ZMP

onecut3

Ensembl ID:

ENSDARG00000056395

ZFIN ID:

ZDB-GENE-050208-744

Description:

Novel protein similar to vertebrate one cut domain, family [Source:UniProtKB/TrEMBL;Acc:Q1LY59]

Human Orthologue:

ONECUT3

Human Description:

one cut homeobox 3 [Source:HGNC Symbol;Acc:13399]

Mouse Orthologue:

Onecut3

Mouse Description:

one cut domain, family member 3 Gene [Source:MGI Symbol;Acc:MGI:1891409]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa7494	Missense	Mutation detected in F1 DNA	Not yet available
sa43821	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa7494

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:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000078885	Missense	49	451	1	2
ENSDART00000135984	Missense	52	447	1	2

Genomic Location (Zv9):

Chromosome 22 (position 20781987)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	20436663
GRCz11	22	20461641

KASP Assay ID:

554-4095.1 (used for ordering genotyping assays)

KASP Sequence:

GGCGACACATAGGAACTTGGTATCATCGCACGGGAGGTCAGCGATGGTGT[C/T]CAGCATGGCCTCGATACTGGACGGGGCCGGGGAGTATCGCACGGACCATT

Long Flanking Sequence:

TGAACAGAGAATGAGGCGCTTTCCTGAACTCAAGAAACACAGAAGAACGTTTATGCTGTCCGGTGCGCGTGCCCGTACACTCAGGCACAACACATCTTAATATATTGCGCGGTCACGAGGCAGACACTCTCACTCGGTCAGCTTCGACTGTCAGTAGTAAGACGCGCGCCACGGCGATAGATACAAGCGTTTAGACACCAGGCGTACGTACATGTGCGTGGTGAAATGCTGGATTGACTAACACTGAAGATCTCGGGATCAATGGCGCGCGGCTTTGAGATCGTTTAAAATTTATTGGAAGGGAGAGTGTGAGAGAGAAAGGAAAGAGAGAGAGGGAAAACAGTGTCTTTCAACAATGGAACTTACAATGGAAAACATTGGGAATTTGCACGGCGTCTCACACTCCCATCAAACGGGAGACTTGATGAACTCTCCTCACGCGCGACAGTCGGCGACACATAGGAACTTGGTATCATCGCACGGGAGGTCAGCGATGGTGT[C/T]CAGCATGGCCTCGATACTGGACGGGGCCGGGGAGTATCGCACGGACCATTCGTTGTCCGGTCCTCTCCATCCAGCGATGACCATGTCGTGCGATTCGAGCATGAGTCTGAGCAGCACTTACACCACCCTGACGCCGTTGCAGCACCATTTGCCTCCCATATCCAACGTCTCAGATAAATTTCACCATCATCCGCACCCTCACGCTCATCACCACCCCGCGCACCAGCGTCTCGCAGCCGGGAACGTCAGCGGCAGCTTTACGCTGATGCGTGATGACCGGGGCCTCGCGTCTATGAGCAACCTATACGGCCACTACTCCAAAGATTTGTCCGGGATGGGACCACCTTTGTCACCTCTTTCCAACGGCCTTGGGTCTTTGCACAACTCTCAACAAACTCTAAGTGCGTACGGTCCGAGTGCTCACCTGGGGAATGACAAGATGATTTCCTCGGGGGGCTTCGAGTCCCATGCTGCGATGCTCGGACGGGGCGAGGAGCACC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43821

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
ENSDART00000078885	Nonsense	180	451	1	2
ENSDART00000135984	Nonsense	183	447	1	2

Genomic Location (Zv9):

Chromosome 22 (position 20782379)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	20437055
GRCz11	22	20462033

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CACCTTTGTCACCTCTTTCCAACGGCCTTGGGTCTTTGCACAACTCTCAA[C/T]AAACTCTAAGTGCGTACGGTCCGAGTGCTCACCTGGGGAATGACAAGATG

Long Flanking Sequence:

GCGTCTCACACTCCCATCAAACGGGAGACTTGATGAACTCTCCTCACGCGCGACAGTCGGCGACACATAGGAACTTGGTATCATCGCACGGGAGGTCAGCGATGGTGTCCAGCATGGCCTCGATACTGGACGGGGCCGGGGAGTATCGCACGGACCATTCGTTGTCCGGTCCTCTCCATCCAGCGATGACCATGTCGTGCGATTCGAGCATGAGTCTGAGCAGCACTTACACCACCCTGACGCCGTTGCAGCACCATTTGCCTCCCATATCCAACGTCTCAGATAAATTTCACCATCATCCGCACCCTCACGCTCATCACCACCCCGCGCACCAGCGTCTCGCAGCCGGGAACGTCAGCGGCAGCTTTACGCTGATGCGTGATGACCGGGGCCTCGCGTCTATGAGCAACCTATACGGCCACTACTCCAAAGATTTGTCCGGGATGGGACCACCTTTGTCACCTCTTTCCAACGGCCTTGGGTCTTTGCACAACTCTCAA[C/T]AAACTCTAAGTGCGTACGGTCCGAGTGCTCACCTGGGGAATGACAAGATGATTTCCTCGGGGGGCTTCGAGTCCCATGCTGCGATGCTCGGACGGGGCGAGGAGCACCTGGCGCGGGGTTTAGGGGGACATGGAGCGGGTATCATGTCTTCTCTCAACGGCATCAATCACCACCACCACCACAGTCACTCGCACTCTCAGGCGAATGGTTCGGTGCTCTCGGAGCGGGACAGGCAGGCAGGAGCCGGCGGACAGGGTGGTGGGTCGGGTCAAGTAGAGGAGATCAACACCAAAGAGGTGGCTCAGCGAATAACGGCGGAGTTAAAGAGGTACAGCATTCCACAGGCCATCTTTGCCCAAAGGATCTTGTGTCGCTCTCAAGGAACTCTGTCGGATCTCCTGCGGAATCCAAAACCCTGGAGTAAACTCAAGTCAGGTCGGGAGACGTTCAGACGGATGTGGAAGTGGCTACAAGAACCAGAGTTCCAGCGCATGTCGGCC

Associated Phenotype:

Not determined