ZMP
cbln1
Ensembl ID:
ZFIN ID:
Description:
cerebellin 1 precursor [Source:RefSeq peptide;Acc:NP_001002520]
Human Orthologue:
CBLN1
Human Description:
cerebellin 1 precursor [Source:HGNC Symbol;Acc:1543]
Mouse Orthologue:
Cbln1
Mouse Description:
cerebellin 1 precursor protein Gene [Source:MGI Symbol;Acc:MGI:88281]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13627 | Nonsense | Available for shipment | Available now |
sa10043 | Nonsense | Available for shipment | Available now |
sa45635 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13627
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 |
---|---|---|---|---|---|
ENSDART00000079926 | Nonsense | 76 | 158 | 1 | 4 |
ENSDART00000145342 | Nonsense | 77 | 190 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 18 (position 17763906)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 18115672 |
GRCz11 | 18 | 18104738 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTTTCCGTGGTGAGAAACACGAACCACGAGCCGTCGGAGATGAGCAAT[C/T]GAACTATGGTGATCTACTTCGATCAGGTACAGTTTCAGTATGGAAAGAGG
Long Flanking Sequence:
TATCAATAATTGAGCGCGCGAGCAGACGGACCCCACGCGCTATGTATTCTACTGCGCGCGAGCAGGGAAAGGGCCTTGATCCGCTTCCAGTCGGCTCTTCTACTACGGACTGAAAGGGAACGAGTGGGGAAACTGTTTTAGTCTTAACTTGAACTGTTTGGAAGGACTTCATTGTACAGTGAGGACAGGTGTGGAGTGTTTTTGGTTCGGGATTTGAGCGGGCTGTGTTGTCTTTGAGAGAAGACTGCTGTTAGGTGCGGAGCGAAGTTGGCATGATGTTGACGTTGGTGCTCGGCGCAGTGTGGTTAGTGTGCCATGCATACGCACAGAACGAGACAGAGCCCATCGTATTGGAGGGGAAATGCTTGGTCGTGTGCGATTCAAATCCCACCTCAGACCCCACTGGGACGGCTCTTGGGATATCGGTGCGCTCGGGAAGCGCCAAAGTGGCTTTTTCCGTGGTGAGAAACACGAACCACGAGCCGTCGGAGATGAGCAAT[C/T]GAACTATGGTGATCTACTTCGATCAGGTACAGTTTCAGTATGGAAAGAGGCACGTGTTTTGTTTAATCTTACTTTTGACGCGTTGGGATCAGTGGGATGTTTTTTTGTGTCACGGTTACAAATGCAAACCAGATCGCAAAATCAAAGAAATATCGCAGCAATGAAAGCTTTAACTGATACGTGTAATCTAGGGAGATGTCACATTTCCTTCCACTTCGTTAAAGGTCAATTACAGGCTAATGGCTTTCAATTATATCTAATAGCCGTGAACTTCTTTGTCGTGTCTTAAAACTATCCTCCATCTGCTCTTGTATGTATAATCAATTGATTTGCTGCTTTGTACAAGCGAGTTTTCACTGTAAAACTTCAAGAGACAAAACTTATTGTAATAAGGCGTTTTTAAGCGATGTTTGGCTTCGATTCTGATGTCTGCATCCTCCTTCAGGTACTGGTCAACGTTGGTAGAAGTTTCGACGAAGAAAGGAGCAATTTCTTCGCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10043
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079926 | None | None | 158 | None | 4 |
ENSDART00000145342 | Nonsense | 179 | 190 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 18 (position 17768297)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 18120063 |
GRCz11 | 18 | 18109129 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGCGCCTACCTCAAGCTGGAGCGAGGCAACCTGATGGGCGGCTGGAAATA[T/G]TCCACCTTCTCCGGCTTCCTGGTCTTCCCCCTGTAGAGGAGGGGTGTACC
Long Flanking Sequence:
AAGTGTTTCGGGTGTATGGCCATACACACTCGAGAAATTTGTATTTTTTTGCTTGTTCAAACTACTTATTTAAAATAAGCTGAAACAACACAATTCTTGATATTTCATTGGAACAACTTAATTTTTTTATGTCAGATCCACATAAATTAGTTAAAAGTGTTACGTTAACTTAATCAATTTGTGTTGGGACAACATTAATGAATTGTGTGGAACCCTGCATTTTTACAGTGCACGATAAATGCGCTATATAAACACACACTACATTTGTTTGAATTCCTTCAAGCATAATTAGGTAGATTAAGCATTGGTCTCGCTAATTGAAATGCTTCCATGTTACAGGTGAGCCTGATGCACAACGGCTGGCCAGTGATCTCCGCCTTCGCTGGGGATCAGGACGTCACACGTGAAGCAGCCAGTAATGGCGTCCTGATTCAAATGGAGAAAGGTGACCGCGCCTACCTCAAGCTGGAGCGAGGCAACCTGATGGGCGGCTGGAAATA[T/G]TCCACCTTCTCCGGCTTCCTGGTCTTCCCCCTGTAGAGGAGGGGTGTACCACAGAAGGACTATTGCTCTTTAGCTCGCCGGCTTGTGGGAGAAAGAAGGGATACGAGGGCGGATGAGAGATAGAATGATAGCAAGAATGTAAAGAAAACTATATAGGAAGAGAATATTTAGTGTGGCAGGCTCTCAGTCGCACTCACTTTGCTATGCTGCTTGACTACAGCTCTGGACAGCCAAAACTTTTTTTTATTATCCTTATGATAATTGAAGTAATACGGAAAGAAAGCATACAGAGGATCGTAGCCCTATCCCACCCCTCTCTTACACATCCTATCCACACTCCTCTGCTTTAAGGATCGTCCTTCAACAGACCCCCATTTCACAGCGGTCACATCTTTGTATATTCTCTCCATACGTACATACCGTGAGTCTCAAACGCCATTGTCATTCCTCTCAGTCCAGTCGCCCCTTCTTTCTCTGGCTCACCCTTTCTTGTTTCTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45635
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 |
---|---|---|---|---|---|
ENSDART00000079926 | Nonsense | 149 | 158 | 4 | 4 |
ENSDART00000145342 | None | None | 190 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 18 (position 17768796)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 18120562 |
GRCz11 | 18 | 18109628 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCAGTCCAGTCGCCCCTTCTTTCTCTGGCTCACCCTTTCTTGTTTCTG[T/A]GAGGGCGTCTGTTCTCTGAAGGATCTCTGAATCCCCACGAAAAGACTGCA
Long Flanking Sequence:
ATTCCACCTTCTCCGGCTTCCTGGTCTTCCCCCTGTAGAGGAGGGGTGTACCACAGAAGGACTATTGCTCTTTAGCTCGCCGGCTTGTGGGAGAAAGAAGGGATACGAGGGCGGATGAGAGATAGAATGATAGCAAGAATGTAAAGAAAACTATATAGGAAGAGAATATTTAGTGTGGCAGGCTCTCAGTCGCACTCACTTTGCTATGCTGCTTGACTACAGCTCTGGACAGCCAAAACTTTTTTTTATTATCCTTATGATAATTGAAGTAATACGGAAAGAAAGCATACAGAGGATCGTAGCCCTATCCCACCCCTCTCTTACACATCCTATCCACACTCCTCTGCTTTAAGGATCGTCCTTCAACAGACCCCCATTTCACAGCGGTCACATCTTTGTATATTCTCTCCATACGTACATACCGTGAGTCTCAAACGCCATTGTCATTCCTCTCAGTCCAGTCGCCCCTTCTTTCTCTGGCTCACCCTTTCTTGTTTCTG[T/A]GAGGGCGTCTGTTCTCTGAAGGATCTCTGAATCCCCACGAAAAGACTGCATACTGGATATATACATATATAAATACATAAAAAAATTTCTATATGATTATGATATACTCAATGCCTAAATGAATCTGGTCGACTCTCTGTATTTCTGTATTTCAGTGTTAATACTTAGTGATTGTGTGTGGATTTTCAGGCTGCTGTCCAACTACCAATGCTTCTTGTTTTTGTTTCGGTCGAAAAAAAAATGTGGCTAAGATGAAACTATATCAGAAATACTATAAAGTACAAAGTTTTATTATCATTGATTGTAATATATATGTGAATATTTAGCAGACGAAATCCTCCCTTTTAATCAATTAACCATTGTTTTTTTTTTCTTTGATTCAATAAAAATTAAATGGTACTTTTTATTTTTCTTAATCTGATTCTGTGCTTTGAAATTGGAAGATCGTCGCCCGCAGGTTTTAAAGAGCAGCAAACATTAATCATTTCACTAAAACGACT
Associated Phenotype:
Not determined