ZMP
zgc:73311
Ensembl ID:
ZFIN ID:
Description:
selenoprotein U [Source:RefSeq peptide;Acc:NP_001180454]
Human Orthologue:
C10orf58
Human Description:
chromosome 10 open reading frame 58 [Source:HGNC Symbol;Acc:28651]
Mouse Orthologue:
5730469M10Rik
Mouse Description:
RIKEN cDNA 5730469M10 gene Gene [Source:MGI Symbol;Acc:MGI:1917814]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13116 | Nonsense | Available for shipment | Available now |
sa42175 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13116
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080025 | Nonsense | 29 | 229 | 1 | 7 |
ENSDART00000122300 | Nonsense | 29 | 229 | 1 | 7 |
ENSDART00000133062 | Nonsense | 40 | 101 | 2 | 3 |
ENSDART00000134740 | Nonsense | 18 | 104 | 3 | 5 |
ENSDART00000141647 | Nonsense | 18 | 102 | 1 | 3 |
ENSDART00000147905 | Nonsense | 18 | 212 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 18712672)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 18532707 |
GRCz11 | 13 | 18663699 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGCATGTGGYCACTTGGCCTTGGGGCAGTAGGTGCCGCTATTGCTGGCT[T/G]AATACTTGCAAACACTGACTTCCTGCTGACTAAATCTGCACCTGCTACTG
Long Flanking Sequence:
TGTTTGTGTGAATAATAGTGATGTGATGTACAGGGTCTCTGTGTCACAGTCTGCCCGGCCTTTAGCTTCTTATAAGACAGTTAAAGCTTATAACATTCCTCCAAAACATCTTCCATTGACCATCTCAACATGGCGACTGGCAGTCAAGACATTAGCGCTCCCCACTGCTGTCAACTCGCTATTCTTTCAAGCTTTTCCAACAAATCGGCACTTTTCAAGCGAAAGCCAGAATGGCAAGCCTTCTTTTAGTCACAAAAAAGGTACTGCTCTTGCCCCAGCATGTCTTGGGGTTATAGAAATTACATGCTTGTCTTCAGTACAAAATTAAGCGGTTGTTTATGCAAAGAAAGCTCATGAAAAGACTAGAGCATTTTACTGTACTGTTTGATTTAATCTACCATATTTGTTCATTTCAGCATCATCTGTCCTGGAGGGTGAGACGCTAGCCATGGGCATGTGGTCACTTGGCCTTGGGGCAGTAGGTGCCGCTATTGCTGGCT[T/G]AATACTTGCAAACACTGACTTCCTGCTGACTAAATCTGCACCTGCTACTGTAGACTATCTTGCGAACGCTGACCTCAAAACCATTGACGGTGGTAAGAAATTATCTGAAATCCCGTGGAAGTGATCCTTGGGATTTTTAAATCATTTTGTACAATTTCCATTCAGCCATCATGGTAAGCCTGCACTGTTTTTCCATCTAAATCCATTCAGATGAGAGGTCTTTAAAAGCAAAAGCTCTTTGGGAGAAGTCAGGTGCAGTGATTATGGCTGTCCGGCGACCTGGATGATTTTTGTGCAGAGAGGTAAGTGGTCATAATACTCTTTTTTATTTGAAAGAGACTACTTTAATTTTTATAAAATATTTATAAAGAAACATCACCATATCCATGTTTTCAGGCAAGTTTTCTGACACTTATGTGGGAAATTCCCTCCTCAACCCACCAAAATAAACAGGGATTGGACAATTAAACTGAAACACTTGCCAATTTAGTGTTGGAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42175
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080025 | Nonsense | 82 | 229 | 2 | 7 |
ENSDART00000122300 | Nonsense | 82 | 229 | 2 | 7 |
ENSDART00000133062 | Nonsense | 93 | 101 | 3 | 3 |
ENSDART00000134740 | Nonsense | 71 | 104 | 4 | 5 |
ENSDART00000141647 | Nonsense | 71 | 102 | 2 | 3 |
ENSDART00000147905 | Nonsense | 71 | 212 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 18712948)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 18532983 |
GRCz11 | 13 | 18663975 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCAAAAGCTCTTTGGGAGAAGTCAGGTGCAGTGATTATGGCTGTCCGG[C/T]GACCTGGATGATTTTTGTGCAGAGAGGTAAGTGGTCATAATACTCTTTTT
Long Flanking Sequence:
AGCATGTCTTGGGGTTATAGAAATTACATGCTTGTCTTCAGTACAAAATTAAGCGGTTGTTTATGCAAAGAAAGCTCATGAAAAGACTAGAGCATTTTACTGTACTGTTTGATTTAATCTACCATATTTGTTCATTTCAGCATCATCTGTCCTGGAGGGTGAGACGCTAGCCATGGGCATGTGGTCACTTGGCCTTGGGGCAGTAGGTGCCGCTATTGCTGGCTTAATACTTGCAAACACTGACTTCCTGCTGACTAAATCTGCACCTGCTACTGTAGACTATCTTGCGAACGCTGACCTCAAAACCATTGACGGTGGTAAGAAATTATCTGAAATCCCGTGGAAGTGATCCTTGGGATTTTTAAATCATTTTGTACAATTTCCATTCAGCCATCATGGTAAGCCTGCACTGTTTTTCCATCTAAATCCATTCAGATGAGAGGTCTTTAAAAGCAAAAGCTCTTTGGGAGAAGTCAGGTGCAGTGATTATGGCTGTCCGG[C/T]GACCTGGATGATTTTTGTGCAGAGAGGTAAGTGGTCATAATACTCTTTTTTATTTGAAAGAGACTACTTTAATTTTTATAAAATATTTATAAAGAAACATCACCATATCCATGTTTTCAGGCAAGTTTTCTGACACTTATGTGGGAAATTCCCTCCTCAACCCACCAAAATAAACAGGGATTGGACAATTAAACTGAAACACTTGCCAATTTAGTGTTGGAGGATTCCTGGCTAAATTTGACCAGCCCGGTGGTCAATCTTCGTTGATTGCACATTCTACTTGTAAGAGCAGAGTATTAGCACAGTTTTGGCTAAAAAGCCCTTATTCTGCATTACAAAAAGGTCATATTTTGGTTTTGGGGGTCTCCAACAGTATGTTGAAATGCATGCAAGAAAAGAAAAAAAAAACACTTTCGTTGTTTTATAATATGCATTTATTTTTACAGAATTATCTCAACGATTCCAATATGACTTGTTCAGCGATTCATTTGTTCCCAATC
Associated Phenotype:
Not determined