ZMP
HNRNPUL1 (1 of 2)
Ensembl ID:
Description:
heterogeneous nuclear ribonucleoprotein U-like 1 [Source:HGNC Symbol;Acc:17011]
Human Orthologue:
HNRNPUL1
Human Description:
heterogeneous nuclear ribonucleoprotein U-like 1 [Source:HGNC Symbol;Acc:17011]
Mouse Orthologue:
Hnrnpul1
Mouse Description:
heterogeneous nuclear ribonucleoprotein U-like 1 Gene [Source:MGI Symbol;Acc:MGI:2443517]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa10200 | Essential Splice Site | Available for shipment | Available now |
| sa17734 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10200
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113508 | Essential Splice Site | 254 | 875 | 4 | 16 |
Genomic Location (Zv9):
Chromosome 5 (position 64864526)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 61139170 |
| GRCz11 | 5 | 61801907 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGATGAGAGTCGAGGATATGGYTACTACGAGCACCGTGAAGAAAGAAGG[T/G]CAGTTCTGTGTGCTTGGGAYTAYTTTTTTGTGTTGCTCAATCTGACTGTT
Long Flanking Sequence:
AGCATTCTTGAAAGTGCAATGTTTACATTTTGCATTTTGTTTAGCCATATTAGTTATTTTTATGTCAAACCTGTAATCATTTGTTTTTTAAAAGTGTTTTATATTTTATTAATATTTTACATCACATATCACATGAATGATTAAATGTGTGTGTGTGTGTGTGTGTATAAGTGTGTGTGTGTGTGTATATATATATGTATGTGTGTATATATATATATATATATATATGTATGTGTTTATGTACACACATTTTAATGTAGAAAGAAATAGTTGTTCACATGTGGCCTATAACTTTTTCCTTTTCCCAACCTTTTACAGGGCGTTATGATGTGAAGTCCGAGTATAAGGCTGATGAGGATGCACCACAGCAGGCTGAGCGGTCCAGCGAGTGGGATGCACAGGCCAAATCAGAGGATGACCGACACAGCTCACATAGTCGTAAAAGATCCCATGATGAGAGTCGAGGATATGGCTACTACGAGCACCGTGAAGAAAGAAGG[T/G]CAGTTCTGTGTGCTTGGGACTACTTTTTTGTGTTGCTCAATCTGACTGTTCCTTTGGTTGTTATAGGGGAAGATCACCTCAGCCTCCAGCTGAAGAAGAAGAGGAAGACATTGATGATAATCTTGTTGTAATTGACACCTGTGAGTATAAAGAGTTTTTATTTTGTTAACTGAGCCTTCATTTGCAAAGCTGTTTTGTGTGTGTGTTAGAAATACAATTAATCCTATTCCGTACTTGTACTCTTTCTTTTTAAAAATAGCAGAGTGCTCAGTGTTTGTGTTCACACAATGAAGCATTGACTGTTGCAGAGAGAGAGCACAGTGTAAATACTTAGAGATGTCTGAGCTCTGTTTTGCACTATGTAGCAAAATCTGTTTTCATCAACCCAATCATAGGTGTAAACAGAGTTTAAGGATGTACTCACTCTAGGCATGGTTGCCTTGAACTGAGTGCACCTTTAGTCAATATCAGGTTTGCGTAAAGTTACAATTAATTGCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17734
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113508 | Nonsense | 855 | 875 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 5 (position 64881710)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 61157200 |
| GRCz11 | 5 | 61819937 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCAGTGGCAGCAGTACTACCAGAACCAGAGCCAGTGGAACCAGTACTA[T/A]AACCAGTACGGCGGTTACGGCAACTACCAGCAGGGAGCTCAAGGCAGCCA
Long Flanking Sequence:
CAGGTACAGATGCTATAAAGGCACCAGGTTTCGGTACCCAACCCTAATTTTGGCCAGATATTTTTCTAAAACCGGGATCACCAAACTTAAAAAAAAATATCACAATGTCAGCTTTTTCCAGTATCCTGCAGCCCTAATCATGAGTAAATTTCTTCCAACCATTAAAAAATGTTCTATATAATATTAATTTAACTAAATTGAACATAGCCAATATGCAATGCATTTGTCTTGTTGACAATGTATGCATTTTCCCCTATTTAAATTCACACATTCATTATTTTGTCAATTACTCCTCTGAATGCTCAGTTGTAAGGAAAATGAAAATTCTGGGCAGAAACTAATAATTCTGCCAACTATACACCGCACACACCTGGTCAGACACTGTTCAGTATTGTGTTATCGAAGCATGTGTTTATTTACACACTGTATCTTTGCTTTCCTCAGTATGCTCAGCAGTGGCAGCAGTACTACCAGAACCAGAGCCAGTGGAACCAGTACTA[T/A]AACCAGTACGGCGGTTACGGCAACTACCAGCAGGGAGCTCAAGGCAGCCAGGGAGCCCAGGGAACACAGTAGTAGCAGCAGCATCAGCGCCGTCTCCTGCAGCCCATTCCCTAAGCAGCATTCCTCAAGCCTTTTCCCTCATCCTTCCCAGTCTTACCTTTTTCTTCGCCCGCGTAACCATTTATCCGCTCCCTATTTATGCCAACCCTAAAGATAACCACACTTCTGTGGACCTCCATTGCTCTCTTTGAGTTTTGGTGACAGGTGTCCCTTTTTTTTGCTCTTCTACTAAATATTTGTTTACATAAAGCTTTGTTTTCCCCCCTCTATGTGTACTTGTAGATGAGAGATTTTGAATTTAGTAACGTGTGGTTTAGTCGACTCCAAAACTGCTCACACACTATGATGTGCTTGAATGTTTCGAAAATAGAGCAGGAAATATTGAGGAAGCTTTGCTTGCTTGCATTTACATCTGATGTATAGAGAAAGAGGCAGGGTGT
Associated Phenotype:
Not determined