ZMP

LOC569773

Ensembl ID:

ENSDARG00000074526

Human Orthologue:

ZBTB16

Human Description:

zinc finger and BTB domain containing 16 [Source:HGNC Symbol;Acc:12930]

Mouse Orthologue:

Zbtb16

Mouse Description:

zinc finger and BTB domain containing 16 Gene [Source:MGI Symbol;Acc:MGI:103222]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa12417	Nonsense	Available for shipment	Available now
sa35853	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa12417

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000114159	Nonsense	84	659	1	6

Genomic Location (Zv9):

Chromosome 15 (position 17302653)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	18423026
GRCz11	15	18359048

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CCAACATTACACTCTGGACTTCCTCTCACCAAAGACCTTCCAGCAGATTT[T/A]GGAGTACGCCTACACYGCCACGCTCCAAGCCAAGCTGGARGACCTGGAYG

Long Flanking Sequence:

TTGTGACGATTGGCTAGTGCTTCTTTATGGCGGTTCAATAACAACAACAACAACTCCCCTTTGACTCTTTCTCAATGCACTCAGTTAACCTGTTTGAGTGATGATTAACGTGACCTGTGTAACTTAGATGAACACATCTGACGTAGTATATTTGGTGCTTGTTTTTGATACACAACTGACTGAATGACATTTGCAGGAGCACTCAAGGAGGGAAGCAGATCTGTGAGATGGTTCGGTAAATCTTGATGTTATGGATTTGACTAAAATGGGTGCGATCCACCTTCAGAACCCCAGCCACCCTACAACTCTCCTGCAGAAGGCCAACCAGATGCGCCTGTCTGGGACATTGTGTGATGTGGTCATCATGGTCGACAGCCAGGAGTTTCATGCGCACAGAACCGTGCTTGCATGTGCTAGTAAGATGTTCGAGATCCTGTTCCACCGCAACAGCCAACATTACACTCTGGACTTCCTCTCACCAAAGACCTTCCAGCAGATTT[T/A]GGAGTACGCCTACACCGCCACGCTCCAAGCCAAGCTGGAAGACCTGGATGACCTGCTGTACGCCGCAGAGATTTTAGAAATCGAGTACTTGGAGGAGCAATGTCTGAAGATTTTGGAAACCATCCAGGCATCTGAAGAGAACGATACAGATGTGAACATGAATGAGAATGGTGCCGAGGATGTTGAAGACCGCAGGATCAAGTACCTTAAGAGTGCATTTATCTCTAAAAAGCATTCCATACAAGATGGCGGTTATGGCACCGCTGCCCGCCATCGCCTGGCTCTGGTCAGCATGGTCGATAAAAGATCTTCAGAGTCTGCCCAACTGGGTCTTTCAACTGTCAGCCCTACTAAAGCTGCAGTAGAGGGCTTGATGAGCATGGGACAGTCCGTCCTCCAAGGCAACATTGGACAGAGTTTCTCGCACAACATTGGTAACTCATCTCCATTGATAGATAAGATAAAAACTGAGATGATGCAAGTAGACGAGGACTATCAAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35853

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000114159	Nonsense	329	659	1	6

Genomic Location (Zv9):

Chromosome 15 (position 17301919)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	18422292
GRCz11	15	18358314

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTGATAGACATTTCGCTTCGCTGTGCTCCATCCCGTCCAACCATAAGAGC[G/T]AAAGCATGCTGCCCGTGCCTGTGTCCATGGCCTCGTCCCTACATGTGCCG

Long Flanking Sequence:

ATTCCATACAAGATGGCGGTTATGGCACCGCTGCCCGCCATCGCCTGGCTCTGGTCAGCATGGTCGATAAAAGATCTTCAGAGTCTGCCCAACTGGGTCTTTCAACTGTCAGCCCTACTAAAGCTGCAGTAGAGGGCTTGATGAGCATGGGACAGTCCGTCCTCCAAGGCAACATTGGACAGAGTTTCTCGCACAACATTGGTAACTCATCTCCATTGATAGATAAGATAAAAACTGAGATGATGCAAGTAGACGAGGACTATCAACATGAAGGTGGCTTCCCTAGGAACGGGGAGGGTGGCGGTGACTCCAGGCAGCACCGGGACACTCCTGGAACCCCGACCAGAGGCAGCGTCATCACCAGCGCCCGCGAGCTCCACTCCACCGATAGTTCTGTTGACTCCCAAGGGGACAACAACCAAGCCAGTTTGATCAGTATGGCCAGTCTGGCTGATAGACATTTCGCTTCGCTGTGCTCCATCCCGTCCAACCATAAGAGC[G/T]AAAGCATGCTGCCCGTGCCTGTGTCCATGGCCTCGTCCCTACATGTGCCGCCATCCCTGGCCATGTCTATGGATTTCAGTGCTTACGGGGGGCTCTTCCACCAGAGCTTGATTCAGAGGGAGTTCTTTAGCAAGCTCGGGGATTTTGCAGTAAATGTGAAACATGAAGTCCATACCCAGAAAGAGCGGTGTGAGGTGTGTGATATGGAGCTGCCCGATAATGAAGCTGCTGAACAACACAGGTAAGTCAAGTTACTTGATGATTTCCTTTTACTTTGCAATTCTACTCTGTGTGTATATTTATATATAGAAAAAAATAAATAATTTGATTTAGTGGTTATATTTAAATAAAAAAACAAAAGTGAATGGTCACCAGAAATGATACAAAAGCAATATAAAAGCTGTGTATTTTACTGCTGAATATAAATAACTTCAAATTCCCTGCATCAAAATCAGTTACAAGGCACATGAGAAGCAATGCTTTTTAGTGTTATTGATAAA

Associated Phenotype:

Not determined