ZMP

si:dkey-197d18.1

Ensembl ID:

ENSDARG00000092692

ZFIN ID:

ZDB-GENE-041014-155

Description:

Novel protein similar to vertebrate PIM family oncogenes [Source:UniProtKB/TrEMBL;Acc:Q5RI90]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa43519	Nonsense	Mutation detected in F1 DNA	Not yet available
sa37141	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa43519

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
ENSDART00000100697	Nonsense	32	463	1	7
ENSDART00000137422	None	None	202	None	4

Genomic Location (Zv9):

Chromosome 20 (position 43493823)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	43564982
GRCz11	20	43462060

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAAGAACCATCAATTCCACCGTCTCAGGTCAAGATAAAAACTTCGACCGT[C/T]AAGAAGAAGGATTGGTCACGGGATCCAACGTGGCCACCAGTGATGGTAAA

Long Flanking Sequence:

ACAGGAAATATTTACGAGTCAAACAAAGAGTTCCTAAAAAATCTGTTTATTTTGCTCCAAAAAAATAAAGGAAACACACAACCGCTAACTAGAGAAGATTAAAGATACACAGCGCAAAACTGACCAATCACGTATCAGTTGGCTGGGAAACGCTGGAACACATTCGAATTCTTACGAGAGACACCTCTTACATTCCACATTCGCCATTACTCTTACTTGACAAAGTGTTTAGTTGAGTTGTACAAAGTTTGCTTTGATTAATTTGCTTTTCGTACATTGTCAACTGATAGCGTACGATTTATTAAGGCTTACTCTGACAAACAAGCTTTACTTACAGTGAATTTCAGTATTTCTTGTAGGTTTATTTAACATTTCTCATATTTAAGTGTACGGAAATTAAACCAAAAATGTTATTTACCGTACTCGGAGTTATTTCTCTCTTCCTGAGAAAAAGAACCATCAATTCCACCGTCTCAGGTCAAGATAAAAACTTCGACCGT[C/T]AAGAAGAAGGATTGGTCACGGGATCCAACGTGGCCACCAGTGATGGTAAATAATGTTTTGTGTTATAAGAACATGTTGCTCATTTTGGATGCTGGAGTCTGTGTAGGGCTCTACCCTGATTTTACCTTAATGTAAAAATTATTTTTTAAGTGAATAATAATACTGGCCTTATAAAAACTGCTGTTTTAATCACATGTGGTGTCAAACATTCGTCACACAAACGTGTCTAATATGGTGCCAACAATAATATAAAATAACAGCTTTTGTCTGGTTTCTAGTCCAGATATCTCAAAATTCTTAAATAAAGAGTCTTTTTTCTAGACAAGCAAAAATATTGTCTGGTTATCATAAATAATAAGTCAAAAATTAAATTTTTTCCCCCTTAAAATACCAAAATTATCTGCCATCGAGAAAGCAAAATAATGCTTTGAAATACATTTGACTTCCCCTCTGGCAGATTATTTAGCTTGTTTTAAGAAAACCCCAGTTCATTTGTACAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa37141

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
ENSDART00000100697	Essential Splice Site	46	463	1	7
ENSDART00000137422	None	None	202	None	4

Genomic Location (Zv9):

Chromosome 20 (position 43493777)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	43564936
GRCz11	20	43462014

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCGTCAAGAAGAAGGATTGGTCACGGGATCCAACGTGGCCACCAGTGATG[G/A]TAAATAATGTTTTGTGTTATAAGAACATGTTGCTCATTTTGGATGCTGGA

Long Flanking Sequence:

TTATTTTGCTCCAAAAAAATAAAGGAAACACACAACCGCTAACTAGAGAAGATTAAAGATACACAGCGCAAAACTGACCAATCACGTATCAGTTGGCTGGGAAACGCTGGAACACATTCGAATTCTTACGAGAGACACCTCTTACATTCCACATTCGCCATTACTCTTACTTGACAAAGTGTTTAGTTGAGTTGTACAAAGTTTGCTTTGATTAATTTGCTTTTCGTACATTGTCAACTGATAGCGTACGATTTATTAAGGCTTACTCTGACAAACAAGCTTTACTTACAGTGAATTTCAGTATTTCTTGTAGGTTTATTTAACATTTCTCATATTTAAGTGTACGGAAATTAAACCAAAAATGTTATTTACCGTACTCGGAGTTATTTCTCTCTTCCTGAGAAAAAGAACCATCAATTCCACCGTCTCAGGTCAAGATAAAAACTTCGACCGTCAAGAAGAAGGATTGGTCACGGGATCCAACGTGGCCACCAGTGATG[G/A]TAAATAATGTTTTGTGTTATAAGAACATGTTGCTCATTTTGGATGCTGGAGTCTGTGTAGGGCTCTACCCTGATTTTACCTTAATGTAAAAATTATTTTTTAAGTGAATAATAATACTGGCCTTATAAAAACTGCTGTTTTAATCACATGTGGTGTCAAACATTCGTCACACAAACGTGTCTAATATGGTGCCAACAATAATATAAAATAACAGCTTTTGTCTGGTTTCTAGTCCAGATATCTCAAAATTCTTAAATAAAGAGTCTTTTTTCTAGACAAGCAAAAATATTGTCTGGTTATCATAAATAATAAGTCAAAAATTAAATTTTTTCCCCCTTAAAATACCAAAATTATCTGCCATCGAGAAAGCAAAATAATGCTTTGAAATACATTTGACTTCCCCTCTGGCAGATTATTTAGCTTGTTTTAAGAAAACCCCAGTTCATTTGTACATTTCTGAAAACAAGACAGTATTTTTACTTGTCAAGAAAATGCTTCTT

Associated Phenotype:

Not determined