ZMP
zgc:153935
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC777611 [Source:RefSeq peptide;Acc:NP_001071187]
Human Orthologue:
CXorf38
Human Description:
chromosome X open reading frame 38 [Source:HGNC Symbol;Acc:28589]
Mouse Orthologue:
1810030O07Rik
Mouse Description:
RIKEN cDNA 1810030O07 gene Gene [Source:MGI Symbol;Acc:MGI:1916405]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa10183 | Nonsense | Available for shipment | Available now |
| sa38093 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10183
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 |
|---|---|---|---|---|---|
| ENSDART00000053562 | None | None | 303 | 2 | 9 |
| ENSDART00000125806 | Nonsense | 58 | 414 | 1 | 9 |
| ENSDART00000131437 | None | None | 67 | 2 | 4 |
| ENSDART00000140663 | None | None | 321 | 2 | 9 |
| ENSDART00000142962 | None | None | 50 | 2 | 5 |
| ENSDART00000148121 | None | None | 173 | 1 | 6 |
The following transcripts of ENSDARG00000036888 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 25 (position 28588987)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 27279081 |
| GRCz11 | 25 | 27722283 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTTATCACAAGGCTCTGCTAAACAAACAGCAGCTCAGTGGACAACGTTG[T/A]GAGCAAACCTGCAAAAATAATAAGGTAACGTAAATCGTACATAGAAATTG
Long Flanking Sequence:
GAATTTAAGAATAGCTTAGCAAAATAAGGAATTAAAATTTGATATGGTATTTAACTTGTATTTTTTTTCTTTTTTTTCTCCTCTCCTCCTACTCTTCTTCCTGTTCTCTCTTCCCTTTGGTAATCTCATCCCTCCATTCGTATCATATCTTTTGTACTCATGCTTTTTCCTACATTATGCGCTCCACACTCCTATCCAGTAGGTGGCGGAAATGCACCATATAAGTTGGTCTGCCAACCACCATTAACCCCATAAGAAGAAGAAGAAGAACACAAAGAAGAAGAGGAAGTTTTGCAGTTTGCATTATTGATATTTTAATTAGCCAAAATGAGCAACTCACAACCTTACAGACGCTTTAGTGATGAAAATTACAAAAACTGGCTAAAAATAGCAGAGAGTCTTCACATACTGCGAAACAGCATGCAGGACTTTATTGAAAAGGAAACTGAAACTTATCACAAGGCTCTGCTAAACAAACAGCAGCTCAGTGGACAACGTTG[T/A]GAGCAAACCTGCAAAAATAATAAGGTAACGTAAATCGTACATAGAAATTGTAAATTGTACCTGGAAATCTAAGCTTAAGTAAATACTGGAGTCGGGGTTCAATCTTCAACTGGCTGGCAGGAGTGATAAAACATTGTTTTGTCATTCAAAACTATTCTGAGAAAATATTAGTGTGAAAGTTTGTAGAAAAATGTTAACACGAGTCCACAGCTGACAAAAATAATGAGTCCTTAATAGCTCAGTTAGTGGAGTCCCCAACAGCTCACATGTCGCTTAATGCGTGTGCTTTAACTACTTGAGTTCGAATCCCGTTGATGACATACACATTATAATTATTTTTTAGATTAATTTAGGTTATATACTGCTGTGTTACACAAATATTAAAATAAAAAAATGTTTACAATGACACTGACATCAAGTAATAAAAATATTTATTTGGTATGGGCTTGTTTTGCTGCTGTGGAAAAAGTAACGAATCTGCCAATCTGCAAGCATGAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38093
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 |
|---|---|---|---|---|---|
| ENSDART00000053562 | Essential Splice Site | 41 | 303 | None | 9 |
| ENSDART00000125806 | Essential Splice Site | 152 | 414 | None | 9 |
| ENSDART00000131437 | Essential Splice Site | 59 | 67 | None | 4 |
| ENSDART00000140663 | Essential Splice Site | 59 | 321 | None | 9 |
| ENSDART00000142962 | Essential Splice Site | None | 50 | None | 5 |
| ENSDART00000148121 | None | None | 173 | None | 6 |
The following transcripts of ENSDARG00000036888 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 25 (position 28585072)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 27275166 |
| GRCz11 | 25 | 27718368 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTAAACATTTTAAGCCATTTTTGACTAAGGGGGAAAATGTGAAAAAGG[T/A]AAATACTGTTTTCTACCCCTAAGATTTTTCTTTTTGATGTTAAATCATTA
Long Flanking Sequence:
AAATACAGAACTCCCAGTTGTGTCTTAACCTGCTTTTTAGATTTTTTTTTAAAATGTAGAGTCAAAGATTATTGGAGTATCTGTACGTTTCTGACTGTGTACTGCTGCTTCCACCAGTCTCTCTGCCAACTGTGTGAATATTGGAAGAATGAAATTGTGACCAATCACAATGAGGGTGGTAGAAATGTACACTGGGACAATTGCCGGCCACATCTATGGGCCACAAATAAATGGGAAGTTGCAAAGGTAAGAACATTTTATCGTTAAAAACAATCACCTGTTGCGTTAACTTGTTGTATATTTGCTGTCAGTGAACAAATCTATGTCCATTATATTTTTGACTGCGTGTTTTTCATACTTTTATCGACAGGCATACATGCCACGTGGGCACAAACAGCATTGTGAGTTTGCCCAGTTTGATATTTCTGCCATTCTTAACTTTCTGAGTGCCTGTAAACATTTTAAGCCATTTTTGACTAAGGGGGAAAATGTGAAAAAGG[T/A]AAATACTGTTTTCTACCCCTAAGATTTTTCTTTTTGATGTTAAATCATTATAAACCTTTTTATCTGTTCTTCTCCAATATTATTATGTGCTGGAAACCGGCTAAACTGTATTGTTACAGATATTCAAACATCAAATGTCACTTTATATAAGATTATTACAACTGTATATTTTGAATAATTCAGGTTATAAATGTTCGGAATGTTGTGATGCACTCCCCTGACCTTAAAATGAACAATGAGGATATGAACAGACACCTTGAAACAATTTTCCAGTTTGCCGATATGCTTAATTCCAAGGTATCAGCACTCTCAGTCTTGAGAGAGAAGATAGAACAGGTGAATGAAATCCAGATTATGATAAGCCTGTTTTTTTTATCACATCCTTTTATTATTTATACTTGATTTCAGCACTTGACTGAAATTTTTTTGTTTTACATTTTCTGAGTAGTTTAACAACATTTTGGACAAGAATTTCAATCAAACAGAAGTAGATGGTCAAC
Associated Phenotype:
Not determined