ZMP

si:dkey-204a24.9

Ensembl ID:

ENSDARG00000019299

ZFIN ID:

ZDB-GENE-041111-214

Description:

Novel protein similar to vertebrate zinc finger protein 592 (ZNF592) [Source:UniProtKB/TrEMBL;Acc:Q1

Human Orthologue:

ZNF687

Human Description:

zinc finger protein 687 [Source:HGNC Symbol;Acc:29277]

Mouse Orthologue:

Zfp687

Mouse Description:

zinc finger protein 687 Gene [Source:MGI Symbol;Acc:MGI:1925516]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa23443	Essential Splice Site	Available for shipment	Available now
sa45658	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa23443

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:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000007137	None	None	736	None	2
ENSDART00000104703	Essential Splice Site	758	1431	2	9
ENSDART00000123058	Essential Splice Site	758	1393	2	10
ENSDART00000132336	Essential Splice Site	758	1431	3	10

Genomic Location (Zv9):

Chromosome 19 (position 8450912)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	7909451
GRCz11	19	7828376

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAACGCTTAATGTCATACACTCAATGCTGAATGCCAAATGTTCTGTTTGT[A/T]GGTATGCTTTCTCCGTCACTTTCCTCTCCACCTTTGACATCCTCCACTAC

Long Flanking Sequence:

ACCAGCATCTATCGTCAACAGCACTGGTGCTGTTATTTCTCGAAGCCAGTCCAGCCTAGTCGAGGCCTTCAACAAGATCTTAAATAGCAAGAACTTGCTTCCTAGTTACCGTCCAGATCTCTCAACCCCTCCACCGCCTGAATGGGGTCTTCCTATGCCTGCCGCTGGCTACCGCTGCTTGGAGTGTGGAGATTCGTTCGCTCTGGAGCGCAGCCTGGCTAGACACTACGACCGTCGCTCTTTAAGAATAGAGGTGACCTGCAATCACTGCGCAAAACGGCTGGCTTTCTTCAACAAGTGCAGTCTGCTGCTACATGCTCGCGAGCACAAGGAACGAGGCCTGGTCATGCAGTGCTCACATTTGGTTATGAGACCAGTTACAGTGGAGCAGATGATTGGCCAGCAGGACACTACCCCCATTGGTAACTTCAAAATTCTGCAGTTTTCTGTGAACGCTTAATGTCATACACTCAATGCTGAATGCCAAATGTTCTGTTTGT[A/T]GGTATGCTTTCTCCGTCACTTTCCTCTCCACCTTTGACATCCTCCACTACCCCTGCAGGGACGATTCCTGCACCGTCCACTTCCAGTCCACTCAAAGACTCCCCCTCTCCAGGCACGGCTTCAACTCAGCCCAGTCCTGCCCGTCGTGGACCCCAGAGTCCTCAGGCATTGATGCCGCTGCCCTGCAAGAAAGGCGAAGCTCTGCAATACCACAACTTCAAGTGTCCAGAATGTCAAGCCCAGTTTTTAAGCAAGGCTGAATTAGTGACCCATTTCCAGCAAATCAGAGCTACTCCAAACTCAGTAAGTTCTAATACTATAAACATACTAGAATTGTCTAGAACACTTTTTCTATATCTGATGACCTGGTTGGACGAGCAGGTCTGATTTTTTTTTCTGCAGACGTTTGAACCAACCCTGCATCATTTTGTTTAAACACTATTTTTCAGCATCATGATTATATGTGTGTGTACTATAAAATGACTCCATGGTGCAACACA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa45658

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:

A > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000007137	None	None	736	None	2
ENSDART00000104703	None	1079	1431	6	9
ENSDART00000123058	Essential Splice Site	1079	1393	None	10
ENSDART00000132336	None	1079	1431	7	10

Genomic Location (Zv9):

Chromosome 19 (position 8447714)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	7906253
GRCz11	19	7825178

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAACCCAAACCAGCAACAGAAAACAATTCAGATGAGCTGAGCCAGGGCCC[A/G]GGAGAGGAGGAAGAGGAAGGGGAAGACGAGGAGGGAGAGCAGGAAGGAGA

Long Flanking Sequence:

TGTGTACATTGTGTTCATTTTTATAATATTTTATGAAATAGTAGTTATTATTGTTATTTAAATAACTATCTTTTTTTAAAATCATTATTTTATTATGATACAATGCATTTAAGGATTGTTTAAATGAAAGAATACATTGTCATTTTGCCTTTTGTGTTACCCATTCTTTTCACATTCCCTGAAGAATGTGGTGTCAAAAAAGGCATACAGTAATACTCTTGGTTAGGCATTTACAAAGTGATTTCTCTGTATCACGCTGTCTAAAGCTCAAACCAAGTACAACAGCCGCCTCGGTGTGCAAATTATCATGCTATCCATTCCGTATCGCTTTAACCAAAGTCGTCTTTTAATATTTCCCATTAGACTGCTCACAGAGGCTTGTCTGTCAAAGCTGAGACTCCGCCCACCACCTCTTCTCCCGTCTCCGCCCCTGCCGGTAACTCCACCTCTAAACCCAAACCAGCAACAGAAAACAATTCAGATGAGCTGAGCCAGGGCCC[A/G]GGAGAGGAGGAAGAGGAAGGGGAAGACGAGGAGGGAGAGCAGGAAGGAGAAGAGAGAGAAGATGAAGAGGAGGAGGAGAATGAGGAGGAGGAGCAGGTGAGCTCTCCAGAGAGCGGGAATATGGAGTGGAGGTGCAAGGAGTGCAAGAAGCGATTTCCAGAGAGAGAGGATTACATCGACCACATGAAGAATGAACACGGAACGGTTGGTACTCTTAAAAAAATAACAGAGTAAGCACAAGTAAACTGATCAATTGAGCTTCTAGCAATTTCTTGTGACTGCTGTAAGAGAAATAATATATTTAGTTTTATATATTTTGAGATCTGCTTTAGAAAAGCTTATTGTTAGAGTATATGTGTGGTGTTTTTGTTTTTTCTTTAAAATCCATTACATGCAGTGCTTCTCACACATACACTTTACTTGGTCAGGCCGCCCAGATATATTAACAGCCGCCCAATTATATTTAGTATATTTAGGCCCAATCCCAATTGTACTTTGGT

Associated Phenotype:

Not determined