ZMP

hoxc8a

Ensembl ID:

ENSDARG00000070346

ZFIN ID:

ZDB-GENE-990415-114

Description:

Homeobox protein Hox-C8a [Source:UniProtKB/Swiss-Prot;Acc:Q68EH7]

Human Orthologue:

HOXC8

Human Description:

homeobox C8 [Source:HGNC Symbol;Acc:5129]

Mouse Orthologue:

Hoxc8

Mouse Description:

homeobox C8 Gene [Source:MGI Symbol;Acc:MGI:96198]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa39422	Nonsense	Mutation detected in F1 DNA	Not yet available
sa15792	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa39422

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
ENSDART00000103139	Nonsense	12	250	1	2

Genomic Location (Zv9):

Chromosome 23 (position 36153024)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	36002677
GRCz11	23	36101480

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTAATGCTAGATAAACATGAGCTCTTATTTTGTTAACCCTCTTTTTTCC[A/T]AGTACAAAGGCGGCGAAACATTAGAGCCAACTTACTACGACTGCAGGTTT

Long Flanking Sequence:

TTCAATAAAAAGACTGACAACTGCGTTTCCCCTTCAAGGTAGACGCCTGTGGACGCTCTGGAAGATGAGGAGCCAAAGGGTGGGGTGTAGGGGACAAGGGGTGGGGGGGTGAGTCTCATTGTAGTGGGGGTGGCTGGTGGGAGGCAAAAAAAAAGTATGAGCTTGTGACTGAGCCGTCGGAGCTAGCCAGCTTTAACCTTAACACACATCCACCGTGCACGCCATGATTTGAGGCTGCAAAAGGAAAGGCTGGCGATAGGAAGAGAGAGAGAGAGAGACTAAGCGAAAGGAGCTGAAGTGGGAGCTGCCTCAGATTGTCCGAAGGGGCAGCATTTCTCCATCTAGTTCCGGTTGCTGTGTCTGCGTTGCATGCCATTTGGAACTGCAACAATAGGTTGCCACCATTAGGAGAGGAGAATACATATATTTTTTCCAAACAGACTGACTCTTTTTAATGCTAGATAAACATGAGCTCTTATTTTGTTAACCCTCTTTTTTCC[A/T]AGTACAAAGGCGGCGAAACATTAGAGCCAACTTACTACGACTGCAGGTTTCCACAGAGCGTTGCCCGAAGCCACACGCTTGTGTACGGACATGGAGCAGCTGCGCCGGGGTTTCAACACCCGTCGCATCACGTACAGGACTTTTTCCATCACGGAACCACAGGTATCTCCAACCCTGGGTATCAACAGAACCCCTGTGCATTGGCATGTCACGGAGACGCTACGAAATTTTATGGATATGAAGCCCTTCCGAGGCAACCGCTTTATGGTACCCAGCAAGAGGCCACCTTAGCGCAATACCCAGACTGTAAATCGTCCAATAGCACTAACCCTGGAGAAGGACAAGGCCACTTAAGTCAAAACTCCTCTCCGAGCCTCATGTTCCCTTGGATGCGGCCTCACGGTTAGCACTTATTATTTCACATTATGTTCAGTTACTGTGTGTGAGTTTGTCCGTGTGACTGCGTCAGTGTGTCAAGATTCTAATTATTGTGTAGCTTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa15792

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
Order Allele From EZRC

Mutation:

T > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000103139	Nonsense	129	250	1	2

Genomic Location (Zv9):

Chromosome 23 (position 36153376)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	36003029
GRCz11	23	36101832

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AGACTGTAAATCGTCCAATAGCACTAACCCTGGAGAAGGACAAGGCCACT[T/G]AAGTCAAAACTCCTCTCCGAGCCTCATGTTCCCTTGGATGCGGCCTCACG

Long Flanking Sequence:

TGCTGTGTCTGCGTTGCATGCCATTTGGAACTGCAACAATAGGTTGCCACCATTAGGAGAGGAGAATACATATATTTTTTCCAAACAGACTGACTCTTTTTAATGCTAGATAAACATGAGCTCTTATTTTGTTAACCCTCTTTTTTCCAAGTACAAAGGCGGCGAAACATTAGAGCCAACTTACTACGACTGCAGGTTTCCACAGAGCGTTGCCCGAAGCCACACGCTTGTGTACGGACATGGAGCAGCTGCGCCGGGGTTTCAACACCCGTCGCATCACGTACAGGACTTTTTCCATCACGGAACCACAGGTATCTCCAACCCTGGGTATCAACAGAACCCCTGTGCATTGGCATGTCACGGAGACGCTACGAAATTTTATGGATATGAAGCCCTTCCGAGGCAACCGCTTTATGGTACCCAGCAAGAGGCCACCTTAGCGCAATACCCAGACTGTAAATCGTCCAATAGCACTAACCCTGGAGAAGGACAAGGCCACT[T/G]AAGTCAAAACTCCTCTCCGAGCCTCATGTTCCCTTGGATGCGGCCTCACGGTTAGCACTTATTATTTCACATTATGTTCAGTTACTGTGTGTGAGTTTGTCCGTGTGACTGCGTCAGTGTGTCAAGATTCTAATTATTGTGTAGCTTGGGCTGTTCATAAACAGAAATTAAAACAGGTGGGGTAGCCTATGCTTTTCAGGTCACGAAATTGTAATAAGTGTTACTGCAAAGTGTCGTATTTTAATAACTCAAAGGACCATCAAGGTTTATTTATGTAAAAACAAATGATGTGGTTTTGATTACTGGCTAGATTGTGTAGACAGAGCTATGTCGACATTAATCGAACCCAGATTATTCTAGTTAGAAACATCCACCTGTCTTAACAGTTTTGGGATAACTAAAAGTAGAAATGAGTGTAATGTGTGGTGGTAAACTGTAATGTTAATGTCATATAATTATTTTGATTCCAATTGACGCTGTGCCCTTTTCATTTAAAGGCG

Associated Phenotype:

Not determined