ZMP

itgbl1

Ensembl ID:

ENSDARG00000040985

ZFIN ID:

ZDB-GENE-050522-410

Description:

integrin beta-like protein 1 [Source:RefSeq peptide;Acc:NP_001019243]

Human Orthologue:

ITGBL1

Human Description:

integrin, beta-like 1 (with EGF-like repeat domains) [Source:HGNC Symbol;Acc:6164]

Mouse Orthologue:

Itgbl1

Mouse Description:

integrin, beta-like 1 Gene [Source:MGI Symbol;Acc:MGI:2443439]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa41453	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa41454	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa41453

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000060054	Essential Splice Site	31	406	1	8
ENSDART00000139584	None	None	186	None	5

Genomic Location (Zv9):

Chromosome 9 (position 32786160)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	31942106
GRCz11	9	31752852

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTTCATCTTGCTCTCTGCCATTCGAGGAAGTTTACAGCAGTCGCTAAGG[T/G]GAGTTTAAGCTGTGTTGTTTTCTTAAACCAATTTGGCTTTTCCACTCTAT

Long Flanking Sequence:

TTGAAATACTCTTTTACAAATTATTTAATAATCATCTGCATCTTATCAATATTTCCTGTTCTACGTCCATATAATTATAACCCCTTTTAAAGTTACAAAACTTTTTTCTTAGCCAGCTGTGAGAGAGGAGAAAAGGACACCAATGCTAAGATACAGAAAGCTAAACCTTCAATCATCTGTATGAACAACTGTTTTGAATTATAGTGACCAAGTTTTCTTTTCTGGCACTTTATCTCTTACTGCTGCCTTTGTACAGAGAGTCCCCGCTAATCAAAGGCATTCATATGGAGTGCGCTGTTGGCCTCTGAAACGTCGGAGCTAGATTTGGCCAGCCCGTTCTCCCTCTGTTTTGGAAAGTGGAAATTCCTGAAGGCACTTCACTTCAGGTTTCTGGTGGGGATCTAAACATGCATGCAGAGACTTTGGTGAACTCCGTCTTAGTTTCTTTGCTTTTCATCTTGCTCTCTGCCATTCGAGGAAGTTTACAGCAGTCGCTAAGG[T/G]GAGTTTAAGCTGTGTTGTTTTCTTAAACCAATTTGGCTTTTCCACTCTATAACCACATTTTGCTGACAGACTGGATTTGCAGTCACAGCTAAAGAACTAGTTCAAGGCTTGTAGGCTTATATTTAAACTATTCCGTTTTTCCACCTATTTAGCTATGGTTGCAGCAATGTTTTAGTTGTCTTACTTGGTGCTTCAAGTCAGATTTTACAGTACATAATACAGCAGCATAAACTTAAAAAAAAGAAAAGTGATGTTTTTTTTCTTGTTATGGTTTTTGATTTTGAAATTGCATGATTGTTATTTTGCACAAATAACTTAAGCAGTTTAAACATAGCAGGTGCACACTGACCATTATACAAGCATGTGCGTACCATAATGCATGTTTACTGTATGCTCACATTGCGCTGCACATAATCAAAGACAGAGACCGCAATCAGAAAGTTAAAATGCTTTTGTGGCTGACAAAACTTTTCCATGTAAGTATACAGTAACCATACCAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa41454

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000060054	Essential Splice Site	148	406	3	8
ENSDART00000139584	None	None	186	None	5

Genomic Location (Zv9):

Chromosome 9 (position 32815753)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	31971699
GRCz11	9	31782445

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGCAAAGACCTCTGCCGCAATGCTCAGGGTGTAGTTTGCTCCAATGCAGG[T/C]AAGATACACATCACCCAGAGACTTATAGTGTTGAGAAAGGCATACAGTAT

Long Flanking Sequence:

GAATTAATGTGTGATATGATTAAACAGTGTTCATACATTTCTAATAGATCATGGGGAACAATTTTTCATAAATAGTAAGCTATTTTTTTTTTTAATCAGAAGGAAATAACATCTTTCACCACATGTGTGAAACTCCTCTCACTACTAAGCATTGATGTCACCCTGTCCTTCACCTCTCTCCAAACACCTCTCAAATGTGCTACTAATCGCAAAATCTATCTCATAGTTAGCTCTTTGGCCCCTGTCATTCCTTATCAACCCATTTACCTTTACATCATGGGTCTGTTCCATGACCGCATGTTACTCAAAACAATCAATATCTCAATCAATCCTGTTTGTGTTTCCACTGCAGATCATGGGATATGCAACTGTGGCAAGTGTTTCTGTGATGAAAACTGGTTTGGTGAATCCTGTCAGTACGAGGAGGAGTGTTCGCTCTCCAGCAAAACCAGCAAAGACCTCTGCCGCAATGCTCAGGGTGTAGTTTGCTCCAATGCAGG[T/C]AAGATACACATCACCCAGAGACTTATAGTGTTGAGAAAGGCATACAGTATACAGAGCTCTGCACAAATAATTGCACCCGTAAATATAAAAATGGTCTTGAGCTTCACAAATTAGGACGTGGTTGTAAGAAAATAAAACAAAACAACAAAATTGGCCACACTGTAAAACATTATTGCTGACAACCAAAGGAACTTTTATAGTCATCTGAACTGACATCAATTACACTGAATAAAATGTTAGGTTAAACTTTGTAAAACTAAACAAAGTCAGTTGAAATCTGATTAACTGATTATTGGTTAAAGTAATATAAAAACATGTTTCCATGGCTTTTTGTCATATCATTTTTCATGGTGCATATTAACCATTAAGGCAATAACATAAATTTCAGCATCACTTTCTATGAAGCCCATGCTCACAATGTATTATACTTTTATTTCTAATTATTTATAATGAAGCATAACAATCATATAAATGTATCATATACAGTATAAAGAGATACA

Associated Phenotype:

Not determined