ZMP

si:dkey-225n22.2

Ensembl ID:

ENSDARG00000076373

ZFIN ID:

ZDB-GENE-091204-64

Human Orthologue:

VOPP1

Human Description:

vesicular, overexpressed in cancer, prosurvival protein 1 [Source:HGNC Symbol;Acc:34518]

Mouse Orthologue:

Vopp1

Mouse Description:

vesicular, overexpressed in cancer, prosurvival protein 1 Gene [Source:MGI Symbol;Acc:MGI:2141658]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa37803	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa39432	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa37803

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000108762	Essential Splice Site	36	175	2	5
ENSDART00000139748	None	None	73	None	2

Genomic Location (Zv9):

Chromosome 24 (position 529874)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	469846
GRCz11	24	199505

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCTAAGAAGTACTGCTGGTATTCTGAGGGAGGATACCCCCTCTTCTTTAT[G/A]TAAGTACAGTGCTGTGGTGTTACGTGCTGATCTGGAGTCAGTGTTAGGGT

Long Flanking Sequence:

CACTCACAAGAGATCCACTAATAGCAAATGTAATGGAGATCAGCTGAGATTTACTGACAGATCTAAATCCGTTTGATGTTTTATTATAAAGGTATGATGTGTGATTTGATGGAATATACTGTCCTGGCATATTTTAGCACATGATATGTTTTAAAACACGTGTATTCATGTATACAATACACTGACCTCAATGGAAAAACTGAACTTTCACATGTTTAGTGTCACTGATATACTCAGGAATCAGAATGCAGAGCTCTCAAATGACTAATCGCAGTCAAACTTTTGTATTTATATAATGTGTGTACTCACTGTGTAAGAATATTGCGTGTATATATAAACAAAATGATCTTTTGAGAGCCCTAATTAACAGATATCGTGTAACTCATTCAGTAATTACTAACGATATTCACTGACTTCAATGTCTTTGTCTTGTTTCTGCAGTGTGTGGAAGCTAAGAAGTACTGCTGGTATTCTGAGGGAGGATACCCCCTCTTCTTTAT[G/A]TAAGTACAGTGCTGTGGTGTTACGTGCTGATCTGGAGTCAGTGTTAGGGTTTCTCTCTGTGTTGCTTCTTCATTGGTTTGAACGTCAGACATAACGTTCAGTGAATTCTGCCGTTCGTCAAGATCTGCTCATTACCATTAAACACTTTACTGGAGGATGAAGCACGCACGCACACTAAAACTTGCAATAAAACACTCACACATGCACGTGCATACACACACTCGCATTAAAACTAAAAACACACACACATATATACTAAAACAGTCTCTAGCAGAAAGCGAGGAGAACCAGCAAAAGGAAAAGCTCAATATACTCTCAGTATAGGTGGCATATAAAGTTGTCAGTATGGTAAATATAAAGTAAAATGCATCTGTGATTGAGTGTAGTGAAATTTCAGTAATAACAACAACAACAACATCCACAGCAGCAATAACAACTACACCAACTGCTACTAATACTAACAGTACACCAACTACTAGCAATATTGTTCAACCAACATG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39432

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000108762	Nonsense	59	175	3	5
ENSDART00000139748	Nonsense	23	73	1	2

Genomic Location (Zv9):

Chromosome 24 (position 527377)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	467349
GRCz11	24	197008

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCTGTGGAACCCGCTGCTGCATCAGGGCTCTCTCCATACAGAGACTCTG[G/A]TACTTCTGGTAGGATCAACTTTTATTAAATAATTCATTAAATGTATTAGA

Long Flanking Sequence:

GGTTAATGAAGCCGTGTTCACCTTGAGGACGTTCACAGCACCACAAACCGACCTGCTCCACCAAAACACGTCAGATCAGCTCACAATCTCATCATTACTTCTCATTTTGTGAGAACATGAACAAAACAGGAAATAACTTGAGTAAATATATTGACCGAGAAGTCTGAGAGATGTTTTGAAGAATGTTCCTGCTGCACCTTATGAAGCATTTAATGAATGAGGGCCGCAAATGAGAATCACAGCAAGCTGAATAAAACAGGACTGAATGTATTTAATCCAGCTTCATCAGCTCATCTGGAGCGCTGCCAGAAGTCTGTTTGTAGAGGATAATATTATAATAACACGTTAGAATAACCAGCACGTGATGATTCATTTATAGCAATTTACAATTGTGTGTGTGTGTGCGCGCGTGTGTGTGTGTGTGTGTGTAGATGCCGCTCATATGAGGACTGCTGTGGAACCCGCTGCTGCATCAGGGCTCTCTCCATACAGAGACTCTG[G/A]TACTTCTGGTAGGATCAACTTTTATTAAATAATTCATTAAATGTATTAGATATTTATAAATTTTCCTGCATTAACTACATCTCCTACATTTATTACAGTGGAATAATCTGAGAAGTGGTCAGCAAACGGTTCATTTTACTCAGAAATACATCAGTTTTTAATCTGTGTGTGATTAAATTATTATTAAAATGTCAAATGTAACATTTTAAAGCAGAAATATGGAAAATATGTACTTGAATTAGTGGTGGGCGTGTCCTTCATGACTGCTGCTCTCTGATAGGCTGCTGCTGATGATGGGCGTGTTCTTCTGCTGCAGCGCTGGATTCTTCATTCGCAGGCGCATGTATCCGTCAGTGCTGAGCGACGAGCCCGCCTTCAATGTGTCCTTCACCAGACAACCCGTCAGCACACCTGGTGCCAACACACACACACACACATACTAAACACACACTCAACAAACACTCAACACACATTAAACACCATTCAGATGCTTATTCGGA

Associated Phenotype:

Not determined