ZMP
hnrnpa3
Ensembl ID:
ZFIN ID:
Description:
heterogeneous nuclear ribonucleoprotein A3 [Source:RefSeq peptide;Acc:NP_001038904]
Human Orthologue:
HNRNPA3
Human Description:
heterogeneous nuclear ribonucleoprotein A3 [Source:HGNC Symbol;Acc:24941]
Mouse Orthologues:
AC114648.1, Gm7551, Gm8991, Hnrnpa3
Mouse Descriptions:
heterogeneous nuclear ribonucleoprotein A3 Gene [Source:MGI Symbol;Acc:MGI:1917171]
predicted gene 6793 (Gm6793), non-coding RNA [Source:RefSeq DNA;Acc:NR_033513]
predicted gene 7551 Pseudogene [Source:MGI Symbol;Acc:MGI:3648704]
predicted pseudogene 8991 Pseudogene [Source:MGI Symbol;Acc:MGI:3644227]
predicted gene 6793 (Gm6793), non-coding RNA [Source:RefSeq DNA;Acc:NR_033513]
predicted gene 7551 Pseudogene [Source:MGI Symbol;Acc:MGI:3648704]
predicted pseudogene 8991 Pseudogene [Source:MGI Symbol;Acc:MGI:3644227]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16864 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16864
Status:
Available for shipment
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For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102934 | Nonsense | 140 | 234 | 4 | 8 |
ENSDART00000135273 | Nonsense | 140 | 312 | 4 | 11 |
ENSDART00000137210 | Nonsense | 140 | 234 | 4 | 8 |
ENSDART00000144822 | Nonsense | 140 | 241 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 9 (position 1687746)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 1696251 |
GRCz11 | 9 | 1698399 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTGAGTGCTACGGCAAGATTGAGACCATYGATATCATGGAGGAGCGCT[C/A]GACTGGGAAGAAGAGAGGATTCTGCTTCGTCACCTTCGACGATCACGACA
Long Flanking Sequence:
AAGCATTACTGACTTGGCTTTGTTTACTGCAGCAAGTTGGCATGGCAACTGTTTCAAACCATTCCTGAGCGCTGCGTTTCACGTTTTAAGTGCAGAGATGCATTCTGCGTGAATGTCTCCCAAATCCGCGCATGTGGTGGACATTTTGCAGTAAAAACTGCCTGGTCGCACACAACAATTTTATGCACTCGCACAAATGCTCCCAAATATATTTTGAGGTCGCATAGATACAATTTCGGGCGCATATGCGGCCAAAATGGTCACATTTCTAGCCCTGCAACAGGCTTCCATACACTCAGTTCACTCTGAAATAAAGATCTCTGCATAATGAAGATGTAATTGAACATTCATTATCCAGGACTCTAATAAACCCGGAGCTCATCTGACAGTGAAGAAGATCTTTGTCGGCGGGATTAAGGAGGACACAGAGGAGTATCACATCAGGGAGTACTTTGAGTGCTACGGCAAGATTGAGACCATCGATATCATGGAGGAGCGCT[C/A]GACTGGGAAGAAGAGAGGATTCTGCTTCGTCACCTTCGACGATCACGACACCGTCGACAAAATTGTTGGTAAGCTTGAATGGAAAGGATCACTTTCAATGGCTAGTCAGACAAAGCAGAATACATATTTTATCTGTAAATTACAAGACTAAGTAAAAATAAACAACATTTTATGATGTTTTTATTTATTATTATTTTTAATTATTAGTGTGCATGCAGTAGGTCTGCATGATACTGAGAAAATATGCAAAATTCGACGTTGTCATTGAATACTGCGAACAATATTTCTTACAGTTTAACATTTTCCTACAGAGATACTGTTTTATTTGTGAATTGTGTTTCATTTATGTAATGATCATACTAAAATCAACAGATATTACATATTTTTCGTATCTAATTCAAGCAAAACAAAACTATTACGAGGCGCTAGCATTCACAACTGTTTCAGAGGCGAGGCGTAAGGCTAGTCTTAAATCAATTTACATTCATTCATTTTCATTC
Associated Phenotype:
Not determined