ZMP

cald1

Ensembl ID:

ZFIN ID:

Human Orthologues:

AC026150.5, AC091304.2, AC100756.2, AC135983.4, AC138749.1, CALD1, GOLGA6L1, GOLGA6L2, GOLGA6L6

Human Descriptions:

Uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:C9IYW0]
caldesmon 1 [Source:HGNC Symbol;Acc:1441]
golgin A6 family-like 1 [Source:HGNC Symbol;Acc:37444]
golgin A6 family-like 2 [Source:HGNC Symbol;Acc:26695]
golgin A6 family-like 6 [Source:HGNC Symbol;Acc:37225]

Mouse Orthologue:

Cald1

Mouse Description:

caldesmon 1 Gene [Source:MGI Symbol;Acc:MGI:88250]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa24667	Essential Splice Site	Available for shipment	Available now
sa38064	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa24667

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

Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000121989	Essential Splice Site	67	778	2	16
ENSDART00000142781	None	None	297	None	9

Genomic Location (Zv9):

Chromosome 25 (position 20670296)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	20081085
GRCz11	25	20178739

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CGAAACATGGAGAATGAAGAGTCCAGTAATATTACAACAGAAAGCAACAG[G/A]TAGTTTTACTTGCTAGCACAAATATACAGTTTTTTAGTGAATTTGCATGG

Long Flanking Sequence:

AGGATGTCATTCCTACAGGTAAATGTGTGTTTTGTGTCAAATATGAGCATAAAAGCATGCTAACTATTAATGAAAGCTGTTTATCCAGTAGGTAAATTGACTGAACTGCAGTCTTGGTTTATCTGTTATTTCTCTCTGTAATGTAAAGCCTATAATGCATTAGCACAATTTTAGCACAATCAGTGTGGAGTCATTTTCAAGATCGCGTTTGCTCGTGTAATCATTAATGCCTTTTCAGGTTTATGTAAAGTTTATGAAGGTTATTTCCCACCCGCTCTGTCAGTGATGAGCCAGGAAGCCTTCATATATCTGTCAGTGTCTGCATTTGCGTTGAAGAATAAGAGACTTTACTCACGTGTCTGTATCCCATCACTCTACAGGATGAACTCTTATGATGATGATGAGGAGGCGGCTCGCGAGCGCCGGAGACGAGCTCGTCAAGAACGCCTGCGAAACATGGAGAATGAAGAGTCCAGTAATATTACAACAGAAAGCAACAG[G/A]TAGTTTTACTTGCTAGCACAAATATACAGTTTTTTAGTGAATTTGCATGGTGCAACCCTGCCAACCTGATTTCACCAAGTAGAATATGTTCCTGGATTAACATCTATGTTGATCCTGGAACAACATTCCTATAAGCCAATCAGAACTAAGAGATACCTCTACCGTTTATTTTAGGTTTAGGCTTACGGTTAGGTTTATGTACTTCTACATGATTGCTATTAAGATAATTCTGCCTTGTAAATCCATTTTTGCAAGTGTTTAAGACACTGTGAGAAATTAATGAAAGCATATAATGTGTATTATGAGGAATGTTTGTTGCATTGTATATTGTGTGTCATATATCATGAATGGATTTTCACACAGTTTCACACAATTCATTCATGTTGTCCCAACACAAATTGTTTAAAATTATTCACTCATTCATTTCCTTTTCGGCTTATTTTGGGATAATGTTAGTACACAAGTCAGCAAAATACAGCACTGTTCTTGTTCTTTGTGGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa38064

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000121989	Nonsense	336	778	5	16
ENSDART00000142781	None	None	297	None	9

Genomic Location (Zv9):

Chromosome 25 (position 20677707)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	20088496
GRCz11	25	20186150

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTGTGAAAGAGCAAGAAAAACCTAGTGAAATTGTTGAAGAAACACCAAAG[A/T]AATCCATAAAGGAAATTGAGGTAAAGGCCAAAATCCCAAAGAAAGAAGAA

Long Flanking Sequence:

GGTTGGATTAGCATGGTGTTGAGGAAATAATTGTTAACTCATAGTAAAACGTAATAAACAGAATGTGGAAGCTGGTAAATTTGGTAAATGTCTTTTTAAAATGTCTTTTTAAATTTGGTAAATGTAATTATATGTTGTTGATTATTTAACATTATTTGTTGTATTTTTAGGAAGAATCTGTCAGTGCAATTATAGAGATTAAAGAACAAACTAATAGAGATTTAGCAAGTGCAGATTTAGAATTGAAAAAGGTGGAAGATCAAAGTTTGATACCAGAACCAGCAAATGAGAACAAAATAGAGGTGGAAGTCAAAATGGAGGCAGACACACCAAAGATTGAGGAGGAAAAGCTGGTGATGAAAGAAGATGTGGAGAAACCTGAAGAAAAACTTGTTGAGGCGAAGGCTCAAATTCAAGATGAAGCTCCAGTGAAAAAAGAGATTGAAAAACTTGTGAAAGAGCAAGAAAAACCTAGTGAAATTGTTGAAGAAACACCAAAG[A/T]AATCCATAAAGGAAATTGAGGTAAAGGCCAAAATCCCAAAGAAAGAAGAAGAGAAACCACAACTGAAGAAAGAGTTTGTAGAAAAACCATCAACCCCACTGAAGAAGGTTGAGGAGAAACCATTGACCCCAAAGAAAGAAGCTGAGGAGAAAATTGTGGCCCCAAAGAAAGCAGTTGAGGAAAAAACTGTGACTCAGAAAAAAGAGGTTGAAGAAAAAACATTTATTCCAAAGAAAGAGGTTGAGGAAAAACCTAAATGGAAGAAAGAAGCTGAAGAAGCGAAGGCCAAAGTTGAAGAAAAGGTCAAATCAAAGAAGGAAGAGGTATTCACCTCTTACCTGAGTGACGCATAGGAATCACAAATATACGCACAGACCACGCTTTTAATGTGCTTTATCGGACTGGGTGAATGCAGCGTTTTTTTGTGTGTGTGTGTGGATATCACAAAATCTGTAAGGAACATGTCCAGGTCTTTAACTTTTTTATATGAGATTTTTCAT

Associated Phenotype:

Not determined