ZMP

nr2f6a

Ensembl ID:

ENSDARG00000003607

ZFIN ID:

ZDB-GENE-030131-4362

Description:

nuclear receptor subfamily 2, group F, member 6 [Source:RefSeq peptide;Acc:NP_991120]

Human Orthologue:

NR2F6

Human Description:

nuclear receptor subfamily 2, group F, member 6 [Source:HGNC Symbol;Acc:7977]

Mouse Orthologue:

Nr2f6

Mouse Description:

nuclear receptor subfamily 2, group F, member 6 Gene [Source:MGI Symbol;Acc:MGI:1352453]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa19746	Essential Splice Site	Available for shipment	Available now
sa39819	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa19746

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000022379	Essential Splice Site	122	402	3	5
ENSDART00000133818	None	None	88	None	2
ENSDART00000135323	Essential Splice Site	113	243	2	3

Genomic Location (Zv9):

Chromosome 2 (position 23487358)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	24721137
GRCz11	2	24376788

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAATACTGCCGTTTAAAGAAGTGTTTCCGAGTGGGAATGCGTAAAGAAGG[T/C]AATTGTTTGATGCAAACACACTGATTTGTCAACGTAATATTAGATGTATA

Long Flanking Sequence:

TGCCGACAGCACGTTTGGGAGTATCATTCTTCCTCGGTTGTGCTGAGAACTAAGCGATGGCCATGGTGAGAGGGGGGTGGGGAGATCCCAACGGGGAAACAAATGGACTTGGTGACAAGGGTTACCTGAGGGGAGATGAAGATGACGGGTCACCGCAAGGAGGCGGCAGCGACATGGAGGCCGGTGAGGATGATAAGGGATGTGTGGTGGACTGTGTTGTCTGCGGCGACAAGTCCAGCGGGAAACACTATGGTGTGTTCACCTGTGAGGGCTGCAAGAGCTTCTTTAAACGAAGTGTCAGACGAAACCTTAACTACACCTGCAGGTAATGCACAGAACTGAAGCAGTGATTATTAATGCAGTTGCTTTGCATGCTAATGTGAAGCTGTTTTGGTGCCTTTCAGATCAAACCGAGACTGCCAAATTGACCAGCATCATCGCAACCAGTGTCAATACTGCCGTTTAAAGAAGTGTTTCCGAGTGGGAATGCGTAAAGAAGG[T/C]AATTGTTTGATGCAAACACACTGATTTGTCAACGTAATATTAGATGTATAGTTAACAAAGAAGCTGTATCACTTATGTCCAGATTTAGACAATGTTTTCAAGCATACATTACCAAAATTCTGGGCTTGGCAAGTTTTTTTTATTTTATTTTTTTATGTTTCTTAAGTCTCTCAATCTTCTTTTCTTTGAAAAAGAATAAAACATGAATGGCATAAATTTCATTCAAATAATATTAAATGTGAAAATGTCTGATTTTTAAATATTTTTAAATTGGTTTGTCAAAAATAATTGTCTTTTGGTCAGTATGCTGTTGGTCACAACTCGCAGGCCTTTCCCAATTCCATCCCCCTCTCTCTCCCACGGTACTTTCTGTCTATGTACTGTCCTATCATATTAAAAAGAAAAATGACAAAAATCCTTAAATTATCATTTAAAAAAAGATAATTTTTTTGTTGGGAATAAAAATTATCATGTTAAGCTGTTCCGTAAAAAATGTAGAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39819

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
ENSDART00000022379	Nonsense	180	402	4	5
ENSDART00000133818	None	None	88	None	2
ENSDART00000135323	Nonsense	170	243	3	3

Genomic Location (Zv9):

Chromosome 2 (position 23482328)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	24726167
GRCz11	2	24381818

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTCCCAGCTCCTGCGGGCAGAGCCTTACCCTAACAGCCGCTACAGCCAC[C/T]AGTACAACCAGCAGATGCAAGGCGGTGGTGGCGGTGGATCTGGCATGGGC

Long Flanking Sequence:

ACATGATGAAACGTGCATCAAAGCCCAATGACCTATATATCTTATCTCCTCAACAGTTTTGCCTTTAAAACTGAGCGTTTTATATAAACACACACACACACACACACACACTGCTATTTATATTATTACATTTTCTCTTTATATTTGTCTAGTATTCCCCTTTTCATTTCATCATTTATATCCAAAAGCTTGCATAATAAAGCTTGGGATATTTCGAAGCCCTCTATACTCTCTCTACCAGATGTTGCATGAACAAATAAGAAAGTCATCCCTCAAGCTCTTCATCTCCATCACGACTCCCTTCTCTCCTCTTCTTCTCCCCTTTAGCAGTTCAGCGTGGACGGATCCCACCTTCACATTCGAGCCTGAGCCCATCTACAACTCCAGTAGGCGGTAATGCCGGCGGTGGTGTGAGCGAGTTCTACAATGGGCAGCCGGTGTCCGAGCTCATCTCCCAGCTCCTGCGGGCAGAGCCTTACCCTAACAGCCGCTACAGCCAC[C/T]AGTACAACCAGCAGATGCAAGGCGGTGGTGGCGGTGGATCTGGCATGGGCATCGACAGCATCTGTGAGCTCGCTGCCAGACTCCTGTTTAGCATCATCGAATGGGCCCGAAACATTCCGTACTTCCCCGAATTGCCAGTATCGGAGCAGGTGGCCTTGCTGCGGCTCAGCTGGAGCGAACTGTTTATTCTGAACGCAGCTCAATCTGCCCTGCCACTGCACATGGCCCCGCTGCTGGCCGCCGCAGGCTTCCACTCCTCACCCATGTCCGCGGAAAGGGTGGTGTCCTTCATGGACCAGGTGCGCGTCTTCCAGGACCAGGTGGAGAAGCTGACGCGTCTGCAGGTGGATTCGGCAGAGTACAGCTGTCTCAAGGCCATAGCGCTCTTCTCGCCAGGTAAACTGCATTTATCCAGGTGAAAGGTGATGGAATGTGTAAATGATCCAAATGGTGGAGAGTAGAATTGTGTTTTGTGCTAGGAGTTAGGGTAGTGCTAGCTC

Associated Phenotype:

Not determined