ZMP

hoxb8b

Ensembl ID:

ENSDARG00000054025

ZFIN ID:

ZDB-GENE-980526-291

Description:

Homeobox protein Hox-B8b [Source:UniProtKB/Swiss-Prot;Acc:Q8JH55]

Human Orthologue:

HOXB8

Human Description:

homeobox B8 [Source:HGNC Symbol;Acc:5119]

Mouse Orthologue:

Hoxb8

Mouse Description:

homeobox B8 Gene [Source:MGI Symbol;Acc:MGI:96189]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa42040	Nonsense	Mutation detected in F1 DNA	Not yet available
sa45461	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa42040

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000076154	Nonsense	34	247	1	2

Genomic Location (Zv9):

Chromosome 12 (position 28688946)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	27026555
GRCz11	12	27117915

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATTCTCTGCGCTCCAACTACTATGACTGCCCAAGCTACACGCCGGATCTT[G/T]GAGGCAGACCATCTGTGCTGTACGGTCACAACACAGGATCTGCGTTTCAG

Long Flanking Sequence:

TAAGACTCGTACTCCGCCTCCCCCTCTACCTCCGAGAACTCCCTCTCTCCCCTTTTTCATCTCTTTTCAGTCTCTTCTGCTCTTCCTATCACAAGATCGCGCTTTGTCTGTTTGGAGATTGTGCGCGCATCCAATGATACAATGATAACTGACGCCCATATGAAATGAGTAAAAAAGGAAAACTATTTATTGCTCGGGGACCGTCACTAAGGAGTCATGTGGGTGCAGCTACGGATACATTTGTTTGCATGAATATTTACGACATTTTACGCATATAATTTCCACCTGGATGAATTCGTTTTTATTGCAATAGCAGGCCTCAAGCAACATAATTTATCTAGAGATTTCTTTATCTCAACACTGATTGCCAAAGTTTCACCGGGGAGTTGATCTTTCAAGCAATGAGTTCCTACTTCGTCAATTCCCTCTTCACTAAATTTAAAGGAGGCGATTCTCTGCGCTCCAACTACTATGACTGCCCAAGCTACACGCCGGATCTT[G/T]GAGGCAGACCATCTGTGCTGTACGGTCACAACACAGGATCTGCGTTTCAGCACGCGGCTCAGTTCCCGGATTTCTACCACCACGGTACATCATCATTCCCCCACGCGTCTTACCAGCAGACCCCGTGCGCAGTTGCGTACCCTGGAGATGCCACGGGAAACATCTTGGGCCAGGACGGTTTACAGAAACAGTCGTTCTTTGGCGCGCCAGATTCGGATTTTACGCAGTTTGGGGATTGTAATTTAAAGGTCAGCGGTATCAGGGATGATCTGGAGAGTGCAGAACCGTGCACAGCGCAACTCTTCCCATGGATGAGACCACAAGGTGAGATGAGTGAAGAGAAACACCTAGTCTGTTATAGTCCCATATAAAACACTGCAGACAATGCTAGGCCTCTTATTACCCCCAATTAAACGCTTTATGGCACCTATAGATTACTAAGGAATTAACACCTTTTAAGAATATCCGGATTACGTGTGTACACATTGTGTTATGACAGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa45461

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000076154	Nonsense	82	247	1	2

Genomic Location (Zv9):

Chromosome 12 (position 28689090)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	27026699
GRCz11	12	27118059

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CATTCCCCCACGCGTCTTACCAGCAGACCCCGTGCGCAGTTGCGTACCCT[G/T]GAGATGCCACGGGAAACATCTTGGGCCAGGACGGTTTACAGAAACAGTCG

Long Flanking Sequence:

ATAACTGACGCCCATATGAAATGAGTAAAAAAGGAAAACTATTTATTGCTCGGGGACCGTCACTAAGGAGTCATGTGGGTGCAGCTACGGATACATTTGTTTGCATGAATATTTACGACATTTTACGCATATAATTTCCACCTGGATGAATTCGTTTTTATTGCAATAGCAGGCCTCAAGCAACATAATTTATCTAGAGATTTCTTTATCTCAACACTGATTGCCAAAGTTTCACCGGGGAGTTGATCTTTCAAGCAATGAGTTCCTACTTCGTCAATTCCCTCTTCACTAAATTTAAAGGAGGCGATTCTCTGCGCTCCAACTACTATGACTGCCCAAGCTACACGCCGGATCTTGGAGGCAGACCATCTGTGCTGTACGGTCACAACACAGGATCTGCGTTTCAGCACGCGGCTCAGTTCCCGGATTTCTACCACCACGGTACATCATCATTCCCCCACGCGTCTTACCAGCAGACCCCGTGCGCAGTTGCGTACCCT[G/T]GAGATGCCACGGGAAACATCTTGGGCCAGGACGGTTTACAGAAACAGTCGTTCTTTGGCGCGCCAGATTCGGATTTTACGCAGTTTGGGGATTGTAATTTAAAGGTCAGCGGTATCAGGGATGATCTGGAGAGTGCAGAACCGTGCACAGCGCAACTCTTCCCATGGATGAGACCACAAGGTGAGATGAGTGAAGAGAAACACCTAGTCTGTTATAGTCCCATATAAAACACTGCAGACAATGCTAGGCCTCTTATTACCCCCAATTAAACGCTTTATGGCACCTATAGATTACTAAGGAATTAACACCTTTTAAGAATATCCGGATTACGTGTGTACACATTGTGTTATGACAGTTAATAGAAGCTGTGAGGTTTTTTGACACTTCGTTACTTTATTAACAGATAGCCTAGATATATATGCCTATCCACCTTATTTCACAACATGTGTTTTTTATTTAAATACGCAGACTTCGTTATAACCACTCTTAATTTGTTTGAC

Associated Phenotype:

Not determined