ZMP
si:ch211-266a5.1
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC556936 [Source:RefSeq peptide;Acc:NP_001038282]
Human Orthologue:
CCDC87
Human Description:
coiled-coil domain containing 87 [Source:HGNC Symbol;Acc:25579]
Mouse Orthologue:
Ccdc87
Mouse Description:
coiled-coil domain containing 87 Gene [Source:MGI Symbol;Acc:MGI:3026882]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45171 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9070 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18779 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33424 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45171
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 |
---|---|---|---|---|---|
ENSDART00000067165 | Nonsense | 58 | 825 | 2 | 19 |
ENSDART00000141395 | Nonsense | 43 | 734 | 2 | 18 |
ENSDART00000144310 | Nonsense | 43 | 246 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 4 (position 12681046)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 13617673 |
GRCz11 | 4 | 13616522 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGAATCATGCAGATATCACAGCGTTACTCCATCTGTGATGAAGACCGA[C/T]AGTCTCTGGTCAGACAGATTAAAAATATATTGCAGACATTGTCTAAAAGC
Long Flanking Sequence:
CCGAATGAATGCGGAAACTGGATGCTGTTTTTCTAAAACTCTGAAGATGTTTTTTAAATATAATTTTGTTTGACCATAATTTCTGACTATTTGACTAGTTAGTTTTACCATAAGACTGTCAGACATTCCTCTTGTGCAGTGACTTTTTGAGAATGACTGGGGAAATTATTAAGGATTTCTTAACAATGTGATGTGATCTACAAATGATGGTCACTATCAAGATATTCTTCAGAGATCACTTTCATTTTTCAGCCATATGGACGTCCGTGTTGGAAGGATGACAGGTTTGTACTTATTCAACTCTCAAATGTTTGTCATTGAAATAACAGTAATGCTAATTCATAAATTCATCTGCAGACAGGTCTAAGGAAGTGATGTTGGAGTCTTCAGTTAACAATAAGAAAAGATGCATCCCGAGTTCTCTGACACAATTGTGCAAACAGCTTGAGGACAGAATCATGCAGATATCACAGCGTTACTCCATCTGTGATGAAGACCGA[C/T]AGTCTCTGGTCAGACAGATTAAAAATATATTGCAGACATTGTCTAAAAGCGTTTGTGAGAAATTAATAAAAGTCATCATTTACTAACCCTTTACTTGTTTCAAACTTTTATGTGTTTCTTTCTTCTGTTGAACACAAGATACAATAGTTTCAAAACATTTTGAAAACGGTAACCATTGACTTCCATTCTAATTGTTTTGTTATTTACCATGGAAGTCAATGGTTACAGGTTTCTAACAATATTCTAAATATCTTCTTTCATGTTCAACAGAGGAAAAGCCCACTTGCGAGTGAGTAAATGGTGAATAAATCTTAATTTTTTGAGTGAAATGTCCCTTTAAGTGACTGCACACTCTCAAAAAATAAATAAAAAAAGGCGAGCATTTCAGTCACACACTGACCCTCGTCAACGCCAAGCTATTGTTACTTTATCTCCCTTGTGTCCTTTTTGTATTTTTGAGAGTTTACATTGTCTGCAGACTTTTTCATTCATTCAGATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9070
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067165 | Nonsense | 539 | 825 | 13 | 19 |
ENSDART00000141395 | Nonsense | 524 | 734 | 13 | 18 |
ENSDART00000144310 | None | None | 246 | None | 5 |
ENSDART00000067165 | Nonsense | 539 | 825 | 13 | 19 |
ENSDART00000141395 | Nonsense | 524 | 734 | 13 | 18 |
ENSDART00000144310 | None | None | 246 | None | 5 |
Genomic Location (Zv9):
Chromosome 4 (position 12685582)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 13622209 |
GRCz11 | 4 | 13621058 |
KASP Assay ID:
2259-4681.1 (used for ordering genotyping assays)
KASP Sequence:
GTCTTGGCTTCGAAGGACTCTGATTATCTGCCAGTKCTGTTTCACTTGTA[T/G]GACAGTGACGATGATGRTGAAGAGGCAGAGAGACACAAGTTGGATCAACT
Long Flanking Sequence:
AAATCGTCTTTTGATCCATCTTCTAAAGGATCCCACTATCGAGCCTTCCTTGAAAAATCCCTTATGTCTACCAAAAAGAATAGTTAATGACAAACTAATAAACCAATCACTCAGGAGGCCCAATCCATACAACATATCCCACAGGTACTGTTCTACATTATTATCTGTGAATTTGTTGTACTTTGATATCACAAAATTACATTTAATCTTGCATCAAATATGCAGAAAGAGAATCGAGAGGAATGTAAACAGAAAGAGGCCTGAAGATGTGACCACAAGAGCGTACAGAGCCTGGTTCCAATGGTGGAGGTGTCAACTATCACTAGATGATTATCTGGACTACATTTCCAATCAGGTAAGTTTATAATATGTGGGTTTGCTAATGGCTGATGAGTATAGTCAGACTGGTGGGTCATTTGTGTACTTCAGTAGTTGTGATTGTTTTTTTGTGTCTTGGCTTCGAAGGACTCTGATTATCTGCCAGTTCTGTTTCACTTGTA[T/G]GACAGTGACGATGATGGTGAAGAGGCAGAGAGACACAAGTTGGATCAACTCCAGAAAGCGGAGAGGAGAAGGTCTGGTATTAATATCTGGATTTTATGTTTAGTTCTTCTTCCCTAATTTATTTGGAGATTGACACATGATTTGGTGAGTCTTCATAATTGGCCTCATAGTTGAAAAAACAAGCACAAAACAATGTGCAATACTAGTAATGTGAGATTCCAGTTATTCTATGTCTATAATTAAAAATGAACTCGAAGATTAATCTTATCAATATTATCTGATGATCATCGCTTTCAGAAAGCAGCAGGAAAGGATCGATTCACTTAGGAGATGCAAACAGGAGTTTGTTCCTGGGTTCTGGAACATCAACACTATAGAGATGGGGGGACTGGGGAGAGAACCAGAACTGGATGGCATGTTATTTTTCTTTAGAAACAAAAATAATACTGGTCTGTTTATGAAAATGTGCTATTTACACATGGAATATCTGTGTTTCAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18779
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067165 | Nonsense | 539 | 825 | 13 | 19 |
ENSDART00000141395 | Nonsense | 524 | 734 | 13 | 18 |
ENSDART00000144310 | None | None | 246 | None | 5 |
ENSDART00000067165 | Nonsense | 539 | 825 | 13 | 19 |
ENSDART00000141395 | Nonsense | 524 | 734 | 13 | 18 |
ENSDART00000144310 | None | None | 246 | None | 5 |
Genomic Location (Zv9):
Chromosome 4 (position 12685582)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 13622209 |
GRCz11 | 4 | 13621058 |
KASP Assay ID:
2259-4681.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTTGGCTTCGAAGGACTCTGATTATCTGCCAGTTCTGTTTCACTTGTA[T/G]GACAGTGACGATGATGGTGAAGAGGCAGAGAGACACAAGTTGGATCAACT
Long Flanking Sequence:
AAATCGTCTTTTGATCCATCTTCTAAAGGATCCCACTATCGAGCCTTCCTTGAAAAATCCCTTATGTCTACCAAAAAGAATAGTTAATGACAAACTAATAAACCAATCACTCAGGAGGCCCAATCCATACAACATATCCCACAGGTACTGTTCTACATTATTATCTGTGAATTTGTTGTACTTTGATATCACAAAATTACATTTAATCTTGCATCAAATATGCAGAAAGAGAATCGAGAGGAATGTAAACAGAAAGAGGCCTGAAGATGTGACCACAAGAGCGTACAGAGCCTGGTTCCAATGGTGGAGGTGTCAACTATCACTAGATGATTATCTGGACTACATTTCCAATCAGGTAAGTTTATAATATGTGGGTTTGCTAATGGCTGATGAGTATAGTCAGACTGGTGGGTCATTTGTGTACTTCAGTAGTTGTGATTGTTTTTTTGTGTCTTGGCTTCGAAGGACTCTGATTATCTGCCAGTTCTGTTTCACTTGTA[T/G]GACAGTGACGATGATGGTGAAGAGGCAGAGAGACACAAGTTGGATCAACTCCAGAAAGCGGAGAGGAGAAGGTCTGGTATTAATATCTGGATTTTATGTTTAGTTCTTCTTCCCTAATTTATTTGGAGATTGACACATGATTTGGTGAGTCTTCATAATTGGCCTCATAGTTGAAAAAACAAGCACAAAACAATGTGCAATACTAGTAATGTGAGATTCCAGTTATTCTATGTCTATAATTAAAAATGAACTCGAAGATTAATCTTATCAATATTATCTGATGATCATCGCTTTCAGAAAGCAGCAGGAAAGGATCGATTCACTTAGGAGATGCAAACAGGAGTTTGTTCCTGGGTTCTGGAACATCAACACTATAGAGATGGGGGGACTGGGGAGAGAACCAGAACTGGATGGCATGTTATTTTTCTTTAGAAACAAAAATAATACTGGTCTGTTTATGAAAATGTGCTATTTACACATGGAATATCTGTGTTTCAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33424
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 |
---|---|---|---|---|---|
ENSDART00000067165 | Nonsense | 671 | 825 | 17 | 19 |
ENSDART00000141395 | Nonsense | 656 | 734 | 17 | 18 |
ENSDART00000144310 | None | None | 246 | None | 5 |
Genomic Location (Zv9):
Chromosome 4 (position 12687843)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 13624470 |
GRCz11 | 4 | 13623319 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTGCATTTGTCCTATCAGGCTATTGCTGCATGGGAGCAGGCCACCTGTT[T/A]GATCCAGAAGAGGGAGCTCTTGCTTTCCAGGTTGGAGGACTTTGAGAAGG
Long Flanking Sequence:
GAGGGTCTGATGAATGGACCAGGAAACGTATGGATGGATTAATGTAGAGACTGATGGATGAATAGAAGGAGAGACTGATGGACTGAATTATGGAGAGACTGGTTGAAATATGGATGGATGCAGAGACAAACTGATGGATGGATTGATGGTTGTTCTGGACAGGAGGGTGAAGGTCCAGCTTCTGGTCTGCTGGATACTGAACAGTTGCAGCTCAGGCTGGAAAGGGTCTGGAATGCCCTGCATCTGCCAGAAGGACAGCGACTAGACATGGCCATTAAATACAGCTCATACGAGCACAGGGACCATCTGCAGGAGGTATACAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAAATAAACTATCCTGGCTATGCATCATCATCTTCAGTGTTGTCACATAGTTGCATTTGTCCTATCAGGCTATTGCTGCATGGGAGCAGGCCACCTGTT[T/A]GATCCAGAAGAGGGAGCTCTTGCTTTCCAGGTTGGAGGACTTTGAGAAGGAGGCATCTGATCCCAACAGATTTTTCCAGCCGGGTACATTAGACACACAGAATAATGAATTCTGCCCTGTTGAGATGATGGATTGCATGCATGGGACTATATCATACATTTAGTACAGATGTAATGTGAATACACAGGTTTTCCTGGCTCATCTATGGCTAGAATGGAGGAGGCGACTCAAAGGGAGAAGCTCAACTCTCAAATTTCAGTTGTAGATGAGGAACTGTCCCAGATAATAGGCCAAATCACAACCCGTTTTCATGACAACATCAGCTATAAGGTGAGAGCGTGACTGTTTGTATACACTATTGTTAATTTGCTTGCAGTTGTCCTTCTTTGTCATTGTTTTTGGCTGTCCCAGGGTCGCCCATACAGGGAGAAGATGCGCTGGGACCGGACTGAGATGTTGTACTGGCTGCAGCAGGAGAGACGGGTTCAATCTCTGGAGAT
Associated Phenotype:
Not determined