ZMP

ntf3

Ensembl ID:

ENSDARG00000059043

ZFIN ID:

ZDB-GENE-031118-66

Description:

Ntf3 protein [Source:UniProtKB/TrEMBL;Acc:Q568T2]

Human Orthologue:

NTF3

Human Description:

neurotrophin 3 [Source:HGNC Symbol;Acc:8023]

Mouse Orthologue:

Ntf3

Mouse Description:

neurotrophin 3 Gene [Source:MGI Symbol;Acc:MGI:97380]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa11980	Nonsense	Available for shipment	Available now
sa38419	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa11980

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
ENSDART00000082046	Nonsense	98	243	2	2

Genomic Location (Zv9):

Chromosome 4 (position 4270837)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	4389213
GRCz11	4	4398126

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGCTACGCCAGTACAAGCGCTACAACTCTCCRCGTGTCCTCTTAAGCGAC[C/T]GACCTCCAATGCAACCRCCGGCTTTCTACCTCATGGATAAATTCATCAGC

Long Flanking Sequence:

TCCCCCCAATGTGTAAAGTGCTTTGAGTGTCCAGAAAAGCGCTATATAAATGTAAGGGGGAAAAGTACAGTACATAGTGCATAGTGTGCCATTTGGGACGCAGCTTGAGATTCATGAGAATTCAATCATGTCTCTAGTTCATTAAAATCATTTCATTTGCTCAAAGCGTCTCTCTTGTTTCTCCACAGATCTTACAGGTGAATCTAGTGATGTCCATCTTGCTGTACGTGATGTTCCTCGCGTACCTTTATGGTATCTCCGCCTCTACAATGGACAAGCAGCGGCCCATGCAGGATCCCATCAGTGCGCTCATCATAAAGCTCCTGCAGGCTGATATCAGCCGCCAGAAACAGGGCGACGTCATTCCCTCCTCCACCTTAAATGTGTCCACAGTCGCAGACTACAAGGAAAAAGACAACAATACCCCCATGGTGGACAGTTCGGAGGAGCTGCTACGCCAGTACAAGCGCTACAACTCTCCACGTGTCCTCTTAAGCGAC[C/T]GACCTCCAATGCAACCACCGGCTTTCTACCTCATGGATAAATTCATCAGCGGTCAGGACTCCAACAAGACGCGGCAGAAACGCTTTGCCGAGCACAAGAGCTACAGAGGAGAGTTTTCAGTGTGCGACAGCGAGAGCAATTGGGTTACAAACAGGACCTCAGCGGTGGATTCTCGTGGAAATCATGTCACCGTTTTGAATTCCTTCACTGTAAAACAGAAATACACGCAGTACTTTTATGAGACCAAGTGTAAAACTCCTCACTCCCACCGCAAGAGCCGATGTTTAGGTATTGATGAGAAGCACTGGAATTCGCAGTGCAAAACCACGCAGACTTACGTACGAGCGCTTACTCAGCACAAATCGCTGGTTTCTTGGAATTGGATACGGATAGACACGGCATGCGTCTGCGCGCTCTCAAAGAAACATAGAAGGACGTGAAAAATGGTGGAAAAAACACTTTCAATTCTCCATTGTCTTGCTAGTGTTTCCTGGGGGCTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa38419

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000082046	Nonsense	212	243	2	2

Genomic Location (Zv9):

Chromosome 4 (position 4270495)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	4388871
GRCz11	4	4397784

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTGATGAGAAGCACTGGAATTCGCAGTGCAAAACCACGCAGACTTACGTA[C/T]GAGCGCTTACTCAGCACAAATCGCTGGTTTCTTGGAATTGGATACGGATA

Long Flanking Sequence:

GCCAGAAACAGGGCGACGTCATTCCCTCCTCCACCTTAAATGTGTCCACAGTCGCAGACTACAAGGAAAAAGACAACAATACCCCCATGGTGGACAGTTCGGAGGAGCTGCTACGCCAGTACAAGCGCTACAACTCTCCACGTGTCCTCTTAAGCGACCGACCTCCAATGCAACCACCGGCTTTCTACCTCATGGATAAATTCATCAGCGGTCAGGACTCCAACAAGACGCGGCAGAAACGCTTTGCCGAGCACAAGAGCTACAGAGGAGAGTTTTCAGTGTGCGACAGCGAGAGCAATTGGGTTACAAACAGGACCTCAGCGGTGGATTCTCGTGGAAATCATGTCACCGTTTTGAATTCCTTCACTGTAAAACAGAAATACACGCAGTACTTTTATGAGACCAAGTGTAAAACTCCTCACTCCCACCGCAAGAGCCGATGTTTAGGTATTGATGAGAAGCACTGGAATTCGCAGTGCAAAACCACGCAGACTTACGTA[C/T]GAGCGCTTACTCAGCACAAATCGCTGGTTTCTTGGAATTGGATACGGATAGACACGGCATGCGTCTGCGCGCTCTCAAAGAAACATAGAAGGACGTGAAAAATGGTGGAAAAAACACTTTCAATTCTCCATTGTCTTGCTAGTGTTTCCTGGGGGCTGTACATATATAAATTATTATTTAAGTTATATAGAATGCATATAGTTTATACATGTCTATGTATAATGTATAAAGATACTTGTTATTTATTTAAAAGTTATAAAATCTTTGGAAAAAAAATGAAAGACAGACTTATGAGAACATGCATTGCCGCTAAGCTAACAGGAGCATTGAATGCTGAATTGTGCCTTGCTCGCGTATCAGAGTCAGAGGACACTCCACTAGACCTGGACCTTGGGAACAGTTGCAATGGAAAAACACACAGATCGCTCAATATCATGTTAACTTCAGTATTGTTCACGAAAACCAGTTTTTCTACTGAAACGGGCTGCCAGTATATCCTC

Associated Phenotype:

Not determined