ZMP
zgc:55582
Ensembl ID:
ZFIN ID:
Description:
myomegalin [Source:RefSeq peptide;Acc:NP_956195]
Human Orthologue:
CDK5RAP2
Human Description:
CDK5 regulatory subunit associated protein 2 [Source:HGNC Symbol;Acc:18672]
Mouse Orthologue:
Cdk5rap2
Mouse Description:
CDK5 regulatory subunit associated protein 2 Gene [Source:MGI Symbol;Acc:MGI:2384875]
Alleles
There are 20 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23850 | Essential Splice Site | Available for shipment | Available now |
sa12833 | Nonsense | Available for shipment | Available now |
sa32328 | Nonsense | Available for shipment | Available now |
sa23849 | Nonsense | Available for shipment | Available now |
sa37218 | Nonsense | Available for shipment | Available now |
sa23848 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23850
Status:
Available for shipment
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:
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031425 | Essential Splice Site | 96 | 1209 | 4 | 28 |
ENSDART00000122131 | Essential Splice Site | 96 | 2784 | 4 | 49 |
Genomic Location (Zv9):
Chromosome 21 (position 4940512)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 4517924 |
GRCz11 | 21 | 4682489 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGTGTGCAGCAGAAATGTGACGACTCCACAGAGGACATTTACAAAACGG[T/A]AACATTATTTATTTTTGGATATGAATGCAAAGAGGTGCTTTTTTGTGCTC
Long Flanking Sequence:
GACCCACACACAGCCTGTTATAGTCGCTCTGTTTCTCTTTTAGCGCTCGTCCCCTCCTTTCCCATCTCCCTTTCAGTTATTTGCAGAACAGCTTTGCTCATGTTTATTCATGAAGGAGTCTGAATATTGTAATGAGGAACAACTATATAGTCATAGAACATCAAAAAACTCAGGGAAGAAAGGTTTTGTCCAATTTGCAAATGAATAGTTTAGTCTGGTGTTGGATTATGTAAAGATCCAAATTAATCTGATTTGTTTTCTGCAAATAATACTATACAATTCACTTAAGTTACTAAACTTATAAAGAAAATAAAAGATGTAGCAACGTTTTCTCCCTGTTTGTATTGTCTGTCTGTGTACACTGAAGATATGCATGTTTCCCTTGCAGCAAATCACAGCACTAAAAAAAGAAAACTTCAACCTGAAGCTCAGGATCTATTTTCTAGAAGAGCGTGTGCAGCAGAAATGTGACGACTCCACAGAGGACATTTACAAAACGG[T/A]AACATTATTTATTTTTGGATATGAATGCAAAGAGGTGCTTTTTTGTGCTCGAAGGCCACAATTGATTGTTTGTTTTATGTCTGTGTAGAACATTGAGCTGAAGGTGGAGGTGGAGTCAATGAAACGAGATCTGGCTGAGAAACAGGAACTGCTCGTGTCCGCATCGTAAGTCGTGCTTGTTTACTTCCTATTTTTTTGTACACTACCTGACAAAAGTCGTCAGGTAAAAAGTTGCCGCCTGTCCAAGTTTTAGTAGCAACGAATAATGACTTCTAGTTGTTCATTTGGTATCAGAAGTAGCTTATATGAAAGGCAAAGGCCTCTAGATTACGCTTATTTTACCAAAATAAAATATGATCATGCCTTGTTATTTAATTATTTCATTAGGACAGTAAGGTCTGACTTTGCTTAGACAAAAGTCTCTTCACTGAACAGAAATAATGTCCAGTATAGAATATAAAGTCCTGCTGCAGTGGAGACAGAATGAATATTGTGTCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12833
Status:
Available for shipment
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:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031425 | Nonsense | 286 | 1209 | 9 | 28 |
ENSDART00000122131 | Nonsense | 286 | 2784 | 9 | 49 |
Genomic Location (Zv9):
Chromosome 21 (position 4934183)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 4511595 |
GRCz11 | 21 | 4676160 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTTAGGGAAGAACTTGACCAGGGAAAAGAAAATGCAGAAAGGGACAAA[C/T]AGGTAAGCGGAAAGCCATTYAATTATAATGCWTACCAGGACGATRAMCTT
Long Flanking Sequence:
CCACTGCTTTGCTCATTTAGCGAAAGGGACAAAACTTTCAGGCACTGATGTTGGATCCGTTTATTTATTTTGCAATGTGAAATCAAAATTCTCCTACGAGAGGGATTATACAGCCTCTCGATGGTGAATGCAATTCTACTCATGGCAGGTATTATTTGGTAGTTTGGTCATTTATTTCACTGATTTGGCAACCATTGGTGTTCCATTTGGGATGACACTACACTACATACATATATTATGCTGTTGAGTGTGTAAGTGTATAGTGGGCCATTTGGGACGCAGCTTTTGTGTATGCAGTTGGAATTTATGTTATTTTCCCACCTCTGAACCACTTCTGTGGCCTCTTTGCTGTGTTAATTTGGTATTTGTCATTGATACTCCATGTTAATGCTTTCTCAAACACACATACTTAAACAATGATTAATGTTTTGTTTATTTTTGGTTTACAGGCTCTTAGGGAAGAACTTGACCAGGGAAAAGAAAATGCAGAAAGGGACAAA[C/T]AGGTAAGCGGAAAGCCATTCAATTATAATGCATACCAGGACGATAACCTTAGCATCTCTGAGTGACAAGTTACTATTTGTTTATGTTGTAACTGATTTGAGCAACGTTAAAAATTCAGGATTTGTGCACTCCAAAACAGTCAAAAACTGTTCATTTAAAAGCATTGTTCCTCATCCATACTAATATCCCTGTAAAATGATTAGGAAGGATCCTATCTTGTAATTAAATATGACAGAAAAGCTCAAAGAGTGTGGGAACCCTGTAGAATGGCAACACACTAAGCTGGATTAGTTAGCTGAAATCTGTGTCTGTCGTAAATGCAAATGAAATATTATAATGAATCCTCCCAGGTCCTGTGGTCAGCTTGGACAGGAGTATGTGTAGGGCTGTACAATAAATCGTTTCAGAATCGACATCGCAATGTGTAAACCTGCAAAAGTTACATCGTAGGATCTGTAATGTCAAATTGATATTATAATTAACCAGAAAACACAGTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32328
Status:
Available for shipment
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:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031425 | Nonsense | 505 | 1209 | 14 | 28 |
ENSDART00000122131 | Nonsense | 505 | 2784 | 14 | 49 |
ENSDART00000031425 | Nonsense | 505 | 1209 | 14 | 28 |
ENSDART00000122131 | Nonsense | 505 | 2784 | 14 | 49 |
Genomic Location (Zv9):
Chromosome 21 (position 4925066)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 4502478 |
GRCz11 | 21 | 4667043 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCTGACCGAGAGAACGCTCTAGATCAACAGCGTCTAGAGCAGCAGGAA[C/T]AGATCCGAGCATCAGAACAGAAGATGCAGAACGCCATGGAGAGACTCACA
Long Flanking Sequence:
TGCTTGCACTGAGAGTGTGCCTCACAACCATGTAGACATTTGTGTAAAATGATTCGGGACATATTTACTTTGATGCAGATCCTGAAATATATCTATTTGAACCAGAATACATGGAAGTTAGCAGATTTTCAGGTGATTTCTCAGGGTCAAAAATGACAGAGTTTCAGTAATGTATTTTAAAGCTTGACTCAAGAGATGAGTGGATCTTTACATTTAAAATCATCTTGCATCATTTTTGAGTGAGATGCTAATGGTCTAATCCATTTCAATGATCTATGCTAAGCTAAGCTAAAAGTGCTCCCGCCAGACCCAGAGGTTGTTTTCAAGCAATCAAAAATGATAAAGCACAGCTGTTTAACACCTATGCGAGTTGTAAAATGAGCTTGTTTTCAGAAAATTGCTTAATTTTGCAGGATCTTCAGAACCAGTTAAAGAAGCTCAATGGTACTCTGGCTGACCGAGAGAACGCTCTAGATCAACAGCGTCTAGAGCAGCAGGAA[C/T]AGATCCGAGCATCAGAACAGAAGATGCAGAACGCCATGGAGAGACTCACAGCCAGCCTGAATCATAAAGACCAGCAGCTTCAGGTACACACAAACACCCACACAACCACACACACATACTCGTATATATGGTTTACTAGGACTCTCCATTGGTTTAATACATTTTATACCGTAAAAAAAGCTTATTATATGGCCTCACACCTTAAACTAAACCCAACCCTCACAGGAAACATGTGGAGATTTTAATGTCAAAAGACCACTAAGTATGTTTCAAATTCTGAGGACACACCGCTTGTCTTAATAAACCCCTTAAAGGGATGGTTTACCCAGAAATAAATACTCACACATTATTATTTAGTCTCCCTTAAGAGTTTCCAAATTCAGTGCTTCCCACACATAGACTTTCTTGGGTGGACCACCCCGGTATAATAACGACCGCCCATGTATATTTAGTGACACATATTTTTACTATTATTATCATCTTTTTACACTTTTTTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23849
Status:
Available for shipment
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:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031425 | Nonsense | 505 | 1209 | 14 | 28 |
ENSDART00000122131 | Nonsense | 505 | 2784 | 14 | 49 |
ENSDART00000031425 | Nonsense | 505 | 1209 | 14 | 28 |
ENSDART00000122131 | Nonsense | 505 | 2784 | 14 | 49 |
Genomic Location (Zv9):
Chromosome 21 (position 4925066)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 4502478 |
GRCz11 | 21 | 4667043 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCTGACCGAGAGAACGCTCTAGATCAACAGCGTCTAGAGCAGCAGGAA[C/T]AGATCCGAGCATCAGAACAGAAGATGCAGAACGCCATGGAGAGACTCACA
Long Flanking Sequence:
TGCTTGCACTGAGAGTGTGCCTCACAACCATGTAGACATTTGTGTAAAATGATTCGGGACATATTTACTTTGATGCAGATCCTGAAATATATCTATTTGAACCAGAATACATGGAAGTTAGCAGATTTTCAGGTGATTTCTCAGGGTCAAAAATGACAGAGTTTCAGTAATGTATTTTAAAGCTTGACTCAAGAGATGAGTGGATCTTTACATTTAAAATCATCTTGCATCATTTTTGAGTGAGATGCTAATGGTCTAATCCATTTCAATGATCTATGCTAAGCTAAGCTAAAAGTGCTCCCGCCAGACCCAGAGGTTGTTTTCAAGCAATCAAAAATGATAAAGCACAGCTGTTTAACACCTATGCGAGTTGTAAAATGAGCTTGTTTTCAGAAAATTGCTTAATTTTGCAGGATCTTCAGAACCAGTTAAAGAAGCTCAATGGTACTCTGGCTGACCGAGAGAACGCTCTAGATCAACAGCGTCTAGAGCAGCAGGAA[C/T]AGATCCGAGCATCAGAACAGAAGATGCAGAACGCCATGGAGAGACTCACAGCCAGCCTGAATCATAAAGACCAGCAGCTTCAGGTACACACAAACACCCACACAACCACACACACATACTCGTATATATGGTTTACTAGGACTCTCCATTGGTTTAATACATTTTATACCGTAAAAAAAGCTTATTATATGGCCTCACACCTTAAACTAAACCCAACCCTCACAGGAAACATGTGGAGATTTTAATGTCAAAAGACCACTAAGTATGTTTCAAATTCTGAGGACACACCGCTTGTCTTAATAAACCCCTTAAAGGGATGGTTTACCCAGAAATAAATACTCACACATTATTATTTAGTCTCCCTTAAGAGTTTCCAAATTCAGTGCTTCCCACACATAGACTTTCTTGGGTGGACCACCCCGGTATAATAACGACCGCCCATGTATATTTAGTGACACATATTTTTACTATTATTATCATCTTTTTACACTTTTTTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37218
Status:
Available for shipment
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:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031425 | Nonsense | 1167 | 1209 | 28 | 28 |
ENSDART00000122131 | Nonsense | 1167 | 2784 | 28 | 49 |
Genomic Location (Zv9):
Chromosome 21 (position 4905960)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 4483372 |
GRCz11 | 21 | 4647937 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAGAGCTTGAGGCAGTAAATGCTGAATTACAGAAGAAGCTGGTTCTGT[T/A]GGAGAAAGACACTGTGGGAAATGCTCCAATAGGCTCTCACTCTCAGAAAG
Long Flanking Sequence:
TTTACACAAATATTTCTTATTCAAATCTTTAGCAACGCTATTTAACTTGTGAATTTGTTTTACATTTATTTACACCTTGACCGATTTATGTATGGCATGGCCATAAAAAATACAATGTTCCTTAACCAGATGGTTTTTCAAGCTACTTTTAAAGAGAGTGTTACTTCAGTCATGTAGTTGTAATGTTTTCAGAAGACTAGTAAGACAATAAAAAAAAAATCGAAATCGTTAATCGGTCAAACTTTATACAAAACCTAGATTTTTTATTTTTTTTTGCCAAATCGCCCAGCCCTACTATGGATTATGGGTTTCTTCAAAATATTTTCTTTAGTGAAGAAAAAAACTCAAAGGTTTTTAACCACTCGAAGATTAGTAAACGGTAAATAAATGTTAATTTTTTAGAAAATTTTTACTATTAATTTAAACTGCATTTTAACCTAATTTTCAGGTTTTAGAGCTTGAGGCAGTAAATGCTGAATTACAGAAGAAGCTGGTTCTGT[T/A]GGAGAAAGACACTGTGGGAAATGCTCCAATAGGCTCTCACTCTCAGAAAGAACCAGATCTTATCGACCTCTCAACTCCTACCAAGGTATTACAGTTTACAAGTTCAGGAGCATGTTTTAGATTCCATTAGGATAATAAATTTTCCAAAAAACACATTACTTGTCTTTACTAAACACTGTTGCTGCAGCTCTTTTCACACTCTTTCTAAAATGCTCAGATTTAGTTTCTGTCTGTTTATAACCTGCTTTTCCAAAAAGCCTAGTGTGTTCTGGCCAATCAGCTTTCTTTTTTATTGGTCAAACACTTCGCTGCTACCTGTTATTTGGATGATAAAAAATGTGAAATTTCTAGGAATGTTCTAATACACTTTTAATTTTCCCAATACCGATTCCAAATACCTGGGCTCAGTGCATCTGCCGATGCAGAGTACTGAACGGATACCTGAGTGTGTATCTTTAGAAAGAGTTGTGTATATTATTAGGCCTATATTAACTGGCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23848
Status:
Available for shipment
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:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031425 | None | None | 1209 | None | 28 |
ENSDART00000122131 | Nonsense | 1449 | 2784 | 32 | 49 |
Genomic Location (Zv9):
Chromosome 21 (position 4900985)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 4478397 |
GRCz11 | 21 | 4642962 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCCAGTAGGAGTACCGGACAGAGTTCTGAAGATCTGAGTGAAGTAAATT[C/A]AGACCACATTCAACCCAAGAGAAAAGACCACCAGACTGGGGCAGAAGAGT
Long Flanking Sequence:
TCAAACGACTTAAACGATATAACTAGAGAAATCTCCACTGTGTTGAGCGAGAGCACAGCCCAGCATCGATGACGTAATCGTACCCAGGCCCGAATGTAATGTGAGTGCGGGCCGTCGGGGGAGACGGGAGGGGGACAAGCATGCTTTGGCACGGTTCATCGAAACTGTACATAGTGTGAGTACGCCCTAAGAGTTCTCTGAACAATACAAATAAAATTAACTAAGTTAGCGATGTTCAAGAGCTCAAAATGTGCATTGAACATGCAAACTTTAATTGCCAATCTAAAGCATTATCGAGTATGCCACATCACCAATTTTTCCTACTTACAATGTGGAGATGCTTCCAATGCTTCACTGATTTTTTTTCCATTTGTTTCAAAAGATCTGATCAGTAAAATAATGTTGTTTGTATTAGGCATATGTGAAATCTCGGCTACCAGTACCTGTGAGGTCCAGTAGGAGTACCGGACAGAGTTCTGAAGATCTGAGTGAAGTAAATT[C/A]AGACCACATTCAACCCAAGAGAAAAGACCACCAGACTGGGGCAGAAGAGTCTGATTATAGCACTGACAGTAAGATGTCCTCAAGATCATCTCAGAAGGGACACCTCGAATTAGACCAGGTTAAAGATGCTCGGCTTAGTCCAACCAGTGGAACAAAACAAGACAATTACACGGATGATTATCTTGAATCCGAGCTCATGGCACAGTTAGAGTTGTTGAATCAAGAATGCCAAGAGAAGGAGGAGCTAATCTCTCACCTGAAGCAACAAGTTCAGGAATTGGATGAACTGCAGGTAGAACTACAGAAGAAGGACAAGCTCAACCGAGAGTACCTGGAAGCCCTGCAAGCAGCAGAATCCACTATTGCATACCTTACCGCTTGTAGCTTGGACTCAGAGTGTGGAATTGGTCAAACAGGAGATGTAACATTGCAACAACGCTGTGCAGAACTGCAAAAGGCCATCGAGGAGAAAGACAGAGTCAATACTCAGCTCTTGGAGT
Associated Phenotype:
Not determined