ZMP
zgc:65979
Ensembl ID:
ZFIN ID:
Description:
Nucleoporin NUP53 [Source:UniProtKB/Swiss-Prot;Acc:Q6P6X9]
Human Orthologue:
NUP35
Human Description:
nucleoporin 35kDa [Source:HGNC Symbol;Acc:29797]
Mouse Orthologues:
AC160535.1, Nup35
Mouse Descriptions:
nucleoporin 35 Gene [Source:MGI Symbol;Acc:MGI:1916732]
nucleoporin NUP53 isoform 1 [Source:RefSeq peptide;Acc:NP_081367]
nucleoporin NUP53 isoform 1 [Source:RefSeq peptide;Acc:NP_081367]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21442 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21442
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 |
---|---|---|---|---|---|
ENSDART00000032344 | Nonsense | 130 | 308 | 5 | 9 |
ENSDART00000131766 | None | None | 112 | None | 4 |
ENSDART00000136558 | Nonsense | 130 | 230 | 5 | 8 |
ENSDART00000144734 | Nonsense | 135 | 227 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 9 (position 12542486)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 12295051 |
GRCz11 | 9 | 12266254 |
KASP Assay ID:
2260-1564.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATGCTATTTTGTTCTATAGTTTCTAACTTTTTTAGTCCCGTGAGTCAG[C/T]AGAGGAAAACAACCCTTTCACCAGCTCAAGTAGATCCGTTCTTCACACAA
Long Flanking Sequence:
CACAGGTGTCAAAGTCGGTTCCTGGAGGGTTGCTGCTCTGTACAGTTTAGTTCCAACCCTAATTAAACCCACCTGATCGAACTGAGTCCTTTAGGCTTGTTTAAAACCTACGGGTGAGTGTGTTGGAGCAGGGTTGGAAATAAACTTTGCAGGGCTGCAGCCCTCCAGGAACTGATTTTGACACCCCTGGTTTTAGTGAAAAACGAGTTTTCAATGAGTTGTTTACATTTAATCTCGTGACATAAAGGCACAACTTTGCTGAACACGCAATTGATCTTTCTTATGAGTGTACAGTTAAAAATTATATCCTAGAACGCCATCTGCTGTTAAAAACTAAGCTCAGCCTCAGAATTGATTCTAGAGAGAATATCGATGAGAGAAGCGATTTGCTACAGCTCTGTTATTTAATTTAAAAACATATTAGTTGTTCACTGTCTAAAAATAGATGCCTAATGCTATTTTGTTCTATAGTTTCTAACTTTTTTAGTCCCGTGAGTCAG[C/T]AGAGGAAAACAACCCTTTCACCAGCTCAAGTAGATCCGTTCTTCACACAAGGAGATGCTCTGTCCTCTGAAGACCAGCTCGATGACACCTGGATCACAGTGTTTGGGTGTGTATGTTTTACTTTTTTTTTTTTTTTTTTTTTTTACATTTTACTTTTTGTAGGTTATCTGTTGTATTTTTTGTACTTTATTTCTTGCATTACATTAAGTCATTAATCTCATCACAATTAAGATGTTTTTTTATGGCATCCACGTTTACATATGAATAACATTTTTACTTCTTTGTCCACAGGTTCCCTCCAGCATCTGCTTCATACATCCTTTTACAGTTTGCACAATATGGAAACATATTAAAACATGTAGTAAGTACAGGTCAGGTTGCATCATTGCATTCTGGTTTATTTATGATTTATGGTCCATAAATGTATATTTTTTTTCATTCCAAGATGTCTAATACGGGCAATTGGATGCATGTTCAATATCAGTCAAAACTGCAGGCGA
Associated Phenotype:
Not determined