ZMP
zgc:162724
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100038788 [Source:RefSeq peptide;Acc:NP_001083037]
Human Orthologue:
C3orf32
Human Description:
chromosome 3 open reading frame 32 [Source:HGNC Symbol;Acc:24809]
Mouse Orthologue:
D630042P16Rik
Mouse Description:
RIKEN cDNA D630042P16 gene Gene [Source:MGI Symbol;Acc:MGI:2443733]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa44990 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa37553 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44990
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000024756 | Nonsense | 59 | 417 | 3 | 14 |
| ENSDART00000060014 | Nonsense | 23 | 381 | 2 | 13 |
| ENSDART00000130604 | Nonsense | 55 | 413 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 22 (position 33709470)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 31071008 |
| GRCz11 | 22 | 31020203 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACAGTGACCAGGATGGCGCGTCAGGTCCAGGCAGATCTTATGGAACTTG[T/A]ACAGGTAATCAATATTTATTTTTCCTAAAGTTGAACTCAAATATCTCTTT
Long Flanking Sequence:
CTTTGTTTTTGTAGTAAACCACTTCTCATTGGAATGTATCATGAGATCGTCACGTTGCGCTGCTGCTTCCTGACTCTCAAAACGAAAGTTGACAGTTCACTTGCTACAATGGACAAGACGCACTTGTTGAGGTATGATCGAGAAAAAAAACAGCAAAATCACGAAGAAATGTCTGTTAGGACAAACGTAAATTAAACATTATTTAAGGTAGCGAGGAATTACTTATAAGACATATTTTAAAAAAGCAACAAACAAAAAAAATACTGAAAAATACGGTCGTTTGTTTTGGTCAGTGAGGGAAATAAGTGTCTCAGTTCTCGTTTTTTTTTTCTGACGGTTTTGTTGTCAACTTTTATTTATCGCTGTACTTTTGTACATATTGAATAAAAACACGTGTTTGTGGCTTACAGTTCTCTCTCTCATACTCTTTCTCTCTCTCTCTGTGTGTGTGACAGTGACCAGGATGGCGCGTCAGGTCCAGGCAGATCTTATGGAACTTG[T/A]ACAGGTAATCAATATTTATTTTTCCTAAAGTTGAACTCAAATATCTCTTTACACATATTTATTTCTCTAAAATTTAAAAGTGCACATTTACACAAGATACAATCCCAAAAAGGTTTATATTAGATAATATCTAATATATATTCATAAATACTGTCAAAAATAGTTCACCCCTGTGTTTACATCAGCAAAAGTAACATGAGAGAAAAAAAAGTTTCCTGTTTCTGCTGTTTCCTCATTGCAGGAATAGCTTAGTCACAGCTGAAAAAACAAGAGTTCAAAGAGTGACAGATAGTATGATGAAATGTGTTTTTTATTATTTTTTTTGTACATTCACTAGATCCAAACATGGAGGCAAATGATGGGGCGACAGCTCCTCCTGCTGATATGATGCCTGTGGTTCCTGGATATGAGAATTTGGGACCTAATGGTGAGAAAAATTTCAGTAGTTTAAGCTGAATCTATGCATGATGTATTGATGTTGCTAATGAATATGATAGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37553
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 |
|---|---|---|---|---|---|
| ENSDART00000024756 | Essential Splice Site | 91 | 417 | 4 | 14 |
| ENSDART00000060014 | Essential Splice Site | 55 | 381 | 3 | 13 |
| ENSDART00000130604 | Essential Splice Site | 87 | 413 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 22 (position 33709041)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 31070579 |
| GRCz11 | 22 | 31019774 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGATATGATGCCTGTGGTTCCTGGATATGAGAATTTGGGACCTAATGG[T/C]GAGAAAAATTTCAGTAGTTTAAGCTGAATCTATGCATGATGTATTGATGT
Long Flanking Sequence:
TCTCTCTCTCTCTGTGTGTGTGACAGTGACCAGGATGGCGCGTCAGGTCCAGGCAGATCTTATGGAACTTGTACAGGTAATCAATATTTATTTTTCCTAAAGTTGAACTCAAATATCTCTTTACACATATTTATTTCTCTAAAATTTAAAAGTGCACATTTACACAAGATACAATCCCAAAAAGGTTTATATTAGATAATATCTAATATATATTCATAAATACTGTCAAAAATAGTTCACCCCTGTGTTTACATCAGCAAAAGTAACATGAGAGAAAAAAAAGTTTCCTGTTTCTGCTGTTTCCTCATTGCAGGAATAGCTTAGTCACAGCTGAAAAAACAAGAGTTCAAAGAGTGACAGATAGTATGATGAAATGTGTTTTTTATTATTTTTTTTGTACATTCACTAGATCCAAACATGGAGGCAAATGATGGGGCGACAGCTCCTCCTGCTGATATGATGCCTGTGGTTCCTGGATATGAGAATTTGGGACCTAATGG[T/C]GAGAAAAATTTCAGTAGTTTAAGCTGAATCTATGCATGATGTATTGATGTTGCTAATGAATATGATAGTGACTTTATGAGTGAATATGAGTGACTTTTTATTTCATCCTCAGTTATTCCGCCTTCACATTTTGGATCATCACAACCACAAGCCCCACCCCGAGCTCCAGAGAGACGCTTTGAGTAAGAAAATGAAATGATTCATGATTTCAGTTTTAATTATTTGAATAGTTCTACATGAAGTCTAAGCACCAAAACGTTTACTCGTTCTTTATTCTGTGTATGCAGTGGTGCAAAGTAACAAGCTACAAATACTCAAATTAAGTTTTTCCGAGAAATTGACATTTGCTAAGTAATTCTAAAAATATGTACTTTTATGTTCTCTAAGTATATTTTTAGTGCTGTATCGGTACTTTTACTCCACTATTTTGTTTTTTGGCAAAGTAATGGAACTTTTGCTTGAGGATGATTTTTTTACAACATCACAATAAAAGCAACCTT
Associated Phenotype:
Not determined