ZMP

zgc:92429

Ensembl ID:

ENSDARG00000030176

ZFIN ID:

ZDB-GENE-040801-194

Description:

hypothetical protein LOC445063 [Source:RefSeq peptide;Acc:NP_001003457]

Human Orthologue:

ITGB1BP2

Human Description:

integrin beta 1 binding protein (melusin) 2 [Source:HGNC Symbol;Acc:6154]

Mouse Orthologue:

Itgb1bp2

Mouse Description:

integrin beta 1 binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:1353420]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa30630	Nonsense	Mutation detected in F1 DNA	Not yet available
sa20919	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa30630

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000048050	Nonsense	233	387	9	11
ENSDART00000145186	Nonsense	233	281	9	10

The following transcripts of ENSDARG00000030176 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 7 (position 24898386)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	23460138
GRCz11	7	23731295

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TATTTGGTCTGTAGGATAAAAAGAAGGTGGCCTGTCGACATGATTGGCAT[C/T]AGACTGGAAGCCAGGTTGTTGTCACGATCTACGCCAAAAACTGCAATCCA

Long Flanking Sequence:

TGATCTGAGCATCCCCCGGAGAAACGTTAGTATTTCGATCGATGATTTGCTTCTTTACTAGTAGGCTGGGCTTTTTTCGCCATATTGACTGTTACAATTTTCCCTGTTGAGTGACATGTCTTATGTGTTTTATATAGTCTTTGTATTAGTCTAGTGTAAAAGTCTTGTAATAACCCCCAGTAGTAGTTTTTTTTTTTTTTTTTTTCCAATGAATGCATGTTAATTCTCATCTGCTGCTCACTTTTTAGATACAAATACTGGAACTGCTGCTGTATAAAAACCACCGACTTTAACGCCTTCCTGGACCAGAAGGGCTGTACATCTGGAAAGCATTGCTGGATCCCCAAACAGGTGCTCATGGACTTCACACTGTTGTTGTTTACGTGGGCACACATTGTATAATCAGCAAACGCCCCACTGGTCCTCTCTGAGAAATGTGCATGTTGTGTTTATTTGGTCTGTAGGATAAAAAGAAGGTGGCCTGTCGACATGATTGGCAT[C/T]AGACTGGAAGCCAGGTTGTTGTCACGATCTACGCCAAAAACTGCAATCCAGATCATTCCTATGTGGAGGCCAACCGCACTGTGGTAAGTTCAAAACTTCGGATGTTCGATTTGCACATCAGCGTCCTGTCAGATTCTTCATGCAGTGCTCTGTGTCTGTTTTTGTGTTCTCCGTCAATCTGCAGTTAACCTGCCACATTCAGTTCGAAGGCGACAAAGTGTTCCATAAGGACATCCACTTATGGGGGGTAAGACTGCTGTGCATTCATCACTCCTTAGGATTTAGCAGTGACCAACAGTTGAGGTCAGAATTATTAGCCCCCCTGTATATTTTCCCCCAATTTTTGTTTAATGTAAGGAAGATTTTTTTTGAACGTAATAGTTTTATAACTAATTTCTAATAACTGATTTGTTTTATCTTTGACATGATGACCACAGAATATTTTACTATATATTTTTCAAGATACTATTTAGCTCAAACTGCAGTTTAAAGATGTAACT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa20919

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:

G > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000048050	Essential Splice Site	281	387	10	11
ENSDART00000145186	None	281	281	10	10

The following transcripts of ENSDARG00000030176 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 7 (position 24898138)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	23459890
GRCz11	7	23731047

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTCAGTTCGAAGGCGACAAAGTGTTCCATAAGGACATCCACTTATGGGGG[G/T]TAAGACTGCTGTGCATTCATCACTCCTTAGGATTTAGCAGTGACCAACAG

Long Flanking Sequence:

ATACAAATACTGGAACTGCTGCTGTATAAAAACCACCGACTTTAACGCCTTCCTGGACCAGAAGGGCTGTACATCTGGAAAGCATTGCTGGATCCCCAAACAGGTGCTCATGGACTTCACACTGTTGTTGTTTACGTGGGCACACATTGTATAATCAGCAAACGCCCCACTGGTCCTCTCTGAGAAATGTGCATGTTGTGTTTATTTGGTCTGTAGGATAAAAAGAAGGTGGCCTGTCGACATGATTGGCATCAGACTGGAAGCCAGGTTGTTGTCACGATCTACGCCAAAAACTGCAATCCAGATCATTCCTATGTGGAGGCCAACCGCACTGTGGTAAGTTCAAAACTTCGGATGTTCGATTTGCACATCAGCGTCCTGTCAGATTCTTCATGCAGTGCTCTGTGTCTGTTTTTGTGTTCTCCGTCAATCTGCAGTTAACCTGCCACATTCAGTTCGAAGGCGACAAAGTGTTCCATAAGGACATCCACTTATGGGGG[G/T]TAAGACTGCTGTGCATTCATCACTCCTTAGGATTTAGCAGTGACCAACAGTTGAGGTCAGAATTATTAGCCCCCCTGTATATTTTCCCCCAATTTTTGTTTAATGTAAGGAAGATTTTTTTTGAACGTAATAGTTTTATAACTAATTTCTAATAACTGATTTGTTTTATCTTTGACATGATGACCACAGAATATTTTACTATATATTTTTCAAGATACTATTTAGCTCAAACTGCAGTTTAAAGATGTAACTGCATTAATTAGGTTAACTAAAATAATAAGGCAAGTCATTGTACAATGATGGTATGTTCTGTAGACTGTTGAAAAAATATATATTGCTGAAGGAGGCTAATATTCACCTTAAAATGCTTTAAAAAAAAATAAAAACTGCTTTTATTCTAGCTGAAATAAAACAAATAAGACTTTCTCCAAAAGAAGAAATATTATCAGACCTACTGTGAAAATTCCCTGTCTCTGTTAAATATTATTTTGGAAACATTA

Associated Phenotype:

Not determined