ZMP

zgc:154073

Ensembl ID:

ENSDARG00000062374

ZFIN ID:

ZDB-GENE-061013-607

Description:

leukocyte receptor cluster member 9 [Source:RefSeq peptide;Acc:NP_001070766]

Human Orthologue:

LENG9

Human Description:

leukocyte receptor cluster (LRC) member 9 [Source:HGNC Symbol;Acc:16306]

Mouse Orthologue:

Leng9

Mouse Description:

leukocyte receptor cluster (LRC) member 9 Gene [Source:MGI Symbol;Acc:MGI:2444509]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa36067	Missense, Nonsense	Mutation detected in F1 DNA	Not yet available
sa28608	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa36067

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:

Missense, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000090183	Missense	68	542	4	7
ENSDART00000132982	Missense	68	225	4	7
ENSDART00000144856	Missense	68	542	5	8
ENSDART00000146719	Nonsense	83	140	4	6

Genomic Location (Zv9):

Chromosome 16 (position 15566676)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	13925135
GRCz11	16	13815255

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCACAGTGTGCTTGACGTCCCACAAACCACAAACTCCGAGAAAGACGATA[C/T]AGCCGTCACAGAAAAGCAGAGCAAGAGCCGAAAAAATGGGAAAAAATGTC

Long Flanking Sequence:

TGCACTGAAACAGACATAAGCCTCAGATTTGCATTTTTGTTAACCATAACTTTTCTTTTATTTCAGAGTTATAAATAAACATTATGATAATATGTTTATATTAATACATTGTTTTCATTTCTGTGAATGATTTTACTCAACTTCCTCTCCTTCCCTTCATATGACTTCAGATGAGATTAAACAAGAAACTGGCCCAAATATTTGCCAGCACTTCCTCATGGGCAGATGTCATTTTGGAGACAGATGTCGTTTGTCTCACAGGTCTGTCAGTCACCGGATGGTAGAGACTCAACTAGTGAACTTATGTAATGCTAGACATGATTTATTATCTGTATATTTTCTTTGCAACTGCAGTTGGAACAGCGTCTTGTAAAAGATGTAAAATGTGATAGATCTTGGCAATACACATTGAAGCTTAGTGGATAAATAATGCATGGCTTTTTCCTAACTTCACAGTGTGCTTGACGTCCCACAAACCACAAACTCCGAGAAAGACGATA[C/T]AGCCGTCACAGAAAAGCAGAGCAAGAGCCGAAAAAATGGGAAAAAATGTCACGCAGACATACAGCATGAAAAGATTGAGAAAAAAGGTGTGATGATCAATTTAACAATGAAGACACTTTAACATTCCGATTCAATCTTCACATTTACAAATATACGCCTCCCTCAGGATCTAAGAAGAAGCCACGGATGCGTACAGCTGATGAAGTCATCTCCAGAATCATCTGGGATGCATCAGTGGACCCTGATGATTTTATAGTTGGCCACCTAGACCGCTTTCTAGGAGTGCTGGAACGCCCCTTCTCTGATTTCTCATGGGACACTCAGGTTGAAGAATCAGTAATATTGTTAAAGAAAAACTCCAGTTTAAATAAGAAAATAGGCTCATTTTACATCTTTCCTTGAGTTAAACAGTTAAGTTTTACCAATTTTTAATCCATTCAGCCAATCTTCAGGTTTGGCAGGAGCACATTTAGCGTAGCTTAGCATAGATCATTGAAATT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa28608

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
ENSDART00000090183	Nonsense	311	542	7	7
ENSDART00000132982	None	None	225	None	7
ENSDART00000144856	Nonsense	311	542	8	8
ENSDART00000146719	None	None	140	None	6

Genomic Location (Zv9):

Chromosome 16 (position 15562233)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	13920692
GRCz11	16	13810812

KASP Assay ID:

2260-9376.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTACTTTAAATCATTTGGCTGGAAATCTGACTATCACTCAAAAAGATGAA[C/T]AAGCGGAAATAGCGGAGGAATGGAAGGACAGCTGGGATGGAGTGAGTGGC

Long Flanking Sequence:

AGTCAAGTGATTCAATTACTTATTAAGTAATTACAGTACTCTTCAGATAAAGTAATCAGAAAATTAATTTAACTACATTTTGATCATGTAATTAATTACTTTATTTTGAGGTAACTTACTCAACATTAAATTGGTTAAAAAAGTTTAATGATTACTCTAAACAATAATGCAATCATTCAATTTCAGACAATCTAACATCTGACACTGGACAACAAGAAGAATCCACCAATGCAGCAGATGTTTCCACTGACCCTGATCAATCGACTGAATTATCTGAAGTACAGGATGATGTTGCATCTGTAATAACACCATCAAAAAACAAACAATCACAGGGAGACGCCCTAAATCACTCAGCAAATGAAAACGCAGAGGAAGAAACCAAAGACCACATCCTACTCTCCCAAACAGAATCTGCACCAGAAGGCGAAAACACAGCAACTGCCGAAGATCCTACTTTAAATCATTTGGCTGGAAATCTGACTATCACTCAAAAAGATGAA[C/T]AAGCGGAAATAGCGGAGGAATGGAAGGACAGCTGGGATGGAGTGAGTGGCTCAGAAGCAGAACTAGCGTCGGCCATCCTGCCACAACCACAGTCCAAACGGCCACCACCACGCAAGCCCACCCACTTCATCTGCTTCCGTGTGGATTCTCCCGCTGCTCTCCAGGCCTTCCAGCGAGTTCAGAGAAAAGTTCTGTCCACCCTCCCTCAGTCAGAGCCAATGTGGGTTAATCCGGCAACTTTACACGTCACCCTCTCCTTACTTGTGCTCAACAGTGCAGAGGAGGTCAGTGCTGCCGCTGAGCTCATGCGCACCATAGTCCGAAGCTCCCACAAACCTCCAATTTCCGTGACGTTCGCACCTAAACTGAAGCACTTTAATGGAACCGTTCTCCACGTAGTCCCACAGCCGTCCTCAGATGTGCAGAGTCTGAATTCGCCCCTTCAAGAAGCCTTCAAAGATAAAGGTTGGCTTCACCGGCATTCCCGATGCCCGTCGTAC

Associated Phenotype:

Not determined