ZMP

ENSDARG00000027310

Ensembl 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
sa12994	Nonsense	Available for shipment	Available now
sa19369	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa12994

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
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Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000067030	Nonsense	46	568	2	13

Genomic Location (Zv9):

Chromosome 25 (position 32186834)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	30766087
GRCz11	25	31343563

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ATGCTGAGGAGATTGAGAGAGAAAGGCGCCGTCGGGCCCGGGAGGCTTTC[C/T]GAAATCAGCACAGCCTGTCTGGATCTGCTGGATCCCCTCAGGASARCGYG

Long Flanking Sequence:

CAAACGATTTATATGGGCTGATTTTAAATTATATAATTACAAATATAAATTATAAATATAATTATAATAATGCAAATTGTTTGCAACCACTTACATAAAAAAAGTAAATCCAATTAATCTTTTTTCAGTGTAGGATAAAGAGTGTGTTTGTTCTGTAAACAGGCTAGATAAACACAGAATGTGCATTGTATCCAGCCTCTTTTGGTTGAGAACTTGCGGTGTCGAATGCCAGAGCAGATGTTATGCCGGCTCCAAATCTCAAGCAAGGGACTAAACAAAGCATTGCAAGAGATTTCTTTAAGAGCTCCATGCATCATAGTCAACTGCTCTCCTCTGGGCTAAGGGTCATTCATCATTCCACATGGGTCAAGAAAGAAAAATGGTTGTCTTGTGGTGTAACACGGGTCTCATTCTATTCCTGCAGAGTAACGGCTCAGCGAAGTATCGAAGATGCTGAGGAGATTGAGAGAGAAAGGCGCCGTCGGGCCCGGGAGGCTTTC[C/T]GAAATCAGCACAGCCTGTCTGGATCTGCTGGATCCCCTCAGGACAGCGCGAACCCACCTGAGGCCAGCCTGTAAGTGTGGACGTCATTCTGTTCGACACACTTCACCTGGTATTTGTTAGGCTTGTTTTGTAGCCTGGCAGATTTCCATTTGAAATATTGGCTTGCAGTGTGTCTGGTTCTCATTGAAGTTTATTCTGCCCAAGAGCTGTCCAGTTAGGCAGATGGAGATTGTCTGACTGACATGTAAAGCAACTGACTGGAGTTTGTTACAATTTTTGGATCAAATAATGAACAACTGAGAGAAGATTCTTCCAAGACATTTTTAAACAGAACAAACTAATTTCTTTGTTTTCTGGCACGATGACAGTGCATGATGTTTTACTAGTTATTTTGCAAGGTACTACTATTAAGTTTAAAGTGCAATTTAAAGGATTTAATTAGGTGAACTACGCAAATTAGGTTAATTAGTCAAGTCATTAGACAACATTGGTTTGGTCTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa19369

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000067030	Nonsense	320	568	5	13

Genomic Location (Zv9):

Chromosome 25 (position 32200828)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	30780081
GRCz11	25	31357557

KASP Assay ID:

554-6236.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAACCCGTGAAGAAGAAGAGCGGAGGAGAGAGGAAGAGGAACAGCTGAAG[C/T]AGACCAAAAAAGAGGTGGCTGAGATAAACAGAAATACTAGCCTATTCTAT

Long Flanking Sequence:

TTGGCTCACCCTAATGCTTATTCTGGCCAAGACTTACCCACTTTAACAAAATGAGACATTTGATGAACATCTAAAGCTACCAACCACTGACATTTGGTCTTAGGAGGTTAGGTTAGGATACTATGTTAATAATTAATTGTGTGGAAAAAAATAATCTCTTCAAATAAGCAAACACCAAATGTATGACTGATCAGAACATCAGTGCAAACGTAAAACGTACATGACTAACGTCAATCTTATTACTATTCTACAGCAGAATCGTTGATACCAATCAGGTCTTCGAGACTAAGAAGGACACACATGCCGTCCTGGAGACAGAGCTGAAGCTGGAGAAGATTAGACGTAGCCATCAGGAAAAGGAGAATCAGGAAATGGAGAATCTACGACAGCGCCAAGCCGAGGCTGAGCTAGAGCTGGAGGAACTGAAGAAGAAGAGAGAGGAACGGCGCAAAACCCGTGAAGAAGAAGAGCGGAGGAGAGAGGAAGAGGAACAGCTGAAG[C/T]AGACCAAAAAAGAGGTGGCTGAGATAAACAGAAATACTAGCCTATTCTATTTTGATTGTGGAAAAAAATAAACGTTCAGTACTAGTACACTGTAAACCCAATTGTGTAATCAAACCAATGAAACAAGAAACAAAATGAAAGGTGAACTTGGATTGAGTAGAAGCAGGTTTTGAGGAAAATAAGTGCTGAAATTGAGGATAAGGGTCTGGCCGCAGAGATGAACTTGCATCTTCAGGCTTGCACTCTCGGGCTTGCATGCTCAGGCACCCACGCTTCCTATGCAAGTGACACCTGCACCTGTCATGTCACTTGGAATCAACACAAATAAACTAAAAGTAAGTTTCCAGATCGTTTGCATTGCCAGTGAAGACGTTGTCAAATAATTCTAAGTAGACTACTTACGTACAGTAGTACAACATGACAGCCCGCACCCCACCCCCCGAAAAGCAGTTAGTATGTTTACTGTATGATTATTTGCTGTGATGTAAGCAGGCTACTAT

Associated Phenotype:

Not determined