ZMP
si:ch211-137i24.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein containing a DHHC zinc finger domain [Source:UniProtKB/TrEMBL;Acc:A2BEM9]
Human Orthologue:
ZDHHC23
Human Description:
zinc finger, DHHC-type containing 23 [Source:HGNC Symbol;Acc:28654]
Mouse Orthologue:
Zdhhc23
Mouse Description:
zinc finger, DHHC domain containing 23 Gene [Source:MGI Symbol;Acc:MGI:2685625]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20407 | Essential Splice Site | Available for shipment | Available now |
| sa40419 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa31434 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20407
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000041905 | Essential Splice Site | 44 | 407 | 1 | 4 |
| ENSDART00000143563 | None | None | 363 | None | 3 |
Genomic Location (Zv9):
Chromosome 5 (position 25951628)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 23778893 |
| GRCz11 | 5 | 24282693 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGAGTACTGCTGCTGTGACTGTGAAGAACTCGACGATGCCTGCGAAAGG[T/C]TAGAAGTCAACTGTTTTAAAGGAACCTACATCTTTTCATACAAGCTTTTA
Long Flanking Sequence:
ATGAAGAATATGTATTTATATGATAATTAATTGTCATTCATGATAGATTTGTAAGTCAAGTTCAAATATCAAGTTCAACCTGAATTTGTTTTTTAAACTGTGAAATAATGAAAGCATTTACAGCTCTATTGGTAACGATTAATACTTTTTTTCCCCCAGCCTGTGTTTTACACAAAGCCTCTGATGTGAGGAGCAGCAGATGACCAGTAAAGGAGCTGAATGAGAAATCTGCAGTCATCTGTTCTGTCAGCTAACTGCTAAAACTACCAACAGCCCTGAATCAACTCTGTTCCAAGTTGATTTAATCCTTTCCACTCACTTGAATCAATGTGATCTAATCTAACCCTGAAGAAGCAGGTATTCTCTGACATAAGGAGATGAAACGAGAACGTTTTAAGCCACCAGAACCAGATGACCCTCTGTGCTGCTGTGGGGACATCGACCAGCAAAGGGAGTACTGCTGCTGTGACTGTGAAGAACTCGACGATGCCTGCGAAAGG[T/C]TAGAAGTCAACTGTTTTAAAGGAACCTACATCTTTTCATACAAGCTTTTAAGGGTTTTAAGGGTTTTACAGTGTTTGATGTAATCTCAGCTGAAAAATTAAGAGAGGGTGAAACATAGAGTAGCTCCTTTTCTTTTATAAAAGAGCCAATAGGACTTAATTTTTTTATCATCCGCTTGTTAAGTCTTCGCTTAAGTAATACTGTTTCCGGGTCCAAGCCGCTACTCTTTTGAATTGAGAAAATATTAGTTTATGGTCACTTTTTATCACACATTAAAGTTAATTTTTTATAAAATCATAGTGTACACATCAGTTTCTGGACTCGCTGCATCACAAATACAAAAGTTTTAACAATTTATAAAAACTAATCACTTTCTGGCCATCAGATATTAGGCATGGATATATACATTGCGATCAGGATTTTCAAAAGTACCACATTGCTTTGTAAACGTTTATTATTACCATTTAATGAGTCTCTCCATACAGTTTGATAGAGCGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40419
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000041905 | Essential Splice Site | 44 | 407 | 2 | 4 |
| ENSDART00000143563 | None | None | 363 | None | 3 |
Genomic Location (Zv9):
Chromosome 5 (position 25956858)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 23784123 |
| GRCz11 | 5 | 24287923 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAATTGTATTGAATTTGTATTTTTTCTGTTTTTCCTCTATTTTTATTTA[T/A]AAGGTTACTCAGAGGAGAGCCAGACAAGCCAGACGTGTTTTCGCGTTTCA
Long Flanking Sequence:
GTATATGTGTGAATACAAGAGTGTATTCCCAGTGTTTGGTTGCGGCTGGAAGGGCATCCTCTGTGTGAAACATATGCTTGATAAGTTGGCAGTTCATTCCACTGTGGCGAGCCCAGATTAATAAAGAGACTAAGCCGAAAAGAAAATGAATGAACGTTTAAAGGGTGTAACCATCTTGTTATTTTTTCTTTTTTGGGTGGAACCATAATAGAGTTTTGTTTCTTGACTATCTTCTTTCTTACTGTCTCCTTTTGTTTTCTTTGGATTCGGCATATTTCTCTGAATGTATGTAGTATAGCAAGTACATTTTGTAGTTCATTCGTAGTTTAAACATTTTAAGCAGGATTATTGAAACTTATTTGGAGCTCTGTGCACCACATCTCTTCAGAAGTCACCCGTTTTTACATTTTGTGACTGTACTTTTTAATTGTATTTAATTCAATTGTCAATTAAATTGTATTGAATTTGTATTTTTTCTGTTTTTCCTCTATTTTTATTTA[T/A]AAGGTTACTCAGAGGAGAGCCAGACAAGCCAGACGTGTTTTCGCGTTTCATCTCTCGTATGGCTGATCGTTTGGGTGTGTCATGTTGCACCGTAGGACCTCTTCGACTGGAACTCTCTGTTTTACCTCCCATGGTTTTAATCCCTGGCCTGTTGCGAGTCGCAGCGATTAATTGCTTGTTGGGAGTTATAATCCTAACAGCGCTTCCACTACTGGTGCTTTGGTATTACTATATGACTCACAGAAGAAAAAGACGCACATTATTTTTCCTCAGTTTGGCACTTTTTTCCCTCGCCTACATGTACTATCTTTTCCTGACTGAGATCGTCCCCAGAGGAGATGTAACTCATCTGCAGGTGGTTACCGCAACGACGGGCATGATGCTGACGCTCATCTCCCTTGTGCGCACCAAACAGGGACCGGGCTTTGTCAAATCCCAGTCTTTAGCTCTGGGAATCAACAGTAGCCTTGCAACCAATCGAAGCACAAACTTAACATTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31434
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 |
|---|---|---|---|---|---|
| ENSDART00000041905 | Nonsense | 90 | 407 | 2 | 4 |
| ENSDART00000143563 | Nonsense | 46 | 363 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 5 (position 25956996)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 23784261 |
| GRCz11 | 5 | 24288061 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCGTAGGACCTCTTCGACTGGAACTCTCTGTTTTACCTCCCATGGTTT[T/A]AATCCCTGGCCTGTTGCGAGTCGCAGCGATTAATTGCTTGTTGGGAGTTA
Long Flanking Sequence:
AAAGAAAATGAATGAACGTTTAAAGGGTGTAACCATCTTGTTATTTTTTCTTTTTTGGGTGGAACCATAATAGAGTTTTGTTTCTTGACTATCTTCTTTCTTACTGTCTCCTTTTGTTTTCTTTGGATTCGGCATATTTCTCTGAATGTATGTAGTATAGCAAGTACATTTTGTAGTTCATTCGTAGTTTAAACATTTTAAGCAGGATTATTGAAACTTATTTGGAGCTCTGTGCACCACATCTCTTCAGAAGTCACCCGTTTTTACATTTTGTGACTGTACTTTTTAATTGTATTTAATTCAATTGTCAATTAAATTGTATTGAATTTGTATTTTTTCTGTTTTTCCTCTATTTTTATTTATAAGGTTACTCAGAGGAGAGCCAGACAAGCCAGACGTGTTTTCGCGTTTCATCTCTCGTATGGCTGATCGTTTGGGTGTGTCATGTTGCACCGTAGGACCTCTTCGACTGGAACTCTCTGTTTTACCTCCCATGGTTT[T/A]AATCCCTGGCCTGTTGCGAGTCGCAGCGATTAATTGCTTGTTGGGAGTTATAATCCTAACAGCGCTTCCACTACTGGTGCTTTGGTATTACTATATGACTCACAGAAGAAAAAGACGCACATTATTTTTCCTCAGTTTGGCACTTTTTTCCCTCGCCTACATGTACTATCTTTTCCTGACTGAGATCGTCCCCAGAGGAGATGTAACTCATCTGCAGGTGGTTACCGCAACGACGGGCATGATGCTGACGCTCATCTCCCTTGTGCGCACCAAACAGGGACCGGGCTTTGTCAAATCCCAGTCTTTAGCTCTGGGAATCAACAGTAGCCTTGCAACCAATCGAAGCACAAACTTAACATTAGACACAGACCTGCGTAATGGAGTCAGCCATTTAAAGGGAGAGAAGGATGTGAAGAAGAAGTGTCCTGTGTGCCAACTGGTGCGCCCACCAAGGGCGGGGCACTGCAGAATCTGTGGGGCATGTGTCCTACGAATGGACC
Associated Phenotype:
Not determined