ZMP
zc3h14
Ensembl ID:
ZFIN ID:
Description:
Zinc finger CCCH domain-containing protein 14 [Source:UniProtKB/Swiss-Prot;Acc:Q5TYQ8]
Human Orthologue:
ZC3H14
Human Description:
zinc finger CCCH-type containing 14 [Source:HGNC Symbol;Acc:20509]
Mouse Orthologue:
Zc3h14
Mouse Description:
zinc finger CCCH type containing 14 Gene [Source:MGI Symbol;Acc:MGI:1919824]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa15419 | Essential Splice Site | Available for shipment | Available now |
| sa29458 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa17062 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15419
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 |
|---|---|---|---|---|---|
| ENSDART00000060695 | Essential Splice Site | 12 | 669 | 1 | 17 |
Genomic Location (Zv9):
Chromosome 20 (position 46743341)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 46588624 |
| GRCz11 | 20 | 46492344 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAACCAAATAAMCATGGAGATCGGAACGGAGATTAGCAAGAAAATAAGGG[T/A]AAACCGTTTYAAATRCTTAGCACTCACCGCTTTTTAGCATGCTAGCTTAG
Long Flanking Sequence:
TGAATTTTAAAGTCGTTTATCCGTTTTCCTACCCTAAACCAAAAAACGAAAATCCAGCCAAAATCTCGTTTTTTCGTTTTCTCGTGAGCAAAAGAAAAACGGAAAAACGGCCGTTTTCTCCATTTCCTTTATTCCGTTTGAAAATGGAAAACAAATGAACAAAATGTACACGGACCATTATTGTTGTTATTATTTAACCCAATACATTTATATCAGTAGTAGACTTTTGGCACTCGTAAATTTGATTACAACAACAGTCCATCATGATATCTACAAACGAGTGATCTGTTTTGCAAAAACACTCTAAACATAGTACTGAATGAGCCGCGCATGCGCAGTAAGAATAGATAAGCTTCACGCGAGGCCTAGCCACAACAAAATCCTTCCTCTTTCTTCTTTTCCTAATGTTCTCCTAATTTAAATAGTCTTTTAAGTTCGAGAGGGAAGCAAAAACCAAATAAACATGGAGATCGGAACGGAGATTAGCAAGAAAATAAGGG[T/A]AAACCGTTTCAAATACTTAGCACTCACCGCTTTTTAGCATGCTAGCTTAGCTTATGTTTCGATACATGTTGTTTGTTGTAAGTGCGCATTTCCCGTTCTTCTAGGTTTTATATCTCTCTTTTATTAGACGTGCTTTATCTATTTATAAGAATAAATATGCTTTGGCTTTTATTGGTGTTTGTTGTGATGGTAATGTTTTGCACGAAGTAACATTAACTTAGTACGTTATTATGTGAAGGACGTTGTGTAAATAACGTCAAGTACTAATATATTGCAAATTGCCTGGTTGTTGTTTGTTGTACCATGTTTTCACTACAGTATTGTTTTGAAAAGGTCAAAGGTGGTCGCTAAACGTCAGTGTCTAAATGTAGTTAAAGTTGTTTATTTATATTGAGGTAAAGTTTGTTATATATTCGTAATTTCGTACATTCGTTTAGTGACAACTTGTGACTCGCTCCCTATATTGTTTACCATGTTACTTTGAATATTCGGTCTGCAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29458
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060695 | Nonsense | 203 | 669 | 6 | 17 |
Genomic Location (Zv9):
Chromosome 20 (position 46753504)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 46598787 |
| GRCz11 | 20 | 46502507 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTATACAGCCGTTCAACAGCAGAGAGGCAGAGACCTGCAGTGGAGTCCT[C/A]GAGACGGACAGCAGACACGTACAGATCCTCTGACATCTCCAGAGGTCAAG
Long Flanking Sequence:
TTAATACTGTATACCGCGAAACCGTCAAACCGTGGTATTGTTTTAGACGATTATCATACCGTAAAAAATTCATACCGTTACAACCCTAGTCTCAGTACAAGATGTAACTACAGAAGGAAATTCATTAATTCATAAAGGATTCAAAAATTTATGCTATGTCAAATGTAAAATGAGCATGTTTGGAGGAAAATTGGAGTATTCCTTTAAGAACAAACACCAAAGGAATAATGGAGGAATAAATAAAAAAATACTAATAATCACAAACTCTCCTGTTTTTGTGTTCTCTAGTAAGAGAGGCTCTTCTGAAAGACCCTCCAGATTAACATCCGCCGTCAAACCGCTGATGGAGGCATCAGCTGAAGCTGTGATTGACATCAAGCCAGATCTAGATGATGACCTCATTTCCTATGACCCCGTGGAGCATAGCTTGACTTCGGGTCACAGTCAGGCTTTATACAGCCGTTCAACAGCAGAGAGGCAGAGACCTGCAGTGGAGTCCT[C/A]GAGACGGACAGCAGACACGTACAGATCCTCTGACATCTCCAGAGGTCAAGACAGGTCAGAGCGAGGCTACAGGAGCTCAGCAGAGAGCAGCAGGGTCAGTCCAGATTCACAAGCTTTTATTTTCATCCATTTATTTTTCTGCACATTTTAAAGGGCTCATATGGTTTCATGAAAGCTTTGAAAAGTGCTTAACCCTTGTGTGCTGTTAGGGATGTTTTCATCCACTCTGGGGGGATTTTGAGTCTTAATTTGGCCACATCTTTCTCTGTGTTTCAGCAAATGGAATGATTTTCGACACACATTTTGGGAAAATGATTTTAAAACTTTAAAAGATTCAACAATACACTCAAATTACTACCCTTTCGTTATGTTGGTTGCTGTTTTTGGCTTTCATTATAATAACATTTTTTGGTTGCAAAGCCATGAGAGTATATAATAATCATGCATTCTTGATAGTTGCTGGTTTTCCCTATTGGGAAGAGGGACATTTTGTAATTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17062
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 |
|---|---|---|---|---|---|
| ENSDART00000060695 | Essential Splice Site | 390 | 669 | 10 | 17 |
Genomic Location (Zv9):
Chromosome 20 (position 46760352)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 46605635 |
| GRCz11 | 20 | 46509355 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGCAGTTGGAGGTTCCAGAGGAGGACAGTCRAGAACCRCATGAATATGG[T/A]KAGATATACTGACATTKTTTWGCTTTTGACATACATTTCTRTTCAAAGTG
Long Flanking Sequence:
AGTGAGCATCTTCTGCTTTAAGAAATAATGCTCTCATTAAAATTAAAGCCTGATCGATTTAATACATCCTTTCTCAATACTATGTTTATCTATAAACCTCATTTAAATACAACCAGAGTTGACCAAATTGCTGTACATGATAGAGCGAAAAAAGGTAGAGAATAAGAACTAAAAAGGTAGAATGAGCAATCAAAACTATCACATTTAGAAATTTAACAAGATTATTAAAAATGTCTTTTTCAAGCAGACTTGAAGGCAGAAATAGAGGGAGATAGCTGAATATGCTGTGGTAGAAAGTGCGATGTACTTCATTTTTAATATCGATCTAGGTATAATAAATGTGACATATGTAAGATACAAAATTTCACATTTTTATTAATTAAATAATTATTATAAACTAAATTTGATTTTGTTTGCTTTACAGCACAATCCAGAGGTTTAGCTTCACGTCTGCAGTTGGAGGTTCCAGAGGAGGACAGTCGAGAACCACATGAATATGG[T/A]GAGATATACTGACATTGTTTTGCTTTTGACATACATTTCTATTCAAAGTGACAAGGCATTGGCTGGTATAAGATTCTGATAGTATGATTACCTTGAAAAAAAAAATCACGGTTTCATGATATCACGGTATTGTGATTACTGGTCTAAAATATATTCTTTTTTAAACAAAACCGTTTTTCCCCGTTGAACAAAATATGTTTTATTATGAGAAACATTTAAAATATTTTGGAGCAAATACATTTCAGGCTAAATAATTCAAATGGATCATTGACTTCTGCTGTCTTCATTTGTTTCAAAAACACAGATTTCTTTACAATTTTAAAACGGCATCTTTGGATGTCTTTTCTGCTGGTAATACTGTTGTCCTAAAAACAACAACAAAAGATTGTAAATAAAACATATTGCACATACCATAGGAACGGTACAGCAGAACATTTTGGCTGTTTTAAAACCTTGACTTTTCCAAACCGCTGTATACCTTGAAAACGGTTATCGTCCCA
Associated Phenotype:
Not determined