ZMP

si:dkeyp-117b8.1

Ensembl ID:

ENSDARG00000059553

ZFIN ID:

ZDB-GENE-060526-361

Description:

Novel protein similar to vertebrate symplekin (SYMPK) [Source:UniProtKB/TrEMBL;Acc:A2CET0]

Human Orthologue:

SYMPK

Human Description:

symplekin [Source:HGNC Symbol;Acc:22935]

Mouse Orthologues:

AC148019.2, Sympk

Mouse Description:

symplekin Gene [Source:MGI Symbol;Acc:MGI:1915438]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa20564	Nonsense	Available for shipment	Available now
sa11725	Nonsense	Available for shipment	Available now
sa9377	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa20564

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

Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000082879	Nonsense	116	1108	5	24
ENSDART00000132452	Nonsense	90	1223	6	27

Genomic Location (Zv9):

Chromosome 5 (position 64928200)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	61203690
GRCz11	5	61866427

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAGACAATGAGCTTCTGCTGCGGCTGATTGCCAACCTGAACATGCTGATG[C/T]GAGATGAGAGCGTGAACGTGGTGAAAAAGGCCATTCTGACACTCACTCAG

Long Flanking Sequence:

GGTGTTAATAAACTTTACACAAACCTTACACAAAAATTACACAGTGTTACTCTGTTTCAGCTTTAGTCGACTGTTTTTATTTGTGATACTAAAAAAGGAAAAGAAAACAAACCAATATACAGTGTCTAAGAATGTATATACTATAATATATATATATATATATATATATATATATATATATATATATATATATATATATTATTTACTGTCATCATGATAAAGATAATTAAAAAAATCTGTTATTTTAAATGAGTTATTAAAGCTATAACTTTTAGAAATGTGTTGAAAAAGATCTTTCTGTTAAACAGAAATTGGAAAAAAAAAACAGGAGGGCTAATAATTCTGACCTCAGCTGTATATCGCACAACTCCACTATCTACTACATAATATTTTGACAAATATTTCACCAAGCTTTCTCTAAAGAGTTGTTTTTTATTCCATTCAGTAAAAGAGACAATGAGCTTCTGCTGCGGCTGATTGCCAACCTGAACATGCTGATG[C/T]GAGATGAGAGCGTGAACGTGGTGAAAAAGGCCATTCTGACACTCACTCAGCTCTACAAAGTGGCTTTACAGGTATCAGTTATTACACACTATTTAATATTAGACTGAGCTGATATTTTTAGGTGTCTTGATGGATGTTTGATTTGTTCTACTAGTGGCTGGTGCGCACTAAGAGTGTCACAGACATGCAGGAGGCATGCTGGGATATGGTAACTCAAATGAAAGGGGATGTCCTGGCGTTGCTTGATTCAGATAACGATGGAGTCCGCACTCACGCCATCAAATTCACAGAGTCCCTCATCATCACTCTGTCACCTCGAACGCCCGACTCTGACACACCCAAGAAGCAGGAGGGCGACATAAGCCTGGATAAAATCCCCAAAGACCACACATATATTCGATACGGTAGGAGCAGGGTCACAATTTTTGGGAATTATTCACACTTTTATTTATTTATTTATTTATTTATTTTTTGCTAATGACAAATAGTGCTACATAATT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa11725

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000082879	Nonsense	684	1108	14	24
ENSDART00000132452	Nonsense	658	1223	15	27

Genomic Location (Zv9):

Chromosome 5 (position 64937470)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	61212960
GRCz11	5	61875697

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TTGTGTTGGAGGCTCCGATCATYACAGATTCAGCACTGGAGGTCATTCAG[C/T]GATACTGYGAGGACGAGGTCTGCAACATCCATACACTCCCATTTCTGATA

Long Flanking Sequence:

ACAACTCATTCCTGTGGTGCAGATGATCACAGAGAGTTGGAACAGATCTTTTAATCCTATTTAAAAAAATCCTGTTCTGTGGACATGTTTTTATACGTTACTACAGAGACATGTCAATACACGGCAGTCAGTCAATTCGGTGGGCAGGGAAAACAGCACTTCTACGTCACCTTGCAGTCGGCCTCAAAATCACTGGCATTGGGATCCTATTTTAATGTCAGAAATAATAATAATAATAAAAAAAGATCTTATTGTGTTTCTATCATTTCTATATGACAGTGAACACACTATACAGACACACAGTTCTGTCCAAACAGATTACAAAAGTTGGTTTTGCATCATAGGTGCCCTTTAAAAAAAAAAGAAGAAAAAAAAAGTTTTGTTAACTACTTGCGTGTATATTCTGGCGTGTTTAAAATGTCTGTCTTATTCACAGGCTTTTCACCAAGATTGTGTTGGAGGCTCCGATCATCACAGATTCAGCACTGGAGGTCATTCAG[C/T]GATACTGTGAGGACGAGGTCTGCAACATCCATACACTCCCATTTCTGATACAATGTTTTAAAACCGTGTTTTAATTGTGCTTTATTTTAGTCTACATAAATGTGTTTCTTTCTCAGAAACCCCCTAACTGTTGACCACATTTTGAGTTCACAATTGAAACTTGTAGGTGATAAAGGCATATTACACACAGTCTGTCAAATTAAGTTCAAATTTAAACAAACAAATAAAATTAATTAATTACTAAACAATTTCCTAGTCATATAAAATGCTAACTTAAAATGATACTTCTAACTCGTTACAAATTAAGCTGCGACTGATCTGAACACTTTTAACCTGCCATTGCACTCACAAGCTCAACAGAAACATATTATTAGTTTCAGTTTCAGTCTTGGAAATCTCATGCAACGTGGTGATTTAAATACAATGCCACATAATGACACTCAGACATTTTCACATTAATTTTAACAACCATAATAGCTCTTGTTTTTGCCTCCTTACCT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa9377

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 > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000082879	Essential Splice Site	777	1108	17	24
ENSDART00000132452	Essential Splice Site	751	1223	18	27

Genomic Location (Zv9):

Chromosome 5 (position 64939736)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	61215226
GRCz11	5	61877963

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GCAATAATAGTGTNAAATGAACTAAATGAATGGTGAATCTGTGTCCTCCA[G/T]AGGTGGCAGCTCCCTGGACGGAGGAGACGGTGCGCCAGTGTCTTTACCTC

Long Flanking Sequence:

ATTTTGTAAGAAGCTCTAGCGTTCTTTGTTTGTCTTTCAGTCACGTGTTTACCTGGGCATGTCCACATTAAAGGAGCTCATCTTCAAACGGCCCTCCAGACAGTACCAGTACCTCAATGTCCTGCTGAATCTCACCTCTCATGAAAAAGAAAAGGTGGATTTCGACTCGTGTGTCGTTCATTATTGCTCTATATTCATTTTCACAGCAGTATAATAACAATCCCGATGTTGTTTAGGTGCGGTCGACTGCTCTTAGCTTCATCAAGCGCATGTACGAGAAGGAACATCTGAAGGACTGCATTGAGAAATTCGCTCTCACCTACATGCAGTTTCTGGTCCATCCCAACCCCCCATCTCTTCTGTTCGGAGCTGGAGAAGATACAGGTTTAGAAACATTTCCTAAACTTAAGGGCTCCCGGTGGCGGTCATTTCACAATAAATAATGCTGATGCAATAATAGTGTAAAATGAACTAAATGAATGGTGAATCTGTGTCCTCCA[G/T]AGGTGGCAGCTCCCTGGACGGAGGAGACGGTGCGCCAGTGTCTTTACCTCTACCTCTCCCTCCTGCCCCTCAACCATCGTCTGGTGCATGAACTGGCTGCCGTCTACACCGAGGCTATCGCTGACATCAAGCGCAGTGTGCTGCGGGTCATCGAGCAGCCTGTAAGAACATCTCGCACCACTAATGCTGCTCATACAAAAGTGGATTTCTTTACTATTATACTTGTCGTAATGTTGCTGTTTAAGAATGAAAAAGATCTGCAACGCTAAAAAGCAGGAAAATATAGTAGGTGAGATCTACTTAATATCACTAAGCATTGCTTCTGATCTCCATCAAACGCTTTAATTCTAGCCGAGAGTTTTTTGGGGGAATGCATGTATCACAATATCCCAAAATCAAATAATTCCCACTCAAGTGGCCGAGGCTTGGTTAAATTGCATTAGTGATGTGTTGTCTTTAGGACCAAGAGATGCTGTTTCACAGATCTAATATACTGATAC

Associated Phenotype:

Not determined