ZMP
si:dkey-216e9.3
Ensembl ID:
ZFIN ID:
Human Orthologue:
CHMP5
Human Description:
chromatin modifying protein 5 [Source:HGNC Symbol;Acc:26942]
Mouse Orthologue:
Chmp5
Mouse Description:
chromatin modifying protein 5 Gene [Source:MGI Symbol;Acc:MGI:1924209]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa717 | Nonsense | Available for shipment | Available now |
sa39848 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa9007 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32944 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa717
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056731 | Nonsense | 14 | 251 | 1 | 8 |
ENSDART00000132645 | None | None | 219 | None | 8 |
Genomic Location (Zv9):
Chromosome 2 (position 30609471)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 30911106 |
GRCz11 | 2 | 30894639 |
KASP Assay ID:
554-0625.1 (used for ordering genotyping assays)
KASP Sequence:
ACTTTTATTATGGTGTGTATTCCACGACCAACCGGAAGAAGCGCGTTGTG[G/A]TGGTCGGCATTTAAATACCTCTACAAAGCAAATAAGTGTCATTCCCATAT
Long Flanking Sequence:
GTAAATAATTAAACAAATTGCACAAAATAAGAATATATATATATATATATATATATATATATATAAATATTTTAGATGATTTATTTATAAATGTCTGTTTCATTTTTACACACTTGTTAGCCAAATTTATATATATTTCCACCATGCAAGATTTATTTTCCACCTCATGTAAATTTTCTATGAATGAAAGGAAGGTTAGGGTTAGGGAAAATTTTTAGGAAATCATTTTTAGGAAATTATGTAAGTAAACAAATAAATAGACCAAAAATAAATATTCGTAAGAGCAAGACAACTGTAATTATATATAGTGTTGGAAAGGGACATGGGACAAAACAATTTCATGGAAAAAATAAAAAGAAGAAAGAGGAACACATAAGCATCGAGATTAACAGCATTATTACATTCTTACCAGTGACAAACAAATGGAAAAGAGAACAATCCGCAGCCGTGACTTTTATTATGGTGTGTATTCCACGACCAACCGGAAGAAGCGCGTTGTG[G/A]TGGTCGGCATTTAAATACCTCTACAAAGCAAATAAGTGTCATTCCCATATAAATATGAACCGAATTTTCGGTCGGAGCAAACAAGCGGCGTCTCCCAACCTTTCTGACTGCATAGGCAATGTAAGTACCGTGGATTTAAGAATTTATTGCCGAGCATCAGTCGAGCGTCCTGATTGGTGTTTTGATGTCAGACATGGATGTGCTGTGGATGCTGAGTGTTCATTATCCCGTTATTCTGCAGGTGGACACGAGGATTGAGTCAATCGACAAGAAAATAGCGAGAATCGATGCCGAGCTCATGAAGTATAAGGACCAGATGAAGAAGATGAGGGATGGACCCTCAAAAGTGAGCATCAGAAAGTCGAGTTAAATAAAGCAAACATTTTAATAATAAAAACAGGCAGCTTTATAAGTCTGTGATCACTGTTTGTTTTTAATGCATCTTTTACATATTATATAATATTATCATTGTAACGTGTAAATGTTTCTTTAAATTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39848
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 |
---|---|---|---|---|---|
ENSDART00000056731 | Essential Splice Site | 105 | 251 | 3 | 8 |
ENSDART00000132645 | Essential Splice Site | 73 | 219 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 2 (position 30611724)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 30913359 |
GRCz11 | 2 | 30896892 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAATACAGTGAAGCAGAAGGCAATGAGAGTGCTGAAACAGAAGAGAATG[T/A]GAGTTTGTTTGGAGACTAATGTGCATTTACAATGTATGAAATGTTTCAAT
Long Flanking Sequence:
TTCAAAAGAATCACTCTTACACATAAATAAAAATACAATAAGTTTGTTTGAATGTGTTTCAGTTAACATCATATTTATGCCAAGAACTAAAAAGTTATATTTTTTTCAAAACATGATGGTCGTGTATATCAGAAAAAATTTCAGAAGGACCCAAAATCCTTAAGTACATCAATAAAGATCTTAAGTTTAAATTGATGGATGACTTTAACTATAATATTGAAATTATGCATTGAATTTTTTTAATTTTTAAAAAAGCCTAGAATATAAAATTAGATTTTGAATTTCACTTAAAACTAAAATATTGTATTTAATCTATCCGTAAGACTGATTCATTTAGTTTAAAATAAATGTAAGGGAAAATTTAGAAACATAGAAATTTATTTTTAAAAATATTTGTATCTCACTGTTAATCGTAAACAGTTGTAAGTATGAGCTGAATGATCTCTTCACAGAATACAGTGAAGCAGAAGGCAATGAGAGTGCTGAAACAGAAGAGAATG[T/A]GAGTTTGTTTGGAGACTAATGTGCATTTACAATGTATGAAATGTTTCAATATCAAGAATTGTGTTTTCATTTAACCCTGGAAAAAAATGTTTAAAAAAAACTTGTTTTTAATAATAATGTAAAATAAAATTATTATTCGTTCTTTCTCCACCACTATTTTTCAGGTATGAGGGCCAAAGAGATCAACTTTCTCAACAGTCTTTTAATATGGAACAAGCCAACTATACAATCCAGTCTTTAAGGGACACCAAAACAACAGTAAAGACTTGTTATTTTACATTACATCTGTCATTATTACTGCCAGTATTAGTTTCTGTTTACTTTAAATCACACGCAACCTTTGATTTGCAAAGATCCAGCTTATTTCATGTGATTTCTCTAATAAAATGATTGCATAATAATTTTTTCTTCCATAGTGTTCCCAGCACATCTGACATTTACATTTATTTGATAATGATTTAATAGATTAAAAGCATGCCCATTTTTTGTAAAGATGGTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9007
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 |
---|---|---|---|---|---|
ENSDART00000056731 | Nonsense | 125 | 251 | 4 | 8 |
ENSDART00000132645 | Nonsense | 93 | 219 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 2 (position 30611949)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 30913584 |
GRCz11 | 2 | 30897117 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAAGAGATCAACTTTCTCAACAGTCTTTTAATATGGAACAAGCYAACTA[T/A]ACAATCCAGTCTTTAAGGGACACCAAAACAACAGTAAAGACTTGTTATTT
Long Flanking Sequence:
TGCATTGAATTTTTTTAATTTTTAAAAAAGCCTAGAATATAAAATTAGATTTTGAATTTCACTTAAAACTAAAATATTGTATTTAATCTATCCGTAAGACTGATTCATTTAGTTTAAAATAAATGTAAGGGAAAATTTAGAAACATAGAAATTTATTTTTAAAAATATTTGTATCTCACTGTTAATCGTAAACAGTTGTAAGTATGAGCTGAATGATCTCTTCACAGAATACAGTGAAGCAGAAGGCAATGAGAGTGCTGAAACAGAAGAGAATGTGAGTTTGTTTGGAGACTAATGTGCATTTACAATGTATGAAATGTTTCAATATCAAGAATTGTGTTTTCATTTAACCCTGGAAAAAAATGTTTAAAAAAAACTTGTTTTTAATAATAATGTAAAATAAAATTATTATTCGTTCTTTCTCCACCACTATTTTTCAGGTATGAGGGCCAAAGAGATCAACTTTCTCAACAGTCTTTTAATATGGAACAAGCCAACTA[T/A]ACAATCCAGTCTTTAAGGGACACCAAAACAACAGTAAAGACTTGTTATTTTACATTACATCTGTCATTATTACTGCCAGTATTAGTTTCTGTTTACTTTAAATCACACGCAACCTTTGATTTGCAAAGATCCAGCTTATTTCATGTGATTTCTCTAATAAAATGATTGCATAATAATTTTTTCTTCCATAGTGTTCCCAGCACATCTGACATTTACATTTATTTGATAATGATTTAATAGATTAAAAGCATGCCCATTTTTTGTAAAGATGGTATTTTCTTTATATAATAAATGTTTATTCTGTATATTTTTGTAACTTTCTTAAATGTCATTCTGGAAAAAAAAAACATTTTCAACTACTGAACTAAAAAATGTATTCATTTATAACATAAGACATTGTCTTCTTAAAATAAATAAAATCAAAATTAATTCAAATTCATAAAGTTAATCTGAAAAATAATTACTGGTGTCATTTAAAAAATTTACGAATATTCTAGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32944
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056731 | Nonsense | 134 | 251 | 4 | 8 |
ENSDART00000132645 | Nonsense | 102 | 219 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 2 (position 30611974)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 30913609 |
GRCz11 | 2 | 30897142 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTTAATATGGAACAAGCCAACTATACAATCCAGTCTTTAAGGGACACC[A/T]AAACAACAGTAAAGACTTGTTATTTTACATTACATCTGTCATTATTACTG
Long Flanking Sequence:
AAAAGCCTAGAATATAAAATTAGATTTTGAATTTCACTTAAAACTAAAATATTGTATTTAATCTATCCGTAAGACTGATTCATTTAGTTTAAAATAAATGTAAGGGAAAATTTAGAAACATAGAAATTTATTTTTAAAAATATTTGTATCTCACTGTTAATCGTAAACAGTTGTAAGTATGAGCTGAATGATCTCTTCACAGAATACAGTGAAGCAGAAGGCAATGAGAGTGCTGAAACAGAAGAGAATGTGAGTTTGTTTGGAGACTAATGTGCATTTACAATGTATGAAATGTTTCAATATCAAGAATTGTGTTTTCATTTAACCCTGGAAAAAAATGTTTAAAAAAAACTTGTTTTTAATAATAATGTAAAATAAAATTATTATTCGTTCTTTCTCCACCACTATTTTTCAGGTATGAGGGCCAAAGAGATCAACTTTCTCAACAGTCTTTTAATATGGAACAAGCCAACTATACAATCCAGTCTTTAAGGGACACC[A/T]AAACAACAGTAAAGACTTGTTATTTTACATTACATCTGTCATTATTACTGCCAGTATTAGTTTCTGTTTACTTTAAATCACACGCAACCTTTGATTTGCAAAGATCCAGCTTATTTCATGTGATTTCTCTAATAAAATGATTGCATAATAATTTTTTCTTCCATAGTGTTCCCAGCACATCTGACATTTACATTTATTTGATAATGATTTAATAGATTAAAAGCATGCCCATTTTTTGTAAAGATGGTATTTTCTTTATATAATAAATGTTTATTCTGTATATTTTTGTAACTTTCTTAAATGTCATTCTGGAAAAAAAAAACATTTTCAACTACTGAACTAAAAAATGTATTCATTTATAACATAAGACATTGTCTTCTTAAAATAAATAAAATCAAAATTAATTCAAATTCATAAAGTTAATCTGAAAAATAATTACTGGTGTCATTTAAAAAATTTACGAATATTCTAGAAGGAGTCACTTTTTGTGCATACGGGAT
Associated Phenotype:
Not determined