ZMP

si:dkeyp-117h8.4

Ensembl ID:

ENSDARG00000043004

ZFIN ID:

ZDB-GENE-030804-4

Description:

hypothetical protein LOC572032 [Source:RefSeq peptide;Acc:NP_001076347]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa37036	Nonsense	Mutation detected in F1 DNA	Not yet available
sa43442	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa37036

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
ENSDART00000063137	Nonsense	405	660	7	10
ENSDART00000082099	Nonsense	319	573	7	10
ENSDART00000137457	Nonsense	298	552	1	4
ENSDART00000138997	Nonsense	321	535	2	2
ENSDART00000144230	Nonsense	405	669	7	10

Genomic Location (Zv9):

Chromosome 20 (position 25672384)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	25743687
GRCz11	20	25642777

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTCCAAATGGGAAAAGCACCTTCAGACCAAGCATTCTGAACATGGAAAGA[C/T]AAATAAACTCGATAGGAAGTCCAAACAGAAGGTCTTCTGTAATCCACCAA

Long Flanking Sequence:

TACAAAATCTACTCAAGAACAAACTAAAGTCTTCTCCACTCAATATATCCTACGAGTCCAGTGCCTGTTTTTACTCACCCAGAAGGAACAGCGTAGATGTGAGCGGTGTGACGGATCAGTCTGCATGGATTGATGTAGCTTTAACCAGGAAGCCGGAGCAGAATCCTGCTCGTGTGATTGACTTCTCAACACCTTCATATTCTGGTTCCCCTTCACATAGTGACAAATCTCCAGATCTGGACCAGACCTATGATGTTGAACCAACATCTCCTGCTGTTCCAACCTTATCGATCTTGACTTCTCCACAACAAAGCAGAGCAGGTCTGTCTATTACTGACCAGAGAGAAACATCAATAATCTCCCAACTCTCCTCATTGGACAAAGACTGTTTCAGGGACCGCCTACATCCTCCTGTTCCCTCGCCTCACCGTAGCTTCATTGGTGTCTTATCTCCAAATGGGAAAAGCACCTTCAGACCAAGCATTCTGAACATGGAAAGA[C/T]AAATAAACTCGATAGGAAGTCCAAACAGAAGGTCTTCTGTAATCCACCAAGAGCTTCTTAGATCTCCTTATGGTGCCAAACAGGTGCCATTTTCATCACAAAGACGACCTGTTTATGACAACACTGATCAAACTTCCTCTAAGGTAGAGAGTCGGTCCCATTTTACACCATTAAAACGCCAACGCTCTTTTTCTGGCTCCCCGTCCTCATACTCATTCAGTGGATCTCAAATTGATGCGGAGTTCAGAAAGCTGTACCACCACTTCATCTGCCGTGGAACATCATCACCCTGTGCTTCCTCCCATTGTCATCTGTGCGAAAGACACACAAAGGAGAGCTTCCAAAGCCCTGGCTTTTCCTCCTCCAGCATGTCTGCTCTGGCTTTGACGCCTCTGAGAGCCAAACTTAAGAAACGGAGCCGTCAGCCTGAAGTGGAAGAGTCACTCCGGTTTAAACGCTTCAGAGAGAGTCGCTCCCCACTGAAACATTTCCAGCTGACA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43442

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000063137	Essential Splice Site	631	660	8	10
ENSDART00000082099	Essential Splice Site	545	573	8	10
ENSDART00000137457	Essential Splice Site	524	552	2	4
ENSDART00000138997	None	None	535	None	2
ENSDART00000144230	Essential Splice Site	631	669	8	10

Genomic Location (Zv9):

Chromosome 20 (position 25671259)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	25742562
GRCz11	20	25641652

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TAACCTCTTTTGCAGAGAGATGCCCCAAGCGGAGTCCACCTACTTGAAGG[T/C]TTGTAGCCACATTTTATAACATAAAAACCTCATCATGCTATCTGTATTTC

Long Flanking Sequence:

ACCAACATGCTCTGTCTTGGGTAAAAGCATTATTGGTGTGACTATTTACATATTTATAAGGACAGTTCACCATGAAGTAAAAACCTGTCATTAGTTATTTGCTTTATTAAAATATTTTAAACAATTAACAAATAAAATTTCTTAGCAATAAAAATATGAAATATTTTGTTTCTGATATTTTGTTGCTTTGATTTTTAGTTCCTAATCTTTTTTTTAAGTGTATGACAATATAAACAAAAATATTGATCTTAGCATATTGGTGATTTCTAAAGGACCATGCGGCACTGAAGAATTACAATTTAGCCTAAGAAAAAGTGTTAATTAAAAATATTTAGTATAATTTATAAATATTTCGTGTATTTTTAATCAAATAAATGCAGGCCTAGTGAGCATTAAGAGCATCTTAATCATTATAAAAGTACATAAATGCAGTTAAACAGTGATTTTCCCTAACCTCTTTTGCAGAGAGATGCCCCAAGCGGAGTCCACCTACTTGAAGG[T/C]TTGTAGCCACATTTTATAACATAAAAACCTCATCATGCTATCTGTATTTCGCCGTTTTAAACACACATCAAGTCTTTGTTTTATTTCAACAGCTGCGTCACCTATGAGACATTTTAACCAAGCTACCGCTTCACACTCTCCAAGGTAATTACATCACGGTCACAAAAAATACCCACTGTCTTAAATATCTAGAAATAAAATGTTCTGCTAATATTTACCTAAATTAATTATTTTAAATACTGTATTATAGTTAGACATTAGGATTTTCTAGATATTACATCCGATAGTGTTCCTAAACGAATGAAGTTAACTTTTAACGTAAAAATGGGAGGACAGTTTTACAGTTAAATATCAGATATAGCAAAAAAACATGTTATTGTGTATATTGACGTTTTTCAATATACATGTCAGTATATGCTAATGAATTATCCAGATTTTGCTGTTTTGCTCTAAAGTCAAACTCATATTGGAGGACTGTTAAAGATGGCCTGAATTGCTGT

Associated Phenotype:

Not determined