ZMP

VGF

Ensembl ID:

ENSDARG00000091371

Description:

VGF nerve growth factor inducible [Source:HGNC Symbol;Acc:12684]

Human Orthologue:

VGF

Human Description:

VGF nerve growth factor inducible [Source:HGNC Symbol;Acc:12684]

Mouse Orthologue:

Vgf

Mouse Description:

VGF nerve growth factor inducible Gene [Source:MGI Symbol;Acc:MGI:1343180]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa16922	Nonsense	Available for shipment	Available now
sa34068	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa16922

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000130710	Nonsense	106	642	1	1

Genomic Location (Zv9):

Chromosome 7 (position 27352634)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	25955573
GRCz11	7	26226766

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GGGCACTAAACCAGAAAGAAAAGATGAGTGAACGAGAAGATGAGGGAACT[G/T]AAGGGSAAAAGGAGAGGGATCTTCAGGGCGCAGACAGAGACAGAGATGGT

Long Flanking Sequence:

ACGTGATGCACATGACTGTATTCAATTTATTCTAGCATTATTTTGACGTAAATATTTTAGGAAAACATGCTTTATGCCTTTTATTAAAAAGCAATTACTTGATTTGCACCTTGAGATCAAATTTGAGCCATCTTTGATGAATTTTGAACTTCTTTTGTCTTTCAGGTTCACACATATGTGCGGTCATGACCTGGTGCCAACACACTTCAAATATTCCCATCATTTTCCTGTTCATGTTATTCAGTCTCACAGTCAAGCCTGCAGCCTTTAGTCCAGTGACAACAGACAGAAACACAGTAAGTGAAAACTATGCAGCTGCCTCCTCTGCTCAGCAACAGGCTCTATATACTCAACCAGCCGAGGAGCAGGGCACGACACATGATGAAAATGAAGATGATGATGAGCTTTTTAAAGACGTGGATCCTAGAACCCTAGCAGCAGTTCTTCTCGGGGCACTAAACCAGAAAGAAAAGATGAGTGAACGAGAAGATGAGGGAACT[G/T]AAGGGGAAAAGGAGAGGGATCTTCAGGGCGCAGACAGAGACAGAGATGGTCACAAAGAACTGGAACTGGTGATGGCAGCTGCGCAAGGAAACGATGAGAAAGAAAGAGAGGAAGAGGAGAAAAAAAGGGCTGAAGAGGAGGAAAGGATGACGGAGAAAGTGACAAGCCGCACCACCAGCCAGACGGTACCCATTAAGGAGCAGGTGGCTCCGCAGGAGGAGGCCACACAAGAGGACGTGACCAAGGAGGAGGAGAGGCAGGAGCCGGAGGGAGGAAAAGCAGAGGAGGAGGAAGAGCAGCTGAGTCCTGAGGAGGTGAAGAATCTGGAGACTATGCTGGAGGAGTTTCAGAGCTATAGCACAGCTGCTAAGAGAGAGCGTGACACCAGACAGAGGGAGAGCCGTGGGGAGTATTTCGATTACCTGGACCGCAATGGCCTCATGAACAATGAGATCAAGCCTAAAGCTAAAGGCAATGACCTAGCCTTGTCCAAGAAGAAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa34068

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000130710	Nonsense	427	642	1	1

Genomic Location (Zv9):

Chromosome 7 (position 27353597)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	25956536
GRCz11	7	26227729

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTCCAGCAGACGATGTGGTGGACATCATTAATGATGTGGAGAAGAAGAAG[A/T]AAAAAGATGCTCCTGAAAATCTGCCATGGCAACATCCTCTTGTGCCGCCT

Long Flanking Sequence:

AAGCTAAAGGCAATGACCTAGCCTTGTCCAAGAAGAAGTTAAAGTGGCAGCTCGAACAAGAGAAAAACAGAGTTCAGCCTTTACAAAGAGGGGGCAACTTCATGGATGACTTTAGCAACAACCTTGCTGACCCAGAGGAAGAAGATGAGGAAGATCAGGAGGATGAAGAACAGCTAAGCCCTGAAGAAGAAGAAACACGGGCCAAAGCTGAGCAAGAGGAGGTACGCAGACAAGCAGCAGAGGCTCAAAGAGCCAAAGCAGAGGAGGAGAAGCTTGCAGATATTGCATCTGACATGCTTCTGAAGTACATTGTAAAACAAGACAAGAAAAAGTACCAAGACAACAATGGTGCTGAAGATAAGCGCTCTGATGAGGACACTAATGATGATGATGAGGACATTGACCCACAGACTATTGATAAGTTGATTGAGATCTCCAGCAAACTGCATCTTCCAGCAGACGATGTGGTGGACATCATTAATGATGTGGAGAAGAAGAAG[A/T]AAAAAGATGCTCCTGAAAATCTGCCATGGCAACATCCTCTTGTGCCGCCTCCAGCCCCCGCTGCACCTTCAACAGTGTTACGTAAACCTCCTCCCTCGAAGCCTCCTCAACCAAACACCAACCCATTGAAAGCCTGGTTCAAAGACAGGGCCTCGGTCAAGCCCAGCAAGCAAGACATGTGGGCAAGGCAACAGTGGCCCTTTCGTACCTACCCTTCCTACAACTCCTATCAAAAACCCTACCGAGGCTACTACCCCGTCTACATCCCACCTCCAAAACCAAAGTCCCGCTACTATTCCAAGCCCTCTTTCTCACTTAATGATGTTCTGGGAAACTCACTGGACTATGACTTTGATTACTCCCCCAGACGGAAGTCCCGTCCTTGGGCGCAGCCTCGCCAAAGAGTCCAACCTGCCTTCCAGAGGAACCTCTACTTCCCTCACCCTCGGACTTTCAAAGCTGTTCCCATGCCTAAACCCCGGTCACCTCCACGTCGTTGG

Associated Phenotype:

Not determined