ZMP

insrb

Ensembl ID:

ENSDARG00000071524

ZFIN ID:

ZDB-GENE-020503-4

Description:

insulin receptor b [Source:RefSeq peptide;Acc:NP_001116701]

Human Orthologue:

INSR

Human Description:

insulin receptor [Source:HGNC Symbol;Acc:6091]

Mouse Orthologue:

Insr

Mouse Description:

insulin receptor Gene [Source:MGI Symbol;Acc:MGI:96575]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa16909	Nonsense	Available for shipment	Available now
sa32383	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa16909

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
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Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000105823	Nonsense	310	1348	3	21

Genomic Location (Zv9):

Chromosome 22 (position 11063496)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	10923664
GRCz11	22	10953346

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GCATACGTCATCCACAAYGGGGCCTGCATCCCAGAATGCCCRTCCGGATA[C/A]ACCACCGTCAACTCCACCTCGTACGTATCAATTTTCTCCTCAACAAAATA

Long Flanking Sequence:

GTAAACCTAGAATGGATTTAGAAACAGATATGCTAATGCTTGAACCTGCAAGTGGACAGAGCACATCATCCTACCCGAGTGTACAACACACAATGAAGAGTGCGGGAGACGTAACTCTAAGACGTATTTACATTGTTCGCCTGTATTATTCTGCCTATTTCATTGACAATCTAACAATATTTCCTTTTTTTTCCTTCAGTTTGTCCTTCTGAATGTGTCCACGGAGCCTGTACGTCCCATAAGGAGTGCTGTCACGAGCAGTGTCTGGGTGGCTGCTCTGTGCCGGGGAACTCCACCAAATGCGTGGCCTGCCGCAACTTCCTGTACGGCGAGGCGTGCGTGGACCGCTGTCCGCCAGGATACTACACCTTTAAGAGCTGGCGCTGCGTGTCCCTTCAGTTCTGCCAGGACCTGCACAACCAGTGTAAGGACAAGAGCGGAGACTGTCACGCATACGTCATCCACAACGGGGCCTGCATCCCAGAATGCCCGTCCGGATA[C/A]ACCACCGTCAACTCCACCTCGTACGTATCAATTTTCTCCTCAACAAAATAAAGAAATGCCATTTTTCATGTGTAACAGAGGCCAGCTAGTGAAGTGCTATACAGGTAACCCTCACTCCTCTGAGATCTAAAGGTGCTCTAGCATAAGATGCTAGAGGTCATGGTCTTTAGCCCTACTTGTCAGAGCAACCGACTCCCATGCAAAGAATTGCCGGTTCGATCTTAGCTCAGACCGGGTTGGGTACAGTAGGACCGGTGGGTTAAATTTAAGGGCTCGTCCGGGATGGGAGTGAGGTTTAGGGGGTTAGTGTAACAGAGGCCAGCTAGCGAGTTTCTATGCAGGTAAACCTCACTCTTCTGAGATCTAAAGGTGCTCTAGCCTCAAGTGCTAGAGGTCATGGTCTTTAGCCTTCTTGTTAGAGCAACCGACTACCATGCAAAGAATTGCCGGTTTGATCCTAACTCAGACCGGGATGGGTACAGTAGGACTGGTGGGTTAGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa32383

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
ENSDART00000105823	Nonsense	858	1348	12	21

Genomic Location (Zv9):

Chromosome 22 (position 11041591)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	10901759
GRCz11	22	10931441

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TACATCAGATGGAAAGAGCCCAAAACTCCTAACGGCATGATCATACTGTA[T/A]GAAGTCAAGTATCTACGGATGTCTGATAACTACGTAAGTGTTATAAATTA

Long Flanking Sequence:

TGGAGGACTATCAGCACTGCAAGTTTTAGATGTCTCCTTTGTCTGTCACACCCGTTACAGATCTTTAAGCCTCTGCTCAAATGATCTGAATCTGGTGTATTTGGGTAAGGAGACATGGAAGATGTGCAGAGCTGGTGGTCCTCCAGGAACGAGGTTGAGAAACACTGCTTTAGATCATTGTATCCCAACCCTGTTCCTGGAGGCATACCAACAGAAGATTTTTGGATGTCTCCCTTATCTAATCATTAACTTCAGGATTCAGCTGTTTGATTATGGGGAGGTTGAAAATGTTGTGTTGGTGTGCCTTCAGGAGCAGGGTTGAGAAACACTGCTTTAGATTATAGAAAGGTATTGGAATGTATTGAGTTTCCACTTGTTTTCATAGTGAAAGCTGATGTCATTGCCGAGCCAGTGACTCACGAATTTTTTCCTGACGAGCCGGATGTTGTTTACATCAGATGGAAAGAGCCCAAAACTCCTAACGGCATGATCATACTGTA[T/A]GAAGTCAAGTATCTACGGATGTCTGATAACTACGTAAGTGTTATAAATTATGGTGTGTATGTATATGCCATAGACATAAAAATGTCTACCTGCTGTAATGTTTTTAAATGTTTTTGGTCTCTCAGGAGGATCAAATCTGCGTGTCCAGAATTTCCTATGAGAAAAACCATGGCTATCGATTAAGAGTAGGGCATCCTGGGAATTACAGTGTGCGAGTTCGTGCCACCTCGCTGGCTGGCAATGGTTCTTGGACTGATCCTGCATACTTTTATGTTCAAGACAGTAAGCTTTACTTTATGTACTATACCTTTTTTCTGAATTTAGCAGCACTTCTGTCTCTAACAAACATGTTTTGCAGGGGAAATGAGCATGAAAATCGTTATCATCCTAGCCATCTGCATTTTCTTACTGGTGATTCTGGCCAGCGTAGGCTACTTTGTCTTGAAGAAGAAGTAAGTTTAAGACATTAAATCAAGCCCTTATTCATCGCATAAACAGTG

Associated Phenotype:

Not determined