ZMP

Ensembl ID:

ZFIN ID:

Description:

semaphorin 4B [Source:RefSeq peptide;Acc:NP_001121824]

Human Orthologue:

SEMA4B

Human Description:

sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (se

Mouse Orthologue:

Sema4b

Mouse Description:

sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (se

Allele Name:

sa32209

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000042074	Nonsense	2	827	1	14
ENSDART00000143899	Nonsense	2	830	2	15

The following transcripts of ENSDARG00000074414 do not overlap with this mutation:

• ENSDART00000144145

Genomic Location (Zv9):

Chromosome 18 (position 25638953)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	25868726
GRCz11	18	25855258

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa11928

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
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Mutation:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000042074	Essential Splice Site	113	827	3	14
ENSDART00000143899	Essential Splice Site	113	830	4	15

The following transcripts of ENSDARG00000074414 do not overlap with this mutation:

• ENSDART00000144145

Genomic Location (Zv9):

Chromosome 18 (position 25603995)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	25833768
GRCz11	18	25820300

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa36655

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000042074	Essential Splice Site	183	827	5	14
ENSDART00000143899	Essential Splice Site	186	830	6	15

The following transcripts of ENSDARG00000074414 do not overlap with this mutation:

• ENSDART00000144145

Genomic Location (Zv9):

Chromosome 18 (position 25596034)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	25825807
GRCz11	18	25812339

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa11879

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000042074	Nonsense	449	827	10	14
ENSDART00000143899	Nonsense	452	830	11	15

The following transcripts of ENSDARG00000074414 do not overlap with this mutation:

• ENSDART00000144145

Genomic Location (Zv9):

Chromosome 18 (position 25575727)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	25805500
GRCz11	18	25792032

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype: