ZMP

ENSDARG00000012764

Ensembl ID:

Human Orthologues:

HNF4A, HNF4G

Human Descriptions:

hepatocyte nuclear factor 4, alpha [Source:HGNC Symbol;Acc:5024]
hepatocyte nuclear factor 4, gamma [Source:HGNC Symbol;Acc:5026]

Mouse Orthologues:

Hnf4a, Hnf4g

Mouse Descriptions:

hepatic nuclear factor 4, alpha Gene [Source:MGI Symbol;Acc:MGI:109128]
hepatocyte nuclear factor 4, gamma Gene [Source:MGI Symbol;Acc:MGI:1353604]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa21135	Nonsense	Available for shipment	Available now
sa41076	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa21135

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024443	Nonsense	56	463	2	19

Genomic Location (Zv9):

Chromosome 7 (position 70190827)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	68795470
GRCz11	7	69032075

KASP Assay ID:

2259-9786.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATCCACTAATGCCAGGTCACGCGTCTGCATCAGTCCCCGTGGTGGTCCCA[C/T]AGCAGAGCAGCATGAGTCTCTGTGCCATCTGCGCAGACCGAGCCACTGGA

Long Flanking Sequence:

AACAATAGGGTTCTGGAAGTAAAAAGTGCATGACAGCTATGCTCATTCATGTTTGCTATTTCACAACTGGTTCATCAGATTTACAATTTTTTTTTAGGGTAAGTGGTTGCAAACAATTGATTTGGGCTGAATTTCAACAAACACATTAGGTTGAACTTGACTAAATTTAACTTGTTTGTTTAAATTCCGCCCATATAAATAGTTACCACTTACCTAAAAATATTGTAAATCCAATTAATCATTTTTTTTTCATTGTAGATTAATTGGCCAGCATAATACTTGACAATATTTCTGATTTTACTATGCTTTGATTAAATAAATAAGTAGTCTTGATATCAGAAGAGATTTTTTTCGAAAACACTGACAACTTTCACTGGCCCCAAACTTTTGAATGGTTTTGCATATGAACTCAAACTAATTGTGTTTTCCCACTCTATTTTTCCATCTAAGATCCACTAATGCCAGGTCACGCGTCTGCATCAGTCCCCGTGGTGGTCCCA[C/T]AGCAGAGCAGCATGAGTCTCTGTGCCATCTGCGCAGACCGAGCCACTGGAAAACACTACGGAGCGTCCAGCTGCGACGGCTGCAAGGGCTTTTTCAGGAGGAGTGTGCGCAAGAACCATGCCTACACATGCAGGTGAAACCAGTATCACATATAGCTAAGTCAGAATTATTAGCCCTCTTGAATTATTGTTTTGGTGTAACGTCACTTATCAGTCATTCTGGAGTCCTTTGGCTCTTGTACCCCAGACATACTTCCTCTTTCTCCAGCCCTTCTCTGCATACCCAAACTGAACAATTAAGTGCATCTTCAATATATTTCACAACTTCTACAAGCATCATGCTCCTTGTGACCTGTCTAGACTTCTTATTAGACAGCGGTCTGGAACAAGGGTCCCCGCCCTAAAAAAATTCTTCTTCTTCTGCTTTTTGTCAAAAGTTTCTTCTGAAAAGTATGCAGCACAGTAAAAAAGAAGAAGTGTGTCTGGTCAATATATGGTATC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa41076

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024443	Nonsense	139	463	4	19

Genomic Location (Zv9):

Chromosome 7 (position 70195821)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	68800464
GRCz11	7	69037069

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATGAGTGTGTTGTTTATCTGTGTCTCTCAGCTGTCCAGAATGAGCGCGAC[C/T]GAATCAGCTGTCGGCGAGAAAATCAAGGAGTCGGGACTCTCACCATCGAT

Long Flanking Sequence:

CCAGTGTGCAGCATCCACCTGAATGACGTGACGGCAGCCATTTTGCATCAGACCGCTCACCACACACCAGCTGATTGGTGGAGAGGAGACAGTGATGAAGCCAATTGGTTATGGGGATGGTTAGGAGGCCATGATGGACAGAGGCCAGTGGGCCGATTTGGCCAGGATGCCGAGGTTAAACCCCTACTCTTTTCGAAGGACATCCTGGGATTTTTAACGACCACAGAGTGTCGGGACCTCGGTTTAACGTCTCATCCGAAAGACGGATGAGACGTTAAGTGAATTAGGTAACCTAAATTGGCTGTAGTATATGAGTGTGTGAGTGTGTTTCCCAGTACTGGGTTGCAGCTGGAAGGGCATGCGCTGGGTAAAACATATGCTGGAATAGTTGGCGGTTCATTCCGCTGTGGGGACCCCTGATATATTGGGGGGTGAGAGGAGGGAAAATGAATGAGTGTGTTGTTTATCTGTGTCTCTCAGCTGTCCAGAATGAGCGCGAC[C/T]GAATCAGCTGTCGGCGAGAAAATCAAGGAGTCGGGACTCTCACCATCGATGTGCTGATGCAGGCAGAGGCGTACACTCATCAGGTCAGCTTTCTGATCAGTTCATCATCTAAACAATAATTTTTAAGAGAATTGTCTGTCCAAGACATTTAAATACCTATTATACAGTTAAAGTCAAAACTATTAGCCCCCCTTTGAATTTCCTTTTCTTTTTGTAATATTTCCCAAATTATGTTTAGCAGAGCAAGAAATTTTTCACAGTATGTCTGATAATATTTTTTCTTCTAAAGAAAGCCTTATTAGTTTTATTTTGACTGGAATAAAAGCAGTTTTTAATTTATTTAAAAGCATTTTAGGGTCAATATTATTAGCCCCTTTATTGATTGTCAACAGAAGAAACCTGTTATACAAGGTCTTGCCTAATTAGCCTAACTCACCTAGGTAACCCAGTTAAGCCTTTAAATGTCACTTTAAGCTGAATACTAGTATCTCAAAAATATC

Associated Phenotype:

Not determined