ZMP

si:ch73-257c13.3

Ensembl ID:

ENSDARG00000069808

ZFIN ID:

ZDB-GENE-081104-270

Description:

Novel protein similar to vertebrate osteopetrosis associated transmembrane protein 1 (OSTM1) [Source

Human Orthologue:

OSTM1

Human Description:

osteopetrosis associated transmembrane protein 1 [Source:HGNC Symbol;Acc:21652]

Mouse Orthologue:

Ostm1

Mouse Description:

osteopetrosis associated transmembrane protein 1 Gene [Source:MGI Symbol;Acc:MGI:2655574]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa14055	Nonsense	Available for shipment	Available now
sa37077	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa14055

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000101887	Nonsense	90	329	1	6
ENSDART00000145269	Nonsense	72	311	1	6

Genomic Location (Zv9):

Chromosome 20 (position 32517251)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	32575491
GRCz11	20	32478370

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGTATCAAAGGCGAACAGTTTRGAGTTTTTCTACTCTCTCAGCCTTTCAT[C/A]ATTTCCAGAGGACTTGGAAGTGAACGAGTATTGTATTGAACTGCTTCGCA

Long Flanking Sequence:

ACATAATCAGAAACATCATTGACTTAACCTAAATTAGCTTTTTTTGCTGCAACACGTTTAAAGATTCAGTGTTAAAAGTCTATCAAAATACAATCAAAATTTTTTTTTTCATTTTACAGACACAAATAGCTGAAAGCTGCTTTACCTGGGCTCCTTTACACTTCTTTTAGTTTTGGACGTTTTAAGACAGGTGCACCGGTCATGTAAATCCCGTTCATCGCGAGATTAGAACATGAGTCATGTGACTGACACAGGACAAAAAGAAAACAGGAAGCTCTGGAGTTTTGCTGTGGACTGTATTCAGTGTAAATTAGAGATGGATTTATCAAAATGTACTATTGCGGTGTTATGTTCGTTTGTAGCATGGACTATTACATTAATGAACTGTTTGATTTCTCCAGCGGAGATGAGTGGTGATGTTGCAGTAAAGCTTCCAGGAGCAGTCATTCCTGTATCAAAGGCGAACAGTTTGGAGTTTTTCTACTCTCTCAGCCTTTCAT[C/A]ATTTCCAGAGGACTTGGAAGTGAACGAGTATTGTATTGAACTGCTTCGCATTTACGGCCAGCGCTACGTGACTTTCGCTAACTGTCTTGTGTTTTATGCACGACCTGTCAAAGTCTGTCAGAACTGTTACACTGGCTTTAAAGGTCTGAAGGAGATATATCTAAATATATCATCAGGACAAGTGAGTGCTAATTTCAAACATTCGTTTTCTCGACATCTAACGTTATGACAGCAAATATGCCGTGTTTTTTAAGGCTGTTTGACACAATTTCCCTACCGCTGGTCACATGTTCTTGTGTCTCGTGATTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTCAACATAACCTGACTCACACCGACTCTGGAACTATTTAGTGAGCCTAAAAGTCTATTTCAAGTTGAAGTGGCAAATTTAGAATACGGCTTCATAGGGTTATTACATTTTTTTTCATAAATATAACAAACTATATAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa37077

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000101887	Nonsense	129	329	1	6
ENSDART00000145269	Nonsense	111	311	1	6

Genomic Location (Zv9):

Chromosome 20 (position 32517369)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	32575609
GRCz11	20	32478488

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTGACTTTCGCTAACTGTCTTGTGTTTTATGCACGACCTGTCAAAGTCTG[T/A]CAGAACTGTTACACTGGCTTTAAAGGTCTGAAGGAGATATATCTAAATAT

Long Flanking Sequence:

GACACAAATAGCTGAAAGCTGCTTTACCTGGGCTCCTTTACACTTCTTTTAGTTTTGGACGTTTTAAGACAGGTGCACCGGTCATGTAAATCCCGTTCATCGCGAGATTAGAACATGAGTCATGTGACTGACACAGGACAAAAAGAAAACAGGAAGCTCTGGAGTTTTGCTGTGGACTGTATTCAGTGTAAATTAGAGATGGATTTATCAAAATGTACTATTGCGGTGTTATGTTCGTTTGTAGCATGGACTATTACATTAATGAACTGTTTGATTTCTCCAGCGGAGATGAGTGGTGATGTTGCAGTAAAGCTTCCAGGAGCAGTCATTCCTGTATCAAAGGCGAACAGTTTGGAGTTTTTCTACTCTCTCAGCCTTTCATCATTTCCAGAGGACTTGGAAGTGAACGAGTATTGTATTGAACTGCTTCGCATTTACGGCCAGCGCTACGTGACTTTCGCTAACTGTCTTGTGTTTTATGCACGACCTGTCAAAGTCTG[T/A]CAGAACTGTTACACTGGCTTTAAAGGTCTGAAGGAGATATATCTAAATATATCATCAGGACAAGTGAGTGCTAATTTCAAACATTCGTTTTCTCGACATCTAACGTTATGACAGCAAATATGCCGTGTTTTTTAAGGCTGTTTGACACAATTTCCCTACCGCTGGTCACATGTTCTTGTGTCTCGTGATTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTCAACATAACCTGACTCACACCGACTCTGGAACTATTTAGTGAGCCTAAAAGTCTATTTCAAGTTGAAGTGGCAAATTTAGAATACGGCTTCATAGGGTTATTACATTTTTTTTCATAAATATAACAAACTATATAATGACTCATGTTTTTACCATGATTTATAGAATAAACCCACTCAAAAGTCATAAGTTGTCAAGTTCTAAACAACAACAACCATTTGATCACATGTCAAGTATATTTCATTCATTAAATCA

Associated Phenotype:

Not determined