Busch Lab

ZMP

NID1 (2 of 2)

Ensembl ID:
ENSDARG00000060675
Description:
nidogen 1 [Source:HGNC Symbol;Acc:7821]
Human Orthologue:
NID1
Human Description:
nidogen 1 [Source:HGNC Symbol;Acc:7821]
Mouse Orthologue:
Nid1
Mouse Description:
nidogen 1 Gene [Source:MGI Symbol;Acc:MGI:97342]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa13713 Essential Splice Site Available for shipment Available now
sa38863 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa13713
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085724 Essential Splice Site 1069 1242 16 21
Genomic Location (Zv9):
Chromosome 11 (position 45443935)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 44335927
GRCz11 11 44597959
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAATGACCTCATAAACCCGCGGCCAATCATCGCAGAGCCTGTAWATGGG[T/G]ACGAATGCATGACACRGCTAAAACAYGCTWAAGTAGAGCAGCGCGARYGT
Long Flanking Sequence:
CAGAAATTCATCAGTTTTAAGTCATTATGATTGTATTTCCTACAATGTGGGCATCAAATATCCCCACAAGTATAGTAATACCAGTACATTTTGACCTTGTGGGAACAATTTCTTTGGTCTCCATCAGAACAACAGCTCTTTTTTAATTTTTTAAATGTAAAAATGCAGATTGTTTGCTGTGATGATTTATTTAGGGGGGGGGGGGGATACAGTACAGTACAGTACAGTAGAAACCTCATTACACCTGTAAAGAAAGATGTACAAGTGTGTGTGTGCTGATTACTGTCTGGACTCTAGTATTGACCTCTGCTGTGTGTTTTCCTGCAGATCTGGGCAGTCCTGAAGGAATCGCCATCGATCATCTGTCCAGAAACATGTACTGGACGGACTCAGTGCTGGACCGGATCGAGGTTTCCCGTCTGGATGGCAGTAACAGACGCGTTCTGTTCGACAATGACCTCATAAACCCGCGGCCAATCATCGCAGAGCCTGTATATGGG[T/G]ACGAATGCATGACACGGCTAAAACACGCTAAAGTAGAGCAGCGCGAACGTTTAAAATCAGAATCAGAATGAGCTCCAGAATGTGCAAACATACAGAGTACAAACACACACACATCAACACAAGAAGACATTGAAATAAGTGGAATAATGAAGTAAAAAATAAGATGTAGGAGCCGGGGCTTTCTGTTGCGAATCATTCCCTTAAAGGAATCTAATGGTTAGAGAGGATATCAAACAAATGTTATCATCGGATCAATCAAATCAGTGCATCTGAATTGGTTTTGAGCGCTATACTAAACACATGCAGACGAGTGACTCTAGTTTTCCCTGTCCTGCAGTCGTCTGTACTGGGCTGATTGGAACCGAGATGGGCCGAAGATCGAGAGCTCCAGCATGGATGGGACAGAGCGCACGGTTTTGGTGCAGGACGGCCTGAGCCTCCCCAACGGTCTGACCTACGACAGCCAGAGCCAACTGCTGTGCTGGGCCGACGCTGGTGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38863
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
ENSDART00000085724 Nonsense 1078 1242 17 21
Genomic Location (Zv9):
Chromosome 11 (position 45444298)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 44336290
GRCz11 11 44598322
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTCTAGTTTTCCCTGTCCTGCAGTCGTCTGTACTGGGCTGATTGGAAC[C/T]GAGATGGGCCGAAGATCGAGAGCTCCAGCATGGATGGGACAGAGCGCACG
Long Flanking Sequence:
TGTCCAGAAACATGTACTGGACGGACTCAGTGCTGGACCGGATCGAGGTTTCCCGTCTGGATGGCAGTAACAGACGCGTTCTGTTCGACAATGACCTCATAAACCCGCGGCCAATCATCGCAGAGCCTGTATATGGGTACGAATGCATGACACGGCTAAAACACGCTAAAGTAGAGCAGCGCGAACGTTTAAAATCAGAATCAGAATGAGCTCCAGAATGTGCAAACATACAGAGTACAAACACACACACATCAACACAAGAAGACATTGAAATAAGTGGAATAATGAAGTAAAAAATAAGATGTAGGAGCCGGGGCTTTCTGTTGCGAATCATTCCCTTAAAGGAATCTAATGGTTAGAGAGGATATCAAACAAATGTTATCATCGGATCAATCAAATCAGTGCATCTGAATTGGTTTTGAGCGCTATACTAAACACATGCAGACGAGTGACTCTAGTTTTCCCTGTCCTGCAGTCGTCTGTACTGGGCTGATTGGAAC[C/T]GAGATGGGCCGAAGATCGAGAGCTCCAGCATGGATGGGACAGAGCGCACGGTTTTGGTGCAGGACGGCCTGAGCCTCCCCAACGGTCTGACCTACGACAGCCAGAGCCAACTGCTGTGCTGGGCCGACGCTGGTGTGTGCCGTTCTGAAAATATATAATTAAATATATATAATAAAATAATTCATAAATATAATAAATCATATATAATAAAATAATTACTCATTTTTGTCATTTAAATATTTGTTAGTTATTTTCATATATTATAATTTTTTACATTTAAATGTTATTTATTTAGATCACTATTTTGTGTTAATTCTTGATATTTTGATTATATATTTTTTTATAATTTATTTTTATTTTTTTGTAATTATTTTACTGTTTTTTATTTTATAGTTTTTTGATAGATTTGTTTAGTTTTTCTTTGTTTTTTCTTTATTTAATTATTATATTATTTATTTAATTATTTTATTTAATTATTTATTTTATAGTTTTTAATTTAT
Associated Phenotype:
Not determined