ZMP
si:dkey-238m4.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
CGN
Human Description:
cingulin [Source:HGNC Symbol;Acc:17429]
Mouse Orthologue:
Cgn
Mouse Description:
cingulin Gene [Source:MGI Symbol;Acc:MGI:1927237]
Alleles
There are 9 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa11671 | Essential Splice Site | Available for shipment | Available now |
| sa15682 | Essential Splice Site | Available for shipment | Available now |
| sa36111 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa12730 | Nonsense | Available for shipment | Available now |
| sa28647 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa32088 | Nonsense | Available for shipment | Available now |
| sa18067 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11671
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000077998 | Essential Splice Site | 403 | 1182 | 5 | 20 |
| ENSDART00000131657 | None | None | 763 | None | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 24724469)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 22628785 |
| GRCz11 | 16 | 22544175 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGGAACAGCTGGGGAGGAAGAACACAGAACTGCACCAAACACATTCAGA[G/T]TAAGAAGAAATACAYTTGTTTGCCATTATAAACATTCAGACATCTACAGT
Long Flanking Sequence:
GTTAGTTTGTTTATTTATTTATTTTTTTATTTTATTTTATTTTATTTATTCATTTTATATCATATGGAGGTTTTTAATACGTTAGATTTATTGTTTTGTTTTTATATTGTGTACTGCTACTTTTGTCATTTTTTTGTGATGCAGAAATTCGCCTTGGGACAAAAAAGTATACCTTAACCGAAGTATTATATCATGAAATGCTGCAAGCAGTTATTGACATTTGAAGCAGTAAAGGATAAATTGTAAAAGCACAATAATATTATGATCTCTATTTTTAAATATCCTAAACATCTTTCACCATCTAAAAGGGGAAAGTAAACGTGAGAAAATTGATATCTAATCTTATGAAGGCAGTCATATAATCTATTCTCTCTCGGATTTCAGGCAAGCAGATCTGATGACTCCTTAAAACATGAGCTTGAGAAATGTCTGGATGAAAATATCCAGCTGCAGGAACAGCTGGGGAGGAAGAACACAGAACTGCACCAAACACATTCAGA[G/T]TAAGAAGAAATACATTTGTTTGCCATTATAAACATTCAGACATCTACAGTTAATAAAACCTTCAGCATTAATTATAGTTAACCCATGTTGTTTTTGTGTGCTTTTTTTCCTCAGTCTTACTCAGTTACGTATGGACAGAGAGAACGCAGAGTCTCATGTTAGAGAGTTGGAGGATCAGCTGGCAGGACTGCAGGAGGAGCTGAGGAGAGAAACTGAAAACAAAGCTCAAGCTGACACAATGCACATGGTAATCACACACATAAGCACACACACACACACCCCAGAGAAAGGCTAAAATGGTCACAACTAACAGATAAACAAATTTATGACAAATCAAATCATTTGAATATGTTTATCTTTTTAAAACATGTGAAAGTCAAAATTATTTGCTCTCCTGTGAATTTTATTTTATTTTTTTATTTTTCAAATATTTTCCCAAATGTTTAACAAAGCAAGGAATTGTTCACAGTATTCCCTATACTATTTTTTTTCTTCTGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15682
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 |
|---|---|---|---|---|---|
| ENSDART00000077998 | Essential Splice Site | 403 | 1182 | 6 | 20 |
| ENSDART00000131657 | None | None | 763 | None | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 24724355)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 22628671 |
| GRCz11 | 16 | 22544061 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCATTAATTATAGTTWACCMATGTTGTTKTTGTGTGCTTTTTTTCCTCA[G/A]TCTTACTCAGTTACGTATGGACAGAGAGAACGCAGAGTCTCATGTTAGAG
Long Flanking Sequence:
TGCTACTTTTGTCATTTTTTTGTGATGCAGAAATTCGCCTTGGGACAAAAAAGTATACCTTAACCGAAGTATTATATCATGAAATGCTGCAAGCAGTTATTGACATTTGAAGCAGTAAAGGATAAATTGTAAAAGCACAATAATATTATGATCTCTATTTTTAAATATCCTAAACATCTTTCACCATCTAAAAGGGGAAAGTAAACGTGAGAAAATTGATATCTAATCTTATGAAGGCAGTCATATAATCTATTCTCTCTCGGATTTCAGGCAAGCAGATCTGATGACTCCTTAAAACATGAGCTTGAGAAATGTCTGGATGAAAATATCCAGCTGCAGGAACAGCTGGGGAGGAAGAACACAGAACTGCACCAAACACATTCAGAGTAAGAAGAAATACATTTGTTTGCCATTATAAACATTCAGACATCTACAGTTAATAAAACCTTCAGCATTAATTATAGTTAACCCATGTTGTTTTTGTGTGCTTTTTTTCCTCA[G/A]TCTTACTCAGTTACGTATGGACAGAGAGAACGCAGAGTCTCATGTTAGAGAGTTGGAGGATCAGCTGGCAGGACTGCAGGAGGAGCTGAGGAGAGAAACTGAAAACAAAGCTCAAGCTGACACAATGCACATGGTAATCACACACATAAGCACACACACACACACCCCAGAGAAAGGCTAAAATGGTCACAACTAACAGATAAACAAATTTATGACAAATCAAATCATTTGAATATGTTTATCTTTTTAAAACATGTGAAAGTCAAAATTATTTGCTCTCCTGTGAATTTTATTTTATTTTTTTATTTTTCAAATATTTTCCCAAATGTTTAACAAAGCAAGGAATTGTTCACAGTATTCCCTATACTATTTTTTTTCTTCTGGAGAAAGTGTTATTTGTTTTATTTAGGCTAGAAGAAAACAGTTTTGATATGTTTTAAAACCATTTTAAGGTCAATATTATTAAACCCCTTAATTGATTTGCCTAATCAATCTAACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36111
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000077998 | Essential Splice Site | 447 | 1182 | None | 20 |
| ENSDART00000131657 | Essential Splice Site | 40 | 763 | None | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 24724220)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 22628536 |
| GRCz11 | 16 | 22543926 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGAGGAGAGAAACTGAAAACAAAGCTCAAGCTGACACAATGCACATGG[T/A]AATCACACACATAAGCACACACACACACACCCCAGAGAAAGGCTAAAATG
Long Flanking Sequence:
CACAATAATATTATGATCTCTATTTTTAAATATCCTAAACATCTTTCACCATCTAAAAGGGGAAAGTAAACGTGAGAAAATTGATATCTAATCTTATGAAGGCAGTCATATAATCTATTCTCTCTCGGATTTCAGGCAAGCAGATCTGATGACTCCTTAAAACATGAGCTTGAGAAATGTCTGGATGAAAATATCCAGCTGCAGGAACAGCTGGGGAGGAAGAACACAGAACTGCACCAAACACATTCAGAGTAAGAAGAAATACATTTGTTTGCCATTATAAACATTCAGACATCTACAGTTAATAAAACCTTCAGCATTAATTATAGTTAACCCATGTTGTTTTTGTGTGCTTTTTTTCCTCAGTCTTACTCAGTTACGTATGGACAGAGAGAACGCAGAGTCTCATGTTAGAGAGTTGGAGGATCAGCTGGCAGGACTGCAGGAGGAGCTGAGGAGAGAAACTGAAAACAAAGCTCAAGCTGACACAATGCACATGG[T/A]AATCACACACATAAGCACACACACACACACCCCAGAGAAAGGCTAAAATGGTCACAACTAACAGATAAACAAATTTATGACAAATCAAATCATTTGAATATGTTTATCTTTTTAAAACATGTGAAAGTCAAAATTATTTGCTCTCCTGTGAATTTTATTTTATTTTTTTATTTTTCAAATATTTTCCCAAATGTTTAACAAAGCAAGGAATTGTTCACAGTATTCCCTATACTATTTTTTTTCTTCTGGAGAAAGTGTTATTTGTTTTATTTAGGCTAGAAGAAAACAGTTTTGATATGTTTTAAAACCATTTTAAGGTCAATATTATTAAACCCCTTAATTGATTTGCCTAATCAATCTAACTTGCCTAATTAACCTGATTAAGCCTTCAAATTGCACTTTAAAAGGCACCAATGATGAAAATCATCTTTTAGAAGCTGTTTGGACAGAACTGTGTGTAGGTATAGTGTGTCCACTGTCATATTGGGGTGATACACAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12730
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 |
|---|---|---|---|---|---|
| ENSDART00000077998 | Nonsense | 464 | 1182 | 7 | 20 |
| ENSDART00000131657 | Nonsense | 57 | 763 | 2 | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 24721252)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 22625568 |
| GRCz11 | 16 | 22540958 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGARTTGATGGCATTGAGAGCTGAATTGGATGAAGCTGCAGTGCTGAGA[C/T]AAAAGCAGGAGGACATTCAGAGGCAAAGAGAGAGGGAGCTGACGGCCCTG
Long Flanking Sequence:
GCGCGCCCAAATAGACACTCCCATACCAAGCCTCTTTTCTTCCTCCGACACTCCCCCCTAAACAGAGCTGGACACGCCCACTTTTCTGACTTTTTCCAAAGTAGAGGTGTGAAAACACACTGCTGAAACGAGGGGGTTTCATGGCCCTTTAAATCTTGAAAAGGGGGTAAAATATGTGTCCTTTTAAGCTTAATATTAGTATATTGAACAATATCTGGTAAAATATGTTATGGCAAAGATAAAAGAAGTCAGTTATAAGAAATAAGTTACTAAAACTATTATCTTTAGAAAATAAATTTCTTTGTGTTAAACACAAATTGGGGAGAAAAAGGAAGGCTAATATTTCAAGAAGGCTAATAATTCTGACTTTAACTGTACTTCATACAGTTGTCTGCTGACCAAAGCAGGTATTAAAATTTAATTTTAAAATGTTATTATTTGTTTGTGTACAGGAATTGATGGCATTGAGAGCTGAATTGGATGAAGCTGCAGTGCTGAGA[C/T]AAAAGCAGGAGGACATTCAGAGGCAAAGAGAGAGGGAGCTGACGGCCCTGAAGGGGGCATTAAAAGATGAGGTCTCCACCCATGACAAGGAGATAGAGGCTCTCAGAGAGCAGTACAGCCAAGACATGGAACAACTGCGAACAAGCATGGCTCAGGTGTCACAGGTACACATCCAATAGTTTGAAAAAAAAAAAAAAAAACTCAGACAGGTCCTGGACTAACCCCTGGGGAACACCCGTTTTAAAGCTATATAGGCATGGGAGTATTGTACATTTAAACTACTTTGTGAAGGAATCCTGTTGCACATAAGTACATCAGTATCTCTGTGTCTTAGTCTCAGGCAACTATTGAAGCCGAGCGCCACCGTGTAAACTCTACGTTAAGGTCTCTTCAGCAGCAACTGGAGGAGAGCAGAGATGAAGGAAACCACTGGAGAGAGCAGTTCCAGTCCAGCAGAGAAGAGCTGCGTAACACCAAACAAGAGTGAGTCACACTTAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28647
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 |
|---|---|---|---|---|---|
| ENSDART00000077998 | Essential Splice Site | 977 | 1182 | 15 | 20 |
| ENSDART00000131657 | Essential Splice Site | 558 | 763 | 10 | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 24713495)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 22617811 |
| GRCz11 | 16 | 22533201 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAACAGTGCAGAGATGCTGACAGAAAGAATCACCAGGAGCCGAGATCAG[G/A]TACATTATATTTAGTACACTCAACATTTTTGGGACCCAAAACTGAATATT
Long Flanking Sequence:
TTTGTTATCCTGCTATATTAATGATTTTTCAGCTGGGCCGTGTAAAGAAAGAGCTGTTCTCCAGTTATGAGGAAAGAGACAACGCTTTATTAGACAAAGAGATGCTCACCAACCGCCTCAAACATCTGGAGAGTGAGATGGAGACTCAGCGCAACACACAAAACGACCGCTCAAGAGAGATCCGCAGTTTAGAGGTGTGTTTGTATGTGTGTTTGTATGTGTGTTTGTATGTGTGTTTGTATGTGTGTTTGTATGGTGCTTGTGTGTGTGTTGTGTTTGTGTGTTTGTGTTGTGTTTGTGTGTGTGTTGTGTGTGTGTGTGTGTGTTGTGTGTGTTTCACATTCACATCTGCTGTCTGGGAGATCAGAGTGATTCTCCTGACTATATGTCATGTTTGTCTCCACCTGCAGGACAAAATCAAGCATTTGGAGCTCGAGTTGGATGAGGAGAAGAACAGTGCAGAGATGCTGACAGAAAGAATCACCAGGAGCCGAGATCAG[G/A]TACATTATATTTAGTACACTCAACATTTTTGGGACCCAAAACTGAATATTCAGTAATTTATTCATCCTGCACTTGTTACAAGCCTATTTGAGTTTCTTTTATTCTGTTGAACACTAAGGAAGATGCACTGAAGAATGTTGGGGGAAAAACAGCCATTGACCTCCATTGTATTTAGTTTGTTCTTGCTATGGATGCGAATGGCGGCTTTTTTCAACATACTTCAAAATATATTGTTTTGTGTTCAACAGAAGAAATTTTACAACCAGTCAGAATTGAAATTTTTGGATAAACTAGCCCTTTATCAGTATACACTACCAGAGAAAAGTCTTGTCGTTGATCCCAGTTGTAAGAGCAACAGATAATAACTTGACTTCTAGTTGATATTTTGGAACAGTAGTAGAAGGTCAATTTTTTTTTTTCCTCAATGAATCATCTGTTGAACTCCATCCTAAACATCACAAATACTGCAGAAGACCTATTGAAACCCCCATGGATCCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32088
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 |
|---|---|---|---|---|---|
| ENSDART00000077998 | Nonsense | 980 | 1182 | 16 | 20 |
| ENSDART00000131657 | Nonsense | 561 | 763 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 24711434)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 22615750 |
| GRCz11 | 16 | 22531140 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCACATTGATGCAATGTTAATGTTTTGATATAATCTTCTGTAGATTGAA[C/T]AGCTGCGTGCAGAACTCATGCAAGAGAGATCCTCCAAACAAGACCTGGAG
Long Flanking Sequence:
TAAGCACTTGACAGTGTTTGTGGAAAATGCTCTTCATGTTATTACAAAAACAAGCATGTGTTGTTAGGAGTGCCAGTGGAATATAAAGCTAAAGTACAATAGGTTGGTTTGTGTACACAGTTTGAATGTAGAGGTCATCAGGAACAGCAGCAAGGAGTAAAGCTGTGCTTGTCAGCTTTCTTCAGTATTTGCATAAGATGTAATGCCTCATAAGATGTAATAATCCAGACAAATGGCAATGTTGTCATGACATAACACAACATCTGTATTGCATAACCATTTTTCGTTGCTGTTTTTGCAGTATTCCTAACACCTGCAGCATCATGGCAAGACAAACTAGATATGGACACTTGCAATGTACTGTGGATAGTCAGACATTCAGATTGAAGTCACATACACAAATAATGGAATTTGAACCGACAATCTGAACAGAAGTGATTAGTAAATGATATCACATTGATGCAATGTTAATGTTTTGATATAATCTTCTGTAGATTGAA[C/T]AGCTGCGTGCAGAACTCATGCAAGAGAGATCCTCCAAACAAGACCTGGAGCTAGACAAAAACGCTCTGGAGAGACAGGTACATTATATAACTGCTGAACAGTTTTATAGATTCATCTCGTACTGTATGCTGCATTTTCCTTGCCTGAGTTTCTGTGCGAACACGTGATAAGAGTTAGGCTCGTGTAACTTCACGGTGCTTTAATTCAAATTGGCCACAGGGTTTCATTTAATCTGCTTTATTTTTTTTTCTTTCAGATAAAGGAGTATAAGACTCGTGTAGCTGAGATGGAAGGCCAGTCACGTTCCTCCACTGGTGTCTCACAGCTGGAGAGCAAAATCCAGGAACTCGAGGAACGACTGCGCACAGAAGAGAGGTTAAAAAAAGACTTTTGAACTGCAGATTTTAACCCACTAACATGAAGTGGCAGAAACAATTACATTACTCACAAAGTACTGGAGAACGCTTGAGAAAAGCACTTTTCTTTAATTGAAAGCACTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18067
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 |
|---|---|---|---|---|---|
| ENSDART00000077998 | Nonsense | 1019 | 1182 | 17 | 20 |
| ENSDART00000131657 | Nonsense | 600 | 763 | 12 | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 24711138)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 22615454 |
| GRCz11 | 16 | 22530844 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTCTTTCAGATAAAGGAGTATAAGACTCGTGTAGCTGAGATGGAAGGC[C/T]AGTCACRTTCCTCCACTGGTGTCTCACAGCTGGAGAGCAAAATCCAGGAA
Long Flanking Sequence:
TGCAGTATTCCTAACACCTGCAGCATCATGGCAAGACAAACTAGATATGGACACTTGCAATGTACTGTGGATAGTCAGACATTCAGATTGAAGTCACATACACAAATAATGGAATTTGAACCGACAATCTGAACAGAAGTGATTAGTAAATGATATCACATTGATGCAATGTTAATGTTTTGATATAATCTTCTGTAGATTGAACAGCTGCGTGCAGAACTCATGCAAGAGAGATCCTCCAAACAAGACCTGGAGCTAGACAAAAACGCTCTGGAGAGACAGGTACATTATATAACTGCTGAACAGTTTTATAGATTCATCTCGTACTGTATGCTGCATTTTCCTTGCCTGAGTTTCTGTGCGAACACGTGATAAGAGTTAGGCTCGTGTAACTTCACGGTGCTTTAATTCAAATTGGCCACAGGGTTTCATTTAATCTGCTTTATTTTTTTTTCTTTCAGATAAAGGAGTATAAGACTCGTGTAGCTGAGATGGAAGGC[C/T]AGTCACGTTCCTCCACTGGTGTCTCACAGCTGGAGAGCAAAATCCAGGAACTCGAGGAACGACTGCGCACAGAAGAGAGGTTAAAAAAAGACTTTTGAACTGCAGATTTTAACCCACTAACATGAAGTGGCAGAAACAATTACATTACTCACAAAGTACTGGAGAACGCTTGAGAAAAGCACTTTTCTTTAATTGAAAGCACTCCACATTGCTAGAAAATACACAGACTGCAGTCTTCAAAGTAGATTGTGAATACTTCTACTTGTTTGCGTTTTGTCAGTTGTGATTTTTTTATTAAATTGGCAGAATCTAAATCTGATCAAGTATCAAATATAACTCCTTATAATGTCCTGATGTATCACTGATATATTTGTGAACAAATTAACAAATCATATTGGAGATCATTTAGTTGTATAATATGTCATAACCAAACACTACACGCAAGGGCTGCAAGATAAATCAAAATTAAAGGGCACCTATGATAAAAATTCCCTTTTAGA
Associated Phenotype:
Not determined