ZMP
si:dkey-181m9.10
Ensembl ID:
ZFIN ID:
Description:
transmembrane protein 59 [Source:RefSeq peptide;Acc:NP_001104658]
Human Orthologue:
TMEM59
Human Description:
transmembrane protein 59 [Source:HGNC Symbol;Acc:1239]
Mouse Orthologue:
Tmem59
Mouse Description:
transmembrane protein 59 Gene [Source:MGI Symbol;Acc:MGI:1929278]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9519 | Nonsense | Available for shipment | Available now |
sa39840 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9519
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 |
---|---|---|---|---|---|
ENSDART00000003946 | Nonsense | 115 | 330 | 3 | 8 |
ENSDART00000126826 | Nonsense | 115 | 329 | 3 | 8 |
The following transcripts of ENSDARG00000019033 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 26768129)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 26964325 |
GRCz11 | 2 | 26619959 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCAGTACGCCTGCAATCTAGGATGCCAGAATCAACAGCCATTTGCAGAA[C/T]AAAGAAWGGAGCAGGTGTGAAAAACCTTTGTCAAWAATTGCCTTTGCGTG
Long Flanking Sequence:
GGCGCTGTACGCCTGTCAGAGAGGATGTCGCCTCTTCTCCATCTGCCAGTTTGTGGGTGACAGCAAAGATCTCAACGAAACCAGATCCGAGTGCGAGTCAGGTAGGGTTATAGCACTGAAAACTGCCAGTTTGTTGTGCAAACAGTTGTGTGTGTTTGACATTGAGATAAGTTTGGTTTCATATTCACTCGGAATTTCTCCTGTATTAAGAGGTCTTGCAAACTATAAAATAGTGAAATACTATTATCAGCCAAAGACAATCAAAGTACAGCAGTGTTCACAGTCAAATACGTAATGTTAAGGTTGTTTTGAAGTCATACTTGCATGTGATTTCAGATTGTATATTTAATGTACCATGGTAAACAGTATACACAACTTGTCACTGAACCAACTCAACTCAATGTGTTTGACTTTCTGCAGCCTGTCGTGAAGCCTACAGCCAGTCAGACGAGCAGTACGCCTGCAATCTAGGATGCCAGAATCAACAGCCATTTGCAGAA[C/T]AAAGAATGGAGCAGGTGTGAAAAACCTTTGTCAAAAATTGCCTTTGCGTGATCTGTTTTATTTGCACGTCACCCAGGTGCAGTCTGACGTCATCCTATGTTTGTTCTTTTGTTTCGGATGAGAAGTTGACGATGATGATGCCCAAAATCCATCTGCTGTACCCGCTGACTTTGGTCAGGGGTTTCTGGGAGGATATGATGAGCCAAGCCCACAGCTTCATCACCTCATCCTGGACATTTTACCTGCAGGCGGATGATGGCAAAGTAGTCGTTTTCCAGGTGATAATTTTATGTCTTTTTATTATTAGACTGTGTTAAACGAGTATATTAGGCTGAGATGCTGAAATTGAGGGCTGTGGGCCAAAGTTTGCCTGTCGTGCATGCAATATAACAATATAACAGGCATTGTGTTTATTTTATTTTTGTTAGCTGTGTGTTGAAATGAAAATGCATTTTTATATCATATTGTCAGTTTTAATACTTCTTTTGCTTTTACTGCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39840
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 |
---|---|---|---|---|---|
ENSDART00000003946 | Nonsense | 298 | 330 | 8 | 8 |
ENSDART00000126826 | Nonsense | 297 | 329 | 8 | 8 |
The following transcripts of ENSDARG00000019033 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 26761297)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 26957493 |
GRCz11 | 2 | 26613127 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCATATATGGAGACATGGAGTACATGAAGGAGCAGAAGCTGAGCCCGTA[T/A]CTGCCGTCGTCTCTGGTCATCATCAGATCTCCTGGCTTTGAGGAGCAGCA
Long Flanking Sequence:
TACATTTCCTTTTTACAGTTTTACCTTATGTTACTAGGTTAGCTTATGTTAGGTTGTTACATTGCATTGTTGAATTGCTCTGTTTTTGTTACGTAATGTTGTTACATTGAGCTATGTTGTGTTGCATTGAATCCATTGTGGAACACATTATCAGATTGCGATATATCTGAAATGGCTTAGCATGTCATTTTACTTAACGAACACTTAGCTCATGAACATTAAATACTTAAATACTGAAATTTTCTCCATGTGATGTTAATAAAGACAGATGAGGTGGGCAAGTAACTAAACGACATCATCATCGTAATGGTGACAACATACCACTAAAGCAGACACAATGTTAAAATTTACGATCAATCGATGAAATGATTGTTAAACAAAGATCAATCATGGGAATTTAGTACATTGAAACCCAGAGTCTAAATGTTCTCCTCTTTTCAACAGAAGCTGAGCATATATGGAGACATGGAGTACATGAAGGAGCAGAAGCTGAGCCCGTA[T/A]CTGCCGTCGTCTCTGGTCATCATCAGATCTCCTGGCTTTGAGGAGCAGCAAGCAGGACCTCTCCCTTCAAAGGTCAATCTGAATCAGTCTAGCATTTAACTAGTCCAACATCCAAAGAAACTGGAGGCTCCTGGTACATGTTTGCTACTTTTCCTGTCAAAGTTGTGATTTTTTTTTTTGCTTTAATATGGGTATATGGGGAATATATTTTATTGGCGTTTTGGCACTTTAAAAGCATTACCTATCAGACGGAAAGCTCGGTAGGATCTGTTTTTCCTGTTTACTACACATTTGTAGAGATGAAGACTTTTTGGTTTCCTTTATTATCACTTCTTGAGTGTTCTCAGTGTGATCAGTAACAGCTTGTGATTTAAGGTTCAAGATGTGTTGCACAATGAAAAACATTAACATTTTGATTTATGCTATAGTTGCAGGGAATGCAAATTGTCATAGAAACAGGGATAGGGAAGTCAGTAATAGGCAATGTGATATTTTGCAAC
Associated Phenotype:
Not determined