ZMP
nfia
Ensembl ID:
ZFIN ID:
Description:
nuclear factor 1 A-type [Source:RefSeq peptide;Acc:NP_001073431]
Human Orthologue:
NFIA
Human Description:
nuclear factor I/A [Source:HGNC Symbol;Acc:7784]
Mouse Orthologue:
Nfia
Mouse Description:
nuclear factor I/A Gene [Source:MGI Symbol;Acc:MGI:108056]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16768 | Nonsense | Available for shipment | Available now |
| sa24138 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16768
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 |
|---|---|---|---|---|---|
| ENSDART00000063467 | Nonsense | 232 | 524 | 4 | 12 |
| ENSDART00000090237 | Nonsense | 232 | 481 | 4 | 11 |
| ENSDART00000090242 | Nonsense | 232 | 507 | 4 | 11 |
| ENSDART00000138233 | Nonsense | 232 | 507 | 4 | 11 |
| ENSDART00000138382 | None | 254 | 254 | None | 4 |
Genomic Location (Zv9):
Chromosome 22 (position 17121642)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 16873400 |
| GRCz11 | 22 | 16899670 |
KASP Assay ID:
2261-6671.1 (used for ordering genotyping assays)
KASP Sequence:
GTTTCGTCACATCAGGTGTCTTCACCGTCTCTGAGCTAGTGCGAGTCTCA[C/T]AGAGTAAGATCTCCACATCTTATAATGATTATTCTTCCTKTTGGGACATC
Long Flanking Sequence:
GAGGCCGCAGGATGTGTGGCAGGTCCTGGGTCAGCTGTAGTCAGCATTATGAACACAGTAATTGTGGTCTGTCTGCTGGAAAAGGCAACCGACTGCCTGCCGAACAAAGAATGCTTTTGACCGAGATTCCACCACGTATCATATGTAAACAGATAATAATTGTGAATTCTTGGGCTTAGCATACAGCTCCTCGTTGTGTGTGTGTGATGCACTGCACTGCGCCTCTGCCCCACTGTACTTCAGACACTCATGGGACCGAATCCAGATGTGCTCTACCCTCTGTGTCACTCAAAACACTCCCTATTCTCTTTCCCACTGGGACTATGTGTGCGTGTGAGTGTGTTGTTGACATAGAGGCTGTCTTTGCTCTGTATTCTGTCATGTTCATTCAGATAACAGTCTTTCTCCTCTTTCATTTTTGTCTCCTAGGGCACCTTGGCTTCCAGGACAGTTTCGTCACATCAGGTGTCTTCACCGTCTCTGAGCTAGTGCGAGTCTCA[C/T]AGAGTAAGATCTCCACATCTTATAATGATTATTCTTCCTTTTGGGACATCATTGAGCGTCTTTGACTCATCTGTTTATGAATGAATCAGTCTCTGAAAACAAGTCTTATTATCTTAGCAGTGTTGCCTTTCAAAGTGTGCCGTCTTTTAAGTAAAAACTCCTTAGGTCAGTTATAATTTGACTTGAACCATTAAAATCAATTTATTGAGCTTTCATAATCAACCTAAAATTAGGTTAGTTGAATTCAATAAAGATGTCGTGGAAGGGTCATAACCTTCAGCTTAGCTTTATTTGTGGCGGTGAGGTTTCCTAAGACCAGTTTCGCCCTATTACATGAAGGCCTTTAGCAGATTAAAACCACAATGTCCAAATCATGTTAGTTCAAGCGTCTCAAATTCCGCTCAAAGGTAGGATGAGGATAGTGATTAACCAGTGTGCAGGAGGAAAGCTTCTTTGGTTTCTCAGCTCGGTTTTTCAGAACAATGGGTTGAATCCACTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24138
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 |
|---|---|---|---|---|---|
| ENSDART00000063467 | Nonsense | 367 | 524 | 8 | 12 |
| ENSDART00000090237 | None | None | 481 | None | 11 |
| ENSDART00000090242 | Nonsense | 350 | 507 | 7 | 11 |
| ENSDART00000138233 | Nonsense | 350 | 507 | 7 | 11 |
| ENSDART00000138382 | None | None | 254 | None | 4 |
Genomic Location (Zv9):
Chromosome 22 (position 17096610)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 16848368 |
| GRCz11 | 22 | 16874638 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTGCCTTCGCAGACCGCTTCCCCCCGAACGGCATTCACACACCATCAT[C/T]GACCTGTCATTACAGGACCCAGAGGTGAGGTCCCAACACCCCACCCTCCT
Long Flanking Sequence:
AGCACACTCTCGAAAGACTGATTGGATTCGTAACATACAACTTAAGTGCTTTTTAAACGCACACTCCTACAGGGATGATAAACAATCCTTGTTTTTTATGGTGAGAAAAGTCACGAGGTCATGCTTAGCGCACATGTCTGTTGAAATGTTGACGTCAAGACTACTTATTCACGTGACCTTGCATTGTACTGGGACAGATCCACTATTCGAGCCCCCATGTAGTGTATCCTGTGCTACACCCTGCTGGGCCTCGCAGTCTCCCCTGCTGTCTTGACCCCCATCCACTCACCCAAACAAACCACCCCCACCCCTCCTATCCACTCTCTCTCCTTTGCGCCAGCCTGTATCTCCATGACCTTGCGTTATTAAATTGCACTTATCAATCATTCTTGCCAGGGATGCCATCGCCTACCACATTAAAGAAGTCAGAGAAGTCTGGTTTCAGCAGCCCTGTGCCTTCGCAGACCGCTTCCCCCCGAACGGCATTCACACACCATCAT[C/T]GACCTGTCATTACAGGACCCAGAGGTGAGGTCCCAACACCCCACCCTCCTCAAACTGCACCCCTCTTCTTCCCCAAAAAATCCCAGCCAGCAGGGCTCCTGCTGTTGTTCAGATCCCTGTTCCTTAAACCCTACAGTGGTCCCTTGTTAGATCAGACCAGAGGAACTTGGGCAAGTTTGATCCTGGAGAGGCACAGTCCTGCAGAGTTACACTTCAACACACCTGAACAAGCTAATTAAGGCCTAGGTGTTTCTAGAAAGTGTACAGTTTTCCAAGGGTTGTATCAAAAGTCTGCAGGACTTTGGTTCTAAAGGACCAAAATTGCCAATTCCAGATTTCAATGAACTCTTCCTATCAGGGTGTTCACACTGAGAGAGATTTGCTGTGTCAAAATATTAGGAAGTAATTCAGTTTTCAATGAAGGTTTGAGATCGAACCAATAGGAGCAGAGATCATCTTCATGCAAATAAGCAGCAACAATGGGACGTTTTCAAGGAATT
Associated Phenotype:
Not determined