ZMP

tgfbi

Ensembl ID:

ENSDARG00000071586

ZFIN ID:

ZDB-GENE-030131-73

Description:

transforming growth factor-beta-induced protein ig-h3 [Source:RefSeq peptide;Acc:NP_878282]

Human Orthologue:

TGFBI

Human Description:

transforming growth factor, beta-induced, 68kDa [Source:HGNC Symbol;Acc:11771]

Mouse Orthologue:

Tgfbi

Mouse Description:

transforming growth factor, beta induced Gene [Source:MGI Symbol;Acc:MGI:99959]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa42397	Nonsense	Mutation detected in F1 DNA	Not yet available
sa39002	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa22487	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa42397

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
ENSDART00000105933	Nonsense	443	677	10	17
ENSDART00000128463	Nonsense	456	690	10	17

Genomic Location (Zv9):

Chromosome 14 (position 27529521)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	26222318
GRCz11	14	26520423

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTGCTGAGAAACCACATTCTCAAGGAGAAGTTTTCCTCCAAGAGCCTTTA[T/A]CATGGGCAGGAGTTGGAGACCCTTGGTGGACTGAAACTTAGAGTGTTTGT

Long Flanking Sequence:

GATGCCATTCATACAATTTGCAATTGCCACCACCAGATTTAAACGAAGTTTGATTTTTGAAGGCTATTTTAGAATCAATGTCATACTATTTTTTTCACTAATTAACAATTCATTTTCTTTAACTTGAAGGTACTTGTTTGAATTTACTCTTGAACCACGTTGTATTCAGCCCTTTCTTGTTTGTTTGTTTTTAGCCAAAACCCTGCTTGAGCTTGCAGAGGGATCTGTTGTTACTACAGCTGCAAAGCTTTTTAAAGATGCTGGTCTTAATGATCACCTGGTCGGCTCTGAGTCTGTGACCTTATTAGCCCCCCTCAACGAGGCTTTTAAAGGTTGGATCACTCAATGTTCTTTAATCTAGCAGTTGAGCCTTACGAAACTCTGTATTAACTCTAATTGTATCATTTGTGTGCAGACAAGAGCTTTGCTATGACTCCTGACATGAAAAAACTGCTGAGAAACCACATTCTCAAGGAGAAGTTTTCCTCCAAGAGCCTTTA[T/A]CATGGGCAGGAGTTGGAGACCCTTGGTGGACTGAAACTTAGAGTGTTTGTGTTCAGAAATGTAAGTGTGGGAATATGCGGATTGGATGGATTTAAAAGAAACCCAAATTGCTGCTATTTTTAAATGAAACATTGATATGTATTGATGCTGATAAAAATGTCCAGTAGAACAGTCATTTTGATGACAGTGGTTAAGGAAATAAATCCCTCTTGACCAGCGCTTGAATTATAACCCAGTTACCAATCCATCAAACACACATAAGAGCCTTTTTTTCCAGCCATGTTGTAGCTGGCAGTGAGGATGGTATAGTTCTGTCTGCACGCTCACATTTCTGCTTTGTAATGGATTTCACAGACCACCGGAAACCTCTCCTTTGGATCACCTTAACGTTTTCCACAGCTCACTTCATGCATCATTATCGTCTTGTGAGAAAAAGAGAGCTTTGAAACGAAAGCGCTGATCTGTATAACCACTAACCTTAACCGTTTCACTTGCTTGGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39002

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000105933	Essential Splice Site	553	677	12	17
ENSDART00000128463	Essential Splice Site	566	690	12	17

Genomic Location (Zv9):

Chromosome 14 (position 27524379)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	26217176
GRCz11	14	26515281

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AACGCTGCTTTCAGTGCATTGCCGTCCGCTGACCTCAACAAACTCATGAG[T/A]AATGTCTCACCTTGTCAGTCAGTCAGAAAAGCAGACGTTTAGTGCATGAT

Long Flanking Sequence:

CTGCTAAAGCCAATTCAAAGTGATAAACTATAAACTACATAACAAAAAGGTTTTAACCTCACACTGATTTACCCAATTTTCCATATAAAAACCTAGAAGAAGAAAAAGTTCCAGCAGAAAGGGTGTAATTGTTTTCACAGTCTTGTTGAAAGAAAATACACAGCTGCTGTTTCTCACCAACATTTACAGGCTTCAGTGTCAATCTCTAAAGCTTTTTCCTAATGATCGTGTTCAAACTTGAGACCGTAATTTCCTCCGATTTCAGATGACCTTTTGAAATGTGCAGTTTGAGCTGTCAGTTTAATTGTCTTTTATAGCCTAAAGATATGTTCCTAATAATGTGCACTAATGAGCTTTCATCTGTGCAGCACTTTGGTTGGCGCCATTCAAAAAGCTGGCTTGACGGAGCTCCTGAATAAAAAAGGAACCTACACCTTCTTCGCACCAACCAACGCTGCTTTCAGTGCATTGCCGTCCGCTGACCTCAACAAACTCATGAG[T/A]AATGTCTCACCTTGTCAGTCAGTCAGAAAAGCAGACGTTTAGTGCATGATTACATATATTCTGGTCAGATTTACTTAAGTGGATGTGCAGCATATTCAACACTTATTGTGACCTTGGATCGCAAAATAAGTGTCTATTTAGGGAAATGAAATGTAATCTGAAAGCTGTATAAATAATCTTTCCATCGATTGGCAATATTTGGTCAAAATACAAATAACCTATTTTAACTAATATTTAAATAATCGAAAAGTTGAGAAAATTGCTTTTAAAGTTCTCCAGATAGAGTACTTAGCAGTGCACACTACTAAACAAAAATTAAGTTATAATGTGTTTACTAGAGATGTCCTGATAAGGGTTTTTTTGCCCCCGAGTCTGAGTCATTTGATTTTGAGTATCTGCCGATACGGAAATCCAATCCGATACTTCTGTAATACGTTAATAAAAATATAGAAGAGTAAAGAAACAAATCCAATATGTTCCTTATTTTTATTTAATTCACG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa22487

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
ENSDART00000105933	Essential Splice Site	628	677	14	17
ENSDART00000128463	Essential Splice Site	641	690	14	17

Genomic Location (Zv9):

Chromosome 14 (position 27522010)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	26214807
GRCz11	14	26512912

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGCTACCAATGGAGTTGTGCACGCTGTTAATGTCATCATCAAGCCACTGC[G/A]TAAGCCAAGGATTCCTTAAACACTGTGATAAAAGAACTATATTGTTTTAA

Long Flanking Sequence:

ATAGCTGAATAAACCAATATTGAAAATACTGACCTTAAACATTTGAATTTTACTGTACATTTATTTCTTTAACAAAAATCTAAAATGATTTAATTACTGTCATGTTAGTTCAAAATATATACTCTAAGAATATATAGTATTACTGTAAATCAATTTGAAAGTGTTTTTGTTTATTTAGTTTATTTTGTGATCTTTTGTCACTAAATATACAATCACACACAATTGAATAATTACATTATTGAACATTTATTTTAAAAATTTCAATAACTTAGAATAACTAAAACAAGAAATAGAATAACTATAATAAAATATGAAGCAATATATATTTAAAAATAAAATATTCCCTACATTTAATAACTCTTTTTGTTCATTCAGTTTTTTTCTTTTTTCTTTTCAGCGTAACTCAACCATATATGTGAACCGTGTGCCTGTGGTGGAGTCTGATCTGATGGCTACCAATGGAGTTGTGCACGCTGTTAATGTCATCATCAAGCCACTGC[G/A]TAAGCCAAGGATTCCTTAAACACTGTGATAAAAGAACTATATTGTTTTAACAGTTCATAACAGCGATGTGTCCATCTGTTTTAGCTCCTAAAATTGTGAGTGACCAGGCCGAAGGCTCAACAATCAGACGCACATCTGCTGTCAGGGTTAGTATATACAATAAACCAATTTTCCAGTACTTTTACTTGTTTATGAATTGTCGTTGTGCCTCTAACTTATTTATAAATGATAAAGAAAAATGTTTATATTGGGTTTTTATTTTTTGTTCTAGGCTGGGTCTCAAGTATCCAAAAATGGTAAGTAATGTTGGCTAACTTCACTTTTCTCACATCAATGCAGTTATTAGTCTCATCTGTACTTTTGTGATGATACTGAAATACAGCATCATTGAGTACACCCCATTTTGAAAACGAATATTTTTATCCATTTAGAGATATTTATTAAAGTCATGCTTTAGTCACCAAACATATTTAGAAATTAAAAGCTAGTCAAATTAAATT

Associated Phenotype:

Not determined