Busch Lab

ZMP

csf3r

Ensembl ID:
ENSDARG00000045959
ZFIN ID:
ZDB-GENE-080104-4
Description:
granulocyte colony-stimulating factor receptor [Source:RefSeq peptide;Acc:NP_001106848]
Human Orthologue:
CSF3R
Human Description:
colony stimulating factor 3 receptor (granulocyte) [Source:HGNC Symbol;Acc:2439]
Mouse Orthologue:
Csf3r
Mouse Description:
colony stimulating factor 3 receptor (granulocyte) Gene [Source:MGI Symbol;Acc:MGI:1339755]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa42647 Nonsense Mutation detected in F1 DNA Not yet available
sa36021 Nonsense Mutation detected in F1 DNA Not yet available
sa39077 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa42647
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000063986 Nonsense 214 810 4 15
Genomic Location (Zv9):
Chromosome 16 (position 4064503)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 3222415
GRCz11 16 3117602
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCGAATGTCTTTGGAAACACAACCACTGATCCTCTGAAACTCACCCCTT[T/A]GAACACAGGTAAACGGGTCATTTAACTGATAAGACTTTAAATGTGAGCTG
Long Flanking Sequence:
TCTTCCTGGCAGAACTATTGCTAAAGCTTTAATTTTTAGTAAGTTGAAACAGTGTCAGTCCAGTTTTCAGAGTTGAAGTTCAGTTTAGTTACATGTTTCACTGCTGAAAGTCCAAAGTTTAAAGGGCAAATCCATAAATGTGCAGCCCCAAAAGTCCAAAACCAAGCAAGCCAGAAGTGACAACCACATTCCTGACAGACAATTTTGTGACAGACAAAGGAGACATCCAAAACATGCAGTGCTGGTGGTCCTCCAGGAACGTGGTTGAGAAACACTGATGTAGAGAAAAATTCAACTTGATTGCTGACGTAACTATTGTACATTTTATTCATTTGATTTTTCCAGGGCCAAGTCACAAAAGGTTTATGCGGTCCCACCCGGGCAGCACTTCTACGTGGTTCCACGGGACGCATACGGCTATTTTACTGAGCTGGAGATTTCTGTGACAGCAGCGAATGTCTTTGGAAACACAACCACTGATCCTCTGAAACTCACCCCTT[T/A]GAACACAGGTAAACGGGTCATTTAACTGATAAGACTTTAAATGTGAGCTGATGAATATAGGGGTTTTGCTAATATATACACTTACCGGCCACTTTATTAGGTACACCTATGTCTTCAGAACTGCCTTAATCCTTAGTGGCATAGATTCAACAAGGTTCTGGAAATATTACTCAGAGGCTGCGTCCGAAACCGCATACTTCTATACTATGCAATATGTATGCGAGCCGAGTAGTGTGTCTGAATTCATTAAATTCGAAAATCAGTATGCGAGAAGTACCCGGATGACTTATGACTTTCGGCGAGATTCCGGAGTGTGTATTCCATGCACGCTGCGCTATCCCATGATACCCCACGAGGGAACTCATGAATGGGTGTAAAGCGACGCAATTGACGCAGGTAGGTCATGTGACTATGACAAAATGGCGGATGTAGTACGTCCAAACTCCATTCATACTTTTCACATTCATACTGTAAAGAACGTACTATTCTAACGGCCGAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36021
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000063986 Nonsense 555 810 11 15
Genomic Location (Zv9):
Chromosome 16 (position 4055255)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 3213167
GRCz11 16 3108964
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATCATCCAAGGATATAGGTTTTACTTCTGGCACAATAAGAACGAAATC[A/T]AAGGTATTTGAGGATTTAAAGTTGAAGTATGATGATTGGCTGGACGATGT
Long Flanking Sequence:
AATTAAATTCAAGTAGTTATTTCAATTCATTATTATAACATCAAATATAGTATTTCTGACAGTTTTCTTTATAATTTGGGTTATGAATTACAGTATCGCAATACTGCTTAGTATCATGATACTTCAGCTGGTATAGTATCGTAAGATTAATTAATGCTATCACGACTACCCTAATTAGATTTTAATTAGAGTTATTAAAACTATTATGTTCAGAAATGTGTTGAAAAAAATCTGCTTTCTGTTAAACAGAAATCGGAGAAAATAATATACAGGGGGGCTTATAATTCAGGAGTGCTAATAATTCTGTCTTCACTTGTATAATGTTAACAAAATCTTGATTATTTTTTTTTATCCCAGCACCCTCTGATGCTCCAGAGCTGAATTATGAGGAGATCAGTCGTTCACACCTCAAATTTCACTGGGGCCAAATCCCCCTCGAAAAGAGAAATGGGATCATCCAAGGATATAGGTTTTACTTCTGGCACAATAAGAACGAAATC[A/T]AAGGTATTTGAGGATTTAAAGTTGAAGTATGATGATTGGCTGGACGATGTTTTTATTAACTATGATGTTTGTGAACCGTTTTCAGAGATAATGACTACGGAGACCAGCGTTGAGGTGAAGGATCTTCAACCACACACTAAATATCATGCCCTTTTATCCATTTGTACCAAGGGCGGATGTGTTAACGGATCATTTTCGACCCTGACAACTGAACGTTTGGGTGAATATTATGATTATTCTACTTTTTAATATAATCAAGGGACATTAAAGATGAGCGGCGGCACTGTCGCCTCGCAGCAAGAAGGTCACTGGTTTGAGTCCCAGCTGGGTCAGTTAGCTTCTCTATGTGTAGAGTTTGCATGTTCTCCTCATGTTGGCGTGGGTTTCCTCCGGGTGCTCCAGTTTTCCCCACAGTCCAAACACATGCGCTATAGTAAATTGCATAAACTAAATTGGCCGTAGTGTATGAGTGTGTATGAGTGTGTTGTGTATGAGTGTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39077
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000063986 Essential Splice Site 633 810 13 15
Genomic Location (Zv9):
Chromosome 16 (position 4052599)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 3210511
GRCz11 16 3106318
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTCCTCGTCATCATTATTGTGTTTACCTGTTTTGGGAAACAAGAACGG[T/G]GAGTTTTACATTCAGTGTAATCACAGTTAATTAAAGAGAAACCCCACATC
Long Flanking Sequence:
TAATAGGTGATTTGAGTCATGTCAGAGATGTATGGATGCAGTCCTCCAAGCTCATGATGGAGTCAGACACAATATTCATTCTGTCTCCACTGCAGCCTGACTTTATATTCTATACTGGACATTATTTCTGTTAATGACAAAACTTTTTTCTAAGCAGTCAGACCTTACTGTCCTGATTAAATCATTAAAAAAATCAAGGCATGATCATAATTTATTTTAGTAAAATACGCATAATCTAGAGGCCTTTCCCTGTCATATAAGCCACTTCTGATACTAAATGATCAACTAGAATCAAGTTATTATTTGTTGTTCCTAAAACTCGATAATATATATAGATAAGGAGTGTGTATAGTCAGACACTTACTATTATCACTGCTTTGACAAACTGAAAATGTTTTTCAGATGGAATTGAGATGGTGATATTTGTTATCCCAGCATGCATTGGTGCATCTCTCCTCGTCATCATTATTGTGTTTACCTGTTTTGGGAAACAAGAACGG[T/G]GAGTTTTACATTCAGTGTAATCACAGTTAATTAAAGAGAAACCCCACATCACAGTAAATAAAACGCAAGATTGTTTTTGTTGTAAAGCATACGCCAATGATCTCATTTACAACTTTTCTATAGTGTGCTAGTAATATACTTTGGCTTCTCATAGGGTGAAGATGTGTTTGTGGCCTATAATTCCCGATCCGGCCAACAGCAGTATTAAGAGGTGGACGACTACAGACTCACTACAGGTATAATTATCTGCTTTTGTTAAGAGACCTATCATGCCTCTTTTTATGATATAAAATAAGTCACTGATGCCCCTAGAGTATGTAAAGTTTAGCTCAAAATACACCACTAATAATGTTTATAACTCTCTGAAACTGACTCTTTTAAGCTTTGATCCTAATTATGTCATTTTGGTGACTGTCGCTTTAAATTCAAATGAGATTGTGTTCTTTTCAAAAGAGGGCGGAGCTACAAATGCCTGTGTGTCAGCTTAGTGGCAGATTCAA
Associated Phenotype:
Not determined