ZMP
zgc:175175
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC797780 [Source:RefSeq peptide;Acc:NP_001120947]
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 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9481 | Nonsense | Available for shipment | Available now |
| sa19303 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa17965 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9481
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109841 | Nonsense | 61 | 211 | 4 | 9 |
| ENSDART00000139706 | Nonsense | 61 | 203 | 4 | 8 |
| ENSDART00000109841 | Nonsense | 61 | 211 | 4 | 9 |
| ENSDART00000139706 | Nonsense | 61 | 203 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 33686023)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 31047561 |
| GRCz11 | 22 | 30996756 |
KASP Assay ID:
554-6169.1 (used for ordering genotyping assays)
KASP Sequence:
CCSTCAGCATTCCTGCGATCAGTGAAGAACTTGCACWGGARGCCTTTACT[G/T]AATATGTGTCCAGCAAATGCWGTTACAGCTCCAAACCAGTCAAAGAGATG
Long Flanking Sequence:
GACTGTGAGTTTTAAACTAGTTGTCCAAATTGTAAGAGCTGAACTTAGAATTAAACTCAGAACTGCTATGTCAACTCAAAATTGCAAGAGGAAGTTTTGAAAAATTGTGAGAAATAAACTCAGAACTTTGAGATATAATATGTATAGAACTATTTGAATTATTAAAAAATATTGCAGATCTGAGGTGGTGATGTGGTCATAGCCTAAAGGGGGAGTCATTGTTTAAATGCTGGCAATTTCTCACAATGTGTGAGACTACTTTCATATATTTCTCATCTATAATATCTACCAACCTTTCTATTGATTTGTTCTTTAACCCCTTTAGCATTCCAGCGTTCTGGTTATTGAGCCATAAACTACTGGAATGCTAAGTGGTAAAGGGGGTTTTGCATACTCAATATTTTGGACAATGTTTGGCTGGTCACATGTGAACTTCACTTTAATCGTGTCCCCTCAGCATTCCTGCGATCAGTGAAGAACTTGCACAGGAGGCCTTTACT[G/T]AATATGTGTCCAGCAAATGCTGTTACAGCTCCAAACCAGTCAAAGAGATGGTGTTCACAGACCTGCAGTCCCTCAACACATATCGGGTCAGCAGCAAAACTCACGAACATCTTACCTCACTATATAATGATGCCATTAACTTACAAACGTATATGTCTTTACAGTACCGACTGGAGACTTTTACAGAATCTAGAAGAACAGAAAGAGACAGTGAACCATACTATGGTAAGAAGAGAGTTTTTTAGTCTCTTGACAGGCAGAAGTCAAGACTCATCATACTAGGGCCATGCTACCTCTAAAACTTTGAACATCTAACAAGAGATCAATCATAGACGAATCATCAAAATCTTGTATATTTTTACTGACATGCCAAATTTAGCCTTCCTTTGGCGAAGACATCTGCGTTTGGATGTCTGTTAGACACCCCTGTGAAATAACATGGTTGTCTATAAGTTAGTGTGCAAAAGAAAATGCATTTAGAAGATACAGTTCAAAGCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19303
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109841 | Nonsense | 61 | 211 | 4 | 9 |
| ENSDART00000139706 | Nonsense | 61 | 203 | 4 | 8 |
| ENSDART00000109841 | Nonsense | 61 | 211 | 4 | 9 |
| ENSDART00000139706 | Nonsense | 61 | 203 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 33686023)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 31047561 |
| GRCz11 | 22 | 30996756 |
KASP Assay ID:
554-6169.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCTCAGCATTCCTGCGATCAGTGAAGAACTTGCACAGGAGGCCTTTACT[G/T]AATATGTGTCCAGCAAATGCTGTTACAGCTCCAAACCAGTCAAAGAGATG
Long Flanking Sequence:
GACTGTGAGTTTTAAACTAGTTGTCCAAATTGTAAGAGCTGAACTTAGAATTAAACTCAGAACTGCTATGTCAACTCAAAATTGCAAGAGGAAGTTTTGAAAAATTGTGAGAAATAAACTCAGAACTTTGAGATATAATATGTATAGAACTATTTGAATTATTAAAAAATATTGCAGATCTGAGGTGGTGATGTGGTCATAGCCTAAAGGGGGAGTCATTGTTTAAATGCTGGCAATTTCTCACAATGTGTGAGACTACTTTCATATATTTCTCATCTATAATATCTACCAACCTTTCTATTGATTTGTTCTTTAACCCCTTTAGCATTCCAGCGTTCTGGTTATTGAGCCATAAACTACTGGAATGCTAAGTGGTAAAGGGGGTTTTGCATACTCAATATTTTGGACAATGTTTGGCTGGTCACATGTGAACTTCACTTTAATCGTGTCCCCTCAGCATTCCTGCGATCAGTGAAGAACTTGCACAGGAGGCCTTTACT[G/T]AATATGTGTCCAGCAAATGCTGTTACAGCTCCAAACCAGTCAAAGAGATGGTGTTCACAGACCTGCAGTCCCTCAACACATATCGGGTCAGCAGCAAAACTCACGAACATCTTACCTCACTATATAATGATGCCATTAACTTACAAACGTATATGTCTTTACAGTACCGACTGGAGACTTTTACAGAATCTAGAAGAACAGAAAGAGACAGTGAACCATACTATGGTAAGAAGAGAGTTTTTTAGTCTCTTGACAGGCAGAAGTCAAGACTCATCATACTAGGGCCATGCTACCTCTAAAACTTTGAACATCTAACAAGAGATCAATCATAGACGAATCATCAAAATCTTGTATATTTTTACTGACATGCCAAATTTAGCCTTCCTTTGGCGAAGACATCTGCGTTTGGATGTCTGTTAGACACCCCTGTGAAATAACATGGTTGTCTATAAGTTAGTGTGCAAAAGAAAATGCATTTAGAAGATACAGTTCAAAGCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17965
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109841 | Nonsense | 188 | 211 | 8 | 9 |
| ENSDART00000139706 | Nonsense | 188 | 203 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 33680680)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 31042218 |
| GRCz11 | 22 | 30991413 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTYTGTGTGGATTCWGTGGTGGCATGGGYTGGACTAACTATGGCCAACGC[C/T]AGTTTTGTGGTGTGTGTGGGGGCAYTGGCAGGCAAAGGTACNNNNTTGAG
Long Flanking Sequence:
ATTAACTAATGAACCTTATTGTAAAGTGTGACCGATTATTGAATATTGTATCTCATTCTTTCTTGCCTAAACATACTCTTCATTTATCAGGTCAGCAGGTGGATGGATCTGGAATTCCTCCCGAACCATGGAGCATCCCGGTGTGCATGCCATCTTTCTTCCAAGATAGTGAGATAACCATCCCCGTTCCTCACACATCAAGTGTCCAAGTAAAACTTGTTCAGTTTTTTATTTGATCACATTCATTGAAAACATATTTTTAGAAGTTTTATTTATCAGTGATCTTTGAATTTAGGATTGTTCGTCATGCTCTACTCTTGGTAGAACTATGTGTCTAAGTTGTGGACGTACAGGCAGGGTGAGTGTTATCATGAAATGTCATTTAAAAGTTTTTCTTTTGCATTAATTTCTTTTTCTATTGTTTAATTATGATATCTTTGTTATTTCAGATTTTGTGTGGATTCTGTGGTGGCATGGGTTGGACTAACTATGGCCAACGC[C/T]AGTTTTGTGGTGTGTGTGGGGGCACTGGCAGGCAAAGGTACAGTCTTGAGAAATTACATGTTGATAAAATGTTGAACGATTACAAATTGGGCAGCTCAGTGGTTAGCACTGTCGCCTCACTTTAAAAAGATTTCTGGTTTGAGTACTGGCTGGGCCAGTTGGCATTTCTGCCTGGAGTTTGCATGTTCTCCCCGTGTTCATGTGGAATTCCTCTGGGTGCTCCGGTTTCCCCCACAGTCTAGCAGGGATGGGCAAACTTGATCCTCGAGGGCCGGTGTCCCTGCAGAGTTTTGTTCCAACACTAGTCAAACACACCTGAACATGCTAATCAGTGTCTTTAAGATCACAAGAAATCTATAAGCAGGTGTGTTTGATTAGGGTTGGAGCTAAACTGTGCAGGACACCGGGCCTCCAGGACCGAGTTTGCCCAACCTTGGTCTAAAGTCATGTGGTACAGGTGAATTGAATAAACTAAATTGGCCGTAGTGTGTGAGAGTGTA
Associated Phenotype:
Not determined