ZMP
si:ch211-287b5.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q1LUH6]
Human Orthologue:
CCDC132
Human Description:
coiled-coil domain containing 132 [Source:HGNC Symbol;Acc:25956]
Mouse Orthologue:
Ccdc132
Mouse Description:
coiled-coil domain containing 132 Gene [Source:MGI Symbol;Acc:MGI:1920538]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10581 | Nonsense | Available for shipment | Available now |
sa32255 | Essential Splice Site | Available for shipment | Available now |
sa23579 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10581
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 |
---|---|---|---|---|---|
ENSDART00000017917 | Nonsense | 43 | 314 | 3 | 12 |
ENSDART00000110699 | Nonsense | 43 | 965 | 3 | 28 |
Genomic Location (Zv9):
Chromosome 19 (position 41356264)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 40808802 |
GRCz11 | 19 | 40395922 |
KASP Assay ID:
2261-3613.1 (used for ordering genotyping assays)
KASP Sequence:
TCTCATTTYTTTTGCTTTTCACACAGGAGGAGCTGAGGGAGCTGAGAGAG[C/T]AGCCCAMSGATCCACAGGCAGAAMAAGAAATCATTGACAGCATAGAGGAA
Long Flanking Sequence:
GCAAAACTCAACTGTGTAAAACTCGAATTACTCTATATCCCAAAAAAGTGGAGTTTTCTTTTAAACCTTGCCTCTGCATTCGCTCTGGGAAGCCAGTGTGACTCAGTAAGTTTATCTCAGTTTGGGTCGCACCATTGTTTTAACCACATTGCATCACGGCATGTGAATCAAGCGTAATGAGCCTCTCAGCAATTTTCTTCAAAGAAAAGAGGACGACTTTGTTTCTTCAAGCTGTTTTGAGTGAAATTGATGTTCTTGTGCTGATCCTCATTAAGGTTCATGAAGGGTGTTCCTCAGGGACGGGTGCTAAGACCACTTAATCTTTGCACTTGGCTTGGCTGTAAGCCAGACTTGAAAATTAATCAATGCTCAGACCCCGTGCTTAGGTGCGAGGCAAGCTTCCCAATGATAGCGTCCCAGAAGCACAGAGATTTCCCTGCCAATACTCATTCTCATTTCTTTTGCTTTTCACACAGGAGGAGCTGAGGGAGCTGAGAGAG[C/T]AGCCCACGGATCCACAGGCAGAACAAGAAATCATTGACAGCATAGAGGAAGTCTACTACTCCAGCGACTCGTTTGACATGGTTCAATATGAACTTGAGGTGTGTGTATGAGAGAATACATATTGCTTGTTGTTGTTTGTTTAACCCTCCTGCACATCTCAAGTCTAACAGTGGGGTTTAGGTCAACTAGGGGTCAATTCTTGTAAAATAAATGGAGCTCTTTCCAAATTTGAGCTCAGTAAGTCTTGTCATCGCCAACCAGGGTGTCCGTGGGGTCCTAAAAAAGTATTAAAAGTTGATAAGTCATTCATTGATTCATTCATTTTCTGCGTAGTCCCTTTATTAATCCGGGGTCGCCACAGCGGAATGAACCGCCAACTTATCCAGCACATGTTTTACGCATAGGATGCCTTTCCAGCTGCAACCCCTCTACGAAACATCCATTCACACTCATACACTACGGACAATTTAGCTTATTCAATTTACCTGTACCGCATGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32255
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017917 | None | None | 314 | None | 12 |
ENSDART00000110699 | Essential Splice Site | 544 | 965 | 18 | 28 |
Genomic Location (Zv9):
Chromosome 19 (position 41512606)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 40964961 |
GRCz11 | 19 | 40552081 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATAGACAACAAAGAAGAGGAGACTGAGGACGTCCTGGCTTCTAATGGGG[T/C]ATATAGTAGTTTGAATGATGGTCATGTTATGTACAGTTTTATATACTGTT
Long Flanking Sequence:
TGATGCGCAGAGTGGTTGAACTATGAGAACTATGCTATTGTGCTTTCACCTTTGCATCTTAGTTCTTGTTTTTTATGACTAGTATATTCAGAATTTTCAATACAAATCTTAATGCATCTGTAATATTTATCAAATACTCCTTGAATGGTTAATAAACACAAACACGCAGTATCATTAAATCCAGTCTTTCACTGCTGATGGCGCAAACACAAATTAATACATCGTTAGCAAACAAACAACATACTCAAAAAACAAGTGCAGGTGGGTGTTTTCATGACCTGTCTTTTAGTTGTTTGATCTGCATGTTTCTCTTCTTTTTCAGGAGTTTAAGTTCATGGGTCAGTGTCGTTCTCCTTCAGTGTCTCCCAGCAGGCAGCCAGAATCCACAGATCTGCTGGAGCTTTCTCTGTTCGAGCAGTACCTGGAGGGTGGAAACCCCTTCGAGATGCAGATAGACAACAAAGAAGAGGAGACTGAGGACGTCCTGGCTTCTAATGGGG[T/C]ATATAGTAGTTTGAATGATGGTCATGTTATGTACAGTTTTATATACTGTTGAATATACAATTATTAGCCCTTACTGAATTATTAGTCCTCCTGTATAATTTCCCTCTAATTTTTGTTTAACGGAAAGATTTTTTTTTTCAATTTCTAAACATAATAGTTTTAATAACTCATTTCTAATAACTGATTTATTTCATCTTTGCCATGATGACAGTACATAGTATTTTACTAGATATTAAGAGTGATATTTAAAGGGTTACCTAGGTTAATTAGGTAAGTTAGAGTTGAGCTTAAAATGTTTTTTTTTTTTTTATCAAAAGCTGCTTTTATTCTAGCTGAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAAATATTATAGGAAATACTGTAAAAAATCCCTTGCCCTGTTAAACATCATTTCGGAAATATTTAAAAAAGAAACAATTCACAGGAGGGCTAATAATTATGTCTTTAACAGTAGATGGTGAAGGGTGAGTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23579
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017917 | None | None | 314 | None | 12 |
ENSDART00000110699 | Nonsense | 646 | 965 | 21 | 28 |
Genomic Location (Zv9):
Chromosome 19 (position 41525869)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 40978224 |
GRCz11 | 19 | 40565344 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCCCATCGCCTTTGATGTCATCCACTGTGTGTCTCAGCTCTTTGATTA[T/G]TACCTGTATGCCGTCTACACCTTCTTCGGCCGCAATGACATGGTATGCAT
Long Flanking Sequence:
ATTTTTAAAGTGACATTTAAAGACTTAATTAGGTTAACTAGGCAGGTTAGGGTAATTAGGCAAGTATTTATATAATGACAGACTATTGAAAAAAAAGAAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACATACACATATACACACATGATAAATGCACTTTATTAATGCACATTACATTACATTCCTTTGTTTTTCTTATTTGAACAATAAGACGTTTCCAAAATATGTATTTTAAAAATGACACAGAAGCTTTGTGGTTGTACTATATATTCCACCCTGTGTATTTACCCTTTTTGTGTATCTCACGTATCTTTTCCTGATTTGTTTTTCTTTGATAGGGAAATACATGCAGATGATGAACATCCTGAAGCCCATCGCCTTTGATGTCATCCACTGTGTGTCTCAGCTCTTTGATTA[T/G]TACCTGTATGCCGTCTACACCTTCTTCGGCCGCAATGACATGGTATGCATTTCAAAAAGCATTGCCTTTCTCCTCCCGGGTTCGTTGTTATTACTTAACATTATGAAATATTTATTATATGCAATTGGAATCTTGCTGTGCTGTTTTGTCTGGAAGGTACATGTTCATTAAGAAAAGCTTTCCCGTATACCCTCATAGTTTTTTTTTCCCCTCTAATGTTTGCAAGGCCTTTGGGCACTGTTCTATAATTATTTCAATTATCATGTGAGCGAGTGTTTAGGCTTTGAGTTTTCCTCAGGAGGCTGGACTTTGAACATCAAAGACAGGTGTAAATGGCTGTTTCTCTTGCGTTCTTGTGAATGAACTCAGAAGACCACAAGCTGTGAGAGTTGAGATACTGAGATCTTCGTGTGGGTCACATGGAAGTTTAAATAGAAAGTAATTGAAACATCACAACATTCATGCAGTGCATTATTATTTTATTTTTATTTTTCAATATA
Associated Phenotype:
Not determined