ZMP
pbx1a
Ensembl ID:
ZFIN ID:
Description:
pre-B-cell leukemia transcription factor 1a (pbx1a), transcript variant 1, mRNA [Source:RefSeq DNA;A
Human Orthologue:
PBX1
Human Description:
pre-B-cell leukemia homeobox 1 [Source:HGNC Symbol;Acc:8632]
Mouse Orthologue:
Pbx1
Mouse Description:
pre B-cell leukemia transcription factor 1 Gene [Source:MGI Symbol;Acc:MGI:97495]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12947 | Essential Splice Site | Available for shipment | Available now |
sa15504 | Nonsense | Available for shipment | Available now |
sa17065 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12947
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 |
---|---|---|---|---|---|
ENSDART00000003750 | None | 48 | 260 | 1 | 5 |
ENSDART00000038419 | Essential Splice Site | 39 | 337 | 2 | 9 |
ENSDART00000073947 | None | 48 | 342 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 2 (position 19717702)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 19085713 |
GRCz11 | 2 | 18734981 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGYCCTGAGAAAGGGGGCGGGTCTGCTGCTGCTGCAGCTGCTGCTGCTGC[G/A]GCAGGCGGYGTCGGCTCCGATAACTCCGCCGAACACTCAGACTACAGGGC
Long Flanking Sequence:
TTCAACTATATATATATGGCAATTTTACTTTAGAAACCACATTGTACATAAATCAGAAGAAACAATATTATTCAGTAATTTTACTGAAATGAATACAAAACTAAAAAAAAAAAAACATTTATTTACACAAAAGTAAGGCTTACTTTAAAGCAGTCTACTTTGTATAGTGCTCTATAAATAAACATGGTTTGGAGAGACTAATAACCAAGCATCTATGTCTCTCAGATGCTTTCTTAACCGCTGTTTTCTCACCATTGTTACCTTTGGTTATTATTTCAAAATAATTTTCTTTATGAAAAATCTATATTAGGAACTCTACAAAACTGACATTTTTTTATCTCTTTCTTTTCTCTCTTAACAGTACTCAGTATCCGTGGAGCTCAGGAGGAGGAGCCACCAGATGCACAGCTCATGCGACTGGATAACATGCTGCTGGCTGAGGGTGTGTCTGGTCCTGAGAAAGGGGGCGGGTCTGCTGCTGCTGCAGCTGCTGCTGCTGC[G/A]GCAGGCGGCGTCGGCTCCGATAACTCCGCCGAACACTCAGACTACAGGGCCAAGCTGTCCCAGATCCGTCAGATCTACCACACAGAACTAGAGAAGTATGAGCAGGTGAGAGGGCACATATGGACTCTGGACTTCAGCAGAGTCACTATAGACCTTGGTTAAAGGATGTGTTCTGTGTGTGACCACCTTTAGACTGTAATGTTAGCATTAACACACAACAGACACATGCTACAAATAAAGTCTTTATAACATTGCATTAGACTGTAATATTAGCATTTAGTCTTAACATGCAACACACACATGGAAGAAATAAAGTCTTTGTAAATTAGACTGTAATATTAGCATTTAGCCTTAACACGCAACACACACATAGAAGAAATAAAATCTTTATAATGTTACATTAGACTGTAATGTCAGCATTTAGTCTTAACACTCAACACACATGGAAGAAACAAAGTCTTTATAACATGACTGTATTGTTAGCATTTAGCCTTAACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15504
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003750 | Nonsense | 209 | 260 | 4 | 5 |
ENSDART00000038419 | Nonsense | 200 | 337 | 6 | 9 |
ENSDART00000073947 | Nonsense | 209 | 342 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 2 (position 19729939)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 19073476 |
GRCz11 | 2 | 18722744 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGTATCCAAYTGGTTTGGAAACAAAAGGATCAGATACAAGAAAAATATT[G/T]GAAAATTCCAAGAAGAAGCCAACATGTACGCTGCCRGAACCGCCGCTAAC
Long Flanking Sequence:
GCCCTATAAAGGAAAAAGAGGAGGAGACGGGGTGGAAAGGGGAATTCTTCAAAATGTAAATGACTAAGGGTATGATGCTTGGTTATTTATACTGAGTTAGGAATCTCCTGATTGGTGGTCCGTACATTAGCTTGACTCGAAGCCAGCAGAGTCAATCATAAGCTTGTGATCTTCTCGAAATTAGTTTATAAATAAACTTCAGGTATTCAAATTCCAGTTGATGTATAAATCTCAATATAAAAAAAAAATTAAGTAATTAAAAATTACATTTACAGCATGTCAGGTTTTATGACCCAAAGTCACAAATGTGTTTATGATTTATATTTTGCAACATAATTTTACAAACATGCAAAACAATGTGCAGTTTTACATAGTCGCTAGATTAAGTGCATGTTTTGTTTGTGTTTTTTGAATTAACAGTCAGATTTAACAGTTGTTAATTCCCTTTTTAGGTATCCAACTGGTTTGGAAACAAAAGGATCAGATACAAGAAAAATATT[G/T]GAAAATTCCAAGAAGAAGCCAACATGTACGCTGCCAGAACCGCCGCTAACGCAACCAGCGTCTCCACCCACGGCAGCCAAGCCAACTCGCCTTCCACACCAAATTCGGCCGGTGAGCATTGCTATAAATCAACACACAAACAACAGATGTGTTTGTTTTTCATTGGCCCGCTTTAGTCCACAGCCCTGCTTTTAGAAGAGAAATGCCAGCTTTAATGTCACCAACTGGCAAATAAATAGTTCACCACTGCAGTGCTTTATATTTTCCTTTTCTTTAAATCATTTCCTTTCCCATAAAGAATCCTTTTTATGCAATTCAAATCTCCCATTTCTTTATCTACGTCGGTAGTCTGTAGACTCTTGCTTTTTTGTTGAAGCATTCATCTTTTACCTTCAAAAATTGTTTGGCTAAAATGCTATTTTGCTTTATCTGGTTTGAACTCACCCAAGGTACTCTGTTGCTGTTGTCTGGTTGACCTCATGGATGTCATTATGATGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17065
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003750 | Essential Splice Site | 246 | 260 | None | 5 |
ENSDART00000038419 | Essential Splice Site | 275 | 337 | None | 9 |
ENSDART00000073947 | Essential Splice Site | 283 | 342 | None | 7 |
Genomic Location (Zv9):
Chromosome 2 (position 19738109)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 19065306 |
GRCz11 | 2 | 18714574 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAGACRTCTTTGTTTTGAACGCTTTTGTGTGTTGTGTTCCGGTGTCTGC[A/T]GGTGGATACTCTTCGCCATGTTAWCAGTCAGACAGGAGGATACAGTGAAA
Long Flanking Sequence:
GGGAATCATAATTTAGATGCATATTTTAAAAACTGTATTTAAATGCATTTATGTACACAAACAAACTGCCACATGTAATTACTTAATAATAACTGTTATTTTCTTTTAAACTTACACATATTTACAAGTATAGTAAAAAAAAAACAATTAAGATTAAAAATGGTATTAAAAATTAAATAAATTAGTTTATTTATATACTTTTTCATATACACATTTTTTTATTATTATAAAATATTTTATTATTATTATTATTATTATTTTATTTTAATCTCAAGTAATTAACTGAATTCCCCCTTATGATTAGACTGTAAACACAGATGTATTCCCTCATCTAAAATCCAGAACAAACCGTGTCTTGTTTGATATCTGCAGCACAAACATTTCATTCAACATTTGATGACCTTTTGGGCTGCCAATATCCTTCTGATATCAGGCTGACCTTTTCTCAGCACAGACGTCTTTGTTTTGAACGCTTTTGTGTGTTGTGTTCCGGTGTCTGC[A/T]GGTGGATACTCTTCGCCATGTTATCAGTCAGACAGGAGGATACAGTGAAAGCCTTGCTGCCAGTCAGATATACAGTCCACAGGGCATCAATGTAAGTCCGCACTCTCTGTTTTTCAAGCTTGTACCTGATTCTGCTGTTGTCTTGATGTGCTGCTGAGTTTGCAAGGGGGATTTGACAGACTGTACTGGGCAGCAGGAGAGACGTGTCAGCAAACATCCGCGTACACTGCTTGTGTTGGGGACATTTAAACAGTCTGACAGAAGATTAGGAAAAAATAAATAAATAAAAAATCTAGAAGGGTAATTGTGGTTCATCAAAGGTAAAAACATGGTATTGTTCAATATATTTGCTGTTTTAAATGTAATGATTACAATAAAATGCATATAAAATGTTTAATTAACTTAAATCCAAAAACTAACACTGAATTTAATCTAAAATCCTACACCTTAAATTGAAATGCATGAAACATGAATAAATAAATAAATAAATAAATAAATAC
Associated Phenotype:
Not determined