ZMP
prdm14
Ensembl ID:
ZFIN ID:
Description:
PR domain zinc finger protein 14 [Source:RefSeq peptide;Acc:NP_001157303]
Human Orthologue:
PRDM14
Human Description:
PR domain containing 14 [Source:HGNC Symbol;Acc:14001]
Mouse Orthologue:
Prdm14
Mouse Description:
PR domain containing 14 Gene [Source:MGI Symbol;Acc:MGI:3588194]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa30745 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa14915 | Essential Splice Site | Available for shipment | Available now |
sa24462 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa30745
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066720 | Essential Splice Site | 292 | 517 | 3 | 7 |
ENSDART00000123674 | Essential Splice Site | 343 | 568 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 24 (position 14357505)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 14308953 |
GRCz11 | 24 | 14453372 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCACCCTCAAAGAGTTCATTGATGACAGTGAAGCTCTCCCGGCAGAAGG[T/C]ACGTGCACAATGCAAATTAATCACTTTTATTATTGATCATTTAACTTTAT
Long Flanking Sequence:
TAGATGGGGGAGGGGGGCATTTATAACATCCTGAAAAATTAGAATTTTTAATTTATTTGTAGTAACTGTACAACCATTATTATTTTTAATATGGGTGGGTTAAAATAGACCACAATTTATCCAAAACATTTGAAAAAAAAACCTCAACCCAGCGCAAAAAAGACAGCATTTTAAAAGATGTGCTTTTCTGATGCTCGCATTTAATTCCAAGCGTGTTCCCCATATGTGTAGATCTTTGAGAACGGCCGCTTGAGTCATTTTGTGGATGGAAGAGGCGCTCCAGGGAATTGGATGTCCTTGGTGAAGTGCGCGCGCTTTCCTGAAGAGCAGAACCTGATAGCGGTGCAGTGTGACGGACAGATATATTATGAGGCCTGCAAAGAGATCCGAGCCGGCCAAGAGCTGCTGGTTTGGTACGGAGATTGCTATGTGCAGTTTTTGGGTATTCCTCTCACCCTCAAAGAGTTCATTGATGACAGTGAAGCTCTCCCGGCAGAAGG[T/C]ACGTGCACAATGCAAATTAATCACTTTTATTATTGATCATTTAACTTTATACAAGATGTCCAGATATGTTTGCAGATTGCTAATGTTTCCTTTTCTTTATTCCAGATTCTGGAGAGGGTTTCAAGTGTGATCGTTGTGGAAAAGTGTTCGCCTATAAGTACTATAGAGACAAACATCTGAAATACACGCGCTGTGTGGATCAGGGCGACAGAAAATTCCCCTGCCACCTCTGCAACAGATCTTTCGAGAAGAGAGATCGTCTTCGAATTCACATTCTCCATGTGCACGAGAAACACAGGCCACATAAGGTAAATATAATACTTGGCATGATCATTTGATGGTTATGGTGCTGAAAGAACAGCTCCTTTGTACAAAAACTGAGAAAAACAGGCACATAAGAGACTAGAACTCGAATTTAAGATGGCTTGGCTTAGAATAAGATTTAATAATAAAATAAAAAATTGGATTTAAGAATCTAGATATCTGTATGGTACTTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14915
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066720 | Essential Splice Site | 359 | 517 | 4 | 7 |
ENSDART00000123674 | Essential Splice Site | 410 | 568 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 24 (position 14357814)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 14309262 |
GRCz11 | 24 | 14453681 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCTTCGAATTCACATTCTCCATGTGCACGAGAAACACAGGCCACATAAG[G/A]TAAATATAATACTTGGCATGATCATTTGATGGTTATGGTGCTGAAAGAAC
Long Flanking Sequence:
GCGCGCTTTCCTGAAGAGCAGAACCTGATAGCGGTGCAGTGTGACGGACAGATATATTATGAGGCCTGCAAAGAGATCCGAGCCGGCCAAGAGCTGCTGGTTTGGTACGGAGATTGCTATGTGCAGTTTTTGGGTATTCCTCTCACCCTCAAAGAGTTCATTGATGACAGTGAAGCTCTCCCGGCAGAAGGTACGTGCACAATGCAAATTAATCACTTTTATTATTGATCATTTAACTTTATACAAGATGTCCAGATATGTTTGCAGATTGCTAATGTTTCCTTTTCTTTATTCCAGATTCTGGAGAGGGTTTCAAGTGTGATCGTTGTGGAAAAGTGTTCGCCTATAAGTACTATAGAGACAAACATCTGAAATACACGCGCTGTGTGGATCAGGGCGACAGAAAATTCCCCTGCCACCTCTGCAACAGATCTTTCGAGAAGAGAGATCGTCTTCGAATTCACATTCTCCATGTGCACGAGAAACACAGGCCACATAAG[G/A]TAAATATAATACTTGGCATGATCATTTGATGGTTATGGTGCTGAAAGAACAGCTCCTTTGTACAAAAACTGAGAAAAACAGGCACATAAGAGACTAGAACTCGAATTTAAGATGGCTTGGCTTAGAATAAGATTTAATAATAAAATAAAAAATTGGATTTAAGAATCTAGATATCTGTATGGTACTTTAAAGGGAAATATCTAAATATATTTTTAATCACTTAAGCATTTTCTTCAACTAAAAAAATCAAGAATGCGTTGTTCATCTAGGTCTAAATAAAAGAGGTTTAAATTTGTTTATAATAAAATATGCACAATTTCTGTATCATCACAGAAAAGGATATTGAAACTTGCATTTGCTTACACTGTAAAAATGATGGGTTCCACACAGTTCCTTTATGTTTTTCCTAACACGTTTTATACATTTAAATAGATTGAACATTTACAGATTGAACATTATTAACAAAACAATTGAGCTGTCCAAAAAAACTTGAGAATTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24462
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 |
---|---|---|---|---|---|
ENSDART00000066720 | Nonsense | 391 | 517 | 5 | 7 |
ENSDART00000123674 | Nonsense | 442 | 568 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 24 (position 14358640)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 14310088 |
GRCz11 | 24 | 14454507 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACACATGCGCGTGCACTCGGGAGAGCGGCCTTACAAATGTGTTTACTG[T/A]AACAAGGTGAGGTTTGCTTGGTGTTTAAACAGGTGTATTCCATTTAAAGT
Long Flanking Sequence:
CATCACAGAAAAGGATATTGAAACTTGCATTTGCTTACACTGTAAAAATGATGGGTTCCACACAGTTCCTTTATGTTTTTCCTAACACGTTTTATACATTTAAATAGATTGAACATTTACAGATTGAACATTATTAACAAAACAATTGAGCTGTCCAAAAAAACTTGAGAATTGTGTTGTTTCAACTCATTTTAAAAAGAAGTTTGAACAATCTTGAGTGTAGCCTACTTTGATTAACATTTTTGTTGTTCACTAAAGTTGATCTTAGTTTTTCATCATCACTTTTACACATATTATAATGATGGGACACGAAAAGCATCCTTATGGAGGAATGACTCTGATTCACTTAAGTTTGGTCAAATTTTTGACTTTTGAATGTAATCTCTTACCTTTTTTCCCTTTTAGTGCTCCGTGTGCGGCAAAAGTTTCTCGCAGTCCTCCAGTCTGAACAAACACATGCGCGTGCACTCGGGAGAGCGGCCTTACAAATGTGTTTACTG[T/A]AACAAGGTGAGGTTTGCTTGGTGTTTAAACAGGTGTATTCCATTTAAAGTCTTGCTTTAAGTATTTTACTATTTTCACGGTGTACCAGCGCGCTCGTTAGCGCCGGACTCGTCCTTAGAAGACACTTAGGCTCTATACATGCTAATTAATGGCAGATGCACCTCCTGTGCATTGTGCGCAAGGATTATGCCTTAATTTATGACTCTCGAGGAGACAAAAGTTCGTCAGTCGCTTTGTTTTAAACTCGCTTATATGCTTAAACACTTACGCGTGCGAGAAGTCTTTTCAGTGGTCGTGTCACTCTCTGTGATTTGTTTGTGGACTGCTACAGACCGTTTTATTTATAAAGTAGCCCGAAAACTATTGTGTTTAGTTTAGGTTTACGTACGCCCACGAAAAATTTTTGTAGTAGAAGTAACGGCTAAAGAAAATGCAGGGAGGCTAGACTGCTAGGTTTTTATTAGGGTATAGGTCTATTGTTTTCGCGTTATAATAATATT
Associated Phenotype:
Not determined