ZMP
hnrnpk
Ensembl ID:
ZFIN ID:
Description:
heterogeneous nuclear ribonucleoprotein K [Source:RefSeq peptide;Acc:NP_998159]
Human Orthologue:
HNRNPK
Human Description:
heterogeneous nuclear ribonucleoprotein K [Source:HGNC Symbol;Acc:5044]
Mouse Orthologues:
Gm7964, Hnrnpk
Mouse Descriptions:
heterogeneous nuclear ribonucleoprotein K Gene [Source:MGI Symbol;Acc:MGI:99894]
predicted gene 7964 Pseudogene [Source:MGI Symbol;Acc:MGI:3646150]
predicted gene 7964 Pseudogene [Source:MGI Symbol;Acc:MGI:3646150]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34499 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34499
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 |
|---|---|---|---|---|---|
| ENSDART00000014895 | Nonsense | 285 | 403 | 8 | 13 |
| ENSDART00000097919 | Nonsense | 285 | 429 | 8 | 15 |
| ENSDART00000137941 | None | None | 148 | None | 7 |
| ENSDART00000140609 | Nonsense | 137 | 281 | 2 | 9 |
| ENSDART00000147309 | Nonsense | 285 | 420 | 9 | 15 |
The following transcripts of ENSDARG00000018914 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 52016536)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 49766923 |
| GRCz11 | 8 | 49755692 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGGCCCACCTCCATCACAGAGAGGAGGAGGAAGAGGACCTCGTCCTCCA[C/T]GAAATATGGGACCCCCACACCACAGGAGAAGGTCAGACACTTTGATAAAT
Long Flanking Sequence:
CATTATCTGCTTCTGTTCCAGAGCACCCAGACCACCATCAAGCTCTTTCAGGAGTGCTGCCCTCAGTCCACTGACCGTGTGGTGCTGGTGGGGGGCAAAGCAGAGCGGGTGGTGCAGTGCATCAAAACTATGCTCGAACTCATCGTGGAGGTCAGATTGAAATCATTTGACTCCTGGTTTGCTTGTTGAACATGTTTCTAATTAGTTCTTTCTCTTTCCAGGCTCCCATTAAAGGTCGTGCTCAGCAGTATGACCCTAACTTTTACGATGAGACCTACGACTATGGCGGCTTCGGTGTGATGTATGAAGAGAGGGGCCGTCGGCCTATGGGAGGCTTCTCTTCGAGGGGGCGCAGCAGCAGCGGTGGATTTGATCGGATGCCCTCTGGCGGTCGTGGCGGCGGACACCACATGCAGAGCAGGAGAGACTATGATGACATCAGCCCACGCAGGGGCCCACCTCCATCACAGAGAGGAGGAGGAAGAGGACCTCGTCCTCCA[C/T]GAAATATGGGACCCCCACACCACAGGAGAAGGTCAGACACTTTGATAAATGTACAAGGGGAAAATAAGTATTGAACACGTTGTCTTGTTTTATCATGGGATTAATATTTCTAAAGGAGCTGTTGACATGGAATTGAATCAGATTTTGCTAAAAAAAAAAAAAAAAAAGTTAAACTAATCAAAAAAAAATCTGAAAAATGTGTTTATGACAATGACATGACACCAGGAGAAAGTCCTGAACTATTCAAATATGTTTTATACTTAATATAAAATGCTATATTGGTGATGGCCGCTTAAAGATGCCTATCATATGGAGTATGAAGACACATTATTTGCTCAGACTTCAAGAGTGTAGAAATCTTGATGCTTCTGTGGGTCTCATCTATCAGATCTGATCTTTATTTTGTGTTTTCTATTGGGTTTAAGTCAGGTGATTGGCTGGGCCATTCTACAGCTCGATTTTCTTTCTCTGAAAGCATTTGAGAGTTGCCTTGGCTGTGT
Associated Phenotype:
Not determined