nacad

Ensembl ID:
ENSDARG00000012347
ZFIN ID:
ZDB-GENE-091020-7
Human Orthologue:
NACAD
Human Description:
NAC alpha domain containing [Source:HGNC Symbol;Acc:22196]
Mouse Orthologue:
Nacad
Mouse Description:
NAC alpha domain containing Gene [Source:MGI Symbol;Acc:MGI:3603030]

Alleles

There are 2 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa5894 Nonsense Mutation detected in F1 DNA During 2018
sa45578 Nonsense Mutation detected in F1 DNA During 2018

Mutation Details

Allele Name:
sa5894
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
ENSDART00000019658 Nonsense 1241 1870 2 9
Genomic Location (Zv9):
Chromosome 16 (position 29858609)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 27695747
GRCz11 16 27630370
KASP Assay ID:
554-3937.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
CGCATAAAGAGACATCAAATTCCAATGAYGTTGTGGGGGAGAAAGTAATT[C/T]AATTAATACCGAACATCAAAAATGAAACAGCAAGTGGTGAAKCTAAAAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45578
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:
A > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000019658 Nonsense 1798 1870 7 9
Genomic Location (Zv9):
Chromosome 16 (position 29854821)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 27691959
GRCz11 16 27626582
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
AGATCGAGGACCTTTCACAGCAGGTGCACAAGGCAGCGGCAGAGAAATTT[A/T]AGGTTCCTCTTGACCCCTCGCCTCTACCATCAGATATTACCCCAAGCTTA
Associated Phenotype:
Not determined

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