ZMP

otomp

Ensembl ID:

ENSDARG00000040306

ZFIN ID:

ZDB-GENE-040709-1

Description:

Otolith matrix protein 1 [Source:UniProtKB/Swiss-Prot;Acc:Q0VIL3]

Human Orthologue:

MFI2

Human Description:

antigen p97 (melanoma associated) identified by monoclonal antibodies 133.2 and 96.5 [Source:HGNC Sy

Mouse Orthologue:

Mfi2

Mouse Description:

antigen p97 (melanoma associated) identified by monoclonal antibodies 133.2 and 96.5 Gene [Source:MG

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa19833	Nonsense	Available for shipment	Available now
sa6858	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa19833

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000126794	Nonsense	201	401	5	9
ENSDART00000130830	Nonsense	201	401	5	9

The following transcripts of ENSDARG00000040306 do not overlap with this mutation:

ENSDART00000058980

Genomic Location (Zv9):

Chromosome 2 (position 41593260)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	41665058
GRCz11	2	41514398

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGGAAGCCGCTTAAATAGTCATCTGCTTCTCCTTGTGATTCATAGCGGTC[G/T]GAGATTTCTTTGGCTACAGCTGCGTCCCTGGCGTGAAGGACCCAGAACAC

Long Flanking Sequence:

ACAAACATACATATCTTGAAATACAGTTGAGTTTTATAAACAAAACATACTGTATGTCTAAATTTAAAGCTTGGATTTTTTTTTTACAATTAATCTTAATTTATAATTATTATTGATGTATGTAGTTTTAAAACTTTTACAATTGCAATTTTAGGAACTATCATTTTATAACTTTCCATTTTACTCCTGTTGAAATTAAAACAAAGGTGAAAAATATGATTCCTCCAAGTGTTCCCATGTTATATTACCATAATTTATTTACATTCCTTTTTTGGCTTGTATCTTAAAGGTATTGTCATTAGATAGAACAGCTGTTGTTTTACAAAAGCACCTAACATCTGGTTTAACGTCTGGTGAGCTGCATATGCACACAAAGTAATGCTCTCAGATATAATATTTGCAGTGCTTACACCTGGCTGAAATGCAAATCGAGATTGTAATTGCAACTTTTGGAAGCCGCTTAAATAGTCATCTGCTTCTCCTTGTGATTCATAGCGGTC[G/T]GAGATTTCTTTGGCTACAGCTGCGTCCCTGGCGTGAAGGACCCAGAACACGATCCCAAAGGAAACAACCCAAGGAACCTGTGTGAGGCCTGCATCGGGGACGAGAATGACCGCCACATTTGTGCCAACAACCCTCGAGAACGGCACTTTGGAGAGGCTGGAGCTCTGAGGTGCAGTAAAGATGTGAAATAATGCATGTTTCCTAGTGGAATCATTATTTAAAATAGGATTTTTGTGTGTGGCCAAGAATATTGAAATGCTTGATGGGCTTGTTAATCTAAATGTTGATGTGTATATGAAACTTTTGAAATTAATTAAAATACCATTTTCTCTGGATTTGCTATTAATATGTACATGTTTTGAGTAAAATGCTTAGTTGTGGCTAATTATTGTTACTTCAAAATAAGATGATTATCATTTAGGGCAATGGTCTCAAACTCAACTCCTGGAGGGCCACAGCTCAGTTCCCACCACCCCATCACACCTGCTTAATAGTCTCTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa6858

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000126794	Essential Splice Site	280	401	6	9
ENSDART00000130830	Essential Splice Site	280	401	6	9

The following transcripts of ENSDARG00000040306 do not overlap with this mutation:

ENSDART00000058980

Genomic Location (Zv9):

Chromosome 2 (position 41595107)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	41663211
GRCz11	2	41512551

KASP Assay ID:

554-5349.1 (used for ordering genotyping assays)

KASP Sequence:

GGCGATGTTGCTTTTGTTAAGCACACTACAGTCTTTGACAACATGCAGGG[T/A]AAGTAGTGCAGGCTATAAGAACATGAGAGGTCAAAAACGTCCCGAWGCAG

Long Flanking Sequence:

ATGTATTGTTTTTAAGTGCAGACAGCTTTTATCTCTTGCTAGATGTGATATTATGATGATGATAATAAAAATAATAATAATAAATGTTTATCATTTGGCCCAATCGGCAACTGCCACCTGGTTTCAAGATGGGCCGACCCAATCCAAGGTTACCCGGACATAATCAAAATCTGGCAAGAATGTCATATTATTTCACCATCTTTACACCAAAATAAATAGTTAATGTGCGTGTCCGTGGGTGGGGCTGTGTCGGTGTGGTAATGTGGGCTGGTGTGGCAACAGTGCCAGGGCTGAATTTTTGTCCCAGTCCGCCCCTGGTCATTACTGTCCTTTATGCTCCATTTCTTGTATCTTTGAAAAACAAAATATGTAAAAACAGTGCTTATATTTTATAAGTATGATTTATATGCATTATTATTTTTAAAATGCAGGTGTGTGGCAGAGAATCTTGGCGATGTTGCTTTTGTTAAGCACACTACAGTCTTTGACAACATGCAGGG[T/A]AAGTAGTGCAGGCTATAAGAACATGAGAGGTCAAAAACGTCCCGATGCAGTAAGATTTTTCAAGTTGGTTTCTTATTAAATGGAATTTTTAAGGGACTGAAGGAGGACAATTGTAGCCTTCACTTGATGATCTGGATCATGTTTCACTGGCTGACAGACACAGGAGGGCAGTATTTCACAACAATGCGTCTCTTTGTGTGCCTGCTGGGATCTGTGAAACCCTTGTATTTAGAATCAGTAAACCCCGTTAGCCAAGTTCAGGGATTATAGATTCTAGTTTTATAGAGATATAGATTTGTTTACCAAAGCCTGCACAACTTTCAAGCTTTTAAACTTTACAAAAAGAATGCAAATGTTACATATCACGCCGAAATTTTCACTGCATGCAAACAACCTTTTTTATTGATGTAAGGTAAGAACCAGGAGTCTTGGGCGCTGGACTTGGAGCTGGAAGACTTGAAGCTCTTGTGTCCTGACGGGAGTGAAGCGAACCTGTTCCA

Associated Phenotype:

Not determined