Busch Lab

ZMP

ccr12.3

Ensembl ID:
ENSDARG00000038541
ZFIN ID:
ZDB-GENE-060503-97
Description:
C-C chemokine receptor family-like [Source:RefSeq peptide;Acc:NP_001038492]
Human Orthologue:
XCR1
Human Description:
chemokine (C motif) receptor 1 [Source:HGNC Symbol;Acc:1625]
Mouse Orthologue:
Xcr1
Mouse Description:
chemokine (C motif) receptor 1 Gene [Source:MGI Symbol;Acc:MGI:1346338]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa33043 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa19895 Nonsense Available for shipment Available now
sa33042 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa33043
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056246 None None 356 None 1
ENSDART00000145888 Essential Splice Site None 355 1 2
Genomic Location (Zv9):
Chromosome 2 (position 50555563)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 50251095
GRCz11 2 49985325
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCTAAGCTGCGGAGAGTTTCACACTCGCTCCTTTACTCAAGCCATCGG[T/C]GAGTGAAGCCAAACATATGATGATCTCAGAATAACCTCAATTTAAAGATG
Long Flanking Sequence:
TCCAACCCGGTAGTTGTAAGGTGTACCTAATAAAGTGGCCGGTGAGTATACTTTTCAGTTTGATCACTTGAACATGTCTGGTAGAATGTAGCTGTCGGTTGACTGTGCAAACCTCAGTTATTATCGTCTATTTATTATTTTCTTATAATTAATATTTATAATATTTATTATTTTCTTTGTTAATGCATGTAGCATTTTAGTCTGGTTTGAACTTGATTGATTTGTGCAGCTGACAATTGAAACTCTTAGGATTACAAAAACATTTGCTTGAATTGTTTCATTGTGGCTCAACTCTCTGTCTTAAAGGAAATGAAAAGAAATGCTCCATGTCATTCTATTAATAGTGTTTTTTGCGTACTGCTGACGGTGTCGGATTTGAAACACTCTTCAGTTTCAGGATGTGTGCTGCTGGGTTTTTCTCGGTAGCCTACATCTCGCTTGCGTCAGTTTATTCTAAGCTGCGGAGAGTTTCACACTCGCTCCTTTACTCAAGCCATCGG[T/C]GAGTGAAGCCAAACATATGATGATCTCAGAATAACCTCAATTTAAAGATGCATACTAATCATATCGATTTTATTCCAGCAGACTGCAAGACACCAAAAATGGTTGACACTAATTGGAGTGATTTCGAGAGTTTTTTCAACGAGACATACAGTGAGGAGACCTATGAAGGCAGCATCGTAACCGCAGAGGTAATTTTATGCAAGAAAGCCGATGTGATTCGATTCAGTGCTGCATTTCTTCCAGCGTTTTACTATATTAACTTCTTGCTGAGCTTGCTTGGGAATGGACTGGTGCTGTGTATCATCTACAAGTTCGAGAAGCTCAGCACGGTCACCAATATCTTCTTACTCAACCTCGTGATATCAGATCTCATCTTCGCCTCCAGTCTTCCCTTTTGGGCAGTCTACCACAAATCCGAATGGATCTTCGGTAAGAATCTTTGCAAGTTTGTCGGCAGCTGTTACTCAGTCGGCTTCAACAGCTCCATCCTTTTCCTCACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19895
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056246 Nonsense 75 356 1 1
ENSDART00000145888 Nonsense 74 355 2 2
Genomic Location (Zv9):
Chromosome 2 (position 50555245)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 50250777
GRCz11 2 49985007
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGCTTGCTTGGGAATGGACTGGTGCTGTGTATCATCTACAAGTTCGAG[A/T]AGCTCAGCACGGTCACCAATATCTTCTTACTCAACCTCGTGATATCAGAT
Long Flanking Sequence:
AATGCTCCATGTCATTCTATTAATAGTGTTTTTTGCGTACTGCTGACGGTGTCGGATTTGAAACACTCTTCAGTTTCAGGATGTGTGCTGCTGGGTTTTTCTCGGTAGCCTACATCTCGCTTGCGTCAGTTTATTCTAAGCTGCGGAGAGTTTCACACTCGCTCCTTTACTCAAGCCATCGGTGAGTGAAGCCAAACATATGATGATCTCAGAATAACCTCAATTTAAAGATGCATACTAATCATATCGATTTTATTCCAGCAGACTGCAAGACACCAAAAATGGTTGACACTAATTGGAGTGATTTCGAGAGTTTTTTCAACGAGACATACAGTGAGGAGACCTATGAAGGCAGCATCGTAACCGCAGAGGTAATTTTATGCAAGAAAGCCGATGTGATTCGATTCAGTGCTGCATTTCTTCCAGCGTTTTACTATATTAACTTCTTGCTGAGCTTGCTTGGGAATGGACTGGTGCTGTGTATCATCTACAAGTTCGAG[A/T]AGCTCAGCACGGTCACCAATATCTTCTTACTCAACCTCGTGATATCAGATCTCATCTTCGCCTCCAGTCTTCCCTTTTGGGCAGTCTACCACAAATCCGAATGGATCTTCGGTAAGAATCTTTGCAAGTTTGTCGGCAGCTGTTACTCAGTCGGCTTCAACAGCTCCATCCTTTTCCTCACCCTCATGACTTTTGACCGCTATTTAGCCGTGGTCCACTCCATCGCAGCAGCCCAGAGCAGGAGAATGGCATATGCATTCGGATCATCCGCCGCTGTTTGGGTGGTCAGTATTGTGGCTAGCATCAAGGATATAGTTCTGTACGACGTAATGAAAACAGAAGACGGTTTGCTTTGCGAAATGACCGGTTACAATCAGACATTCCTCACAAAGTGGGAGCTTATCGGCTATTATCAGCAGTTTTTCCTCTTCTTTATGGTTCCTCTGATTATCGTTTTGTACTGCTATGTTCGGATCACCATCAGAATCATGTACACGAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33042
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056246 Nonsense 214 356 1 1
ENSDART00000145888 Nonsense 213 355 2 2
Genomic Location (Zv9):
Chromosome 2 (position 50554828)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 50250360
GRCz11 2 49984590
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTACAATCAGACATTCCTCACAAAGTGGGAGCTTATCGGCTATTATCAG[C/T]AGTTTTTCCTCTTCTTTATGGTTCCTCTGATTATCGTTTTGTACTGCTAT
Long Flanking Sequence:
TTCTTCCAGCGTTTTACTATATTAACTTCTTGCTGAGCTTGCTTGGGAATGGACTGGTGCTGTGTATCATCTACAAGTTCGAGAAGCTCAGCACGGTCACCAATATCTTCTTACTCAACCTCGTGATATCAGATCTCATCTTCGCCTCCAGTCTTCCCTTTTGGGCAGTCTACCACAAATCCGAATGGATCTTCGGTAAGAATCTTTGCAAGTTTGTCGGCAGCTGTTACTCAGTCGGCTTCAACAGCTCCATCCTTTTCCTCACCCTCATGACTTTTGACCGCTATTTAGCCGTGGTCCACTCCATCGCAGCAGCCCAGAGCAGGAGAATGGCATATGCATTCGGATCATCCGCCGCTGTTTGGGTGGTCAGTATTGTGGCTAGCATCAAGGATATAGTTCTGTACGACGTAATGAAAACAGAAGACGGTTTGCTTTGCGAAATGACCGGTTACAATCAGACATTCCTCACAAAGTGGGAGCTTATCGGCTATTATCAG[C/T]AGTTTTTCCTCTTCTTTATGGTTCCTCTGATTATCGTTTTGTACTGCTATGTTCGGATCACCATCAGAATCATGTACACGAGACTGATGGAGAAGTGCAGGGCGGTCAAGCTCATTTTTATCATTGTGTTCACCTTCTTCATCTGCTGGACGCCTTACAATGTGGTCATCCTGTTAAAAGCCATTAAGACGTACTTCAAGGTCCAGAACGATTGCTCGAATGCTCTCGATTACGCGCTGTATGTGACTCGCAACTTTGCTTATCTCTACTGCTGCATCAGTCCTGTCTTCTACACTTTTTTGGGGAAGAAGTTCCAGAGTCATTTTCTGAAGCTTCTGTCCAAGCGTATACCATGTCTGAAGATTGATGCCATGTGGTCTACACAGAGCAGTAAGAACACGTCATTCAGGAGCCCAAATACTGATTTTTGAGCATTTTTAGTGGCGGACAGGTGAACAAAAGATTTGTTTAGAAATGTGTCATTGAGAGGACACAAAGAA
Associated Phenotype:
Not determined