ZMP
rfx2
Ensembl ID:
ZFIN ID:
Description:
DNA-binding protein RFX2 [Source:UniProtKB/Swiss-Prot;Acc:Q5EAP5]
Human Orthologue:
RFX2
Human Description:
regulatory factor X, 2 (influences HLA class II expression) [Source:HGNC Symbol;Acc:9983]
Mouse Orthologue:
Rfx2
Mouse Description:
regulatory factor X, 2 (influences HLA class II expression) Gene [Source:MGI Symbol;Acc:MGI:106583]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14019 | Nonsense | Available for shipment | Available now |
sa31644 | Nonsense | Available for shipment | Available now |
sa21260 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14019
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 |
---|---|---|---|---|---|
ENSDART00000029939 | Nonsense | 113 | 734 | 5 | 18 |
ENSDART00000122943 | Nonsense | 113 | 738 | 4 | 18 |
ENSDART00000132218 | Nonsense | 83 | 189 | 4 | 6 |
ENSDART00000133141 | Nonsense | 83 | 234 | 5 | 7 |
ENSDART00000147634 | Nonsense | 83 | 170 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 8 (position 20638559)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 20068456 |
GRCz11 | 8 | 20100541 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTTATAAYCCAGAGTCCCAGCTATATGGTCAGGGCAGTGGAAGTGCCTA[T/A]TTCGACTCTCAGGCGGGTGGTGCTCAGGTAACCACAGTCGTCTCTTCTGG
Long Flanking Sequence:
ATCCGCCATTTTGTCATGATCACATGACCTGTCTGCGTCAGTTGCATCACTTCACTCCCATTTCTGAGTTCTCTCGTAAGGCATCATAAGATAGCGTAGAATACATCATATGCACACTTTAGAATTTCACCGGAAGTAGTACGTCATCTGGGTACTTCTCGCATACTGTTTTTTGTATTCTATGATTTTGGACATACTATTCGGCTCGCATACTGTTTTTAGTGTAATGTATAGTATGAACATATGTGATTTCGGACACAGCCAAGGAAAAATGTGTAGAGCTGGTGATCCTCCAGGTACGTGGTTGAGAAACAAATTCACCTGTTTTAAGGTTGTTAAAAAGTTAAAGTCAATAGTTGATTATTTTGAAATGAGTTATTTTGAAAATCGAGACAATAGTTAAAACTAAACACGCCTGTATTTTTATCCTTCTTCAGTCGTGCTGCATACTCTTATAACCCAGAGTCCCAGCTATATGGTCAGGGCAGTGGAAGTGCCTA[T/A]TTCGACTCTCAGGCGGGTGGTGCTCAGGTAACCACAGTCGTCTCTTCTGGTGGAGTGCCCACTCATGGCATGGTGGGAATTGCTATGGATGTGGGTGGCAGTCAGATCATTTCCAGCGGCAGCGCCTACCTGATCCACGGCGGGATGGAAGGTGGCCGCCACCACACCTCTCACTCCTCACGCTCATCATCTGCAATGGTACGTTCCACTGTGCTTAAGTCCTGAACATGGGAGTAACATGGGAGGGGAGTTTGGGGAGCTGTGGTTTAGAAAATGAGCACAGCCTAATAATGCTATATTCCAGATGAGGTGTGACAGGAATGTACAGAGATATGTTTACATGGTCAAAAACAATGACTTATCCCTCAGTTTGCGAAATCTCCCCAAAAAGTTGCGCTTCCAGTTATCACACTAAATGTGTATGCATTGCATCATTATTGCCACTAATATTAAACATTATTGCAGAGTTGGTTTTCCCCTAAATGAAACTTTGTTTATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31644
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029939 | Nonsense | 403 | 734 | 11 | 18 |
ENSDART00000122943 | Nonsense | 403 | 738 | 10 | 18 |
ENSDART00000132218 | None | None | 189 | None | 6 |
ENSDART00000133141 | None | None | 234 | None | 7 |
ENSDART00000147634 | None | None | 170 | None | 5 |
Genomic Location (Zv9):
Chromosome 8 (position 20622040)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 20051937 |
GRCz11 | 8 | 20084022 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCTGGATGTTGTGATGAACCTGCAATTTCATCTCATAGAGAAGCTGTG[G/A]CAGACCTTTTGGCATTCAACAGCGCCCTCTAGTGACGGAGCCACTACCAT
Long Flanking Sequence:
AAAAAAACTTTTAATACAAAAATAATTTGAACATATTGTCCTGCAGTCTGTCACCTTAAACAGAACCTGAAATGAAGTTGAATTTATATATGTGGCTAGTGTTGTGCAACCATTTAGGCAGTTTCTATAAGAAGGTGGGTTGCTTTGAAGATGCTGCTTCAGAATGAGGAGCGAATGAGTTTTGATGGATGGCCGTATTATGAGTGGGCCAAATTCAAGATGAGCCATCAGGAAAGACAAAAGACACTTCAAATAATGGAGGAACACTCATCTCTCACACTCTATATTCATGAGATCTTCCTACAGCCCCCCAAAACACAGCTTTTGTTCCGGAATCATTTGTAATTTTGTTGTTATTGTGTTATCAGGAGAAACATTTTTCCTGTTTAAATGATTTTAATGCACACAAGAAACTTTGTTATAATAAACCTGATTTCTCTCCTTTAGGCTACTCTGGATGTTGTGATGAACCTGCAATTTCATCTCATAGAGAAGCTGTG[G/A]CAGACCTTTTGGCATTCAACAGCGCCCTCTAGTGACGGAGCCACTACCATACCTAACAGGTGCCATGTCTATACAGTTCATAGTTAAAGTAAAAAGGAACGCAACAATTAAAAAACAAAACTCACGCTCATGGAAAACCTGAAAGCATCTAGGATTTTTTTTAAATAATTTGGTGATCTTAGAAAATAATCAACATTTTAAAATATCATTTTTTTTGGTATGATCTGCTATTAAATATAAGCTACTGTAATGTTCCAAAGTTCAAGGTCATTGATATTGCCAATGTTGCATTTGTTATATTATAGTAATACATATATTATATTATAATATTTTATATTATATTATATTACATTATATTATATTACGTTATATTATATTATGTTATATTATGTTATATTATATTATATGTAAAGCTGTAAAAATATTATTACAACGTAAAATAAAAATTACCAAAAACAATCTAAAAACCAAAAACACTGTCAAAACACACCAGTGCTCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21260
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029939 | None | None | 734 | 18 | 18 |
ENSDART00000122943 | Nonsense | 727 | 738 | 18 | 18 |
ENSDART00000132218 | None | None | 189 | None | 6 |
ENSDART00000133141 | None | None | 234 | None | 7 |
ENSDART00000147634 | None | None | 170 | None | 5 |
Genomic Location (Zv9):
Chromosome 8 (position 20612354)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 20042251 |
GRCz11 | 8 | 20074336 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCGTGTGTCTCCTTTAGGTTTTCTGCGACTGTGAAGCAAGAATGTGCTG[G/A]TTTGGTGGCGTGTGGTTTATTTTTCATGTGCCATAGTCTTCTTTCAGTGC
Long Flanking Sequence:
GTCTTGGAAAATGTCTAGTCAAATATTATTTACTCTCATCATGACAAAGAAAAAATAAATCACTTATTAGATATAATATAACTATTATATTTAGAAATGTGTTGAAAAAATCTTCTATAAATATATATTAATGTTTTTCTGTTTATTTTCAGTTCAGTGACCTCAGTTCATTAATGCCATCCCTCAAGGAGCAAGGTAACCCATTCAAACCCCAGCCTAAAATATTGCATTGATTTTGAAGTCTCGTCTTCTCTTCTATTAAACCTCTCTCTCTGTTTTCCCGCATAGACACTTCATTCTCAGACGACATGACCAGCGATGGAGACATGTCGAGGATGAGCGAGAGAAGCCTGACTGAACCAGCGGTAAAGAGAGAAAGAATCGAGATCCCTCACTCCCTGCAGGAGATCTAACAGACACAAACGTCATCTCCGTCTTTAGAGTAGGGTCAGCGTGTGTCTCCTTTAGGTTTTCTGCGACTGTGAAGCAAGAATGTGCTG[G/A]TTTGGTGGCGTGTGGTTTATTTTTCATGTGCCATAGTCTTCTTTCAGTGCCTTAGATGAGAAAAGAAACACTAGAGCTTTCTCTTTGACCTTCTGTCGTTTTCCTCGGCCGTGCCTCCAACCGCAGGATGAATGTATCGTCTATGAACCTCAGATGTCTAAAGCACCTTTTTAAACGGCAGCCACTTTTATTTTTTCCCTCTCTCAGACGTAGATGCAACCTGCTGACCCCAAAGCCGCCCGTTTTCAGCCTCCACCCAAAACTTGCTGCAACACGAGAAAAGCCTTCAGAAGCATCCGTTTGATGAGAGCTCTGGCCGTATGAGATGCCTAGTCTATACCTCAAAGCATTCGTAGGTTTAATCAATTGACGTCCAGCTTTTATGATGTTTTCTAATGAGATGAGTGGATTTGGAAGCCCCGCGCTGTTGTTGGAAAGCTCTCGGGATGTATATAAACAGATTCCGTTGGTCGTTATTGCTCGAGCAAAGCAGAAATGGT
Associated Phenotype:
Not determined