ZMP

hnf4a

Ensembl ID:

ENSDARG00000021494

ZFIN ID:

ZDB-GENE-030131-1077

Description:

hepatocyte nuclear factor 4-alpha [Source:RefSeq peptide;Acc:NP_919349]

Human Orthologue:

HNF4A

Human Description:

hepatocyte nuclear factor 4, alpha [Source:HGNC Symbol;Acc:5024]

Mouse Orthologue:

Hnf4a

Mouse Description:

hepatic nuclear factor 4, alpha Gene [Source:MGI Symbol;Acc:MGI:109128]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa43991	Splice Site, Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa43991

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:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000028236	Splice Site, Nonsense	216	463	5	11
ENSDART00000122938	Splice Site, Nonsense	180	427	6	11
ENSDART00000124103	Splice Site	None	42	6	11
ENSDART00000138907	Splice Site, Nonsense	194	274	5	7
ENSDART00000145426	Splice Site, Nonsense	216	463	5	10

The following transcripts of ENSDARG00000021494 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 23 (position 26148100)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	25934220
GRCz11	23	25860761

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGGAATGGGCAAAATACATCCCTGCATTCTGCGACCTCCCGCTGGATGAT[C/T]AGGTAGGACAAGTTCCTCTTATTTATCTACAAATGTGTCCTTGCAATATT

Long Flanking Sequence:

GTCACGAGTGTCTGAAGGGGGTCATATTGAACATCTATGAACTTGTTTTCTACTGAAAAAAAAAACGTTGTTAAGTACTCATCACATGGATTGATTATACGAAGTTCCATCATGTTTCTTTGATTAAATTTTCAAAGTTGTGGTATTCTTTTTGAATCTCCCCATTATTATTATATTCATTAAAGAAAGTAAAAATTTTGAGCAGCTGTGGTGGTCTCATAAATATGTTAGTGGTCTAATAATATTGTTATGCACTGTTTATAAGTAATAATAATAAGATTTAGTAGTAATGTTTATGTTTAAGAGATGTATAGCAAAATACTTATAAAGTATATACCCTCATATAGATTTCATCACCGGGTCCAATCTTGAATGGTGATATCAGAACAAAAAAGGTAGCCGCAATAATGGATGTGTGTGAGTCTATGAAACAGCAGCTGCTGGTGCTGGTGGAATGGGCAAAATACATCCCTGCATTCTGCGACCTCCCGCTGGATGAT[C/T]AGGTAGGACAAGTTCCTCTTATTTATCTACAAATGTGTCCTTGCAATATTTACTTAAATGCATGTTGGTGTCGACTGAATCCGTGTTTTGTTTTCATTGGAAAAAAAGTTCAGAGATCTCTAGTTTGGGTGGTTAATGTATTTGGATGGCTCAGGTTAGAATATGATGAGCTGGTTTGAAAGTTACATCTCTTCTTGAGACATTCAGAATCATTAACACGCTGAGCACTGAGGCATGCTAACTTATCAGTGTTTTAGCTGTGGGTGAGAGCGTCTCAAACCGCATCTTCTCACACATGGAGACACGCTAAGACTAACCATATGGTCATCATAGAGACTTTAAACAATTCATTGATTTTATATGAAATATTCTAGACATGAAAAGAACTCTAAAGAAAATGTAAAAAAATAATAATATATTTCCATGTTTATTTGTCTCAGGTGGCTTTACTGCGAGCTCACGCTGGAGAACACCTCCTACTAGGAGCTGCCAAACGCTCC

Associated Phenotype:

Not determined