Busch Lab

ZMP

ccdc132

Ensembl ID:
ENSDARG00000094936
ZFIN ID:
ZDB-GENE-060503-325
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.
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.
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