ZMP
wu:fk86g11
Ensembl ID:
ZFIN IDs:
Description:
Novel protein similar to vertebrate netrin G1 (NTNG1) [Source:UniProtKB/TrEMBL;Acc:B0S6C7]
Human Orthologue:
NTNG1
Human Description:
netrin G1 [Source:HGNC Symbol;Acc:23319]
Mouse Orthologue:
Ntng1
Mouse Description:
netrin G1 Gene [Source:MGI Symbol;Acc:MGI:1934028]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19708 | Nonsense | Available for shipment | Available now |
sa25783 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19708
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105742 | Nonsense | 13 | 355 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 2 (position 15610765)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 16121592 |
GRCz11 | 2 | 15790182 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATCCGCAACCATGCATTTTCTGCTAGCGTTTGTACTACAGGCCCTGTG[G/A]GTGAATTGGTGTCACGCCACACAGCATTACCTGGCCTCGTGGGGGCATTA
Long Flanking Sequence:
TGAAGTCCGTCTCGGCTATAGAAAACACTTGACCTGCACCTCCTCACCTTTTCCACCAGGCTCCTCGTTATTTGCACAACACCATTTCTAAAAGCTGACACACTCTCGTTTCCCTCTCTTTTTCTTCTCATCCCCACAGACTTCAGAAAGTACACAGGGAAATGGCGATGGACAGCCGGATGATCCGAAATGGCCTCCACTAATGGCGTCAAGAAGGAATTAATACCACTCATTCACACCGGTGACCCACAGCTTTGTCAAAACACGTTCAAGCAACACAATCAGATGAAAGGAAACAAACAAATGAAATTAAAGCAGCTTAAAGAAGCAGAGTCAAAGCTGGCACAGATGCTGGCCTCTTTCCCCCTTTAAAGTTGAATTTTGCGGTCTGCCTCATCACCCTCTGCCAGCTTATTGTTTATCAGACTCTGTTTAATGAGGCATCAGAAGAAATCCGCAACCATGCATTTTCTGCTAGCGTTTGTACTACAGGCCCTGTG[G/A]GTGAATTGGTGTCACGCCACACAGCATTACCTGGCCTCGTGGGGGCATTATGATGTTTGTAAGTCTCAGGTACATGCTGAGGATCGCCTAGCCTGGCATTACATGGCCTGCCAGCCTGAAGCCACTGATATGACCCAATACCTGTCTATGGTGTCTTTGGATCCACCCAATATCACCTGCGGAGACCCACCTGAGATGTACTGCGCACTGGTGAGTTTACATTTTTGTATTGTTTATTTTTCTTTAATAATCGTTTTACTGGTGTATTAATATATATGACAACATCAGGCGCCAAACCATACTACTTTGGTATTACTATCTACTATTGGTATCATTGTACTTCTTTATTATACATGTCGTGCAGTCAATTTCTTGTATAGAATTACTTGTGTACATGAATCTTCTTAGTTTTTTCTCTTCATAGATAATGAAATAAGTGACTCTTAAATCAATATTTTTGTCTATTTATTTATTTAAATTTATTCTTTATTTTATATGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25783
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000105742 | Nonsense | 21 | 355 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 2 (position 15610787)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 16121614 |
GRCz11 | 2 | 15790204 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTAGCGTTTGTACTACAGGCCCTGTGGGTGAATTGGTGTCACGCCACA[C/T]AGCATTACCTGGCCTCGTGGGGGCATTATGATGTTTGTAAGTCTCAGGTA
Long Flanking Sequence:
AAACACTTGACCTGCACCTCCTCACCTTTTCCACCAGGCTCCTCGTTATTTGCACAACACCATTTCTAAAAGCTGACACACTCTCGTTTCCCTCTCTTTTTCTTCTCATCCCCACAGACTTCAGAAAGTACACAGGGAAATGGCGATGGACAGCCGGATGATCCGAAATGGCCTCCACTAATGGCGTCAAGAAGGAATTAATACCACTCATTCACACCGGTGACCCACAGCTTTGTCAAAACACGTTCAAGCAACACAATCAGATGAAAGGAAACAAACAAATGAAATTAAAGCAGCTTAAAGAAGCAGAGTCAAAGCTGGCACAGATGCTGGCCTCTTTCCCCCTTTAAAGTTGAATTTTGCGGTCTGCCTCATCACCCTCTGCCAGCTTATTGTTTATCAGACTCTGTTTAATGAGGCATCAGAAGAAATCCGCAACCATGCATTTTCTGCTAGCGTTTGTACTACAGGCCCTGTGGGTGAATTGGTGTCACGCCACA[C/T]AGCATTACCTGGCCTCGTGGGGGCATTATGATGTTTGTAAGTCTCAGGTACATGCTGAGGATCGCCTAGCCTGGCATTACATGGCCTGCCAGCCTGAAGCCACTGATATGACCCAATACCTGTCTATGGTGTCTTTGGATCCACCCAATATCACCTGCGGAGACCCACCTGAGATGTACTGCGCACTGGTGAGTTTACATTTTTGTATTGTTTATTTTTCTTTAATAATCGTTTTACTGGTGTATTAATATATATGACAACATCAGGCGCCAAACCATACTACTTTGGTATTACTATCTACTATTGGTATCATTGTACTTCTTTATTATACATGTCGTGCAGTCAATTTCTTGTATAGAATTACTTGTGTACATGAATCTTCTTAGTTTTTTCTCTTCATAGATAATGAAATAAGTGACTCTTAAATCAATATTTTTGTCTATTTATTTATTTAAATTTATTCTTTATTTTATATGGTGGCCAACAAAACACGAACACAT
Associated Phenotype:
Not determined