ZMP
cic
Ensembl ID:
ZFIN ID:
Human Orthologue:
CIC
Human Description:
capicua homolog (Drosophila) [Source:HGNC Symbol;Acc:14214]
Mouse Orthologue:
Cic
Mouse Description:
capicua homolog (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1918972]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11051 | Nonsense | Available for shipment | Available now |
sa13638 | Nonsense | Available for shipment | Available now |
sa14154 | Nonsense | Available for shipment | Available now |
sa13672 | Nonsense | Available for shipment | Available now |
sa12482 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11051
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 |
---|---|---|---|---|---|
ENSDART00000077862 | Nonsense | 1435 | 2623 | 5 | 20 |
ENSDART00000140674 | None | None | 1128 | None | 14 |
Genomic Location (Zv9):
Chromosome 16 (position 12897576)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 11302819 |
GRCz11 | 16 | 11193721 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCGAATCAGGACAACCGCACTGTCAGCAAAATACTCGGAGAGTGGTGGTA[C/A]GCCCTGGGACCCAAAGAAAAACAGAAATACCACGACCTCGCATTTCAGGT
Long Flanking Sequence:
TGAGCCATTATTTTAACCATTAATTTAATGATTACACTTAAACAGTGATTCTGTGTTGAAATTGAAATCAATCAATATTTTAGGCTCAATCAACAGACCACCCGGTCATAAAGAAAGCGTTGATTCATCATTCATGGGCAGTCGCCTTGAAAGGATGCTACAAAAAAGATATCACTTTGCGTGTTTGTGTGTATGTAAATTGTTTACAGTCTAAAATGTATGAAATATTTATTTTTATGTAAACACAATGGGAATATATATTACATAATCTAACTATGGACAGTTGAACAGTTGTGTATTTTTTCATAATAATACTCTATTGCTCAGGCATGTTCAATCATTCCTTCTTGTTCTTTTACTTTAAAGAGGGAAAAAGATCATATCAGGAGGCCTATGAATGCATTTATGATCTTCAGCAAGCGACATCGCGCACTGGTTCATCAGAGGCACCCGAATCAGGACAACCGCACTGTCAGCAAAATACTCGGAGAGTGGTGGTA[C/A]GCCCTGGGACCCAAAGAAAAACAGAAATACCACGACCTCGCATTTCAGGTTACTGGAACTTTTCTCACACTGGCAGATACGCATGCTGAGACTCCAAAATAACCCAATTAAGTCCCTCTAGCTCTTTTAAATGTCTCTGCCACTCATTTACAGGTAAAAGAGGCACACTTTAAGGCACATCCTGACTGGAAGTGGTGTAATAAGGACAGAAAGAAATCCAGCAGCGAGGGACGTGGTGTTCCAGGAGGCAAAGACATCCGCGAGAGGAGCATGTCAGAAACCACAGGTGTGGAACAGAGCAGCACGTGCCTCTTCAATTGGAATAGTTTCACAGTTTGAGTAGCTGTGATCTATTTCAATATTTATTATCTTTTTTTAATATCTCAAAAAGTTTTTAATTTAAATTTAATTAAAGTTTTTTATTATTATGAGTTATAATTATAATTTGCTTCTGGGCTTATTAATGTATTATTTTATTTACTTACATATATTATTTATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13638
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 |
---|---|---|---|---|---|
ENSDART00000077862 | Nonsense | 2022 | 2623 | 13 | 20 |
ENSDART00000140674 | Nonsense | 527 | 1128 | 7 | 14 |
ENSDART00000077862 | Nonsense | 2022 | 2623 | 13 | 20 |
ENSDART00000140674 | Nonsense | 527 | 1128 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 16 (position 12910483)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 11315726 |
GRCz11 | 16 | 11206628 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGCTSCCTAATCTGAACATCACGTTGTCTCCCACAGAATCACTTATGTA[C/T]AGTCCACTCCTGGGGTTCCTTCTCCTTTGCCATTAGTTCCCTCAACTACA
Long Flanking Sequence:
CTACTATTGTCATAACAAAGAACAATATAACTTATTGAATCAATGCAGGATATGACAGCTTTAAATAATGCCTCATTTGAAACTTATAAAAAAAACTGCTGTTTGAAATTAATGTAATAAATCAACCTAATCAGCTTGCTTTCCTGTTTTTCTTCTGTCTAGATTATTCAGATCGCTCCGATGCCAGTCGTGCAGTCTCAGCTCCCCTCTGCAGGCCCAGTGCAGCCTGGGAGCCCATTTTCAGTTACTATGGGAACAGCTACAGTAGTGGCCCCAGGCTCTACCCCGTCTCAGACCGTGCTGCTACCGCCTCCACCTACCAGGTAAAATGTCCGCTCTCACCTAGCCGCACACACACAAACATCTCCACCACTCTTATCTCAGCAACTCCTACACTCCTGAAGCACAGAAGCACTTGAGAGTAACCCTGCCCTGCTGTGCTCACTTTAAAAGCTGCCTAATCTGAACATCACGTTGTCTCCCACAGAATCACTTATGTA[C/T]AGTCCACTCCTGGGGTTCCTTCTCCTTTGCCATTAGTTCCCTCAACTACAGGCTCCTCGTCTCAGACAGTTTCAGCAGCACCTGGATCTGCATATGTTTCCTCACCCTTGGCCACGTTTGCAGCTATCGCTCATCCGGGACAGACACTGGTGCAGCCGCTGATTGCAGGTCAGTGGACTCACATTTGATGTACTCAAATGCTGCTATTTTGGTCAGTCATGCTGCTTATCGATTTTAAGATCACATTTGCATATGTATTGACAAACAGTCACAGGCAAATTCTGAACTTTAGTGACAAGCCAGCACTGACATTCCTGTCTACTAGGGCTGCACAATATATCGTTTCAGCATCGATATCACAATGTGCGCATCTGCAATAGTCACATCGCAAGATCTGCAACGTTGAGTCTGAATCATAGTTGACCAGGAGCCATAGTGTAGAGTCACTGCTTAGTTTAATCATAACAGAGTGAACGTTTACCATTTGCATGTGTTTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14154
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 |
---|---|---|---|---|---|
ENSDART00000077862 | Nonsense | 2022 | 2623 | 13 | 20 |
ENSDART00000140674 | Nonsense | 527 | 1128 | 7 | 14 |
ENSDART00000077862 | Nonsense | 2022 | 2623 | 13 | 20 |
ENSDART00000140674 | Nonsense | 527 | 1128 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 16 (position 12910483)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 11315726 |
GRCz11 | 16 | 11206628 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGCTSCCTAATCTGAACATCACGTTGTCTCCCACAGAATCACTTATGTA[C/T]AGTCCACTCCTGGGGTTCCTTCTCCTTTGCCATTAGTTCCCTCAACTACA
Long Flanking Sequence:
CTACTATTGTCATAACAAAGAACAATATAACTTATTGAATCAATGCAGGATATGACAGCTTTAAATAATGCCTCATTTGAAACTTATAAAAAAAACTGCTGTTTGAAATTAATGTAATAAATCAACCTAATCAGCTTGCTTTCCTGTTTTTCTTCTGTCTAGATTATTCAGATCGCTCCGATGCCAGTCGTGCAGTCTCAGCTCCCCTCTGCAGGCCCAGTGCAGCCTGGGAGCCCATTTTCAGTTACTATGGGAACAGCTACAGTAGTGGCCCCAGGCTCTACCCCGTCTCAGACCGTGCTGCTACCGCCTCCACCTACCAGGTAAAATGTCCGCTCTCACCTAGCCGCACACACACAAACATCTCCACCACTCTTATCTCAGCAACTCCTACACTCCTGAAGCACAGAAGCACTTGAGAGTAACCCTGCCCTGCTGTGCTCACTTTAAAAGCTGCCTAATCTGAACATCACGTTGTCTCCCACAGAATCACTTATGTA[C/T]AGTCCACTCCTGGGGTTCCTTCTCCTTTGCCATTAGTTCCCTCAACTACAGGCTCCTCGTCTCAGACAGTTTCAGCAGCACCTGGATCTGCATATGTTTCCTCACCCTTGGCCACGTTTGCAGCTATCGCTCATCCGGGACAGACACTGGTGCAGCCGCTGATTGCAGGTCAGTGGACTCACATTTGATGTACTCAAATGCTGCTATTTTGGTCAGTCATGCTGCTTATCGATTTTAAGATCACATTTGCATATGTATTGACAAACAGTCACAGGCAAATTCTGAACTTTAGTGACAAGCCAGCACTGACATTCCTGTCTACTAGGGCTGCACAATATATCGTTTCAGCATCGATATCACAATGTGCGCATCTGCAATAGTCACATCGCAAGATCTGCAACGTTGAGTCTGAATCATAGTTGACCAGGAGCCATAGTGTAGAGTCACTGCTTAGTTTAATCATAACAGAGTGAACGTTTACCATTTGCATGTGTTTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13672
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 |
---|---|---|---|---|---|
ENSDART00000077862 | Nonsense | 2551 | 2623 | 20 | 20 |
ENSDART00000140674 | Nonsense | 1056 | 1128 | 14 | 14 |
ENSDART00000077862 | Nonsense | 2551 | 2623 | 20 | 20 |
ENSDART00000140674 | Nonsense | 1056 | 1128 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 16 (position 12924900)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 11330143 |
GRCz11 | 16 | 11221045 |
KASP Assay ID:
554-4410.1 (used for ordering genotyping assays)
KASP Sequence:
CTGCGTTCCAGGCACGGTATGCTGATATCTTCCCAACAAAGGTGTGTTTA[C/A]AGCTCAAGAWTCGAGAGGTCCGGCARAAGATCATGCAAAMGGCAGCTCCA
Long Flanking Sequence:
TCAATGGTGAACGTGTCAAGTATAAAAGCCTTAATCCGTTTCGTGAGTTGTGCGATGCGGTGCCGGGTGAAAGTATAAATCTGCATTAAGATGTTTGTTTTTTCTGTAGTTCAATAGTGCATTTAACCTGACTTTAGTACTGTTCAATTTAAATAACTTGATTTTACCCCTAATTTTGTGCTTTTACATTTTCTCTCGCGTGTTTTTGATATTGCGATATAGGTCTTAAATTTAATACTTAATGGTCTTAAAAAGGTCGTAAAAGGTCTTAAATTTGACATTATAATATCTGCAGAGACCCTGTAAAAACATTGCTATTAAACTTTGGTCCCTATGTTTGCAGAGAGTGTTGGCATCTTCTAGGATTGTATTTTCTTAAATCTAATTAAATCTTTCAAATCTCTCTCTTATTTTCTCCTCCTTCCACCCAAACAATAGCTCAAGCTACTGCTGCGTTCCAGGCACGGTATGCTGATATCTTCCCAACAAAGGTGTGTTTA[C/A]AGCTCAAGATTCGAGAGGTCCGGCAAAAGATCATGCAAACGGCAGCTCCATCAGAATCTGCTGGTATTTCAGACCTTTCATTACCGGGACCTTCCGGAGTGGTGACAATGGACCCAGCTTTAGGGGCAGACCCTCTGGAGAAGGAGGTTGAGCGAGAGGGTGAACAACACAGCCCAGAGGAGCCTAGAAACGCTGGCGATTCACAGGACTCCTCAAGATGAGGCTAATGTCCAAACGGACAGCTCGAAGACCTGAAGTCTCCCCTCAACATCTGCACGATCTACATTTGTTGTCCTGTCTCTGCTATGACCGCTTCCGAAGGACATAGCGAGAAAAAGAGCCAAATTTTCATGTGTGTGAAGCGGATGAGGGGAGACACCTCAAAAGATGTTGGGGTTTTGAAACTTCTCAGTATTTTTCGTGATGTGGACTTACATACATAGACATTTGCCTACACAGACACTCTTGAACATACACTCTTGAATTTACAGCATTATCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12482
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 |
---|---|---|---|---|---|
ENSDART00000077862 | Nonsense | 2601 | 2623 | 20 | 20 |
ENSDART00000140674 | Nonsense | 1106 | 1128 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 16 (position 12925050)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 11330293 |
GRCz11 | 16 | 11221195 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGTGACAMTGGACCCAGCTTTAGGGGCAGACCCTCTGGAGAAGGAGGTT[G/T]AGCGAGAGGGTGAACAACACAGCCCAGAGGAGCCTAGAAACGCTGGCGAT
Long Flanking Sequence:
AAATAACTTGATTTTACCCCTAATTTTGTGCTTTTACATTTTCTCTCGCGTGTTTTTGATATTGCGATATAGGTCTTAAATTTAATACTTAATGGTCTTAAAAAGGTCGTAAAAGGTCTTAAATTTGACATTATAATATCTGCAGAGACCCTGTAAAAACATTGCTATTAAACTTTGGTCCCTATGTTTGCAGAGAGTGTTGGCATCTTCTAGGATTGTATTTTCTTAAATCTAATTAAATCTTTCAAATCTCTCTCTTATTTTCTCCTCCTTCCACCCAAACAATAGCTCAAGCTACTGCTGCGTTCCAGGCACGGTATGCTGATATCTTCCCAACAAAGGTGTGTTTACAGCTCAAGATTCGAGAGGTCCGGCAAAAGATCATGCAAACGGCAGCTCCATCAGAATCTGCTGGTATTTCAGACCTTTCATTACCGGGACCTTCCGGAGTGGTGACAATGGACCCAGCTTTAGGGGCAGACCCTCTGGAGAAGGAGGTT[G/T]AGCGAGAGGGTGAACAACACAGCCCAGAGGAGCCTAGAAACGCTGGCGATTCACAGGACTCCTCAAGATGAGGCTAATGTCCAAACGGACAGCTCGAAGACCTGAAGTCTCCCCTCAACATCTGCACGATCTACATTTGTTGTCCTGTCTCTGCTATGACCGCTTCCGAAGGACATAGCGAGAAAAAGAGCCAAATTTTCATGTGTGTGAAGCGGATGAGGGGAGACACCTCAAAAGATGTTGGGGTTTTGAAACTTCTCAGTATTTTTCGTGATGTGGACTTACATACATAGACATTTGCCTACACAGACACTCTTGAACATACACTCTTGAATTTACAGCATTATCCTAGTCATTAGGCTTCCTTTGGAACTAGAGGACTGTGGGCCTGTCCTGTTGGCCAGTGAAGTCCCAGTGCTGCTGATGATGTGCGAGGGCACCCGATCCCTTCCACTCTGACTGAGTTTTCGTATGGCCTGATTGGCAATAGCTTGGCCACA
Associated Phenotype:
Not determined