ZMP
zgc:77880
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC393865 [Source:RefSeq peptide;Acc:NP_957185]
Human Orthologues:
ZDHHC3, ZDHHC7
Human Descriptions:
zinc finger, DHHC-type containing 3 [Source:HGNC Symbol;Acc:18470]
zinc finger, DHHC-type containing 7 [Source:HGNC Symbol;Acc:18459]
zinc finger, DHHC-type containing 7 [Source:HGNC Symbol;Acc:18459]
Mouse Orthologues:
Zdhhc3, Zdhhc7
Mouse Descriptions:
zinc finger, DHHC domain containing 3 Gene [Source:MGI Symbol;Acc:MGI:1926134]
zinc finger, DHHC domain containing 7 Gene [Source:MGI Symbol;Acc:MGI:2142662]
zinc finger, DHHC domain containing 7 Gene [Source:MGI Symbol;Acc:MGI:2142662]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14751 | Nonsense | Available for shipment | Available now |
sa32600 | Essential Splice Site | Available for shipment | Available now |
sa17658 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14751
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 |
---|---|---|---|---|---|
ENSDART00000043881 | Nonsense | 6 | 297 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 9481778)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 9621564 |
GRCz11 | 1 | 10305675 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATGACGTCATCARGAAGACCGCAGATGGGAAGATGGCTGCGTTTCGCTG[T/A]CGGCGAGACCCGTGCGGCTTTATTTGTCTYATTTTAACTTACTTCAGCGT
Long Flanking Sequence:
CGACATTCCATAAAATAGGCACATTCAAAACTGAGAAAACATTCTAAAAACATGAGAACATTCCAAAACATTGAGAAAAAATTCTAAAAACACGAGAACATTAGAAAACATAGAGGGCACATTACAAAACAAAAAAAAAAAACATTCAGAAACATTGAGGGAACATTCTTAAAACACGAGACGATTCCAAAACAAACAGGGAACATTTAAAAACATTTAAGGAACATCTAAAAAACATAAAACATGGGAACATTCCATAAACATGAGTGCATTATTACAAAACATTGAGAGAACATTCAAAAAACAGGAGAACACTTATTCTTTCGAGTTCACGTTTTTATTAAAACTGTGTCATTTTAAAAGAAGTTAAATCAGAGATGCAGGCTCGCAGGTGGTCAGAAGGATTAATAACAGCAGATGACAACACTGCATACGTAACGCTCGTCCTTTTATGACGTCATCAAGAAGACCGCAGATGGGAAGATGGCTGCGTTTCGCTG[T/A]CGGCGAGACCCGTGCGGCTTTATTTGTCTCATTTTAACTTACTTCAGCGTCTTTTACGCGGACTATGTTGTAATTCAGTATGTATTGATTCCCGCGTATTCTGGAAGGTGAGTACCGCCTTTAAATAGTCGTTTTTGAGTCCACACGCGCTGTTCGTGAGCTCATCATATGATTGTTAATTTTCAAATCAATCACCCATAGCAACAGCAGATCAAAAGCAACGTGTGTGCCAATTCTTACCGCGTTCTGACGGAGTTTCCCGCGAAACGTGTTTCAAATGCGCTTGAACTGTTTACAAACGCATCGGCGCTGTCAGTCAGTCTGCAGTAGTGCATCATTCAGCGGTTTTACTACACTTGTCTCGGTTACATTCGAGGTCTAAGGTTTCAGGTTATCTCGCTTGAAATGAACAAACCACTTTACCTTATAAGACTCTGGTGCATTATGATATTACTCACAGGTCTTTTTGGAAGTGTAACGTGGTACTCTAAAACATTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32600
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 |
---|---|---|---|---|---|
ENSDART00000043881 | Essential Splice Site | 195 | 297 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 9487707)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 9627493 |
GRCz11 | 1 | 10311604 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGATGAAGAGAAAGAAGGAGAAGAAGCTCCCAGCAAACATCTCATTGTG[T/C]AAGTACAATTTCTTTCTGAGAAACTGTATTAATGTTATATAATGGAAATT
Long Flanking Sequence:
CCATGCTTGGTCTTGTTTTCCCAGTGATGGGTTGCAGCTGGAAGGGCATCCGCTGCGTAAAACATATGCTGGATAAGTTGGCGGTTCTTGTGGCGACCCCAGTGAATGTTTGGTCTTGGTTACAATCATATCAACTGTGTCAAATTTAACAGTTTAAAGCAACTTAAATTTATTAATACAACAATATACCATATGTACTGTACAGGTGTTCCTTTTTCTCTTTTGTAGGATTAATAACTGTGTTGGAGAGCTTAATCAGAAATACTTCATTCAGTTTCTTTTCTACACGGGTGAGTTTTAAGATCCGCTCACAGACAATATTTCACAAAGTAAAGGAGCATGAAGTGTTTCAGCAGATCTGCCATGTTGTTTCTGTAGGCATGGCTAGCTTGTACTCCATGGCACTGGTGGTTTCAGCCTGGGTGTGGAGGATAAGGAGTGAAAGAGAAGGAGATGAAGAGAAAGAAGGAGAAGAAGCTCCCAGCAAACATCTCATTGTG[T/C]AAGTACAATTTCTTTCTGAGAAACTGTATTAATGTTATATAATGGAAATTGGTTTTTTTTTGTTCAGCTATTACTACTTCTCACATTGTTTTTTTATTTTTATTTTTTTACAGGGCACATTATATTATTTTACTGGTGGAGTCGATACTTTTTGGAGTTTTTGTCTTGGTAATATTTTATGACCAGGTATGCTTCCACGTTTTTTATTACTGAAATTATATATTAATATCATTTTAAAATTAATCTACAGCCACAGTACTGATTCATTGTTACAGTATGTTTACATGACAGAACTGTGAAATAGTCCGTGTTTTTTTTCTTCACAGTTTGAAATTAACATACACACTACCAGTCAAAACTTGAACACATGAAGATTTAGTAATGTTTTTGAAAAAAACTTCTGTTTACCAAGCATTCATTTATTAGATAAAAATTAAAATAGTTTATTTTTATTATTTTATATACATTTTGTTTTTGAATACATTTTAAAATGCAGTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17658
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 |
---|---|---|---|---|---|
ENSDART00000043881 | Nonsense | 272 | 297 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 9490459)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 9630245 |
GRCz11 | 1 | 10314356 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAATAATRCTAAATGTATTTCTCTCACCTGTCTACAGGYTCTATAYTGTG[T/A]TGGTTATTCCCGCTTCATTCCACCCCTCCTTCTGTTGGCGGCATCAGTTA
Long Flanking Sequence:
CCAAAAAGGTCTCTCAAATAAAATTTTCAATTTCAGCGGTGTAAATTAATCAGATTTAGTTGAAAATGTACAAACGACTCATAGGGGACAATGCAAAAGACTTTGGTGAGTGAATCAAGTCAAAGGCAGCTTCTGCTTGCCTATTGTATTCAGCATTGAACACCACTTTGTTATAAATGTGATTGTTGATGTTTTTAATCAAAATAAGTTTTAATAGAAAAAATTATACTGCATTAGTTAATATAATTCAAAGTAAAGTTTTCTATTTATTATTCAATATTATTAAATAAATTAGGAAATTAGCCATGGCAACTTTAATGTAAATTAGTAAATGGTATATTTATGTTTGGCCCACAGCTATCAATGATATTTGGTTTTTTGGCTCTTCAAAAAAAAAGTTTGGGTACCCCTGCTTTACACATAGTGACCCAACATTCTCAACAGCATTTCTAATAATACTAAATGTATTTCTCTCACCTGTCTACAGGTTCTATACTGTG[T/A]TGGTTATTCCCGCTTCATTCCACCCCTCCTTCTGTTGGCGGCATCAGTTATTCAGCACTTCCTGATTACGACGTGTAACACTAACCAGTTTTTCATCAGTCCTTTTGACCGCTCAATCAGTATGGCAGTATCATATATGTGTGTGTGTGTGTGTTGGGAACTGTGGATATTACGTTACTGAGATGCAGATTTCAGCTCTCATGAATGGTGTGTGAGTGCTTTTGTGTACTTCTGCTTACTGCTTCTCCATTACACACAGAGATTATTACAAGGTACTGAATCTTTTTTCTTCATCTAATCAACTAAATGTTTCTTTTGATATTACCCGGGAGATTTTATGATTTTTTTTTTTTTTTTTTTTTCGGAAGAGTCTTGTTTAAAGTTGTTAAATCAGTATGTTAACCAGCAACCAGTATACATTGTGTTGTATACGGTACAGTAACCACTAATTTGCATTAAGGGACAAGGTCAGCTGTGTTGACTTTATCAGGTAAATGCAA
Associated Phenotype:
Not determined