ZMP

chchd10

Ensembl ID:

ENSDARG00000010717

ZFIN ID:

ZDB-GENE-040426-1753

Description:

coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial [Source:RefSeq pept

Human Orthologue:

CHCHD10

Human Description:

coiled-coil-helix-coiled-coil-helix domain containing 10 [Source:HGNC Symbol;Acc:15559]

Mouse Orthologue:

Chchd10

Mouse Description:

coiled-coil-helix-coiled-coil-helix domain containing 10 Gene [Source:MGI Symbol;Acc:MGI:2143558]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa18461	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa18461

Status:

Available for shipment
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Availability:

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Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024858	Nonsense	89	143	2	4
ENSDART00000146909	Nonsense	89	105	2	3

Genomic Location (Zv9):

Chromosome 21 (position 13909101)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	15610056
GRCz11	21	15706033

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GCCTTCAGTGGAGGCAGCAGTTCAGAGGCACCCAAACCAGCACCCACATA[T/A]CAGGTCATACCCAAAATATTTATTGAAATATTATATTTTTATTTTNTTTTC

Long Flanking Sequence:

GCTAGAATACTAAATTCAAAGTATTGTAATAAACCACATAGAGACCATGTCACAAGTTTTCATTATTTAAAAATGAACAAATGTGCAAATCTAAAACTTTACCTTAACAATGTACTGAAGAATGTTGGGGGAAAAAAACAGTTCTTGGCTTCCATAATATATATTCAATGTATCTTCCTTTCTTCATAAATTTAGAACCACTTGAACGAAAATGGTCATTTTATGGTGACCTGTAAATTTAAATCTCTTTAACATATTTTATCCTGTTTTCTTCCTAGTGCTCCTGCCCCATCCTATGCTCCAGCTCCTGCAGCTCCTCCTCCGATGGCAGTGGCCCCTGCTGCGGCTCAGCCTAAGCAGCCAGGTCTCATGGCCCAGATGGCCACCACAGCGGCCGGAGTGGCCGTTGGTTCAGCTGTTGGGCATGTGATGGGCAGTGCCATCACAGGTGCCTTCAGTGGAGGCAGCAGTTCAGAGGCACCCAAACCAGCACCCACATA[T/A]CAGGTCATACCCAAAATATTTATTGAAATATTATATTTTTATTTTTTTTCCATGGAGTGTAACCAACAACTCTTTAAGTGGCATTGAGTCAAAGTATTTTTCATATACATGATTTTTAAAAATCTTCATTAAAATGTTTTAAGTCGTAGAGTTTAATCACAACATTACAAATTTATTTTGAAGAAATGTATTTAAAAATATGAAGGTACAAGACTAGACTGTTTTACGTAGAGAATGAATCACAATCCCATGAGTCTATCTCAGAGCTTGACATTAGCTTTTTTGATCACCAGCCAGTGTGGCTTGTAGTTTTCCAATATTACCAGCCATTTGCCATTTTTACTAGCCACAATTTTGTTGTTGGGAAAATATATTTTTTAAGCTTATAATTAGACTTTGGCATGCTAAAATGACTTGATTTAGATTTTGTGTTATTTCCGTATGCCTCATTCATTTCACCTTTGTGTGTTGTGTATGACCTTGCTCAATGAGCAACCTAT

Associated Phenotype:

Not determined