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 |
sa43334 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa29252 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa3030 | Nonsense | F2 line generated | Not yet available |
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
Mutation Details
Allele Name:
sa43334
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:
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 | 687 | 965 | 22 | 28 |
Genomic Location (Zv9):
Chromosome 19 (position 41548586)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 41000941 |
GRCz11 | 19 | 40588061 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGATTGAGGACCACTCTCAGCCGAATCCAGGAGAGCCTAATAGACATG[G/A]TGAGTAAAACATGACTCGTTTAATGCACTCTTTCAGTTTTCCCCCTGTCT
Long Flanking Sequence:
TTCGAGTGTGGTCCTGATAAATCTTTGTTTGAAGGGGTTGTATAGTATACCCAATAGGTTTCTTCCCAGCTCTGCTGCCTGGCCCCTAATTATGGAGAAATAGTAGTAAGAATATAAATAGAAAATAAAAGAAATTATAACAAAATATTTAAAGACTTTTGATATAGAGTATCTGGCTGTAGATAAAAGTATGAAAAAAAATTCTCGAGGTTTCCTATAAGGGTTGGGTTTAGAACACACAATACATTTTGTCAACGACGAGTCCTCATCAACCACCAAAACAAGTATGTGTGTTTGTGCCATTTTTAGGATATGATCAGTAGCATGTATCCTTTCAAGTTTGGGTTTGTGAAGTGTGTGTATTCCCAGTGGTCAATAAAATCTCTTTCACACGCAGTGTGTTCTGCTCTCACCTACAGTATGAATCCTCTGGCCTGGGTTTGATCAGCAGCAGATTGAGGACCACTCTCAGCCGAATCCAGGAGAGCCTAATAGACATG[G/A]TGAGTAAAACATGACTCGTTTAATGCACTCTTTCAGTTTTCCCCCTGTCTCTCTTACTCCAATGGTTCATCTGTTGGTCTCTAATACATAACCATTATAAATCCAAGTGGAAATGCATTTATCCGAGTCCCTTATAGCCTCTCATTGGGCCTGTCATCTTTTGCCCCTTCCTACTTTCAGCCGCAGCATCCACAGGTGAGTTAATCACACTTCCATGGCCCTGCGCTCTTGTAATAAATGTCCTTTGGTTTCCATGGCTGCACCCATTACGGCTCTCTGGGCCAAAGGTTTGATACCCACAATGCACCATAAACCTCTATTTGCAGCACAAATGGCCAGTCATTATATGGGATCCTTTTCCCCCAGATGTCTGAGTGTCAAAGAGCACAACGAGGTACTTATTTGCAGTATTCAATCAGGCTTGAGAGTTGTAGTGTTCCGTCTGAGATTATGGGCTGTTTCTACCTGGTATTAACATTCAATTTCAGTGATTTGATTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29252
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017917 | None | None | 314 | None | 12 |
ENSDART00000110699 | Nonsense | 776 | 965 | 25 | 28 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 41613297)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 41065551 |
GRCz11 | 19 | 40652671 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGACATTTTCCGCTGCTGTTTTCTCTACAGACTGTATCAACGGCCAGC[G/T]AGCTCCGCAAGCCCATTTACTGGATCGTGGCAGCCAAAGCCATAGATTAT
Long Flanking Sequence:
CTGTCAGTTCGTCTTTCTGTTCGTCTGACTGTCTGTCAGGCTGTTCGTCCGTCCGTCCGTCTGTTTGTCTGTCTATCTGTCTGTCTGTCTGTCTAATGCAGCAGACTGAAAATGCAAGCTTGTGCAATGAGTTTTACATGGATGCTGTGTTCTAAAGTTCAAGCTTGGTGTACTCTGTTCTGTGAAATGAATTTACATATTGTTCTATTAGTCCCTTTTGGAAATCACTTTTGATAAACACACCTGTCATGTGATTCAATCTAAAAGAATTCCTGACCTCTGCATAAAGTAGTACATTTCAGGATTTACATTTCAATATGCAGTTTACATTTCAAGCACAAGCCACTTTCAGCATGACTTTCACAACTTGTTAGTTTTTGGATAATCGACAAATACTAAACTGCATTTATCACCCCTGATGTCTGGCGGTTATGTATAGGAGCTCTTAATTTTGACATTTTCCGCTGCTGTTTTCTCTACAGACTGTATCAACGGCCAGC[G/T]AGCTCCGCAAGCCCATTTACTGGATCGTGGCAGCCAAAGCCATAGATTATGAGCAGATGCTGCTGCTGATGGCTGGAGTGAAATGGGACATTAAAGAGATAATGTCACAGCACAACGTCTACGTGGATGTCCTTTTAAAGGTAATGTGTTTGTGTGCGCAGCGGTCTTTATGTGCAACGATAATGTGTTGTTCATTACACACTAGAGGAGAGAGCAGGTGGGAGAATATCAGTAGAGATTAGCCAACCTTTACTTCATCTATCCACCTTTTTCCTACAGCTCCGTGATTTTTGGCGTGAACTATGTTGGCGTGAACTTCTGTTAAGCTGTGAACAGTCAGTGAAGTGTTATTAAAAACTGGGGTGGTATTGTTCTGCTCACAGTTCATCAAAACAAATTTTACTATGCAATATTAAAGACATGTTAATGTGACTGTATTGTAAAGAATATACAGTGGGGGAAATACGTAGGGTTGGGTATCGTTTAGGGTTATTTCGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3030
Status:
F2 line generated
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017917 | None | None | 314 | None | 12 |
ENSDART00000110699 | Nonsense | 950 | 965 | 28 | 28 |
ENSDART00000017917 | None | None | 314 | None | 12 |
ENSDART00000110699 | Nonsense | 950 | 965 | 28 | 28 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 41645988)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 41098242 |
GRCz11 | 19 | 40685362 |
KASP Assay ID:
554-3435.1 (used for ordering genotyping assays)
KASP Sequence:
TGACTAACCTGGTCAACGTCTGCCTCGGGTCCCACATCAACAAGAAAGCA[C/T]GACAGAAACTCCTCGCAGCCATTGATGACATTGACCGGCCCAAAAGATAA
Long Flanking Sequence:
TAAAATAAAAAGGGATAATAATTAAAAATGGTGAATGCAATTTAAAAAAAATTTAAATAATAATTTAAAAATAATGCAAATGAAGGGTAGCTTATAATAATTCGTTTAAACAAAATCACATTTTATTCTTTTCTTAGAAGTGCCTTGTCAAACCTTTTTATGCTAATGTTCGGATCAAACATTCTTGCATATACTGTAAAAATCGAATCTCATATTCTAATGAAGCATTAGCATATTTTATAAATGACGCATCACTAAATGTTTGCCTTTTAAATGTCAAGACAAACGCTGGCTTGGCTCCAAATGTGCTTGTGATGTTGCTTAGTAAGGCATATCCTGCAAGACTGGCTTTAATTCTCCATTAAAGAGATGTATGGTTATGACTGTCATCTCCGCTCGATTTATCACCAGTTTGTTTTGTATTTACCCAGGAGTACTCGATGAAGCAGCTGACTAACCTGGTCAACGTCTGCCTCGGGTCCCACATCAACAAGAAAGCA[C/T]GACAGAAACTCCTCGCAGCCATTGATGACATTGACCGGCCCAAAAGATAAATCACTGTCATCAAAAATACACCACAAAAGTCACACACACCTACACTGTTACGCGTCCCGTATCTGTCTTGCGTGGTCTGCAGTTTGTTTGTCAACCATGAAAACGTTTACGGTTTCTGTTTGCGTTTTGTTAGGAATGTAAGCAGGACGTGCTGTGACTACATATGAAGCGGCTGTAAAAGATAATGGGTAATGAAAGTGTTATCAGCATCACTTGAATCACAACATGAGTGAATGTCTCAGGCGCTGTTAAACCCTAATTTAAGCAGAGCTGTGGATGAGCAGCTGAATTTTTCCTTGTTGAGGAATATATGAGGGTTTTGTAGCATGAGGCTTTTTAATATGGTATAAAGACGTCCTTTAAAGGGACAGTACACTCAAAAATGAAAATGTTGTCATTTAATCATCTTCCACTTATTCCAAACTTGTATGGGTCACTTTGTACTGTTG
Associated Phenotype:
Not determined