ZMP
narf
Ensembl ID:
ZFIN ID:
Description:
Nuclear prelamin A recognition factor [Source:UniProtKB/Swiss-Prot;Acc:Q6DHP6]
Human Orthologue:
NARF
Human Description:
nuclear prelamin A recognition factor [Source:HGNC Symbol;Acc:29916]
Mouse Orthologue:
Narf
Mouse Description:
nuclear prelamin A recognition factor Gene [Source:MGI Symbol;Acc:MGI:1914858]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa22143 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22143
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 |
|---|---|---|---|---|---|
| ENSDART00000007053 | Nonsense | 122 | 465 | 5 | 12 |
| ENSDART00000142716 | Nonsense | 122 | 131 | 5 | 5 |
The following transcripts of ENSDARG00000024184 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 34960716)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 33364825 |
| GRCz11 | 12 | 33465808 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGTGCCATTTTTTGCTGTTAAATTTCAGTTGGACGTTTCAGCAGCTGCA[C/T]AGAAACTTTGTGGCTTCCTCAAGAGTGTGGGTACGTCTGGACGCCATATT
Long Flanking Sequence:
GAGGTACTCTATTGTCTTTTATTTTATATACTTTGTGTATCAGACACAGTGCAATCTGATAAGCTGCGGTCTGCATCTGTTGTTTTGTTTGTGTTTGTATTGGGGTTGGATGAAGAAATGCAAACCTCATTTGTTTTGGACGCGTGCATAATCTGATACGTGAATTTATTTGTTTTTCGTCCCAGGTGAGAGAGTCTACCTCAGTTCAGCAGGTGTTGCTGAGTGCGTGTCTGTCCTGTGACGGCTGTATATCGGAGGATGAAGGCAAGAGAATATCACAGCAGAATCTGGACGAGATCAATCACGTGCTTGCTCTCAACAAGGTAGCGTTTGCCTGTCATGGATTTGGAAAGATGGTTTGTTGATGTATCTTACATTTGTCTTTTTATTTTTGGCAGAAATGTGACACTTCGAAGCACAAAATTCTCGTAGTGTCCGTGTGTCCACAGTCGGTGCCATTTTTTGCTGTTAAATTTCAGTTGGACGTTTCAGCAGCTGCA[C/T]AGAAACTTTGTGGCTTCCTCAAGAGTGTGGGTACGTCTGGACGCCATATTTCATCTTTCTACATCCAGCTGGTTTTTCTGTTTTTAACCGAGTCAAGATGTGCACATTGCAAATATTTACTGCAATGCAGTCTATGCTCATTTGCACATATTAGGTTTATTTTAGTATCGTTTCTAATATTATTTTATATTGGCTTATATATTAAGTTAATTTTATTAAAGTATCAGAAACGCCAGTTCCCTGGACTGTTTTAAGAAACTTCTCAAAACTCATCTTTTTATTATTGCTTATAACTTATGAGGCCTTCTTGTAATATGTATATTTTTAGCATTATTATCATTCTTACTTTTTTGTGTATTTCATGTTCTTCTGTGTGTTGATGCTCTTGTTAGCGCTTTGAGTTTGAGAAAAGCGCAATATAAATAAAATGTATTATTATTATTATTATTATTATTTTATTATATTACTTTATTAATGTTAAAGTTTTAATATCGTTTTTG
Associated Phenotype:
Not determined