ZMP
zgc:172056
Ensembl ID:
ZFIN ID:
Description:
nuclear pore glycoprotein p62 [Source:RefSeq peptide;Acc:NP_001107068]
Human Orthologues:
NUP62, NUP62CL
Human Descriptions:
nucleoporin 62kDa C-terminal like [Source:HGNC Symbol;Acc:25960]
nucleoporin 62kDa [Source:HGNC Symbol;Acc:8066]
nucleoporin 62kDa [Source:HGNC Symbol;Acc:8066]
Mouse Orthologues:
Nup62, Nup62cl
Mouse Descriptions:
nucleoporin 62 C-terminal like Gene [Source:MGI Symbol;Acc:MGI:2685565]
nucleoporin 62 Gene [Source:MGI Symbol;Acc:MGI:1351500]
nucleoporin 62 Gene [Source:MGI Symbol;Acc:MGI:1351500]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa28269 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa28269
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 |
|---|---|---|---|---|---|
| ENSDART00000041523 | Nonsense | 474 | 507 | 12 | 13 |
| ENSDART00000131295 | Nonsense | 474 | 507 | 12 | 13 |
| ENSDART00000136480 | None | None | 214 | None | 5 |
The following transcripts of ENSDARG00000020527 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 10854546)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 10349903 |
| GRCz11 | 14 | 10655917 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGATCTGCAAAATTCTCAATGCACACATGGACTCCTTACAATGGGTG[G/T]AGCAAAATTCAGGTCAGTATCCACTTAAATTCGATACATATTTCGCTACA
Long Flanking Sequence:
ACATAAAGTTTAACTCGCCCTCAGGGTCTTGAATTGATATTTAATTGAAATCCAGAAGACCTAATTAGGGAGTGAATGTAAACAGCTTCATTGTCATAAGTTCCGATCTGTCTACATGTACTCTGGAGTTATGTGGATGCCAGACATAATCAAAACAAAAGTTTAAATGAACAAAAAAAGTGTAAATGTAGTGTCAATCAACCCTGTCAGAAGCTCACGTTTTCTTCAAATACTAATAATCTTTTATCCAGGTACAAGTTGGCTGAAAATGTGGATGCTCAACTCAAAAGAATGTCCCAAGATCTAAAAGAGATTATTGAACACCTCAACACCTCCAGTGGACCCGCTGACACTGCTGACCCGGTATGCACAATATAATCTATATTTGTAAAAAATCAATGCTGTTACCTGGACCAAGACTGACTTGTGGTGTCTTTTTTTTCCAGCTTCAGCAGATCTGCAAAATTCTCAATGCACACATGGACTCCTTACAATGGGTG[G/T]AGCAAAATTCAGGTCAGTATCCACTTAAATTCGATACATATTTCGCTACACAGTCTTTTTTGGAATGTTTCATTGAATCCTTTGCATACATTTGCTTATGTGCAGTTTTACTTCAGAGGCGAGTGGAGGAGGTCTCAAAGTTGTGTGAGAGCCGCAGCAAGGAGCAAGAGAAGAGCTTTCGTTTAAACTTCCAGTGATCATGCATAATCATGTTGTTTTTTCTTCAGTCAGATGTAATGAACGTCTTTGTTTTTGATATTTGCTTCAAAATAAAATTAGCTTGGTTTCCTCTTAGTTTATGTATTTGTATTGATTGTCAATTCTCCAAAATCTGGAGTCATTTTAAAGATCTAAAACGAACAAATCTACAGAGCAAGGCTTTTATTTTCCTGCTTTACGGTTATGGGATGAAACGAGCCAATCAGCTGGATGGAGCTCCACCATAGCAACATGGATCCTGGCATTGTTTAATATCAAGCATTCCTGCGACTACGTCGAGC
Associated Phenotype:
Not determined