ZMP
ccdc132
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q1LYA7]
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 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa29252 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa3030 | Nonsense | F2 line generated | Not yet available |
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 |
---|---|---|---|---|---|
ENSDART00000146468 | Nonsense | 89 | 278 | 3 | 6 |
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 |
---|---|---|---|---|---|
ENSDART00000146468 | Nonsense | 263 | 278 | 6 | 6 |
ENSDART00000146468 | Nonsense | 263 | 278 | 6 | 6 |
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