ZMP

btbd9

Ensembl ID:

ENSDARG00000068983

ZFIN ID:

ZDB-GENE-040704-39

Description:

BTB (POZ) domain containing 9-like [Source:RefSeq peptide;Acc:NP_001157304]

Human Orthologue:

BTBD9

Human Description:

BTB (POZ) domain containing 9 [Source:HGNC Symbol;Acc:21228]

Mouse Orthologue:

Btbd9

Mouse Description:

BTB (POZ) domain containing 9 Gene [Source:MGI Symbol;Acc:MGI:1916625]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa31963	Essential Splice Site	Available for shipment	Available now
sa35580	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa31963

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:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000074765	Essential Splice Site	62	602	None	10
ENSDART00000099990	Essential Splice Site	62	602	None	11
ENSDART00000141298	Essential Splice Site	62	183	None	3

Genomic Location (Zv9):

Chromosome 13 (position 45398574)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	44642073
GRCz11	13	44778977

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GATTTCCTGCACACAGGGTCATTCTAGCGGCCCGCTGCCAGTATTTCAGG[T/A]TTGTGAGATGATATCACTTGTCTGTTGGGCTGATTTTGGGTGAAATCACC

Long Flanking Sequence:

TTTGGAACAAAAAGCTTGTCAAATAGCACTAGCTGAAAAGAAAAGAATGCATTGAATTTGCTCAACTTAAAACATTTCACACATAATTTCATTTAAAGTTCAATACGTCATATTCCACAAATTCCTTCTAGAATTCACTATTCACCAAGCTTTATATTTTCAAACACTTTTGACAATTTTTCTTCCATAAAATAACTCTCATATGTGCTCTACTTCTTTAGTGGTAATGCTATTTATTTACTTTACTATTCACTATTTTCACTGACTGGCTGAAATGTTTGTTTGAGTTGTGAAGGTGTTGTCCAGCTGTGGTCATGAGTGACAGTCATCCTCTGCGGCCGATGAACTCCGCGTCTGAGATCGACCACCTGCATCTCCTGTCAGAGCAGCTCGGTGCTTTAGTTCCTGGTGAAGAGTACAGCGATGTCACATTCGTGGTGGAGGAGAAGCGATTTCCTGCACACAGGGTCATTCTAGCGGCCCGCTGCCAGTATTTCAGG[T/A]TTGTGAGATGATATCACTTGTCTGTTGGGCTGATTTTGGGTGAAATCACCTTAAGTAGGGCTGCACATTATATTGTTTCAGATTCGATATCAGCAATAGTCACATGGCATGTTCTGCAATGTCAAGTTGGGATGATAATTAACCAGAAAACAGTTCAGAACTAATGTTTAACCTTCAAAGAGTGAATTTTTTTTGTCACAGAAAAAATATTCTGTAATTATGTATGATTTCAAGTGCATTTGAGTCATTTGTGTACTTTAAATTATAAAATTTGTTAACAAGGGTGCTTTTTTTTCTACAGTAGAACATTAAAGAAGGTTTTCAGCTGAAACTGTGATCCTTGGTAATACATGAAATGCATATGCAAGTCAATGGTTACCGGCACTTTGAGAGCCAAAAAATAGACAAAACAAAAATAATACCTGTGGCTCCTGATGAAACATTGAGGTCTTATGAAGAGAAATTACCATCTGTAAAGGAACTCCGAAGGTTATTAGCTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35580

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000074765	Essential Splice Site	487	602	7	10
ENSDART00000099990	Essential Splice Site	487	602	8	11
ENSDART00000141298	None	None	183	None	3

Genomic Location (Zv9):

Chromosome 13 (position 45389929)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	44633428
GRCz11	13	44770332

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAGCCATCGTCATCCAGCTTGCTCAGCCATACATGCTTTGCTCCATGCGG[T/C]ATTTTGTTTATCACAAGAGTTATTATTATTATGATGTCTTAAATGTTCCT

Long Flanking Sequence:

AAGCCAAAAAAAAAGATTCCAAAGGCTGCACCGCTCGTACATGAAGAAAAAGGTCAATAGAAAATCATCTGTGAAAATCTATACCTTTACTCACAGTACACCAGCTTTCAAAAGACTTTCAGGGAAAAGTTGTAAAAAGGCACGGATTAGAAGAAGGCTACAAAAACTAAGGATGGGAAAGTTATTTAGAGTGTGATTGGATTTCAGGCTGTATGACAAATAAAGAAAATGTTTTAAAGGGGTTTGATGACTCTATTGGTACTCTACATCACCTACTGAAACTTATCCCATGCCTTTTTCTCCCTGCAGTTCCCACAGAGAACGTGGCGACCGTGCAGGCATGTGCCAGTGTGGTGGAGGGTGTGAGTCGCAGCAGAAACGCCCTGCTGAATGGAGACACCAGCCATTACGACTGGGACTCGGGATACACCTGTCACCAGCTGGGCTCTGGAGCCATCGTCATCCAGCTTGCTCAGCCATACATGCTTTGCTCCATGCGG[T/C]ATTTTGTTTATCACAAGAGTTATTATTATTATGATGTCTTAAATGTTCCTAATTTAGCTTTGCGGGTTGTTAGTATAGGTTTACATCTATCTAAAATTGCATTCTTTGTCAATGCTGCTACATTACACATTGTGTGATTGGTTCCACACAGAATCTGTGCACATTTTTTGTGATGTCTGCACATAATTTGTCTGTGGATTTATGCTAAATGACTTGGAGTATAGTAACTACAGATATAGCACATGAGATAATAACATGAGAATAATAACTTTTTAAGTTTCATTTAAGGTTTTCTCAATGCAAATGCACTTGTTTGGTAAACAAAGCATGTCTCTAATATATCTACTGAAAGACAGAGAATAGTACTTCACAAACTGTATTGCACATAAGTCAGAAACAATTAAAACATTTGCATGTTATGCAATATTATTACTGGAATTAAAAATAAAAACTGAATAAATATATACTCCCCAACCACTTTATTTGGTACACCTTACAGT

Associated Phenotype:

Not determined