ZMP

lgals9l1

Ensembl ID:

ENSDARG00000025903

ZFIN ID:

ZDB-GENE-030131-9543

Description:

lectin, galactoside-binding, soluble, 9 (galectin 9)-like 1 [Source:RefSeq peptide;Acc:NP_956366]

Human Orthologues:

LGALS7, LGALS7B

Human Descriptions:

lectin, galactoside-binding, soluble, 7 [Source:HGNC Symbol;Acc:6568]
lectin, galactoside-binding, soluble, 7B [Source:HGNC Symbol;Acc:34447]

Mouse Orthologue:

Lgals7

Mouse Description:

lectin, galactose binding, soluble 7 Gene [Source:MGI Symbol;Acc:MGI:1316742]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa11406	Essential Splice Site	Available for shipment	Available now
sa42572	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa42571	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa11406

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000048729	Essential Splice Site	151	320	5	12
ENSDART00000100145	None	None	310	None	10

Genomic Location (Zv9):

Chromosome 15 (position 30338439)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	31160146
GRCz11	15	31040887

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GCACATGTGGTCATWACAAATCTTTTCTCACAAATGACTTCCTTTTTCTG[A/C]GCCATTTTGGCAATCATTTGCTWGTATGTTTTGAAATRATGTGTGAAATC

Long Flanking Sequence:

TGAACCTTCAGTGTGGTTCTCATTCAGAGGCTAACGTTGCTCTTCATTTTAACCCACGCTATGAGGACACTGACTATGTAGTAAACAACTCATATCTGAACAGGACCTGGGGCTCAGAGGAGCGCAAGTATGAATCTCCCTTTGCTCAAGGTCAAACATTCACCCTGCAGATCCTTGTCGCTCAGGACAGATACAAGGTACAAGTACATTCACTCCGTTTCTGAAGTGTTTTTAAACAGCATTAGCCCCATTGAGTTATAAATGGTTTAATATCTCAGGAGTTTGACCTCTTCTTACTTTTCTGGATCTGTCTAGATATCTACAAATGGCAGACATTTTATGGACTACAAACATCGTATACCATTCACTCAGGTCGACACAGTCGCAGTGGAGGGAATGGTGGAAGTGAACTCTGTTGCCTTCCAGAATCCTGCGGTAAGGGAAAAAAATGCACATGTGGTCATTACAAATCTTTTCTCACAAATGACTTCCTTTTTCTG[A/C]GCCATTTTGGCAATCATTTGCTAGTATGTTTTGAAATGATGTGTGAAATCAAAGGGCAACTCTGAGAGTAATTCATCACATGAATCACTATATTTATAAACCAGGCTACAAGGATCATGACGATATAAACTGAGATTAGATGTAGCTTTAAATGCCTTAGAGAATACAAAAACTTGTTTAAAGTTTAGATTTTTAAATAAATCTGTCTTAAAGGTCTCATGAAATTAAAATAAAATTTTTTAGATGTTAGTATCGGTATTGTCAGTTTTCAAGATGTCTTAAGTGACACAATTTGCATTTAGAAAGTAAAAAACTGATATAAACATGTAAAGCTTGTAGTTTGTCACTTCCTCCTAAATGGATCAACGGTTTCATTTATGTCAACCCAAACAACAGTTTCTCTTTAAAACATGCATCACCACCCTCAAGATGTAAGATTTGGGCTGTTTCTGAATTCCAAGAACACAGAAGTCGAACTTGCGTTCTCATGGAGAGGAGTC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42572

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
ENSDART00000048729	Essential Splice Site	220	320	10	12
ENSDART00000100145	Essential Splice Site	210	310	8	10

Genomic Location (Zv9):

Chromosome 15 (position 30333165)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	31154872
GRCz11	15	31035613

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGGCAAAAACATTGTCATCAATGGAGTTGTCAACCCTAATGCTAAAAGG[T/C]TAGACATTTAATTGGAACAGTGTTGTTTGAATTTCAACTAACATTTCTTA

Long Flanking Sequence:

AAAATATTTATTGAGCATTATTTAACAAAAACATTTTTTTTTTCAATAAATTTTTAAACATGATAGTTTTAATAACTAATTTCTTATGTCTTTGATCTGGGGACAGTACATAATATTATTAGCTTATTTTGCATGATAGTAATAGGCTCAAAGGGCAATTTAAGTACTTAAGTAGGTTATTATGTTAACTAGGCAAGTTATTGGATAACAGTAGTTTTGTTCTGTAAAGGGCCTAATAATATTGCCCTTAAAATTATTTTGAAAAAAAAAAAAAAAAAAAAACCTGCTGTTATTTCAACTAAACAAAAAGAAAAAAACTTTCCACAGGAAAACTATTATGTTAAATTTGACTTCACTTGTACATTTTTACACTTCTTTTTAAATATATCTTTTTTGTCACCCACACTTAGACTATCCCACACAAAACGGTCATGAATGGGGGACTTCACCCAGGCAAAAACATTGTCATCAATGGAGTTGTCAACCCTAATGCTAAAAGG[T/C]TAGACATTTAATTGGAACAGTGTTGTTTGAATTTCAACTAACATTTCTTATTAAATCATTTTGTAAATCTGCTTTATTGAAATTAATTCCGCCATTTTGCTGCTTCCATCAGCATAATATTCAACCTGTGCTACAGAAGTGGGATTGCGTTTCACTACAATCCCCGTTTTGATGAGAATGTTGTTGTGAGAAACACCAATCAGATGGAGAAATGGGGTGCGGAGGAACGGTTTGGAGGGCTGCCATTTCACAAAGGACAACCTTTTCAGGTAGAACTTACCCTGAACATATGAAATTGTTGCTTTTAAAGAGATTGTTTACCTTTAAATGTTTATTAACCTTAAGTATACCCTCCAAACAGATTGAGAAAACACAAAACACTTTTTAAAGAATGTTGGAATCCCACAGCCATTGACTTTTATACAATTTTTGTTCAAATATTATGTATAGGAGAAAAAGGAAACTCATAAATGTTTGGAACAACTTGGGGCTAAATTCAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42571

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
ENSDART00000048729	Essential Splice Site	272	320	11	12
ENSDART00000100145	Essential Splice Site	262	310	9	10

Genomic Location (Zv9):

Chromosome 15 (position 30332894)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	31154601
GRCz11	15	31035342

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGAGGAACGGTTTGGAGGGCTGCCATTTCACAAAGGACAACCTTTTCAGG[T/C]AGAACTTACCCTGAACATATGAAATTGTTGCTTTTAAAGAGATTGTTTAC

Long Flanking Sequence:

AAAAAAAAAAACCTGCTGTTATTTCAACTAAACAAAAAGAAAAAAACTTTCCACAGGAAAACTATTATGTTAAATTTGACTTCACTTGTACATTTTTACACTTCTTTTTAAATATATCTTTTTTGTCACCCACACTTAGACTATCCCACACAAAACGGTCATGAATGGGGGACTTCACCCAGGCAAAAACATTGTCATCAATGGAGTTGTCAACCCTAATGCTAAAAGGTTAGACATTTAATTGGAACAGTGTTGTTTGAATTTCAACTAACATTTCTTATTAAATCATTTTGTAAATCTGCTTTATTGAAATTAATTCCGCCATTTTGCTGCTTCCATCAGCATAATATTCAACCTGTGCTACAGAAGTGGGATTGCGTTTCACTACAATCCCCGTTTTGATGAGAATGTTGTTGTGAGAAACACCAATCAGATGGAGAAATGGGGTGCGGAGGAACGGTTTGGAGGGCTGCCATTTCACAAAGGACAACCTTTTCAGG[T/C]AGAACTTACCCTGAACATATGAAATTGTTGCTTTTAAAGAGATTGTTTACCTTTAAATGTTTATTAACCTTAAGTATACCCTCCAAACAGATTGAGAAAACACAAAACACTTTTTAAAGAATGTTGGAATCCCACAGCCATTGACTTTTATACAATTTTTGTTCAAATATTATGTATAGGAGAAAAAGGAAACTCATAAATGTTTGGAACAACTTGGGGCTAAATTCAGTGTCCTACCTAAAGTTCAGTTCCAGACCTGCTCAAACACATCTGTAGTTCATATTTAACTGGTTCAGTTGTACTTGATCAGGGTTGGAGCTAAAGTTTGCAGGAAAGTAGAAGAGGATTGGGTACCCTGTTTTAGCAAGTTTAACTTTAATTAGCATGTTGCTAACATGTTTTCAGTTTGTTTATATGCGTGCAGGACAGAATGTTGCTTGTATGTTGTAGCACTGTTAAATGTTTTGAAAGTACTTTAGCACACTTCTAGCATGAATGAG

Associated Phenotype:

Not determined