ZMP

LOC566587

Ensembl ID:

ENSDARG00000086098

Human Orthologue:

ERRFI1

Human Description:

ERBB receptor feedback inhibitor 1 [Source:HGNC Symbol;Acc:18185]

Mouse Orthologue:

Errfi1

Mouse Description:

ERBB receptor feedback inhibitor 1 Gene [Source:MGI Symbol;Acc:MGI:1921405]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa43961	Nonsense	Mutation detected in F1 DNA	Not yet available
sa39405	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa43961

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
ENSDART00000127628	Nonsense	42	365	3	4

Genomic Location (Zv9):

Chromosome 23 (position 21129472)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	20914016
GRCz11	23	20840359

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGTTTTTTAGATTTGGTTCGGAGTCCATGGATCACAGCTTGAGAATGTAT[C/T]AGCAGAACTCTGCGAATGTGGGCTTTGAAAGTGAGTGAGTGCTTGATATT

Long Flanking Sequence:

TTCTTTACAATTTTAATATGAGAGGGACAGTGAAACATTTAACTGAGCTTTTAACTTGACCAAAATGGTTACATTAATTTTAACAATATCTGACCATTTGAGAAAAATGGCTCTATTTAACATTGTTGAACATTGTCAATATATTTCATTGATTTTTTTTTTCCACACAGGGTTTCTCATTGCCATTATAAAAGTGAAGTATTAAAGTCCTGTCTTGCTTGCCCATGGCTGGATAATGAGTTGTGCTGGTTCGGGAAGGTGGAGACCCCCTCAGGCCTAAACAAACCTCCACTCTCTCTCCAACAGTATGGCCTCAGCCCAAGCGTACTGGGATCAACACCATGACCATGACACCATGGATAAGTGAGTGTGAATGCAGTCTGTATTATAGACCATCTGTTGCTCCGGTCAACCGGTTTTGACACATTCCATTTTGTCTTTTTTTCAGGCTGTTTTTTAGATTTGGTTCGGAGTCCATGGATCACAGCTTGAGAATGTAT[C/T]AGCAGAACTCTGCGAATGTGGGCTTTGAAAGTGAGTGAGTGCTTGATATTGAATTAAATCAGCTCTATTGCAATCTGGTCACCCTCTGTTCTATGAGCTTGTTGCGGATGTTTCTCAGGAAGCGCAGAAGGTTATAGGAAGTTGGTTGTATGATTGTCTGATAAGTGAATCCTTTGATAAAGTCCCTATGTTGAGGCTGAAACTGTATCAGGAGAAAGAGCCATTGAAAATAACACTTACATTAGGTTGACGACTCTGTTAAATGTTTAGATCACAGGTTTTCTATCTTTTAGCTTAAATTTGATCAACCTTGAGGATTTTTAGTGGGCAGCTGTAGAAATTCTTAGTTTCTCTGGGTTTATTAGATGTATGTTTGAGTAAAAGGCTTATATTTGCTTTATTTTATAAAGTTCTGATAATGCTCCTTATTTTTAAAATACAAATATTGTCATTTAGAGCATTTTTATGTTTCTTAAGAAGTTAAAACATTTAAAACATAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39405

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
ENSDART00000127628	Nonsense	313	365	4	4

Genomic Location (Zv9):

Chromosome 23 (position 21131747)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	20916291
GRCz11	23	20842634

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCCTCCTACTCAGAGCTTTGCTCCCTATCCGGAGTATGTCAGTAAGGCT[C/T]AACACAAGCAGATCTGTCAAGGCTTGCCTTCTCCTCGTAGTCCCTGTATT

Long Flanking Sequence:

AAACCTCATCCTTCCAGTATGGCCTGCCAGGAAGACGCAGTTTTCGGGGAAGTGGTCAGATAAATTTTGCATATTACGAAGGCCTACAGGAACATCAGAAGCTATGCGGGATGAAGCCCCAATGGGAGCAGGCGGTAACGGAGAACCAACAACGACCACAACGCCGACTTCATCGCTCCAATTCTGGCCCTGCTGGATGCTTTAAAGCTGCCAATTTCGAATTGACCAGCCTTCACCATTCTCATCCTGCTTACTCGCAGGAAAAGCCCGAAATCCCACCTCGAGTTCCAATCCGTCCTTGTCTCAGTGAAAGCACAGACCTCAGGAGAACATCAACTGATGACTTTGATGCAGACAAACCTCCCAAAGTGCCTCCTAGAGAGCCCATTCCTCAGGTCATCCCTCGTGCTATTAGTCCCAAAAGTCTACCAATTTATGTCAACGGCGTGATGCCTCCTACTCAGAGCTTTGCTCCCTATCCGGAGTATGTCAGTAAGGCT[C/T]AACACAAGCAGATCTGTCAAGGCTTGCCTTCTCCTCGTAGTCCCTGTATTTTACCCATTATTGAAGATGGAAAGAAAGTGAGCAGTACCCATTACTTCCTGCTCCCTCATCGGCCTGGCTACTTGGACAAGTTTGAGAGGTTTTTCAGAGAGTCAGACTCATAGTGTTTTAAAGTCTGAAGTTGTTTGCTTGAGCAAAATAAGAGAGAGAAAAAAAAAAAGGCAGGATATAAAGTGTTGTTTGACTGAACTGATTCTCCAGTGTTATGAATTACTGTTGTGTTTAGGGAATGGACATGATGTCCTCAGAGAAGAACTGGTTTACCGCTGCTTGAATATGCAGGATCACTCTGTCAGAAGTATCCTTTGTTTGTTAGGGCTGCATGAGTGTTCCTAATGAAACAAAAATTGTGAATATAAAACCTCAGCAAAAGAGAAGCTTTAAGGTCTCTTTGTAGTTTTTTACCTTAAAAGCTAGATGGTTTATTATTTGAAAATGAA

Associated Phenotype:

Not determined