Busch Lab

ZMP

calml4

Ensembl ID:
ENSDARG00000059347
ZFIN ID:
ZDB-GENE-071009-6
Human Orthologue:
CALML4
Human Description:
calmodulin-like 4 [Source:HGNC Symbol;Acc:18445]
Mouse Orthologue:
Calml4
Mouse Description:
calmodulin-like 4 Gene [Source:MGI Symbol;Acc:MGI:1922850]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa37975 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa30175 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa37975
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000082447 Essential Splice Site 11 155 1 5
Genomic Location (Zv9):
Chromosome 25 (position 1389363)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 1242943
GRCz11 25 1323588
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTCTTATGTTCTTACAGGCGAAATTCCTCAGTCAAGATCAAATCAACG[G/A]TAAGCAGGTCTCTGCATTATAACGTCTCTTATAGATATTGTGTAAATATT
Long Flanking Sequence:
GGTCAAGTATAATGCTTAAATATTTTAATAATGCTACGATTGGACAGAATTTAATTTATTTCGTTTCTCGGCGTCAATCAAGCGTAAAATCAAATCTGACAACAGTTGACGCAAATGTCACGTGACCGGCGCTTTTCCCTCAGCGCTTACTTGTTTAGTGATTGTCAAATGTTTGTTACTGGAGACATTTAAAAATTAAAATGATTGAATACCACTCTGTTACTTGCGTTACACATTTACTATATGTTTTAATCCCGCCTCGAGACCAGTGAATGGGATTTGATGGAGATTTTGCTTTCTGTCGTCGAGCGCCATCTGCCGGAGTGAAAGTTCGCTTCATTACAAACACCTGACAGCACTTAGAGAAGGACTGAACACCAACATGGTCAGTTTGCCATCTCTTTCTATGTATTATTTTCATGTAAAACAATATACTAACTAATTAAATTGGCTTCTTATGTTCTTACAGGCGAAATTCCTCAGTCAAGATCAAATCAACG[G/A]TAAGCAGGTCTCTGCATTATAACGTCTCTTATAGATATTGTGTAAATATTTATCAGTTTAGTTCGATAAATTCGGTTTTATATCGTTCACAAAACTCCCAAAATATGATTAATACGCAACCTAAACACATTAGCTGTCAATAACACTATCAAACTGAGAGATAAAAAGTCAAACTATGGATGAAATAGCCTAATGTTTAGTCTTTATTCAGTATTGTGATATGGTTATTTCATGTACTGTACATCCTTTTCTGGCCTGTGTTTATTTATATGTAAACTAATTAGTGAACGTAGTCAATTTAAATGCTGTGTTAAATAATAGAAAACACTGATGTCAAATGGGTGAGAATTAGTGTTTTGAAGGATCAATACCCTGATAATAATTAATATTTCAGACGACAACTAAGCTGATATTGCGGCTGAAATTAACAGATTTTAATATTTCAATAAATGATTCATGTTCTAATATTATAAATATAATCTCTTTTTCTGAGCTGAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30175
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000082447 Essential Splice Site 12 155 1 5
Genomic Location (Zv9):
Chromosome 25 (position 1389364)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 1242942
GRCz11 25 1323587
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCTTATGTTCTTACAGGCGAAATTCCTCAGTCAAGATCAAATCAACGG[T/G]AAGCAGGTCTCTGCATTATAACGTCTCTTATAGATATTGTGTAAATATTT
Long Flanking Sequence:
GTCAAGTATAATGCTTAAATATTTTAATAATGCTACGATTGGACAGAATTTAATTTATTTCGTTTCTCGGCGTCAATCAAGCGTAAAATCAAATCTGACAACAGTTGACGCAAATGTCACGTGACCGGCGCTTTTCCCTCAGCGCTTACTTGTTTAGTGATTGTCAAATGTTTGTTACTGGAGACATTTAAAAATTAAAATGATTGAATACCACTCTGTTACTTGCGTTACACATTTACTATATGTTTTAATCCCGCCTCGAGACCAGTGAATGGGATTTGATGGAGATTTTGCTTTCTGTCGTCGAGCGCCATCTGCCGGAGTGAAAGTTCGCTTCATTACAAACACCTGACAGCACTTAGAGAAGGACTGAACACCAACATGGTCAGTTTGCCATCTCTTTCTATGTATTATTTTCATGTAAAACAATATACTAACTAATTAAATTGGCTTCTTATGTTCTTACAGGCGAAATTCCTCAGTCAAGATCAAATCAACGG[T/G]AAGCAGGTCTCTGCATTATAACGTCTCTTATAGATATTGTGTAAATATTTATCAGTTTAGTTCGATAAATTCGGTTTTATATCGTTCACAAAACTCCCAAAATATGATTAATACGCAACCTAAACACATTAGCTGTCAATAACACTATCAAACTGAGAGATAAAAAGTCAAACTATGGATGAAATAGCCTAATGTTTAGTCTTTATTCAGTATTGTGATATGGTTATTTCATGTACTGTACATCCTTTTCTGGCCTGTGTTTATTTATATGTAAACTAATTAGTGAACGTAGTCAATTTAAATGCTGTGTTAAATAATAGAAAACACTGATGTCAAATGGGTGAGAATTAGTGTTTTGAAGGATCAATACCCTGATAATAATTAATATTTCAGACGACAACTAAGCTGATATTGCGGCTGAAATTAACAGATTTTAATATTTCAATAAATGATTCATGTTCTAATATTATAAATATAATCTCTTTTTCTGAGCTGAAAAA
Associated Phenotype:
Not determined