ZMP

ccdc57

Ensembl ID:

ENSDARG00000089863

ZFIN ID:

ZDB-GENE-090603-1

Human Orthologue:

CCDC57

Human Description:

coiled-coil domain containing 57 [Source:HGNC Symbol;Acc:27564]

Mouse Orthologue:

Ccdc57

Mouse Description:

coiled-coil domain containing 57 Gene [Source:MGI Symbol;Acc:MGI:1918526]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa13752	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa13752

Status:

Available for shipment
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Availability:

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Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000124982	Nonsense	266	1022	5	19

Genomic Location (Zv9):

Chromosome 12 (position 34866211)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	33270320
GRCz11	12	33371303

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GATTGCWATTACTGATTTATAGGATAAAGGAGCTTGAGGAAACACTGAAA[C/T]AAYTAGAGAACAACTGTAAAAAAGAACAGGAAGCCTACGACAGGAAGTAA

Long Flanking Sequence:

TTCACACACATACACTACGGACAATTTAGCTTACCCAATTCACCTATACTACATGTCTTTGGACTTGTGGGGGAAACCCAGAGGAAACCCAACCAAACACTAGGAGAACATGCAAACTCCACACAGAAATGCCAACTGACCCAGTCGCGGCTCGAACCAGCGACCTCCTTCTTGCCACCGCTCTGCCGAGTGATGTACAGTTTATGTTAATTTCTGAATTAAACTGTCCAGGAAAAACTATTGAGCAAAGAGTTAGAGGTCCATGCCAAAGCACACAGCCAAGCAACTGAAGCCCTGCAGGCCTCTGAAGAACTTTACCAGCAGGCTCAAAAAGAGATCCAGCATCGAGACTGGGACCTAAAAAACACCACCGCAATGAAAGACTCCAGGTAAACTGACAGATTAATACTAGTATAGAAAGTTTTTTTTGTTTAATTTAGGATACCATAAGATTGCAATTACTGATTTATAGGATAAAGGAGCTTGAGGAAACACTGAAA[C/T]AACTAGAGAACAACTGTAAAAAAGAACAGGAAGCCTACGACAGGAAGTAAGTAGCACTACATCTTGAATATATCGACCCAGTCTAGTCAAATCAAATAATTAAACATTCATTGAGAGCAACTGACATGCTTAATATGCATAGCTCAGATTACTCTTGTAGGCCATGATATCTTGCTTCGATGTTTTGAAATTTGATATTTGCAGGCATGCAGAGCTGGAACGAAGGACTCGGGAGAGCAAAGATGCATTGGACCGCTTGAGAGAAGCTCATGCCAGGGATCTCCAAGAGGAGAGGGAGAAATCCTCAGAATTACAAGCCCAACTGGACAGGATGATCCTGGAGCTGGAGAGGAGAGAAAAAACCCGTACAGATGACCTGGAACATAGAGACCAGCAGATACAAGAGTAAGACAGCTTAGAAATTTGGCATTGGTGTATATTATCTCATAACTATTTGCTTTTTTGTGTGTATGTGAAATGTTATGGTCCATCTGTGTGTT

Associated Phenotype:

Not determined