ZMP

crlf3

Ensembl ID:

ENSDARG00000070261

ZFIN ID:

ZDB-GENE-050417-354

Description:

Cytokine receptor-like factor 3 [Source:UniProtKB/Swiss-Prot;Acc:Q568M3]

Human Orthologue:

CRLF3

Human Description:

cytokine receptor-like factor 3 [Source:HGNC Symbol;Acc:17177]

Mouse Orthologue:

Crlf3

Mouse Description:

cytokine receptor-like factor 3 Gene [Source:MGI Symbol;Acc:MGI:1860086]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa10525	Essential Splice Site	Available for shipment	Available now
sa40110	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa10525

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000075903	Essential Splice Site	None	444	None	9
ENSDART00000147712	Essential Splice Site	None	148	None	4

The following transcripts of ENSDARG00000070261 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 3 (position 35897424)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	35682620
GRCz11	3	35812128

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CGGAACTCCGCGGCAGAAGTTAATATGACACAAGACAGGATCGCTTAAGG[T/C]ACTGTTAAAAAATAACCGCCTATGTTTTTGCTACACTTYATCATTCATTG

Long Flanking Sequence:

ACATATTACTATTAAAAAACGTGGTTTATTTTCGTACGAGTAAAAACGCAAAATAAAACACATTAGCCAAATAAACAAACCTGCTTTCATACTTTCTGCTTTCACAGAAGTTTTGTATTCCGCATTTTGATAAAGTTGCCTGTAAATAACTCTGTTGAAAGTGTTGGACTTTGGTACTTCTCCATAATCAATAAATACGCACAAGACAATCAGTTTTACTTTGTGATAAACACAATCTGACGCCAGGGAGCTCTGCATTGACGCCTTCGTGTGCTTTGGGTTTTTAACAAAAGATGAGGCGGGGACAGAAGAAGTTAAATCATCTGATTGGCTAAAACTGACAGTAGACATGAGGAAAACACAGCGATGCGGCCTCTGATTGGATGAGGGGTTTGTATCAAAGTGAAAATATGTGCCTCAAGCCCTTTACTGTTGCCAGGGCGTCAATGGCGGAACTCCGCGGCAGAAGTTAATATGACACAAGACAGGATCGCTTAAGG[T/C]ACTGTTAAAAAATAACCGCCTATGTTTTTGCTACACTTCATCATTCATTGCTTAAATATTCGGTCTCCAAATAATCATGTGTATGGGTGGAGTTTTAAGAGCTTACATTAAAACTCTGAAGAGTAAAAGTGATGATGAGTGTTGGTGTGGCAATACTCGCTGAAGAGCCTCGTGAACTGCCACTGCTGCTGCTGCTTTATGAGTTTCAAAATAACTACTTATATTTTCATTTTGTGAGCTGTTTTTCAAAACTTATTTTTATATTTGATCTTATACATCTTTACCATCTCTACTACCTTTAATCTCCTTACGTTTGCCTTTTATTTTCATTTGTTTTGGACTTGTTTACACCTCTTGAGTGTTCACGATGCATCAGTTTGGTCCATAGAGAATTGCTGCACGTTTACATAACTGTCCTCTAATACTCTAATGTTTTTATGTAAGAGCATAACTGTAAAGCTGATGGATAAGCAATAGTTCTGGGAGTTTATAAATAATTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa40110

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
ENSDART00000075903	Essential Splice Site	39	444	None	9
ENSDART00000147712	Essential Splice Site	39	148	None	4

The following transcripts of ENSDARG00000070261 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 3 (position 35902445)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	35687641
GRCz11	3	35817149

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAGTGAACTACAGCAGAGACTGCATGGACTCAGTCAGGCACGCAAACAGG[T/G]ACGAGTCTCTGCACTGCCACTGAAAGAATAAATCAGTGTCAGCAAAAGCA

Long Flanking Sequence:

CATCCGTTTGCGCAGAACTTTAACAGATAAGGCTGCGAACGTTATTATGATTCAAAACACGCTTCCCTTGCCTCCACATGAAGTGGAAACGATGGCCTGATTTTTCATAATGTTGCTGTTAAATTTTTATGAGTGCTGACCATGAGAAACAGGCCCATTTTTGGGGGAAGGGGGCTTATGTGGAATTTTATACTCCTGTTTTTTATTATTTTAGCTTTGTTACTGTGACATTTTCCGAAATGGGTGTGTCTTGGCTTTTTTTTTTGTCTAAGGTTTTCCATAGTGAAACATCCAGTCAAACAAAAAAGTTATCGCTATCAGTGGAAATGTTTTCTTGCACTTTACCTTGGTATTTGTGGTGCTTTTGCAGAGGTCAACAAGGATGTCAATAGAGGCAGAGGCGTTGCTGCAGGAGGCAAAGGAGAGCATTGAGGCGGCCCAAAACTACAGAAGTGAACTACAGCAGAGACTGCATGGACTCAGTCAGGCACGCAAACAGG[T/G]ACGAGTCTCTGCACTGCCACTGAAAGAATAAATCAGTGTCAGCAAAAGCAGTTGGTGTTCAAATCGTGGGAGTGTTTTGGTGAAATTTGTTGATTGCATTTGTGTAAGAGTTGAAAATGGAGACGTGAAGTCGGTCTGCTCATGTAATGTTTGCATACTTTTGTCACAGATGATGTTGATTAGATGCAGTACTTGTCAAATACGCAGAGTTTCAGATATTCTCATGTAGCTACAATAACACTTTATTCAGTACTCTATATGCCTTTAAGGGACTTGCATAGAAGTCAGAAACCCTTGTTATTAGTGAAAGTGGTGGCTGTTAAGTGAACTGTACGCAACAACTTATTGCTCATGCTTGCACTCGTGCACATGTACTGTATAGAGTGCACTGAGTGATCATTGTACCCCATGGCTAGGCCCACACGGAATCTGCGCATGCAGATTTTTTAGCCCATCATTAATTCTGTTTATTTACTTCTGTAAATGTGTGTAAATTCATA

Associated Phenotype:

Not determined