ZMP
chmp2b
Ensembl ID:
ZFIN ID:
Description:
chromatin modifying protein 2B [Source:RefSeq peptide;Acc:NP_001116769]
Human Orthologue:
CHMP2B
Human Description:
chromatin modifying protein 2B [Source:HGNC Symbol;Acc:24537]
Mouse Orthologue:
Chmp2b
Mouse Description:
chromatin modifying protein 2B Gene [Source:MGI Symbol;Acc:MGI:1916192]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34606 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa31708 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34606
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 |
|---|---|---|---|---|---|
| ENSDART00000055866 | Nonsense | 64 | 216 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 9 (position 19666161)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 19040403 |
| GRCz11 | 9 | 19048115 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAAATGGCCAAGACTGGAAACCGTGAAGCCTGCAAAATATTAGCCAAA[C/T]AGCTCGTACAGCTTCGAAAACAAAAGAACCGAACCTACGCTGTGAGCTCT
Long Flanking Sequence:
TTGAACACTCACTGCTGATTTGCCATTTTTTGCCATCACATCGATCAGCTGGTTTGTCTATAAGCTGAAAAAGGAGCGATCCACTGATGAATCATGGCTTTAAAATGCTCCAGTGTCTCTGTATCTGTGGTTACACACAATGAACAGTGGTGAGTTTGATGAACTGATGACCTTCACGGCCAATTACAGTCATTTCTGTTGAGCACCTGAACACAATGGCAAATCAGCGCTGTTTAAGAACGCGCTCAACAGTGCTCAAATGTTAGCGGGGAATGTACATTTTTAAAATTTCATAATTAATTGATACCAAATTCCAGTATTGTGACAACTATACAGTAGTTACACATCAGTATAAAATGACACTGCTTGATTTCTCTGTCCCTCTGGGTTATGTATTGGTTTGTTCTAGACTTAGTTTTGTTTTTTATTGTTAACAGGAAATGGAAATCAAAAAAATGGCCAAGACTGGAAACCGTGAAGCCTGCAAAATATTAGCCAAA[C/T]AGCTCGTACAGCTTCGAAAACAAAAGAACCGAACCTACGCTGTGAGCTCTAAAGTCACATCCATGTCCACGCAGACCAAAGTCATGAACTCTCAGATGAAGATGGCAGGAGCCATGTCCACCACAGCGAAGGTAAGAAGCTCAAACTGCTGAATTAATCTGCATTTCTGCATCTGTTTCTGGAGGTCTACAGAATGCAACCAACGCATCCTTTGTGGCCCAAACTTTTCCAAGATTCACTGCGCTACAGAGGCAACACATTGGGTCTCATTTATTAACGAGGCGTACGCACAAAATAGGGGCGGAAATGTGCGTATGCCACTTCCCACATGAAAAGTTGTGGTCTATAAAAAAAAATTACTTGACGAAAGAATGTAAATAAACTGTAAGTAAACATATTTAACTTCAATTTTGACTTGAACCTGTTTAAATCATCATATGAGCCATAATCATTAATAAATACATTTATTCTGGTGAACATTCAGGAAGGTTTCTATGCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31708
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 |
|---|---|---|---|---|---|
| ENSDART00000055866 | Nonsense | 71 | 216 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 9 (position 19666182)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 19040424 |
| GRCz11 | 9 | 19048136 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCGTGAAGCCTGCAAAATATTAGCCAAACAGCTCGTACAGCTTCGAAAA[C/T]AAAAGAACCGAACCTACGCTGTGAGCTCTAAAGTCACATCCATGTCCACG
Long Flanking Sequence:
GCCATTTTTTGCCATCACATCGATCAGCTGGTTTGTCTATAAGCTGAAAAAGGAGCGATCCACTGATGAATCATGGCTTTAAAATGCTCCAGTGTCTCTGTATCTGTGGTTACACACAATGAACAGTGGTGAGTTTGATGAACTGATGACCTTCACGGCCAATTACAGTCATTTCTGTTGAGCACCTGAACACAATGGCAAATCAGCGCTGTTTAAGAACGCGCTCAACAGTGCTCAAATGTTAGCGGGGAATGTACATTTTTAAAATTTCATAATTAATTGATACCAAATTCCAGTATTGTGACAACTATACAGTAGTTACACATCAGTATAAAATGACACTGCTTGATTTCTCTGTCCCTCTGGGTTATGTATTGGTTTGTTCTAGACTTAGTTTTGTTTTTTATTGTTAACAGGAAATGGAAATCAAAAAAATGGCCAAGACTGGAAACCGTGAAGCCTGCAAAATATTAGCCAAACAGCTCGTACAGCTTCGAAAA[C/T]AAAAGAACCGAACCTACGCTGTGAGCTCTAAAGTCACATCCATGTCCACGCAGACCAAAGTCATGAACTCTCAGATGAAGATGGCAGGAGCCATGTCCACCACAGCGAAGGTAAGAAGCTCAAACTGCTGAATTAATCTGCATTTCTGCATCTGTTTCTGGAGGTCTACAGAATGCAACCAACGCATCCTTTGTGGCCCAAACTTTTCCAAGATTCACTGCGCTACAGAGGCAACACATTGGGTCTCATTTATTAACGAGGCGTACGCACAAAATAGGGGCGGAAATGTGCGTATGCCACTTCCCACATGAAAAGTTGTGGTCTATAAAAAAAAATTACTTGACGAAAGAATGTAAATAAACTGTAAGTAAACATATTTAACTTCAATTTTGACTTGAACCTGTTTAAATCATCATATGAGCCATAATCATTAATAAATACATTTATTCTGGTGAACATTCAGGAAGGTTTCTATGCCAATTTTATAAATCAGGCCCATT
Associated Phenotype:
Not determined