ZMP

immt

Ensembl ID:

ENSDARG00000057454

ZFIN ID:

ZDB-GENE-030131-5417

Description:

mitochondrial inner membrane protein [Source:RefSeq peptide;Acc:NP_001001401]

Human Orthologue:

IMMT

Human Description:

inner membrane protein, mitochondrial [Source:HGNC Symbol;Acc:6047]

Mouse Orthologue:

Immt

Mouse Description:

inner membrane protein, mitochondrial Gene [Source:MGI Symbol;Acc:MGI:1923864]

Alleles

There are 5 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa22456	Essential Splice Site	Available for shipment	Available now
sa42380	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa38989	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa35678	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa22456

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000080120	Essential Splice Site	188	757	5	14

Genomic Location (Zv9):

Chromosome 14 (position 20032529)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	15797264
GRCz11	14	16102827

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCCCGCACCAGGTACAAGTGATGAAAGCCCATCTGGCCACTCGGCGGCAG[G/A]TCAGCATTGGATCATTCACAGTCTTCTGCTTATGACAACTGATCCACAGC

Long Flanking Sequence:

ATGTCATGTTGTCCTTGCGAATCACATTGCATTCTTGCCATTTCCAAATCTCCTCCCGTGGCCTAATGGGTAAAGTAAAGGGAGTAAAGTGTCCATTAAATGCACATTTAGAAACAGGTCATCCAAGTACTTTTCTCCTTTGATTTTGTATAAATTTGGAAATACCACTCATTACATTCTGAAATGTATGTAATTGGATATATTCATACACAGGGTGGTCATTTGAGTTTTTAAGCAGATACACGCACACACACAGTAACTGAATGTCTAACTTTATCTTAAGTCTACATATGCAAATGATCAAAGGATCACATGTCAGCAGATGTTGGATAACTGTCATTCACATCTGCTGAGCCGTGAACTTAATTTCTGATCAGGTCCTGTTGTTGTTACAGAAGCCTCAGCAGAGGCGGCTCATATTATTTCGGCTATCAGCGAAGTGCCCTCTGTGCCCGCACCAGGTACAAGTGATGAAAGCCCATCTGGCCACTCGGCGGCAG[G/A]TCAGCATTGGATCATTCACAGTCTTCTGCTTATGACAACTGATCCACAGCCTGAAAGATCAGTTAATAGGCAGAAGCACAGTGTCTCGTTTTCTCTGCATGTTCTCAAACATCACACCTTCTGGTTCATTTCCAACCATCTGCACGGTTCTGTCCTGTGACCCATGCTAACAGTTTCTGTTCATTGTAACTGTGTCCCATATCAGAGGTTGCATCCTTAAAGTAATGGTACTCTCAAAAATGATTATTATTCCATAACTTACTTGCTCTCAAGACATCCTCTGTGTAAATGACTTGCATTTGTCAGAAGGACACAGAGTAGTTTTAATAGTTTTTCCTGTGATCTTTCATGCTCTGTAATGGTGTTGGGCAGTGGCCCTTTTACGCTTGCCTTGACCCAACTTCTACTCTAAATTGTGTGTTGATGCTCATGTTGCAAATAGGCTGAATTATGATAGAAAAGGTAAGTCAACAGTTTGTTGTTTTGGCCTTAAGATGCAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42380

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:

G > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000080120	Essential Splice Site	273	757	8	14

Genomic Location (Zv9):

Chromosome 14 (position 20040740)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	15805475
GRCz11	14	16111038

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGTGTGTGTGTGCGTGCGTGTGTGCATGTGTGTGTGCATGTGTGTGCCCA[G/T]ACTCCTCCAGATGAGAAGTCCACTCAGGCACTGAATGAGGCTCTGAACGA

Long Flanking Sequence:

ATCCTGCTTTTACAGGGCTACTTGCCACAAAATTAAAAAAATTAGACACAAAACATTGTTCTGATGTGTAATAGTTTATTATTTATCAATTAAATGCAAAGCTGACAGAAAAAAAATATATCTGTAGCACAAACTAACCTATGTATTATTCAGTCATAAGATGGCCCCAAACCATCTAGTCAAAAACATCAAAATGACAGACAATATATATAAATCTGGATCTAAATGTATTCACTGGGGGTCAAGATGATTCAAAGTACCAGATTGAGAATGCGTTATTAGTGTTAATGGTTGTTGTCTGGGAATAACATACCTTGGAATGTTGTTACTGACCAATCAGAATCAAGTGTTTTAGAGAGCACTGTGATAACATTTTATGACATTAAATGTCAAATGTAGCTAGACTATTTTCTGCTGGGTTTAACATGGTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGCGTGTGTGCATGTGTGTGTGCATGTGTGTGCCCA[G/T]ACTCCTCCAGATGAGAAGTCCACTCAGGCACTGAATGAGGCTCTGAACGAGAGGGCCAGAGCTGTGGACGATGCTGGAGAAGCCCTGTTCAAAGCCAAGTGAGATCTGCTTCTGATATCTTTAATTACAATTTCAGTACTTTGACCAAAGGGTGGACAATAGGAACAAAGCCTTATCATACTATGTTGCACATGGTAAATAGACAGGCAAATGTGTCTATCAGTATTGTGCAAGCTACTTGAAAAATGTAGTGAGATTAGCTACTCTTCTCAAAATGTAGCTGAAATACACTAAAAGCTACTCTATTGAAAATGTAGCTAAGCTAAAAGCTATTTGGCAAAAGTAGATTAGCACCATCTAAGCTATTTTATTGCAATAAAAAATACATCTAAGCTATTTTTGCAATTTTCATTTTTAAACTGAAGCAACTTGAATCCAAGGCTTCGTTCACACTGCAAGGCTTAGTGCTCAAATCAGATTTTTTTCGCATGGCTGTTTAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa38989

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
ENSDART00000080120	Essential Splice Site	394	757	10	14

Genomic Location (Zv9):

Chromosome 14 (position 20044730)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	15809465
GRCz11	14	16115028

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAGCTTGCCAACATCACACCTGAGATCCAGGCCAACTGGAAAGGACTATG[T/A]AAGATATCACACTCTTTACATGGATTCAAGTTCTCTACATTTTATATTAA

Long Flanking Sequence:

TGTAAATATGTACACTTGGTATTTCACAAATTACACTCAATTTTTTTTCATCTCTATATATATTTAGAGGAGAGCTTGAAAAGCTGCGTAGTGTGATCGACAAAGCAAAACAATCCAAGATTGATTCGGCGAGACCGCAGATCCTGGCCGCTGAGGAGAACTTGCACAGCATGATTGTGGATCTGGACAAAGTTGTAACCAAGGTAAGTATTGTAAACATCACAACATAAATGTGCTCTGAAGAAACCCCCTGTTCATATTAATGAGATTTGTGCCTGTAATCTATTTAACTTTATGCTCTCAGTGACTATTAGTGCATCCCATCTGGATGTGTAACTCAATCCTAGGTGTTGTCTGTCTCCTGCGCAGGTGCAGACGGCACAGTCCGAGGCCAAGATCGTGTCTCAGTACAGTGAGCTGGTAAATGAAGCTAAAGCTCAGTTCCAGCAGGAGCTTGCCAACATCACACCTGAGATCCAGGCCAACTGGAAAGGACTATG[T/A]AAGATATCACACTCTTTACATGGATTCAAGTTCTCTACATTTTATATTAATAAAAGCTGATGATGGTTTATTAAAGTGATGTAAAGGGGATTACATGTTTTTCTCAGCGGGAAAGCTGAGCGCAGATGATCTGAACTCTCTGATTGCTCATGCCCACCGGCGCATCGACCAGCTAAACCGAGAGCTGGCAGAGCAGCGCGTGAGGGAGCAGATCCACATTGAAGTGGCTCTAGAGCAGCAGAAGCTGGAGGATCAGAAAGCGCAGGAGAGAGCCGTGATTTCTGCTCTGGAGCACAGCCGAGAGGACATGAGACTCGAGCAGGAAAAAAAGGTCTGGTATTCACTGCTGTACTGTTATGCAAAGTATTAAATCGCTAAATAATGAATATGTTTTTTAAGAAAGTCACATTTAGAATGATGTGTTAATATTCTCTGTAGCATCAGTAAGGTAGGGTCTGAATGGGTCATAAAATGAATTTTCCAAAATGTTTTTTTTTTTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35678

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000080120	Nonsense	561	757	14	14

Genomic Location (Zv9):

Chromosome 14 (position 20052194)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	15816929
GRCz11	14	16122492

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATTTTTCACATATCAAATATTTGTTTTGTCTTCAAGGTCATGTGATTGCT[G/T]AGGAAGAGGCTCGTAAAGCTCACCAGCTGTGGCTTTCGGTTGAAGCTCTA

Long Flanking Sequence:

ATGATTCGAAATGATCTGATTCTGCAGCAGAAAATTTACCTTGCAGCTTTTTTAGAAAATTACCTGTAGATGGCGCTACTTTTTACTTTTCTCTATTATTTGTTTAAGTTGCACTTCTGTGGCTTTGGGTTCAGTGTCTGTCCAAACTATTTTTGTACTTTTATTACTAAAAAGTTTGAACAAGGGTTAAATTAAGCTGCGCAAACATTAAACTTTGCTGTGGTCTAGACTGGACATAATCTGTTAACTTTGTTATACTAGAATTACTAAAACTACATGTATCAGAACTAAACAGAAAATGTGTTCCCATGAACAAATCTAAATTAAAACAAAAAAACCTGCTAAATGAAATTTAAAGCAATTTTTAATATATTATTGAATTAAAAACAAACTAAAAATGCTGACCTAAAAAACCTTGATCTCGATGTGACTTGACTGATGTTGTTTCTCATTTTTCACATATCAAATATTTGTTTTGTCTTCAAGGTCATGTGATTGCT[G/T]AGGAAGAGGCTCGTAAAGCTCACCAGCTGTGGCTTTCGGTTGAAGCTCTAAACTACACGCTGAAATCTGCAGGTGCTGATTCCCCCACTGAGCCTCTAGAGGGCGCTGTACGTGCTATTAAAGAAAGCTGCGCAGAAAACGAATTTGCACAGGCACTGGCCATCGCCATTCCTGAAGAGTCCCTCAACCGAGGAATCTACAGTGAAGCTTCCCTTCGCGCACGTTTCTACGACATCCGCAGGCTCGCACGACGTGTGGCGCTTATCGACGAAACCCGCAACAGCCTTTACCAGTACTTCCTGTCCTACCTACAGTCCGTCCTTTTGTTTGAGAGGGATCAAGAAGCGCCACCTGCGAAACTAGCCCCTGAAGATCTTGACACATTCAAGCTGCTAGCCTACGCTACTTACAGCATCGAGCGCGGCGACCTGGAACTAGCCGCTAAGTTCGTCAACCAACTTCGCGGAGAGTCACAGCGCGTGGCGCAGGACTGGCTCAAA

Associated Phenotype:

Not determined