ZMP
pacsin1b
Ensembl ID:
ZFIN IDs:
Description:
protein kinase C and casein kinase substrate in neurons protein 1 [Source:RefSeq peptide;Acc:NP_001
Human Orthologue:
PACSIN1
Human Description:
protein kinase C and casein kinase substrate in neurons 1 [Source:HGNC Symbol;Acc:8570]
Mouse Orthologue:
Pacsin1
Mouse Description:
protein kinase C and casein kinase substrate in neurons 1 Gene [Source:MGI Symbol;Acc:MGI:1345181]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44647 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38582 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44647
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 |
---|---|---|---|---|---|
ENSDART00000056830 | Nonsense | 109 | 445 | 4 | 10 |
ENSDART00000128456 | Nonsense | 109 | 445 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 6 (position 54211800)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 54248534 |
GRCz11 | 6 | 54256642 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGAGCGAATTGCACCAGGAGGTGAAGAATAATCTGCTGAATGAGGACT[T/A]GGAGAAGGTGAAGAACTGGCAGAAAGACGCCTACCACAAACAAATGATGG
Long Flanking Sequence:
GGCCGATAACGATAGAGCCGCCGATATAGTGCATCCCTACTTATAATATAAGGAGAACATTTTAATGAAATAAAATAAATGCCAAAGCATTTTGGTTTAAAAGCCTTCCTCAGGGCACAAGAACACATCATTTAATACAAGTGTTGCTGGAGAGCCCTATTTTTATTATGTTTACATTAATGAATTACGCAAATGGTGAATGTTTTCAGCATAAAACTCAGAAATATATTCAGAAAATATGAATTATGATCATTAAAGTTGATGTTAAACTGGACATTAGTTAGACATTTAGTTTTTCAACCTTAAATGTTTCAAATAAAAAATAAGGGTTTATATCATGCACCTAAAATATACAATTTTGGCATTGTTTTTTTTCTCTGAATGGTTTGCAGGGCCGCAATACGGTACACTGGAGAGAGCCTGGTTAGCTGTGATGACCGAAGCTGAAAAAGTGAGCGAATTGCACCAGGAGGTGAAGAATAATCTGCTGAATGAGGACT[T/A]GGAGAAGGTGAAGAACTGGCAGAAAGACGCCTACCACAAACAAATGATGGGCGGCTTCAAAGAAACCAAAGAAGCGGACGAGGGCTTTCGGAAAGCGCAGAAGCCTTGGGCCAAAAAACTCAAAGAGGTGAGACAGAACATCTCCTTTAAGTCCTAAAGTGACAGTGCAGTCTGTAAAATGGCGAGTCTGGAAACAGAGATGAGGATGTACATGCAGTTTGTTAGGAAAATAGGCAGGCAACAGTCAAACATGTACAAACTGGAGCATAGTGATGTGACGTTGTGCATAGCTCGATTTATTTTGCCATAATCAAATGATCAGTGACGTCTGAAGCTTCATTTTCACGTATACCCACATGACTGCACTGAATTTTGATTCAAAAGTTTAAACACTCTCGTGGGTTAGTAAAGTGTATAGGGAGAGATTAGGCATCGATTACATACATTTCTACGGTTTCAAAGCTCTGCACCAGTCCCGCGCACCAGTAATTCAACTAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38582
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 |
---|---|---|---|---|---|
ENSDART00000056830 | Nonsense | 390 | 445 | 9 | 10 |
ENSDART00000128456 | Nonsense | 390 | 445 | 9 | 10 |
Genomic Location (Zv9):
Chromosome 6 (position 54221529)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 54258263 |
GRCz11 | 6 | 54266371 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGTGAAACCAACGGTGGAAATCCATTTGAAGAGGACAGTAAAGGAGTG[C/T]GAGTGAGGGCGCTGTATGACTACGAGGGCCAAGAACAAGACGAGCTCACA
Long Flanking Sequence:
ATGAATGAATGAATGAATGAATTACATTCAGTAAAGGTTGTGGAGGGACTTCTCAACATAACAGCTGCCTGTTTTTACTATTTATCATAGGTCATGGAAATTCAGCTTTTTAGTCAGTGAAAGTAAGAGAAAGGGTCCAGTGTTTCTCAACCATATTCCTAGAGGACCACCAACTCTGCATATTTTCTTTATCTCCTTAACCAAATTCAGGTCATCAGCTTATTAGCAGAGACTGAAAGACCTGTAATGATTGTGACAGACAAAGGAGACATCTAAAACATGCTGTATTGGTGGTCCTCCAGGAGCATGGTTGAGAAACACTGATTTAGTCTAAAGAAAGGCTAACTCGTGCTTCTCATGTTGTCCTCAGTGTGAGCAGTTATGAGAAGAACCAGCAATATTCTGCAGAATGGTCTGATGATGAACAGCCGCCCACTGCCGCACAATCAGCCAGTGAAACCAACGGTGGAAATCCATTTGAAGAGGACAGTAAAGGAGTG[C/T]GAGTGAGGGCGCTGTATGACTACGAGGGCCAAGAACAAGACGAGCTCACATTTAAAGCAGGTGAGAGGCATCTTATGCTCACTTAGGCTGCCTTACATTGTTTAAAAATACTGTCAAATGAACTGCATTATTACAAGTCAAAATAAGTGTGTTCTATTTGAAAAGCTGCATTTTCAGCATCACTCCAGACTTCAGTGTCATGTGATCCTTCATGAAACATTTACTATTGTTTTAAGGTTTGCTGATGGATAGGAAGAATCTATCAGTCTATCGTTTTTCTATCTATCTTTCTATCTATCTATCCATCCGTCCGTCTGTCTGTCTGTCTGTCTGTTCGTCTGTCCATCTATCCATTAATCCATCCGTCCGTTCGTCTGTCCGTCTATTTATCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTTCATTTGTCCATCTATCCATCCATCCCTCTATTCATCCGTCTGTCTATCTGTCTGTCTCTCTGTCT
Associated Phenotype:
Not determined