ZMP

LOC100333037

Ensembl ID:

ENSDARG00000039884

Human Orthologue:

IL16

Human Description:

interleukin 16 (lymphocyte chemoattractant factor) [Source:HGNC Symbol;Acc:5980]

Mouse Orthologue:

Il16

Mouse Description:

interleukin 16 Gene [Source:MGI Symbol;Acc:MGI:1270855]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa20867	Nonsense	Available for shipment	Available now
sa11532	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa20867

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

Mutation:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000058342	Nonsense	249	1521	6	22

Genomic Location (Zv9):

Chromosome 7 (position 12330296)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	11215852
GRCz11	7	11512662

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTGTGTATTTTTGCAGATGCCAATTATAAAGGTGTCAGACGATGATGTC[A/T]AAGACATTGACAATGAAGACCAGGGCTGCCAAGAAATGTCCTGCAAAAGA

Long Flanking Sequence:

AGTCTACAGAACAAACCATCGTTATGCAATAACTTGCCTAATTACCATAACCTGTCTAGTTAACCTAATTAACCTAGTTACGCCTTAAAATATTTGGGGACAAATGAATCGCTGAACGAATCAAATGGGAGCCGCTGGGATAATTGTGTAAAAATAAATGCATATTACAAGACAATGAAAGCATTTTTTGACCTTGCATGCATATCAGCCTGTTGTTGGAGACCCCTAAAAATAAAATATGACCTATTTTAATGCTAAATAAGGGCTCTTTAAATATAACAATTATAACAATATCAAAAGCTGCGCTCACAAACAATACGCAGCTGATTGGGTGGTTGCCTAGCGACATAAAAAGCGCAGCACACTAAAAAAGGCAACAAAAAAAGTCGGTGTGTCTTATGTGTCAGGTTGGTGTGTCTTATGTGAACCAATAACTGTTTACTGTCCACTTTTGTGTATTTTTGCAGATGCCAATTATAAAGGTGTCAGACGATGATGTC[A/T]AAGACATTGACAATGAAGACCAGGGCTGCCAAGAAATGTCCTGCAAAAGATCTCGCTCCAACTCCACCAGTGAGACAAACAAACCTGCAGGAACACACCTGACTTCTGTCACTAAATGCAACCAGCACAAATTCACTGTCCTATTATTATTAAAGGTGCAGTATGTAAGTTGGATTGGTTAGATGGTTTTGCACGCCTGGTTCAAAACACATGCAAGCGCAGGTTGCCAGATTGACAGCATCAACATAATTGTTCACACAACTATTGTGCCTAAAGGCTGATTTCTCGTGTTCTAAATAAAAGCAACAACACTCGATAGAAGGAATATTTTCCATCAAGTTTTTGTCCTAGATTATAAACCTTACCATTTCACTGGAGTGCAGTGAGTGCACTATTCTGTGCTTCTGAACGGCTGCATTTAAATTTCTGTGCTGTTTCGACTGGTGCAAACAACCCAATTGCTTATCACTGCAAATCTCGTCACATAGCCTGTTGTTAGG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa11532

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
ENSDART00000058342	Essential Splice Site	769	1521	15	22

Genomic Location (Zv9):

Chromosome 7 (position 12357615)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	11243171
GRCz11	7	11539981

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TTCACCAGTTAAGGAGGAAGATTTGATGCTCTCACAAAGCAATTGCCAGG[T/C]ATGGMCNNATATWTACTCKATGAAATGATCAATTATGAAGTTTATGTCTTTK

Long Flanking Sequence:

GAAGTGACTGAAGTGTCTGATCTTAGGTCTGAGGAGACCCGAGTCCTGTTGCCACAGCAGGCAGAAGTGCATGCGCTGCGTGGACCGGAGCACCAGTCAGCTGACCTGCAGACGCACACAGAAACCCATGATCCGCTCCTGCAGCGAAGGCGCTTACAGCCAACGCTGCTGCATCCCAAACAGCACCACCGCTCAATCCTTCCTACACACGGACCACGTCTCTCTAACAACCAACAGTGAGACCTCACTCAACAACACACTGTCTCAATCCTCCTTCACCGATGACGACTATAACATTCCCTACAAATGTCCAGTGAACTTCAATGGAAAGCAGACATTTGATGTGAACGCAAGTTCAGGACTAGTAAACCAGCCCCGAAAATACTGTAGACAGCAACAGGAAGTCAGCAGTCAGGAAGCACTGAATGTTTCGAGCGGCTCTAGTCGAGATTCACCAGTTAAGGAGGAAGATTTGATGCTCTCACAAAGCAATTGCCAGG[T/C]ATGGCCATATTTACTCTATGAAATGATCAATTATGAAGTTTATGTCTTTTTTGTTGTTGCTGTTTTGATACATTTAAGGTTTCTGCTGATTTAAAGTCAAATTAGAGACTCTTAAAGACATTTTAAGACCATTACTGATGAAATTTCAGACTTGCACAAAGCTAAACGCTAAGGTTTTTTTCTAATGGCCCAGTCGGGAAAAGAGTTTCACTTGGCCCATTAACAAAATTTATTTGTATGAAACGATGGAATAAGATGTTCATTTCTATGTTGTTGCTGATTTTGTAATCACAATCAGATTTTCTGTAAATTAAAAGACCTTTAAAGACATTTTTATGACCAACTTTCAGCCTAATACAGAGCTAATAGTCCTGTTGGGACAAGATTTTTACTTGCCCCATTAAAAAAAATCTAAATAATTATTTCGGTCACACTTTATTTTGATGTCTGTTTGTTGAATATAAGTAACGTTGCATCTACATGTCAACTAATTCTCGTTA

Associated Phenotype:

Not determined