ZMP

si:ch211-194c3.6

Ensembl ID:

ENSDARG00000074036

ZFIN ID:

ZDB-GENE-090313-64

Description:

Novel protein similar to vertebrate kyphoscoliosis peptidase (KY) [Source:UniProtKB/TrEMBL;Acc:B8JIN

Human Orthologue:

Human Description:

kyphoscoliosis peptidase [Source:HGNC Symbol;Acc:26576]

Mouse Orthologue:

Mouse Description:

kyphoscoliosis peptidase Gene [Source:MGI Symbol;Acc:MGI:96709]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa31912	Nonsense	Available for shipment	Available now
sa42158	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa31912

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000111463	Nonsense	275	866	4	7
ENSDART00000131255	Nonsense	93	477	3	6

Genomic Location (Zv9):

Chromosome 13 (position 13611936)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	13619931
GRCz11	13	13750923

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGAGTACGATATAGAGGGATACCTTGGTCTTTCTCAGAAGATTTGTTCTT[T/A]AGATGAAGTCATCAGGAATGGAAAAGGTGTATGTAGTGGTTACTCCAATC

Long Flanking Sequence:

ACTAATATTTAAATTTGTCTGAGGATCTGAAACATTAAAGTGTGACAAAAATAAGAAATTAGTAAGGGTGTAAACACTTTTCTACACCACTGTACTGCACAATATATCCAGATGTTCATTCAATGGGACCATTAAAATCTGCTAACACTTTATTTTAATGGTCCCTTAAGAGCTTATTCCACTTCCCCTAACCATAACCTTACTGTCTGCTAATACCCTACTTTTACTTTAATTCTATTTATTTAACATGTTTTTATTTAATATGTAGTTGCAAAGTTATCATAGTCAGATCAATGTCTAAATTTGATTATTAAAACATAGTGTATAGGAAACCATATTGGTAAATTGTTTTAATAAAGACTATTAAAACTTTGTCAAAAGATCAAGAAAATCCATGACCCTGTAAATGTATTTCCTGTTTAAAAAATGTTTTCTTGTGTTTCCATGTGTAGAGTACGATATAGAGGGATACCTTGGTCTTTCTCAGAAGATTTGTTCTT[T/A]AGATGAAGTCATCAGGAATGGAAAAGGTGTATGTAGTGGTTACTCCAATCTCTGTGTGGAAATGTGCAGGTAAATGACCAGCGGTATTTAGAAACACACATCATGCCAGAAGAATGTGGCTCTGAACTTTCCCTTTTTTCTCTAGGGAGGTGGGCATTGAGTGCGTGGAAGTAAGCGGGTACAGCAAAGGTATCGGATACCAGGCCAGGCACAGTTTAGCTGAGGAGTGTTCTGATCATGAGTGGAATGCTGTCTTCATAGACGGTCAGTGGTGGCTGCTTGACGCTTGCTGGGGTGCTGGCACTGTGGATATGAAAAGCAAAACATTTGTAAAGAGGTCAGGCTCCCCGGAGTGTCAGTTATGCATTTCATACGATACAGACATACCACATACATTATGACTTGACAAATCATGTGTTGTTTTTACATACAGTTATAGCTAGTAGTGCCTATGACATTTTTTTTTAAAATCAACATTAAGAAAATATATTTTTTGATAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42158

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
ENSDART00000111463	Essential Splice Site	425	866	6	7
ENSDART00000131255	Essential Splice Site	243	477	5	6

Genomic Location (Zv9):

Chromosome 13 (position 13608682)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	13616677
GRCz11	13	13747669

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCAGTTGGGACTGACCCTCATACATCCCAAGCAGTATAAGACAATCACAG[G/A]TGTACATATGCACACAAAACATACACTATTAACGTAAATATGCTCATGCA

Long Flanking Sequence:

ATAGGTGTGTACAGCCCACTTGGAGCTCAAAGGCCCACCCACTTGGAGCTCAAGTCCTACCCACTTGGAGCTGACTGCGACCTCCGTTTATACCTTTGTCGGTATAGGGGGTGATTTCGGATACAATGTGTACCACCTAGATTCTTAAAGTTGCATTAAAAAGGTGTACCTAATAAAGTAGGCATCATCTTTCTCTATAGGGAAATTTGACAAAACAATATTGAGTGATATTAAGTGCAATGCTGCACTAAATGGAAAGGATAAATCAATACAATTCCACTATAATAATGTCTGGTTTCTTTTGTTCAGGTATGATGACTTTTATTTCCTGACTGAACCCAGTGAATTCATAAACTCTCATTTCCCTGATGACCAAACCTGGCAACTGCTTACCACACCCATCTCCATACAAGAGTTTGAAATGAGACCCTTGAGGACATCAGCATTTTATCAGTTGGGACTGACCCTCATACATCCCAAGCAGTATAAGACAATCACAG[G/A]TGTACATATGCACACAAAACATACACTATTAACGTAAATATGCTCATGCAAAACAAAACATAGCACAAACACAAAAGGGAGATTAGTGAAGCAAACACAATGTCTGTCACACTGTAATGAGATCATAGGAGGCGACTGGCTTCAGCTTGTGTCGAGAAACTCTGAGAAAACAGATTAGAACGTTTGCTGCAGAGATTAGGCCGTCGCATAAGAAAAAAGTTATTGTAATTGAAACTTCTTGAAGAATATCTAAAGCATGCATTGCAGAAAATGCAGGCAAAAGCATTAGGAAAGTGCAAGCATTTAGGGAGGCAAGAAAACAGCTTGACAAAGGCTCAGCTGGTAACTTCTGGGCACTAAATGGCTCCATACGCACTGAAGGCTAAATGTGGTTTCACCCCTGGGTCTTGAGATGACAAAATGTGAAAATTAAGCAGCGAGAGTCTAAGCGAGACACATTTATCTAATATGCTAAGCCAGCTGGTTGGAACTGTGTGTGT

Associated Phenotype:

Not determined