Busch Lab

ZMP

cplx4a

Ensembl ID:
ENSDARG00000059978
ZFIN ID:
ZDB-GENE-060526-116
Description:
complexin-4 [Source:RefSeq peptide;Acc:NP_001070768]
Human Orthologue:
CPLX4
Human Description:
complexin 4 [Source:HGNC Symbol;Acc:24330]
Mouse Orthologue:
Cplx4
Mouse Description:
complexin 4 Gene [Source:MGI Symbol;Acc:MGI:2685803]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa14594 Nonsense Available for shipment Available now
sa44957 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa14594
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000084011 Nonsense 26 159 1 3
Genomic Location (Zv9):
Chromosome 21 (position 9275604)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 10647657
GRCz11 21 10740285
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TKGGGAACCCATTGAAAGGAATGGGACTTGGAGGAGGAGATGAAAAGGCT[G/T]AAGAGGAGACCCCTAAAGACCCTGCKGCCGCYGCYGGGATGACTCGAGAA
Long Flanking Sequence:
AGTGGGTGGACACAAATGAGACATCTAAAACCGAGGCCGACCTAATCTCCAAAACACAAAATATAGAGTTTTCCACTTTCTCTCAGGTTGTTCTGTGTCGCTGATATTTTAGTTGCAACTCCTGATGGATAAATGCATGGAGGTCTTTCACTTTTACAGTGCAGCAAAGCACACAGCCATCTGCCTCTGTGTAGACGGACGCATCTTAATCCAGATTATGGCTGCAGCATAAACGTTTTTTTTTTTTTTTCCCCCCTAGTCAACAGTGTGTCCTTGATAGCACAGGCAGGTCGGTTAGCCTAGCTCCAATTTGACCACCAGCAATCAATCTAAAGGACTTCTATAGTGGAAATCGAGGATTCAGACCCAAATATTTCAGGAAATCGCAACTTGGCATCAAGCTAGAGACTCCGGCGTGGTAAATAATGGCGTTTTTAATCAAAAGTATGGTGGGGAACCCATTGAAAGGAATGGGACTTGGAGGAGGAGATGAAAAGGCT[G/T]AAGAGGAGACCCCTAAAGACCCTGCTGCCGCCGCCGGGATGACTCGAGAAGAATATGAGGAGTACCAGAAACAGCTTGTGGAGGAGAAGTAAGTCACGTTTAGGCCCTAATTTTGCTTGCATACATGACATTAAATGACCTTGACAAAGTGGATTGGAGAATCTTATATGTTGCATCTTGCAGTTAAAGTTGCTGTTATTTCCACTTTTAAGATTTATTATTAGTTCTTAGTGAGATTTAATACAATCCCAATGTTATCAAAACTCTAAGCAAGTTGATTTTGGATTTCCTTCTGTATTTTCCACTCTCAAAGTCAATCATACATCACAGAAAATGTGTGTTCAGATTAAATTGTAATGCATTGATTTCCATTGCTATACAAGCAATGATGCATCCTCATGAAGGCATTATTTATTCTCAGTATTAATGCAAAACTACTGGTAGTCATACCTCATCAGGATGCATTAAATATGATAACGTCAATGATGAAAGATGAACAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44957
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
ENSDART00000084011 Nonsense 139 159 3 3
Genomic Location (Zv9):
Chromosome 21 (position 9283126)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 10655179
GRCz11 21 10747807
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATGGGCCAGATTCAGAATCTACAAAACATGGACATGGATCAGATCAAA[G/T]AGAAAGCCAGCGCTACGTTGACAGAGATGAAGTCCAAGGCCGAGGAGAAA
Long Flanking Sequence:
TAAGTTTCCTTTTCTGTTGAACACAAAAGAAGATTTTTCCATAGTAGGAAAAACAAATACTATAGAAGTCAATATTTACTGGTTTCCAGCATATTTTACATGATTTTCTTTTGTGGTTAACAGAAGAAAGAAACGAGCATTAAAAGTTTATGAAGTGAAACAATCAGGTCTGTAAAACAAACTAAACATATCTTTACAACAGTATTACCTTTAATCTGCTGCCTCGCCAAACAGCATTTGTGACAATCTGGATTACTGAACTATCCCTGTATTTATCTCTGTTTGTTCCGAGTCCTCATCCAGCACTATATGAGCTTGTTTACCCGTTTTCTCCTCAGAGCGAGCAGGACGAGAACATGCTGCAGATGGCCGGAGACGATGTGGACGTTCCTGAAGAGCTACTGAAGATGGTGGATGAGGATGCCACAGAAGAAGAGGAGAAGGACTCCATCATGGGCCAGATTCAGAATCTACAAAACATGGACATGGATCAGATCAAA[G/T]AGAAAGCCAGCGCTACGTTGACAGAGATGAAGTCCAAGGCCGAGGAGAAATGTTCTGTCATGTAGGGGTTTAACAAACTTGCGCATTTCTACACACAACATTAACAACAACAAAAAAGGTCAGGATTTTGATTTGGAGGAGATTTGAGGAGAAAAAAAATGTGCACTGCAAAACAAAAAAAGGCTTTTCTTACCTGAAGTTTTTGTCTTGTTACTATATAGTGCAAATATCTAAAATTAAGAAGCATTTTTAGACAAGTAATGTTTTCAGAAACAATGTCAAATTCTTATCCCGAGTTCAGACTGCATGATTTTAGCCCCTAATTTTGACTTGCCAAGAGTTTTTGAGAAATCGCAGACAAATGACTGAAATCACAAGCAAATCGGTGCTCTTTCACGTAAGTAACAATCACACAGTGTGAACTATCAAAGATCTGAGAGAATCGCTGATGAGTTGCACAACGCCCGTGAGATATTTGGCATGCTAAACATCTGGAGCTG
Associated Phenotype:
Not determined