ZMP

LOC792560

Ensembl ID:

ENSDARG00000087417

Human Orthologue:

ZDHHC5

Human Description:

zinc finger, DHHC-type containing 5 [Source:HGNC Symbol;Acc:18472]

Mouse Orthologue:

Zdhhc5

Mouse Description:

zinc finger, DHHC domain containing 5 Gene [Source:MGI Symbol;Acc:MGI:1923573]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa35763	Nonsense	Mutation detected in F1 DNA	Not yet available
sa15335	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa35763

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
ENSDART00000128508	Nonsense	288	658	7	11

Genomic Location (Zv9):

Chromosome 14 (position 51275632)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	50028348
GRCz11	14	49016105

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGTCTGTTCAGGTCCAGCCACCATTTCTGCGACCGCCTTTATCTGAAGCT[C/T]AACTAGCAGCTAAAGTCCTGGATAACGGCATCCAGCAGGTATTAACACAT

Long Flanking Sequence:

CATACACTATGGACAATTTAGCTCGCCCAATTCCCCAATAGTGCATGTGTTTGGACTGTGGGGGAAACCGGAGCACCCAGAGGAAACCCATGCCAACACGGGGAGAACATGCAAACTCCACACAGAAATGCCAACTGACCCAGCCATGACTGGAACTAGCGACCTTCTTGCTGTTAGGTGACAGTGCTAACCACTGAGCCACCGTGCCGCTTTTAAATGCGTCTTTTAAATAGGCCTTTACACACCTCTATACTTATTACAGCCTACATGTGTGCAAAATACTGCAATTCAAAAGAACAGGATTCATTAAACAGAATCAAGTGTAATGCATTTCTAACTATGCTGAACTCTAACCACATGCGTTTGTGCTGAGGGTGATTGTGTGTTTTAATTGTATGTGATTTATGAACTTGTTTTAATGCAGGTATCTTGGTCGATTGCGAAAGCCTCAGTCTGTTCAGGTCCAGCCACCATTTCTGCGACCGCCTTTATCTGAAGCT[C/T]AACTAGCAGCTAAAGTCCTGGATAACGGCATCCAGCAGGTATTAACACATCATTCATACCTTTTTTATTTACACTACCTGACAAAAGTCTTGTTGTTGATCTCAGGTGTAAGAGCAACAAATATTAACTCGACTTCTAGTTGATCATTTGGAAAAGTGGCAGAAGGTGGATTTTTTTTTTTGATGAATTATCTGTTGAACTGCATCCCAATCATCACAAATACTGCAGAAGACCTACTGGAACCAGCATAGACCCAAGCTTCTTATAGAAATCAGTCAAGTTTTCCAAATCGAAGATAAGGCAGTAGGGTAAAATTGGTCTAGTTATTGTAAGCTTAGATCAATCTGATTGGGTTATTACTGATTACAGATGAGAGTCCAGCCGTGCTCAATCATCACGTGCTCCTCTCGAATTTAGTTTATAAAACTTCACTTAAGTACATTAACTTGTGCCACATGTCAATATAGAAGCTTTTTTTGGTCATTGTATATGAGATTAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa15335

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000128508	Nonsense	650	658	11	11

Genomic Location (Zv9):

Chromosome 14 (position 51288085)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	50040801
GRCz11	14	49028558

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ACACCCACTCACACAAACCCGCCAGAGGGGTGAAGAAAGTGAGCGGTGTC[G/T]GAGGAACCACCTATGAGATTTCAGTATGAACGGTTATTGARTCTCCGATC

Long Flanking Sequence:

ATTTGGTAAAGGCGTAAGAGCAACAAAAAAATCAGAAGTTTGAAAATGCGTCTAAAAATTCAGCCTTAAAAAATTTAGTTGTCTTAAATTTCAGATGTTTAATATTTGAGTTATGAAATTCTAATTAAGAAATTCAAATTAAGAAATTCAAATTCAAAACATTTAAATGACATATATAAAAATTCAGATTTATCTAATTACAATTGTCAACCATTCAAATTAACACAAATTCAGATTGTTTTGGCATATTATTAGCTCCATATTATGGAAATAACTATAATTTTGCGATTTATATTTTGCAGTTCTACTTTCAATGCATCCCAAAAGTGTTTTTGTCTGTTTAACCTTTTCCACATGCACCATATATTCACCTGTCTTTTTTTGTTTTGTTTTACTTGTTTACCCACCAACCATTCAGCTCGACTATTAAACAAAACGTGGCCAATCATAACACCCACTCACACAAACCCGCCAGAGGGGTGAAGAAAGTGAGCGGTGTC[G/T]GAGGAACCACCTATGAGATTTCAGTATGAACGGTTATTGAGTCTCCGATCGGATGGATGTAAAGCTGCTCAACCACACATGCAAAAAAGCATACAAGACTGCAAAACAAAGACAAAAGTCAAACTTCAGTCACTGTGGAGGACGCACACCAAAAAAACAAACAAAAACACGTGGACCAGTGAAGACGAGTCTTGCAGTTTTGTTTTCCGAATATCAATATATGGTACACAAAGAACTTTTTCTTATTTAAGAGTCATTTGGTACTTCAATGCATTGATTTGTACGTCTGTCCAATGATCACTGGACATTCAGCCTTTCTAGGCGGGACCACTTGAAACCCGATGATGTCACGTTCGGAATGACATTAAATCAAATCATGAGCCTCTCAGCAGTCAGCCAATCAGCAACGTGATTCACTGTTCTGTTTTGCATATTCAACAGCACGCTTTCACACCCTTATAGGGGACAGTTCACCTAAAAATGCACATTCTGTTATGATT

Associated Phenotype:

Not determined