ZMP

si:dkey-196h17.3

Ensembl ID:

ENSDARG00000058160

ZFIN ID:

ZDB-GENE-081107-56

Description:

Novel protein [Source:UniProtKB/TrEMBL;Acc:B8JIB7]

Human Orthologue:

TNFAIP2

Human Description:

tumor necrosis factor, alpha-induced protein 2 [Source:HGNC Symbol;Acc:11895]

Mouse Orthologue:

Tnfaip2

Mouse Description:

tumor necrosis factor, alpha-induced protein 2 Gene [Source:MGI Symbol;Acc:MGI:104960]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa22211	Nonsense	Available for shipment	Available now
sa28061	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa1956	Essential Splice Site	F2 line generated	Not yet available

Mutation Details

Allele Name:

sa22211

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000080975	Nonsense	312	613	4	11
ENSDART00000143326	Nonsense	8	309	1	8

Genomic Location (Zv9):

Chromosome 13 (position 6787188)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	7114035
GRCz11	13	7446237

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCCTGGAGGGATGGGAAGCTTCCACAGCTGATGGACCAGGTGTACTGCTG[T/A]CCTCAGGCCATCGATGTGATCCAGGTAAGGAAGAAAACTATGGATCAATC

Long Flanking Sequence:

GATGCCCTGAGCGTTTTTATGGGCGAGCATTCTCAGTAGACATGTAAACTTGCGTCCATATGTCTATACAGTTACATATAAACATGATCCTTTAATCACTTTATTCTGTTGAGCACAAAATAAAATAGTTTGAAGAATGTTGGAAACCTGTAACCATTGACTTCCGTAGAACACTATGGAAGTCAATGGTTACAGGTTTTCCACATTTTACAATATGTTCTCTTTTGTGCTCAGAACCAAATATGGTCAAGGATGAGGTAAATTATGAACAAATAGTAATTTTTGAGTGAACTATCCCTTTAAGTGTCCCATTTGTTAAAATAGGCAATAAAAAGTGATTAATACATCACAATTCTCCAAACAGCCCCTTTAAAGCTTCGATTTCAATTTGCTTTTCACCAGAGGGAAGTGAGCAAATGCCTCCACAATATTCTGGACAGAGAAGAAACAGCCTGGAGGGATGGGAAGCTTCCACAGCTGATGGACCAGGTGTACTGCTG[T/A]CCTCAGGCCATCGATGTGATCCAGGTAAGGAAGAAAACTATGGATCAATCTTTCAATTTCGTTCTATAATGAATCATTTAGTAACATTTTTTTTTTCTCATTTCTTCCTAGTTCTTTCACAGACATGTAGAGTTCACTGAACAGGTGCTTGGTGATAAGACAAAAGCACGGAGGATCACTTGCCAGATGAGCAATTTTCTGAAAGAGTAAGCATTTAGTTAAGCTGTTTAGTTTCATATTAATTTCTGAACATAATTTATAAATATATCTGTGGACAAAATCACTATAATCAACTCAATTTATGTCTATACAGTTACAGAGCTTTTCATGCTAAAGTCATTAAGAGCAAGCAGCCCAACACTGAAGTCGTTTTGATGGTCAACCTCTCATATCTTATACAGTGCAGGTACGTATCATCTACAGTTGAAGTGATAATTATTAGCCCCCTTGTTTATATTTTTCCCAGATTTCTGTTTAACGGAGAGAAGATTTTTGTCAAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa28061

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000080975	Essential Splice Site	519	613	9	11
ENSDART00000143326	Essential Splice Site	215	309	6	8

Genomic Location (Zv9):

Chromosome 13 (position 6782246)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	7118977
GRCz11	13	7451179

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGCCCTCTGCTTCAACAGTGAACGCATACATACTTTCCTCACTTCAGCT[G/A]TAAGTACTCACCAAAACAAGTGCATCAGACATGCCATGTATCATTAAAAT

Long Flanking Sequence:

TGACCTGTGAAATCACATCACATGACTTTGTGAGACCAATCAAAGATCAAAACATGACTTCTCTTTACAGAAACTTAAAATATAAACCAATCAATTGATTTTTTTTTTTTTTGTCTAATCATCTTGTTTATTCCCGCCCCTTCCCACAGCACTATATGACAGAGTTTTGCAAGCTCAAACTCTAGTGTGACTGCGGCACTAGTCAGACAAAAGATGACTTATGTGCTAATAATAATAGATAATAATAATAATATAATAAATGATAATAATAGCTCCATTTTATAGTGATTGTTTGGTTGACTGATTGATTAGTTGGTTGATTTGTTTGCTTGTTTGATGATTAGGAGCTGCTGGGTCGGATACATAAGGAGTTTCTAGCTGAATATATACGGAAAATGATGAAGCAAAAGATCAAACTTTCCAATAAAGAACAGCAACAGTTGGCAGCATCAGCCCTCTGCTTCAACAGTGAACGCATACATACTTTCCTCACTTCAGCT[G/A]TAAGTACTCACCAAAACAAGTGCATCAGACATGCCATGTATCATTAAAATAACAGTTTAGCATTCATACATTACAGAAATATTGACCTAATAAACAAATATGTCGGTTACATCATGACATTATTCTAATGCTTTATTTCCAGGGTTCAAACATGGACTGGTTGAAAGACATTCTTCCCAAGTTAGCCGGACTGCTGAAACTTCAGGATCCAGACAGTGTGAAGTTAGAGCTGGTGAATCTGATGAGAGCTTACCCTGACCTCAGGTATGTCAGGTTCTGGTGTGCCACTGTAACAAACATATGTGTTAATTAACAGTATCTGTTTTGTGTTATTCACTAGGTGATTTTATGTTGGATTATGGGAAACTTATCTCTTTTTTCTCAACTTTTAATGTAAACAATTCTACTTCACAGTATAACAAAGGGCTTTTTATTGACATTTTGCTACTTTGTATTATATTATGTATAAAAAATTATATATACACTGTAAAAACATCCTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa1956

Status:

F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

A > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000080975	Essential Splice Site	520	613	10	11
ENSDART00000143326	Essential Splice Site	216	309	7	8

Genomic Location (Zv9):

Chromosome 13 (position 6782105)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	7119118
GRCz11	13	7451320

KASP Assay ID:

554-1944.1 (used for ordering genotyping assays)

KASP Sequence:

TAAACAAATATGTCGGTTACATCATGACATTATTCTAATGCTTTATTTCC[A/G]GGGTTCAAACATGGACTGGTTGAAAGACWTTCTTCCCAAGTTAGCCGGAC

Long Flanking Sequence:

TCCCACAGCACTATATGACAGAGTTTTGCAAGCTCAAACTCTAGTGTGACTGCGGCACTAGTCAGACAAAAGATGACTTATGTGCTAATAATAATAGATAATAATAATAATATAATAAATGATAATAATAGCTCCATTTTATAGTGATTGTTTGGTTGACTGATTGATTAGTTGGTTGATTTGTTTGCTTGTTTGATGATTAGGAGCTGCTGGGTCGGATACATAAGGAGTTTCTAGCTGAATATATACGGAAAATGATGAAGCAAAAGATCAAACTTTCCAATAAAGAACAGCAACAGTTGGCAGCATCAGCCCTCTGCTTCAACAGTGAACGCATACATACTTTCCTCACTTCAGCTGTAAGTACTCACCAAAACAAGTGCATCAGACATGCCATGTATCATTAAAATAACAGTTTAGCATTCATACATTACAGAAATATTGACCTAATAAACAAATATGTCGGTTACATCATGACATTATTCTAATGCTTTATTTCC[A/G]GGGTTCAAACATGGACTGGTTGAAAGACATTCTTCCCAAGTTAGCCGGACTGCTGAAACTTCAGGATCCAGACAGTGTGAAGTTAGAGCTGGTGAATCTGATGAGAGCTTACCCTGACCTCAGGTATGTCAGGTTCTGGTGTGCCACTGTAACAAACATATGTGTTAATTAACAGTATCTGTTTTGTGTTATTCACTAGGTGATTTTATGTTGGATTATGGGAAACTTATCTCTTTTTTCTCAACTTTTAATGTAAACAATTCTACTTCACAGTATAACAAAGGGCTTTTTATTGACATTTTGCTACTTTGTATTATATTATGTATAAAAAATTATATATACACTGTAAAAACATCCTGGTTGCCTTTAACTTTTACCCTGAATCAAATTTACCTTATGAGTCCATTGAACTTATATGATGTTAAACTTACTTGAAACAGCTTGCGCAACATACAAAATTAAGCTATAACATGATTAACTTAGTTTACTAAGTTACAATG

Associated Phenotype:

Not determined