ZMP
zgc:153153
Ensembl ID:
ZFIN ID:
Description:
Coiled-coil domain-containing protein 61 [Source:UniProtKB/Swiss-Prot;Acc:Q08CF3]
Human Orthologue:
CCDC61
Human Description:
coiled-coil domain containing 61 [Source:HGNC Symbol;Acc:33629]
Mouse Orthologue:
Ccdc61
Mouse Description:
coiled-coil domain containing 61 Gene [Source:MGI Symbol;Acc:MGI:2685005]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43627 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23916 | Splice Site, Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43627
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 |
---|---|---|---|---|---|
ENSDART00000089651 | Nonsense | 89 | 511 | 4 | 13 |
ENSDART00000108978 | Nonsense | 89 | 525 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 20094463)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 21229952 |
GRCz11 | 21 | 21266588 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTGTATTTTACAGTCCAGCGACTCCGTGACCCTTGACCTTTTGACGTA[T/A]TCTGACCTCGAGCTTCTGCGAAACAGAAAGGCAGGTGTCGTCGGCCGTCC
Long Flanking Sequence:
GTGTAGAGTTGGTATGTTCTCCTCGTGTTGCCATAATCCGACAGCGGAATGAACTGTCAACTTATCCAGCTTATGTTTTATGTAGCGGATGCCCTTCTAGCTGTTACCCATCACTGGGAGACACCCATACACTCTCATTCACACACATACACTACAGACAATTTAGCTTACCCAATTCACCTGTACTGCATGTCTTTGGACTGGAGCACCCAGAGACAACCTAAGCGAACACGGGAAGAACATGCAAACTCCACATAGAAATGCCAACTGACCCAGCCGAGGCTCAAACCAGCAACCTTCTTGCTGTGAGGTGACAATGCTATCCACTGCCCCACCAAGCCACGCCTAGTTTTGTTTTTATTTTTGTTAAACATTCTCATCTAATACTTCAAGTTAAAATATATCTCTGATAGTAATCATATCTAAATAAATATCTGATTTACCCTTTTGAATTGTATTTTACAGTCCAGCGACTCCGTGACCCTTGACCTTTTGACGTA[T/A]TCTGACCTCGAGCTTCTGCGAAACAGAAAGGCAGGTGTCGTCGGCCGTCCTCGTGCTCAGCCACAGTCTCCTGCTCTGAGTGCTAAACGATACCTCATCCTCATCTACACGGTGGAGTTTGACAGGTGTGTCTAGTGTCATCACTCTGTCTGCTTTGTTCATGTTTAATACAGCAGTTTTACATCAAGCATTTTTTTGTAGGATACATTATCCACTTCCACTTCCGTATCTCGGCAAACCTGATCCTGCAGAGCTTCAGAAAGAGATCAGAGCTCTGAGGTCCGAGCTGAAAACACTGGGACTGAGAGGAGACCACAAAGTATCAGACCAGGAAACACGCAAGCTGCGCACTGAGTCAGTTCTTTCTTTGTTTTATATAATGTAATACATATTTCAGATGTTTTCATATATAAACATCCCTTGCACATTTTGGTTATAGCTTGTAAATAATTTTTCTTTCAAAGAAAGACAATCTGTAGAGAAAATCTTTTTTTATTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23916
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089651 | Splice Site, Nonsense | 249 | 511 | 6 | 13 |
ENSDART00000108978 | Splice Site, Nonsense | 249 | 525 | 6 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 20097239)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 21232728 |
GRCz11 | 21 | 21269364 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCAGCGGTCTGCAATCAAGAAGAGCCAGGAACAGCGCCTCCTGGTGGAA[C/T]AGGTCAGTGTACACATTACATTGGTACAGTTATGAGATAGACAAACTGAT
Long Flanking Sequence:
TGGCCCTAGCCATTAGCTATAGTTTCCACTCTTGTCATTGAACGTTGAAAACAGCAAGTGATGTTTGGTCAAAAAGCATCAAAGGCTGACATGTGTGTGTCAACAACACAAAGAATTTGCAAGTGAATTCTGAATCATTTGACAAAGTGATTATCGTAACAGTCTAAAAAAAATATTTTATGTGTTCGGGTTGAAATTATATTCTACAAATTAAACCCACCAATTTTTTGCTTATTATAAAGTCACAAAACATTTCAACATTTTACAAAATGCTTTTATTATGTTATGTGCGCTTGATCAGGTTGGCTTTGGTGAGAGATGAAAAGGAGGCCTTGGCCAAGGCTCTGGATCGTCTGCAGATGGTGGGGTCCGGATCTGCTCCTGGAGCTCGGGGGCTCAGAGAGGCAGTTCACAGCCTGGAAGAACAGCTGCTGAAGGAGAGGGCAAAAAGCCAGCGGTCTGCAATCAAGAAGAGCCAGGAACAGCGCCTCCTGGTGGAA[C/T]AGGTCAGTGTACACATTACATTGGTACAGTTATGAGATAGACAAACTGATCATCCAAAGCATTAAAATATTCAATTGACTCTGTCGGCAGTTAGAGGAACTTAGAGCCTCCGAACGAGCTCTTCGAATACGGGTTAAAAGTCTGACCACTGAGTTGGCCTTGTTACGATGTGGGTAAGATGGTTAAATCAAAATTTTGTATTTATTTTTTTATGAAAATGTTGCATGTTTTAGAGCAAATGTTAATTATATGAATTTTTCAAAAAACTTTGACAGCCGAGCAACTCCAGTCTTGTCTGACCGAGGTGGACTGAGAGGTGATGGTGTGGTTCATCGTTCTTTATCCAGAGAGCGCAGTTTGACTCGTGTTGGTATAAGAGCACGCTCTGGGTCGAGGGAGAGGATAGAGGACAGGGGTCGAAGGTCAGAGGAAAGAGTTAGGAGGGCAGACTCTTCAGGGTTGAGGAACTGCATCACAAGACCCTCGCCGTCTCCAACAGG
Associated Phenotype:
Not determined