ZMP

Ensembl ID:

ZFIN ID:

Description:

hypothetical protein LOC404610 [Source:RefSeq peptide;Acc:NP_996961]

Human Orthologue:

FAM49B

Human Description:

family with sequence similarity 49, member B [Source:HGNC Symbol;Acc:25216]

Mouse Orthologue:

Fam49b

Mouse Description:

family with sequence similarity 49, member B Gene [Source:MGI Symbol;Acc:MGI:1923520]

Allele Name:

sa6147

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
ENSDART00000066784	None	None	325	None	10
ENSDART00000102484	Nonsense	54	383	1	11
ENSDART00000132282	None	None	331	None	10

The following genes are also affected by this mutation:

• ENSDARG00000093657

Genomic Location (Zv9):

Chromosome 24 (position 10669484)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	10756887
GRCz11	24	10897254

KASP Assay ID:

554-3694.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa44097

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000066784	Essential Splice Site	148	325	5	10
ENSDART00000102484	Essential Splice Site	206	383	6	11
ENSDART00000132282	Essential Splice Site	152	331	5	10

Genomic Location (Zv9):

Chromosome 24 (position 10602612)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	10661496
GRCz11	24	10801882

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype: