ZMP
cpne5
Ensembl ID:
ZFIN ID:
Description:
copine V [Source:RefSeq peptide;Acc:NP_957322]
Human Orthologue:
CPNE5
Human Description:
copine V [Source:HGNC Symbol;Acc:2318]
Mouse Orthologue:
Cpne5
Mouse Description:
copine V Gene [Source:MGI Symbol;Acc:MGI:2385908]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41760 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa41761 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41760
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000050098 | Essential Splice Site | 247 | 429 | 10 | 14 |
ENSDART00000104503 | Essential Splice Site | 392 | 574 | 17 | 21 |
ENSDART00000126071 | Essential Splice Site | 375 | 557 | 16 | 21 |
Genomic Location (Zv9):
Chromosome 11 (position 3152935)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 3104423 |
GRCz11 | 11 | 3172583 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTTGGTTTAAATGAAGATGCAAATATGATCCACTGATCTCTGTCTTTC[A/T]GAATGGAAATATTGAGAATCCCTACTGTAATGGTATCGAGGGGATACTTG
Long Flanking Sequence:
GGTTCTCAATTGACTTACCTGGTTAAATAAAGGTTATTATTATCAAAAGGTCCATTGTTATTGTTATCAATTAAAAAAACAACGTGTGACCGCTGAGCAGAATCTCGGAAAATAAACCAAACTCTGACCAATGTGTGGAGAGTTGACTCGTACACGACTTGTTTTACTTTTGGTCCTTTAAAAAACTTTGTCGTGTGAAAACATCGTACCAGTTTTTCGGAAACAAATCAATTGATCTACAGGTGTGAAAGCAGCCTCAAAGAGTTTGCTGATGCAAGCATCTCGCTGTCCTTCGGTTTTACTTTCCCAGTTGTAAACTTGAGCGTGAGATTCTGTTGATGATCTGGAAGTGGTTCGATCCCACTGTATGGGAGACGTCTATAATTGGCAACGTTAGCTTGTCGTATTGATTGACATAATCCATGTTTTCTTTTTCTCTGGGTTGTTTTTCTGTTGGTTTAAATGAAGATGCAAATATGATCCACTGATCTCTGTCTTTC[A/T]GAATGGAAATATTGAGAATCCCTACTGTAATGGTATCGAGGGGATACTTGAGGCGTATCATCAGAGTCTGAAAACTGTCCAGCTATACGGCCCGACTAACTTTGCCCCTGTTGTAAATCACGTGGCCAGGTACGTTTTTCCAAACGTCTGTTTTAAAGTCAACACAAACTGTTTAGTTGGGCTATTATGCCAACTTAAAAATAAGATATAATTGGTTTGATGTCAGATTAATGATAATCAGTGATAAAAAAAACAGGGGGTCGCGGTGGCTCAGTGGTTAGTACTGTCACCTCACAGCAAGCAGGTCGCTGGTTCGAGTTCTAGCTGGGCGAGTTGGCATTTCTGTGTGGAGTTTGCATGTTCTCTCCGTGTCGGCGTGGGTTTCCTCTGGGATCTCCGGTTTCCTCCACAGTCCATGAACTAGAATTGGATAAACTAAATTGGCTGTAGTGTATAAGTGTGTGGGTGAATGTGAGTGTGTATTGGTGTTTCCCAGTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41761
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 |
---|---|---|---|---|---|
ENSDART00000050098 | Nonsense | 295 | 429 | 11 | 14 |
ENSDART00000104503 | Nonsense | 440 | 574 | 18 | 21 |
ENSDART00000126071 | Nonsense | 423 | 557 | 17 | 21 |
Genomic Location (Zv9):
Chromosome 11 (position 3155621)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 3107109 |
GRCz11 | 11 | 3175269 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGTGATTTTTAATTTTTTTCTGTTCTGTGAAGGTACGCAGCTGCTGTA[C/T]AGGACGGCTCGCAGTATTTCATTCTCCTCATCATCACAGACGGGGTCATC
Long Flanking Sequence:
ATTTCTTAATAAATAAATGATAATTCAGTTTTTGTGTGTGCATTTTGTTTTTTTTATATTAATAAGTTAATTAATTATGAAATGAAGAAAAATTCTGCATTTTGTTGACCTACAATGTTAGCAAACATGTAGCAAGATGAAATAATAACTTAAGATGAAGTAAATAATTTTGCATATCTTTTTCTAGATTGCTTTTGAAAACACTATTGGTTGGGTTTAGGGAAGAGGGTGGGTGCGGGGTTCGGTCGGTGAATTAGTCAGTCAGTCAGTCGCTAGAGAAATTTGAGATCTGAAAAAGCGTACACAGTGGTCTCTGGTGGATTCGCGAAAACAAAAACTGCAAAAAACAAAAAAAAACATAGCTCCTGGGATGTATTTGGCGCTCTCCAATAATGTATATAGGGGTACATTTTTTGAATGAGCCTGAGTTGGTTTCGAGTGTAAAGAGTTGATGTGATTTTTAATTTTTTTCTGTTCTGTGAAGGTACGCAGCTGCTGTA[C/T]AGGACGGCTCGCAGTATTTCATTCTCCTCATCATCACAGACGGGGTCATCTCAGATATGTCGCAGACCAAAGAGGCCATTGTTAATGTGAGTTTATGAGCACAAATGCCACAACTGGGGTCTCATTTATAAACATTCATAAGCGTAAGTACTAAACAGCGGCAAACAACGTGCATACGCCACTTTCCACACAAAAATTTTGATCTTTAAAACAAATAACTTATTTGATAGGAGAATATGCGCATATGTAAACTCCAAAACATATTTAACCTAAGTGTTGACTTAATTGAGAGAGAAAGAGTTTATTGCCATACCAGCTTTTTTGGCTATTTCATAGCAAAATCAGATCAAATTTACAACATTTTATAAATATCAGTTTTTTATAAAAAAAATATTAATGATGACAAAAAAGACAAGATCATCAATAAATAATACATATGATAAAAAATCTAAAAGGTTTACTTAACACTTTTAATAAATTTGTAGAATTTGTTAAGGATT
Associated Phenotype:
Not determined