Busch Lab

ZMP

BTBD16 (2 of 2)

Ensembl ID:
ENSDARG00000088482
Description:
BTB (POZ) domain containing 16 [Source:HGNC Symbol;Acc:26340]
Human Orthologue:
BTBD16
Human Description:
BTB (POZ) domain containing 16 [Source:HGNC Symbol;Acc:26340]
Mouse Orthologue:
Btbd16
Mouse Description:
BTB (POZ) domain containing 16 Gene [Source:MGI Symbol;Acc:MGI:3045247]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa18423 Nonsense Available for shipment Available now
sa41978 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa18423
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000129408 Nonsense 94 138 3 4
Genomic Location (Zv9):
Chromosome 12 (position 12713856)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 11569509
GRCz11 12 11607812
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCGATCAGTGCGCTTTCACATCACAGTGCAAAGYTATGCCAACGGAGAGT[G/A]GCAAGAGCACAGCAGTGGAACTGTCAATCAACACTTCGGCTTATGCAAGC
Long Flanking Sequence:
AATTAAACAAACAAAAAGGTTATATTATATAGAAACCGCAGACTCTAAATCATCCTCATAATTCTTCTTAAATGAGATGGTGGGCAAAATCAAAAGTTAACATGGGCCAACTTTGGCCTGTGAGCCCTAGTTTGGGCATTCCTGGTTTATGGAATAAAATATAAGTTATTACTCAAACACACAACTATAAATTGTAAACCCAAAGAAACTTAGACCTTTAGAGTTGTCTTTATTGTATTTAATTGATTGCTTTTTTTACTTTTAGCTGTGCATGAAATCCTCAGAATAAGAAAAATTCATAATGTCATGAAAAATTATTTTCGGGGGTTAATTATTACTTGGAATTCATCCTTTCCCACCTCACCCTCTCTCTGTGTAGAGGTTAAGACACTGGGATCCTGCTGTACCCCAGTCTTCCGCTGTGAGCCATCCGTACTGCATGAGGGCTGATCGATCAGTGCGCTTTCACATCACAGTGCAAAGCTATGCCAACGGAGAGT[G/A]GCAAGAGCACAGCAGTGGAACTGTCAATCAACACTTCGGCTTATGCAAGCGCCTCAGCAGGAGCAAGGTACCAGCACTCAAAGACTGACATACAACTCAAGAAATCTTCAGAACAAAGTTACACAAAAACAACAATAATCTAAACAGCAGTTGCTGATTGCCCAAAACACTCAAGATTTAGATTTTATACATCAAATTATTAGCAATCAGTCTTACTTTAGTATTTTTCATGTTTTGCTTGATGTGTTTTTAATTAGATGGAAGGAAATTATTAGTTTCATAATTAGGATCAATCGAAAGGCAAAAGAGAAAGTTGTTGATTTTAATAAGTTTTATTTATAAAATTTTTTTTTGCATGTGTAGTGGCTGTGTAGTAGAACCACCAGAAGGGTTGCATAACACAAAAGAAGGGACTAAGCTGGTTGAATTAAAGTAATTTATCTAAAACTATGCACAGTAGTCTGTCCTGGCTAAAGGTCCCAGATTACCAGTTAACTATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41978
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
ENSDART00000129408 Nonsense 104 138 3 4
Genomic Location (Zv9):
Chromosome 12 (position 12713827)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 11569480
GRCz11 12 11607783
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGCTATGCCAACGGAGAGTGGCAAGAGCACAGCAGTGGAACTGTCAAT[C/T]AACACTTCGGCTTATGCAAGCGCCTCAGCAGGAGCAAGGTACCAGCACTC
Long Flanking Sequence:
TAGAAACCGCAGACTCTAAATCATCCTCATAATTCTTCTTAAATGAGATGGTGGGCAAAATCAAAAGTTAACATGGGCCAACTTTGGCCTGTGAGCCCTAGTTTGGGCATTCCTGGTTTATGGAATAAAATATAAGTTATTACTCAAACACACAACTATAAATTGTAAACCCAAAGAAACTTAGACCTTTAGAGTTGTCTTTATTGTATTTAATTGATTGCTTTTTTTACTTTTAGCTGTGCATGAAATCCTCAGAATAAGAAAAATTCATAATGTCATGAAAAATTATTTTCGGGGGTTAATTATTACTTGGAATTCATCCTTTCCCACCTCACCCTCTCTCTGTGTAGAGGTTAAGACACTGGGATCCTGCTGTACCCCAGTCTTCCGCTGTGAGCCATCCGTACTGCATGAGGGCTGATCGATCAGTGCGCTTTCACATCACAGTGCAAAGCTATGCCAACGGAGAGTGGCAAGAGCACAGCAGTGGAACTGTCAAT[C/T]AACACTTCGGCTTATGCAAGCGCCTCAGCAGGAGCAAGGTACCAGCACTCAAAGACTGACATACAACTCAAGAAATCTTCAGAACAAAGTTACACAAAAACAACAATAATCTAAACAGCAGTTGCTGATTGCCCAAAACACTCAAGATTTAGATTTTATACATCAAATTATTAGCAATCAGTCTTACTTTAGTATTTTTCATGTTTTGCTTGATGTGTTTTTAATTAGATGGAAGGAAATTATTAGTTTCATAATTAGGATCAATCGAAAGGCAAAAGAGAAAGTTGTTGATTTTAATAAGTTTTATTTATAAAATTTTTTTTTGCATGTGTAGTGGCTGTGTAGTAGAACCACCAGAAGGGTTGCATAACACAAAAGAAGGGACTAAGCTGGTTGAATTAAAGTAATTTATCTAAAACTATGCACAGTAGTCTGTCCTGGCTAAAGGTCCCAGATTACCAGTTAACTATACATAAATGGAGAGTTAATCTCATATTAAA
Associated Phenotype:
Not determined