ZMP
coro1ca
Ensembl ID:
ZFIN ID:
Description:
coronin, actin binding protein, 1Ca [Source:RefSeq peptide;Acc:NP_958452]
Human Orthologue:
CORO1C
Human Description:
coronin, actin binding protein, 1C [Source:HGNC Symbol;Acc:2254]
Mouse Orthologue:
Coro1c
Mouse Description:
coronin, actin binding protein 1C Gene [Source:MGI Symbol;Acc:MGI:1345964]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16635 | Essential Splice Site | Available for shipment | Available now |
| sa11685 | Essential Splice Site | Available for shipment | Available now |
| sa11512 | Nonsense | Available for shipment | Available now |
| sa33570 | Essential Splice Site | Available for shipment | Available now |
| sa40394 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa14944 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16635
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 |
|---|---|---|---|---|---|
| ENSDART00000004217 | Essential Splice Site | None | 474 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 5 (position 22102997)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 19815869 |
| GRCz11 | 5 | 20319669 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAAAATTAAAGTCGGGCTTGGATATATTTTGCCTACGACAGCTGAGAAG[G/A]KAAGGATAAGGACAWACTCTCTCTGAAGCGTAATGTTTGCAGAAYGAAGC
Long Flanking Sequence:
GCAATTTCCCGTGCAGGAAAATAAACCTCACCATACAGGTTGCATCTCAGTACAAAAATGCCAAATGCCTACCCAAAATACATTGTACTTACACCACATTGCGTCCACGATACCATCTACTAATCGACGTAACTAAACGTTGACTGACCTCACTACAGGTATGACGTCAGGAGCAATAAACCGGTTTCACCAGTAATTTCAGTCACGTCGTCCACACTGAACTTCATACCTGTTTTACACTCCTAATAGGCGGGGCTACGTTGAATGTGTATGGTGATTGGTGAGCTTTGACGCCACTCAGTGCTCATTTCTCCAATCCGGTTTGTTGGGGGCGTGGATAAGAAAACAAGGCGTGCCTTCCGGCGAGTCTCGGACAAGTTGAGTGAGGCAGAGGCATAGGGAACATTCGCGCGATAAGGGACTGCTGCTGGGAAACTAAAGCTGTCTAGTACAAAATTAAAGTCGGGCTTGGATATATTTTGCCTACGACAGCTGAGAAG[G/A]TAAGGATAAGGACATACTCTCTCTGAAGCGTAATGTTTGCAGAATGAAGCGAAGATTGGGTTGGCGTGTGTAAGTTTTAAGGATCTGTCCATGCGAAGGGATCATGGCAGCGTGGATCAGGCCAGATGGGCTGATCTGCAGTGCTCAAAACGGGGGATTGCTTTAACAAATTTTCATGTTCCATATCTGAGCTGACAAGCTTTCAGGATGGAACATGTAATGCTGTGTGATTTGTATGGATGGATTTAGGAACCTCCTTGGCTCAGTGCTCAAACTGTGGGAAGCGAAAGTTGCTGCATCTGGGGCGGTTTAAGAATTCTTCAAATAAAAAAAAAACTACTACAGAATTTTCAAATCTTAGAATTCCTAAGGTGTTTTTATGGAATTTTGGAATTCCTGATAAAAAAAAAATAGCTCATTTGAAATCTTACGATCTTTGTTTGCTCATCAAATTAGGGTGAGTGATCACTAAACAAATAAAGCTGAAGTTTAACTACTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11685
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000004217 | Essential Splice Site | None | 474 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 5 (position 22102998)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 19815870 |
| GRCz11 | 5 | 20319670 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAAATTAAAGTCGGGCTTGGATATATTTTGCCTACGACAGCTGAGAAGG[T/G]AAGGATAAGGACAWACTCTCTCTGAAGCGTAATGTTTGCAGAAYGAAGCG
Long Flanking Sequence:
CAATTTCCCGTGCAGGAAAATAAACCTCACCATACAGGTTGCATCTCAGTACAAAAATGCCAAATGCCTACCCAAAATACATTGTACTTACACCACATTGCGTCCACGATACCATCTACTAATCGACGTAACTAAACGTTGACTGACCTCACTACAGGTATGACGTCAGGAGCAATAAACCGGTTTCACCAGTAATTTCAGTCACGTCGTCCACACTGAACTTCATACCTGTTTTACACTCCTAATAGGCGGGGCTACGTTGAATGTGTATGGTGATTGGTGAGCTTTGACGCCACTCAGTGCTCATTTCTCCAATCCGGTTTGTTGGGGGCGTGGATAAGAAAACAAGGCGTGCCTTCCGGCGAGTCTCGGACAAGTTGAGTGAGGCAGAGGCATAGGGAACATTCGCGCGATAAGGGACTGCTGCTGGGAAACTAAAGCTGTCTAGTACAAAATTAAAGTCGGGCTTGGATATATTTTGCCTACGACAGCTGAGAAGG[T/G]AAGGATAAGGACATACTCTCTCTGAAGCGTAATGTTTGCAGAATGAAGCGAAGATTGGGTTGGCGTGTGTAAGTTTTAAGGATCTGTCCATGCGAAGGGATCATGGCAGCGTGGATCAGGCCAGATGGGCTGATCTGCAGTGCTCAAAACGGGGGATTGCTTTAACAAATTTTCATGTTCCATATCTGAGCTGACAAGCTTTCAGGATGGAACATGTAATGCTGTGTGATTTGTATGGATGGATTTAGGAACCTCCTTGGCTCAGTGCTCAAACTGTGGGAAGCGAAAGTTGCTGCATCTGGGGCGGTTTAAGAATTCTTCAAATAAAAAAAAAACTACTACAGAATTTTCAAATCTTAGAATTCCTAAGGTGTTTTTATGGAATTTTGGAATTCCTGATAAAAAAAAAATAGCTCATTTGAAATCTTACGATCTTTGTTTGCTCATCAAATTAGGGTGAGTGATCACTAAACAAATAAAGCTGAAGTTTAACTACTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11512
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 |
|---|---|---|---|---|---|
| ENSDART00000004217 | Nonsense | 7 | 474 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 5 (position 22149799)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 19862671 |
| GRCz11 | 5 | 20366471 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAKCATTCTTGTCTTGTTTTCSTTTGCAGATATGTTCAAACGGGTTGTA[C/T]GACAGAGTAAGTTCCGGCATGTGTTCGGCCAGGCGGTGAAGAATGACCAG
Long Flanking Sequence:
TAGTTCTTAGAAAGAATCTTAAATTGGCAAAAATAGGTAAAAAATAATAATAATAACAACATTTGTTGTTGTTGTTATTACTATTAGTTCTTAGAAATAATGTTCTGTCCGCAAAAAATCTGTAAAAGCAGAATCTGCAAAAACGATAACGGCTGGTCACACTTACCACAATATTTAAATCTGCCAATAAAATTACAAACGGAGCATCAGAAAATGATATTTAAACTAGTAAGTCAAAACACAGTTCACGCACCCTAAAGCTGCTATTTACACTGAGACAACTGTCGAAAACACCATTGAATTACAGATTAAAGTGCACAAATGATCAAATCAGATTTTTGCTGATGTGCTTGTCAGTATAAGCTAATAATGAATGTGTGTAGACATGCTGTACAAGGCTTTGCTCTGTGAAAGCGCTCAAGCGTTTGTGTCATGTGACGACGGCTTCATTCATCATTCTTGTCTTGTTTTCCTTTGCAGATATGTTCAAACGGGTTGTA[C/T]GACAGAGTAAGTTCCGGCATGTGTTCGGCCAGGCGGTGAAGAATGACCAGTGCTATGATGACATCAGGGTGTCCCGGGTCACATGGGACAGCGCGTTCTGTGCAGTTAACCCCAAATTTGTTGCCTTAATTGTGGAAGCCAGCGGAGGCGGAGCGTTCATGGTTTTGCCTCTACACAAGGTGAGAGTTGCAGAAAGCTTTTGTTGCTTTTTGGGTTATATTCTTTTAAGAAGACTTGGGAAATAATTGTTGTTAAAAAAAATGTTGACAAAACTGAAACGTTATCAAAACTAGAGATTTATTTTTCTTTTTTTTCATATTTTTTTCATGTCTAGGTATTTTGTACACACAGTTGTTCTGAAGTTTGGAAGATGTTGAACTTTTATTTAGATAAAATTCTTGTCAATTGTAAAATTGTTGTAGCTTTAAGAATTTTTTCTACATCTAAAGCATTTAAAAGTGTAAAATATTGTGTTTTAGTGTAAATTGCAATATTCTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33570
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000004217 | Essential Splice Site | 67 | 474 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 5 (position 22180267)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 19893139 |
| GRCz11 | 5 | 20396939 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTGAATGCTTTCATATTTAATCTGATATTAGGCTTTGTCTCTGTTTGC[A/T]GACGGGTCGTATAGACAAGGCCTACCCTACAGTATGTGGTCACACCGGCC
Long Flanking Sequence:
GAATTTCATTTTAATCAAACAATGTAACTATAAATCCGCTCCTCAGAATCTGAGAATTTCTATGTAGTCTCTTTTAAATTTTTCTGTGGCTGTTTAGTAAAACCTCCTCATTTATGGGTTTTCTCACACTCTGCCTGAACCTCCGTGTGACCTTTCACTCCTAATGAAAGGGTCAAGGGCCTGTCGCACACGCACTTCTGTCTCTGCTTTTGAAAACAGAGATGCAAGAACAAAAGCTGCAATCTGTTTTTATTATAAATCAGCTGTCGTGTGTAAATGTTTCTTCTGTTTGCGCTGAATGACCGGATGAGCTATTGTTTGAACATTTGGAAATGAATGGCTTTTTGACCCCCTCCTGATTTGACGAATGCAGGCCAGGCTGTAAGTGTTTGTTTTGGTGCTACACAGACATTTGCTGGCATTGTTAGATCTCATTTCTCTTACCAAAAGAACTGAATGCTTTCATATTTAATCTGATATTAGGCTTTGTCTCTGTTTGC[A/T]GACGGGTCGTATAGACAAGGCCTACCCTACAGTATGTGGTCACACCGGCCCTGTTCTGGACATCGACTGGTGCCCTCATAATGACCAGGTCATCGCTAGTGGATCTGAAGACTGCACCGTCATGGTATGTCAACATTTTTTTCTTCATTTTAGACTTCTGAAAGTGGTTTTACAAGCTTTTTGTGTTAGAAAACTATCAAATTTAATATAGGTTATTAAACGTTTGATTGCGGTGTTTATTTTCATTAATAAAAATAGAGAGAATAATTATAGTGTTTGATATAATAGTATTTTAAAGTCTGCTTGAAATAAAAATTTACAATGTTGATTTTGCTAGCTCACATCGTTATCCTGAAGGTGAATAATTAATCTGTTTAAGTTAGTCCTCTAAAATGGTTTGATTTGGTTATCTTCTATTAAGATGGATGGGTGTGTGGCTGTATGGGTAAAAGGATGGTTTGATGGATGGATGGATGGATGGATGGATGGGTAGATGGATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40394
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000004217 | Nonsense | 109 | 474 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 5 (position 22183440)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 19896312 |
| GRCz11 | 5 | 20400112 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATTACAAGGGGTAAAAATTAAGATGTGTTAATTGTTGTTGTCAGGTGT[G/A]GCAGATCCCAGAGAACGGGTTGGTGACTTCCATGTCAGAGCCAGTGGTGG
Long Flanking Sequence:
TAATTATTATTATTAATGATAATAATAATAGTTATTAATAATAAATAATAAATATAAATAACTTAGTATATATATATTTGTTTTTATTATTCATTTACTTATTATTATTATTACTAATGATAAAAATTTAATATTGATGATGATGATGATGATGATGATAACAATAATAATAATATTATAATAACTATTTTATTATTTTAAAATAACTTAACAATTATTTATTTATTTCTTTATTTACTTGTTATTAATATTGTTGTTGTTTATTATTATTTTTTTATTAATATTGATACTACTACTACTACTACTACTACTACTAGTAGTAGTAATAATAATAATAATAATTGTCATTGATAATAATACTAATACTAATGACAATAATAATATTTGCATTTCTGGCAACTCAAATAACAACCATAGTTAACAATACACACCACATCACTTAATTACAACAAATTACAAGGGGTAAAAATTAAGATGTGTTAATTGTTGTTGTCAGGTGT[G/A]GCAGATCCCAGAGAACGGGTTGGTGACTTCCATGTCAGAGCCAGTGGTGGTTCTGGAGGGTCATTCAAAAAGAGTGGGAGTTGTTACCTGGCATCCTACTGCACGCAACGTCCTCCTCAGTGCAGGTATGAAAGGTTTCGGCAATCATCTAGAATAGATGCCCTAATCAATGCCTATCAAAAAAAAACTTAAATAGATAAAAACTGCTCAGTATCTGTGATATAGATTTTAGACATGATAGTTTTTAGCTTGCCTCTATAAATCGTTATTTTATTCACTAAACAAATGAATTTCAACATTTGACAGGATAGAAAAGACTGAACTTTGACAATTGTTGGTATAAGTGTTCTATTATTCCATGCGAGTTCAATACAAACTCAGGAGGCAGAAATAGAATTAAAAAATATTAGTAATTTATTAAGTACAAATGAATAATTCGATTAGGGCCCTGGGTCACCCAAATGTGTCCTATTGGTTATACAATGCTATCCAAGAAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14944
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000004217 | Essential Splice Site | 151 | 474 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 5 (position 22183567)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 19896439 |
| GRCz11 | 5 | 20400239 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGTTGTYACCTGGCATCCWACTGCACGCAACGTCCTCCTCAGTGCAGG[T/A]AWGAAAGGTTTCGGCAATCATCNNNNNTAGATGCCCTAATCAATGCCTAT
Long Flanking Sequence:
TTAATATTGATGATGATGATGATGATGATGATAACAATAATAATAATATTATAATAACTATTTTATTATTTTAAAATAACTTAACAATTATTTATTTATTTCTTTATTTACTTGTTATTAATATTGTTGTTGTTTATTATTATTTTTTTATTAATATTGATACTACTACTACTACTACTACTACTACTAGTAGTAGTAATAATAATAATAATAATTGTCATTGATAATAATACTAATACTAATGACAATAATAATATTTGCATTTCTGGCAACTCAAATAACAACCATAGTTAACAATACACACCACATCACTTAATTACAACAAATTACAAGGGGTAAAAATTAAGATGTGTTAATTGTTGTTGTCAGGTGTGGCAGATCCCAGAGAACGGGTTGGTGACTTCCATGTCAGAGCCAGTGGTGGTTCTGGAGGGTCATTCAAAAAGAGTGGGAGTTGTTACCTGGCATCCTACTGCACGCAACGTCCTCCTCAGTGCAGG[T/A]ATGAAAGGTTTCGGCAATCATCTAGAATAGATGCCCTAATCAATGCCTATCAAAAAAAAACTTAAATAGATAAAAACTGCTCAGTATCTGTGATATAGATTTTAGACATGATAGTTTTTAGCTTGCCTCTATAAATCGTTATTTTATTCACTAAACAAATGAATTTCAACATTTGACAGGATAGAAAAGACTGAACTTTGACAATTGTTGGTATAAGTGTTCTATTATTCCATGCGAGTTCAATACAAACTCAGGAGGCAGAAATAGAATTAAAAAATATTAGTAATTTATTAAGTACAAATGAATAATTCGATTAGGGCCCTGGGTCACCCAAATGTGTCCTATTGGTTATACAATGCTATCCAAGAAAACACATCAGGCTCTCTGAGTGTTTCTTAGGACTAAACACCAAGTTTATATTCACAGAAGAAGAAGGCGGGTTGTCTTCGTTCGCTTTTCTGCACCGTCTGTAGTTCCCCTTTTCTCCACAGAAGAACTGA
Associated Phenotype:
Not determined