ZMP
prdm5
Ensembl ID:
ZFIN ID:
Description:
PR domain zinc finger protein 5 [Source:RefSeq peptide;Acc:NP_001002301]
Human Orthologue:
PRDM5
Human Description:
PR domain containing 5 [Source:HGNC Symbol;Acc:9349]
Mouse Orthologue:
Prdm5
Mouse Description:
PR domain containing 5 Gene [Source:MGI Symbol;Acc:MGI:1918029]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37594 | Nonsense | Available for shipment | Available now |
sa24242 | Nonsense | Available for shipment | Available now |
sa31079 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa14875 | Nonsense | Available for shipment | Available now |
sa7503 | Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37594
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 |
---|---|---|---|---|---|
ENSDART00000127443 | Nonsense | 109 | 634 | 4 | 16 |
Genomic Location (Zv9):
Chromosome 23 (position 2047085)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 2015180 |
GRCz11 | 23 | 2025588 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACTCTGTGTGTGTGTGTGTGTGTTCACAGGATGGAGAGAATATCTTTTA[T/A]CTGGCGGTTGATGACATCGAGACGGACACGGAGCTGCTGATTGGTTACCT
Long Flanking Sequence:
CAATATAAAAGCCAGACACTAAGCTTTCTTTGCACTGCAACTGATAATCAACAGTCAAAATGGCAAGTTGTATCTCTTCCCAACAGAGAAAACCAGCAACAATGAAGAATGCATGACTATATGGAGTCATGGCTTTGCAATAAATAAATGTGATTATAATGGAAGTCAAAGGGGCAAAAACAGCCCCCAACACAACGAAAGGGTAGTAAATTTGCCTTTAAATTTGTGCATTGTTGAATTTTTGACAACTGACAAAGCATTTTCCAAAATATGTGTCAAAATAAGATTTAAAATTTATCCCCAAACATCCTCCCATTTGCCGATACACGGAAAAAGCTAATACTAAATCACCAGTGCAACATCAAGCAGCATAACAAGCTGATTTTAACTTTTAAAAATCTGCATATCGTCTTTTCTGACCCGTTTAATATATCTCAATGTGCTTTCTCTCACTCTGTGTGTGTGTGTGTGTGTTCACAGGATGGAGAGAATATCTTTTA[T/A]CTGGCGGTTGATGACATCGAGACGGACACGGAGCTGCTGATTGGTTACCTGGACAGTGATATGGAGGAGGAAGAGGAGGATCTGGAGGAAGAGCAGGACATCAAAGATGAAGACGAGAACAGTAAAGACAGCAAACAACTCAGTGCAGACACAGGTGTGTGTTCAGTGGCTCTCTAAAGGCCTAGTTCTCACTACATGACTTAAAACATAGGCAGATCACTGTGCTGTTCAGACTACCTGACTTGATTTATTCATTCATTCAGTTTCTTTTCGGCTTAGTCCCTTTATTAATCCAGGGTCACCACAGTGGAATGAACCGCCAACTTATCCAGCACGTTTTTATGCAGCGGGTACTCTTCCAGCCGCAACCCATCTCTGGGAAACATCCACACACACTCATTCACACTCATACACTACGGACAATTTTGCTTAGGAAATTAACCTAAAAATAAACGAAAGACACTTGGCAAATGATCATTTTGACACCAGGCATGATCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24242
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 |
---|---|---|---|---|---|
ENSDART00000127443 | Nonsense | 155 | 634 | 4 | 16 |
Genomic Location (Zv9):
Chromosome 23 (position 2046949)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 2015044 |
GRCz11 | 23 | 2025452 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAAGAGCAGGACATCAAAGATGAAGACGAGAACAGTAAAGACAGCAAA[C/T]AACTCAGTGCAGACACAGGTGTGTGTTCAGTGGCTCTCTAAAGGCCTAGT
Long Flanking Sequence:
GCAATAAATAAATGTGATTATAATGGAAGTCAAAGGGGCAAAAACAGCCCCCAACACAACGAAAGGGTAGTAAATTTGCCTTTAAATTTGTGCATTGTTGAATTTTTGACAACTGACAAAGCATTTTCCAAAATATGTGTCAAAATAAGATTTAAAATTTATCCCCAAACATCCTCCCATTTGCCGATACACGGAAAAAGCTAATACTAAATCACCAGTGCAACATCAAGCAGCATAACAAGCTGATTTTAACTTTTAAAAATCTGCATATCGTCTTTTCTGACCCGTTTAATATATCTCAATGTGCTTTCTCTCACTCTGTGTGTGTGTGTGTGTGTTCACAGGATGGAGAGAATATCTTTTATCTGGCGGTTGATGACATCGAGACGGACACGGAGCTGCTGATTGGTTACCTGGACAGTGATATGGAGGAGGAAGAGGAGGATCTGGAGGAAGAGCAGGACATCAAAGATGAAGACGAGAACAGTAAAGACAGCAAA[C/T]AACTCAGTGCAGACACAGGTGTGTGTTCAGTGGCTCTCTAAAGGCCTAGTTCTCACTACATGACTTAAAACATAGGCAGATCACTGTGCTGTTCAGACTACCTGACTTGATTTATTCATTCATTCAGTTTCTTTTCGGCTTAGTCCCTTTATTAATCCAGGGTCACCACAGTGGAATGAACCGCCAACTTATCCAGCACGTTTTTATGCAGCGGGTACTCTTCCAGCCGCAACCCATCTCTGGGAAACATCCACACACACTCATTCACACTCATACACTACGGACAATTTTGCTTAGGAAATTAACCTAAAAATAAACGAAAGACACTTGGCAAATGATCATTTTGACACCAGGCATGATCAAACTGTCTATACTAGATGTTGAATTGGACATAGGTTGACTCATTTGTATATACTACTTAATGAAGCACCTCCTAAGTGTAATTACTGCCAGGCTGCTCCTACCATAAAACATATTTTGTTGGATTGTGGAAGTTTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31079
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127443 | Essential Splice Site | 161 | 634 | 5 | 16 |
Genomic Location (Zv9):
Chromosome 23 (position 2043660)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 2011755 |
GRCz11 | 23 | 2022163 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAAAGCTCATATAGTTCACCAATGTGTGTGTGTGTGTGTGTGTGTGTGT[A/G]GAGCTGATGATCAAAAAGGAGGATTACCCATGTCTGCTGTGCGAGAGCAG
Long Flanking Sequence:
AAATGCACACACACACACAAACATTTGCACATACACACACATGCGCATATACATGCACACACATTCATGCACACAAACTTATGCACACATTTGCATGCACACACTCAAACGCGCAAACACACACATATGCGCATACGCACACATATGCATGCACATACAAACATATACACACGCTTACACGCAAGCATATGCACACATACATTACACACACATGCGCATATATATAGACTGACATGCATGCACACACAACTGTAAATTCACATATGCACACACACATAGGCACACACTTGCATGCACAAACACAAACGTGCGCGCACACACACACATATACACACATAAGCACACACACACAAACTTGCAAAGGTTGTCCCACCTCCGAGTTCTTCTGATTGGTGCACTGCTGTGGAACTGACAGCAATGAGCGGCGCTGCCTCGGAAAGTTCATTATTTGCAAAGCTCATATAGTTCACCAATGTGTGTGTGTGTGTGTGTGTGTGTGT[A/G]GAGCTGATGATCAAAAAGGAGGATTACCCATGTCTGCTGTGCGAGAGCAGCTTCCCCAGTGAAGACGTGCTAGCAGAGCATCTCCAGAGCCTCCACAACAGAGGAAGTGCTGAAGACAAAGAGTTTAAGTGTCGATCCTGCGGAAAAGAGTTTCCCGTCAGACAAGCCCTGCAGCGCCAGTCAGTACCACACACACACACATACACGCAAACAAACACACGCAAACATACATATATACATGCATACAGTATGTACAACAAGCATACATAAACACACACATGCACACTCAGTGTCATGTGCTGTAATGCTTACTCGCTCAAACACACAGAAACAATCACACAAACACAAACAAATACACACACACACACACAGACACACACACACACACACTAACAAACACAATTTTATTCTCATACACGCAATCACTTTCGCACACAAATGCACACAGACTCACACAGCACACAAACAGTAATGCTGATGTCCTGTGTGTGTGTGTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14875
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 |
---|---|---|---|---|---|
ENSDART00000127443 | Nonsense | 347 | 634 | 9 | 16 |
Genomic Location (Zv9):
Chromosome 23 (position 2027417)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 1995512 |
GRCz11 | 23 | 2005920 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAAAAAGTTCATCTCCACCAATCAGCTGAAGAGACACATGATCACACAYT[C/A]AGGTAAATTCACACACTAGTAAAGGTGATGATACACAGGCGACTTTAMAA
Long Flanking Sequence:
TGCCAAAACTGCTATTGAAGTAATAAAAACCGCAATATCGAAGTGTGAACTCTTGAAATGACATTTGAGAATAATATTTAATCAGACACATTTAAACATGTCAATTTATTTGTTCATTTTTATTTTTAGTCATTTATATGCATTGTTATGCTTCAATTATTAAATTAATATTTTGATCATTATAACTGGAACTCCTGCTCCCCCAAACTGCTTATGTGTGCGACTTTTCAAAATGCGCGAGACTTGAGTGTAATGGTCATGCATGTCCATCAATTGCATGGTTACAATAAAAAACAATGCACAAGTAGCGCACTGGAATGAAAAACAATGCATTCTGTTTGAATAAGCTCTAAAGTGTGCACTTATTGTTTTGAAGGTGTATGAATTATACACTAATTACATGTTGGTGCATTTTCAGGTTCATGAGGTGTTTGACTGCGACGCCTGTGATAAAAAGTTCATCTCCACCAATCAGCTGAAGAGACACATGATCACACACT[C/A]AGGTAAATTCACACACTAGTAAAGGTGATGATACACAGGCGACTTTACAAGCAACTTTTTCACAATATTACCCTTATTAGGCAACCAAATGAGAAACATGGCGACTATTTAGCGTTCTGGAGATTAGGCAACAGCCATTCTGCCACCACCATGCTATGCTGTAGGAATGGTATTAGCCTGGTGATGAGCGCTTCCTGGTTTTCTCCAAATGTAACACCTGGCATTCACTTCAAAGAGTTCAATTTGAGTCTCATTAGACCAGAGAATTTAGTTTCTTATGGTCTGAGAGTCCTTCAGATGCCTTTTGAGGCAAATTCCAGATTGGCAGTGGCTTCCATCTGGCCACTCTACCATACAGGGCTGATTGGTGGATTGCTGCACAGATGGTTGTCCTTCTGTAAGGTTCTCCTCTCTCCACAGAAGAACGCTGGAGCTTAGAAAGAGTGACCATCAGGTTATTGATCACCTTCCTGACTAAGGCCCTTCTCCCCCGATCACTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7503
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:
G > A
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127443 | Missense | 467 | 634 | 12 | 16 |
Genomic Location (Zv9):
Chromosome 23 (position 2009948)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 1978043 |
GRCz11 | 23 | 1988451 |
KASP Assay ID:
554-4281.1 (used for ordering genotyping assays)
KASP Sequence:
ACTCAACGTGCACATTCARGTGGTTCACGACGGACACAAGAAGTACAAGT[G/A]TGACCTGTGTGAGAAGGCCTTCGTCACGCCGTCYGTGCTCAAGAGCCACA
Long Flanking Sequence:
GCATTTCTGTGTGGAGTTTGCATGTTCTCCCTGCGTTCATGTGGGTTTCCTCCGGGTTCTCTGGTTTCCTACACAGTTCAAAGACATGCGGTACAGGTGAATTGGGTAGGCTAAATTGTCTGTAGTGTATGAGTGTGTGTGTATGTGTGGATGTTTCCCAGGGATGGGTTGCAGCTGGAAGGGCATCCGCTGCTTTAAAACGTGCTGGATAAGTTGCCGGTTCATTCCGCTGTGGCGACCCAAGATTAATAAAGAGACTAAGCCGACAAGAAAATGAATGAATGATTGTATTGCCTTTTGTAAAGCTCCTTTGATACAATAATGCCTGTGAACAGCGCTATACTTATAAACTTGAATTGAATTGGACGTCTGAATGCAATCTTTTCTCTGTCCAGATGAGAGGACGTTTAAGTGTGACCATTGTGACGCCACTTTCAAGCGTAAAGACACACTCAACGTGCACATTCAGGTGGTTCACGACGGACACAAGAAGTACAAGT[G/A]TGACCTGTGTGAGAAGGCCTTCGTCACGCCGTCTGTGCTCAAGAGCCACAAAAAGGTGCGTTCATAATCACACGCCTTTGAGCAACACACACACACACACACACACACACACACACACACACACACACACACACACACACAAACACACATGTTTGTTTTTGTGAAAAGTGGGGACATTACATATGTTTCCATTCATTTTATACAGTCCAAACCGTATATTGTATTGCCCTAACCCCACCCCACCCCTAAACCCAACCATCACAGCAGACTGTGTGCAGCTTTACTCTCTCATTAAACTCATCCTGTGTGATTTATAAGCATTTTGAGAAACGAGGACGTCACCAATGTCCTCATATTTCACCTGCTTTTTGTAATACCTGTGTCATACCCATGTCATTATACAGATTTGTGTCCTGATATGTCACAAAAACACGTACACACACACACACACAAAGTCAAGTCAATGTATTCAGAAGCACATTTGAAGCTCAATGGGGTGC
Associated Phenotype:
Not determined