ZMP

nr2f1b

Ensembl ID:

ENSDARG00000017168

ZFIN IDs:

ZDB-GENE-000112-32, ZDB-GENE-040426-1438

Description:

Nuclear receptor subfamily 2 group F member 1-B [Source:UniProtKB/Swiss-Prot;Acc:Q6PH18]

Human Orthologue:

NR2F2

Human Description:

nuclear receptor subfamily 2, group F, member 2 [Source:HGNC Symbol;Acc:7976]

Mouse Orthologue:

Nr2f2

Mouse Description:

nuclear receptor subfamily 2, group F, member 2 Gene [Source:MGI Symbol;Acc:MGI:1352452]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa34990	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa34990

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000027242	Nonsense	79	389	1	3

Genomic Location (Zv9):

Chromosome 10 (position 45299809)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	43950872
GRCz11	10	43797669

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCGGGAAGCACTACGGACAGTTCACCTGCGAGGGATGCAAAAGTTTCTTC[A/T]AGCGAAGTGTCCGGCGGAATTTATCGTACACGTGCCGCGCCAACAGAAAC

Long Flanking Sequence:

AAAAGTGCGGTCATGTACATCTCCATCATGCCGAAAAGAGTTGAGTTTTCACGGATGCTCCAAATAAATCTGTTATAGTCAGCAATCCTCCACTCATGCTCCTGTCAATCATGCCGACAGCGCGGTATCTGTACTCCCATTGGATCTGATTCATCTGGGGTTTCCGATCGTCCCTTTTACGCACGGAGTTGCTTCAAATCGCGCGTTTAGGGAAATGCGTGGATAAAACCGGCTTTCTTGGTTAATTCGCGTAAAAGATTCCAGCCATGGCCATGGTGGTGAGCGCGTGGAGAGATCCGCAGGAGGAGCTGGCAGCGGTGGATGATCAGAGCGCGGCCGGGAGAGAGCACCTCCAGCACCGGCACTCGCCGAAGTCCGCGGAGGAAAAAGCGCAGATCGCGGCGCAAAACCAGCAGCACGTCGAGTGTGTGGTGTGCGGGGATAAATCCAGCGGGAAGCACTACGGACAGTTCACCTGCGAGGGATGCAAAAGTTTCTTC[A/T]AGCGAAGTGTCCGGCGGAATTTATCGTACACGTGCCGCGCCAACAGAAACTGCCCGGTGGATCAGCACCACCGCAACCAGTGCCAGTACTGCCGCCTGAAGAAGTGCCTGAAAGTGGGCATGAGACGCGAAGGTGAGTACATCTTGTGTGGGGGAAATCTGCATTTATGCAACCTGCGATAATTACTGATTGTGTCATAAAATGGTAGAAATAAATAAAAATAAGCGGATGATTTTCAATCAATATTTACAATGATTTATTTGCAAACATTTTAATTTTTAAATACCTAAACTTATTCATCATACTTGGAAAAAAATATTATAGTAATTTGTAGTTAGTCTTTTGAATTATGGGAAAGTACTTGAATTAATAAGGTTTGGTTGTTCTATAGTTGGTTACAACAACTGTTGTAAAATAAACAAGACAATGCTGTATTTTTTTTAGAAATATAAAAAAATATTGTACTAGCAAAAAAAATTACATTAGTAAACACTGATATT

Associated Phenotype:

Not determined