ZMP
pa2g4b
Ensembl ID:
ZFIN ID:
Description:
proliferation-associated 2G4-like [Source:RefSeq peptide;Acc:NP_997806]
Human Orthologue:
PA2G4
Human Description:
proliferation-associated 2G4, 38kDa [Source:HGNC Symbol;Acc:8550]
Mouse Orthologue:
Pa2g4
Mouse Description:
proliferation-associated 2G4 Gene [Source:MGI Symbol;Acc:MGI:894684]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18591 | Nonsense | Available for shipment | Available now |
sa16995 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18591
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016248 | Nonsense | 288 | 394 | 10 | 13 |
ENSDART00000131486 | None | None | 207 | None | 8 |
The following transcripts of ENSDARG00000070657 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 25585830)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25371950 |
GRCz11 | 23 | 25298491 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATTGTTCACTTTGCATGTGTGTTTTTTCAGGGCATTTGAAGATGAGAGT[A/T]AAGCTCGTCTTGGTGTGGTTGAGTGTGCCAAACACGAGCTGCTGCAGCCC
Long Flanking Sequence:
TTCTCTACTTAGTAATTTTTCCTGAAATGGTGACAGCTGAATTTGAAAATCATTACTTTAGAAAAACATTTGGTACTCAACAATCATTTATCAATTTTGGTAACAGCTTGTGGAAGCCATGATGCTTTTCTGTAAAAACTAAGATTCTCTAAATACTGAGATCAAAAAAACAACAGTGCATCAATTAAATGCACCTTACTAACTTATGGTGTAGTTCCTCAAATATTTGTATACAGCCTTTTAAACAGTGCAGTATAACTCATATAAAAACATTGAATAAATAAATAAGCTTTAAGTATTAGATCAGTCAAATGTGCAGATTTTGACTTGCTATATACATTTTCTGTATGTATAAGTGCAATTTGCTTCCAATCAGACCTACAGTATGCATTTGACATTGTTACTAGCTGAACTAAAAGCAGATAATGGCACAAGACAAAATCTCACCACAATTGTTCACTTTGCATGTGTGTTTTTTCAGGGCATTTGAAGATGAGAGT[A/T]AAGCTCGTCTTGGTGTGGTTGAGTGTGCCAAACACGAGCTGCTGCAGCCCTTCAGCGTCCTGCATGAGAAGGAAGGTGAGGCGCAAGCACATCAATCAGAAAATGTCACTTTTATATGTAAAACGCTCAACCAGGCATGACGATGATAAGGTTAAAGCTTTGCTAAATGAAAATGAAAAATAATTTCCTGTCACGTCGGGGCTCAGAGAAGCGCAGCCAGCACATTTGCCGCATGAGCAGGTCAAAGACTGTTCCTATTTTAGGAGTTGGGTGCCATCAGCACAGTCTCAAGAGTCACATTGTCAAACCTTCTGTCTCTTTTTCTCTTTCAAGGTGAACATGTCGCGCAGTTTAAATTCACAGTGCTGCTCATGGCAAATGGCCCTCTGCGCATCACCAGTGGACTCTTTGAACCAGAGCTTTACAAGTCTGAGTATGAAGTACAAGACCCAGAGCTCAAGGTGAGAGACTTTAATGCATGGAAATAGTTTTTGTGTGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16995
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016248 | Essential Splice Site | 313 | 394 | 10 | 13 |
ENSDART00000131486 | None | None | 207 | None | 8 |
The following transcripts of ENSDARG00000070657 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 25585907)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25372027 |
GRCz11 | 23 | 25298568 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCAAACACGAGCTGCTGCAGCCCTTCAGCGTCCTGCAWGAGAAGGAAGG[T/C]GAGGYGCAAGCACAKCARTCAGAAAATGTYACTTTTATATGTAAAACGCT
Long Flanking Sequence:
CAACAATCATTTATCAATTTTGGTAACAGCTTGTGGAAGCCATGATGCTTTTCTGTAAAAACTAAGATTCTCTAAATACTGAGATCAAAAAAACAACAGTGCATCAATTAAATGCACCTTACTAACTTATGGTGTAGTTCCTCAAATATTTGTATACAGCCTTTTAAACAGTGCAGTATAACTCATATAAAAACATTGAATAAATAAATAAGCTTTAAGTATTAGATCAGTCAAATGTGCAGATTTTGACTTGCTATATACATTTTCTGTATGTATAAGTGCAATTTGCTTCCAATCAGACCTACAGTATGCATTTGACATTGTTACTAGCTGAACTAAAAGCAGATAATGGCACAAGACAAAATCTCACCACAATTGTTCACTTTGCATGTGTGTTTTTTCAGGGCATTTGAAGATGAGAGTAAAGCTCGTCTTGGTGTGGTTGAGTGTGCCAAACACGAGCTGCTGCAGCCCTTCAGCGTCCTGCATGAGAAGGAAGG[T/C]GAGGCGCAAGCACATCAATCAGAAAATGTCACTTTTATATGTAAAACGCTCAACCAGGCATGACGATGATAAGGTTAAAGCTTTGCTAAATGAAAATGAAAAATAATTTCCTGTCACGTCGGGGCTCAGAGAAGCGCAGCCAGCACATTTGCCGCATGAGCAGGTCAAAGACTGTTCCTATTTTAGGAGTTGGGTGCCATCAGCACAGTCTCAAGAGTCACATTGTCAAACCTTCTGTCTCTTTTTCTCTTTCAAGGTGAACATGTCGCGCAGTTTAAATTCACAGTGCTGCTCATGGCAAATGGCCCTCTGCGCATCACCAGTGGACTCTTTGAACCAGAGCTTTACAAGTCTGAGTATGAAGTACAAGACCCAGAGCTCAAGGTGAGAGACTTTAATGCATGGAAATAGTTTTTGTGTGGTTGGGGAAATAATTAACACAAGATGGCTTCCAAAGTGTCACATTGGGAAGAAAATTAATAAGTAATTAATTCATTATA
Associated Phenotype:
Not determined