Busch Lab

ZMP

pacsin1b

Ensembl ID:
ENSDARG00000042128
ZFIN IDs:
ZDB-GENE-050913-35, ZDB-GENE-050913-35
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.
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.
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