ZMP

zbtb12.2

Ensembl ID:

ENSDARG00000070658

ZFIN IDs:

ZDB-GENE-060503-27, ZDB-GENE-060503-27

Description:

zinc finger and BTB domain containing 12, tandem duplicate 2 [Source:RefSeq peptide;Acc:NP_00103834

Human Orthologue:

ZBTB12

Human Description:

zinc finger and BTB domain containing 12 [Source:HGNC Symbol;Acc:19066]

Mouse Orthologue:

Zbtb12

Mouse Description:

zinc finger and BTB domain containing 12 Gene [Source:MGI Symbol;Acc:MGI:88133]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa32245	Nonsense	Available for shipment	Available now
sa36850	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa32245

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000079344	Nonsense	109	538	2	4
ENSDART00000103955	Nonsense	109	538	3	5

Genomic Location (Zv9):

Chromosome 19 (position 27448086)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	27378198
GRCz11	19	26962421

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTGCAGTTCAGCGCCAAAGAGATTGTGAACTACTTGACTGCTGCCAGCTA[C/A]CTGCAGATGGAGCATGTGGTGGAGAAATGCAGAGGAGCACTGAGCCAGTA

Long Flanking Sequence:

ACCTCATCTAGCTATGAGAACTGACTTGTTACTTCGATTTTTTTGGGCTCTGATATGCTACCAGAACATTGTGTCTCTAAAATATAGCAACGCTGTCTCTAATCAATGGTATGAGTTCAGAAAACCTATTTGAGTTAAGTAAATATTCTCGGGAAATCTTAGTGCTGAAATAAAAGTTTGCTCTGTTTTCATATTTGTTTTCTAAATGTGTATTCATCAACACATACAGTCGTGGTCCAAACTATTGGCACCCTTGGTACACATGAAATGTTTCCTGTATTCCTTATTTCTTTATTCTCTAAGTAAAGCTGCCTTCGTTCAAGTAACAATTGAAATTGTTGGTTTGATTGTGAACAAACAGTGGCTCTGTCTTTCTCTTTCCAGCAGGTTTCAATGTTGCACAGCTCAACAGTGGTATTTGAACTCCTCCAGTCCTGTTATACAGGGATACTGCAGTTCAGCGCCAAAGAGATTGTGAACTACTTGACTGCTGCCAGCTA[C/A]CTGCAGATGGAGCATGTGGTGGAGAAATGCAGAGGAGCACTGAGCCAGTACATGCAGCCCCGGAGTCGCAGTCCCATTGTAAGTATCTCAACCTCAAATAATGGTCACTATTACAGACCTTGTTTCTTCTTAATTAAAAAGTTCAGCCAGAAATTCTTGAAAGTACTGACTTGTTAAAGATATTTGATGTACATTTACATATATGCAGATTCTTAACACATGCAATGTTTTAGTAGTTTGGGTAGAGGATGATTGCTCATTTAAGTTGAAAGGGTCTGTCTTGGAAATCGACTTTATCCCTTGTTGTCTAGGTAAAAAACAATGCTCTTTCGTTGCATACACACTTGTAAGAGTGCATTAAGGTGATGTTTACATTATTCCATTTTTGATTCATTTCACTAAATTGAAACTCTCTTTGTAGAGCCTGGAGTTTTTATTGTGTTTCAGAAAAACGATCTCTGTCCAAACTTTACACACCAATAGATGACCATTTGCGCTCA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36850

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
ENSDART00000079344	Nonsense	111	538	2	4
ENSDART00000103955	Nonsense	111	538	3	5

Genomic Location (Zv9):

Chromosome 19 (position 27448082)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	27378194
GRCz11	19	26962417

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGTTCAGCGCCAAAGAGATTGTGAACTACTTGACTGCTGCCAGCTACCTG[C/T]AGATGGAGCATGTGGTGGAGAAATGCAGAGGAGCACTGAGCCAGTACATG

Long Flanking Sequence:

CATCTAGCTATGAGAACTGACTTGTTACTTCGATTTTTTTGGGCTCTGATATGCTACCAGAACATTGTGTCTCTAAAATATAGCAACGCTGTCTCTAATCAATGGTATGAGTTCAGAAAACCTATTTGAGTTAAGTAAATATTCTCGGGAAATCTTAGTGCTGAAATAAAAGTTTGCTCTGTTTTCATATTTGTTTTCTAAATGTGTATTCATCAACACATACAGTCGTGGTCCAAACTATTGGCACCCTTGGTACACATGAAATGTTTCCTGTATTCCTTATTTCTTTATTCTCTAAGTAAAGCTGCCTTCGTTCAAGTAACAATTGAAATTGTTGGTTTGATTGTGAACAAACAGTGGCTCTGTCTTTCTCTTTCCAGCAGGTTTCAATGTTGCACAGCTCAACAGTGGTATTTGAACTCCTCCAGTCCTGTTATACAGGGATACTGCAGTTCAGCGCCAAAGAGATTGTGAACTACTTGACTGCTGCCAGCTACCTG[C/T]AGATGGAGCATGTGGTGGAGAAATGCAGAGGAGCACTGAGCCAGTACATGCAGCCCCGGAGTCGCAGTCCCATTGTAAGTATCTCAACCTCAAATAATGGTCACTATTACAGACCTTGTTTCTTCTTAATTAAAAAGTTCAGCCAGAAATTCTTGAAAGTACTGACTTGTTAAAGATATTTGATGTACATTTACATATATGCAGATTCTTAACACATGCAATGTTTTAGTAGTTTGGGTAGAGGATGATTGCTCATTTAAGTTGAAAGGGTCTGTCTTGGAAATCGACTTTATCCCTTGTTGTCTAGGTAAAAAACAATGCTCTTTCGTTGCATACACACTTGTAAGAGTGCATTAAGGTGATGTTTACATTATTCCATTTTTGATTCATTTCACTAAATTGAAACTCTCTTTGTAGAGCCTGGAGTTTTTATTGTGTTTCAGAAAAACGATCTCTGTCCAAACTTTACACACCAATAGATGACCATTTGCGCTCACTGG

Associated Phenotype:

Not determined