ZMP
csf2rb
Ensembl ID:
ZFIN ID:
Description:
colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) [Source:RefSeq pe
Human Orthologue:
CSF2RB
Human Description:
colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) [Source:HGNC Symbo
Mouse Orthologues:
Csf2rb, Csf2rb2
Mouse Descriptions:
colony stimulating factor 2 receptor, beta 2, low-affinity (granulocyte-macrophage) Gene [Source:MGI
colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) Gene [Source:MGI S
colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) Gene [Source:MGI S
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa19999 | Essential Splice Site | Available for shipment | Available now |
| sa19998 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19999
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 |
|---|---|---|---|---|---|
| ENSDART00000115283 | Essential Splice Site | 74 | 696 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 24620432)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 24198643 |
| GRCz11 | 3 | 24329191 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGATCCACGTGCTAACTTCACTTTGTATTACTATGACAAATATAAGAA[G/A]TAGGTGATGAAAGACACAATAGATGAAATAAAGTGACAGGAATGAATAAA
Long Flanking Sequence:
ACCAAAAAGCACTTGTTTACTTAACTTTTATTATTGCTATGTCTCATTTACATATGCTTCTAACTTAATTGCACTGCATAGAAAAAGACTTGATCATCTCAGTCAATCAAAATTGATTAAATCTTTCCAACTAGAGTGATTCAAATCATCTGGTAAAATTATATTCATATTGCAATATGTATTGCAGACAAAAAATATCATAATGATAGAGCTTTACAATATTATGCAGCCCTAAAAGGTATTACAAAAAAACACAACAGAGGCATTTAAGCATCATTTGCCTCAAACCAAAACTAAAACGTATCTGGGCAGCTTTTGATGTTAAATAAATGTGACATGAACAGAAGTCACCGTCTTAAATGCTTTTAAACTCTTGTTTTAGACTCTGCAGTGATGGATTCTTTGCTGTGCTACAATGACTACAAATCCTATACAGAATGTACATGGGAGACTGATCCACGTGCTAACTTCACTTTGTATTACTATGACAAATATAAGAA[G/A]TAGGTGATGAAAGACACAATAGATGAAATAAAGTGACAGGAATGAATAAAAGAATACAATGAGGAACTTTTGTCTCTCCCTCTCTTCAGAGCAGAAACACTTTGCCTCTTGAATAAACCCCATGTAGTTTTACCCAATGGGAAGTTTTCTCACGTGTGTCGCTATAACACAGGGAGATTTTCACTTAACACCAATCACACCCTATACTTCAAAGTACAATGTGGAAATACTCCCACATCTCTCCGAGTTGCTCAGCATGGTAAGTGTGTTTCGTGAATGCATTTACCTTTTAAAACATCTCTGCAGTGGAAAAGTCCTTTACTGTCATGTGCATGATTTCAGGGAAAGTTAGAGCCCCGGTCAGCTTGACGGAGATGATGACTGATGGAGGAGGTCGCCTGCTGTCCTGGAAAAGTCCGTATCCTGCATCCTCAAATATCACAAGGTCTCTCATGTACCAGCTTCAATATCGCAGACACATGCATGACTGGACTGTGAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19998
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 |
|---|---|---|---|---|---|
| ENSDART00000115283 | Nonsense | 501 | 696 | 11 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 24610514)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 24188725 |
| GRCz11 | 3 | 24319273 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGTCTTATGGAAGGGATCGATTCCATCACCCATAAAGAGCAAAGTACTC[G/T]AGGGGGTGATCAAGGTGAGCCTTTATTGACTGATCTTGCAAGTGTTTAAA
Long Flanking Sequence:
ATAAACAGGGGGGGCTAATAATTCTTAACTTCAACTGTATATATTTTTGATGAACTATCCTTTTAGGCTTAGGGGAAGAGTGGACAGAACTGAATGCGTATGTAATGTATAAGAAAAACTTTTTTGTATGTGCAGCTTCGTCACCCATCAATCATCTCATCCAACCGTCATCCAACATTCCACTAACCTACATTTTGGCTGGTGTGCTTGTACCAGTGTTAATCGGCATCCTATACAGTGCTCTTCCAGCATGCCACAGGTAAAACAAATGGCATGTTTACATTTATGCATCACCCAAACATACATTAAGTCAATGAATTGATCAATTTCTGCATTTCCTGGAAAAGTCATTACATTAAAGTTGTATATACTTGCTGTGTGAGCAACAGGAACATTTATCAAGTGTAGCTGTTTTTGTATGTGTTTGTAACAGAAGGATTAACAGAAAGATCGTCTTATGGAAGGGATCGATTCCATCACCCATAAAGAGCAAAGTACTC[G/T]AGGGGGTGATCAAGGTGAGCCTTTATTGACTGATCTTGCAAGTGTTTAAATTGTTGTGAGCATACTACATTATTTCTTTCTTTCTCCCTCTCTCTCTCTCTCTCTTAGAAATATCCAGCCGGGTGGCCGTATCTTCAGAGTGAAAAAGAGACAACCTCTGTTTGTGTACTGCTGGCTACTGACAATATCAGTGTCTGCAATAAGTAAGATCTCAATTATTCATGATAGCACTAATTAAACTGTAACGTCAACAAAAATTGATTTTTTTCAGTTTTAATTTACCCTAAAAATGTTAATTAAATCGATGATGGATATTGGTCTTTGCAAATGAAACTGAACATTATATACAAGGCTATTATTACCTTTTATTCACAGCTTTTGTAAATAAGAGCTTCAATAAGGAAATAAAAGACCTTAATGTATTATAAGGAGACATAGCCTTAATTTGGTTTTGCCTGTATATGTCTCAAAAATACTAGAAATTGTTGAATTAGCTTTAC
Associated Phenotype:
Not determined