ZMP

LOC100334900

Ensembl ID:

ENSDARG00000078018

Human Orthologue:

ZNF70

Human Description:

zinc finger protein 70 [Source:HGNC Symbol;Acc:13140]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa11683	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa11683

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
ENSDART00000114505	Nonsense	546	793	2	2

Genomic Location (Zv9):

Chromosome 16 (position 26979937)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	24825612
GRCz11	16	24740644

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CCACCCKAACATTCCKGKTTCTACACCTTCAGTAGTGCGTCCCTTGTTGT[T/A]GAATCCACCGAGGTTGACTATTCGTGTCCCTACGCCTTCCAGTCGTCCTC

Long Flanking Sequence:

GGTGGCATGCAAGAATGAAGAGTCGCTTTTAAAGCACATGACCGAAAAACACCCTAAGACTTCATATATCTGCTCGACCTGCCGCAAAGTTTTCCCTAGACAGGAAAATTTAAAAAATCATGTGTGCTTGATACCTAGAGGCAACATGGTCACCCCTCTAACCCAGTTACCCAACATGCCTTTGCCTTATAGCAGCGGTCAGGGAAAGCCCATTGCCTCTGCTTTGCACACCAATCAGAGCACTGTTAAAATTCTTAACTTTATTCCAGCAGTTAACAAAGTTTCCACTGATCCTCCACGCCCAGTGGCGTCCTTGGGGTCTACAGAAGCTCTGACGCTGCACCGACTGCTTCAGACCACTCCTGCGGTCACTCCTAAGGTGACTAATTTGGTTCCACAAGTTGTAGCTGTCCCACAAACTCTTATGAGATCCAGTTTCGCATTTGTTTCCCACCCTAACATTCCTGTTTCTACACCTTCAGTAGTGCGTCCCTTGTTGT[T/A]GAATCCACCGAGGTTGACTATTCGTGTCCCTACGCCTTCCAGTCGTCCTCTTCCAATTGTCGTTTCTTTTTCCCCCACTGTGAACACCATCACGCCTGCTCTGGTATCCTCCAGCAGGACTGCTCTCAGACAAAGGCCTGTGCCTAAGATTAGACCTGTACCAGTCAACATCCCGCCGGTCACCTCAGTTGCCTGTCCCACCCTGGTAAGCGCTCTTACCAGGAATAACCAATCTCAGGTTCCTCCTGCCCAGATTCAGGCTCCGTTACGAATAGTCGGCATGTACATGAACCACATGGCTCTGCAAAAGCCTCTCGAGCAGAGCTGGAGCTCCAAGACCATCTTTCCCTGTCGTCACTGCGGTGCTGTTTCCAGACAACCGTCGATGAGGGTCCGCCATCGCTACCTTCACCGTGGGTCAAGGTTGTACAGGTGTCAGTGTGGAAGGTCTTTTCAAAGGCAGCTGCATTTGCTGAGGCATCAGGTCCAGCATGCAGAGT

Associated Phenotype:

Not determined