ZMP
paxip1
Ensembl ID:
ZFIN ID:
Description:
PAX-interacting protein 1 [Source:UniProtKB/Swiss-Prot;Acc:Q5XIY8]
Human Orthologue:
PAXIP1
Human Description:
PAX interacting (with transcription-activation domain) protein 1 [Source:HGNC Symbol;Acc:8624]
Mouse Orthologue:
Paxip1
Mouse Description:
PAX interacting (with transcription-activation domain) protein 1 Gene [Source:MGI Symbol;Acc:MGI:189
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39846 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32937 | Nonsense | Available for shipment | Available now |
sa9641 | Nonsense | Available for shipment | Available now |
sa17872 | Nonsense | Available for shipment | Available now |
sa5145 | Nonsense | F2 line generated | Not yet available |
sa32936 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39846
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031130 | Nonsense | 419 | 935 | 7 | 22 |
ENSDART00000144672 | Nonsense | 419 | 1122 | 7 | 21 |
Genomic Location (Zv9):
Chromosome 2 (position 29628900)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 29930535 |
GRCz11 | 2 | 29914068 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACTGCAACAACAGCAGCAGCAACAGTCACATCAGCTACAACAGCAACAG[C/T]AGCAGCATCAGATGGCACAACAACATCCCATGATGCTGCCACAGGTCATG
Long Flanking Sequence:
TTTTCTACAATGTATATAAATGATTGCAGGTTTCCAACATTAATCAAAATATCTTATTTTTTGTTTAACTGAACAAAAATATATATAATTAGTTTAAAAAATCGAGGTTGAGTAAATGGTGACAATTTGCATTCATTCAGGCTGCAATTTGTCAATTCTGTCTAAAAGCACACAGTGAAACTTCATGCGTATAAAAAAAAAACTAATAAAGGATCAAAATTAAATATCTTTGTAGTATTTTTATAATTTAATTTGTACAAAAGGCAGAAGTGTCTTTATGTATTTTTAAAGTTTAATGAAACATATGCATTTTTCTACAGATCATCCAGAGTTTTTCCGCATCCTCTAAAGGTGTAGTGGATCATATGGGAAATCAGGGCCAGTCTGGTATTCCCAACCAGCTTCTGTTAAAAGCCCAACAGCAGCTTCCTCCTGAAGCACAGCAGCAGTTACTGCAACAACAGCAGCAGCAACAGTCACATCAGCTACAACAGCAACAG[C/T]AGCAGCATCAGATGGCACAACAACATCCCATGATGCTGCCACAGGTCATGCAGATGCACCACCATCAACAACAACAACAGCATCAGCCGCCGCCACAGCAACAACAGCAGCAGCAAAACCAACAAGGCTTTCCTCAAATGCCTCCACAATCGCATCAGTTCTTACAGCAACAGATGCATCAGCAGATGTATTCCCAACATCAACAGCAGCAGCAGCAGCAGCAACAACAGCAGCAGCAACAACATGCATTCCCACAACAAATGCGACCCCAACAGCTTCCGAGGCTGCCCTTGCAGCATCAGCAGCAACATGTGCTGCAACAACAGTTACAGTTACAGCAGCAGCACAGACTTCAGTTGCAGTTGCAACAACAACAACAACAGCAGCAGCAACAACAACAACAGCAGCAGCAGCAGCAGCAGCAACAACAACAACAAAAACAACAACAGCAGCAGCAGCAAAACCAGCAGCAGATGCACCAACAGCATTTGCAGCAGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32937
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031130 | Nonsense | 442 | 935 | 7 | 22 |
ENSDART00000144672 | Nonsense | 442 | 1122 | 7 | 21 |
Genomic Location (Zv9):
Chromosome 2 (position 29628831)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 29930466 |
GRCz11 | 2 | 29913999 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAACATCCCATGATGCTGCCACAGGTCATGCAGATGCACCACCATCAA[C/T]AACAACAACAGCATCAGCCGCCGCCACAGCAACAACAGCAGCAGCAAAAC
Long Flanking Sequence:
TGAACAAAAATATATATAATTAGTTTAAAAAATCGAGGTTGAGTAAATGGTGACAATTTGCATTCATTCAGGCTGCAATTTGTCAATTCTGTCTAAAAGCACACAGTGAAACTTCATGCGTATAAAAAAAAAACTAATAAAGGATCAAAATTAAATATCTTTGTAGTATTTTTATAATTTAATTTGTACAAAAGGCAGAAGTGTCTTTATGTATTTTTAAAGTTTAATGAAACATATGCATTTTTCTACAGATCATCCAGAGTTTTTCCGCATCCTCTAAAGGTGTAGTGGATCATATGGGAAATCAGGGCCAGTCTGGTATTCCCAACCAGCTTCTGTTAAAAGCCCAACAGCAGCTTCCTCCTGAAGCACAGCAGCAGTTACTGCAACAACAGCAGCAGCAACAGTCACATCAGCTACAACAGCAACAGCAGCAGCATCAGATGGCACAACAACATCCCATGATGCTGCCACAGGTCATGCAGATGCACCACCATCAA[C/T]AACAACAACAGCATCAGCCGCCGCCACAGCAACAACAGCAGCAGCAAAACCAACAAGGCTTTCCTCAAATGCCTCCACAATCGCATCAGTTCTTACAGCAACAGATGCATCAGCAGATGTATTCCCAACATCAACAGCAGCAGCAGCAGCAGCAACAACAGCAGCAGCAACAACATGCATTCCCACAACAAATGCGACCCCAACAGCTTCCGAGGCTGCCCTTGCAGCATCAGCAGCAACATGTGCTGCAACAACAGTTACAGTTACAGCAGCAGCACAGACTTCAGTTGCAGTTGCAACAACAACAACAACAGCAGCAGCAACAACAACAACAGCAGCAGCAGCAGCAGCAGCAACAACAACAACAAAAACAACAACAGCAGCAGCAGCAAAACCAGCAGCAGATGCACCAACAGCATTTGCAGCAGCAACAGCATTTCCTACAACAACAACTCCAACAGCAGCACATGCAACAGCTGCAACAACAGCAGCAAATGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9641
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031130 | Nonsense | 580 | 935 | 7 | 22 |
ENSDART00000144672 | Nonsense | 580 | 1122 | 7 | 21 |
Genomic Location (Zv9):
Chromosome 2 (position 29628417)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 29930052 |
GRCz11 | 2 | 29913585 |
KASP Assay ID:
2259-2128.1 (used for ordering genotyping assays)
KASP Sequence:
AACAAAAACAACAACAGCAGCAGCAGCAAAACCAGCAGCAGATGCACCAA[C/T]AGCATTTGCAGCAGCAACAGCATTTCCTACAACAACAACNNNTCCAACAGCAG
Long Flanking Sequence:
AGCTACAACAGCAACAGCAGCAGCATCAGATGGCACAACAACATCCCATGATGCTGCCACAGGTCATGCAGATGCACCACCATCAACAACAACAACAGCATCAGCCGCCGCCACAGCAACAACAGCAGCAGCAAAACCAACAAGGCTTTCCTCAAATGCCTCCACAATCGCATCAGTTCTTACAGCAACAGATGCATCAGCAGATGTATTCCCAACATCAACAGCAGCAGCAGCAGCAGCAACAACAGCAGCAGCAACAACATGCATTCCCACAACAAATGCGACCCCAACAGCTTCCGAGGCTGCCCTTGCAGCATCAGCAGCAACATGTGCTGCAACAACAGTTACAGTTACAGCAGCAGCACAGACTTCAGTTGCAGTTGCAACAACAACAACAACAGCAGCAGCAACAACAACAACAGCAGCAGCAGCAGCAGCAGCAACAACAACAACAAAAACAACAACAGCAGCAGCAGCAAAACCAGCAGCAGATGCACCAA[C/T]AGCATTTGCAGCAGCAACAGCATTTCCTACAACAACAACTCCAACAGCAGCACATGCAACAGCTGCAACAACAGCAGCAAATGCAGCAGCAACAGCAACAACATCTGCAGAACCAGCAGCCTCTGCAACATCAGAACCAGCAGGTTAATCCACATCAGACACAGACTATGCTTCAACCTCCAATCACATCTGCACAGCTCTTTGGACACGAGCCTGGCCATGACAGTAAGTGCAATTACTTTACGATATCACCCAGCTGCACATTGTTTTGTGAGCACAATACATATAGTCTGTCTTTGTGAGAAAGTAAAAACGGAAACAGTGACTTCTCCTGAATAGAGTTGTATTAATTTATAATATTCTACGGTGACATTTATCATTACCTTTTCAGTACCTGAAGAGGGATTCCTGGTTGGCTGTATTTTTGCCATTGCTGACTATCCAGAACAAATGGCTGATAAACAGTTACTGGCCACATGGAAAAGGGTAAGCGACTCCGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17872
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031130 | Nonsense | 586 | 935 | 7 | 22 |
ENSDART00000144672 | Nonsense | 586 | 1122 | 7 | 21 |
Genomic Location (Zv9):
Chromosome 2 (position 29628399)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 29930034 |
GRCz11 | 2 | 29913567 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCAGCAGCAAAACCAGCAGCAGATGCACCAAYAGCATTTGCAGCAGCAA[C/T]AGCATTTCCTACAACAACAACNNNTCCAACAGCAGCAYATGCAACAGCTGCAA
Long Flanking Sequence:
AGCAGCATCAGATGGCACAACAACATCCCATGATGCTGCCACAGGTCATGCAGATGCACCACCATCAACAACAACAACAGCATCAGCCGCCGCCACAGCAACAACAGCAGCAGCAAAACCAACAAGGCTTTCCTCAAATGCCTCCACAATCGCATCAGTTCTTACAGCAACAGATGCATCAGCAGATGTATTCCCAACATCAACAGCAGCAGCAGCAGCAGCAACAACAGCAGCAGCAACAACATGCATTCCCACAACAAATGCGACCCCAACAGCTTCCGAGGCTGCCCTTGCAGCATCAGCAGCAACATGTGCTGCAACAACAGTTACAGTTACAGCAGCAGCACAGACTTCAGTTGCAGTTGCAACAACAACAACAACAGCAGCAGCAACAACAACAACAGCAGCAGCAGCAGCAGCAGCAACAACAACAACAAAAACAACAACAGCAGCAGCAGCAAAACCAGCAGCAGATGCACCAACAGCATTTGCAGCAGCAA[C/T]AGCATTTCCTACAACAACAACTCCAACAGCAGCACATGCAACAGCTGCAACAACAGCAGCAAATGCAGCAGCAACAGCAACAACATCTGCAGAACCAGCAGCCTCTGCAACATCAGAACCAGCAGGTTAATCCACATCAGACACAGACTATGCTTCAACCTCCAATCACATCTGCACAGCTCTTTGGACACGAGCCTGGCCATGACAGTAAGTGCAATTACTTTACGATATCACCCAGCTGCACATTGTTTTGTGAGCACAATACATATAGTCTGTCTTTGTGAGAAAGTAAAAACGGAAACAGTGACTTCTCCTGAATAGAGTTGTATTAATTTATAATATTCTACGGTGACATTTATCATTACCTTTTCAGTACCTGAAGAGGGATTCCTGGTTGGCTGTATTTTTGCCATTGCTGACTATCCAGAACAAATGGCTGATAAACAGTTACTGGCCACATGGAAAAGGGTAAGCGACTCCGCCACACTCCAACAAATACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5145
Status:
F2 line generated
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:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031130 | None | None | 935 | 19 | 22 |
ENSDART00000144672 | Nonsense | 1038 | 1122 | 18 | 21 |
Genomic Location (Zv9):
Chromosome 2 (position 29619928)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 29921563 |
GRCz11 | 2 | 29905096 |
KASP Assay ID:
554-3520.1 (used for ordering genotyping assays)
KASP Sequence:
ATTTTTTNATTTTTACAGGGGAAGTATTTCTATATWACTCCAGGAATCTG[T/A]CCCAGCCTCAGCACAATGAAGCTTATAGTGGAGAGTGCCGCAGGGAAAGT
Long Flanking Sequence:
AATATTTTTTGGACTTTTTTTTATTTTTTGGAAGTTGTACTTGCAAGTGTTTGTTCATTTGTGTTTATCTGTGTGTGGTCCATACTGCATATCAGATCATTAATTGACTTTTAATAGTGGCTTGACATTTTAAAAACGTTATATTAGCTCTCACAGATATATTGTGCATCTTTAGTGCTAATTAGATTTGGCTTTGTGTTTGCAGATGAGCAAAGCTACATGCTGCGAGATGCAGAGGCTGAGGTGCTGTTCTCTTTTAGCCTGGAGGAGTCACTGAAGAGAGCTCATGCAGCTCCGCTCTTTAAGGTTTGGAGCTTTGAGAAAATTGATATACTGTGTAACTTTATTGTGTTCATGTTTACTCACACATAGTCGTGACTCTGCACTGACATGTGACTTAATTTGAGATCACAGGGAAGCATTGGGTGTCTGTTCAGCAGTCTCTTTATTATTTTTTTATTTTTACAGGGGAAGTATTTCTATATAACTCCAGGAATCTG[T/A]CCCAGCCTCAGCACAATGAAGCTTATAGTGGAGAGTGCCGCAGGGAAAGTGCTCTCCAAACAGCCCTCCTACCGCAAGATCATGGAGCACAAGCAAAACAAGGTACACTAATCAGATCCTCAATACGGGTGCTTGTGGGGCTGTTGTTTTGATGAAGATGCTGGGTCAGACTCGACTCTTTCACTTAATGAACTCCTATTTACAGCCAACACAACAGAGCTGTTCTCTGGATTTGGTGCTCTGTTAAATCATTTGGCCTGTTGAATCACAATGACCATGTAAATACTACAGCTGAATTCAGTTGTCAGTTCAGATTTCAGTATGTAATCCTGCACACATAGTTTAGTCATTTATGGACATTTAAGTAATCTTTGCAACTAGATTACCTCCAGATGGGAAAATCCAGGTAGTGGCAACAATATTTGTGACCCCCCCCCCTCTGTGAAACCTCCGCTTAAGTCATGGTATTTATTTTTTGAGAAAGCGTCAAAGAGGTATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32936
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031130 | None | None | 935 | 20 | 22 |
ENSDART00000144672 | Nonsense | 1098 | 1122 | 19 | 21 |
Genomic Location (Zv9):
Chromosome 2 (position 29618288)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 29919923 |
GRCz11 | 2 | 29903456 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGTGAAAATGACTCTCATCTGTGCCGAGAGTATTTCCTGAAGAACATC[G/T]GTAAGATGACGCTGTTCCCATCTCAGCATTTACATTTAACACAAAACCAT
Long Flanking Sequence:
GAAGAGGTCACATTTATAAAATAGTTTGTTTATGACGTGTTTAAACATGGTCATTAACCACATATTAAAATATCACAAACTGCACTTGCCTACATTTATGCCTTCTTAAACTGTAAGTGTTGAAATATAATCGTTTATATTAAGTGAACTTGGCAATGCTTCAAGAGCATACTTTGCAAGCAGCCTCCCACACAAAATAAAAATCACATCGTAGACCAACCCAAGTTTTTAAAATGGTAATTCATAATATTGTTTTAAAGCATTGTATTATTTGAGATGTTACCAAATGCTTTTATAAAAGGATTCAATAAATATGGTTCAAGCGTGCTGGAAGAGCACACTACCTGATTTTGAAATGAGAGTTTTGTTGGTGTTTATATGTCTGGCGCAAAATCAAACTTGTGCTCTTCCTGTGTTTGTTTTAGAATTTACCGGAAATCATACTAATAACCTGTGAAAATGACTCTCATCTGTGCCGAGAGTATTTCCTGAAGAACATC[G/T]GTAAGATGACGCTGTTCCCATCTCAGCATTTACATTTAACACAAAACCATGGTTAAAAAAACAAACAAACTACATGGTGTGCATTTAATATCCGAGATGTACTCTACAATTAATGCTTAATTGATTTCTTCTGTCTTTATTTCAGAAGTGTACACTGCTGAGCTTATATTGACAGGGGTGTTGACTCAGTCCTTGGATTATGAATCATATCCTTTTAAAATAAATGCAAGATTGAACAGACAAATGATAAACAATCGCCTTTGAGTGACTTCTGAATCAACATATGGTTGACTGAACCACAAAACTTTGCTGTCATTGATATCGGACTTGAATCTTAGCAATTTTACAGAATTTTATCTTCTATGTTTTTTAATGCTGGGTTTATTATAATTTTTTTTAAAGAATCCTTTTATTTTAATTTGTTTGAATTGATTTGTGGATGTATGTTCTATTTGTTTCGCTCCTTAACAATCTCACGTATAAATTCACATGATGTCCTT
Associated Phenotype:
Not determined