ZMP

zgc:153219

Ensembl ID:

ENSDARG00000054054

ZFIN ID:

ZDB-GENE-060929-144

Description:

hypothetical protein LOC767641 [Source:RefSeq peptide;Acc:NP_001070049]

Human Orthologues:

ITLN1, ITLN2

Human Descriptions:

intelectin 1 (galactofuranose binding) [Source:HGNC Symbol;Acc:18259]
intelectin 2 [Source:HGNC Symbol;Acc:20599]

Mouse Orthologues:

Gm9765, Itln1

Mouse Descriptions:

intelectin 1 (galactofuranose binding) Gene [Source:MGI Symbol;Acc:MGI:1333831]
predicted gene 9765 Gene [Source:MGI Symbol;Acc:MGI:3642721]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa9989	Nonsense	Available for shipment	Available now
sa7071	Splice Site, Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa9989

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
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Mutation:

T > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000076181	Nonsense	48	325	3	8
ENSDART00000142450	Nonsense	48	325	3	8

Genomic Location (Zv9):

Chromosome 7 (position 34466846)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	32861186
GRCz11	7	33132336

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GATGTCAGCATCAACCCTGAGATTGCAAAATTTGTGRACAGAATTAAATA[T/G]GTTGSTCRAAGYTGCAAAGARATCYGTGACAAGTACCATGTTTATGARGG

Long Flanking Sequence:

TATCTGCTAAATCAGAGGAAATAGTCAATCAAGCTGATATCTTATTTTATGATAAAATAATCTGCATAACATTTTTGTTGCATTTTTTTTAAACAACTAGTGCAAACAACAGTAACTGCTCTCAAAATCCTCTCAAAGCTAAATATTTTTCTCAATGAACAATTCAGTGTCACCAGAATAGCAAACTGTTGTCTTTGTTCACAAACAACAAATTAAAAAAAAATTTCCCTGTTGCTATTGGCAGGAATAAAACATGTTTTCAGAACTCATCATCCTCTCACTGAGTTTTTGGTTCTGTAACACTGCACAAAGTAAGTGTAATTTATCAAAAATAAAAGTTAAGACTTGAAGATTGGTATGTCAATTTTTATATCAGTTTTTTTATTACACCATGTCCTTATCTTTCACATTGTAGCAAACCAACAAGAAACATCATCTACTAATATTGATGATGTCAGCATCAACCCTGAGATTGCAAAATTTGTGGACAGAATTAAATA[T/G]GTTGCTCGAAGTTGCAAAGAGATCCGTGACAAGTACCATGTTTATGAGGGTATGATCTCATACTGTATCTTTTATTTGTAATGTTAGACAGCATCTGCATGTGTGTGACTGAGGAATGCTTGTGTTGACACACAGATGGCCTGTACTATCTGATCTCTTCAAGAGGAGTCCTTTACCAGACGTTCTGTGACATGACCACTGCAGGCGGCGGCTGGACGCTGGTGGCCAGTGTTCACGAAAACAACATGTATGGAAAGTGTACAGTTGGTGACCGCTGGTCTAGTGAACAAGGCAGCAATGAAAACCGGCCTATAGGTGAAGGCACATGGGCAAACAAAGTCACATTTGGAGCCGCAGAGGCCGCAACAAGTGATGATTACAAGGTATTACAATAATGCACTCACAATCTAAAAAGTTTATCTAGAAATAGAATCATATAAAATCTGTATTCTGTTATTTACCAATATTCAGAAATAAAATAGATTAGATTGAGATTACTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa7071

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:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000076181	Splice Site, Nonsense	242	325	7	8
ENSDART00000142450	Splice Site, Nonsense	242	325	7	8

Genomic Location (Zv9):

Chromosome 7 (position 34467938)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	32862278
GRCz11	7	33133428

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AGAAAAYTTTATKACATCATTAATAATATATTCTCTGTGNTTTTTTCAGCA[C/T]AATTTGAGCCTGGATTCATCACATTCAGAGTCTTAAATWATGAAAAGGCA

Long Flanking Sequence:

TATGACATTGCAGCTCAGGATGTTTCTGTGTGGCATGTGCCTAATAATATGGAGTTGGAACACTGGAGCACTGGCTCCATTCTCAGATACCACACTGAAAATCACTTCTTAACCCTACACGGAGGAAACCTATTCAAGTTATTTACGGTAAGATTACCTTTGACACCACTTTTAGTTGGAAACATTAACTGAAATTTAGCCATTTTGAATTTTGTGTGGGAAAAAAAACACTTAATGAATCTTTTTTAACTGCATTTCCCAGAAATTCCCTGTGAGGTTTGGAATCGGCTCCTGCAACATTGATAATGGACCTGCTGTCCCGATCGTGTATGATACTGGAAATGAAGAATCTACCAAAAAACTGTATGGTCCAAGTGCAAGAAGTAGGACAGAACCTCTTCTAGTGCTTTTTAAGCTGACACATTAATCTGGTTACTCGAATGAATTGAAAGAAAACTTTATGACATCATTAATAATATATTCTCTGTGTTTTTTCAGCA[C/T]AATTTGAGCCTGGATTCATCACATTCAGAGTCTTAAATAATGAAAAGGCAGCTATGGCACTTTGCTCTGGGGCTAAGCCAACTGACTGTAACACTGAGCATGTGAGTTATAAATCACAATGGATTATTTACAGCAACATTTGTACACAGCAAACAACATACAACAACATAAGTCATGCATTAAATCAACTGCACCAATGTCATATAGAGAAATGCATGGGTATATGTTGTGTTGTAAGTAATGCACTCCTACTGTATTCTTGCAGTTTTGTATTGGTGGAGGCGGACACTTTCCTGAGGGTTACCCTAAACAATGTGGAGACTTTACGGGTTTTGACTGGAATGGCTATGGTACTAATACAGAATGGAGTGCTTCCAGAGAGATAACTGAAGCAGCTGTGCTTCTCTTTTATCGCTGAAACTTGAGTATATCAGAGTTTTAAGAAGAGACTTGTTGTGATGTACTTGCTGGAGCTGTCTCATAAAAGTATCCTGAGCAAC

Associated Phenotype:

Not determined