ZMP
ENSDARG00000087019
Ensembl ID:
Human Orthologues:
CGN, CGNL1
Human Descriptions:
cingulin [Source:HGNC Symbol;Acc:17429]
cingulin-like 1 [Source:HGNC Symbol;Acc:25931]
cingulin-like 1 [Source:HGNC Symbol;Acc:25931]
Mouse Orthologues:
Cgn, Cgnl1
Mouse Descriptions:
cingulin Gene [Source:MGI Symbol;Acc:MGI:1927237]
cingulin-like 1 Gene [Source:MGI Symbol;Acc:MGI:1915428]
cingulin-like 1 Gene [Source:MGI Symbol;Acc:MGI:1915428]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39487 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30277 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8721 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15716 | Nonsense | Available for shipment | Available now |
sa11668 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39487
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123347 | Nonsense | 73 | 507 | 3 | 14 |
Genomic Location (Zv9):
Chromosome 25 (position 29822598)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 28512692 |
GRCz11 | 25 | 28955894 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTTGCCTCTAAAGTACATGTATTTTTAAATATTTTGGGTCTTCAGTTG[A/T]AAGAAAAGCTGTCGTCTAACCTAACCAAGGCCACAGAGAGACTACAGGTG
Long Flanking Sequence:
ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACATAGTATTTTTTAGAACAAAGCTTTTTAAAACTTTTTAAAACATCTTGCATTGTGCAAGTATGTTCTAAAAACAATAATATGCTCAGCTTCCAGAAATGATCAGATGTGCTCCAACATTAGGCACATTCAAATCAAGACTGAAAACACATTTGTCTAGCTGTGCCTTTACTGAAAGAGCTCTGTGTTCCTCTGTCTTTATCTTCTTCTTCATTCTTTAATAACCTGTTTTTAACACATTTTAATCGTAATCCTATTTACTATTTGTTTTTATTTCCTTATACTTTTCTCTTTTATTCCTGTTTATGTAAAGCACTTTGAATTGCCACTGTGTATGAAATGTGCTATATAAATAAACTTGCCTTGCCTCTAAAGTACATGTATTTTTAAATATTTTGGGTCTTCAGTTG[A/T]AAGAAAAGCTGTCGTCTAACCTAACCAAGGCCACAGAGAGACTACAGGTGACCCTTAACCAGTTACACGAGCTGGAGGCGGAGAAACTAATCCAAACCAATCAGATTACAGCGCTGGAGACTGAACGCTTGCAGCTGATTGGAGAGAAGGAGGAGCTAAGGAAAACATTTGATGATGGTCTTCATGAAAAAATTAAGCAGCTGGGAGAGAGATGCTGCCAACTCAAGTATGAATAAACAAATATTACATAATATATAGATTGTTTAATTCTATTTCTAATCTGGGTTATTCCCGTCTCAAATCAAGGAAACAGCGGGACAATCTGGAGCAAGAAAATCAGCGTCTGCAATTCAAACGTAAAGAACTGGAACAAAAAATAGAAAGCCTGGAGGCGGGGCAGCAACACAAAAAAGAGGAGGAGCATCATATGTGGGCGGAGTTTGAGCGGGAGAAGGAGGAATTAAAGAAAGTGGCAGCTCACTGGAACGAGAGATGGCTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30277
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123347 | Nonsense | 229 | 507 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 25 (position 29823146)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 28513240 |
GRCz11 | 25 | 28956442 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGATGTGGCGATGACGTTATGCTCAACTCAGGAAGAACTAGATGTGCTC[A/T]AAAGTCAACAGCAAGAGAAAGACGGAGTATGTTTTTGATTTAATCATTTG
Long Flanking Sequence:
GTGACCCTTAACCAGTTACACGAGCTGGAGGCGGAGAAACTAATCCAAACCAATCAGATTACAGCGCTGGAGACTGAACGCTTGCAGCTGATTGGAGAGAAGGAGGAGCTAAGGAAAACATTTGATGATGGTCTTCATGAAAAAATTAAGCAGCTGGGAGAGAGATGCTGCCAACTCAAGTATGAATAAACAAATATTACATAATATATAGATTGTTTAATTCTATTTCTAATCTGGGTTATTCCCGTCTCAAATCAAGGAAACAGCGGGACAATCTGGAGCAAGAAAATCAGCGTCTGCAATTCAAACGTAAAGAACTGGAACAAAAAATAGAAAGCCTGGAGGCGGGGCAGCAACACAAAAAAGAGGAGGAGCATCATATGTGGGCGGAGTTTGAGCGGGAGAAGGAGGAATTAAAGAAAGTGGCAGCTCACTGGAACGAGAGATGGCTGGATGTGGCGATGACGTTATGCTCAACTCAGGAAGAACTAGATGTGCTC[A/T]AAAGTCAACAGCAAGAGAAAGACGGAGTATGTTTTTGATTTAATCATTTGGGAAGTGTGTGGTCTTACTGTGTTTTACAAAGGACCACAAGCAAGGTCTGGAATTTTATTAAAAGTAAAGATTTCCCACTCTTTCCTAATGTTGGGATCAGACGGAAGGCAATACAAAAGATTGTATTCCATTACTTAAAGTCATCCTTATCGTTGGGCTTGTTGCTTTTATTTTTGTTTACCTGTTGAATACATGAAATGGTTGGCGGAGCTAAACTGTGATGTAGAAGTTGGTATTGATCATCTGTGGAACCGTATTTAGCCACAATCTCAGGTAGTTTCAGATCAAGTTTAATTTTTAATTTTTAATATTTTGGAAGCCATTAGCCACTGACATCCAAAGTAGGAAAAATAAAACTGTCTTACAGCAAGAGGCTGATGTATATATGTGTGTGTTTATAAATTTATAATGCATTTAAAGGTGGTTCTTTCATAATGTCAGTTTGTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8721
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123347 | Essential Splice Site | 272 | 507 | 6 | 14 |
Genomic Location (Zv9):
Chromosome 25 (position 29823865)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 28513959 |
GRCz11 | 25 | 28957161 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTKAAATYCTGAAGAAGGAYGGACATCAGATTTTTTYCCCCATGTTTTTC[A/T]GGAGTCACAACAGAGTRATAAAGTCCAGAARCTGGAGAAGCTGCTCTCAA
Long Flanking Sequence:
TTATTTTTGTTTACCTGTTGAATACATGAAATGGTTGGCGGAGCTAAACTGTGATGTAGAAGTTGGTATTGATCATCTGTGGAACCGTATTTAGCCACAATCTCAGGTAGTTTCAGATCAAGTTTAATTTTTAATTTTTAATATTTTGGAAGCCATTAGCCACTGACATCCAAAGTAGGAAAAATAAAACTGTCTTACAGCAAGAGGCTGATGTATATATGTGTGTGTTTATAAATTTATAATGCATTTAAAGGTGGTTCTTTCATAATGTCAGTTTGTAACAATGTAAGTACTGTTAATGCTCAAACTTTCTTCATAGGTGTCTTGTGAAGACCTGAATGGAGAGCTGGAGGAGGAGCTACTTAGGTTGAGAGACATGCTGAAGGTCAGAGATGCTGAGCTGCAGTCTGTTCTCAATCAGGTGAGGCCAGCAAACCTGACCTGAGATCTGTGAAATCCTGAAGAAGGACGGACATCAGATTTTTTCCCCCATGTTTTTC[A/T]GGAGTCACAACAGAGTAATAAAGTCCAGAAACTGGAGAAGCTGCTCTCAAAGAAGGAAAAGGAATTGATGGAAAAGTATGTACATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCATCACATTAGTATAGATGTAGAGGAAATGTTCTGTGAGATGTAAATTAGTGACACAGAGATAGGTCCAATTTAACAGACGTAACATCTGTTGCTGACACAAGGAAATGTGCTCCAGAAAAATTATTCTAAAATAGGGAACCTATTACAAGATATAAAATAAGTCTCTGATCTTGAGTGTGTATGTGAAGTTTCAGCTCAAAATATCCCACAAACAAATTGTTTTATATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15716
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123347 | Nonsense | 293 | 507 | 6 | 14 |
Genomic Location (Zv9):
Chromosome 25 (position 29823931)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 28514025 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TRATAAAGTCCAGAARCTGGAGAAGCTGCTCTCAARGAAGGAAAAGGAAT[T/A]GATGGAAAAGTATGTACAKCTATCTATCTATCTAWCTATCTATCTATCTA
Long Flanking Sequence:
TATTGATCATCTGTGGAACCGTATTTAGCCACAATCTCAGGTAGTTTCAGATCAAGTTTAATTTTTAATTTTTAATATTTTGGAAGCCATTAGCCACTGACATCCAAAGTAGGAAAAATAAAACTGTCTTACAGCAAGAGGCTGATGTATATATGTGTGTGTTTATAAATTTATAATGCATTTAAAGGTGGTTCTTTCATAATGTCAGTTTGTAACAATGTAAGTACTGTTAATGCTCAAACTTTCTTCATAGGTGTCTTGTGAAGACCTGAATGGAGAGCTGGAGGAGGAGCTACTTAGGTTGAGAGACATGCTGAAGGTCAGAGATGCTGAGCTGCAGTCTGTTCTCAATCAGGTGAGGCCAGCAAACCTGACCTGAGATCTGTGAAATCCTGAAGAAGGACGGACATCAGATTTTTTCCCCCATGTTTTTCAGGAGTCACAACAGAGTAATAAAGTCCAGAAACTGGAGAAGCTGCTCTCAAAGAAGGAAAAGGAAT[T/A]GATGGAAAAGTATGTACATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCATCACATTAGTATAGATGTAGAGGAAATGTTCTGTGAGATGTAAATTAGTGACACAGAGATAGGTCCAATTTAACAGACGTAACATCTGTTGCTGACACAAGGAAATGTGCTCCAGAAAAATTATTCTAAAATAGGGAACCTATTACAAGATATAAAATAAGTCTCTGATCTTGAGTGTGTATGTGAAGTTTCAGCTCAAAATATCCCACAAACAAATTGTTTTATATCTGTTTGAAACATCCCTTTTTAGGTTTTGATCCAAATTGTGCTTGTTATGGTGACTGTCACTTAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11668
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 |
---|---|---|---|---|---|
ENSDART00000123347 | Nonsense | 432 | 507 | 12 | 14 |
Genomic Location (Zv9):
Chromosome 25 (position 29839118)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 28529212 |
GRCz11 | 25 | 28972414 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATGTGAAAYGTGTTCTATTCAGATCTTCAGTGTTCCCAAGAAGACCTTA[C/A]TTGGCTGATAATTTGGTCCAAAATGCTTCAGATATTAAGGTAAACAWGCA
Long Flanking Sequence:
ATATGTCCAGTACCTCGTTGAATGCCATGAAGGCAGAAGCCATGATTAAGGCAGTTCTGAAGACTAAAAGGGATCCAACCCAGTACTAATAAGGTGTACCTAATAATTTGGCCAGTGTGTATATATAAAAGTCAAACTCTTTGTTTCTAAATTGATATAATCGATATAAATCAAGATATTGTTTTTATTCAGGTAGTTTACATTTAACATTTTGTTTACTTTTTTTGTATTTTAGTTTAAGCTTTTGTTAATGATAATAACCTTCCTCCCAACTCTCCCTCAACGGATCAGTGAATGGTGTGAACCCTGGCTCAGGAAGAGGAGTGGGGGTGGGAATACTGGAATTTTCCCAATGTCATAATTCACATTTGGCATGTGGCGACGTTAAAACTGTCTTGGAAAAGAAGCTATGAATCAAATCTTATTGACATTTGACAGAAAACATATATGTATGTGAAACGTGTTCTATTCAGATCTTCAGTGTTCCCAAGAAGACCTTA[C/A]TTGGCTGATAATTTGGTCCAAAATGCTTCAGATATTAAGGTAAACAAGCACATTTTTCGTTTTTTAGGCCATAAATCGGGATGTCTTTTGATACGGAAATTAATAACAGCTGTGTGACACATTTAGAACTGGAATGCTGTTGACGTGAACCATCAGGGAAGAGAAACGCAGACACCGGAGCAAGATCCCCAACAGGGGGCAGCAAAACCATGTCCATCCCAGATCTCAGACGGAGGATCAGACAGGTCTGCAGGAGGGGTGGAGGATAAACAGCCAATCAGCGTCAAGCATTCCAGCAAGACTGCCCAGGTATGGTGAGAATCTGCGCTGCCGATCTTAGTTTGATAGCATTTTTGATTGGCTTATGGTGCTCTTCTAATTCAAGCTCAACTAAAAATTAATTGATTTTAATCTTTGAGTAAAGTTTAACAGAACAACTCACAAATCACATCATAGACTCTAATTATAGTGTCCTGATCTCACATTTTATGTTAATCAAA
Associated Phenotype:
Not determined