ZMP
si:dkeyp-55c8.1
Ensembl ID:
ZFIN IDs:
Description:
calsyntenin-2 [Source:RefSeq peptide;Acc:NP_001153311]
Human Orthologue:
CLSTN2
Human Description:
calsyntenin 2 [Source:HGNC Symbol;Acc:17448]
Mouse Orthologue:
Clstn2
Mouse Description:
calsyntenin 2 Gene [Source:MGI Symbol;Acc:MGI:1929897]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25875 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19831 | Nonsense | Available for shipment | Available now |
sa45114 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19832 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa25875
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 |
---|---|---|---|---|---|
ENSDART00000085675 | Nonsense | 179 | 937 | 4 | 17 |
Genomic Location (Zv9):
Chromosome 2 (position 39098281)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 39428446 |
GRCz11 | 2 | 39394085 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTATGACAGCATCCTGCAGGTGGAGGCCTGGGATCAGGACTGCTCTCCA[C/T]AGTACAGCCAGATCTGCAACTATGAGATTGTCACACAGGATACACCCTTC
Long Flanking Sequence:
AAATTCACTTTAAACACTAATTTGAGACATTATTTATTTAATTTGAGCAATTTAAGTGCAGTTAAAAGAGACTGGTCAATTTTGACAAGGAACACTAAAGTAAGAGGTGGGAGATGAACATGACAGGAGGATGACAGGAGGTTTAAAGAACTATTTTTTTATCATTAACATAAATATTTACAGTCAGACTAACCACTTGGGGTCTCAACACAGTGACTGCTTTCTGTTTTCATTAATTTCCCTTGAATGTAACCTATTAACTCAGAGGTGTTCAGAGGTGTTTTAGCAGTGCGACTTGAGTCTATTAACACCTCTGTGTTCTATAATTAACATCTCTTCTGATTGGTTGGTGTTGCAGGGCGGTGGTTCATATCCAGGTGGATGATGTAAACGAGTTCTCCCCAGTGTTCAGAGAGCCGTTGTATCGCGCCACTGTAACTGAAGGGAAGATCTATGACAGCATCCTGCAGGTGGAGGCCTGGGATCAGGACTGCTCTCCA[C/T]AGTACAGCCAGATCTGCAACTATGAGATTGTCACACAGGATACACCCTTCGCCATTGATCGAAATGGTAAGTTCTAGTGTAAAAGATGTGTAAAAAGTTCAATAAATGTAATAAATCAAGATTTCAATTTGTCAGAAGAGCAAAACGTTTGAAAACAGTACACTAATTGAAGCATTTAACTACAATTTTAAAGAGACAGATGGTGTAAATCTCACTAAATTTATTAATTGAGTTTTTATTAGTTAATCTGATGTAGTCAAAGAGAAATGTACAGTTTTCTTTAAGTTTGGGATCAGTGATAATATGGTTATGTAAAAGTGTGCATTAAACTGATCAAATATGACAGTAAAGACTTTTACGCTGGGAAAAATATATTGATTAACAGTTTCCGTATTTTGTGATTCACGTTTTTTATTTATTTATGATTGTGAATTAAATTATGGGATGTTGATCTCTGAAAATTCAACTCTACAGTTAAAGAAAGTGAGTTTTGTTGATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19831
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085675 | Nonsense | 245 | 937 | 5 | 17 |
Genomic Location (Zv9):
Chromosome 2 (position 39115301)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 39445466 |
GRCz11 | 2 | 39411105 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAGGGCGATGGAGAGCGTTCCAGTTCACATTGACGTCAAACCAGTGTG[C/A]AAGCCAGGCTGGCAAGGTCAGTGGATACTTAATCTGTTGACTTATGCTTT
Long Flanking Sequence:
TGCCATGAATGCAGATAACCATTACAAAGCCTTGTGAAATACAAAATACAGAGATTAGATGTAATTATTTTTATTCTAATTAGCAGCATTGCAAACGGTCTGGCAGATATAATCCATAATTGCTGAAACAGGGACACTAACGCTGTTGAAATTACATTTGTGATTGAAAACATTTGGCCAGAGTCATTGTATGGGAGCTTAATTATTGTTTAAAAGCATATGTTGTTGTGGTTGTATCTCAGGCTGGCAGCTGCAACGATTACAGATTGCTCTTTTAAGTTTTGCTTTCCATTTTCCACTTAGTGTGTTTAAATTTATTTTGCAAATGTTCTCACGTTTTGTGGCCTTGTTTTATTCATCTCTGCAGGCAACATAAGAAACACAGAGCGACTGAGCTTCGACAAACAACAGCACTATAAAATCATGGTGACGGCCTACGATTGTGGCCAGAAGAGGGCGATGGAGAGCGTTCCAGTTCACATTGACGTCAAACCAGTGTG[C/A]AAGCCAGGCTGGCAAGGTCAGTGGATACTTAATCTGTTGACTTATGCTTTTCACCATTCAAATTAGCTTCATATTCTGTAGTTTTCTAAGCAGCATCTTTTGCTAATATCACACTGTAGCGTTCATCCATTGCAATTATCTTTTTTTGTTGCTTAAGGGTTTTTTTTATTTTTTTGTGTGTGTGTGTGCTCTCTTTGACATTGCTTCTTGTGATTCACACTATTGTTCTGTGATTCTATTGGGGGAAAAGCGAGAAATTTCATTTAGCAGTTGTCATGTCATGTAGCAGTTGACCGACTATCATTGAGATGAATGGAAATGCTAACAAATCGGTTTCTCCAGATACTATTGACTTTTTTCTGGGGTTTCAAGGCTGCGTCTTTTTCAAAAGAAGTCTTTTGTCTTTTTTTCACAAATGTCTCAGATACCCTTCGGCAATGGTTTTCAACATGTTGAAGGTCACTGAGGGTTTTTTGGAGGTCAACTGTTTGTATTCATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45114
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 |
---|---|---|---|---|---|
ENSDART00000085675 | Nonsense | 353 | 937 | 7 | 17 |
Genomic Location (Zv9):
Chromosome 2 (position 39138409)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 39468574 |
GRCz11 | 2 | 39434213 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACAGACAGTGGCCGAGACAGTGACCTCATCTTCCGATTTGATGGACGA[C/T]AGGCAGCCAACATCCCAGATTGGGTTGTGCCACAGAACCTGACAGATCAG
Long Flanking Sequence:
GAAAGTTTATTAAAAACAAGAAATATTTTTGCGGATTTAATTAGGACATATGCTTTTCAAGCACAAACTCAAACTCTCTTTCCCCACGTGAGCACCCTAGCTTATCGAGTGTTGCTAGGCCGCGACTCTGACAGCAGTGAGTTTCATAATGAGACGTTTGCTTTCAGAAATGACATTTCAGTCAGGCTTGAATGTGGGTCCTGGAACCAAATGTTATTTGCTTTTCATCTCTAATTTGATTTGAAGTGTGCTGTATGCACAGTATATTTGAATGCCAGGGCAACTAACATGATTTTAACTCTTTATGACAGACAGCTTGTAATTTTTCATCACTGCCTCTTGAAGTAACCTGAACTAACCTCAGTGCTTTTATCTCTGCAGGAGCAGCCTCGGGCAGCACAGACCTTCTCCCGGCTCCTAGCACATCCACCAATTGGACGGCATCCCTGCTGACAGACAGTGGCCGAGACAGTGACCTCATCTTCCGATTTGATGGACGA[C/T]AGGCAGCCAACATCCCAGATTGGGTTGTGCCACAGAACCTGACAGATCAGTTCACCATAGCAACATGGATGAAGCATGGGCCGAGTCCTGGACTGAGAGCTGAGAAGGAGACGTTGCTCTGTAATTCAGATAAAACTGGTGAGTTATGAAGACTGAATAGGACTTTAAGAGGGCCATGGCCTTTGATTAAGTGGTGGATAAGTGCACATTCTTCTTTTCTCGTTAGGTTTAGGTCTTTTTTAAGTTTTGAAAAGAGTTTTTTTTTTCACTGTAACAAAGTATTACATTTAAAAACAGTCTTAAAAGTCCAAATATACTCATTAAGGGATGATGCTTGAAGATATTTTTTGATAAAAAAAACAGTGGCCATATACAGTATTACCATGTAGGCGCGTAACTGAGGCCAGCCAGCGAAATGCTGTACAGGTAAACCTCACTCCGCTCAACCCAAAATGGTGCTGTAGCGACAGACACTAGAGGCCATGGTCTTTAGCCTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19832
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085675 | Essential Splice Site | 399 | 937 | 8 | 17 |
Genomic Location (Zv9):
Chromosome 2 (position 39147346)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 39477511 |
GRCz11 | 2 | 39443150 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTAGTATTTGACGCATGTACAATAATGCTTCTCTGTGTTTTCTTTTCGC[A/T]GAGATGAACAGACATCATTATTCTCTGTATGTCCACAACTGCCGTCTGGT
Long Flanking Sequence:
TATTCAAAGTAAAATCTAATTTATTAAACAGTTTCACATGATCTGTCAGAAATCATTCTCTTACCAAATTCACAAGAACATTTTGATTAACAATAGAATGTTCTTTTTCTGACTATTTAAAAGTGTTAACTGTGGATTTTGGCCAGTTTAATAGGTTCCTGCTGAAATAAAAGCCTTAGTCACTATAAAATTACAGCTTTCAAACTTCACATTTTAAGAAATGCCTAGATTTTGCCTAAATTAGTCAGTCCATTCCAAGCTTAAAAATGACTTCATTTGGTTTTTCTGCAGAGCAGTACTTGTTAAATTCCTTCTGTGTCCATACGTTCCTTCTATAATCTATAAATGGAAATCTTAAATCAACATCTACCTCTTACTTTGCCAACCATTCAGAGTGATTTGTAGAAAATCCTTTTAGCAGTTCTAAAAATAATCTATGTCACCTATAAAATTAGTATTTGACGCATGTACAATAATGCTTCTCTGTGTTTTCTTTTCGC[A/T]GAGATGAACAGACATCATTATTCTCTGTATGTCCACAACTGCCGTCTGGTGTTTCTTCTGAGGCGCGACTTCATTCAGCTGGACTCCTTCAGACCGGCCGAATTTCACTGGAGACTGGAACAGGTGAGCCACACATTCATGTCAACTTCACATGCAGCCCTTGGATAAACAGGACGGGAAAAATGCCACACGGATCGGGCTCCATTTATAGTAATCACTTGTGAAGTGAAGTTCGCTCTGTATAATTTTCAATTACCTGTTTCTGAATTATTCATTATCCGTGTGACTGATCTTTCTGTTGCGATGAGTGATCTGTCACTGGTGAAATGATTATTATCAGAAGGACAAATTGGAAAGCCGACGCAAAAGACAGCGCTCACGTTTTCTCTCCCAGCGCTTATTTGCTTCATAATCAGCCTAGTTTTTGTTTGGAAACACCTTGATTTTCTCATATTTTCAGCATTTCCCTTGGCTAACGGAGAGTGCGGACTAATCTCTTG
Associated Phenotype:
Not determined