ZMP
si:ch211-255l14.7
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q1MT95]
Human Orthologue:
ZCCHC14
Human Description:
zinc finger, CCHC domain containing 14 [Source:HGNC Symbol;Acc:24134]
Mouse Orthologue:
Zcchc14
Mouse Description:
zinc finger, CCHC domain containing 14 Gene [Source:MGI Symbol;Acc:MGI:2159407]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38022 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa6798 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38022
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 |
|---|---|---|---|---|---|
| ENSDART00000005778 | Nonsense | 251 | 754 | 8 | 12 |
| ENSDART00000144728 | Nonsense | 273 | 776 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 25 (position 13368046)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 12494171 |
| GRCz11 | 25 | 12590676 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTATTCACTTACAGTTCCTCGCGCTCACAGAAGAGGATCTCAACAAATA[C/A]GACCTCACTCAGGGGGCCAAGAAGAAACTAAAGACTCAGCTGGAGCTTCA
Long Flanking Sequence:
CAAAATAAAAGTTTTGTTATTATTATTTCAGATTACAGTAGTCAACATTTAAAGTGAATCAGACAAGTTTATCAAAGCTGTCTAAAACTAACAACAATTTAATAACATTTAATCTTGTCTTAGGACAGTTTTGATGAATTTTTTGATTCACTTCATATGTTGACTACTGTATATCCAATATAAATATATAGCAATATAATGTATGTCGGAATATAAGAAATAAGATAGTGAAATACTATAAATAAGACATTAATATATTCATTATTGTCTGACAAGTAAACTAAAGATTATAAAAGCCAATGACGATTCTATTGCCAAAGTGTCCACAGAGGATTGGATATTTGAAGGAGATGCTTAGGGAAGGGATTTCAGATATTGTAGCCAAGGAATACATATTTTCTTCCTGACACTGATATCTCTCCCACTGCAGTTAATCTAAATGCTGATCTCTTTATTCACTTACAGTTCCTCGCGCTCACAGAAGAGGATCTCAACAAATA[C/A]GACCTCACTCAGGGGGCCAAGAAGAAACTAAAGACTCAGCTGGAGCTTCAGAAGTGAGTTTGGTTTGGGTGACACAATGTGACAGGAGAAAGAAGTGCGTTCATAATTACCATAATTACAAGAATCAAACTTGTAAAAGAGTTCAGCTTAGAGGTAACTTGTCAACTGGGGATTTATAGCTATGCCGTGTACCATGTGATCAGCAGTCAGGTGGTACGGTTAAAGGGATAGTTTACCCAAAAATTTAAATTCTGTAATCATTTACTCACCCTTAACTTGTTCAAATTCTATTTGATTCTTTCTTTTGTTTCTTCTTATTTACATAAATAGATATTTTGAAAAATGCTAATTGCTGGCACTTATTGTCTTTTATAGTAATAAAAAAAGAAATTCCCACTATGGGAGAAGTTGATGGGTACAAGCAATCTTCAAAATATCTTCAGAAAGAAACTAATGAAGATTTAAAAAAACACGAAGGAGAATACATGATGAGGTCATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6798
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000005778 | Nonsense | 724 | 754 | 11 | 12 |
| ENSDART00000144728 | Nonsense | 746 | 776 | 11 | 12 |
Genomic Location (Zv9):
Chromosome 25 (position 13376968)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 12485249 |
| GRCz11 | 25 | 12581754 |
KASP Assay ID:
554-4623.1 (used for ordering genotyping assays)
KASP Sequence:
AAACAGGGAATGTGTCTTGCTATAACTGTGGGCTGAGTGGGCATCATGCA[C/T]AAGACTGYAAGCAGCCAGCMATGGAYTCTGCACAACAAGGTAACAASTAR
Long Flanking Sequence:
CCGGCCACACCTACTGTGTAAACAATACACCCACAATTACGCCCTGTTCTAGCCCAGCCTCCACAGAGAATAGCAGCTACGTCTCGGTGCAAGCGAACAGTGCTAACTCCAGTTCCTCTTTGTGCGTATGTAGCTCGTGTGGTTGTAGCGGCAACTGTGGCTCCTATGGGGCACTTCCGGCAAGCTACACCGGCTACTTTCCACATCCCTTTTCAGGAACGTCAGTATTCACTTTAGGTCCATTGCTTCATTTTAGTCCACTCCTTACAGGAAGCGGTACCGCCTCTCCTTTTTCATACCCTTTGGTGGCCCCGCCTATTTACAACAACAGCCTATCACATGACTCACAACAGAATCTTGTGCTTCCGCCAGTGCAGGGTTTTCTTGGGGGAGGGGGCGCTGTCTACCAGCCCCATGGAATGATGGGAAACGGAAGCACCGGACATAAGAAAACAGGGAATGTGTCTTGCTATAACTGTGGGCTGAGTGGGCATCATGCA[C/T]AAGACTGTAAGCAGCCAGCCATGGACTCTGCACAACAAGGTAACAAGTAGTGTTTTTTAAGCACTTAAACACCACTTTCACACGAGGCATCAGTGTCAACGCTTCCCTTTAACTTAGAATGGGTGACGTCAAACATTGCTGAACTAAATTGTGGGTCCGTAACGGAAGCTTCAGCCAATCAGATCACTTTATGCAAATATTCCATCTCAGACAGTAGCTGATTACAGACTTATTTCATTGGCTGATGCTGCTATGATGATTGTGTCAGCCCCAACTTCAAACACGCCCTCCGTCAAGCATTGACGCTGAATCCCTGTGTGAATTGGGTGCAAAGGCTGATTAATACTTTTTCGTCGAGTGATCGGCGTGACCCATGGCACCTGCCTCTTGCATAGTCGTGTATTTATACCTCTGCATGCCGTTTGTGTTGCTCTGCAATAACACTTCCGAAACGCTAGCTGGCAGTAGGTTTTTATGTTCCTCTGTGTCAAGTTTCTTCA
Associated Phenotype:
Not determined