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  Domain Name: IG_like
Immunoglobulin like. IG domains that cannot be classified into one of IGv1, IGc1, IGc2, IG.
No pairwise interactions found for the domain IG_like

Total Mutations Found: 770
Total Disease Mutations Found: 215
This domain occurred 377 times on human genes (952 proteins).



  ACHONDROPLASIA
  AGAMMAGLOBULINEMIA 6
  AND CATARACTS
  ANTLEY-BIXLER SYNDROME WITHOUT GENI
  ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STE
  ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS,
  AORTIC ANEURYSM, FAMILIAL THORACIC 7 (AAT7)
  BLOOD GROUP--LUTHERAN NULL
  BLOOD GROUP--OK
  CARDIOMYOPATHY, DILATED, 1CC
  CARDIOMYOPATHY, DILATED, 1G
  CARDIOMYOPATHY, DILATED, 1KK
  CARDIOMYOPATHY, DILATED, 1MM
  CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 22, INCLUDED
  CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4
  CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4, INCLUDED;;
  CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 4
  CD64 DEFICIENCY, FAMILIAL
  CD8 DEFICIENCY, FAMILIAL
  CHARCOT-MARIE-TOOTH DISEASE, TYPE 1B
  CHARCOT-MARIE-TOOTH DISEASE, TYPE 1B, INCLUDED
  CHARCOT-MARIE-TOOTH DISEASE, TYPE 1B, WITH FOCALLY FOLDED MYELIN SHEATHS
  CHARCOT-MARIE-TOOTH DISEASE, TYPE 2I
  CHARCOT-MARIE-TOOTH DISEASE, TYPE 2J
  COLORECTAL CANCER, SOMATIC
  CONGENITAL SHORT BOWEL SYNDROME
  CRANIOSYNOSTOSIS, NONCLASSIFIABLE AUTOSOMAL DOMINANT, INCLUDED;;
  CRANIOSYNOSTOSIS, NONSYNDROMIC UNICORONAL
  CROUZON SYNDROME
  CROUZON SYNDROME, INCLUDED
  CYSTIC FIBROSIS,
  DEAFNESS, AUTOSOMAL DOMINANT 4B
  DEJERINE-SOTTAS SYNDROME, AUTOSOMAL DOMINANT
  ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1
  ESOPHAGEAL CARCINOMA, SOMATIC
  GASTRIC CANCER, SOMATIC, INCLUDED
  GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS
  HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION,
  HYDROCEPHALUS DUE TO STENOSIS OF THE AQUEDUCT OF SYLVIUS (HSAS)
  HYPOCHONDROPLASIA
  HYPOCHONDROPLASIA, INCLUDED
  HYPOGONADOTROPIC HYPOGONADISM 2 WITH ANOSMIA, SUSCEPTIBILITY TO
  HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA, SUSCEPTIBILITY
  HYPOGONADOTROPIC HYPOGONADISM 2 WITHOUT ANOSMIA, SUSCEPTIBILITY TO
  HYPOTHYROIDISM, CENTRAL, AND TESTICULAR ENLARGEMENT
  IGG RECEPTOR I, PHAGOCYTIC, FAMILIAL DEFICIENCY OF
  INCLUDED
  JACKSON-WEISS SYNDROME
  JACKSON-WEISS SYNDROME, INCLUDED
  JACKSON-WEISS SYNDROME, INCLUDED;;
  LEFT VENTRICULAR NONCOMPACTION 10, I
  LETHAL CONGENITAL CONTRACTURE SYNDROME 4
  LUPUS NEPHRITIS, SUSCEPTIBILITY TO
  MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A
  MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2B, REMITTING,
  MENTAL RETARDATION, APHASIA, SHUFFLING GAIT, AND ADDUCTED THUMBS SYNDROME (MASA)
  NARCOLEPSY 7
  NEPHROTIC SYNDROME 1 (NPHS1)
  NEPHROTIC SYNDROME, TYPE 1
  NEUROPATHY, CONGENITAL HYPOMYELINATING, AUTOSOMAL DOMINANT
  OSTEOGLOPHONIC DYSPLASIA
  OVARIAN CANCER, SOMATIC
  PFEIFFER SYNDROME
  PFEIFFER SYNDROME, INCLUDED
  PFEIFFER SYNDROME, INCLUDED;;
  PFEIFFER SYNDROME, TYPE III
  PSEUDOMONAS AERUGINOSA, SUSCEPTIBILITY TO CHRONIC INFECTION BY, IN
  RADIN BLOOD GROUP ANTIGEN
  ROBINOW SYNDROME, AUTOSOMAL RECESSIVE
  ROUSSY-LEVY SYNDROME
  SCAPHOCEPHALY AND AXENFELD-RIEGER AN
  SCIANNA BLOOD GROUP SYSTEM, SC:-1,2
  SCIANNA BLOOD GROUP SYSTEM, STAR ANTIGEN
  SPONDYLOEPIMETAPHYSEAL DYSPLASIA AGGRECAN TYPE (SEMD-ACAN)
  THREE M SYNDROME 2
  TO
  TRIGONOCEPHALY 1
  UROFACIAL SYNDROME 2
  VARIANT OF UNKNOWN SIGNIFICANCE
  WITH MENTAL RETARDATION
  WITH OR WITHOUT MENTAL RETARDATION


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Range on the Protein:  

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