Busch Lab

ZMP

si:ch211-141h20.2

Ensembl ID:
ENSDARG00000059965
ZFIN ID:
ZDB-GENE-070912-80
Human Orthologue:
CAMSAP1L1
Human Description:
calmodulin regulated spectrin-associated protein 1-like 1 [Source:HGNC Symbol;Acc:29188]
Mouse Orthologue:
Camsap1l1
Mouse Description:
calmodulin regulated spectrin-associated protein 1-like 1 Gene [Source:MGI Symbol;Acc:MGI:1922434]

Alleles

There are 7 alleles of this gene:

Allele Name Consequence Status Availability
sa33015 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa6020 Nonsense Mutation detected in F1 DNA Not yet available
sa14892 Nonsense Available for shipment Available now
sa33016 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa33017 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa33015
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083957 Essential Splice Site 56 1407 None 18
ENSDART00000135582 None None 93 None 2
ENSDART00000139154 None None 325 None 6
ENSDART00000144704 Essential Splice Site 47 187 None 3
ENSDART00000147245 None None 124 None 3
Genomic Location (Zv9):
Chromosome 2 (position 45346966)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 45447654
GRCz11 2 45300652
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGATATCCTGCAGTTTGACGTGGCTCATCGCCAAAGCCTTTGGATCTGG[T/G]AGGTGGCGCTTAAAGGTTTGAAAATGCACATTTTGAGTTCAGGGGAAGTT
Long Flanking Sequence:
GGAAGAAATCATGACACCAAACGGTCAGCTCATCGATCGCCTCTCCTCGCCATTCAGCGTGACATCCCTCATCATGGCGCTCGTGTCACACATGAGATATTGATTTTTGGCATCGACACCAACTTGAGGATAATATGCCGGGAAACGGATGAGAACTAACGTTACCGCAGTCGCCTGGATTTGCTTTTTGGATATTGAATCCTGTGCTCGGGGGTTCGTTTTTCCACTCGTGTAGCCTAATTAGTGTTTGAGAGGAGAGTTACCGGATCCGTTATTTTCCAGATCATATTTGAGCATGGGAATGTCGTCTCTGAGCTCATAGTCCCGCGGGAAATGATGCAGCCGCGCGTGGACGTCAAGATGGGAGATGCCGCAGAGATCAAGGAGAGCAGGAGGACCTTCATCGTGCCCTCCATCAAATCTATGGATCACTATGACTTCAGCAGGGCCAAGATATCCTGCAGTTTGACGTGGCTCATCGCCAAAGCCTTTGGATCTGG[T/G]AGGTGGCGCTTAAAGGTTTGAAAATGCACATTTTGAGTTCAGGGGAAGTTGGAGCAATTATCAAAACACTGTATCTAAATCAAAATAAGACGTGATGTAATCTGTGCTGGGCGTCCAAAATGATCGCATCCAAATTAACCTTGTTTTGACATGTGTGTGTGAGCGCTTGTGTTTGTATTATATATATATATATATATAATAATATATATAATTTTACACATAATTTGTACCATATGCTATACAGTTGATGTCAAAAATATCCCTCCTGTGTTTTTTAATGTTTAATAGAGCAAGGAATTTGTACAGTCCTTTCTATAATATTTTTTTTCTTCTGGTGTAAGTTGTTTATTTCGACTAAAATAAAAGCCGTATTTAAAAAAGCAACAACAAAAAAACATTCTAAGGTCAATATTATTCACCTCAACAAAACAAACCATAGACTTGCCTATACCCTAACTTGCCTATTTAACCTAGTTAAGCTTTTAAATGTCACTTTAAGC
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa25904
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083957 Nonsense 685 1407 12 18
ENSDART00000135582 None None 93 None 2
ENSDART00000139154 None None 325 None 6
ENSDART00000144704 None None 187 None 3
ENSDART00000147245 None None 124 None 3
Genomic Location (Zv9):
Chromosome 2 (position 45413722)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 45505432
GRCz11 2 45358430
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAAACACACCTGAAACTGCTGAACTGAACGCCACAACTCCAGGAGCATA[C/A]GGGACAGTTCGGTCAGTTACTCCTGACACACATAGTCCTGCTCGAATCAC
Long Flanking Sequence:
ATCATCCATGACTCTGAGCGACCCCAGAGCAGCTTGCCGCCACCATCTGGGGACAGCGCCTTTTTCTTGCACAACCCATCTTCCTCTAACTCTGCCTCTGACCCCAATGAACCAGAGGACTCACTTAACAAGGCCAGAGCAGATGATGCTGACCTGAATTCCACGTCTACTGACATGGACACTGGAATCCACGTACGTACAGAGGACATTCAGGATGGACAGGATGAGGATTCGTCCTTGAAGGACTACTCAGACATGGACCAAGACTATGAGGCTCGTTCCTGTCCACTTCCAGACACGTCCGGCAGTCCGTGCCCAAGTCTTTTAGGAACAAGATCTTTGGCAACCAGCATGGCCTCCTCATTGGGCTCAGCGATACGCATGACCAGCTTTGCCGAACAGAAGTTTCGCAAACTAAACCACGGCGATGGCCGCAGCAGTGGCAGTGGTGGAAACACACCTGAAACTGCTGAACTGAACGCCACAACTCCAGGAGCATA[C/A]GGGACAGTTCGGTCAGTTACTCCTGACACACATAGTCCTGCTCGAATCACATCCCCTCGTGATCCTTCACACCTTCTGGCATCCGAAATGGTGCAGTTAAAGATGAAGCTGGAGGAGAAACGCAGAGCCATCGAGGCCCAAAAAAAGAAAGTGGAAGCTGCTTTTACGCGTCACCGTCAGCGAATGGGCAGAACCGCCTTCCTCAATGTGGTCAGACGTAAAGGAGTCGTTTCGCCACTTGGGGGCAGCAGTGAAGGCCCGGATGGTCGAGAAAAGACAACCAATGATCCAGAACCCCAAAAGTCACCCTTAACTTTAAACGATTCCAATGCTAGGCTTGAGAGATGCCGACCAGATGGCGCTCCACCAAAATCTCCTCTGGAGGATGCAGGAGTAGAGGTGGACCTGACAGAGTACACTCGGTCAATCGAACGCTTGAACACGTCTCTGGGCTTCCTGCAGTCGGAGATGCAGCGGTTGGCACAACAGCAGGAGCGAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6020
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
ENSDART00000083957 Nonsense 1033 1407 12 18
ENSDART00000135582 None None 93 None 2
ENSDART00000139154 None None 325 None 6
ENSDART00000144704 None None 187 None 3
ENSDART00000147245 None None 124 None 3
Genomic Location (Zv9):
Chromosome 2 (position 45414764)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 45506474
GRCz11 2 45359472
KASP Assay ID:
554-3917.1 (used for ordering genotyping assays)
KASP Sequence:
CAAAAGCATTGACATCTGAGGTCACGGCCAGTGGGAACACAAATGAAGAA[G/T]AGTCTGAGGAGAGTAAGGAKTTRATTGAGGTKCCTCTCTCGGTTCTGAAG
Long Flanking Sequence:
CAGATCCTTCACCGCGGAAACAATTTCGTGAACTGCGCAGTAGCAGTGTAGTTGGCCGAGGTTCGGTGGGATCTCTCTCTCCTATTTTATCATCCACCGGCTCTCCGCGCACTACACACCGCTCACCTTCTACAATCAAAAGGAAATCAGCATCTTTTCATGCAAGGACACCACGAACGCCAAGACCCAACGACCTTAAGGTCACTTCCTTCAGCCGCATGCTTAACACGCCGCAGTCAGTGGACAGCCTTCCTCGACTTAGACGTGTCTTACCAAGTCAGCCGCAAATCAGTTCATTCGCCTATTTGGGATCTGATGAAAGAGCTTTAAGTAAAGAGCAAAGCGATAAAGAAAAGCCATGTAAACCTGAATCCAAAGACACAGCTGCAGATCAGATGAGTGAAAAACAGAAAGAGGAAAAAAGAGGTACTGGAGAGAGTGACAAACTCACAAAAGCATTGACATCTGAGGTCACGGCCAGTGGGAACACAAATGAAGAA[G/T]AGTCTGAGGAGAGTAAGGATTTGATTGAGGTTCCTCTCTCGGTTCTGAAGCCTCTGGATGGACATGAGTTGGAGAGCAGCAGGGAAACAGAGACTGGACTAGGATCCAAACCAGATCAGAAGATGTGCTGTGGGTTCTTCTACAGGGTGAGACTCAAATATTGCATGTTAAAGCAGTGAGGGTTTACTGACATTTTCGCTGAACTTGCTGCTTTAATTAACAGTATTAACATTTAACATAATTTTATTAACCACTGAAGACTGGAGTAGTCCTATATTAGCTTATATTAGTCATATAGCTCTTTTATAAATCTTCCATCATATAGTCCTATGATCTGCTCATATGAGGAAGGCGCTGACAAAATGCAAGATATTGAAATCATTTTGAATGCGTGCACTGCTGTGCACACTTTTCCCCACACTTTTTACGACCACATGTACATTATTATAAATAAAACCGCAGGACACACATTTGTTATTATCCTCTGCAAGTCATTTGTC
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa25905
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083957 Nonsense 1121 1407 13 18
ENSDART00000135582 None None 93 None 2
ENSDART00000139154 Nonsense 40 325 1 6
ENSDART00000144704 None None 187 None 3
ENSDART00000147245 None None 124 None 3
Genomic Location (Zv9):
Chromosome 2 (position 45417425)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 45509135
GRCz11 2 45362133
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGAGAAGGAGATGCAGATCAAGAAACAGCAACAGGAGGCTGAGATAGAA[C/T]AGAAGAAAGAAGCTGCACGGTATGAACATACACCAACACTACAGAGAAAG
Long Flanking Sequence:
AATGTTGAAAACGGTTTCTGCAAAAAAAAATTTTTGTGGTACTTTTTTTTGTACAGAAAATAGAGAAATTATTCACCTTGGAGACATTAAATTGAACAAAAAGGTGTCAGTAAAAACACTTCAAATATTACAAAAGATAACAGAAGATGAAAGAATTTTTGAGCACCAAAAAAGCATATTCAAACAATCTAAATTAGTCTTTTGAGTTGTTTTATTTGAATTAAAATCATCTTAAATACGTGCTTTCATGACATGGACCTTCTTTGTTTTAAAAATTTTTGTTTTTCTTCATGACACGCATTACAGTGTTCAGTGAATGAGTGTTTTGTGCATCCAGCTGTACATGAGGCCTGAATGATTGTTTGTCTGTGGCTGTGACTCAGGATGACCTGCAGGGAGAGGAGGACATTGCACAGAAGAAAGCAGCTCTGATGGAGAAGAGGCTGCGGAGGGAGAAGGAGATGCAGATCAAGAAACAGCAACAGGAGGCTGAGATAGAA[C/T]AGAAGAAAGAAGCTGCACGGTATGAACATACACCAACACTACAGAGAAAGGTCAAATGCACATAGCAACCAAATGTGGTTGTCAGGATGGGTCAATTACAGAAACTTGGCTCCTTTTTTACTTAAGCTGAACAAATATTTGTTGAAGCAATGAACAAAAAAGCAAATAAGTGCAAATCCATATAAAATATCTAAAAATCTATCTAAAAGATAAATGACACGCATTAAAATTGCACATACTTCATTAACTCCATAAGCTGGGTTGTGCAAATCCAAAGAAAATATCTTAAAGGGCACCTATAATAAAAATCATCTTTTGTAAGCTCTTTGGACTGAACTGTGTGTAAGTATAGTGTGTTCACAGTCATATTGGGATGATATGAACACAATAAGTTTCTTTTTTTAATTTCATGATGTTAAAATAGGAGCCTAATCCTTTTGAGGCTGACCGCAACGTGATGTAGAAGTGTGTTTTCCCTGCCCTCCAAATTGAATGACAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14892
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083957 Nonsense 1226 1407 15 18
ENSDART00000135582 None None 93 None 2
ENSDART00000139154 Nonsense 145 325 3 6
ENSDART00000144704 None None 187 None 3
ENSDART00000147245 None None 124 None 3
Genomic Location (Zv9):
Chromosome 2 (position 45425552)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 45517218
GRCz11 2 45370216
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCCAGCATATCACTCGCCTCCCTGAACTTAGCAGACAATGAGAGCATC[C/T]AATCAGATAAGAGAACATCCAGGTRAGACTRWGGCTAATTTACTGTAAAA
Long Flanking Sequence:
ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATATGTATGTATATGTATGTATGTATGTATATATATATATATATATGTATGTATGTATGTAAAAATACACACACACACACACACACGTGTATATATAGACAATTTTTACAATTATTTTTACACTGTAAATTTAAAAAATAATAGCAAAATTAATTTAACAAATATTGCACATTTTGTGTCTTGAAGCATTTCCAAAGTTTTGTTCTGTTTATAAGAACTATTAATTTTAACCTGTGGGTACATCTTTTTTTAAACTGTATTAAAACTATACACTCAAAAAAGTATGAATATTTGCCACAGCAGGCTAAAAACAGGAAAAAATGTGTATATGATAATGCGTAAAATTGTGTCTTTATGTGTCCAGGGTCACGTCCTCGTGGATATTCTGTGTCCAGCATATCACTCGCCTCCCTGAACTTAGCAGACAATGAGAGCATC[C/T]AATCAGATAAGAGAACATCCAGGTGAGACTGTGGCTAATTTACTGTAAAATATCATTCAAGTACAATGACAGTTTCTACTGAGACCTATTGAGTTGTTATATTAATCAGTACTAGGTCCTAAGTTCCTAACACTGTGTGTGTGTGGTGTGTGTGTTTTCTCTGTGCTGGTTGCTCAGAGGCAGCAGACTGTCTCCTGGTAGTCTGTGTTTCTTTCTGAGCTCTCCTAAAGGGAGAAAGGGAAGGTCAGTTTGCGGACGGCATCACATTCATATCATCAGCTCACAAGGGCTGATCACTGTCATTTCAGCTTCAGTGATGGACAAACTCATTCGCTTTTTACAGATCACTTCACTCGTTGATCAGCTGTTGTATAATCATTACTTCGGAATCATTTATGTGATAAAACTATGAATGGGACATCGTACAGCTTTGCAGTTCTTGCTTACGTAATTTATTTATTTATTTTGCTGTTTGTTGTTGGCTTTCTTATTATTTTTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33016
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083957 Essential Splice Site 1233 1407 15 18
ENSDART00000135582 None None 93 None 2
ENSDART00000139154 Essential Splice Site 152 325 3 6
ENSDART00000144704 None None 187 None 3
ENSDART00000147245 None None 124 None 3
Genomic Location (Zv9):
Chromosome 2 (position 45425575)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 45517241
GRCz11 2 45370239
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAACTTAGCAGACAATGAGAGCATCCAATCAGATAAGAGAACATCCAG[G/A]TGAGACTGTGGCTAATTTACTGTAAAATATCATTCAAGTACAATGACAGT
Long Flanking Sequence:
TATATATATATATATATATATATATATATATATATATGTATATGTATGTATATGTATGTATGTATGTATATATATATATATATATGTATGTATGTATGTAAAAATACACACACACACACACACACGTGTATATATAGACAATTTTTACAATTATTTTTACACTGTAAATTTAAAAAATAATAGCAAAATTAATTTAACAAATATTGCACATTTTGTGTCTTGAAGCATTTCCAAAGTTTTGTTCTGTTTATAAGAACTATTAATTTTAACCTGTGGGTACATCTTTTTTTAAACTGTATTAAAACTATACACTCAAAAAAGTATGAATATTTGCCACAGCAGGCTAAAAACAGGAAAAAATGTGTATATGATAATGCGTAAAATTGTGTCTTTATGTGTCCAGGGTCACGTCCTCGTGGATATTCTGTGTCCAGCATATCACTCGCCTCCCTGAACTTAGCAGACAATGAGAGCATCCAATCAGATAAGAGAACATCCAG[G/A]TGAGACTGTGGCTAATTTACTGTAAAATATCATTCAAGTACAATGACAGTTTCTACTGAGACCTATTGAGTTGTTATATTAATCAGTACTAGGTCCTAAGTTCCTAACACTGTGTGTGTGTGGTGTGTGTGTTTTCTCTGTGCTGGTTGCTCAGAGGCAGCAGACTGTCTCCTGGTAGTCTGTGTTTCTTTCTGAGCTCTCCTAAAGGGAGAAAGGGAAGGTCAGTTTGCGGACGGCATCACATTCATATCATCAGCTCACAAGGGCTGATCACTGTCATTTCAGCTTCAGTGATGGACAAACTCATTCGCTTTTTACAGATCACTTCACTCGTTGATCAGCTGTTGTATAATCATTACTTCGGAATCATTTATGTGATAAAACTATGAATGGGACATCGTACAGCTTTGCAGTTCTTGCTTACGTAATTTATTTATTTATTTTGCTGTTTGTTGTTGGCTTTCTTATTATTTTTTGCAAAAAACAGCTCATCTTTTAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33017
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083957 Essential Splice Site 1269 1407 16 18
ENSDART00000135582 None None 93 None 2
ENSDART00000139154 Essential Splice Site 188 325 4 6
ENSDART00000144704 None None 187 None 3
ENSDART00000147245 None None 124 None 3
Genomic Location (Zv9):
Chromosome 2 (position 45429620)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 45521286
GRCz11 2 45374284
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGGAGCTGGAATCAACATCATCCGCAGCATCTAACACAGAATACACAG[G/A]TAAGATGACAGTCCTGCAGTATTATATGAACCTATTATATTCCATCTGAA
Long Flanking Sequence:
TCTTTTCACAATTTTTTGAAAATCAGAAAAAATAACGGGACTAAAACTTTAAATTTTAAACGTTAAAACTATTCAATTCTATTCATTAAATAATTTGAGAACAAATGGGGCCCCCTGGTGGTTTGGAGACCTTAAGAATATTGTGTACATTGTAAATAGGGAGGCATAATTAAACAATGCAATAAGTACACTATTTCTGCTCCATTCATCCTTTGCTTCTGTGATTTTTGCATCACGGCTTTCTGGCATCACATGTGGATTTATGCTTACTATTTTCTATTAATTTTGCAGCTTTATGGTTACCTTTTCCAGCAGCAATAAAAGCTCAAGAGTTAAATGAATATTTCAGATCTGTTTATTGTGAGTGTGTGTGTGTGTGTTCATTGTCAGGCCGGAGTCTGCAGAGGGCTTTCTGTCACCCTGTCCTTCTGTTAGTGGAAACGGGGAAAACTGGGAGCTGGAATCAACATCATCCGCAGCATCTAACACAGAATACACAG[G/A]TAAGATGACAGTCCTGCAGTATTATATGAACCTATTATATTCCATCTGAAAAAAGTTAAACTTTTATTTTGCACGCTACCAAATGTCCAAACCTTAACCCTCCTTATTAGTCTGCTCACAAAGCTTTGATGGTTTCTTTAATTCTCATGTCTTTTCTTCTGCAGGGCCAAAGTTGTACAAGGAGCCCAGTGCGAAATCAAATAAATACATTATCCAGAACGCACTGGCGCACTGCTGCCTTGCGGGCCGCGTCAACGAGGGACAGAAGAACAAGATCCTGGAGGTCACTTTAGATCTATTATGACTCAAACTTATTATTATTTTTATTGTTATTAGTAAGGGTGTCATGATCCTCCAAATCCTCGATTCGATTACATTTTCGATTCTAAAGGCACGATTCAATTCGGTTTTCGATTATGAATAATTAATTAATTAATGACCAATTAATTATTTGTAGCCTACCGTTTAAACTACCTGACCTGCATGGTCTTTGTTTTACC
Associated Phenotype:
Not determined