ZMP
prdm16
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens PRDM16, PR domain containing 16 (PRDM16) [Source:UniProtKB/TrEMBL
Human Orthologue:
PRDM16
Human Description:
PR domain containing 16 [Source:HGNC Symbol;Acc:14000]
Mouse Orthologue:
Prdm16
Mouse Description:
PR domain containing 16 Gene [Source:MGI Symbol;Acc:MGI:1917923]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31682 | Nonsense | Available for shipment | Available now |
sa14462 | Nonsense | Available for shipment | Available now |
sa14438 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31682
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086053 | Nonsense | 403 | 1200 | 9 | 16 |
ENSDART00000122737 | Nonsense | 134 | 927 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 8 (position 50650246)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 48502656 |
GRCz11 | 8 | 48491425 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTAATCAGTCATGTGTGTTCTCCCAGGTGAGGTGTGTCACAAATCGTA[T/G]ACCCAGTTCTCTAACCTGTGCCGTCACAAACGGATGCATGCAGACTGCCG
Long Flanking Sequence:
TGAATTAATGTCTTCATACAAAACTGAATTCAAAATAGTATATCATTACTTGTGAGAGCTCAACAAGTAGGGTCTGAACAAGAATCTAATCCATCTGAATGATTTATCAACTACTAAAGAACAAACAAAGGGCAATCGATGGTACTCGAATACACTCACTTGCTTTCATCAACTCCTTTAAGTGGACTATATTAGGGAATAGTGAATGATCATATAGGGGTCAATTTCATATAAAGTAATCCTGAACACCTTGATAAGCTGTTTCAGGTGTGTTTATTAAGGATTGGACTTATTTTTCTCAGGAAGGTTTCCTCCTGGAGCAGGGTTGACCACCCCGATGTAGACAGTGTCATGATTGTTGATCATAATAAACAGCATGCAGAGTTTATTGGTTGATCTAATCAGCTGCTGAATTATCACTGCTACCAAATTAAAACAGTATGTTAATAGAATTAATCAGTCATGTGTGTTCTCCCAGGTGAGGTGTGTCACAAATCGTA[T/G]ACCCAGTTCTCTAACCTGTGCCGTCACAAACGGATGCATGCAGACTGCCGCACCCAGATCAAGTGTAAAGACTGTGGGCAGATGTTCAGCACTACCTCCTCCCTCAACAAGCACCGGCGCTTTTGCGAGGGAAAGAACCATTATAATCCCGGAGGCATATTCACACCGGGCATACCAATGACATCCAGTCCTATTTTAGGCAAGTCCAAGTCTCATCCTGGCTTGAACCATAGTGGACTTGGCTTTGGTGATTACTTCCCATCCAGGCCACATCATGCAGGTTTACCCTTTTCCCCAGGACCACCTGCATTCCCAGCCATTTCCCATGGATTTCCAGGGATCTTTCCCCCATCACTATATCCTAGACCACCATTGTTACCTCCTAGCTCACTTCTCAAGAGCCCACTTAATAACAGTCAAGATGGGAAACTGCCCCATCTTGATGCTCCTGCTCTTTCTGTCGCCTCGTCAATGAACAACAGCAATGGCAACATAGGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14462
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 |
---|---|---|---|---|---|
ENSDART00000086053 | Nonsense | 884 | 1200 | 9 | 16 |
ENSDART00000122737 | Nonsense | 615 | 927 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 8 (position 50651689)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 48504099 |
GRCz11 | 8 | 48492868 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATCRCTCCCCCAGCCACCTGTTCCCCAGCAGCWGCCATCGCTTCACTA[T/A]GCCAAGCCCTCGCCATTCTTCATGGACCCTATTTACAGGTATTTCAACCC
Long Flanking Sequence:
GAGAAGAAGATGGGCTCCTTAAATTACCATTCCATGTTCCCCTTCCAGTTTCTGCCCAACTTCCCACATTCCTTGTACCCATTTACAGACAGAGCACTCAATCCTGGCATGTTCTTCAAACCTGAGCCTAAATCCCCTCGTGAGCACATACAGAAATTACATACGGCCACTGGTGCAGATTCACCCTTTGACCTAACCACCAAACCCAAGGAGATAAAGCCTCTTCCACCTCCCCCAAGTAAGCCAGCCTTGCCATCCAATGCTCTCTTGGCCTCCGGCGAGGAGCAACCTCTGGACCTCAGCATAGGCAGTCGAAGCCGAGCCAGCCACAATGGTGGCACACATGAACAGCGCAAGAATCACGTCTATGGCACAAACTGCAAAGCAGCTAAAGATGAACACCCAGCACTAAATCAGAACTTGCACCAGCCCCAAATGCCTCAGCAGCATACATCGCTCCCCCAGCCACCTGTTCCCCAGCAGCAGCCATCGCTTCACTA[T/A]GCCAAGCCCTCGCCATTCTTCATGGACCCTATTTACAGGTATTTCAACCCGAGTATGTCTTAATATACAGTAAAAGCCAATATAAGCACAACCTAACACTAGAGCTTGTGATATATTTAAATGAAATAAAATATTGAGAAGGTATTGATATTTGCAATCAACCTTCGTTCGTACGTAACCCTTGGTGTTGTTGTCCAGCAGGGTGGAAAAGAGGAAGTTATTAGACCCAGTAGGAGCTCTGAAGGAGAAGTACCTGAGACCGACGCCACTACTTTTCCATCCTCAGGTATTCTTTCTATACATTTGTTTTACCTGTTCTGATCCCTTGGTAAAAAATTCTGCTCTTTATTATTGCAAGTACAGGGGATTATTCTAAGACATCAAAAACACCTTCCTAGTGCCCTAGATTTTAGACTTCCTTGGGAAATCTGATGGTATTTATTTTCATTAGATTATTTTCATCATGAAGATAATCTCAAAAGGGGTATTGCCTGTTCTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14438
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 |
---|---|---|---|---|---|
ENSDART00000086053 | Essential Splice Site | 1197 | 1200 | None | 16 |
ENSDART00000122737 | None | 928 | 927 | None | 10 |
Genomic Location (Zv9):
Chromosome 8 (position 50672465)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 48524875 |
GRCz11 | 8 | 48513644 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGATGAGGAGCCCACCCCTCTGCCTATGTCTTATGAACACACGCGCAGG[T/A]SAGCAGAMCATTCAGTAAAACACTCAGACTTWAATCAACACTCTTGCTAG
Long Flanking Sequence:
AGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATTTGTTTGTTTTTTGCATTTGAATATGGCTTACCTTGTTTACATATTAACAAAATTCTAGTATTCAAATTATTCAAATAACCATATTTACTTACCAAGTAATTGAAAGGCTAATTTTACTACTATACACATGTGGTTAACATATAGATATCCTTTAAATACAGTAATAAAGGTAATGGCGATATGTAAAGCTAAATGACCTGTGCTTCTCATCTGCAGGTCAGAGCTGGCGGAGGAAGAGCATCCTCAGAGTCACACTCTCACTGCTTCTAAACTGGAGGAGGAGGAAGAGGAGATGGAGGGCGACGATGAAGATGAAGAAGGCTCGTTGACAGAGAAGTCGCAGGATGAAACAGCCTCTCCCGCCACTATGGTGCAGGGCACTTACGACGAGGATGAGGAGCCCACCCCTCTGCCTATGTCTTATGAACACACGCGCAGG[T/A]GAGCAGAACATTCAGTAAAACACTCAGACTTAAATCAACACTCTTGCTAGTTGGACATCATTGTAGACATACTGTACCTTTCTGTTTTTCTGAAAGTGGAGCTTTTTTTCTGCATTATGATGCTCCAGTAGCAAAAATTGCTGCACTTAGATTAATAGTGTGCTATTATTTAGCTTGGAGAAAATGCACAGAATTATTTTCAATAGGAACAGTGTAAAGAGTCTCTTAAACGTAAAAAATATCATCACAATTTAACAACTCAAATTCAATTTACTTTTGGATTTAAGGCAGCCGTTACTCATTCTTCACGTGATCCTTCAGAAATAATTTTAATATGATGACTTGGTGCTTAAAACATGTTTTATTCAGTAAGAATCAATTCAGTTCATTAAAAGTGACATTAATAAATACTATTTACAATAAATGAGGTTTACTGAACTTTCTAGTGAACAAATGATTCAAAACAATAATATGATTTTGTGTGTGTGTGTGTGTGTGTG
Associated Phenotype:
Not determined