCAGCTCACACCTGAAAAGGTTAGTCCTCGTTTGAACCTTCATATATCCTGTAAATAGCTGTAAAGTTGTTTAAACAGTTTGAGGGTTTCCAGGTGTTCAAGGATCTGGCCGAGTTTGATGTATCTGATGCCTTTGGGGTACCCAAAGATGAGGGACATTTTTGGTGGCCCGGATTGTCTTCACGAAGGCGACGTTCCTCCGTGTTTCCATGGCACTGGGACATCACTAAAGATGCCCGTTTTGCTTTTACGG[T/A]GAGGACATGACTTTCTCCACTTCCCCGTATTGTTTTAAGCTCAGGCAGCATAGTAGCTAAGTGGTTAGCACTCACAGTAAAGCTGCGGTCACAGTGCACTTTTCACCCCATAGACTTTCCTTCATAGGAACGAGAAACACCAGAAATGCAAGCTTGTGCAACAAGTTTCACAGTTTGCTAGTTGCGAAGTTCAAACTTGGTGAATTCTGACCTGCGAAATCGCTTCATGTGACTGCATGAGACCAAGAGAAGATCAGATGACCTCTCTGTACAGAAATGTAAAATATGGACCAACTGCATGCTTTTTCTAATCATCTTGTTTAATACCGCCCCTTTTCACAGCACCATACAACAGAATTTTGCATGCTAAAACTCTTGTGTGACCACGGTACTAAAAGTTTGCTGATTTGAGTCCCAGCTGGACCAGGACGTCATTCTGTGTGGAGTTTGCATGTTCTCCCTGTTTTTGAGTTGGTTTCCTCTGGGTGCTCCAATTGCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43830
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079046 | Nonsense | 705 | 1749 | 17 | 39 |
ENSDART00000134893 | None | None | 734 | None | 18 |
The following transcripts of ENSDARG00000056530 do not overlap with this mutation:
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 21587647)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 21240895 |
GRCz11 | 22 | 21265873 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACCTGCGTTTCAACCACACACCTCTACCCTGGTGGCAGCTATGCACTCC[C/T]GATCTGGGACACGGTACACATGCTCACAGTGTCTGAAATTTTAAGGTTAA
Long Flanking Sequence:
CTACATTCCAAAGACAGGCAGTATAGGTGAATTGAATAAACTGAATTGGCCATAGTGAATGAGTGTGTATGGATGATTTCCAGTAAAGGGTTGCAGCTGGAAGGGCATCCTCTGTGGCAACTCTTGATGGATAAAAGGACTGAATAAATGAAATTGACCACAGTGTGTGAATAGAAGAGTGTGGGGGTGTTTCTCAACACTGAGAGTTTTACTCAATGCTGGGTTGCGGTTGGAAAGGCATCTGTTGTTAAAACATATGATTGAGTAGTAGGTGGTGGTTTATTCCTCTTTGAAGACCACCAAATGAAGGGGGAAGCCGAAGTTAAGTAAATGAGTTCAAATTATAATATGCTTGTGTACCCGTGTTGTAGGAGACAGGGCTGGTGGTGATGACAGACATGGTGAGTCTCAATCACAGACAGAGTGGAGGGATGTACACAGACGAGGCCGTACCTGCGTTTCAACCACACACCTCTACCCTGGTGGCAGCTATGCACTCC[C/T]GATCTGGGACACGGTACACATGCTCACAGTGTCTGAAATTTTAAGGTTAATTTTACAGGCGATTATGGCTAACTTCAGTAAGGGACTTGTTTCTTATGTCAGTGTGTATTTTTCAGGGCAGAGAACCGTAGGCGTACATTCTTTCCAGAAACATGGATATGGCATTGCTTTAATGTCAGGTACTAAACTATTTCTATTATTCAATCAAATAGATAAATGATAATAAAAACATAGTAACCACAAACTTTTGAAGGGTAGTGTGTGTTTATATAGAGCAAGGATCACCAACCCTTCTCCTGAAGATTTCAGCTCCAACCCCAATTAAACACACCTTAAATAGATAATGAAGGGTTGCATGATAATTGTAGGCAGGTGTTCTGGAGCAGGGTTGGGACTGAAATCCGTAGGATAGTTGAACCTAAAGGCGGGCCTACACGATGCAAATTCTGATGGCTTAAAGATCATGAAAGATCAAGATCAGAAATCGCATACTTCCATAC
Associated Phenotype:
Not determined