ZMP
cnst
Ensembl ID:
ZFIN ID:
Description:
consortin, connexin sorting protein [Source:RefSeq peptide;Acc:NP_001020712]
Human Orthologue:
CNST
Human Description:
consortin, connexin sorting protein [Source:HGNC Symbol;Acc:26486]
Mouse Orthologue:
Cnst
Mouse Description:
consortin, connexin sorting protein Gene [Source:MGI Symbol;Acc:MGI:2445141]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45710 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43491 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16439 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45710
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 |
---|---|---|---|---|---|
ENSDART00000062761 | Nonsense | 84 | 398 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 20 (position 35032063)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 35104576 |
GRCz11 | 20 | 35007455 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCATGCGGTGATCTCTCTCTTTCTGTTCAGAGGGTCTTCCTGGGATTT[T/A]GGCACCTGGACCAAGTCCTTCTCTTCTGGCTTCACTGCATGCTCTGGTTG
Long Flanking Sequence:
CCTAAAACAAGTAATTTTGTGTAACTTAGTAATCCTATTTTAGTAAACACACACTTGTATACAGTATATGGTTTATGATACTTTCCATGGGCATCCTTTATATTATACTGTAAAAGCCACTTATTATTACATGGCCTAACCTTACCTTATATGGCCTCACCCCTAAACCCAACCCTCACAAAACCCTGTGGCAAATATGATTGTAAAAAGACTCTGTTAAATATGTTTTTTTATGTTTTTAGAATTACGAGGACACCAGACATGTCCTCGTAAACCACCTTAATAATGTAACACCAAGGTCATACCCATCTCATTACAAATTCTTTTGTCCTCGTAAACCACATAAACAAGTACACAAACAAAAACACATCTTTTATTTTACAGTGATGGTCAAAATCCACCTGCTTTAATAATGTGCTGAAGTAATAATTCTGCAGTGTTTGTGACTTTTCTCATGCGGTGATCTCTCTCTTTCTGTTCAGAGGGTCTTCCTGGGATTT[T/A]GGCACCTGGACCAAGTCCTTCTCTTCTGGCTTCACTGCATGCTCTGGTTGAACACAATGATCACATGCTCCTTCCACATTCCTTACACCAGGTGTGTGTGCTTTGAACGAGTTAATATGAATTAATGTTTCTCTTTTCAATTCAGATGTTTGTTCTATTTTGACCGTAAGTGCCATGCAAAGTTGACTCCACAACATATTTCACCATGATTTCAGTTTGAAGGAAGCATATATGTTTCGTTCAGATGGTATTTCATTGTGTGATACATTCAAAAAATAATATTTCATAGTTCAAACTATAACTTAGGATGCTTTCACACCTGCCTTATTTAGTTCGATTGAATCGCACTAGAGTTTGTTTCCCCTTTTGGTACGGTTCGTTTGGGCAGGTGAGAATGCAGCAATCGTACTCTAGTGCGCACCAAAAGCGGACAAAATAAGCGTACCGAGACCTGCTTGAAGAGGTGGTCTCGGTACGTTTTCAAACGAACCCTGGAGCGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43491
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062761 | Essential Splice Site | 200 | 398 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 20 (position 35024878)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 35097391 |
GRCz11 | 20 | 35000270 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAATAATCTGACAAAACTTTCTTTCAGACCAAACCTCTCTGTGCAAAAG[G/A]TAAAACATTACAACTTCCTTATTCTCCTCCAATGCATTTTATTTTCTCTT
Long Flanking Sequence:
TGTTTTAATCAATTTTGTTTAAATGCACCAAAATACATGATTGTGTATGGGTATTTCCCAGTGTTGTTTCGCAACTGGAAGGGCATCCGCTGGGTAAAACATATGCTGGATAAGTTGGCGGTTCATTCTGCTGTGGTGACCCCTGATTAATAAAGGGACTAAGCCAAAAAAAAATGCATAAATGAAGAAATTATAATTTTTGGGATTAGATACAGAACAAATCACTGCCACTCTAATTAACTTAATTGGACTAGCTGAATTACTTAATTTAGAATTTTAAGCTAAATCCTAGTGTCTTGCAAAAAAAGCTAAATATTATTTACTGTCATAATAGGGAAGACAAAATAAATGAGCTATTAGAAATGTATTATTAACACTGTTATGTTAAAAAAAATTGCCTTCTGTGTACATACAGAATTGTAAAAAACAAAACGAAAATCCATCTCTCCATTAATAATCTGACAAAACTTTCTTTCAGACCAAACCTCTCTGTGCAAAAG[G/A]TAAAACATTACAACTTCCTTATTCTCCTCCAATGCATTTTATTTTCTCTTTCTGTGAGTGTGATCGAAGTGTCTGTTGTTGCAGAACATGGAGGCCGTAAAACTGCGAACTAGCCCAACCCATGAGACTGAAAGCAAATCAAAACAAGAGCAAGCTTCAGTGAACCAGATCTCACTGGAGGCTGAATGCGAGCCAGAAGATGATGGCGAGTTCAGTGAGGAGGAGGAAGAGGAGGATGAAGGTCTCGAGGAGGACGAGTGCTGGAATGAGGAGCTACAGGAGGATACGGAGCTCCAGACTCCTGTGGACGAGTTGGACAACCTCATTCAGGTAGAAGAGGTACGCCACCACAGGAGCCATGTTAATCTCTCTCTTATTACCATCTGCCTTGAGAAAAAACAAGCATGCTGAGACACCATCCGTCTGCTGCAGTCTCAAACAAACCAGAGCTGGGTAATGATTCAGATGTCCTGATTCCATTCCTATTCACAAGCTCTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16439
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 |
---|---|---|---|---|---|
ENSDART00000062761 | Nonsense | 380 | 398 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 20 (position 35016425)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 35088938 |
GRCz11 | 20 | 34991817 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGTACTCGAATGTGTGCATCGACTTCTCTCAGAACATGGACTTTTACTTT[G/T]GACCTGTASGACRAACAGTGRCTGCTCTTACACAGTGGTTCACTTCTGGT
Long Flanking Sequence:
AATTACCCTAACTTGCTTAGTTAACCTTATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGTCTTGAAAAATATCTAGTAAAATATCATGCGCTGTCAGCATTGCAAAGATCAAATAAATCAGTTATTAAAAATGAGTTATTAAAACTATTATGATTAGAAATGTGTTGATAAAATCTCTCATTTAAACAGAAACTGAGAAAATGAATAAACGAGGGGCTAATAATTTAGGGAGCCTAATTATTCTGACTTCAACTGTTTTATACTGATATATATTTGCACAAACGATTGAAATATCTACTTTAAGCAAATTTTTCTCATCTCATGCACACAGAAGAGTCGGCCAGAGCGTCCTGCCTCATCCTTCTCCTCATGTGTGTGGTTACGGTGGTGGTCAGTCTGGGTGGGACGGCTCTCTATTGTCTGCTTGGAGAAGCGTACTCGAATGTGTGCATCGACTTCTCTCAGAACATGGACTTTTACTTT[G/T]GACCTGTACGACGAACAGTGGCTGCTCTTACACAGTGGTTCACTTCTGGTGCTTCATAGCAGCTGCTTCAAGCTAACATAAGTGGAACTCTGACTTTCTATACTAATTTTCCGATGATAACAGTATTTCTGTTGAAAAAAATATGCACTAATGCACAATACCAGACTGGCCTTATTAAATGTTTCTTTAGAGAGTCACACAGGGCTTCCTAATGCATTATTACATTTGTGTAATGTGTTTAATATTGATGCCAAAATCTGTGTTTTAACCTTCGGGTGTTGTTCATTCAAAAGAAACTAAATGATGGTTACCGCTACATTTATTCTTCTATGGCGGGGTGTCACAAAAACATTCAATCCCACCACAGCTACACGGCTACAGCTTCTCATTCAAAACCTTCAGTTGTTGCAGTTGTTTTAAATAGCAGGTTATAACCGCGCAAAAACATATTAAAATGTAAGTGAATTATAACAAAGCAAACTTTTCTAGAATCATAGTAG
Associated Phenotype:
Not determined