ZMP

NAV1 (1 of 3)

Ensembl ID:

ENSDARG00000078011

Description:

neuron navigator 1 [Source:HGNC Symbol;Acc:15989]

Human Orthologue:

NAV1

Human Description:

neuron navigator 1 [Source:HGNC Symbol;Acc:15989]

Mouse Orthologue:

Nav1

Mouse Description:

neuron navigator 1 Gene [Source:MGI Symbol;Acc:MGI:2183683]

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa10965	Nonsense	Available for shipment	Available now
sa16509	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa10965

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000115403	Nonsense	149	2168	1	30

Genomic Location (Zv9):

Chromosome 23 (position 5889501)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	5905662
GRCz11	23	5839634

KASP Assay ID:

2261-7307.1 (used for ordering genotyping assays)

KASP Sequence:

CCAACGGCAACAAGAATTTCCAGAGTGGGATCTTTCGTTCTCAGCCAGGA[C/T]AAATAGACAATGGTAATCTCAGGAGTGTGATCTCAGAACAACTCAAGTGC

Long Flanking Sequence:

CATGCCCTCATGGTATTTATTCTCTTTTTCCCCTCAGCATCTGATCTGGTGCCACCATGAGTGGGGGAGTGAATGTAAAGAGTCTTCCACGAGCCCAGCCGGGCTCAGGCATCCCCCTGCACAGGACCAGACTCCCCTCCCCAAAACCTGAACCTAAAAGCAACAGCAGTAGCCTTCCTAGACCATCTACACACATCCCCAACAGAACCACCTGTAGTAGCAGTCCTACACCCATCTCTTCCAGAGATTTACTAAGGGACAGTACCCTCAGAAATCAGCATCTCTTACTAAGAGGCAGTCCACCCAGTCAACGTTCTTCCACTAGTTCTCAAACACACTCCCAAGACTCTAGATCAGCCCACAGCAGTCCACAAATTAGGCGTAAAGAGTCTTCATTTTCTAGGGGCACACTGGATGGGTCTAAGACAGAGAGTTTGCTTGACCTTCGGTCCAACGGCAACAAGAATTTCCAGAGTGGGATCTTTCGTTCTCAGCCAGGA[C/T]AAATAGACAATGGTAATCTCAGGAGTGTGATCTCAGAACAACTCAAGTGCCATGAGGAGAGCATTGCTTCTGGAAGTGGTCAAAGCAAGACTGGAATCCCTTCATTTAGATTTAGTAACAAAAACTTGAGGCCTGGCCCAGCAGCTGCTAACCTAGAAATGAGTCACCTTAAAGTCCGCAGAGAGCGAGTGTCCCTGCAAAACAGTGCCTCCAGTAGCTTCTCAGATGAGGAAATGTGCACGCCAGATGACTTGAGCCCTGAGATCCCACAGAGACCACCACCTGAGACTGCAATGCTGAAACAGGAGACCTCTAGTGTCGAGCTGCTCAAAACCAAACAGACACCAAAGGTCAATATGGCAGCTGTGGCACCTTTCAGATACAGGTAAGTTATAGATAATTGAAAATGAAAATGTGCTGTTGGTATTAATAGAATTTGTGATTGTAGCTAAGTTGGAATTGGGAAACACACCTCATGTTGGTTTAGTGCAGGTTTAGTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa16509

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
ENSDART00000115403	Nonsense	497	2168	3	30

Genomic Location (Zv9):

Chromosome 23 (position 5922816)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	5938977
GRCz11	23	5872949

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CAGCAAGGCTCAAGAGCCGGCTGATGACAGCAAGTCCGATGATGAGATCT[T/A]GTCCAGCAAGGCTAAAKCTAATGGTAAGAAATCTTTGAGTGGTACTTCGG

Long Flanking Sequence:

AGCCAAGACCCTTCAGGGCCAGGCAGGAGCCAAAGGAGTTGGAGGCATGGCTGCGAAAAGGGGCAAGTCAGGGCTCCCACAGGCTACTCCTCGGGCTGAGCTGAAGGTGTACCGAGCAGGGAACTCTGAGGGTCGTCTTCCAGTGCCTAGCAACTTGCGGAAACAAAAGTCCTTGACCAATCTATGCGTGCTTACAGATGCCGAGAAGAAGATGCACCTGTACCAGCCCAAGTGGTCAGACGACATGGAAAAACCTGGGACAGGTCAGAACAAATCAGGCAAGCTCAGAGATCCCGGAGGGAGCATTGGCAGGGGTATCCCTCTTTCCAAGAACCTTTCAAAATCGGAGCATTCGCTGTTTCAGGGAAAGCCAAAACCCTTTAATCCACCTTCCAGACTAGGGAAACCCAGTCGGATACCTAAAAGTCCTTACGCTGAGGTCAAACCCATCAGCAAGGCTCAAGAGCCGGCTGATGACAGCAAGTCCGATGATGAGATCT[T/A]GTCCAGCAAGGCTAAAGCTAATGGTAAGAAATCTTTGAGTGGTACTTCGGGATCAGCCACCCCAGGAGGAGATGGAGGTGGGAAAGATGGACTGGAACCGGAGGAAGGTGACAAGACCTTTCTAAAGGTGGACCCCGAACTGGTTGTAACAGTGCTTGGGGACCTGGAGCAGCTCCTCTTCAGTCAAATGTTGGGTAAGTAATAACAAGATCCTCTAATCTGCTTGCAATGCCAAGGAATGAGCAATTCTGCCTGGCTGATGCATCCGGCATCACCTTCATAGCTCAACCCAGCCCTGCTCTTGCTTAGCAACCACCTTGCTTTGTATTTCTCATTCATCCTGTGCTGCTCACATAACTACGCGCACCTTCTCTTTTCACGCATCTATTCTTGGCTCAACCTGCATGCCAATAAGTATGCTTCTTGCTTTTTTGTAAATATGTCTGGTTGTGTTGGATATTCGCCGTGTTATTTTTTTGTTTACATTGCAAGCTCATGTC

Associated Phenotype:

Not determined