Busch Lab

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
sa25037 Nonsense Mutation detected in F1 DNA Not yet available
sa15802 Nonsense Available for shipment Available now
sa44869 Essential Splice Site Mutation detected in F1 DNA Not yet available

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:
sa25037
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
ENSDART00000115064 Nonsense 230 1351 3 27
Genomic Location (Zv9):
Chromosome 17 (position 14700817)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 14851645
GRCz11 17 14859578
KASP Assay ID:
554-7876.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCTCGTGTGGGATTTTCCAGAGGAGAGATTTCCTACTTGATTTTTTCT[C/T]GAACAGAAGGGCCGTATTATAGCCTCACCAGCAATGAGCAGTCCGTCAAG
Long Flanking Sequence:
AATAAAACAACGTGTGAAAAACATCAAAAGTTAGCACTGTCGTGAGTAATTCACTAGGCCAGTAAAACAGTTGTTAGAAATGCCATATTTGGAGTCCAAGATGGCCAAGATTTCCAGCAATGATTGATGATCCCAGGAAATAAATCTATTAAAGACCACTTTGTCCAAAAGTAGGGGGGAGTAAGTTCTCTAGTAAAACATTTGAGATAGATTTACAGTATATAATGGAATATTTACAGGTGGTTTGTCTTTTTTATTGCCTTCTAAAAGTGCTGCACAGAAATCTGGAGCTCTGAGTAATGTTCTTCTTTTTCTTTTAGGTAAACACGTTCCAAGTGGTGCTTGCGTACAATGAGAAGGACACTTATGCGCTCTTCCTATACCCTGAGGATGGCCTGCAGTTTTTCGGGACACGGCCCAAAGAATCTTACAATGTTGAAATTGAGCTTCCAGCTCGTGTGGGATTTTCCAGAGGAGAGATTTCCTACTTGATTTTTTCT[C/T]GAACAGAAGGGCCGTATTATAGCCTCACCAGCAATGAGCAGTCCGTCAAGAACCTGTACCAGTAAGCATTGCGGGAATTACCATTTAAGATCAAGCCACCCTGTTGTTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAATAGACGCACACACACACACACACACAAAGTTAAAGTATACACAGTTGAAGTTTTTCCCAATTTCTGTTTAACGGAGAGAAGAAATTTTCAACACATTTCTAAACATAATAGTTTTAAGAACTCTTCTCCAATAACTGATTTATTTTATCTTTGCAATGATGACAGTACATAAAATTTTACTAGATATTTTTCAAGACACTTCTATACAGCTTAAAGTGACATTTAAAGGCTTAACTAGGTTAATTAGGTTAACTAGACAGGTTAGGTTAATTAGGCAATTTATTGTATAACGATGATTTGTTCTGTAGACTATCGAAAAAAC
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

Mutation Details

Allele Name:
sa44869
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000115064 Essential Splice Site 731 1351 12 27
Genomic Location (Zv9):
Chromosome 17 (position 14687849)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 14838677
GRCz11 17 14846610
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCGCATCCTTCGATATGCCATCACCAACAAGATCGGACCACTAGGAGG[T/C]AAGCTTCTAACTGCTCACCATTGAATTCTGTGATTTTAAAAGTGCTGAAT
Long Flanking Sequence:
TGATATCGTTTTATTTTGCTGATAACATTTTAATGAATGACTTAGTTGTATAAAAAAATAAAAGTGAGCTAAAACATAGCTCTTGTGACTCCTCCTGTCTCCTCTATTTTCTTTCAACTGTGTCTGCTCTCGATAAACCCTAAACAAAAGCAGTTTCTGATACCGCTGAACTTAAGATTCCTCAACTTATGGGATTTTGAGTCTTAAGCTGAAGCCCAGAGATTGTTGTGAATTGTTTTCTAAACTCTTGCCTGTTTTTTTCTGTTCTCAGTGATTACTTCCACATCGGTGCGTGAGTTCAAAGTCGTGTCAGCTGAAAACGGAGCAGAAACTTTCACTTTCCAAGTTAAGCAGAACATCACATACAGGGACTGCAGTCACAGGCCCCGCAGCAGACTGGAGACACTGGAGCTGAAGATGGAGCGCGTATTTGTTATGTACGTCAGAGAGGAGCGCATCCTTCGATATGCCATCACCAACAAGATCGGACCACTAGGAGG[T/C]AAGCTTCTAACTGCTCACCATTGAATTCTGTGATTTTAAAAGTGCTGAATGTTCCTACCAAGCCACAGTGAAACAAAAGTTGTGCCATTTTTGGGGGGTTTATTTATCTAAGAGTGTTAACATAGTTTAGGCCCTCATTGCAAAGCCAAAAGTGTATTTTTGTAGCAACAGGCAACCATAAAATGCCGGAGACTGAAGGCTGATTTATACTTCTGCGTCAAACGCCGGCGTATGATACGGCGCTGACGCATAGCACTTCGCTGTGGCCGTCGCCGTCACTGACGTGCACCTCTCAAAAAATGTAACTACACGTCGCAACGACGCGTAGCGTAAGCTCTGTGATTGGTCGGCTTGGAAGCGCTGACGAGTCTGGGCGGGACCGAGAGCCGCGCGAATGGCACGAACCCAATGTAGCGATTGTTTACAAGTGTGGAGTACCGTGAAGGAACTCCGGATGGAAAGTTTTGTTCTGTGTTTACCTCATAGTTAAAGTTGTTGCA
Associated Phenotype:
Not determined