ZMP
rfx3
Ensembl ID:
ZFIN ID:
Description:
Transcription factor RFX3 [Source:UniProtKB/Swiss-Prot;Acc:A0JMF8]
Human Orthologue:
RFX3
Human Description:
regulatory factor X, 3 (influences HLA class II expression) [Source:HGNC Symbol;Acc:9984]
Mouse Orthologue:
Rfx3
Mouse Description:
regulatory factor X, 3 (influences HLA class II expression) Gene [Source:MGI Symbol;Acc:MGI:106582]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31758 | Nonsense | Available for shipment | Available now |
sa16866 | Nonsense | Available for shipment | Available now |
sa17373 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31758
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 |
---|---|---|---|---|---|
ENSDART00000041236 | Nonsense | 40 | 765 | 2 | 17 |
ENSDART00000144234 | Nonsense | 40 | 382 | 1 | 8 |
ENSDART00000144882 | Nonsense | 40 | 542 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 10 (position 612590)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 609363 |
GRCz11 | 10 | 625318 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAGCCTGCGGTCAGTGGCCAGCAGGTGGCGTCTCAGGTGCCCGTCCAG[C/T]AGCAGGTGAGCCTCTGCACACATCTCTCTCTCTCTCTCTGTGTGCTGTGA
Long Flanking Sequence:
ATATATATATATATATATATATATATATATATAAATATATATTTGTGTGTGTGTGTGTGTGTGTGTATATACACTTCCTACTTTCTTTATTGATCCGCAATGACTTCTGAGACATCTAGAGCGAGTGCTGTGCTCAAATCTGCATCATTGATATCAGGTATGCATCAGGGTTCTGTCGCGGGTCCTCTGTTCTTGTGCTCTTGATTATTGGAACTGAACTTTGGTGCTTGATGATGACGTTACATCAATACACAAGACTGCAGCATCGCTTATTAACGCACACGGAGAAATGAAAATTCTGATACTGATATCTAAAAACACTAGTTTAACATCATGCGAGCGTTAATCTGAGACTGATGTTGATTTTGTGTTTTGAAGGCGCCATGCAGACCCCAGAGGCAGGCGCTGACTCCACCGTGTCCACCGTGCCCCTCCAGACCAGCGTGCCTGTGCAGCCTGCGGTCAGTGGCCAGCAGGTGGCGTCTCAGGTGCCCGTCCAG[C/T]AGCAGGTGAGCCTCTGCACACATCTCTCTCTCTCTCTCTGTGTGCTGTGATTGGCTGAGCTTCCTACACATCTCTCTCATGATGACAACTACAACAAACTATTCTTTTATTCTGTATAGCTTCTGCCGGTATCAAATGTTCTTGTGATTAACTGCTGAAGCTTTTATCATGATATACAGTATTTTTATGACATTGACTTCATTTACAGGTATAATAAATGTGTAAATAAACGTTTGCTGCATCCCAATTTGCATTCTTATACATCGTTCTAAAGGTATGCACTTTTTAGTGAAGGAAAATGTACTTACTTTTGAGTGTGTAACAGATGAGTGTGCAAACTTTGGTACATACTGCTTCCTCATTAACAGATCTTTATGTTGCTTAGTTACGAGACCTGTCAATCATCCCGACTCATCCATATTTCTTTCATAATTAATTTCCTACCATATTGGAGATGCAGCTGTGTGTTAATCTGCCATTCACGAGTCTTTCATGCAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16866
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 |
---|---|---|---|---|---|
ENSDART00000041236 | Nonsense | 139 | 765 | 4 | 17 |
ENSDART00000144234 | Nonsense | 139 | 382 | 3 | 8 |
ENSDART00000144882 | Nonsense | 139 | 542 | 4 | 13 |
ENSDART00000041236 | Nonsense | 139 | 765 | 4 | 17 |
ENSDART00000144234 | Nonsense | 139 | 382 | 3 | 8 |
ENSDART00000144882 | Nonsense | 139 | 542 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 10 (position 605029)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 601802 |
GRCz11 | 10 | 617757 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGCTATGGGGCTCACCGGAGGYCAGAKCATCAGCAGCTCAGGAGCTTA[T/A]CTGATTRGAGGAAACTCCATGGATGGCTCCGCCCCTCACGGCGCCGCACA
Long Flanking Sequence:
AAGTATGGCAAGGACGCGTCTCCCTCCCGGTCTTCAAATAAGTCGCGCACCCTTGCCATCGATGCCATCGTCCATAGCGATGTTTCACATTAGACATCGTACGATGCCAAATTGATTCCGGGGGATTATCACTCGTTTGCGGGCATTATGAGTCCCGCAAGTGGATAGAGACTCCCGGAACTTCCGGGACACTTGGTGTCTGAATATCACGTTTAACATCTATAGTGAGACGCGATCCAGCAGTACAGTGATCTATTCTCTAGGATAAATAAAGTAACCTAAGCTTGTGCTGTGTTCAGACGGGCGTACTCGTACTCGGAGCCACAGCTCTACAACCAGAACAGCAGCGGGAACTACTTCGACACGCAGGGCGGCGGAGGCAGCGCGGCACAGGTCAGCACCGTAGTGTCCACTCACAGCATGGCCAACAACGGCAACGGCACCGGCGCTCTGGCTATGGGGCTCACCGGAGGCCAGATCATCAGCAGCTCAGGAGCTTA[T/A]CTGATTGGAGGAAACTCCATGGATGGCTCCGCCCCTCACGGCGCCGCACAGACCACCAGAGCCTCCCCTGCTACGGTAAGCACCAATCACAGAACGGTTTCAGTTGTGTTGCTCTTTTTAAATGCGCAGTTTGAACAAGTCATGTTGGAGTGTAGTTCAGCTACTCCATTTCAAGTTAACAGATCTGTACTCTCTAAATAAAGGCGAGAGGTTCTTTAAAAGCTCTCACTTTAACGGAAGCTAGATATAAACATCTTAAAGCTGAATTAGTCTGGATTGTTTCCAATACTGAATGATCTAGAATCTTTGCATGCATACATACTCATTCAGACAGCTCCTCCTTCAAAATCTGAGCAGAAGCAGGAGAAATAATGAATAAGAGTCTTTATGTCAGAGACACATATGTTGTCTTGCTGTGTTCCCTATGCAGACAACTCATTAGGGTTCGGAACGGAGCCAATGTGTACGTCTGTGGCTAGAACAGATTGATTTGAACGTCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17373
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 |
---|---|---|---|---|---|
ENSDART00000041236 | Nonsense | 139 | 765 | 4 | 17 |
ENSDART00000144234 | Nonsense | 139 | 382 | 3 | 8 |
ENSDART00000144882 | Nonsense | 139 | 542 | 4 | 13 |
ENSDART00000041236 | Nonsense | 139 | 765 | 4 | 17 |
ENSDART00000144234 | Nonsense | 139 | 382 | 3 | 8 |
ENSDART00000144882 | Nonsense | 139 | 542 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 10 (position 605029)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 601802 |
GRCz11 | 10 | 617757 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGCTATGGGGCTCACCGGAGGYCAGAKCATCAGCAGCTCAGGAGCTTA[T/A]CTGATTRGAGGAAACTCCATGGATGGCTCCGCCCCTCACGGCGCCGCACA
Long Flanking Sequence:
AAGTATGGCAAGGACGCGTCTCCCTCCCGGTCTTCAAATAAGTCGCGCACCCTTGCCATCGATGCCATCGTCCATAGCGATGTTTCACATTAGACATCGTACGATGCCAAATTGATTCCGGGGGATTATCACTCGTTTGCGGGCATTATGAGTCCCGCAAGTGGATAGAGACTCCCGGAACTTCCGGGACACTTGGTGTCTGAATATCACGTTTAACATCTATAGTGAGACGCGATCCAGCAGTACAGTGATCTATTCTCTAGGATAAATAAAGTAACCTAAGCTTGTGCTGTGTTCAGACGGGCGTACTCGTACTCGGAGCCACAGCTCTACAACCAGAACAGCAGCGGGAACTACTTCGACACGCAGGGCGGCGGAGGCAGCGCGGCACAGGTCAGCACCGTAGTGTCCACTCACAGCATGGCCAACAACGGCAACGGCACCGGCGCTCTGGCTATGGGGCTCACCGGAGGCCAGATCATCAGCAGCTCAGGAGCTTA[T/A]CTGATTGGAGGAAACTCCATGGATGGCTCCGCCCCTCACGGCGCCGCACAGACCACCAGAGCCTCCCCTGCTACGGTAAGCACCAATCACAGAACGGTTTCAGTTGTGTTGCTCTTTTTAAATGCGCAGTTTGAACAAGTCATGTTGGAGTGTAGTTCAGCTACTCCATTTCAAGTTAACAGATCTGTACTCTCTAAATAAAGGCGAGAGGTTCTTTAAAAGCTCTCACTTTAACGGAAGCTAGATATAAACATCTTAAAGCTGAATTAGTCTGGATTGTTTCCAATACTGAATGATCTAGAATCTTTGCATGCATACATACTCATTCAGACAGCTCCTCCTTCAAAATCTGAGCAGAAGCAGGAGAAATAATGAATAAGAGTCTTTATGTCAGAGACACATATGTTGTCTTGCTGTGTTCCCTATGCAGACAACTCATTAGGGTTCGGAACGGAGCCAATGTGTACGTCTGTGGCTAGAACAGATTGATTTGAACGTCG
Associated Phenotype:
Not determined