ZMP

pou1f1

Ensembl ID:

ENSDARG00000058924

ZFIN ID:

ZDB-GENE-040630-7

Description:

pituitary-specific positive transcription factor 1 [Source:RefSeq peptide;Acc:NP_998016]

Human Orthologue:

POU1F1

Human Description:

POU class 1 homeobox 1 [Source:HGNC Symbol;Acc:9210]

Mouse Orthologue:

Pou1f1

Mouse Description:

POU domain, class 1, transcription factor 1 Gene [Source:MGI Symbol;Acc:MGI:97588]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa8555	Nonsense	Mutation detected in F1 DNA	Not yet available
sa41392	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa8555

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000081878	Nonsense	89	350	2	7

Genomic Location (Zv9):

Chromosome 9 (position 19762052)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	19136294
GRCz11	9	19144006

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CTCCACTACCCGATRCCCCCATKTCACTATAGCAACCAGCAGACCACCTA[C/A]GGCATGATGGCAGGTACGTCAAGTTGCAACTGCGTCAACCATTGCTCTTT

Long Flanking Sequence:

TCATGCTCACCTGTAAACTAATACTGCTCAGATCCCATGGTGACATAAAATTTCTTTAGTAGACTAACTCAAAAAAAATTTTGTTACTAAAAAATCTTTAGATAAAAAAAAAACACTGTTTAAAATTAAAGAACGTCGATAAAAAGTTTCTGTTTCAAAGTGATATTCTTTCTTGTGCTTTTTTCTTTTCCTTTTTTTTTCTTTTTTTTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTCAAGTATAACTTATATTAGTGTCTTCTTTAGTCCCCTCAGGTCTCCCATTGGTCCAGTCGTCCAAGCGCTCTCATATGCACCTGTCCACTTCTGCTTTGGGCAATGCGTCAGCCAGCCTCCACTACCCGATGCCCCCATGTCACTATAGCAACCAGCAGACCACCTA[C/A]GGCATGATGGCAGGTACGTCAAGTTGCAACTGCGTCAACCATTGCTCTTTTATGCATAAACATAATAAACACACAAGCATGCAGGCTTAATGTTGTGTGTGTGTGAGTGAAATGACAGTGTGGTGTATGTGTGTGTGCGTGTGTTTGTGTGCATCTCCAGCACAGGAAATGCTCTCTGCCAGCATCTCCCAGACCCGCATCCTGCAGACCTGCAGTGTACCTCATGCAAACATGGTTAATGGCGCCAACTCACTGCAAGGTACAGCCTGTGCTTAAATCTAGACTTTGAACCCCATGGCACCACCATTAAAGCGGACAGTTCACCCAAATATTTTAAATTGACTCATTATTTACTTCCCCTCAAGTGGTTGCAAACCATGAGTCTCTTTTTTTTTTCTTTCTTTTGAACACAAAATAAGGTATTTTGGAAAAAGCTGGAAATCTGTAACCATTAACTTCAATAGTAGGAAAAACTAATTCTATAGAAGTCAATGGTTACA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa41392

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
ENSDART00000081878	Nonsense	202	350	4	7

Genomic Location (Zv9):

Chromosome 9 (position 19756611)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	19130853
GRCz11	9	19138565

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACATGGACTCGCCTCAGATCCGAGAGCTGGAGAAGTTCGCTAATGACTTC[A/T]AATTAAGGAGGATCAAACTTGGTTTGTCTTTTGATTTCAGTTGCCCATTT

Long Flanking Sequence:

ACCAGTAAATCCGCAGTCCAAGTGGAAATGGGAATGAGATCATTCCTACACAGCATGGGACATTGAATTAAATATCTGATTGAATATTATACACTGCCCATCATCTTCAAAACATCAATCTGGCTTGTTTGATTCTGTTGAAGTTTACACAATGCAAATGTTGGTGCATTCAATAGTATTACAATCTCTTTTATTTAAAAAAAAAAAATGATGGTTTGCTTTCGTGTCTCTGAGATGGGATTATTAGGTATTATTCTCTTGATTTGTGTCCCGCAGGAGCTCTGGCTCCACGTCTCTACAAGTTCCCTGAGCACAGTTTGGCTGGAGGATCCTGTGCTTTGAGCCACGGCTTCGCTCCTCTTCCCCAGACCCTGCTAACAGATGAGCCCATTCTAGGAGACATCAAGCAGGAGCTGCGCAGGAAGAGCCGGACCCTCGACGAGACCCCCGACATGGACTCGCCTCAGATCCGAGAGCTGGAGAAGTTCGCTAATGACTTC[A/T]AATTAAGGAGGATCAAACTTGGTTTGTCTTTTGATTTCAGTTGCCCATTTTAAAAGTGTAGTTCACCAAATGTATATTTACTCCCCATTGACTCATCTTGTGTTTCGAAAAGTGTGGTTCTTTCATCGTTTGAACACAAAAGCAGACATTTCGAAGAATGTAAATCAGTAGCCATTGACTTTTATTTATAGAATTATTATTATTGAAATCAATGACTACTGGTTTCCAAACTTTCTCAAAATAAGAAAGAATAGTGGCGACGCAGTGGGTAGCACGTTCGCCTCACAGCAAGAAGGTCGCTGGGTTGCTGGTTCGATCCTCGGCTCAGTTGGAGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGTGTTCGCATGGGTTCCCTCCGGGTACTCCGGTTTCCCCCACAGTCCAAAGACATCACTTGGTGTCTTCAGACATCATTTGATGTCCAAAGACATGTGGTACAGGTGAATTGGGTAGGCTAAATTGTCCGTACTGTA

Associated Phenotype:

Not determined