ZMP

Ensembl ID:

ZFIN ID:

Description:

Novel protein similar to vertebrate myosin VIIA and Rab interacting protein (MYRIP) [Source:UniProtK

Human Orthologue:

MLPH

Human Description:

melanophilin [Source:HGNC Symbol;Acc:29643]

Mouse Orthologue:

Mlph

Mouse Description:

melanophilin Gene [Source:MGI Symbol;Acc:MGI:2176380]

Allele Name:

sa39853

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 > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000111810	Nonsense	86	1173	2	16
ENSDART00000132955	Nonsense	62	159	2	4
ENSDART00000135668	None	None	193	None	4
ENSDART00000144383	Nonsense	86	313	2	8

The following transcripts of ENSDARG00000075706 do not overlap with this mutation:

• ENSDART00000145505

Genomic Location (Zv9):

Chromosome 2 (position 31366680)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	31667740
GRCz11	2	31650958

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa6849

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
ENSDART00000111810	Essential Splice Site	217	1173	6	16
ENSDART00000132955	None	None	159	None	4
ENSDART00000135668	None	None	193	None	4
ENSDART00000144383	Essential Splice Site	217	313	6	8

The following transcripts of ENSDARG00000075706 do not overlap with this mutation:

• ENSDART00000145505

Genomic Location (Zv9):

Chromosome 2 (position 31356855)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	31657915
GRCz11	2	31641133

KASP Assay ID:

554-5165.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa39852

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000111810	Nonsense	598	1173	10	16
ENSDART00000132955	None	None	159	None	4
ENSDART00000135668	None	None	193	None	4
ENSDART00000144383	None	None	313	None	8

The following transcripts of ENSDARG00000075706 do not overlap with this mutation:

• ENSDART00000145505

Genomic Location (Zv9):

Chromosome 2 (position 31351679)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	31652739
GRCz11	2	31635957

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa44535

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000111810	Nonsense	681	1173	10	16
ENSDART00000132955	None	None	159	None	4
ENSDART00000135668	None	None	193	None	4
ENSDART00000144383	None	None	312	None	8

The following transcripts of ENSDARG00000075706 do not overlap with this mutation:

• ENSDART00000145505

Genomic Location (Zv9):

Chromosome 2 (position 31351430)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	31652490
GRCz11	2	31635708

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa14035

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000111810	Nonsense	810	1173	10	16
ENSDART00000132955	None	None	159	None	4
ENSDART00000135668	None	None	193	None	4
ENSDART00000144383	None	None	313	None	8

The following transcripts of ENSDARG00000075706 do not overlap with this mutation:

• ENSDART00000145505

Genomic Location (Zv9):

Chromosome 2 (position 31351043)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	31652103
GRCz11	2	31635321

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa32949

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000111810	Essential Splice Site	1117	1173	None	16
ENSDART00000132955	None	None	159	None	4
ENSDART00000135668	Essential Splice Site	174	193	None	4
ENSDART00000144383	None	None	313	None	8

The following transcripts of ENSDARG00000075706 do not overlap with this mutation:

• ENSDART00000145505

Genomic Location (Zv9):

Chromosome 2 (position 31343698)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	31644758
GRCz11	2	31627976

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype: