ZMP

B6E448_DANRE

Ensembl ID:

ENSDARG00000079014

Description:

Semaphorin 4f [Source:UniProtKB/TrEMBL;Acc:B6E448]

Human Orthologue:

SEMA4F

Human Description:

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

Mouse Orthologue:

Sema4f

Mouse Description:

sema domain, immunoglobulin domain (Ig), TM domain, and short cytoplasmic domain Gene [Source:MGI Sy

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa34223	Nonsense	Mutation detected in F1 DNA	Not yet available
sa15002	Nonsense	Available for shipment	Available now
sa7607	Missense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa34223

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000126930	Nonsense	98	414	4	12

Genomic Location (Zv9):

Chromosome 7 (position 65958531)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	59140271
GRCz11	7	59442701

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTATGTCATGCTTTACTCTGCTGCCCCTTACAGGATGACTGCAGGAATTA[T/A]GTTCGTTTGCTGGAGTTTTTGGACGATGGCCGCATATATGCCTGTGGAAC

Long Flanking Sequence:

CCTGAAACCTTAAAATTTGAATAAAACAAATGAAAAACAATGAATCAATACAGGCTCGCTTACATATTTAAAGATATGCCAAATGGTGTAAGATAAAAAAAATGGTTTTATCACAATTCCAGCCAGGCCTATCGTCAGGATATATTTTTGTAAGATATATTTGTGCTCCTTTATGCTTTATGAATTGACCCACTGTGAAATGTCAGACATTACTCATTTACTGTACTGATTAGACACAGCCAAGCAGTGTTTGGTTTTCCAATCATTGTTAATAATGCAGAAACACTCTTATTGTGCTCAGCAATTGTTTTAATGTCACACATGACATACAGTATTTATACATAATGTGAAGAGCTTTAGTAAAAAAAAAAAAAAACTATTAGTTTTCAGTGTCTTTTTAATTAATAGAAAATGAAAAAGAGCATTTAATTATATATTATTTGTCTTGCAGTATGTCATGCTTTACTCTGCTGCCCCTTACAGGATGACTGCAGGAATTA[T/A]GTTCGTTTGCTGGAGTTTTTGGACGATGGCCGCATATATGCCTGTGGAACATTTGCTTTTGACCCTCAGTGTGCTTTTATTGTAAGTGTACTTTCAAGTGTTACATACTATTAAGTACCTAGTTTAAAAAGAAGTTTTAAAAGAAATGTGTCACGTTTTGACACATGTACACATGCACTGAAAAAAATTATTGGATTTACAAATTATTTTAAGGTAAATGTATTTGGGCTGAATTTAAACAAACAAATTAGGTTGAACATTACTAAATTTAATTTGTTTGTTTATATTCACCCCATATAAATAGTTTGCAACTGTTTTGCAGAAACCATTATTTCAGTGTTTATGTTGCTGCGAGTGGAATGTGGCAGATAAAATTCAGTTAAAAAAATAGTTTTACCTTACATTTATAATTTTTTTTTTTGCATACTCTTCACTTGTTCTAAACCTGTTTCAGTTTATGTCTTCATTTGAACACAAAAGAAGATTTTAAAGAAAGCTGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa15002

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
ENSDART00000126930	Nonsense	135	414	5	12

Genomic Location (Zv9):

Chromosome 7 (position 65959711)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	59141451
GRCz11	7	59443881

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CTGTCTTGTCTWACTTGTTACAGAACATCTCTACATTCTCTCTGGAGAWA[C/T]AGGATGATGGTTTTATAAAGATGGAGACCGGGAAGGGGAAATGCCCCTTT

Long Flanking Sequence:

CCATTCACTTTGAATGGGTGACCTCAAGCGCTGCTGAACTGAATTGTAGATCCTTGCTGTAGAAGTTAGGAATTTCTCAACATTTCAAGCGTCAATGGAAGCTTCAGCCAATAAGGATGCTTTATGCAAATTCTCAGACAGTAGCCGATTGCGGACTAATTTCATTGGCTGTGATGCTATGACGATCGCATTATCCCCAACTTCAGACATGCCCTCCGTCAAGCGTTGACTCTAAAGCCCCATGTGAATTGATCATAAATGATGACAGATTTTTTTTTTTACTTTCCCTTTACCTCTTAACTTTTTTGATTAGTTTAGAGATTAAAGAAATATTTATTAGATTGCCTCCTTCAGTATACAGGTGTATATACCCCTCTCTCTCTCTCCTTCATACATTTGTTTTTTGCTCAAATTTACAGTATGTACTAGTTTGTAACTACTACGTTTTTCCTGTCTTGTCTTACTTGTTACAGAACATCTCTACATTCTCTCTGGAGAAA[C/T]AGGATGATGGTTTTATAAAGATGGAGACCGGGAAGGGGAAATGCCCCTTTGAGCCTAGCCAGCCTTACACTGCAGTCATGGCAGGTATGAAACTGTAGACATACTGTATCATCTGTTGTTTATGTATTCTGTAAAGCTAACCTTAGATGCTAAAAAAAATTATTCTAAACAAAGAAAGCATTTTTCATTTTGCTTAAATTTTTTGTTTTTCCCCTGAACCTAAAGCTGACATTGGCTGGTCCTCACTAAATAGGCTATTTACAGTGACATTTTTGCAGAAACATTTGGTTGCCTAGATGTGATAGCATGAATTATAGATGTGGCATTAGTATTAGTAAAACAACATATTAATTTTTTTTTCCTTTTCTCTCTTTTTTCAGGAGGTATTCTGTACACTGCTGTCACTAGTAATTTTCTTGGCACAATGTATGACATTTCCAGAGCAACAGGCATCGAGCAGGAACGCATCCGAACTGAGCAATCAATCAACTGGCTTAGTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa7607

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:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000126930	Missense	191	414	6	12

Genomic Location (Zv9):

Chromosome 7 (position 65960175)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	59141915
GRCz11	7	59444345

KASP Assay ID:

554-4258.1 (used for ordering genotyping assays)

KASP Sequence:

TTCTTGGCACAATGTATGACATTTCCAGAGCAACAGGCATCGAGCAGGAA[C/T]GCATCCGAACTGAGCAATCAATCAACTGGCTTAGTGGTAAGATACTAATT

Long Flanking Sequence:

TTGTTACAGAACATCTCTACATTCTCTCTGGAGAAACAGGATGATGGTTTTATAAAGATGGAGACCGGGAAGGGGAAATGCCCCTTTGAGCCTAGCCAGCCTTACACTGCAGTCATGGCAGGTATGAAACTGTAGACATACTGTATCATCTGTTGTTTATGTATTCTGTAAAGCTAACCTTAGATGCTAAAAAAAATTATTCTAAACAAAGAAAGCATTTTTCATTTTGCTTAAATTTTTTGTTTTTCCCCTGAACCTAAAGCTGACATTGGCTGGTCCTCACTAAATAGGCTATTTACAGTGACATTTTTGCAGAAACATTTGGTTGCCTAGATGTGATAGCATGAATTATAGATGTGGCATTAGTATTAGTAAAACAACATATTAATTTTTTTTTCCTTTTCTCTCTTTTTTCAGGAGGTATTCTGTACACTGCTGTCACTAGTAATTTTCTTGGCACAATGTATGACATTTCCAGAGCAACAGGCATCGAGCAGGAA[C/T]GCATCCGAACTGAGCAATCAATCAACTGGCTTAGTGGTAAGATACTAATTGGTCTGTCCATCCATCTCTCCTTGTTGCATGTGATTAGTTGCACAATAACAGGTTACTGCAATTAAATAATTTTTCTGCTAAAGTTACTTTTCATTTTTAAGTAACTTGATTACAGTTACTAATAATGTATTTTAACAGAGTTCAATTTTACACATGGAAAAGGTGGGAGACGGGAAGAATTTAATTACAAAAATAAACAAAACATTCATGTGGTGGCAGTCCCTCACTACAAAAAAAGTTGCAACATAAATGTCCCAGGCCAGGTTCTGTCTTGTCTTCCACTATTGTTACTCCTTGTTTTATCCTTTTAGAGTTTCTCCATTAAAATTGACACTGTTGTGGTCCACAAGTGAGGCTTGGTAATATTTTTCCAACAAGCATTTATCAATACATGAAATACTTTTTATAAACACTTAACACCTTAACATAGCTACATCACACAATTAGCC

Associated Phenotype:

Not determined