Busch Lab

ZMP

marcksb

Ensembl ID:
ENSDARG00000008803
ZFIN ID:
ZDB-GENE-030131-1921
Description:
myristoylated alanine rich protein kinase C substrate b [Source:RefSeq peptide;Acc:NP_001015060]
Human Orthologue:
MARCKS
Human Description:
myristoylated alanine-rich protein kinase C substrate [Source:HGNC Symbol;Acc:6759]
Mouse Orthologue:
Marcks
Mouse Description:
myristoylated alanine rich protein kinase C substrate Gene [Source:MGI Symbol;Acc:MGI:96907]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa39154 Nonsense Mutation detected in F1 DNA Not yet available
sa36365 Missense Mutation detected in F1 DNA Not yet available
sa6465 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa39154
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
ENSDART00000002932 Nonsense 9 232 1 2
Genomic Location (Zv9):
Chromosome 17 (position 15377007)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 15527835
GRCz11 17 15535768
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCATTCATTTGATCTGCGATTCTTTGTTGCGTGTGAAAGCATGGGAGCA[C/T]AAATCTCCAAAAACGGAGCAAAAGACGAGACTGCTGCCGAAAAACCCGCG
Long Flanking Sequence:
AAATTTATTGAGTTAAAACATGAAGCCCCCCCAAGAAAATTATGTTTCGAAATAAAAATAAAGGCAAAGCAATTTGTGACTGTATTTACTGGTTCTGAATCACCAGTTGCTGGTTGCGCGCCCTTCCTCCCCTTCCAGTGCGTGATTGTAGTCCCTCCCCCCTGCTTCACGCAGGCTTCTGATTGGCTCACGCCGCCTTTATGTGACGTCAGGGGTATTTGGGCGTTGTATCTCGCATCTCATTATCAAAAGAGAACAATTTCATTATCTCCATCTCGTATCCCAAAATAATATATTTTATTTAAGAGAGTGCTGTAATTATTACTTCTCCGGGATCAGTAGATCACAGCTTCGCCTCTCGCTTTCTCTTTTCCGCGGTTTTATTTGAAAACAGACGCTCTTGAGAGCGCGCACGCGACGCGTCTGTGAGGGAGAAGCTCGCGCTCTTTGTTCATTCATTTGATCTGCGATTCTTTGTTGCGTGTGAAAGCATGGGAGCA[C/T]AAATCTCCAAAAACGGAGCAAAAGACGAGACTGCTGCCGAAAAACCCGCGGAGGCTGCAAATAAATCAAACGGGCAGGTAATAACTTTAATTATCATCTTTCTACAGGCGTGTGATGTTATGAGGGGGTGTGCGGTTACCAAAAACCAAGTCGGTTCAAATGAACAATGAGCCGATCAACAAAGGGACTCTCCGGTTTCCACGAAATATAGCAATTTTAGTAAATATCGATGCTGTTGTAGATTAAAAATGAATGGTGCGCGTGAACGGCTTCGAGTTGGGGGAAAATCTGTTTTTCACATTTCCACGTTTATTGTAACAGACCACCCAAAAGCAAGCCGAGCTCTTAACGTCAAGTTAATTTTAAAATCGTAAATGAAAAAATTGTGATTAAACCGAAATTCGGCGATAACACGAGGATTTCCTTTGGAAAATGTTTAATATTCGCAGCTTTATCAAGCTTTTCCGTCGTGGATGGCCATTACTGTAAAATCACCACGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36365
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 > C
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002932 Missense 68 232 2 2
Genomic Location (Zv9):
Chromosome 17 (position 15377967)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 15528795
GRCz11 17 15536728
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCAGCAGAAGATGTCCAAGCCAATGGAAAGCATGCTGCCGATGGGGAGG[T/C]AAAAGCCGAGGAGGGAAAGGCAGAGGAAGCAGACGCAGAGAAGGCCGCTC
Long Flanking Sequence:
CTTTTCCGTCGTGGATGGCCATTACTGTAAAATCACCACGCCTTTATCGCATCTAGTTGATAAAATGGATGTACAAATAAGCCACGAGACCCAATCCGTAGATTTAACATGAGAAATGGCTGTAGTGAGAGAAGTGGCCTTGTAAGACTGCTTGTGTGCTCAACACGATGGTCTCCTCGGTTTGATCCTCCAGCGCTGGAGGATCCACTCGTCCATCTTGCAACGCTTTCACTTAGATGGCAACAGCATCAGCCAGACAAAGTGCATGAGACTTTACCCACGTGGCGATCCTATAGCTTACTTTTAATACAGCTTTTCACCTTTTATTGAGTGCACAATGTATGCAAAAAAGTTTAAAATGATACACAATGCAAAAACTATACATTTCATGTTTCCTCAGGAAAATGGCCATGCTAAAACCAACGGGAATGCCTCTCCGAATGCTGAAGCGGCAGCAGAAGATGTCCAAGCCAATGGAAAGCATGCTGCCGATGGGGAGG[T/C]AAAAGCCGAGGAGGGAAAGGCAGAGGAAGCAGACGCAGAGAAGGCCGCTCCGGAGGGTGAAGGAGAGAGTTCTGCTGTTGCAAATGGTGAAGACTCCACCAAGACAGAAGAAAGCGCAGCTACTAGCAGCGAGCCTGCCAAAACCAAAAAGCGATTCTCCTTTAAGAAGCCATTCAAGCTGAGCGGTTTCTCCTTTAAGAAGAGCGCCAAAAAAGAAGCTGAAGGTGGAGAAGCGGCGGCGGCCACCGCTGAGAATGGAGAGCAGAAGAAAGATGCTGAACCCGAGGAGGCCAAGCCCGAAGCTTCCAGCGAAGAGGCCAAGGCGGAGACTCCAGCTGAGGAACCCAAAGCTGAGGAACCAAAAGCTGAAAGCAGTGAGGAGAAACCAGCCAGCGAGGTAGCTGAGGAAAAGCCAGCTGAGGAGAAGCAAGAGGCGGCTCCTCAGGAACCAGCAGCCGCAGAAAGCTCAGAGGCTCCAGCCGCTGCCACAGAGTAAGATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6465
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002932 Nonsense 112 232 2 2
Genomic Location (Zv9):
Chromosome 17 (position 15378098)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 15528926
GRCz11 17 15536859
KASP Assay ID:
554-5296.1 (used for ordering genotyping assays)
KASP Sequence:
CAAATGGTGAARACTCCACCAAGACAGAAGAAAGCGCAGCTACTAGYAGC[G/T]AGCCTGCCAAAACCAAAAAGCGATTCTCCTTTAAGAAGCCRTTCAAGCTR
Long Flanking Sequence:
AAGTGGCCTTGTAAGACTGCTTGTGTGCTCAACACGATGGTCTCCTCGGTTTGATCCTCCAGCGCTGGAGGATCCACTCGTCCATCTTGCAACGCTTTCACTTAGATGGCAACAGCATCAGCCAGACAAAGTGCATGAGACTTTACCCACGTGGCGATCCTATAGCTTACTTTTAATACAGCTTTTCACCTTTTATTGAGTGCACAATGTATGCAAAAAAGTTTAAAATGATACACAATGCAAAAACTATACATTTCATGTTTCCTCAGGAAAATGGCCATGCTAAAACCAACGGGAATGCCTCTCCGAATGCTGAAGCGGCAGCAGAAGATGTCCAAGCCAATGGAAAGCATGCTGCCGATGGGGAGGTAAAAGCCGAGGAGGGAAAGGCAGAGGAAGCAGACGCAGAGAAGGCCGCTCCGGAGGGTGAAGGAGAGAGTTCTGCTGTTGCAAATGGTGAAGACTCCACCAAGACAGAAGAAAGCGCAGCTACTAGCAGC[G/T]AGCCTGCCAAAACCAAAAAGCGATTCTCCTTTAAGAAGCCATTCAAGCTGAGCGGTTTCTCCTTTAAGAAGAGCGCCAAAAAAGAAGCTGAAGGTGGAGAAGCGGCGGCGGCCACCGCTGAGAATGGAGAGCAGAAGAAAGATGCTGAACCCGAGGAGGCCAAGCCCGAAGCTTCCAGCGAAGAGGCCAAGGCGGAGACTCCAGCTGAGGAACCCAAAGCTGAGGAACCAAAAGCTGAAAGCAGTGAGGAGAAACCAGCCAGCGAGGTAGCTGAGGAAAAGCCAGCTGAGGAGAAGCAAGAGGCGGCTCCTCAGGAACCAGCAGCCGCAGAAAGCTCAGAGGCTCCAGCCGCTGCCACAGAGTAAGATGGAGGAGGTGAAAGGCCCGTTTTTAGATGAAGTCCGAGGAGCACAAACATGGAAAATTTGTACAAAAACCAATGACATTTCAAACCTTCTGTTATATCCCATACTTTCACCCATTCCTGTTCCATCCACTAC
Associated Phenotype:
Not determined