ZMP
csf1rb
Ensembl ID:
ZFIN ID:
Human Orthologue:
CSF1R
Human Description:
colony stimulating factor 1 receptor [Source:HGNC Symbol;Acc:2433]
Mouse Orthologue:
Csf1r
Mouse Description:
colony stimulating factor 1 receptor Gene [Source:MGI Symbol;Acc:MGI:1339758]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37380 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24034 | Nonsense | Available for shipment | Available now |
sa1503 | Essential Splice Site | Available for shipment | Available now |
sa43722 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa29665 | Essential Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32360 | Essential Splice Site | Available for shipment | Available now |
sa24035 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37380
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075675 | Nonsense | 369 | 851 | 9 | 23 |
ENSDART00000142718 | Nonsense | 453 | 964 | 9 | 21 |
Genomic Location (Zv9):
Chromosome 21 (position 42270988)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 43870034 |
GRCz11 | 21 | 43865210 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCTCTAATTGCTTTTGATTTGATGGCAGGTGTAGTGACAACCGTACAT[C/A]AGGTGTGGAATTAATGGCCAACCAATCCATTTCTGAGCAAAGCGGAGAGT
Long Flanking Sequence:
TGAGGCGATAGTGCTAACCACTGAGCCACCATGCTGCCTTGATTTTATCAGCTAATTCTATCAATGTGTTTATGTTTGACAGTGATATCTACATGGCCACAATCCGGCTCAAAAATGTTGGAGCACAAGACTACGGTGACTACATCTTCAGCGCCGGCAGCACCAGTGTCAATGCCTCCATTATTTTCACAGTACACGTCTACCGTATGTATAGTTGGTTTATAAAGAACATACTGCCTCACATAGCAAATCCAAAACAGCATCATTTTTGTTCTTTCTAAACCTACAGAGAAGCCAACAACAGTTATTAAGTGGGAAAATGGAGTCGTCAGTTGCGCAGCGACTGGCTACCCCATACCTAGCATCCAGTGGTTCCAGTATGAAGTTAACAGAGCTTTGTATGTGCACTTTTTTGGGCAATTAGTTATGTAAATAGGGTTTGCTACGACATTGCTCTAATTGCTTTTGATTTGATGGCAGGTGTAGTGACAACCGTACAT[C/A]AGGTGTGGAATTAATGGCCAACCAATCCATTTCTGAGCAAAGCGGAGAGTATGAACCAGTGCTGGTGAAGAGTGCATTACCAGAGATTACAGCTAATGCTGATTTAATATTTGAGTGTGTGGCAACAAACACCGCTGGAGACGATTGTGACTTCTATACCTTTACATTTTCAGGTGAGAAAGAATGTGTACCTGCTGTAGTTCAGACAAGACCACTTTTATTTGGTGGTATGGTTCCTAATTAACCGACATAGATATATACATTAGATGTCGCCTGGCCTATTGTTGTCTATTGGACGGAATGCGTCAATAGCGCCGCCATCTTGCTACAGGGTAGCGCTCCTTTTAAATGAATGCGGGACCAGGGTACAGTGGAGGACTGTGGCCATCCAAAGCCAGAGATATACACATATACATGTATATCTATGATCGGGAGTTTTCCTGGATGTTAATATGTCTTTTTTTTTCTAATTACGAAAATTATAATTTTACATTACTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24034
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 |
---|---|---|---|---|---|
ENSDART00000075675 | Nonsense | 382 | 851 | 9 | 23 |
ENSDART00000142718 | Nonsense | 466 | 964 | 9 | 21 |
Genomic Location (Zv9):
Chromosome 21 (position 42271026)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 43870072 |
GRCz11 | 21 | 43865248 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAACCGTACATCAGGTGTGGAATTAATGGCCAACCAATCCATTTCTGAG[C/T]AAAGCGGAGAGTATGAACCAGTGCTGGTGAAGAGTGCATTACCAGAGATT
Long Flanking Sequence:
TTGATTTTATCAGCTAATTCTATCAATGTGTTTATGTTTGACAGTGATATCTACATGGCCACAATCCGGCTCAAAAATGTTGGAGCACAAGACTACGGTGACTACATCTTCAGCGCCGGCAGCACCAGTGTCAATGCCTCCATTATTTTCACAGTACACGTCTACCGTATGTATAGTTGGTTTATAAAGAACATACTGCCTCACATAGCAAATCCAAAACAGCATCATTTTTGTTCTTTCTAAACCTACAGAGAAGCCAACAACAGTTATTAAGTGGGAAAATGGAGTCGTCAGTTGCGCAGCGACTGGCTACCCCATACCTAGCATCCAGTGGTTCCAGTATGAAGTTAACAGAGCTTTGTATGTGCACTTTTTTGGGCAATTAGTTATGTAAATAGGGTTTGCTACGACATTGCTCTAATTGCTTTTGATTTGATGGCAGGTGTAGTGACAACCGTACATCAGGTGTGGAATTAATGGCCAACCAATCCATTTCTGAG[C/T]AAAGCGGAGAGTATGAACCAGTGCTGGTGAAGAGTGCATTACCAGAGATTACAGCTAATGCTGATTTAATATTTGAGTGTGTGGCAACAAACACCGCTGGAGACGATTGTGACTTCTATACCTTTACATTTTCAGGTGAGAAAGAATGTGTACCTGCTGTAGTTCAGACAAGACCACTTTTATTTGGTGGTATGGTTCCTAATTAACCGACATAGATATATACATTAGATGTCGCCTGGCCTATTGTTGTCTATTGGACGGAATGCGTCAATAGCGCCGCCATCTTGCTACAGGGTAGCGCTCCTTTTAAATGAATGCGGGACCAGGGTACAGTGGAGGACTGTGGCCATCCAAAGCCAGAGATATACACATATACATGTATATCTATGATCGGGAGTTTTCCTGGATGTTAATATGTCTTTTTTTTTCTAATTACGAAAATTATAATTTTACATTACTTTTCTACATTGATGGATCAGTGACTGCACGGGCATTCCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1503
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 |
---|---|---|---|---|---|
ENSDART00000075675 | Essential Splice Site | 507 | 851 | 12 | 23 |
ENSDART00000142718 | Essential Splice Site | 590 | 964 | 11 | 21 |
Genomic Location (Zv9):
Chromosome 21 (position 42273132)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 43872178 |
GRCz11 | 21 | 43867354 |
KASP Assay ID:
554-1428.1 (used for ordering genotyping assays)
KASP Sequence:
ACTTCCATACAACAAGAAACTGGAGTTTCCTCGAAATAAGCTGAAGCTTG[G/A]TACTTACACTCTCTGTTTTACTAGAGTATAATTTTGTAATGATAAGAAAT
Long Flanking Sequence:
CTATGTGCATAATAGTAAAAATAACTTTAGTGAACTTAATAGTTTTAAGTTACAACGGATATACTTAAAAATTTTAAGTTAAATGAACCTAAAATTAGGTTTACTCACTTTATAAGTAGTTGCTTAATTTCCTATTTTGCTTTTGAAATGGACCTGTCTTAATGAAGCACCTTAAATGTGTTCATAAGGTCCTCGCCCTACATCGGTGTGGTCAACTTCAGTGCTAATCAGTCTTGGTCTCTCTGGAGCTCTCTCTGTGGCAACTCTATGGATGTTAATTCTCCTCTACAAGAACAGAAAGGTATCTTTTATTTACCTGAGTTATACTCACAATCATGCAAATTTAACAGTTTGTTTAACCTGATACTTTAAGGCACAGAAGTATGAGATTCAATGGAAAATCATTGAGGTAAATGATGGGAACAACTACACATTCATTGACCCCAGCCAACTTCCATACAACAAGAAACTGGAGTTTCCTCGAAATAAGCTGAAGCTTG[G/A]TACTTACACTCTCTGTTTTACTAGAGTATAATTTTGTAATGATAAGAAATAACTACTGCAAAAAAAAACAATGCTTGCACTCCAGGACAGGTTCTTGGAGCAGGAGCGTTTGGGAAGGTGGTGCAAGCAACTGCTATTGGCCTGGTCAAGGATGAAACCATCACACGAGTGGCGGTGAAAATGCTCAAGCGTAAGTTTAATTTAATTATGGCTTTTAAAATTTTTTAAATAATTTTTTATAATTATTTTTAGGGGTTTTCAACTTTAATGTGATAGGACAGTAAAGGACAGTCAGGAAAGCATTAGGAGCAGAGAGAGGGGAAGGATCGGCATAGGACCCTGAGCCGGGAATCAAACTTAGGTCACCGTGAGCACCTTGGGCCTATATGTTAACGCACTAGGCCTCTAGGCTACGCTATTGGCGCAGATGACACTAGAAATTGTTAACCCTGGGCATCCTAAACCCATGGATAAATGGAACCTGTGTCATCTGTGTCATG
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa43722
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075675 | Essential Splice Site | 580 | 851 | 14 | 23 |
ENSDART00000142718 | Essential Splice Site | 663 | 964 | 13 | 21 |
Genomic Location (Zv9):
Chromosome 21 (position 42275102)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 43874148 |
GRCz11 | 21 | 43869324 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACCACATGAAAACATAGTCAATCTGCTGGGGGCATGCACTCAGGGCGG[T/A]AAGTCAAAGTTGTATTTCTACATTGTAGAGATGGATAAAAAAAGGCTGTC
Long Flanking Sequence:
TGATTTTTGTATTTTTGTCTCTGACACTGCACAATAGTCATTAAAATCTGCACTTGGATTCTACACCCGTTTTTGTTCCTGTTTGTAATCCCGTACCGTGACACATTTACATTTAGCAGACGCCTTTGTCCAAAGTGATATACAATTGTGGAGGCATTCAGCGATTCAACAAGAAAAGGCAATACACACAAGTGCTGATTATACAAAGGAACTGTTAGTGCTCAGAAGAAGCAAGTGCTAGAGTTAGGTTGTTTTTATAGATAGACAGAAAAGAGTGTTTTCTACAGGTGGTTTGTCAAGCCCACTCACCTGTGTGAGGCACACTCAGTTTGGGGTTGTCATGTACTGTGAACCTCAGGTTAACTTTCTTACTTTCTGAACCAAACAGCTAGCGCCCGCTTTGAAGAAAGAGAAGCACTCATGTCTGAACTGAAGATCTTAAACTATATTGGACCACATGAAAACATAGTCAATCTGCTGGGGGCATGCACTCAGGGCGG[T/A]AAGTCAAAGTTGTATTTCTACATTGTAGAGATGGATAAAAAAAGGCTGTCAATTAGCACACTGTTTTTCAAAGTGACTTACAGTAAAAATATTAAGTACGTTAACTAAAAATGAGTGGTAGTGTGTTAAAAAAGGTAAGAATAGAAAATACAAATGTAATTTTATTGTTGACATCTAATTAATCTAAGTATAACTCTAATTATTCTCTATCAACAACATAAATTAATGAACAAATCAATCAATAATTCAGCCAGTCTGTGAATGCTGGTGGTTTTAAATTCTTTGCTTGATGTTGATTAATCTCAGAACTTGGTCTGATTTAGGACCCATGCTGATGATCACTGAGTACTGTTGCCATGGCGACCTCCTCAACTTCTTGCGCCAACGAGTAGAAACCTTTGTGAACACTGTTCTTGGTGTTCAGAGTTTTGCCGAAGACTCAAACCTCTACAAAAATGTGACCATCCAAAAGCAACATCCCGCAAGGTTCGTCTCTCAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29665
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
G > T
Consequence:
Essential Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075675 | Essential Splice Site | 666 | 851 | 19 | 23 |
ENSDART00000142718 | Nonsense | 746 | 964 | 16 | 21 |
Genomic Location (Zv9):
Chromosome 21 (position 42278278)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 43877324 |
GRCz11 | 21 | 43872500 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTCTCATTATGCTAATATCTGACTTTTTCAACAGAGTCCTGTAATGAA[G/T]AATTGGAGAACATGCTGTCATTGGATAACATGGATTTGCTTATGTTCTCA
Long Flanking Sequence:
CTGGAAGGACATCCGCTGCATAAAACGTGTGCTGGAATAGATGGCAGTTCATTCAATTGTGGTGACCCCTGATAAATAAGAGACTGAGCCGAAGGAAAATGAATAAATAAATGAAGGTTTATGTGTGTGTGTCGGTTTTTGACCAAAGATTAAATCGAGTCTTAAGAGTTCATATTGATCAAAATGGGCAGACGTAAAAGACTATACTGTATATTGCTTGGGCAGAGAGCAGCTCATGTTTAATAGCTAATAGCTGTTTGATGCTATTCAATCCGATCTAATGCTTTTTTTTTGACCACCTCTGGATGTTTTATTTTTACTTCATTTTTTTAGGAATGCTTACTCTGGTTTAGACAGCTTTAGGGACACACCGTCAGGACAGATGCCAAAAGAGCCTTTTCAGGGTAAAGTAATATAGTACGCCCTTCAAATCATTCTGTGAATGAATGGCATTCTCATTATGCTAATATCTGACTTTTTCAACAGAGTCCTGTAATGAA[G/T]AATTGGAGAACATGCTGTCATTGGATAACATGGATTTGCTTATGTTCTCATATCAAGTGGCTCAGGGAATGGACTTCCTGGCTTCCAAAAATGTAACATTTCTTGGTTATATATCACATATACAGTAGGGAAATTAAGTATTGAACACGTCACCATTTCTCTCAGAAAACATATTTCTAAGGGTGCTGTTGACTTGAAATTTTCACCGGATGTTGGTAACAACCAAAGAAATCCATATATGCAAATAAAACATTATTAATTAGTTTACAAATGAAGTTATGTGTAATAAAATCTAATTATACAGGGAAAACGTATTGAACACATGAAGAAAGGGAGGTGTAGTTCGGCAGTGAAAGCCCAGACAGCAGCTGAAATCTCTCAGTAGTTCTTTAGCAGCCCTCTGCCCTTCCTCAGTGTAAATGAACATCAGCTGCTTCAGTCCAACATCTACATTAGCAGGAGGATGAAGATGAACCCAGGGTGGACATTTCAGCAAGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32360
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075675 | Essential Splice Site | 738 | 851 | 21 | 23 |
ENSDART00000142718 | Essential Splice Site | 818 | 964 | 18 | 21 |
Genomic Location (Zv9):
Chromosome 21 (position 42280762)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 43879808 |
GRCz11 | 21 | 43874984 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTCCTGTCTACTATGAAATTTCTTTACATGCTGTTGCTTTGGTTTTAT[A/G]GGCACGGCTGCCAGTGAAATGGATGTCACCTGAAAGCATTTTTGAATGTC
Long Flanking Sequence:
GACGTACAAAGGTTCAATTCCCGATTGGGCCAGGTTGTATTTTTGTGTGGAGTTTGCATGTTCTCCCCGTGTTCACTGTCATCCCCTTATGATGCCAGGTTGCACCTTTCTGGAAAGGGCTATTAGAGTGATTATGGACTTTGTTGTGTATTTTGACGTGGCATTCCTTTGTTCTGTTTTACCACCACCATTTGTTTATTATCAGTATACTACCTGTTTGCCATTTAGTTCATTCATCTCCATGAGTATTTAGGTTTCGCTTTCTCTTCAGTTTCGGTTATCATCTGTGTGGATGTCTCTAATAAAACTTATGTTGGTGTTTGCCTCTTTGGATTATTAAACCTTTTTGAATTTCCCTAATCTCTCATTAACTCTTTCCTAAACAGACACATGACAAACCCACATGTATTCACAAGAATTTCTTGATTAAATCTTGCATCAGTTCCCACATTCTCCTGTCTACTATGAAATTTCTTTACATGCTGTTGCTTTGGTTTTAT[A/G]GGCACGGCTGCCAGTGAAATGGATGTCACCTGAAAGCATTTTTGAATGTCTGTACACAGTCCAAAGTGATGTCTGGTCATATGGTGTCCTTTTATGGGAGATTTTTTCCTTGGGTAAGTAAATATAACACATACAAACTTACTAACAAAATGTTAGTGTACTGAGGAAAACATTTACTACAAACAAAGTGGTCTTAAGGCATTTTGTTGTCATTAACATGACTAGTATATACATATATATGTCTTGTTTTTCAAGGTATGAGTCCTTACCCCAATGTTGCGATTGATGCCCAGTTCTACAAGATGATAAAAGACGGTTATCACATGCCACAACCAGATTTTGCGCCACATGAAATGTGAGTTTATGAACATTTGTCAAGTTTGGGAAAATAAACAACAAATAGTAAGCCAATTATAAAAGTGACTTAAACTCCTGTAGGTACACTATCATGAAAATGTGCTGGAGACAGGAACCAACTACACGGCCAACCTTTGCTGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24035
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075675 | Nonsense | 755 | 851 | 21 | 23 |
ENSDART00000142718 | Nonsense | 835 | 964 | 18 | 21 |
Genomic Location (Zv9):
Chromosome 21 (position 42280817)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 43879863 |
GRCz11 | 21 | 43875039 |
KASP Assay ID:
2261-6100.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGCTGCCAGTGAAATGGATGTCACCTGAAAGCATTTTTGAATGTCTGTA[C/A]ACAGTCCAAAGTGATGTCTGGTCATATGGTGTCCTTTTATGGGAGATTTT
Long Flanking Sequence:
GCATGTTCTCCCCGTGTTCACTGTCATCCCCTTATGATGCCAGGTTGCACCTTTCTGGAAAGGGCTATTAGAGTGATTATGGACTTTGTTGTGTATTTTGACGTGGCATTCCTTTGTTCTGTTTTACCACCACCATTTGTTTATTATCAGTATACTACCTGTTTGCCATTTAGTTCATTCATCTCCATGAGTATTTAGGTTTCGCTTTCTCTTCAGTTTCGGTTATCATCTGTGTGGATGTCTCTAATAAAACTTATGTTGGTGTTTGCCTCTTTGGATTATTAAACCTTTTTGAATTTCCCTAATCTCTCATTAACTCTTTCCTAAACAGACACATGACAAACCCACATGTATTCACAAGAATTTCTTGATTAAATCTTGCATCAGTTCCCACATTCTCCTGTCTACTATGAAATTTCTTTACATGCTGTTGCTTTGGTTTTATAGGCACGGCTGCCAGTGAAATGGATGTCACCTGAAAGCATTTTTGAATGTCTGTA[C/A]ACAGTCCAAAGTGATGTCTGGTCATATGGTGTCCTTTTATGGGAGATTTTTTCCTTGGGTAAGTAAATATAACACATACAAACTTACTAACAAAATGTTAGTGTACTGAGGAAAACATTTACTACAAACAAAGTGGTCTTAAGGCATTTTGTTGTCATTAACATGACTAGTATATACATATATATGTCTTGTTTTTCAAGGTATGAGTCCTTACCCCAATGTTGCGATTGATGCCCAGTTCTACAAGATGATAAAAGACGGTTATCACATGCCACAACCAGATTTTGCGCCACATGAAATGTGAGTTTATGAACATTTGTCAAGTTTGGGAAAATAAACAACAAATAGTAAGCCAATTATAAAAGTGACTTAAACTCCTGTAGGTACACTATCATGAAAATGTGCTGGAGACAGGAACCAACTACACGGCCAACCTTTGCTGACATCACAGAACTCATTGCAAAGTTACTGCCAATGCAAACCAGTGAGGTGAGCAGTCA
Associated Phenotype:
Not determined