ZMP
camsap1l1
Ensembl ID:
ZFIN ID:
Description:
calmodulin regulated spectrin-associated protein 1-like 1 [Source:RefSeq peptide;Acc:NP_001038461]
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 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa43837 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa44986 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa6710 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa15817 | Nonsense | Available for shipment | Available now |
| sa1309 | Nonsense | Available for shipment | Available now |
| sa24164 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43837
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 |
|---|---|---|---|---|---|
| ENSDART00000089569 | Nonsense | 580 | 1410 | 11 | 17 |
| ENSDART00000142947 | Nonsense | 577 | 1407 | 11 | 17 |
Genomic Location (Zv9):
Chromosome 22 (position 22717102)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 22328738 |
| GRCz11 | 22 | 22353716 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGAGGACATCCAAGAGACACTCGACGAGGACTCATCCCTAAGGGATTG[T/A]ACTGTCAGCATGGAGTTTGACATGGATCAAGACTTTGAGGCGAGAGCTTC
Long Flanking Sequence:
TTTGAAATCCCATTTGATGAAGACAGTAACAACAAAACAACTACTGGCCGAGGGATGACTCGGTCTGTCAGCACTGAAGGGTTTGGTTTCAAGATGCCCCATGGAACCAGAGGCATAAAGAGAAACCTGTCCTTTCAGCCTGTCAATGGCAAGAACATGGGCATTGAGGAGGAAGGCTGTCCTGACACCCTGTCAGAAAATCATAACAGCCGTCTAAATGGCTCAGGGCCACCTAGCATTGAAGAGGCCCTTGAGATCATCCACAACTCAGAGAAAAAATCACAGAGCCCCAGGGCCCATTTGCCCAGTGAAGGCTTCTTTCTTCACCTCCAGAGTAAAAGTGAATTTAACCCCAAAGCAAAGGATAGTCAGCTAGATTCAGTATCAGAATCATCCAAAGGGGTCGCTAGCACGTCCACCACTGAAGTAGACACTGGCATTCATGTGCGGACAGAGGACATCCAAGAGACACTCGACGAGGACTCATCCCTAAGGGATTG[T/A]ACTGTCAGCATGGAGTTTGACATGGATCAAGACTTTGAGGCGAGAGCTTCTCGTAGCCAGGGCTCTACAAGCCCATGTCCCAGCAGCCTTAGTGCCAAGTCCCCTGCAGGAAGTATCCCAACTCCTGCTTTTACACCTGGGATTAAGTTGACCAGCTTTGCTGAGCAGAAATTACGCAAACTGAATCCGAACACAGAAACCAAAAGTGCTCCTTTCCAAGGCACAACACCAGATGGGTCAGATCTCGCCATTCCTCACTCCGTCTCTTGGGCTCCTTCTCCTGAAATCAGCCCTGCGCATCAACCGTCCAAGGACCCAGCTCAGGCCATGGCTGCAGAAATGGTGCAGCTGCGCATGAGACTGGAAGAGAAGCGTCGAGCCATTGAGGCCCAAAAGAAGAAAGTGGAGGCAGCCTTTACCCGACACCGTCAAAAGATGGGCCGCAGTGCTTTCCTCACAGTTGTCAAGAGGAAAGGAGTAGATGGAGCGTCACCATTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44986
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 |
|---|---|---|---|---|---|
| ENSDART00000089569 | Nonsense | 829 | 1410 | 11 | 17 |
| ENSDART00000142947 | Nonsense | 826 | 1407 | 11 | 17 |
Genomic Location (Zv9):
Chromosome 22 (position 22716357)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 22327993 |
| GRCz11 | 22 | 22352971 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTAATCATGCAGATGCGGGAGCAACAAGCTTGGGTTGTGTCACCACAT[C/T]AGCCTTCACCACAAAAGCAGGTACGAGAGCTCAGAGGGAGTGGGGCGCGC
Long Flanking Sequence:
TCGCCATTCCTCACTCCGTCTCTTGGGCTCCTTCTCCTGAAATCAGCCCTGCGCATCAACCGTCCAAGGACCCAGCTCAGGCCATGGCTGCAGAAATGGTGCAGCTGCGCATGAGACTGGAAGAGAAGCGTCGAGCCATTGAGGCCCAAAAGAAGAAAGTGGAGGCAGCCTTTACCCGACACCGTCAAAAGATGGGCCGCAGTGCTTTCCTCACAGTTGTCAAGAGGAAAGGAGTAGATGGAGCGTCACCATTTCAAGAGGACACTCCCACCTCAGAGGAGAGCAAAACACCAGTGGGGACACCCCAACCCGTCAAGTCTCCGCTGAAGTCTGCTGGTGAGGACGGCACATCTGAGGCAGACCTGATGGAATACACACGCTCCATTGAGAAGCTCAATGCTTCTCTAAGCTTCCTGCAGACTGAGATGCAGCGACTGGCCCAACAGCAGGAGGTAATCATGCAGATGCGGGAGCAACAAGCTTGGGTTGTGTCACCACAT[C/T]AGCCTTCACCACAAAAGCAGGTACGAGAGCTCAGAGGGAGTGGGGCGCGCTCTTCTGGGTCTCCCTCACCTGCAGATTCTCCTAGAGCCACACACCGTTCCCCTACTAATCTAAAGAGGAAGTCTGCCTCTTTCCACTCCAAGACACCAAGAACACCAAGACCCAGTGAGCTAAAGATTGCTCCCTTTAATAGAGTTTTGACCGTCCCACAGTCAGTAGACAGCATACCACGCCTAAGAAGATTCTCCCCATCTCAGCCCATGTCCTGCTCATTTTCATATATGGGAAACGAGAAGAAACCATTATCAACAGCTGACAAAGACATTGAACAAGGTCTTGAGGCATTGTCAATTGAATGTTCTTCTGATACTATCACCTCCCCAACCAAAGAAACCCAACAGGCTGTAACTGATGACACTGACCTGCATGCTAAAAAGGCAGAAGATGTAGAAGAGGAGAGCAGGAAGGACATCAAGCAAACAGAAAAAAGGGAAAAGCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6710
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 |
|---|---|---|---|---|---|
| ENSDART00000089569 | Nonsense | 922 | 1410 | 11 | 17 |
| ENSDART00000142947 | Nonsense | 919 | 1407 | 11 | 17 |
Genomic Location (Zv9):
Chromosome 22 (position 22716076)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 22327712 |
| GRCz11 | 22 | 22352690 |
KASP Assay ID:
554-4866.1 (used for ordering genotyping assays)
KASP Sequence:
CGCCTAAGAAGATTCTCCCCATCTCAGCCCATGTCCTGCTCATTTTCWTA[T/A]ATGGGAAACGAGAAGAAACCATTATCAACAGCTGACAAAGACATTGAACA
Long Flanking Sequence:
AGCAAAACACCAGTGGGGACACCCCAACCCGTCAAGTCTCCGCTGAAGTCTGCTGGTGAGGACGGCACATCTGAGGCAGACCTGATGGAATACACACGCTCCATTGAGAAGCTCAATGCTTCTCTAAGCTTCCTGCAGACTGAGATGCAGCGACTGGCCCAACAGCAGGAGGTAATCATGCAGATGCGGGAGCAACAAGCTTGGGTTGTGTCACCACATCAGCCTTCACCACAAAAGCAGGTACGAGAGCTCAGAGGGAGTGGGGCGCGCTCTTCTGGGTCTCCCTCACCTGCAGATTCTCCTAGAGCCACACACCGTTCCCCTACTAATCTAAAGAGGAAGTCTGCCTCTTTCCACTCCAAGACACCAAGAACACCAAGACCCAGTGAGCTAAAGATTGCTCCCTTTAATAGAGTTTTGACCGTCCCACAGTCAGTAGACAGCATACCACGCCTAAGAAGATTCTCCCCATCTCAGCCCATGTCCTGCTCATTTTCATA[T/A]ATGGGAAACGAGAAGAAACCATTATCAACAGCTGACAAAGACATTGAACAAGGTCTTGAGGCATTGTCAATTGAATGTTCTTCTGATACTATCACCTCCCCAACCAAAGAAACCCAACAGGCTGTAACTGATGACACTGACCTGCATGCTAAAAAGGCAGAAGATGTAGAAGAGGAGAGCAGGAAGGACATCAAGCAAACAGAAAAAAGGGAAAAGCTAAAGAAGCCAAAAACTGACATTAAGCCTGCAGTAGAATCTACCGTTTCTGAGGTTTTGTCGCAGATTGTAATGGAGACCGTTATTGTCACTCCCACAGAGCCATTTGACATTGCCCATCAGACCAATAAAAATCTGATTGAGGTCCCACTTTCTGTTTTAAAACCACTGGAAGGAAAGGCATTAGAAGAGGAAGTGGAGAAGGAGGCCTCTGGGGAAAATCAGGATGATGATCAGAAAGCGTGCTGTGGATTCTTCTTCAAGGTAGAGAATAATCCTGTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15817
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089569 | Nonsense | 1078 | 1410 | 11 | 17 |
| ENSDART00000142947 | Nonsense | 1075 | 1407 | 11 | 17 |
Genomic Location (Zv9):
Chromosome 22 (position 22715610)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 22327246 |
| GRCz11 | 22 | 22352224 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAAGGAGGCCTCTGGGGAAAATCARGATGAYGATCAGAAAGCGTGYTGT[G/T]GATTCTTCTTCAAGGTARAGAATAATCCTGTAGATAAATCTTMTGATTAA
Long Flanking Sequence:
CCCCATCTCAGCCCATGTCCTGCTCATTTTCATATATGGGAAACGAGAAGAAACCATTATCAACAGCTGACAAAGACATTGAACAAGGTCTTGAGGCATTGTCAATTGAATGTTCTTCTGATACTATCACCTCCCCAACCAAAGAAACCCAACAGGCTGTAACTGATGACACTGACCTGCATGCTAAAAAGGCAGAAGATGTAGAAGAGGAGAGCAGGAAGGACATCAAGCAAACAGAAAAAAGGGAAAAGCTAAAGAAGCCAAAAACTGACATTAAGCCTGCAGTAGAATCTACCGTTTCTGAGGTTTTGTCGCAGATTGTAATGGAGACCGTTATTGTCACTCCCACAGAGCCATTTGACATTGCCCATCAGACCAATAAAAATCTGATTGAGGTCCCACTTTCTGTTTTAAAACCACTGGAAGGAAAGGCATTAGAAGAGGAAGTGGAGAAGGAGGCCTCTGGGGAAAATCAGGATGATGATCAGAAAGCGTGCTGT[G/T]GATTCTTCTTCAAGGTAGAGAATAATCCTGTAGATAAATCTTCTGATTAAACACAGATTGTGTCTACTTGGTGGCGAATGTGAACTCAAGTGTCAGTATTATTACTCTTACTAATTTGAATGCAAGTTAAGTTTAGCTAATAATAATTCCTGAAATGTTTATTAGAGCATACTCATTTAAGTACAGCTGCCTTGAACCGTGCCAAAGGGCAACTGTCCCCCCTCCCCTCTCCCGATGGCCCGCACACACACTGCATCTTTATCTTACAAGTCAGGGCATGCTTCCGTCATCGATAATGGAACTGGTCAGTAGGTAGGAAGAGAAGCACTCTCGCTTCATACAGTGGCGATTGGTTTAGTTATATCGTTTTAGTTGTTTGGAATGCAGTGGCACGCAGTCAAATATTTTGACAAACAGATCCACAAATTTTTACGCTCATAAATAATCATACAAGTCATCGTGTTGAAGGTATAAGGAGGTTTGCTGAAGGTGCAACTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1309
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 |
|---|---|---|---|---|---|
| ENSDART00000089569 | Nonsense | 1122 | 1410 | 12 | 17 |
| ENSDART00000142947 | Nonsense | 1119 | 1407 | 12 | 17 |
Genomic Location (Zv9):
Chromosome 22 (position 22714479)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 22326115 |
| GRCz11 | 22 | 22351093 |
KASP Assay ID:
554-1224.1 (used for ordering genotyping assays)
KASP Sequence:
GAGAACGGGAAAGCCAGCAGAGAAAACAGCAGCTGGAGGCWGAGCATGAG[C/T]AGAAGAAAGAGGAGGCTAGGTAAGAGCCAGCTCAGCTGTCAATCAAAGAG
Long Flanking Sequence:
TTGCATTCACACCACAAACGTACTACGCCAAAGCCCAACTGAACCGTGCCTGGGCTCGATTTGAAGCACTCACGCTTGTCTAAGGAACCTATAAAAGCGTCTAGTCACAGTTCGGATAGAATAGTGTAAGTGCACCTTTGAAATGTGCAGTCATAGAAAGAGGTTACCTCAGGACAGTTTGCTGGAAAATGCAGCTGTCTTATCCAGGTCAAACTAAATCTGAGGCAAAGAAATAATTTATGATGCTAGCTTTCTGCAGGGACTCTGAGCAGTGTAGCTTATTTAGCTTATCAAGACTAGTCACATCAGCAACAGTAAGACAACAGAGATGATTGATTGATTGATTGATTGATATAATTTTTATAATGTGTTTATGTTGTCAGGATGATATGAAGGAAGAGGACAGCATGGCCTTGAAGCGAGCAGCACTTCTGGAGAAAAGGCTGAGAAGAGAACGGGAAAGCCAGCAGAGAAAACAGCAGCTGGAGGCTGAGCATGAG[C/T]AGAAGAAAGAGGAGGCTAGGTAAGAGCCAGCTCAGCTGTCAATCAAAGAGTCTAAACTCTTGCCCCCTAATTCTGAACTCTAATATATGTTTTTCTCCACAGGTTAAAAGCAGAGGAAGAACGCCTGAAGAAAGAAGAAGAAAAGGCTCGGCGAGAATTTATAAAGCAGGAATACTTGAGGAGGAAACAACTGAAACTGATGGAGGACATGGACACGCTTGTCAAACCGCGGCCTACAGGAGCAAAGCAAAGAAAACCACGGCCTAAGTCCATCCATAGAGATGTGATGGAGTCCCCTAGGACTCCTGTCAGGGCCACAGCAGGTAGAGGGTGACCCCCTACTGGCATAGCCCAGTACTGCATGCTTTGTGCTACTCTCAAGCCTTTCCTTTTCCAGCTCGTCTGCATTTCCTTCTAACTTTACTTGCTCAAAATATCTTCCATTCTAACCAGTTTACATATTGTCTGACTAATCTAACAAAGCAGTTCTAATTCCAATC
Associated Phenotype:
Normal
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa24164
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089569 | Essential Splice Site | 1232 | 1410 | 14 | 17 |
| ENSDART00000142947 | Essential Splice Site | 1229 | 1407 | 14 | 17 |
Genomic Location (Zv9):
Chromosome 22 (position 22712740)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 22324376 |
| GRCz11 | 22 | 22349354 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTCTCTTGGAGATAATGACAGCGTCAACTCCGATAAGAAAACACCCAG[G/A]TAAGAGCCAGTTAGGCAAAAAGAATATTTATTTCCTGTTTCCCAGCAATT
Long Flanking Sequence:
AGGCTTGAATTAACTCCACAACAAATACATCAAATAATCATTGGGAAAGTTCTTACTGTAGTATTTTTCTCAAACGTTACGTGTGATCTGCTACTTTCACGTCTGTCAATGTGCTGTTTATCTGATGCAGCTGAGGCAGAGATTGAGGCACACTCTGACAGACACAATGTTCTGAAAGGTATAATAAATAATCTGATGGGTGTTTTGAGCTGAAATTTAACAGACACATTCTGAAGACACAAAAGTCTTATCTTAAATCTTGAACAAGGGGTAAAATAGTTGCCCTTTAAAGAAGTTTGCAAGATCATTGCAGAGAGCTGTACTGTTATGAGGGTAACACAAAGTTCAGTGGGCTTGCTGTTGTTTTGTGTAACTGTGGGTCCTGTCCCGTTTTGTGTTTTGAATGCAGGTTCACGACCTCGTGTTTTTTCAGTTTCTAGCCTGTCTCTGGCTTCTCTTGGAGATAATGACAGCGTCAACTCCGATAAGAAAACACCCAG[G/A]TAAGAGCCAGTTAGGCAAAAAGAATATTTATTTCCTGTTTCCCAGCAATTGTATATATTTCTGCAACTTTACTGTACAATACTAACCTTGTATACTTGAATCTTCTGTATTTTTTCCTTCATGTTCTTGAATGTTCTGGCTTCTTAGAAGCAATAGCTTAGCATCTGGCAGTCTTTTCTTCTTTTTGAACTCTCCTCGTGTGAGAAATAGAAGGTCAGTCGTAGTCGGATAAGACTTTTTGTGCTTCAATCTTCTGTTCAAGAAGATCATCCTATTTTGCTTTGAGTTCGGCAGCGACACGAGGAATGATCCCCATCTTTGAGCAATAAAGATGGCTACTGTAGTTTACCCATCACTGCTTTTTTGGTTTTATTTTTGTCATTATTAAACTAGCAGATGTTATAATTCACTAACTGGCACTGAATGGCACTGAAACAAAAACTACAATAAAGATCTGCACTTCACACTCTTGTCAGAAGCTTTTAAAAGATACAAAATTA
Associated Phenotype:
Not determined