ZMP

hoxb1a

Ensembl ID:

ENSDARG00000008174

ZFIN ID:

ZDB-GENE-990415-101

Description:

Homeobox protein Hox-B1a [Source:UniProtKB/Swiss-Prot;Acc:O42366]

Human Orthologue:

HOXB1

Human Description:

homeobox B1 [Source:HGNC Symbol;Acc:5111]

Mouse Orthologue:

Hoxb1

Mouse Description:

homeobox B1 Gene [Source:MGI Symbol;Acc:MGI:96182]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa31326	Nonsense	Available for shipment	Available now
sa1191	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa31326

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110682	Nonsense	239	316	2	2

Genomic Location (Zv9):

Chromosome 3 (position 24061630)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	23639841
GRCz11	3	23770389

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAAACACTATTCGGACAAATTTCACAACCAAACAACTGACAGAGCTCGAA[A/T]AAGAATTTCACTTCAGCAAGTATCTGACGCGAGCGCGGCGTGTGGAGATT

Long Flanking Sequence:

ATTGTGTTCTTAAGCTTTCGTCTCCTGTCCCAATAGTGACTCGGAACGATTTAGTGCACCAACTTTTACGCATGGGGTTCACCATTTTGACATACTGTACAAATTGAGTGGTCATAAAGCCATCTTTGGGGAGTATTGAATAGCATGTGTTCAACATAACCCGTTATGTTCTTTCAAAATTGATAACATACAAACAGGGGAATTACGCTAAGGTTAACAAAAGTTCGCAATATTGAATTACTTGTTGAATGTTCTTTAATGCTACTGAAAGTGTCACATGTAATTATTGTTAAAACAATTATTAACAACACATTTAATTGTGTTTGGTGTGTTAACCCAATAAAGTATTATTTAACTGTTTTATGTTTAACATTGTCAAACAGCCATGTAACTGTTCCTTCTCTTTTTTTTTTCTCGCAGGTAAAGTGGCTGAGTACGGACTAGGGCCGCAAAACACTATTCGGACAAATTTCACAACCAAACAACTGACAGAGCTCGAA[A/T]AAGAATTTCACTTCAGCAAGTATCTGACGCGAGCGCGGCGTGTGGAGATTGCTGCCACACTTGAGCTCAACGAGACGCAGGTTAAGATTTGGTTTCAAAACCGCCGAATGAAACAGAAGAAGCGAGAGAAGGAGGGACTCGCGCCTGCTTCCTCCACTTCGTCTAAAGACCTCGAGGATCAATCTGATCACTCAACTTCAACATCTCCAGAAGCCTCTCCAAGTCCGGATTCCTAACCGAGCACAATAACTTTGGGTGCACTGATCAAATGTGAAATATATAGCAAAGTCTATTAATTTAACCATTCCACTGTGGCCCAAAAGACTTGTTCTGTTGGGACAATTAATTGCAGGGAAAAACAACGACAGGCGAAAAAATGTGAAGAGCAAAAAGACTTTCTTTAACAATACAATGTAAAATTCCCAACACTTGCCTAAATTGTTTGTGTGTTATACAGGGTATTTCTGCTGTGATTACAAATATAATGCACTTTCAGAATG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa1191

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:

G > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110682	Nonsense	269	316	2	2

Genomic Location (Zv9):

Chromosome 3 (position 24061722)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	23639933
GRCz11	3	23770481

KASP Assay ID:

554-1100.1 (used for ordering genotyping assays)

KASP Sequence:

GTGGAGATTGCTGCCACACTTGAGCTYAACGAGACGCAGGTTAAGATTTG[G/A]TTTCAAAACCGCCGAATGAAACAGAAGAAGCGAGAGAAGGAGGGACTCGC

Long Flanking Sequence:

TACTGTACAAATTGAGTGGTCATAAAGCCATCTTTGGGGAGTATTGAATAGCATGTGTTCAACATAACCCGTTATGTTCTTTCAAAATTGATAACATACAAACAGGGGAATTACGCTAAGGTTAACAAAAGTTCGCAATATTGAATTACTTGTTGAATGTTCTTTAATGCTACTGAAAGTGTCACATGTAATTATTGTTAAAACAATTATTAACAACACATTTAATTGTGTTTGGTGTGTTAACCCAATAAAGTATTATTTAACTGTTTTATGTTTAACATTGTCAAACAGCCATGTAACTGTTCCTTCTCTTTTTTTTTTCTCGCAGGTAAAGTGGCTGAGTACGGACTAGGGCCGCAAAACACTATTCGGACAAATTTCACAACCAAACAACTGACAGAGCTCGAAAAAGAATTTCACTTCAGCAAGTATCTGACGCGAGCGCGGCGTGTGGAGATTGCTGCCACACTTGAGCTCAACGAGACGCAGGTTAAGATTTG[G/A]TTTCAAAACCGCCGAATGAAACAGAAGAAGCGAGAGAAGGAGGGACTCGCGCCTGCTTCCTCCACTTCGTCTAAAGACCTCGAGGATCAATCTGATCACTCAACTTCAACATCTCCAGAAGCCTCTCCAAGTCCGGATTCCTAACCGAGCACAATAACTTTGGGTGCACTGATCAAATGTGAAATATATAGCAAAGTCTATTAATTTAACCATTCCACTGTGGCCCAAAAGACTTGTTCTGTTGGGACAATTAATTGCAGGGAAAAACAACGACAGGCGAAAAAATGTGAAGAGCAAAAAGACTTTCTTTAACAATACAATGTAAAATTCCCAACACTTGCCTAAATTGTTTGTGTGTTATACAGGGTATTTCTGCTGTGATTACAAATATAATGCACTTTCAGAATGTTTACGAGTCTCTGAGGGAACATAAATGTCTTTACAGGGTTTTGTGTTGTCAAAATATTCATTGATGTTTTGTTGCGTTTTTTATGTATAGT

Associated Phenotype:

Not determined