ZMP

zgc:110200

Ensembl ID:

ENSDARG00000057035

ZFIN ID:

ZDB-GENE-050417-366

Description:

hypothetical protein LOC550523 [Source:RefSeq peptide;Acc:NP_001017825]

Human Orthologue:

STOML3

Human Description:

stomatin (EPB72)-like 3 [Source:HGNC Symbol;Acc:19420]

Mouse Orthologue:

Stoml3

Mouse Description:

stomatin (Epb7.2)-like 3 Gene [Source:MGI Symbol;Acc:MGI:2388072]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa10092	Essential Splice Site	Available for shipment	Available now
sa30938	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa10092

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000079628	Essential Splice Site	171	278	None	7
ENSDART00000081834	Essential Splice Site	108	215	None	7
ENSDART00000132830	Essential Splice Site	173	280	None	7

Genomic Location (Zv9):

Chromosome 10 (position 25073304)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	24672656
GRCz11	10	24642108

KASP Assay ID:

2260-3246.1 (used for ordering genotyping assays)

KASP Sequence:

CCTTGCTGAGGTCCTWTCTGACAGAGAAGGCATCTCCCATAGTATGCAGG[T/C]GAKTGTGGAAAATGAAATAATGKTCTCCTSAGTTGTGYATGCATGATCYW

Long Flanking Sequence:

ACTTTATTTACAAGCTAGTACAAATAGCCTAAAATAGTATGTACAAATTTGGCCCAACTACTCTCATAAAAGAGTATGCAAAAATAGGGATGCCTATATGATTTGTGAATGCAATCAATCACTTATTGTTCTTTCCTCAATAACTCAACGAACCTTTAAGTGAATGATTCTATGCCATAATAGAAAGCAACCAAAAACCTTTTTCTCAGATGCACAGATTGTCAGTCAACTGTTGTATACCTTAATGATCAGTATGTTTAGATGCTAAAATGCCACATTTTTTGCTTCCCATTAGATCTTAACCAAAGACTCAGTGACAGTTTCAGTGGATGGTGTTGTGTACTTCAGAGTAAATGACCCTGTTGCCTCAGTGGCAAATGTCTCCAATGCAGATTACTCAACCCGACTACTGGCCCAGACCACCCTGAGAAATGTCCTGGGCACCAAGAACCTTGCTGAGGTCCTTTCTGACAGAGAAGGCATCTCCCATAGTATGCAGG[T/C]GAGTGTGGAAAATGAAATAATGGTCTCCTGAGTTGTGCATGCATGATCTAAATGCAGGTCTGTTTTCAAGTACCTGAAGTTTTCTTAATATTACTCCTTCCTGCTGTAGACAACTCTAGATGAGGCCACAGATTCATGGGGCATCAAGGTGGAGCGAGTGGAGATTAAAGATGTTAAACTGCCACAGCAGCTGCAGAGAGCAATGGCAGCTGAGGCGGAGGCATCTCGTGAGGCCAGAGCAAAGGTCAGTATTACAAGTTTTATAACTTATTTTAAATTAAAAAAGACACATCTTTCATTTATATTCTAATTGCCCATATGACATCTATGCACATTGACTGTGTCTTCATGCCACACAATAATGGTTTGTGATGATGCAGGTCATTGCAGCGGAGGGAGAAATGAATGCGTCCAGGGCTCTAAAGGAGGCATCTCTGGTGATCGCAGAGTCTCCATCTGCACTTCAGCTCAGATACCTCCAAACCCTCAACACCATTGCA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa30938

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000079628	Nonsense	191	278	6	7
ENSDART00000081834	Nonsense	128	215	6	7
ENSDART00000132830	Nonsense	193	280	6	7

Genomic Location (Zv9):

Chromosome 10 (position 25073137)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	24672489
GRCz11	10	24641941

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TAGATGAGGCCACAGATTCATGGGGCATCAAGGTGGAGCGAGTGGAGATT[A/T]AAGATGTTAAACTGCCACAGCAGCTGCAGAGAGCAATGGCAGCTGAGGCG

Long Flanking Sequence:

TTCTATGCCATAATAGAAAGCAACCAAAAACCTTTTTCTCAGATGCACAGATTGTCAGTCAACTGTTGTATACCTTAATGATCAGTATGTTTAGATGCTAAAATGCCACATTTTTTGCTTCCCATTAGATCTTAACCAAAGACTCAGTGACAGTTTCAGTGGATGGTGTTGTGTACTTCAGAGTAAATGACCCTGTTGCCTCAGTGGCAAATGTCTCCAATGCAGATTACTCAACCCGACTACTGGCCCAGACCACCCTGAGAAATGTCCTGGGCACCAAGAACCTTGCTGAGGTCCTTTCTGACAGAGAAGGCATCTCCCATAGTATGCAGGTGAGTGTGGAAAATGAAATAATGGTCTCCTGAGTTGTGCATGCATGATCTAAATGCAGGTCTGTTTTCAAGTACCTGAAGTTTTCTTAATATTACTCCTTCCTGCTGTAGACAACTCTAGATGAGGCCACAGATTCATGGGGCATCAAGGTGGAGCGAGTGGAGATT[A/T]AAGATGTTAAACTGCCACAGCAGCTGCAGAGAGCAATGGCAGCTGAGGCGGAGGCATCTCGTGAGGCCAGAGCAAAGGTCAGTATTACAAGTTTTATAACTTATTTTAAATTAAAAAAGACACATCTTTCATTTATATTCTAATTGCCCATATGACATCTATGCACATTGACTGTGTCTTCATGCCACACAATAATGGTTTGTGATGATGCAGGTCATTGCAGCGGAGGGAGAAATGAATGCGTCCAGGGCTCTAAAGGAGGCATCTCTGGTGATCGCAGAGTCTCCATCTGCACTTCAGCTCAGATACCTCCAAACCCTCAACACCATTGCAGCCGAGAAGAACTCCACCATCGTCTTCCCACTGCCCATTGACATCATGAACCACTTCATAAGGAAATAAATGCTGAATATTCTTTACATACATATGCTATCCATTTACTTACAACTTGTAATATGTACTTACAAATGTGCCATGTTTTACATTTTTTTTATGTTGAA

Associated Phenotype:

Not determined