ZMP
B0JZN1_DANRE
Ensembl ID:
Description:
LOC561643 protein [Source:UniProtKB/TrEMBL;Acc:B0JZN1]
Human Orthologue:
PWWP2B
Human Description:
PWWP domain containing 2B [Source:HGNC Symbol;Acc:25150]
Mouse Orthologue:
Pwwp2b
Mouse Description:
PWWP domain containing 2B Gene [Source:MGI Symbol;Acc:MGI:2142008]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9575 | Nonsense | Available for shipment | Available now |
| sa11977 | Nonsense | Available for shipment | Available now |
| sa9706 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9575
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 |
|---|---|---|---|---|---|
| ENSDART00000089544 | Nonsense | 396 | 565 | 4 | 4 |
| ENSDART00000089545 | None | None | 231 | None | 3 |
| ENSDART00000089544 | Nonsense | 396 | 565 | 4 | 4 |
| ENSDART00000089545 | None | None | 231 | None | 3 |
Genomic Location (Zv9):
Chromosome 13 (position 53160591)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 51495379 |
| GRCz11 | 13 | 51720795 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTAATTAACTTCCGCAAGAGGAAAGCAGACTCTTCCAGCCTTTCTGTGTG[C/A]AGTAGTGACAGTCTAGACGAGTCCAAATCGTTCAGTTCGGATGGCACGTC
Long Flanking Sequence:
ATCAAGATCTCCTACAGCACTCCGCAAGGCAAAGGCGAGGTCATGAAGATCCCTTCCAGGGTCCATGGATCCGTCAAACCTTTCTGCCCCAAGCAGCTCCTCCAGAACGGACATGGAGATCGAGATTCTTCCAAGGAAACCCCTAAAAAACTACAACCCCCAATGGACGCAATACGAACAGGTCTTACCATTTCCATTCCCAAACTCAAGCTTCCGAAGTTGCCTAGTCCTGATGCGCAGTCGCCTAAGATTCGCTTGCGCTCCCGGGCGGAAGGAGCGGAGCAGATGTCTGTATATGAGGCAGAACTCGTGGACGGAGCTCGGAGGAGAAGTCCGAGAGTTCCCAACTCTGGTTTACCTCAATCCGAGGATGCTGAAGATAAGAATTCACTAGAACTTTGGTCGGGGAGCTGCGGTGGGGAAGTCGAGCGGCACGGAGATCTGACTTTACTAATTAACTTCCGCAAGAGGAAAGCAGACTCTTCCAGCCTTTCTGTGTG[C/A]AGTAGTGACAGTCTAGACGAGTCCAAATCGTTCAGTTCGGATGGCACGTCTCCGGAGCTGTGTGATCTGGCTCCAGGCGATGATATCTCTGTGTCTTCGTCCTCTCAAGGAGAAGGCAAGACGGTTCCTCCGCTGACTGTCCGCCTGCACACGCGCAGCATGAGCAAATGCGTGACGGAGGATGGTCATGCGGTGACGGTCGGGGACGTAGTTTGGGGAAAGATTCACGGCTTCCCTTGGTGGCCGGCTCGGATCCTCAGTATTAGCGGGACTCGCAGAGAGGACGGAGAAGTCGACGCTCCGTGGCCTGAAGCGAAGGTTTCTTGGTTTGGATCTCCGACCACCTCTGAACTCTCAGTTGCCAAACTGTCACCGTTCCGCGAGTTCTTCAGGTCACGCTTCAACCGCAAAAAGAAAGGGATGTACCGGCGTGCCATCATGGAAGCTGCCAAAGCGGTGGGACACATGGGTGCAGAAATCACATCTCTTCTGGCTCACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11977
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 |
|---|---|---|---|---|---|
| ENSDART00000089544 | Nonsense | 396 | 565 | 4 | 4 |
| ENSDART00000089545 | None | None | 231 | None | 3 |
| ENSDART00000089544 | Nonsense | 396 | 565 | 4 | 4 |
| ENSDART00000089545 | None | None | 231 | None | 3 |
Genomic Location (Zv9):
Chromosome 13 (position 53160591)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 51495379 |
| GRCz11 | 13 | 51720795 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTAATTAACTTCCGCAAGAGGAAAGCAGACTCTTCCAGCCTTTCTGTGTG[C/A]AGTAGTGACAGTCTAGACGAGTCCAAATCGTTCAGTTCGGATGGCACGTC
Long Flanking Sequence:
ATCAAGATCTCCTACAGCACTCCGCAAGGCAAAGGCGAGGTCATGAAGATCCCTTCCAGGGTCCATGGATCCGTCAAACCTTTCTGCCCCAAGCAGCTCCTCCAGAACGGACATGGAGATCGAGATTCTTCCAAGGAAACCCCTAAAAAACTACAACCCCCAATGGACGCAATACGAACAGGTCTTACCATTTCCATTCCCAAACTCAAGCTTCCGAAGTTGCCTAGTCCTGATGCGCAGTCGCCTAAGATTCGCTTGCGCTCCCGGGCGGAAGGAGCGGAGCAGATGTCTGTATATGAGGCAGAACTCGTGGACGGAGCTCGGAGGAGAAGTCCGAGAGTTCCCAACTCTGGTTTACCTCAATCCGAGGATGCTGAAGATAAGAATTCACTAGAACTTTGGTCGGGGAGCTGCGGTGGGGAAGTCGAGCGGCACGGAGATCTGACTTTACTAATTAACTTCCGCAAGAGGAAAGCAGACTCTTCCAGCCTTTCTGTGTG[C/A]AGTAGTGACAGTCTAGACGAGTCCAAATCGTTCAGTTCGGATGGCACGTCTCCGGAGCTGTGTGATCTGGCTCCAGGCGATGATATCTCTGTGTCTTCGTCCTCTCAAGGAGAAGGCAAGACGGTTCCTCCGCTGACTGTCCGCCTGCACACGCGCAGCATGAGCAAATGCGTGACGGAGGATGGTCATGCGGTGACGGTCGGGGACGTAGTTTGGGGAAAGATTCACGGCTTCCCTTGGTGGCCGGCTCGGATCCTCAGTATTAGCGGGACTCGCAGAGAGGACGGAGAAGTCGACGCTCCGTGGCCTGAAGCGAAGGTTTCTTGGTTTGGATCTCCGACCACCTCTGAACTCTCAGTTGCCAAACTGTCACCGTTCCGCGAGTTCTTCAGGTCACGCTTCAACCGCAAAAAGAAAGGGATGTACCGGCGTGCCATCATGGAAGCTGCCAAAGCGGTGGGACACATGGGTGCAGAAATCACATCTCTTCTGGCTCACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9706
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 |
|---|---|---|---|---|---|
| ENSDART00000089544 | Nonsense | 476 | 565 | 4 | 4 |
| ENSDART00000089545 | None | None | 231 | None | 3 |
Genomic Location (Zv9):
Chromosome 13 (position 53160831)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 51495619 |
| GRCz11 | 13 | 51721035 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCGGTGACSRTCGGGGACGTAGTTTGGGGAAAGATTCAYGGCTTCCCTTG[G/A]TGGCCGGCTCGGATCCTCAGTATTAGCGGGACTCGCAGAGAGGACGGAGA
Long Flanking Sequence:
TCGCCTAAGATTCGCTTGCGCTCCCGGGCGGAAGGAGCGGAGCAGATGTCTGTATATGAGGCAGAACTCGTGGACGGAGCTCGGAGGAGAAGTCCGAGAGTTCCCAACTCTGGTTTACCTCAATCCGAGGATGCTGAAGATAAGAATTCACTAGAACTTTGGTCGGGGAGCTGCGGTGGGGAAGTCGAGCGGCACGGAGATCTGACTTTACTAATTAACTTCCGCAAGAGGAAAGCAGACTCTTCCAGCCTTTCTGTGTGCAGTAGTGACAGTCTAGACGAGTCCAAATCGTTCAGTTCGGATGGCACGTCTCCGGAGCTGTGTGATCTGGCTCCAGGCGATGATATCTCTGTGTCTTCGTCCTCTCAAGGAGAAGGCAAGACGGTTCCTCCGCTGACTGTCCGCCTGCACACGCGCAGCATGAGCAAATGCGTGACGGAGGATGGTCATGCGGTGACGGTCGGGGACGTAGTTTGGGGAAAGATTCACGGCTTCCCTTG[G/A]TGGCCGGCTCGGATCCTCAGTATTAGCGGGACTCGCAGAGAGGACGGAGAAGTCGACGCTCCGTGGCCTGAAGCGAAGGTTTCTTGGTTTGGATCTCCGACCACCTCTGAACTCTCAGTTGCCAAACTGTCACCGTTCCGCGAGTTCTTCAGGTCACGCTTCAACCGCAAAAAGAAAGGGATGTACCGGCGTGCCATCATGGAAGCTGCCAAAGCGGTGGGACACATGGGTGCAGAAATCACATCTCTTCTGGCTCACTGCGAAACTTAGGTGAGGCTTGTCTTTGCATTTGTTGAGTTTTTTTGCAACAGAGGGAGAAAAAAACTAAACAAAACACAACGTCAATAGTGTTGGAGCTTAGTGTTGTCACGATACTGGAATTTCCAACTTCGATACCTTAAAAAATATATCGATTTTTTTTTATTTTTTTTTATTCCATGGGGACAAAATTTTACAACATAAGTATGCAAATTAAGTACAAAAATAAGTAACTTGAACTA
Associated Phenotype:
Not determined