ZMP

Ensembl ID:

ZFIN ID:

Description:

hepatocyte growth factor-regulated tyrosine kinase substrate [Source:RefSeq peptide;Acc:NP_956162]

Human Orthologue:

HGS

Human Description:

hepatocyte growth factor-regulated tyrosine kinase substrate [Source:HGNC Symbol;Acc:4897]

Mouse Orthologue:

Hgs

Mouse Description:

HGF-regulated tyrosine kinase substrate Gene [Source:MGI Symbol;Acc:MGI:104681]

Allele Name:

sa20125

Status:

Available for shipment
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Availability:

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Mutation:

T > C

Consequence:

Essential Splice Site, Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000019661	Essential Splice Site	249	447	None	22
ENSDART00000056622	Missense	259	773	9	21
ENSDART00000131913	Essential Splice Site	249	721	None	20

The following transcripts of ENSDARG00000020960 do not overlap with this mutation:

• ENSDART00000142009

Genomic Location (Zv9):

Chromosome 3 (position 47669636)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	49060581
GRCz11	3	50095849

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa9499

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

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Mutation:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000019661	Nonsense	338	447	13	22
ENSDART00000056622	Nonsense	353	773	13	21
ENSDART00000131913	Nonsense	338	721	13	20

The following transcripts of ENSDARG00000020960 do not overlap with this mutation:

• ENSDART00000142009

Genomic Location (Zv9):

Chromosome 3 (position 47673447)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	49056770
GRCz11	3	50092038

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa31357

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

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Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000019661	None	None	447	16	22
ENSDART00000056622	Nonsense	500	773	15	21
ENSDART00000131913	Nonsense	484	721	15	20

The following transcripts of ENSDARG00000020960 do not overlap with this mutation:

• ENSDART00000142009

Genomic Location (Zv9):

Chromosome 3 (position 47676100)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	49054117
GRCz11	3	50089385

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa12053

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

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Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000019661	None	None	447	19	22
ENSDART00000056622	Nonsense	639	773	18	21
ENSDART00000131913	Nonsense	623	721	18	20

The following transcripts of ENSDARG00000020960 do not overlap with this mutation:

• ENSDART00000142009

Genomic Location (Zv9):

Chromosome 3 (position 47681402)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	49048815
GRCz11	3	50084083

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype: