ZMP

NID2 (1 of 2)

Ensembl ID:

ENSDARG00000075707

Description:

nidogen 2 (osteonidogen) [Source:HGNC Symbol;Acc:13389]

Human Orthologue:

NID2

Human Description:

nidogen 2 (osteonidogen) [Source:HGNC Symbol;Acc:13389]

Mouse Orthologue:

Nid2

Mouse Description:

nidogen 2 Gene [Source:MGI Symbol;Acc:MGI:1298229]

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa23022	Essential Splice Site	Available for shipment	Available now
sa15802	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa23022

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:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000115064	Essential Splice Site	169	1351	2	27

Genomic Location (Zv9):

Chromosome 17 (position 14713960)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	14864788
GRCz11	17	14872721

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGTGTCAGCTTATGAAGAGGTCGCGCGCAGCTCTAGCCCATCCCATCGGG[T/A]AAGAAAACAGCTTTGAGGTCTTGTTTACACCTGTTGTTAAAGGGATAGTT

Long Flanking Sequence:

AGGAAGATAACTGGAGTGAAAAACTCAGGTTATTTATAATGCTATAAAGCTAATAAGGAGCCAGCCGTGTTGATTATAAGCTTGTGATCCTCTCGAAATTAGTTTATGAATAAACCGCACAAATTGTTTAAAACATGATGCCAGAAAACTATTTATATTACAGACGCTTATATTTTTGTTTTGACTGTCATTGCAGGTGACCACCAATGGAATCATCTCAACTCAGGATCTTCCCATGGAGAAGCAGTATGTGGACGACGGCTTTCCCACCGACTTCCCCGTCATCGCCCCCTTTCTGGCCGACATTGACACCAGCAAAGGAAAAGGATCCATCTACTACCGGCAGACGGAGTCTCCCACCGTGCTGAAGCGTGCAGAAGCGGATGTCAAAAGAGGCTTTCCAGATGCCACGTTCAGCCCTACCCACGCCTTTATCGCCACCTGGGAGAATGTGTCAGCTTATGAAGAGGTCGCGCGCAGCTCTAGCCCATCCCATCGGG[T/A]AAGAAAACAGCTTTGAGGTCTTGTTTACACCTGTTGTTAAAGGGATAGTTCACCCAAATATTTAAATTTACACACTTTAACACAAGTCTGCTTAACACAAAAGAAGATATTGTGAAGAAAGCTGCATAGTAGGGCCATAGTAGGGAAAAACAAATACTGTGGAAGACAATAGTTATAGGTTTGCAGCTTTCTTCAAAATATCTTCTTTTGATTAAACAGATTCCCAGTTCTGGGTTGTAACTGGAAGGGCATCTGCTGTGTAAAACATATGTCAGAGTAGCTGGCGGTTCATTCCAACCAGGAATCAGGGACTAAGCTGAAGGAAAATGAATGAATGAATGAATGATTCAACAGACAAAATAATCTCAAACAGGTTTGGAAGAAGAATTTTCAAGTTTTGAGTGAACTATGCCTTTAAGATGTTTTTTGTAAAACCAATCACAAGTGTGCGGTGATAAATACAGATGTTAATGGGGGCCGAAATGTTTAGAGCTTGTTCC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa15802

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000115064	Nonsense	473	1351	9	27

Genomic Location (Zv9):

Chromosome 17 (position 14695305)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	14846133
GRCz11	17	14854066

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGAWCCATTACYCGACAGATAAYAAAGAGACGTGTGAGCGTTTCCAGCAG[C/T]AGTGCAGTCTAAACGCTCACTGTAYAGATCATTCCACCGGCTTCTGCTGT

Long Flanking Sequence:

AACATAAAAGTGATCCAGTTAATTTTTTAAAAATTCATGTGCACATTTAAATTAAAATGGATGCTTTTCATGAGACAGAGTTTAGCAAAAGGCTAAATGTAACCAAAATAGCTTAGAAATTAAAAAAGCCATATTTATTGTTAGCAAAGGAGCACAAAATATTCCAAACATCACAAAAATACACAAGTCTTTCCCATTGTTTCTCATAATACAGATAAATAGCAAAGCTTGCATTGCCACTGCTTTAACCTCAAAATGCCCCACATTATTCATAAAAGTATTAATGTATTGTGACTTGCATTTCCAGTTACTCAGAATAAATATCTGTCTAGACAATCCAGAGCACCTCAGATCATGTAGGAATTTTACCAATGACTTGTACACTAGCAAGTTTGCCTTTCCTACCCTATTCAAGAGCTCTTTCTCTGTGCTTTTACCTCTGTCCCGCAGTGATCCATTACTCGACAGATAATAAAGAGACGTGTGAGCGTTTCCAGCAG[C/T]AGTGCAGTCTAAACGCTCACTGTACAGATCATTCCACCGGCTTCTGCTGTCACTGCAACTCCGGCTTTTACGGCAACGGCCGCCACTGCCTGCCAAACGGTAAGACTCCGCCAGAAATGCAGTAAAAAGAGCCGTTGTAAAAGCCACACATAACATGACCTTGTGCTGAAAGCATGAACAACATTAGCAGGACACCTCTGGGGATTTATTACCAGTGTTTTTCTTTCCAGCACAGTATTTTTTAGAGGGTAAAGATGTATATTTTTGTTTCGCAAAGGAATTTGGAGATAACATTTGGATTTTGGCAAATACTTTGTGTTGGTTCGAGTGCAGTTATTTTCTGTAGGGTCAAGTCAAGTCCCCCAGTCTAAACTTGTGCTGCCTGTGTCCCAACTATCCATCCTAAACCTTCATTCATTCATTCATTCATTCACAGTCCCTTTTTTTAATCTGGGGTCGCCACAGTGGAATGAACCGCCAACTTATCCAGCTCATGCCCT

Associated Phenotype:

Not determined