ZMP
pcnx
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens PCNX, pecanex homolog (Drosophila) (PCNX) [Source:UniProtKB/TrEMB
Human Orthologue:
PCNX
Human Description:
pecanex homolog (Drosophila) [Source:HGNC Symbol;Acc:19740]
Mouse Orthologue:
Pcnx
Mouse Description:
pecanex homolog (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1891924]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31944 | Nonsense | Available for shipment | Available now |
sa35550 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14634 | Nonsense | Available for shipment | Available now |
sa16965 | Nonsense | Available for shipment | Available now |
sa22351 | Nonsense | Available for shipment | Available now |
sa28165 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31944
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 |
---|---|---|---|---|---|
ENSDART00000015664 | Nonsense | 269 | 2292 | 6 | 37 |
ENSDART00000139593 | Nonsense | 241 | 2279 | 5 | 35 |
Genomic Location (Zv9):
Chromosome 13 (position 36505694)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 35978263 |
GRCz11 | 13 | 36104095 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCACTCACAGTCTTTCCGAAAAGAGTCGTCTCGACCAAGAGGATTGCCT[C/T]GAACCTCAAGTTCTGCGGGATCTGCTTTTCCGGATCCTTCTCTGCCTGAG
Long Flanking Sequence:
TCTTTCAAACTAATGATTGTCATTTTTGCTTGATGTTCACATAAGGTTTTAGACAGGTTTTAGAGGCTTCTTTAATCTGCTTTTGATTCAACAATATATTCCACGAGCAAATATGAATGAATTTAACAGTCCCACTCCTTTTCATGCATTACATTAAGCTTTAGTGAAGAAACTAAATACTAATAACATGCACCAATAAATCATTCACCAGCACATTATCATCTGTTAAGAAACTAACAAAGTTATTGTCATTTTCACACACTCTGCTATGTCTCTTTCACTCTTTAGATTTGATGTCGGACCCAAAGATGTTCTGCCTTGTCTCCAATGACTCTTTTGCCTCCATGCAGCCATCAACCTCATTGGCACAGGACCTTTATGGCTCCACCCCCCACCCTTTCAGTCAGTCCTTGTCCTCCTGTGACACAGAAATTACTGCCCATCTTTCAACTCACTCACAGTCTTTCCGAAAAGAGTCGTCTCGACCAAGAGGATTGCCT[C/T]GAACCTCAAGTTCTGCGGGATCTGCTTTTCCGGATCCTTCTCTGCCTGAGTTCAGCCTGTACCCTCCACCTCGGAGGGGAGGACTTGATCCTGTCTGCGAAATGGATTCGTCTAGATCACAGAGGGCGACGGAGAGCTCTGAGCAGGCCGACTCGGGAACTCCCAGCACTTCAGGAACTGAATGTACCAGATATCACCTGAAGGAGCACCGCAGGTTATCAAGGTCTGTGTCCCGAGAGACAGGGGAAGGAGAGTGTGCTGGGGAAGGGGGATCTGGGCTGTACCGTTCTGAGGGTGTTCAGGGGGGTTGTGAAAGGACAGGTGGACACAGTGCCGAAAGTTTGCGTAGTTTAAGCACACGCAGTAGTGGCTCCACTGAGAGCTATTGCAGTGGGACAGACCGGGATACCAACAGTACCCTGAGCAGCTTGCATAGCGAACAGACCAGCTCCACACATGTGGAGAGTCTGCTGTCTCTCTCCGGGGACGAGAAGGTGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35550
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000015664 | Nonsense | 1252 | 2292 | 21 | 37 |
ENSDART00000139593 | Nonsense | 1239 | 2279 | 19 | 35 |
Genomic Location (Zv9):
Chromosome 13 (position 36478368)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 35950937 |
GRCz11 | 13 | 36076769 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTTGACTGATCTTGTCCTCTTTTATTTCTTCCAGCCATTTTTAAGCTA[T/A]GTTCTGTACGGTCTAGTCGGCTCGGTAGGGCTGTTAACTCACTACCTACT
Long Flanking Sequence:
AACTCAAGTTTTTTTTCACAAATAAACAAAACAAGCCAGGAGAGAGAAGACTCTCCAAACAATCATTCAGTCCGGTTTAAATGGACTTCACAAACATGTCGGCAAGCTTCCACATGCCGACACCTGACTAATGAAACCTGTTGGAGACAGCGGATAAAGGCGGTGAAAAGAGAACCACAACAAAAAGAGACATATACAACAACACAAAGAACTCACTACTTCAAATAAAAAAAAAAATTTATATTATTGTTTTAACAAATAAAAAATATAAATAACAGAGACTTACAAATGAAGATAAAAAGACATAACAACAATAACAGTATATTGTGCATCTTTAACTTTCACCATACATCTCATAGTCCAGCTGCAGGATAACACACTAAAATCTCCAAAAAGATAATCAAGTTGTCATGCTGCTCATATTTTTAATATCCAATGAAGAATAAACAGATCTTGACTGATCTTGTCCTCTTTTATTTCTTCCAGCCATTTTTAAGCTA[T/A]GTTCTGTACGGTCTAGTCGGCTCGGTAGGGCTGTTAACTCACTACCTACTGCCCCAGATGAGGAAGCAGTTGCCCTGGTACTGTTTTTCCCACCCGCTGCTCAAAACCAGAGAGTACTATCAGTTCGAAATCCGGGGTGAGTCACTCCATCACACAAATATTTGTTTCTGGTTATTTAATGAAATAACTCTTGTTCTCGGCTAGCATGAACATTACCTAAACGTGTGTGCTGTTCGTTCAGGTGCTGCCCATGTCATGTGGTTTGAGCGCACTCATGTGTGGCTGCTGTTTGTGGAGAAAAACATCCTCTATCCGCTCATTGTGCTCAATGAGCTGAGTGGCAGCGCACAGGAGCTCGCCGGCCCCAAAAAACTCAACACAGAGTCAGTATTATATCCTTTTTATTATTTCTTATTGACTAAGGGTGCTTTCACACTAGCACTATTTGTCCGCACCTAGGTTGGTTTGATGTCAGAGTTCAGTACGTTTAGATCTTGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14634
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000015664 | Nonsense | 1292 | 2292 | 21 | 37 |
ENSDART00000139593 | Nonsense | 1279 | 2279 | 19 | 35 |
Genomic Location (Zv9):
Chromosome 13 (position 36478248)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 35950817 |
GRCz11 | 13 | 36076649 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGCCCTGGTACTGTTTTTYCCACCCGCTGCTCAAAACCAGAGAGTACTA[T/A]CAGWTCGAAATCCGGGGTGAGTCACTCCATCACACAAATATTTGTTTCTG
Long Flanking Sequence:
CACCTGACTAATGAAACCTGTTGGAGACAGCGGATAAAGGCGGTGAAAAGAGAACCACAACAAAAAGAGACATATACAACAACACAAAGAACTCACTACTTCAAATAAAAAAAAAAATTTATATTATTGTTTTAACAAATAAAAAATATAAATAACAGAGACTTACAAATGAAGATAAAAAGACATAACAACAATAACAGTATATTGTGCATCTTTAACTTTCACCATACATCTCATAGTCCAGCTGCAGGATAACACACTAAAATCTCCAAAAAGATAATCAAGTTGTCATGCTGCTCATATTTTTAATATCCAATGAAGAATAAACAGATCTTGACTGATCTTGTCCTCTTTTATTTCTTCCAGCCATTTTTAAGCTATGTTCTGTACGGTCTAGTCGGCTCGGTAGGGCTGTTAACTCACTACCTACTGCCCCAGATGAGGAAGCAGTTGCCCTGGTACTGTTTTTCCCACCCGCTGCTCAAAACCAGAGAGTACTA[T/A]CAGTTCGAAATCCGGGGTGAGTCACTCCATCACACAAATATTTGTTTCTGGTTATTTAATGAAATAACTCTTGTTCTCGGCTAGCATGAACATTACCTAAACGTGTGTGCTGTTCGTTCAGGTGCTGCCCATGTCATGTGGTTTGAGCGCACTCATGTGTGGCTGCTGTTTGTGGAGAAAAACATCCTCTATCCGCTCATTGTGCTCAATGAGCTGAGTGGCAGCGCACAGGAGCTCGCCGGCCCCAAAAAACTCAACACAGAGTCAGTATTATATCCTTTTTATTATTTCTTATTGACTAAGGGTGCTTTCACACTAGCACTATTTGTCCGCACCTAGGTTGGTTTGATGTCAGAGTTCAGTACGTTTAGATCTTGTGAATGATGTCTTCTGAACTCGTACCTAAGAGAGCCGTACCTAAGTACGCCTGAAAGAGGTGGTCTGGAGCAAGGTTATAATAGTTTTGGATTATTCATTCGTTTTAGTTTCTATTTCGTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16965
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000015664 | Nonsense | 1778 | 2292 | 31 | 37 |
ENSDART00000139593 | Nonsense | 1765 | 2279 | 29 | 35 |
Genomic Location (Zv9):
Chromosome 13 (position 36467139)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 35939708 |
GRCz11 | 13 | 36065540 |
KASP Assay ID:
2260-6738.1 (used for ordering genotyping assays)
KASP Sequence:
CCAGTGGYTAYGTKTTTGTGTTRTTACAGCAATCTGGAGTCAKTCCTGTA[T/A]GGGCTGCATGCCTTGTTTAAAGGTGATTTCCGGATCTCGTCWGTGAGAGA
Long Flanking Sequence:
CTTATTATGCACTTTGATGCCTGACTAACAAGCAATAGTGTCCTGGTGCTGTTAAACAAGCTTATGTAGCACGGATTAAATGCATGCAATTTGTTGATGTGTTTGAAAACATAACATTCTGTAGTGCATTTAGTTATTGTTTAAGGCCATTTGGCTCTGTCATTATGTGTAATAATTTTGCATATTCTTGGACACCTTTTTATTGCTTTAAAGCATCCGTATCTGAAGTTTTTCTGTCTGGTGCAATTTTTCAATGCGCCATTTAATTGGATGGGAATCATAGGCATGATTATTCTACTTAGCCATTCACCTTATACTAGAAAAAATAATCATATTACTGCATGTTGAAGTAAAGCCCTGATACAGCACTTAAAATGTACTCAAGTAAAAGCTCCTGAAAAAAACTACTTGATTATAGTAATCTGAGTAATTGTAACTTGCTACTTTACACCAGTGGTTATGTTTTTGTGTTGTTACAGCAATCTGGAGTCATTCCTGTA[T/A]GGGCTGCATGCCTTGTTTAAAGGTGATTTCCGGATCTCGTCTGTGAGAGATGAATGGATCTTTACAGACATGGAGCTGCTGAGGAAGGTGGTTGTTCCGGGAATTCGCATGTCACTCAAACTGCATCAGGTGAGACTCATCTGTTCTCTGTCATACCTTTTTATGGATTGATGAGGAGATTCCCCCCCATTGTGTAAAGCGCTTTGAGAGCCCAGAAAAGCGCTATATAAATGTAACAAATTATTATTATTATTAATATTATTATTATTATTATTAGTGTGTACCCATAGTGAGTCTAATCTCTCTTTGCAGGATCACTTCACTTCCCCTGATGAATATGAGGAGTCATCGGTGTTGTTTGAAGCCATTTCTTCGCACGAGCAGACACTGGTGATCGCTCATGAGGGGGATCCGGCCTGGCGCAATGCCGTCCTGTCCAACTCTCCCTCTCTGCTCGCTCTCAGACATGTGCTGGATGAAGGGACCAATGAGTACAAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22351
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 |
---|---|---|---|---|---|
ENSDART00000015664 | Nonsense | 1911 | 2292 | 33 | 37 |
ENSDART00000139593 | Nonsense | 1898 | 2279 | 31 | 35 |
Genomic Location (Zv9):
Chromosome 13 (position 36464469)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 35937038 |
GRCz11 | 13 | 36062870 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTGCATTTTCAGGTGAATAAGGAGTGTGTTCGTGGCCTGTGGGCAGGA[C/T]AGCAGCAGGAATTGGTGTTTTTACGAAACCGAAACCCGGAGCGTGGAAGC
Long Flanking Sequence:
ATGCAGCGGATGCCCTTCCAGCCGCAACCCATCTCTGGGAAACATCCACACACATTCACACACACACTCATACACTACGGACAATTTAGCCTACCCAATTCACCTGTACCGCATGTCTTTGGACTGTGGGGGAAACCAGAGCACCCGGAGAAAACCCACGCAAAGGCAGGGAGAACATGCAAACTCCACACAGAAACAACAACTGAGCCAAGGTTCAACCAGCGACCCAGCGACCTTCTTGCTGTAAGGCGACAGCACTACCTGCTAGTTTCAAAACAGCAAAAATAATGCAAAATTAAGCTTTTTTATCTGTATGTATTATTTTTAGAGCAACCCTAATATTTCAAATAATTTGTTTCAGTTTCTGTAAAGGGAAGTTCCCCAAACTGAAAGTGCAGGCTTTAGTTAGTCATGTGGAAAAATATGGAATAAGTTATTTAAAATTTTCACATGTGCATTTTCAGGTGAATAAGGAGTGTGTTCGTGGCCTGTGGGCAGGA[C/T]AGCAGCAGGAATTGGTGTTTTTACGAAACCGAAACCCGGAGCGTGGAAGCATCCAGAATGCCAAGCAAGCACTACGCAACATGATCAACTCATCATGCGACCAGCCAATCGGATACCCAATATATGTATCGCCCTTGACAACCTCTTACTGTAATACACACCCCCAGCTGGGACACATACTGGGAGGACCAATCAGCATTGCCAACATACGAAACTTTATTGTCAACACGTGGCACAGGTGTGTGTGAATTAGAGGAAATGGACATGTTTTGTGTGATGTCATATTAACAGCACGTTTTTTCTCTGATTGCAGACTGCGTAAGGGCTGTGGTGCTGGCTGTAATAGTGGCGGGAATGTCGAAGATTGTGATGCGGGTGGTTTGTCGTGTGGCAGTGGGAATTCTGGGAATTCTGGGACAGGAGCAAGTGATTCCCAGCATAGCTCAGGACCCACAGCGCTACACGCGTACACACCACATTCTCTGGGTAAACACACAGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28165
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 |
---|---|---|---|---|---|
ENSDART00000015664 | Nonsense | 2146 | 2292 | 35 | 37 |
ENSDART00000139593 | Nonsense | 2133 | 2279 | 33 | 35 |
Genomic Location (Zv9):
Chromosome 13 (position 36462199)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 35934768 |
GRCz11 | 13 | 36060600 |
KASP Assay ID:
2260-6736.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCCTGGCCCCTCCAGCTCCCTCTCCGCTCACTCCATCCCGCCCTGCAAA[C/T]GACACGCACACACGCTCGCAGGCCTGCTGGGAAACGAGGCCTTAGTGCTG
Long Flanking Sequence:
AGACAGACAATTGATGGATTGATGAATGGACTGATGGATAGAAGAATTGATTGATTGATTGAATGAATGGACAGATGGATAGATAGATGGATGGGTAATAGACAGAGAGATGAATCAACAGTTATCCATCTGTCCCTGATGTATCCAGTAAATAACACACAGTGTCTCTCTCTCTCTCTTTCTCTCTCTCTCTCTGTTTGTGTTCAGGTACGAGTCAGAGTTCTCAGTCAGTTCAGTCTGGTTTGGTTCGTCAGTCTCCTGCGCGTGCGTCTGTGGTCAGTCAGTCGTCCTCGTACCGCCACAGCAGCAGTCGTCAGTCTTCACTGCGCACATCTGTGACTGGTCTGGAGCCCTGCAGACGCTCCTCCAGCAGCCAGCTCTCGCTCCGCACCCTGCCCACCTCCCTGCAGCTCCGGCTGGGAACCAACTCCTCCATCGCCAACCCCGAGCCCCCTGGCCCCTCCAGCTCCCTCTCCGCTCACTCCATCCCGCCCTGCAAA[C/T]GACACGCACACACGCTCGCAGGCCTGCTGGGAAACGAGGCCTTAGTGCTGGGGACGGACATCCATCCTCACCCCCACCACCACCTCCACTACATCCACCATCACCATCACAACCCCTCGCTGTCATGCCTGAGGAGGGACGACATCTCCTACAGAGTGCAGGTCAGTAGCTACGTTTCCGTCCACCTATTTTCATACGCATTTTGGATATGGGCATAAAAAACGGTTGATGGAAAAGGCAAGACACTCATAAAAAATGTATGCGCATAATTGAGTAGGATAAAGTTTTTGTTCGATAAGAAACATTGCTCAAAAACTACAATGGAAACACTTTTAGCGAACAAATTCCAGTATGCGCATTAAAAAAGGTCATGTGATTTTGTTATAAGAGGTCATGTGATGATAAAAATGTGTGTAAATGGACAAACCAGCAGGCTGAGCACATTGTAAAACATACGAAATGTTGTTTTGGTCATTCTGAAATGCCTTGACTACCTCAGT
Associated Phenotype:
Not determined