ZMP

LOC793246

Ensembl ID:

ENSDARG00000090889

Human Orthologue:

LECT2

Human Description:

leukocyte cell-derived chemotaxin 2 [Source:HGNC Symbol;Acc:6550]

Mouse Orthologue:

Lect2

Mouse Description:

leukocyte cell-derived chemotaxin 2 Gene [Source:MGI Symbol;Acc:MGI:1278342]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa6351	Nonsense	Mutation detected in F1 DNA	Not yet available
sa15673	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa6351

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
ENSDART00000124159	Nonsense	53	165	3	5

Genomic Location (Zv9):

Chromosome 14 (position 38211981)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	36550292
GRCz11	14	36890606

KASP Assay ID:

554-5056.1 (used for ordering genotyping assays)

KASP Sequence:

CTCTGCAGTGGAAACAAAGATAACAYGAAAAGAGGATGTGATGTAAACTA[T/A]GGTTGTGGACAYTATGGAGCCAGCCGGTAAATCGTGACTTTTTGTTTATA

Long Flanking Sequence:

TAACAAAGCATGTAGTGTGCTTCACAAAATAAGCTTAATTTAACGATTTATTGTGTTCTGCAATGTACATTTAATGTTATTAAGTCTATATTACTGTATAAATACTTGTCAAAACATGTCAATTCAAGATTTTCTAGCAAACAGAGCAAGTTTACTATTGCTTTGTGGTGGTGTGTCATTAAAATGCATTGTGAAAAGACTATACAAGTAAATTAACATGCACCATAAACATTGCAAAAGTGATTCAAAAACTGTATGCAAATGAATCTCAATGCATCTCTCTCTTGCAGTGCTCAGCTGCTCATGTGTTAGAGATCGAGGTATGAATGCAAATTAAAAAAAGAAAAGAAACATAAAAACAATTAGACAAATATAAAGATAGAAACAGGAAGCACATAAAACAGAGATGAGTTTTCACACTTTTTTTTTTCCACAGTGAAATTTGGGCCCCTCTGCAGTGGAAACAAAGATAACACGAAAAGAGGATGTGATGTAAACTA[T/A]GGTTGTGGACACTATGGAGCCAGCCGGTAAATCGTGACTTTTTGTTTATAATGCTTCAATTTGCTGATGACACGTTTAGCAAAACATTCTTATTTTGTATCACAGCTGTTATAACAACACTGAATTAAACGTAAAATAAGATATTTTGCAGAATGCTGTCTCTAACCAACTTTTTACAAGGCATAACAAAGTTTAATATAACTGATATCAGATCTACAGTATTTTGATGATCTGCATTATTTTGGTTGTACTTTATGATCAGTGTTGGGTGTAATTATTTACAAAATCAAAAGTTACTGTAATTAAATAGCTTTTCCACTCAATAACTGCATTTTAGGTAGTTTAATTACAGTTGGTTATAAATGCCTTTGTTCTATATAAACAAAGTAATTGTGATTAATTATGCTGAAGAAATTGTTTTAACTTAATTAGTTTGTGACAATACAAGGTCAATGTTTTAATGTCATCTCTCTCTCTTTCACTTTCTGGATACAATTGAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa15673

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000124159	Essential Splice Site	110	165	4	5

Genomic Location (Zv9):

Chromosome 14 (position 38214087)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	36552398
GRCz11	14	36892712

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ATATGGAAATAACAATGYCATTGATGATGGGATAACCTTAATGGSTGAAG[G/A]TTTGTACTGTCATCACATATATAAGTTAGTCAAATGTTTCACAAAGTTCT

Long Flanking Sequence:

GGTCAAAATGATCAGCCCCTTTAAGCTATATATTTTGTTCGATAGTCAAAATAGTAAAATAGTCAAATATTATTTACTGTCATCATAGCAAAGATAACGTAAATCAGTTAATAGAACAGAGTTATTAAAACTATTATGTTTAGAAATGTGTTGAAAAAAATTTCTCCGTTACACAGAAATTTGGAAAAAAACAATTCAGGGGGGGCTAATAATTCAGACTTTAACTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTATTTATTTATAGTATTGGTGTATTTGATTCATGTTATGTGTACCTATGTTACAGTGGGAGCAGGAAACACATGGGTCTGGACATTGTGTGTACTGACGGAGCCTATGTTTATGCTCCATTCGATGTGAGGATAATCGGCAGAGCTAAACCATATGGAAATAACAATGCCATTGATGATGGGATAACCTTAATGGGTGAAG[G/A]TTTGTACTGTCATCACATATATAAGTTAGTCAAATGTTTCACAAAGTTCTTTTAGAGTCTTGATTTCTTTCTTCAAGTAATTCTGCTTAAAATACTTCCTCAAATGACATTTGAAGACTTCATACAAGAAAATCATAATCTTACAATAATGTCATCTGTTTGGCAGGTCTCTGCTTCAAGCTCTTCTACGTACAGCCAGATCTTTTGTCCGGGACCAAATTTAAATATGAAAAGATTGGAAGTCTTCTGCCCATGCAGAAAGTTTATCCTGGCATCACTTCACATGTTCATGTTCAAATGTGTGACAAGTCAGATCCAACAGAGTACTTCTGATGGATCCCATGACCAACTTCCACCATCAAACTTCTGTTGCATTCAACTAAACCAAACGTCAACTTTTTTTGCATTTTGTGTCATTTATCAGATTTAATTCTTTAAACTTACAGAGTTTCAAACTCTTTGTACAGCACTTTGAAACATAACAATAAAGTCATTTAATC

Associated Phenotype:

Not determined