ZMP
nkrf
Ensembl ID:
ZFIN ID:
Description:
Similar to NF-kappa-B-repressing factor (NFkB-repressing factor) (Transcription factor NRF) (ITBA4 p
Human Orthologues:
CDKN2AIPNL, NKRF
Human Descriptions:
CDKN2A interacting protein N-terminal like [Source:HGNC Symbol;Acc:30545]
NFKB repressing factor [Source:HGNC Symbol;Acc:19374]
NFKB repressing factor [Source:HGNC Symbol;Acc:19374]
Mouse Orthologues:
Cdkn2aipnl, Nkrf
Mouse Descriptions:
CDKN2A interacting protein N-terminal like Gene [Source:MGI Symbol;Acc:MGI:1261797]
NF-kappaB repressing factor Gene [Source:MGI Symbol;Acc:MGI:1924536]
NF-kappaB repressing factor Gene [Source:MGI Symbol;Acc:MGI:1924536]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16160 | Nonsense | Available for shipment | Available now |
| sa16364 | Nonsense | Available for shipment | Available now |
| sa31995 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16160
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 |
|---|---|---|---|---|---|
| ENSDART00000077336 | Nonsense | 396 | 858 | 3 | 3 |
| ENSDART00000077336 | Nonsense | 396 | 858 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 14 (position 33713835)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 32516845 |
| GRCz11 | 14 | 32857159 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGCTGACCTTCCTAAAAACAGAAAGGTACCATGTGATGGATATGCGTGT[G/T]AACTGAGGTGTCAGAGTGTATACCTTGCTACAGGTTACTCTGGGAGTAAA
Long Flanking Sequence:
CCTCAAACTTCATGGGCAAAGTGCAGCAGGAGTACACCGCTAAATATGAGGCCCATAATTCCAGGCAGTCTGATTCAGTCTTACACGCAGGCAGATCTGATGGAAGTGGACGGTCTGGAACCTACGAGAGTGGACGGCGTGGATTGGGATTTGGACATCAAGAAAGGCCAACCTCCAGCAAGGCATTCAGCAGGGCATACGACGGACCAAGCAGAGGAGGTACAGGCCTTCTCCCTACACCCTCACTGCCAGCTTCTGTCCCCACAGCCGCAGTTGAAGAAAAACAGAGGCTGATAGTCAGAGTAGCATCAGCCGTTGCCGTCACCCTCAGAGATCCGGCATTTGTGGGTGGACCTGAAGGTCCAAACTACAATTTCATACTTAGCCGCAGCATTCAGGCCTGCAAGACGAACCCAGAGTACATCTATGTCAATTTAAGAGATATCCCACCTGCTGACCTTCCTAAAAACAGAAAGGTACCATGTGATGGATATGCGTGT[G/T]AACTGAGGTGTCAGAGTGTATACCTTGCTACAGGTTACTCTGGGAGTAAAAACGGTGCCAGAGACCGAGCTTCAGAACAGGCAATCAAGCTGTTCATGAGGCCGGTGGAAATTCGTATCTTGCGGCGAGTCTACAAGCGCAGATATGTTAATGACATGGTGGTGTGCCAGGTTAACACTCCAAACCCATCCCTCCCACCACCTCTACGCAACCCTGAGGACAGTCCACCCCCAAGTACTAAGGGCCAATATGTGCCTGACCGAAGCAAACACTGGACAGAATTCGTAATCATGGAGAACGCACATGATGCCATCTGTATTTTAAACAACTCTGCAGCTTTCAACCGCATGAAAGTTGATTACACTTTTGACCCGGTTCCCAACAGCAATTTATGGCTCTGTAATGTGTACTTGCAGGGCGAACTGGTGGCACAAGCCAGAGGGACCAAGAAAAGTGCAAAACACTCAGCGGCAGAGGAGGCAGTGAAGAAGTTGCGAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16364
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 |
|---|---|---|---|---|---|
| ENSDART00000077336 | Nonsense | 396 | 858 | 3 | 3 |
| ENSDART00000077336 | Nonsense | 396 | 858 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 14 (position 33713835)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 32516845 |
| GRCz11 | 14 | 32857159 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGCTGACCTTCCTAAAAACAGAAAGGTACCATGTGATGGATATGCGTGT[G/T]AACTGAGGTGTCAGAGTGTATACCTTGCTACAGGTTACTCTGGGAGTAAA
Long Flanking Sequence:
CCTCAAACTTCATGGGCAAAGTGCAGCAGGAGTACACCGCTAAATATGAGGCCCATAATTCCAGGCAGTCTGATTCAGTCTTACACGCAGGCAGATCTGATGGAAGTGGACGGTCTGGAACCTACGAGAGTGGACGGCGTGGATTGGGATTTGGACATCAAGAAAGGCCAACCTCCAGCAAGGCATTCAGCAGGGCATACGACGGACCAAGCAGAGGAGGTACAGGCCTTCTCCCTACACCCTCACTGCCAGCTTCTGTCCCCACAGCCGCAGTTGAAGAAAAACAGAGGCTGATAGTCAGAGTAGCATCAGCCGTTGCCGTCACCCTCAGAGATCCGGCATTTGTGGGTGGACCTGAAGGTCCAAACTACAATTTCATACTTAGCCGCAGCATTCAGGCCTGCAAGACGAACCCAGAGTACATCTATGTCAATTTAAGAGATATCCCACCTGCTGACCTTCCTAAAAACAGAAAGGTACCATGTGATGGATATGCGTGT[G/T]AACTGAGGTGTCAGAGTGTATACCTTGCTACAGGTTACTCTGGGAGTAAAAACGGTGCCAGAGACCGAGCTTCAGAACAGGCAATCAAGCTGTTCATGAGGCCGGTGGAAATTCGTATCTTGCGGCGAGTCTACAAGCGCAGATATGTTAATGACATGGTGGTGTGCCAGGTTAACACTCCAAACCCATCCCTCCCACCACCTCTACGCAACCCTGAGGACAGTCCACCCCCAAGTACTAAGGGCCAATATGTGCCTGACCGAAGCAAACACTGGACAGAATTCGTAATCATGGAGAACGCACATGATGCCATCTGTATTTTAAACAACTCTGCAGCTTTCAACCGCATGAAAGTTGATTACACTTTTGACCCGGTTCCCAACAGCAATTTATGGCTCTGTAATGTGTACTTGCAGGGCGAACTGGTGGCACAAGCCAGAGGGACCAAGAAAAGTGCAAAACACTCAGCGGCAGAGGAGGCAGTGAAGAAGTTGCGAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31995
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 |
|---|---|---|---|---|---|
| ENSDART00000077336 | Nonsense | 569 | 858 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 14 (position 33714354)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGCAGAGGAGGCAGTGAAGAAGTTGCGAATGAACCAAGCTGCTCGCCAA[C/T]AAGAGCAGCAGCAGCAGCAGCAACAACAACAACAACAATTTTCTGGAGGA
Long Flanking Sequence:
TATACCTTGCTACAGGTTACTCTGGGAGTAAAAACGGTGCCAGAGACCGAGCTTCAGAACAGGCAATCAAGCTGTTCATGAGGCCGGTGGAAATTCGTATCTTGCGGCGAGTCTACAAGCGCAGATATGTTAATGACATGGTGGTGTGCCAGGTTAACACTCCAAACCCATCCCTCCCACCACCTCTACGCAACCCTGAGGACAGTCCACCCCCAAGTACTAAGGGCCAATATGTGCCTGACCGAAGCAAACACTGGACAGAATTCGTAATCATGGAGAACGCACATGATGCCATCTGTATTTTAAACAACTCTGCAGCTTTCAACCGCATGAAAGTTGATTACACTTTTGACCCGGTTCCCAACAGCAATTTATGGCTCTGTAATGTGTACTTGCAGGGCGAACTGGTGGCACAAGCCAGAGGGACCAAGAAAAGTGCAAAACACTCAGCGGCAGAGGAGGCAGTGAAGAAGTTGCGAATGAACCAAGCTGCTCGCCAA[C/T]AAGAGCAGCAGCAGCAGCAGCAACAACAACAACAACAATTTTCTGGAGGAAACTATTTTTCAGAGGAATCCGCTGGTTGCTACTCTCAGCAAAGCAGCAGTGTGGCACAGCTCGGTGAATTGGTCATCCTTGAAAATTCAGATAATGCTATATGCATAATAAACGACACTGCTCAATTTAATAAGGTGTCGGCAGAATACAAATTCACAGTTCTGGCGGACCACAGCTGGCGATGTGAAGTTTACCTGGATGGTCAGTATGTGGCAACAGGGCTTGGTCCCAAAAAAACAGTCAAGCACATCGCGGCCGAGGAGGCGCTTGCCATGCTTCGGCGTACACAGGCTGTGGTGAAGTCCAATCTTAGGAAGGAGGGCCACGCCGATGCAATTTCCAGAGATCAAATCATGTGTCGTTCTGGTGAGGAAGCCGTTCGGCAGGAGATTAAAGAGGACAACATTGGGAACCAGCTACTCCGTAAGATGGGCTGGACAGGTGGAGGC
Associated Phenotype:
Not determined