ZMP

NTNG2 (2 of 2)

Ensembl ID:

ENSDARG00000087100

Description:

netrin G2 [Source:HGNC Symbol;Acc:14288]

Human Orthologue:

NTNG2

Human Description:

netrin G2 [Source:HGNC Symbol;Acc:14288]

Mouse Orthologue:

Ntng2

Mouse Description:

netrin G2 Gene [Source:MGI Symbol;Acc:MGI:2159341]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa9458	Nonsense	Available for shipment	Available now
sa23847	Nonsense	Available for shipment	Available now
sa37213	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa9458

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000124030	Nonsense	189	1579	6	10

Genomic Location (Zv9):

Chromosome 21 (position 4169542)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	3844542
GRCz11	21	4009161

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TCATATTATTAGTCACCAGTGCATCTGTCACACCAGCACCTGAACCTKTT[G/T]GATCAGTGCSGGAGTCTGCCGAGCCAAAGCCAGAGTCGATTCCRAAGCCA

Long Flanking Sequence:

GAATATTTCATTGAGATGTGACTTGCTATTCAATAGTTTTTTGTCAGTATTGTAGTAGTGTTGTGGTAGATGTGGCTTTGTTGATTTTCCCTAATTAATCTGTGGTTTGTTGTGGAGTTTGTCTTGCTATAGAGTATAGGCTGATGTACAGGTTATTTCTAACTAGACTGCTTGTTGTTCAGTTGCTGTTTATAGAGAAAAACGTGCTGTTTGTGTACCAAATTTGTGATTATTCAAGTGATTACAACTAAGAAATCATTACAGCACCACCAGTGGAGGATTCTGGGGAAGTTGAAGAGATTTCTGAAAAGAAAGAGATGACTTCAGGGAGACATGAAGTATCTGAAGATGTAAAGAGAGTGGAGACTTTTCTGGAACATAACAGACACAGGGAAGAAACTGGTATGAAGTGTCTCACTGTGTTCTCAATATATTTGTTCAATTTGTGAATCATATTATTAGTCACCAGTGCATCTGTCACACCAGCACCTGAACCTGTT[G/T]GATCAGTGCGGGAGTCTGCCGAGCCAAAGCCAGAGTCGATTCCAAAGCCAATTTTGGAAACACACAAGCCACTACACAAACCTCAAGTTCATGTGTCTACAGCGGAATCTCATGGAGCAGCACAAACATCACATGAATCAGTAACAAAGCATCATGAACCAATTCAGAAACTTCATGAGTCAACAGTGAAACCTCACTCAATGCATACAACCCATGAGACTATACAGAAACCTCATGAACCAAAAGTGAATTCTCATGAATCAATGCATAAACCCCATGAGCAAATTGTAAATCTTAATGAATCAATGTATAAGCCTCATCAGCCAATATGGGATCCACATTCATCGCCGCAAAAACCTTTTGAGCCAAACGTGAACCCCCTTGAGTCAGTAGTGAATATTCATGAGTCAACGCATAAATCACATGAAGCAGTAGTGAATCCTCAGGAATCAATGAATAACCCTCATGGGTCAGTAGTAAACCCTCACAAGTCAGGGCAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa23847

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

Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000124030	Nonsense	276	1579	6	10

Genomic Location (Zv9):

Chromosome 21 (position 4169804)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	3844280
GRCz11	21	4008899

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCATGAGACTATACAGAAACCTCATGAACCAAAAGTGAATTCTCATGAAT[C/A]AATGCATAAACCCCATGAGCAAATTGTAAATCTTAATGAATCAATGTATA

Long Flanking Sequence:

AGCACCACCAGTGGAGGATTCTGGGGAAGTTGAAGAGATTTCTGAAAAGAAAGAGATGACTTCAGGGAGACATGAAGTATCTGAAGATGTAAAGAGAGTGGAGACTTTTCTGGAACATAACAGACACAGGGAAGAAACTGGTATGAAGTGTCTCACTGTGTTCTCAATATATTTGTTCAATTTGTGAATCATATTATTAGTCACCAGTGCATCTGTCACACCAGCACCTGAACCTGTTGGATCAGTGCGGGAGTCTGCCGAGCCAAAGCCAGAGTCGATTCCAAAGCCAATTTTGGAAACACACAAGCCACTACACAAACCTCAAGTTCATGTGTCTACAGCGGAATCTCATGGAGCAGCACAAACATCACATGAATCAGTAACAAAGCATCATGAACCAATTCAGAAACTTCATGAGTCAACAGTGAAACCTCACTCAATGCATACAACCCATGAGACTATACAGAAACCTCATGAACCAAAAGTGAATTCTCATGAAT[C/A]AATGCATAAACCCCATGAGCAAATTGTAAATCTTAATGAATCAATGTATAAGCCTCATCAGCCAATATGGGATCCACATTCATCGCCGCAAAAACCTTTTGAGCCAAACGTGAACCCCCTTGAGTCAGTAGTGAATATTCATGAGTCAACGCATAAATCACATGAAGCAGTAGTGAATCCTCAGGAATCAATGAATAACCCTCATGGGTCAGTAGTAAACCCTCACAAGTCAGGGCATAACCCTCATGGGTCAGTAGTGAACCCTCACGGGTCAGGGCATAACCCTCATGGGTCAGTAGTCAACCCTCACGAGTCAGGGCATAACCCTCATGGGTCAGTAGTGAATCCTCACGAGTCAGGGCATAACCCTCATGGGTCAGTAGTGAATCCTCACGAGTCAGGGCATAACCCTCATGGGTCAATAGTAAACCCTTATGAGTCAGGGCATAACTCTTATGGGTCAGTAGTGAACCCTCACGGGTCAGTAGTGAACCCTCACG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa37213

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000124030	Essential Splice Site	1406	1579	7	10

Genomic Location (Zv9):

Chromosome 21 (position 4173899)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	3840185
GRCz11	21	4004804

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CGGGAAACAGACTGTACAGCTAAAAGGCATCATATATGACGACTTTCAAG[G/A]TGAGAAAGAATCACAAATGGAATGAGAAAATGAAGATGTTTATTTGATGT

Long Flanking Sequence:

CCTTTTTCCTTGCTTGACCCACACAAACAGTCAAATGAGCACGATATATGGGAGGGTGAAGTGAAGCCAGCGCTTAAGTGGGAGAGAGTAGATGATAAATATATCGATGCTGTGAAGTAGACTAAAGTGCATTTTGGGTTGTGAAGTTTATGGCTGTGTGCTCATAGTATAGTCATTAGACCCCCACATAAACATTGTGCTGTGTTAGCTTCTATAATATCCCACTTCAGGTTGTACTTTTGATAGCACATATGCTTGGTAGTGGATTTTTGGGCTCATTAGATGGCTTAAACGATGATTCTATTCCCTCCCTTAACGGTGTAAATTCATAGCTTGTTATTTGCTTGCCGTAGAGTCAGTTTGCTTTGCCTGTAATAGGGGTCCAGATAAACGAATATAATAATCATACTGTTCATTTTCCAAAGCTCTTATGAAGTTCTTATTATCTGGCGGGAAACAGACTGTACAGCTAAAAGGCATCATATATGACGACTTTCAAG[G/A]TGAGAAAGAATCACAAATGGAATGAGAAAATGAAGATGTTTATTTGATGTTTTAATCATTAGTCTTCAGCCATTCCCTTCTGCTTATTACCACTATAGTTTTAGAATTCACTTTTGTTCCTTACAACTAAAAAGCAACAATGTTCTAGATTCTAGATCCTTTGGGTGTTTCCTTCAACTCATTAATGGTGTACCTTTCAATGTTCCATTCTACTTATCACTGTAATGGTTTCTAGAGCTCTCTCTATTTCACTGCAACGCTTAAACACTGTAACATGTTCTAGATTCTGGACATATAAACTGTTTATTTCTACAAAAACACTAATGTGCTCAAGACTGCACCCATGTTACTTGCATGTCTAACTTTGTAATTTTTAAGGTTCTAGAACATTCAACTGTTCCTTCTACAGTACTCATAAACACGGCAATGTTCTTGAACTCACCTTAATATCAGACAACTGAAAAACACTACCATGTTCTAGATTCTACAATCTTTGACTA

Associated Phenotype:

Not determined