ZMP
cadps2
Ensembl ID:
ZFIN ID:
Description:
Zgc:110135 [Source:UniProtKB/TrEMBL;Acc:Q568R8]
Human Orthologue:
CADPS2
Human Description:
Ca++-dependent secretion activator 2 [Source:HGNC Symbol;Acc:16018]
Mouse Orthologue:
Cadps2
Mouse Description:
Ca2+-dependent activator protein for secretion 2 Gene [Source:MGI Symbol;Acc:MGI:2443963]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12715 | Nonsense | Available for shipment | Available now |
sa6001 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa25229 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24694 | Nonsense | Available for shipment | Available now |
sa24695 | Essential Splice Site | Available for shipment | Available now |
sa24696 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12715
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 |
---|---|---|---|---|---|
ENSDART00000023890 | Nonsense | 261 | 396 | 4 | 6 |
ENSDART00000103500 | None | None | 255 | None | 11 |
ENSDART00000112076 | Nonsense | 131 | 1155 | 3 | 37 |
Genomic Location (Zv9):
Chromosome 25 (position 28986069)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 27676163 |
GRCz11 | 25 | 28119365 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTGTTTTGTGTTTCCYGTGCAGCTKGACAATGTGGACGAGCAGGCAGCG[C/T]AAATYCGCAGAGAGCTGGACGGGCGACTGCAGCTGGCTGAGAAAATAGCC
Long Flanking Sequence:
AGAGGAGCTTATCAAGTGGAAACAGTGCTAAAGAGGGGGTGGTGTATGTGTGTGTATCTATGTGTGTGTGTGTGTGTGTGATACACAGAGATTTCCCACTCATAGAGAGGAAACCCTGTCTTGACAACATGCCAGCGGTGCTGTGTGGGTGTGTTTGTGTGTCACTTTCTGTGTGTGTGTGTTTCACACTCCAAAAACGCTTCATTTGAGGGCATGCCAGAGCCGCTCAGCGAACAGATAAAGACATTAAACATTTTTTTTATGATCTCATATCTTCTCAGTATGGCCCGTCCAAGTGCCATTGCTGCTTCATGAAGCTCAAAAGAGATTACATGAATAATCGGGGCAGATATTAAGCCTGTCTTTTCTGTCTTTTCACTATGGTCAGCTTTGATCTGCTCAGATCTACCTGCAGTCAATGGGTTTACTAACCATGTCGAATAGATAAGCTTTGTTTTGTGTTTCCCGTGCAGCTGGACAATGTGGACGAGCAGGCAGCG[C/T]AAATCCGCAGAGAGCTGGACGGGCGACTGCAGCTGGCTGAGAAAATAGCCAGAGTAAGAAATGTTCACCTGTTTCTGTCTTTACTATGAAAATGTAAACAGATTGTTGTCCAAATTGGGACTGCATGATACATTTAATTTTCTTGAAGAGATGCAGCTTTTTCTTACAGTATTTGTGTTTTGACAAATTCATATTTTTAAAAGGAAGCTTCACAATATTATAATTGTGCATATACATTCGATTAGTTTGTACTAAAGCCAAATCTGTAGTTTATCTAACAAAATGATTTTTGTTAATGGTCCAAAATCTAGTACAGCCAAATTATTAATGTTATAGAAAAATATTAAATGCAAATAAAAAAAAGAAAAATCAAAAGAAGGCAAAAATTTGCAAAACTTAGTTGAAATTATGTAGGTTTTATGTATATATGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTAATAAATATATATATATATTTTTTTGTGGTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6001
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:
A > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023890 | Splice Site, Nonsense | 278 | 396 | 4 | 6 |
ENSDART00000103500 | None | None | 255 | None | 11 |
ENSDART00000112076 | Splice Site, Nonsense | 148 | 1155 | 3 | 37 |
Genomic Location (Zv9):
Chromosome 25 (position 28986120)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 27676214 |
GRCz11 | 25 | 28119416 |
KASP Assay ID:
554-3842.1 (used for ordering genotyping assays)
KASP Sequence:
AAATCCGCAGAGAGCTGGACGGGCGACTGCAGCTGGCTGAGAAAATAGCC[A/T]GAGTAAGAAATGTTCACCTGTTTCTGTCTTTACTATGAAAATGTAAACAG
Long Flanking Sequence:
GTGTATCTATGTGTGTGTGTGTGTGTGTGATACACAGAGATTTCCCACTCATAGAGAGGAAACCCTGTCTTGACAACATGCCAGCGGTGCTGTGTGGGTGTGTTTGTGTGTCACTTTCTGTGTGTGTGTGTTTCACACTCCAAAAACGCTTCATTTGAGGGCATGCCAGAGCCGCTCAGCGAACAGATAAAGACATTAAACATTTTTTTTATGATCTCATATCTTCTCAGTATGGCCCGTCCAAGTGCCATTGCTGCTTCATGAAGCTCAAAAGAGATTACATGAATAATCGGGGCAGATATTAAGCCTGTCTTTTCTGTCTTTTCACTATGGTCAGCTTTGATCTGCTCAGATCTACCTGCAGTCAATGGGTTTACTAACCATGTCGAATAGATAAGCTTTGTTTTGTGTTTCCCGTGCAGCTGGACAATGTGGACGAGCAGGCAGCGCAAATCCGCAGAGAGCTGGACGGGCGACTGCAGCTGGCTGAGAAAATAGCC[A/T]GAGTAAGAAATGTTCACCTGTTTCTGTCTTTACTATGAAAATGTAAACAGATTGTTGTCCAAATTGGGACTGCATGATACATTTAATTTTCTTGAAGAGATGCAGCTTTTTCTTACAGTATTTGTGTTTTGACAAATTCATATTTTTAAAAGGAAGCTTCACAATATTATAATTGTGCATATACATTCGATTAGTTTGTACTAAAGCCAAATCTGTAGTTTATCTAACAAAATGATTTTTGTTAATGGTCCAAAATCTAGTACAGCCAAATTATTAATGTTATAGAAAAATATTAAATGCAAATAAAAAAAAGAAAAATCAAAAGAAGGCAAAAATTTGCAAAACTTAGTTGAAATTATGTAGGTTTTATGTATATATGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTAATAAATATATATATATATTTTTTTGTGGTCAATTGTCATATTGGTTACATCAGGTCAAATGATCTGTACAGGTACAAGTGATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25229
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 |
---|---|---|---|---|---|
ENSDART00000023890 | None | None | 396 | None | 6 |
ENSDART00000103500 | None | None | 255 | None | 11 |
ENSDART00000112076 | Nonsense | 597 | 1155 | 22 | 37 |
Genomic Location (Zv9):
Chromosome 25 (position 29057071)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 27747165 |
GRCz11 | 25 | 28190367 |
KASP Assay ID:
554-7661.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTTCCTCCTTGATTTGACAGACCTGACGGCATGGGCACAGTTACAGAA[C/T]GAGAGAAGGAGGAGTTTGAGGAGATCAGGAGCAGATTGTTGACTTTACTG
Long Flanking Sequence:
AACACTTCAAACAGTGAGATTTTATTTTACTTAAAGATTGTCTTTTTTTCAAAGATATTTTCAATCGTTTTTCTTTTTGCATTGTACCTTAATCTCATTTTCTAAAAACACATTTAATTTGATATTCTTTTGTTTAATGTTTTCGGTTTGTGAAACACTTCAAACAGTGAGATTTTATTTTACTTAAAGATTGTCTTTTTTTCAAAGATATTTTCAATCGTTTTTCTTTTTGCATTGTACCTTAATCTCATTTTCTAAAAACACATTTAGTTTGATATTCTTTTGTTTAATGATTTCGGTTTGTGAAACACTTCAAACAGTGAGTCAACTCATTGTTCGGTTCTGATGGCAGCTTTCAAAAATCTTTTGAGTTTTAAGGTTGCAACAGTGGATTCAAGGGCATTTGGTATGAATGAGCAGGTGTTGTACAGAATAAAGCAAACAATTGAACATTTCCTCCTTGATTTGACAGACCTGACGGCATGGGCACAGTTACAGAA[C/T]GAGAGAAGGAGGAGTTTGAGGAGATCAGGAGCAGATTGTTGACTTTACTGGAGAAGCAGATCACACATTTCAGGTAACTCGAGCTGTCACATTTCCTTCTGTCCATATACAGAGAATATTCAACAGAATCTACATCAGTTTAACTGGAGTTTAACGTATTGTCAGCTAATGGATTGCAGGTAAACTAACCAGTTGTTGTGTCGCTTTTAACCATTCGCTTTTAACCATAACAAAAATGGAAGCCGTTTCATTTTCCACTGTTTTGCTGATAATGAAACCCTTTGGAATGCAGTACAAGTGCGCCAGTTATTGCATTGGCAACATGATCAGATATTTCTGTTTTTGAAACTTCTTTTTTCTCATATTTACAATGTTAGTTGATATTACTAATTGATTTATTGGTTGATTGGTTCGATCATTTGTTCATTGAGTCATTCGTTTGGTTGTTTGTTTGTCCATTGATTTGCTCATTGATCAATTTGTTGTATTATTGATGGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24694
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 |
---|---|---|---|---|---|
ENSDART00000023890 | None | None | 396 | None | 6 |
ENSDART00000103500 | Nonsense | 76 | 255 | 3 | 11 |
ENSDART00000112076 | None | None | 1155 | None | 37 |
Genomic Location (Zv9):
Chromosome 25 (position 29118581)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 27808675 |
GRCz11 | 25 | 28251877 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCATCCCCACATGTCCTGCACGTTATTGCATGAACCCAAGGTTGACCAA[C/T]AGTGGGTAAGTGTCCATTCTACCAAACTTACTTGCATTCAAATAGGACAA
Long Flanking Sequence:
GAAATCTAATCATTCATCTCATTTCAAACTGCTTTTTAAAATTCGGATTGTTCAGACCGTTTCGAGCTGCAAATAAATAAAGAAAATGATTCAGATTTTTTCTCTCTCTCTCTCTCAGAGTAAAGCTTCATAGTTTGCTGTAAGTGGAATGCTAGGTTGCACTTTCATTTGGTCACAATAATTTGTTCTTCAGACATTAAACTGGCAGTTTGCTTGTTTTTTTTATTTTGTAATTTACTGTAAATCTCATTTCACTTGTGAAATGAGCAGGTTTCGCATTGGCTTTGTTTATCGTCTAGTTCAATTTGAGCTAATTAATGTTTAAAATCATGTTTTATTTAAAACGATGTTTTATTTATCTGATGGCTGTCCATTAACCAGCTCTGAGATTACTTTTCATTCAACTGCTTTTTTTCTTTTCTTTTTATTTATTGTCTTTTTTTCCCCCCACTCATCCCCACATGTCCTGCACGTTATTGCATGAACCCAAGGTTGACCAA[C/T]AGTGGGTAAGTGTCCATTCTACCAAACTTACTTGCATTCAAATAGGACAAAATCCAAAGTGTGCAATTAACAATCAAAAGAAGTGAATATTTGTTCATCATTAACTCACCCTCATGTCATTCCAAACCTGTATGACTTTCTTCTGTGTGACTCTTGAAAGAAAAACAAAACATTGGCTTCAATTATAAGGACAAAAACAACAACACTACATTCTTAAAATATCAAAAATGACTGGAATCTCTTGTCGGTGTTATTTTAATATAACCAAATCAGTTACCGCTTCAAATGATTCCGATTTATAAACAACAGCTCGAATTTGATCACATTCGTATTTCTTTCTCATCTTCACATCAGTGCACATTTATATGTATGAAAGCTTCTGAAATAGAAGTAAACTATTTGTTTGTGTAGTTCAGATCTTGCCTCTCTTCTGAATATCACGGTCATTGTCGCTACTACTCTTTTCCAGTCCTAACAAAACAAAAACTGGTGCTAACTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24695
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023890 | None | None | 396 | None | 6 |
ENSDART00000103500 | Essential Splice Site | 77 | 255 | 3 | 11 |
ENSDART00000112076 | None | None | 1155 | None | 37 |
Genomic Location (Zv9):
Chromosome 25 (position 29118588)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 27808682 |
GRCz11 | 25 | 28251884 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACATGTCCTGCACGTTATTGCATGAACCCAAGGTTGACCAACAGTGGG[T/C]AAGTGTCCATTCTACCAAACTTACTTGCATTCAAATAGGACAAAATCCAA
Long Flanking Sequence:
AATCATTCATCTCATTTCAAACTGCTTTTTAAAATTCGGATTGTTCAGACCGTTTCGAGCTGCAAATAAATAAAGAAAATGATTCAGATTTTTTCTCTCTCTCTCTCTCAGAGTAAAGCTTCATAGTTTGCTGTAAGTGGAATGCTAGGTTGCACTTTCATTTGGTCACAATAATTTGTTCTTCAGACATTAAACTGGCAGTTTGCTTGTTTTTTTTATTTTGTAATTTACTGTAAATCTCATTTCACTTGTGAAATGAGCAGGTTTCGCATTGGCTTTGTTTATCGTCTAGTTCAATTTGAGCTAATTAATGTTTAAAATCATGTTTTATTTAAAACGATGTTTTATTTATCTGATGGCTGTCCATTAACCAGCTCTGAGATTACTTTTCATTCAACTGCTTTTTTTCTTTTCTTTTTATTTATTGTCTTTTTTTCCCCCCACTCATCCCCACATGTCCTGCACGTTATTGCATGAACCCAAGGTTGACCAACAGTGGG[T/C]AAGTGTCCATTCTACCAAACTTACTTGCATTCAAATAGGACAAAATCCAAAGTGTGCAATTAACAATCAAAAGAAGTGAATATTTGTTCATCATTAACTCACCCTCATGTCATTCCAAACCTGTATGACTTTCTTCTGTGTGACTCTTGAAAGAAAAACAAAACATTGGCTTCAATTATAAGGACAAAAACAACAACACTACATTCTTAAAATATCAAAAATGACTGGAATCTCTTGTCGGTGTTATTTTAATATAACCAAATCAGTTACCGCTTCAAATGATTCCGATTTATAAACAACAGCTCGAATTTGATCACATTCGTATTTCTTTCTCATCTTCACATCAGTGCACATTTATATGTATGAAAGCTTCTGAAATAGAAGTAAACTATTTGTTTGTGTAGTTCAGATCTTGCCTCTCTTCTGAATATCACGGTCATTGTCGCTACTACTCTTTTCCAGTCCTAACAAAACAAAAACTGGTGCTAACTTTGCGCGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24696
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 |
---|---|---|---|---|---|
ENSDART00000023890 | None | None | 396 | None | 6 |
ENSDART00000103500 | Nonsense | 117 | 255 | 5 | 11 |
ENSDART00000112076 | Nonsense | 1002 | 1155 | 33 | 37 |
Genomic Location (Zv9):
Chromosome 25 (position 29120587)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 27810681 |
GRCz11 | 25 | 28253883 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTACAGTTTGCAGCTGTTTTAGATGGGGTGTTGTCGAAACTGTCACGATA[C/A]GACGAGGGAACATTCTTCTCCTCCATCCTGTCTTTCACGGTGAGGCCTTT
Long Flanking Sequence:
TGGCATAATAGGCCTAATAGCTGCTTAACTCAGCCCTATTGCACAGGGAGGATTTTTCCCTCTCCCGAAATATGTCTTTGTGAGGGTGTTGTTCTTTTAGGATTGCCTCGCGTTGATCCACGTTTAGCCATGGTGTTTGTTGATGTTTCTCCTTTTCTTGTCCCGCAGCAGCAGTACCACTCCAAAATCGATGTCCTGATCGATGAGGCCTTTAAGGAAATGATCTCCTCCTTGGTCTCGAAGGTACAACCATTGTTTGGGTTCTTTTCACAACATTGAGATTTGGCTTTTGAGCATTCTCCTCAGCCGGCCTTCACTCGTGACTCGTGAAACGTTACATACAGAGTGTTCCAGCATATTGTTAGATTTCCAGCGAAGGTTACTTCAGCCTTAATTGTTCATTGTTGCATTCGTGTCTGTCACGCAAACATTGATTTTTTTTTTTTTTTGGTACAGTTTGCAGCTGTTTTAGATGGGGTGTTGTCGAAACTGTCACGATA[C/A]GACGAGGGAACATTCTTCTCCTCCATCCTGTCTTTCACGGTGAGGCCTTTCTCGTTTATCACACCCCTTTTTAGGATCTCGTTTCGAACTGAATGTTTATTGAGTCAAAGATATTCAGCAGGTACTTCTTTATTGTTTTTTAAAAAAAGGTAAAAGCAGCAGCCAAATATGTGGACGTCCCAGTAAGTGTCATTTAAATGGTAGCTGTGTGCATGATGCCGGCTTGCCCTGTGTGAATATTTTTGTGCATGCTGTGTGTGTGTGTGTATTTCATTATTTACTTAGGGAAACAGATTCTCTATTCGGCTTTGCCAAGCATTTCCATCTTGCTTTGTGTTTAATATTTCAAAAAAGGCTTAACGCGTATTATTTCATCATTACTTAACACAATTACATTTTTTTTTGGTTTAATTTGTGATTCGCGGCCAAATGAAAGCGGGATTGGAGCGTCTATCAGAGCTGGCTGAGCAAGACTAATTAGCAACCCGATTGGCTTAAAA
Associated Phenotype:
Not determined