ZMP
NWD1
Ensembl ID:
Description:
NACHT and WD repeat domain containing 1 [Source:HGNC Symbol;Acc:27619]
Human Orthologue:
NWD1
Human Description:
NACHT and WD repeat domain containing 1 [Source:HGNC Symbol;Acc:27619]
Mouse Orthologue:
Nwd1
Mouse Description:
NACHT and WD repeat domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:2442268]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13940 | Nonsense | Available for shipment | Available now |
sa13770 | Nonsense | Available for shipment | Available now |
sa739 | Essential Splice Site | Available for shipment | Available now |
sa35019 | Essential Splice Site | Available for shipment | Available now |
sa4405 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa13940
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111559 | Nonsense | 236 | 1312 | 1 | 15 |
Genomic Location (Zv9):
Chromosome 11 (position 7311965)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 7213387 |
GRCz11 | 11 | 7223226 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAACAAGGAGACACTCTTCTACTCATTCTAGACTCATTGGAGCAGYTTT[T/A]AGARACAAACAAACTTCATAAACTAGACTGGATACCTAAAATAATTCCAC
Long Flanking Sequence:
CAGCAGAAATGCTCTGCAAACCTCAGGAACTTCAGTAGATCCAGTATGGTCCTGGCTAAAACAGGAGATCTTTCATCATGCCAAGTTGAGTGAGGAGAAGTGTGCTGTGTTTAAAGGGAGAGACGACATTCTGGGAAAGATCTCCATCACCCTGTGGGAATCCAATGATGTTTCTCATGGACCTCTTCTAGTCCATGGACCTCCAGGAGTTGGTAAAACAGCTCTGCTTTGCAAACTGGCCAAGGAAATGCGAGCAGTTGTTGACAATCGGGGAGTTGTTCTGCTGAGGTTGCTGGGAACATCTCTGCTCAGTTCAGATGTCGATTCTGTTCTTCGAGGTGTTTGTCTTCAAGTGTGTGGAGCTCTAGGGTTGCAGTCCCCATACTCGCATATAGCGTACACGCATGAAGGGCTAGTTCGATTTTTCCATTCCATGCTGGAAGACGTGTCAAAACAAGGAGACACTCTTCTACTCATTCTAGACTCATTGGAGCAGCTTT[T/A]AGAGACAAACAAACTTCATAAACTAGACTGGATACCTAAAATAATTCCACCCAATGTGCAAATCGTATTCTCAACTTCTAATGAGTGCTTGGACAAATGTAAATCTTTGGTTTCAGCGGAAGAAAACATCTTTAAATTGGAACTTCTCACGAAAGATCAAGGGAGAGACGTCATTGATGCATATATGAGTGCAGCTGAACGCAAGCTGACGGCAGAACAGCAAGACGCAATCTTACGCTACTTTGAGCAAAGTGGAAACCCTTTGCATCTGAAACTCATGCTAGACACTGCCAAACTGTGGTCCTCCTACACCCCCATGTCTAGTGTTCACCTGGACAAGTCGGCGGAGGAAGTGATGACACAGTTTGTCGAGTCACTTGAGGTGAATCATGGGAAGAAGCTAGTCAGTCATGCTCTGAGCTTCATCCTGTTATCAAGGTCAGTCATGTTATTTTAATCATTCACTTTCTGGGCCAAGGGCAACATGGTCGCTTAGTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13770
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111559 | Nonsense | 383 | 1312 | 2 | 15 |
Genomic Location (Zv9):
Chromosome 11 (position 7310998)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 7214354 |
GRCz11 | 11 | 7224193 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAATGAATCTTTAAATGTAATCGTTTACTTTTCACATTTGAAACAGATA[T/A]GGACTTTCAGAGGCAGAGTTACAGGATGKCCTAKCATTAGATAATGATGW
Long Flanking Sequence:
TTCTGGGCCAAGGGCAACATGGTCGCTTAGTGGATTGCACTGTCGCCTCACAGCAAGAAGATAGCGATTGGTAGATTAGTTGGCACCTCCGGGTGCTCCAATTTCCCCCACAGTCCAAAGACATGCACTATTAGTGAATTGAATAAACTAAATTGGCTATAGTGAATGAGTGTGTATGGAGGTTGCCCAGTTCTGGGTTTCATCTGGAAGGGCATTCAATGTGTAAAACATATGCTGGATAAGTTGGCAGAATTCCACTGTGGCAACCCCTGATGAATAAAATGAATGAATGTCTGGGCCAGTAGCCTAGTGGTTAGTGTGCTGACATATAGAGCCAATGCACTTCATGCATCCCAAGTTTGAATCCCAGGGTGTGGACCTTTCCCAATCCTGTCCACTTCTCTCTCTCACTTCACTTGCTACTAGCTACTGTCCTGTTAATAATGGCAAAAAATGAATCTTTAAATGTAATCGTTTACTTTTCACATTTGAAACAGATA[T/A]GGACTTTCAGAGGCAGAGTTACAGGATGTCCTATCATTAGATAATGATGTTCTAGCTGAGATCTATAAATGCTGGCTTCCTCCGAGCCATACGCTCATGCGCTTCCCACGTTTTCATTGGTCAAGACTCAGGCATGACCTGAGTGCTCATCTGACGGAGAGATGGGAAGCCGGCGTTCTTCTGCTGGGTTTCACTCACAGGTAAAGTTTGCCTCAACCTTTCTGTTTGCCAGAAGAAACATTTTCTTGACCATGAATGCTGAAAATTAAGACAGAAACATTCTTAAAACATACCTCTATATACATTTCTGTAGAGCGCCAAATACCAAGGAGCTAGATCTAAGGAGCTACATTTTTTTGCAGATTTCCACCAGAAGCCGCTGTGTATGCTTTTTGAGATCTCAAATTTCTCTCACTAGTGCTATTCGCGCCTGCTGTTACAATGTAAATCCCACAGAGGCCGCTGTTGACTGACTGTTTGAATGACTGAATATCTGACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa739
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:
C > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111559 | Essential Splice Site | 807 | 1312 | 10 | 15 |
Genomic Location (Zv9):
Chromosome 11 (position 7298667)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 7226685 |
GRCz11 | 11 | 7236524 |
KASP Assay ID:
554-0646.1 (used for ordering genotyping assays)
KASP Sequence:
GACATATCCACCGGCACTCAGACTTCCCAGACCCTCCTGCCCTACTCTGC[C/T]GGACACCAYAACATCACCTGCTGTCTCACACTCACCAAACACTCCAAGAT
Long Flanking Sequence:
AGCAATAAATTGTGCCTTATTGCACCGGGTGTATGATAGGGCCCAATATGACAGTTGGTATAAACATGCAGAAAATCTCATTCACATTCATGACATGTCAAGTCACGATTATAAATGTTTAATATCACCTATTTAGGAAAAATGTTATCGATTTGGTAGCATACACAGCAAAAATAAATAAATAAAACTAATACTAGCCCACAACATTCTAGGTTTTACAGTACTTTTGATCAAATAAATACAGGCAGACTTTTCACTATGATAACATCCCGAATGTTGTCAATTTATATGTTCGGATTTCCTTCTCCATCCTTTCATGTGTAGGTTAAAGCTTGGGATTTGGACACTGCAGAGCCTCTGTTTGAGCTGACCGCAGTGATTGGTTCTGTTCTTGGCATTGTGGAAGATGAAATAGCGTGCATATGCAGTGAGGCGATACTCTGCTTTTATGACATATCCACCGGCACTCAGACTTCCCAGACCCTCCTGCCCTACTCTGC[C/T]GGACACCATAACATCACCTGCTGTCTCACACTCACCAAACACTCCAAGATACTCATTGCTTTTGGGGAAAGCCGTCTACATTCGGTTTGTACGCTACCTTTTTTCAGAAAAGTCCAGGCAAAATGTATTATTTCAGTGTTATTCAAAGGATTTGTGTTTGTGTGTGTGCAGGTGTGGAGCCATGAAATGGAGTCTGTGATTGATCTTCCATCTCCAGCTCTCTTTCTCAGAACATCTGAGGATGAAAAACTGCTGCTTGCAGGTGCATTTTCATCTCATTGTCTGGATATAGTTTTTTCTCATTTCATTGATCATTTCTCTCATTTATTAATTATCCTTTATGCGTGCTCTAATAACACCACAATTTTGATCTCTCATTCTTACAATAATCATCTATTACTGTTTGTTACTGGTTGAGCCAGCATTGATTAGATGGTAGGCGAGGCAGTGGCGCAGTAGGTAGTGCTCAGTTGGCGTTTCTGTGTGGAGTTTGCATGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35019
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111559 | Essential Splice Site | 944 | 1312 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 11 (position 7296413)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 7228939 |
GRCz11 | 11 | 7238778 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGCGAAGGTAGCGAAATCATCACGAGTGCCCAGGATCGTATAATACGG[G/T]TCAGTTTAATCCCCTTCTTCCCAGAAAGGTACAGTGTCCTCTCATTTTAT
Long Flanking Sequence:
TTTTTTCTGCTTGGCAAGTTAAGCTGACATGACATGGGAGCGTGACAGCATCGACGATTCCATTTTTTTGATTCGATAATCGAAATTGAGCATGAACTTTGATCGATTTCGATTTTAAATCGAAATCGTGACACCCTTACTGTCTATGGTATGATAAGAGAGCTCTCAGATATCATCTAAAATATCCCTATTTGTGTTCTGAGTATGACCGGTAAGGTTTAGATAAGGTTTTAGGGGATTCGAACAATGTCGCAGAATTTTTTCATCTTGAGTGAACTAACCCTTTAAATAAAACATTGCCTTTAATTTGTACACTTCACTGATGTACCTGTATTTTTTTTTACATTGAAGGATGTGACAGAACATTGTGCGTGTTCCTCGTGACATTGACTTCAATGCACAAGGTTCTGGATCTTCAACATGATGCATCTATCCTGTGCGCCGTGTCAAACAGCGAAGGTAGCGAAATCATCACGAGTGCCCAGGATCGTATAATACGG[G/T]TCAGTTTAATCCCCTTCTTCCCAGAAAGGTACAGTGTCCTCTCATTTTATGGAATGGAACTTGACCTTGTTGTACTGTTGAAGGTATGGAGCGTAACCACAGGAGCCCTGCTGGACTGGATCGGTGTGATGGATTCCTCTGTGTCCTCATTGGCTGTACATCAGCGCTTTATTATTTCCGCCTCTGTTATTGTCAACCAGCTTAAAGTATGGCAGCTTGACCACAACACCACGCACAGGAACAAGAGTTTCATCCCCGCATACTGCCCCTTGGCAGTCCTGTCGAAAGATGGTGATACTGTATTCTATGTCAAGGAGGGAAATAAAACCGAGGTTTTCACCTGGAGCTGTTCGGAAGGTGAAACATGTAATAAAAGGATATTATTTTCCTTTTTAGTATTCATCAGGGTTCCCACAGGTTATGGAATGACATGATATTTTAAAAGTTCTATTCCAGACATTGAAAGTAGGGGAATTTTATATTTGTTTGTCCAATTCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa4405
Status:
F2 line generated
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111559 | Nonsense | 1031 | 1312 | 12 | 15 |
Genomic Location (Zv9):
Chromosome 11 (position 7296069)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 7229283 |
GRCz11 | 11 | 7239122 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATACTGTATTCTATGTCAAGGAGGGAAATAAAACCGAGGTTTTCACCTG[G/A]AGCTGTTCGGAAGGTGAAACATGTAATAAAAGGATATTATTTTCCTTTTT
Long Flanking Sequence:
ATTGAAGGATGTGACAGAACATTGTGCGTGTTCCTCGTGACATTGACTTCAATGCACAAGGTTCTGGATCTTCAACATGATGCATCTATCCTGTGCGCCGTGTCAAACAGCGAAGGTAGCGAAATCATCACGAGTGCCCAGGATCGTATAATACGGGTCAGTTTAATCCCCTTCTTCCCAGAAAGGTACAGTGTCCTCTCATTTTATGGAATGGAACTTGACCTTGTTGTACTGTTGAAGGTATGGAGCGTAACCACAGGAGCCCTGCTGGACTGGATCGGTGTGATGGATTCCTCTGTGTCCTCATTGGCTGTACATCAGCGCTTTATTATTTCCGCCTCTGTTATTGTCAACCAGCTTAAAGTATGGCAGCTTGACCACAACACCACGCACAGGAACAAGAGTTTCATCCCCGCATACTGCCCCTTGGCAGTCCTGTCGAAAGATGGTGATACTGTATTCTATGTCAAGGAGGGAAATAAAACCGAGGTTTTCACCTG[G/A]AGCTGTTCGGAAGGTGAAACATGTAATAAAAGGATATTATTTTCCTTTTTAGTATTCATCAGGGTTCCCACAGGTTATGGAATGACATGATATTTTAAAAGTTCTATTCCAGACATTGAAAGTAGGGGAATTTTATATTTGTTTGTCCAATTCATGGAGCTTTTGTTTGTTGTTTTCAATTTTAGTTTGCATTTATCAAATATTTTGTATCGCTGTTCTTATGGTTAGACTATTCATTTGATGTCTATCAACTGGTAGTCATTCATTCATTTCGGCTTAGTCCATTTATTAATCAAGGGTCGCCTCAGTGGAATGAACCGCCAACTTATCCAGCATGTTTTTTTGCAGTGGATGCCCATCCAGCCGCAACCCAACAATCTGAAACACCCATACACTTTGGTGGGGACGGGTGAATAAAATAAATTGGCCAATGTCAAGAGCAAACTTACACCCTTGCTTCAAATGGTGTTTAAAAAGCAGACGACAGAAAAACTAAATGT
Associated Phenotype:
Not determined