ZMP
npnt
Ensembl ID:
ZFIN ID:
Description:
nephronectin [Source:RefSeq peptide;Acc:NP_001139052]
Human Orthologue:
NPNT
Human Description:
nephronectin [Source:HGNC Symbol;Acc:27405]
Mouse Orthologue:
Npnt
Mouse Description:
nephronectin Gene [Source:MGI Symbol;Acc:MGI:2148811]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15583 | Essential Splice Site | Available for shipment | Available now |
sa19582 | Nonsense | Available for shipment | Available now |
sa19583 | Nonsense | Available for shipment | Available now |
sa19584 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15583
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018469 | Essential Splice Site | 57 | 605 | 3 | 13 |
ENSDART00000134988 | None | None | 87 | None | 3 |
The following transcripts of ENSDARG00000018721 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 50633239)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 49482330 |
GRCz11 | 1 | 50126156 |
KASP Assay ID:
2259-1087.1 (used for ordering genotyping assays)
KASP Sequence:
CACATTTAGACGKAGCTTCCTTCTTTTTTTGTCTGGCYGTTTGTTTTGCA[G/A]CCCTCTACGTCTTAACCCGCAGAGTAATCGGGATAAGGTGTCARCCCCAA
Long Flanking Sequence:
AAAACAAAGCACAAAGGCAGAACATTTCATAGGTAATATTAAGTTTTTTACGTTTTTGTATGTTCTAAAATTTGTGCTAAACAGTAGTGTTATTGATGATAATACAGCCACTTACTGCATTCATCATAAGGCAAAGTAGATCCAATTTGCACTAAACACTCGGCTTATGCTAGTTTTGTTGAATAAAATCAGCAAACAATGCAAAAGAAATATGAAAATGAGACGCTGCAGTGCCAGAAACTTGTATTATTGTCGACTCAGTGAAGGAGTCATTCATAACGGAGATTACCCCCCCCTCAACCCCCCCCCCCCAAGCACATCTTGGTCAGCACATGAACTGTGAGAGACTTAAGCTTTGTTTTGTGTGTGTTTGTGTGTGTGTGTGCTGTATGTGTTGCATTTGTAAAGCTTGTCCATCATCAGCATGGCTCCCATGCAATGTTTTGATCTCACATTTAGACGGAGCTTCCTTCTTTTTTTGTCTGGCCGTTTGTTTTGCA[G/A]CCCTCTACGTCTTAACCCGCAGAGTAATCGGGATAAGGTGTCAGCCCCAAGGTTAGCACCAAATCATCTTTCCTCTGCACTCATCCTGGCTGAGCGTCATGCTTCCGCTCCAGTATTTATAGTCCATCACTCGCGCTTCTCCTCGGAGAATATCCTGATACCCTGTGAACACTTCACACCTGCTCCCGCTCTGAATATCTGAATATCTGGACGCTCCAGGATATTTGGATATCGCTGTTTATTTTCATGTTTGTTTGTTCCGCTGTGTCGAACTCAGAGACATCAGAGCTGATTTCAGTCTACTCAACACTTTTATTTAGATAAAAGAGAAAGAGTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19582
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018469 | Nonsense | 83 | 605 | 4 | 13 |
ENSDART00000134988 | Nonsense | 66 | 87 | 3 | 3 |
The following transcripts of ENSDARG00000018721 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 50639028)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 49488119 |
GRCz11 | 1 | 50131945 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACTGATGATCTTTTTGCCTACAGCGCTATGTCAGCACGGATGCAAGCAC[G/T]GAGAATGCGTGGGACCCAACAAATGCAAGTGCCATCCAGGTTATACAGGA
Long Flanking Sequence:
AATCCTCTTGTCGACATTGGGCGTGATGGGATTAAGCTTTTGTCTTTTGGAATTGCCTCTGTTTTGAAGATGTCTGAGTCGGAATTGACCTCATATCAACCCTCAGTTGCTTCTCCCAGACGAGGATCTTAAGGGGCCGCACGGCGCTGGGCTTCCTCCCAATCCAAATGTGAGATGTAATGAGTCATAAAGCAGAAGTGAGCCGGACCGTACTCTCTGCAGGTCCCAGGTTCATTAAAATGACCAAGGCAAACAATGAATTATTGATGTAGGGGGGCCGGCGTTCCAAAATAATGTTTTTGTGCACCTCTCACTACAGTATCCTCAAGGTCTAATTGCACTGACGATCATTTCCCACAGCAAGAGCAGTGGATTTTTTTCTTCTCAGGCTGTGTTTTGTTACATGTTTTCATGTGTGCTGTATAGACTCTGACATTTGGTGTAAAATGATACTGATGATCTTTTTGCCTACAGCGCTATGTCAGCACGGATGCAAGCAC[G/T]GAGAATGCGTGGGACCCAACAAATGCAAGTGCCATCCAGGTTATACAGGAAAAACATGCAACCAAGGTAAGAGCTGAAGTGTGTGTGTGAATCAGCCTGTCTTGTTTAAAGTGCGTCAATTGTGCTATGTAAAAGCTTGCTGAATTTGTTATGTACATCCAAAGTTTAAAAAACATATTGCAGCACCAGCTCTTTTCCCACAGTGTCTGAAATGGTTGATACAAGTATACGGTTTCTCTAAACCCCGCCTTTTCTAAAAACTCGATTGGTTAGATCAAGCAACACTATATAAACATGGTCACTTTTTTATAAGCGGGTCGCCACAGAGGAATTAACTGTTAACTATTCCAGTGTATGTTTTACGCAGAGCATATCTTTTTAGCCACAACCCAGTACTGGTAAACACCCATGCACTCTCAAAATCAAACACACACTCATACACTACCAATTTGGTATTTTAACAGACACATTTAGCTGCTAGATGTTAGTCAGATAATGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19583
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 |
---|---|---|---|---|---|
ENSDART00000018469 | Nonsense | 226 | 605 | 7 | 13 |
ENSDART00000134988 | None | None | 87 | None | 3 |
The following transcripts of ENSDARG00000018721 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 50678302)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 49527393 |
GRCz11 | 1 | 50171219 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTGCAAGTGCCATGACGGCTTTGACCTTCAGTACGTCAATGGGAAATA[T/A]CAGTGTACAGGTAAACATAGTGCACATTCATGGGATAGCAAGCTTTGATT
Long Flanking Sequence:
GTCAGATTTCCCAGGCTACGTTTAAATATGCAAATCAGACATTGTTGAATGAAATATGCACCATTTATCGTGAAAATCTCAACAGAGAAACATGTTCAAGTTTTTAATTGTTTAAAATTATACAGTGAATGGATTTATGCTACAAAGAGACTCCCCAAAACTGTGTTGTATAATTAATAATGTATACAATTGAAAATGATTAGCCCTCGTGTGAAATTTTAATGTTTTTAAAAAATATTTCCCAAATTCTGTTTAACAGAGAGAGTTAACACATTTTTCAAACACAGTAGTTTAAATATCTTATTTCTTTTGTTTTTGCCACATTTACAGTACATAATATTTGATCAGTACATAATCTTGTGTTTGTTTTTTGCAGATGTGGATGAATGTGCCGCAGGTCTTGCTGTTTGTCCCCGTTTCCGGAAGTGCATCAACACATTTGGGAGTTACATCTGCAAGTGCCATGACGGCTTTGACCTTCAGTACGTCAATGGGAAATA[T/A]CAGTGTACAGGTAAACATAGTGCACATTCATGGGATAGCAAGCTTTGATTTGAACACACTTCATATTTATTTATTCTCATAGTTTATTTTAGAGATAACAGCAGGTCTTAATTTGGGCCGGAACATGCCAGATCCGGATCTGGCACCTCATTTTACTGATCCCCCTTCTCAACCGCTCACCTCCCCCGTCCGTTGTTTACTTTTACTTTCTTGCACAACTCCCCAACCCTCTTCACTTTTGTCCGCGACACCCCTTTCCCATCTAACGCCCGCCATCCCCCCTGCTCTTCACTTTTGTCCGCGACAACCGTAACCAACCCCCCTCCCCCAGTCTCAACTTTTATGCGTGACACCTTTACATCCCCGGGTAACATGCCGGATCCACTACCCCGATCTGTTCACAATTCACAAATTAATCACTGGATGACAGATATAGATAACTACTTTTATAGATAACTGAGACTTTCTATAGATAAAAATATACAATTACACCAGCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19584
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018469 | Nonsense | 281 | 605 | 9 | 13 |
ENSDART00000134988 | None | None | 87 | None | 3 |
The following transcripts of ENSDARG00000018721 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 50685709)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 49534800 |
GRCz11 | 1 | 50178626 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCTCTTTGTTCTCTTTTAGCCATCCCAAAGGTGGTAATTGACCCTCCA[C/T]GACCTGGAAAGACCACACCGAGCAGCAATAACAACAAAGGCGGCAACAAA
Long Flanking Sequence:
GACTAGACAAGTTTTGGAATATTCCAAGACATCTATTAAATTTTGGGACAGCCCAAATTTAGCCTTGTTATAGCCAAGATGACTATACTTAGACATCTATTAGATATCTTTTGTATAAAAAATGTCATTCTGTGTGGTTTATGAGATGTTTTTCCTCATTTAGTCTCCACGATGTGATGAATACAAGGTACACACACAAACATATGAATCGTGTTGACAATGATCGCAAATAAAAAAAAATAAAACTGCTTAAATGAACAGTTCACACAGATACTGAAATTTTAAGTTTAAATTTACTGTTAAATAAGAGAGATTTAAAACTAAAACTAGGACCAGTTAAACCATCTTAGCACCAGTTAGACCAGGTTTAAACCATTACCTATTAAAGAAGAAAATAAACACAAGTTATGACTTGATTTTGTTTTCACATTACCTACAAATAAACAGGCAATCCTCTTTGTTCTCTTTTAGCCATCCCAAAGGTGGTAATTGACCCTCCA[C/T]GACCTGGAAAGACCACACCGAGCAGCAATAACAACAAAGGCGGCAACAAAATTCCAGGATCAGACCAAAAGAGGACCACCACAACAGTAAGACCTCCAGTAACGGCCAAACGCATCTCACCTACAATCACCACCACCACCACTACCACCAAACCTCCTCCAACCAAAAAAATCACCCCTCCAGCAAGAGTCCCGGTGACCACCACCCGTAAGCCATTCATCCCAACAAGGAAGCCCCCTGTGCTGGTGACAACCAAACCTAAGGTCCCGACTCACCAGCACACCACCACAAAAGTCCCAGTGGTTACAGCAGTGGTTCCTTTTATCCCAACACGCAGACCTTTCACCATCCCGTTTGTGACACCAATTGATAACAGCATCAAAGACATCACCCAGAAACAAAGAGGCGATGTTCACAGTAAGTAAATCTTCAATACTTTATAATTATTGTGAAATATTTGCCAATATTTTTGGAGTTCAAACGGGTCCATTGTTTATTGT
Associated Phenotype:
Not determined