ZMP
xpa
Ensembl ID:
ZFIN ID:
Description:
xeroderma pigmentosum, complementation group A [Source:RefSeq peptide;Acc:NP_956765]
Human Orthologue:
XPA
Human Description:
xeroderma pigmentosum, complementation group A [Source:HGNC Symbol;Acc:12814]
Mouse Orthologue:
Xpa
Mouse Description:
xeroderma pigmentosum, complementation group A Gene [Source:MGI Symbol;Acc:MGI:99135]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16787 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16787
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000055566 | Essential Splice Site | 59 | 549 | 2 | 9 |
The following transcripts of ENSDARG00000038114 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 11220514)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 11382790 |
| GRCz11 | 1 | 12069590 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATGCTCAGACAAGCCAGACTYGCCAGCAGAMCGTCCTCCGCYGTAGAAG[G/A]TCTGACTTTTGTTTAAAACCTRCACAAGACATGTACAAATTTAATTTAAT
Long Flanking Sequence:
TTTGAACATGGTTTAACAACAAAAAAACCATGTGCTTTTTTCTTTTTCCTATTGTTTGTTTTACAGTAACTATGGTTAATTTGCATAGAGTATTTTTGCTCACCAAATAAGTATTAAATTGATGACCAACTACATTTAATTTCACGCTTGACTGTATGTAAATTGTTAAAAGTGATGTAGTTTATGTGTAGATATTCACATTCAATAAGATATGTATTTACTTATTCATTTTGTTATTCCTTTGTCTTCAGACATTGTGTTTGAATGAACTTCTGCCTGATTATTATTGTGAGTGTAAACTGTTGTTGGTTATAGGCTGATCATGGAGATGCCAGAGGCCAGTCATTGTCAACACACATCGCCAGACTCTGCAAACTCTTCAAATGAGTCCAGCATGTCTTTAACACCACACATGCTGGCCAAAATTGAGCGAAACCGCCAACGGGCGCTGATGCTCAGACAAGCCAGACTCGCCAGCAGACCGTCCTCCGCTGTAGAAG[G/A]TCTGACTTTTGTTTAAAACCTGCACAAGACATGTACAAATTTAATTTAATTAATACTGTGTGATGAATGTAATATGTTTCAGGAGCTACTCACGCTAAAGTGGCAAAAACTATAGACTCTGGTGCTGGGTTTTTTATTGAAGAGGAGACAACAGAGGACGAGCAGCAGGAGAAGAGAGTCGTTCAACAACCAGGTTTTTGAAACTACCATACTTGCTTTATTTTATTGCACAAACTGAATAGCAGTAAGTTACTTTAGAAAGAGAAGCATTACAATATTGAGTTACTCCTTCAAAAAAGTAACTAGTTGTGTTACTTGGTTACTTTTTATGGAAAGTAATGCGTTACATTACTTTTGAGTTACTTTTGCGTTACTTTTCCTTATCTGGCTGAGGTTTGATCTCTTTCAGAGCTCGCAGGTGTTTTTTCACCTTTTTTTAAAGAGAAGCTCTGCATTTAACAACCACCAATATAACATACAGCTTCATTTTCCTTTAAAAA
Associated Phenotype:
Not determined