ZXDA

Ensembl ID:
ENSDARG00000052351
Description:
zinc finger, X-linked, duplicated A [Source:HGNC Symbol;Acc:13198]
Human Orthologues:
ZNF425, ZNF786, ZXDA, ZXDB, ZXDC
Human Descriptions:
zinc finger protein 425 [Source:HGNC Symbol;Acc:20690]
zinc finger protein 786 [Source:HGNC Symbol;Acc:21806]
zinc finger, X-linked, duplicated A [Source:HGNC Symbol;Acc:13198]
zinc finger, X-linked, duplicated B [Source:HGNC Symbol;Acc:13199]
ZXD family zinc finger C [Source:HGNC Symbol;Acc:28160]
Mouse Orthologues:
Zfp786, Zxdb, Zxdc
Mouse Descriptions:
zinc finger protein 786 Gene [Source:MGI Symbol;Acc:MGI:3026883]
zinc finger, X-linked, duplicated B Gene [Source:MGI Symbol;Acc:MGI:3694898]
ZXD family zinc finger C Gene [Source:MGI Symbol;Acc:MGI:1933108]

Alleles

There are 2 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa40690 Nonsense Mutation detected in F1 DNA During 2018
sa26744 Nonsense Mutation detected in F1 DNA During 2018

Mutation Details

Allele Name:
sa40690
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2018.
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000058028 Nonsense 36 751 2 12
Genomic Location (Zv9):
Chromosome 6 (position 23711542)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 19966988
GRCz11 6 22027210
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GCAGTATTTGCCAAAATTTAAAACGCAAACCATTAACTTGTGAAGAATTA[C/T]AGCCAATGAACCTTTTAACTGTGTCTGGAATGACCAAGAAAGTTTCGCTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26744
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2018.
Mutation:
C > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000058028 Nonsense 614 751 10 12
Genomic Location (Zv9):
Chromosome 6 (position 23721855)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 19977301
GRCz11 6 22037523
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GTTCTGTTGTTCTGCCGTTAGGAAAGCAGTGGATCAGCACGCACAGATTA[C/A]AGGGCCATTCAGCTTGCCAAAAGGAGGAAGCAGAAAGGCTCAAACTCTTC
Associated Phenotype:
Not determined

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